Fractional amplitude of low-frequency fluctuations associated with μ-opioid and dopamine receptor distributions in the central nervous system after high-intensity exercise bouts

Introduction: Dopaminergic, opiod and endocannabinoid neurotransmission are thought to play an important role in the neurobiology of acute exercise and, in particular, in mediating positive affective responses and reward processes. Recent evidence indicates that changes in fractional amplitude of low-frequency fluctuations (zfALFF) in resting-state functional MRI (rs-fMRI) may reflect changes in specific neurotransmitter systems as tested by means of spatial correlation analyses.

Methods: Here, we investigated this relationship at different exercise intensities in twenty young healthy trained athletes performing low-intensity (LIIE), high-intensity (HIIE) interval exercises, and a control condition on three separate days. Positive And Negative Affect Schedule (PANAS) scores and rs-fMRI were acquired before and after each of the three experimental conditions. Respective zfALFF changes were analyzed using repeated measures ANOVAs. We examined the spatial correspondence of changes in zfALFF before and after training with the available neurotransmitter maps across all voxels and additionally, hypothesis-driven, for neurotransmitter maps implicated in the neurobiology of exercise (dopaminergic, opiodic and endocannabinoid) in specific brain networks associated with “reward” and “emotion.”

Results: Elevated PANAS Positive Affect was observed after LIIE and HIIE but not after the control condition. HIIE compared to the control condition resulted in differential zfALFF decreases in precuneus, temporo-occipital, midcingulate and frontal regions, thalamus, and cerebellum, whereas differential zfALFF increases were identified in hypothalamus, pituitary, and periaqueductal gray. The spatial alteration patterns in zfALFF during HIIE were positively associated with dopaminergic and μ-opioidergic receptor distributions within the ‘reward' network.

Discussion: These findings provide new insight into the neurobiology of exercise supporting the importance of reward-related neurotransmission at least during high-intensity physical activity.

Highlights

• Positive mood changes, indexed as elevated PANAS Positive Affect, were identified after high- and low-intensity exercise bouts, supporting previous accounts on mood-improving effects of physical activity.

• High-intensity exercise was found to be associated with distributed changes in fractional amplitude of low-frequency fluctuations, indicating enduring neural activity changes after anaerobic exercise bouts.

• Results of spatial cross-correlations with representative PET neurotransmitter distribution maps suggest involvement of dopaminergic and opioidergic neurotransmission at least after high-intensity exercise, with weak evidence for the endocannabinoid system.

• Utilizing spatial cross-correlations of changes in fractional amplitude of low-frequency fluctuations and representative PET neurotransmitter distribution maps, despite being an indirect metric, provides an innovative methodological framework for human exercise research, as it allows for non-invasive testing of acute exercise-related changes of multiple neurotransmitter.

Introduction

Physical activity is considered one of the most efficient mood-regulating behaviors (Thayer et al., 1994). Much work has been undertaken to unravel the underlying mechanisms of affective changes triggered by physical activity in animal models and in a growing number of human studies (Basso and Suzuki, 2017). Various studies show that moderate exercise regimens induce acute improvements of positive affect, especially immediately after exercise (Reed and Ones, 2006). Moreover, there is some evidence that acute exercise can exert motivational effects (Bothe et al., 2013), including phenomena of transient appetite suppression or altered reactivity to food cues (Dorling et al., 2018; Dera et al., 2023; Thackray et al., 2023).

Meanwhile, the underlying changes in regional brain activity remain understudied. Considering cerebral blood flow (CBF) as a frequently-used proxy for brain activity, human evidence mainly comes from transcranial doppler sonography or near infrared spectroscopy studies. They suggest transient increases in perfusion which may plateau or return to baseline, depending on duration and intensity of exercise bouts, among other factors (Mulser and Moreau, 2023). But these methods provide no (or limited) information about region-specific effects, and there are theoretical accounts which assume that resource limitations may also necessitate temporary downregulation of brain metabolism in certain brain regions (e.g., the reticular-activating hypofrontality model: Dietrich and Audiffren, 2011). Indeed, preliminary evidence from magnetic resonance imaging (MRI) studies using arterial spin labeling (ASL) indicates post-exercise CBF increases in young adults for the hippocampus (Steventon et al., 2020) or posterior insula, but also concomitant CBF decreases in the medial orbitofrontal cortex and dorsal striatum (Thackray et al., 2023). Indirect evidence for region-specific activity changes also comes from resting-state functional MRI (rs-fMRI) studies. Using blood oxygenation-dependent (BOLD) fMRI, most studies examined post-exercise changes in functional connectivity (FC), i.e., the spatiotemporal coherence of spontaneous brain activity fluctuations between different brain areas which are interpreted to reflect integrated functional brain networks (Won et al., 2021): This includes exercise-related increases of FC in sensorimotor networks (Rajab et al., 2014), or affect-reward, hippocampal, cingulo-opercular, and executive control networks (Steventon et al., 2017), but also contrary findings of FC reductions (Alfini et al., 2020). Exercise intensity may also play a moderating role (Won et al., 2021), as suggested by studies observing differential pattern of FC increases and decreases in specific rs-fMRI networks after low- or high-intensity exercise bouts (Schmitt et al., 2019, 2020). Still, rs-fMRI can provide additional brain activity-related markers, including the amplitude of low-frequency fluctuations (ALFF). It represents the voxel-level magnitude of regional BOLD fluctuations in the low-frequency range (0.01–0.08 Hz) which is assumed to be proportional to neural activity (Zang et al., 2007). Fractional ALFF (fALFF) is a normalized index of ALFF which is considered to be less sensitive to physiological noise (Zou et al., 2008). Previous data showed a close association with underlying metabolic activity (Aiello et al., 2015), making it a possible proxy for changes in regional brain activity. While one recent study (Zhang et al., 2022) examined the cross-sectional relationship between fALFF measures and cardiorespiratory fitness measures in trained athletes, studies investigating brain activity responses to acute exercise by means of fALFF are lacking.

Neurotransmitters and neuromodulators are thought to play a crucial role in mediating the mood-regulating effects of exercise, and changes in affective homeostasis, anxiety, and depression have been commonly associated with monoamine (Guszkowska, 2004), endorphin (Boecker et al., 2008), and endocannabinoid (Matei et al., 2023) neurotransmission. In addition, the motivation to exercise and to overcome physical boundaries and pain, as is particularly the case for strenuous high-intensity and/or long-duration exercise regimens, has been particularly linked to the mesolimbic dopamine reward circuit (Knab and Lightfoot, 2010; Lewis et al., 2021). As yet, most of the current knowledge on exercise-induced central neurotransmission has accumulated in animal studies (Basso and Suzuki, 2017) using either ex vivo brain tissue assays with high-performance liquid chromatography/mass spectrometry (Hattori et al., 1994; Gamelin et al., 2016), Western blot and immunofluorescence (Galdino et al., 2014), and autoradiography (Robison et al., 2018); or in vivo sampling with microdialysis (Hattori et al., 1994; Meeusen and DeMeirleir, 1995; Meeusen et al., 2001). In humans, while there is some evidence for peripheral increases of transmitters (or their metabolites) during and after exercise (Goldfarb and Jamurtas, 1997; Marques et al., 2021; Desai et al., 2022), their correlation with central neurotransmission changes is unclear, and only very few in-vivo studies used selective pharmacological manipulations to clarify the roles of dopaminergic (Watson et al., 2005; Roelands et al., 2008; Meeusen, 2010; Roelands and Meeusen, 2010; Klass et al., 2012), opioidergic (Allen et al., 1983; Crombie et al., 2018), and endocannabinoid (Crombie et al., 2018) neurotransmission, especially regarding their mediating role in exercise-induced affect modulation and reward-related behavior. Functional neuroimaging with positron emission tomography (PET) holds unique potential for localizing and quantifying exercise-induced neurotransmission in vivo after acute training sessions, or long-term changes in receptor distribution after repetitive training (Boecker et al., 2012; Boecker and Drzezga, 2016). PET ligand displacement studies allow in vivo monitoring of endogenous transmitter trafficking at the human whole-brain level after acute exercise bouts and, thereby, to identify the link between exercise-induced behavioral measures and endogenous neurotransmission (Boecker et al., 2008). Previous human PET studies reported endogenous dopaminergic (Ouchi et al., 2001; Sacheli et al., 2018; Ando et al., 2024) and opioidergic (Boecker et al., 2008; Hiura et al., 2017; Saanijoki et al., 2018a) transmitter release following exercise challenges, with [11C]Carfentanil PET data indicating that aerobic exercise modulates anticipatory reward processing via the μ-opioid receptor system (Saanijoki et al., 2018b), and 6-O-(2-[(18)F]fluoroethyl)-6-O-desmethyldiprenorphine ([18F]DPN) PET data showing correlations between running-induced opioid release in prefrontal and limbic/paralimbic brain structures and subjective euphoria ratings (Boecker et al., 2008). While exercise increases circulating endocannabinoid levels in humans in an intensity-dependent manner (Raichlen et al., 2013; Desai et al., 2022), to the best of our knowledge, no PET tracer studies on endocannabinoid neurotransmission changes due to acute or long-term exercise challenges were published so far.

It is important to point out that despite the genuine interest in PET displacement studies during exercise challenges, studies are hampered by limited availability, cost, and radiation exposure (Boecker et al., 2008, 2012; Boecker and Drzezga, 2016). The latter aspect is the main limiting factor preventing a comprehensive analysis of the effects of exercise on several transmitter systems at the same time. Indeed, within-subject designs are largely limited to one or maximally two neurotransmitter systems due to radiation exposure limitations, especially in healthy young subjects. Recent rs-fMRI studies have shown that spatial fALFF patterns are associated with the distribution of specific receptor systems targeted by respective PET and SPECT compounds (Dukart et al., 2021) and that this approach cannot only be used to make inferences about the status of various neurotransmitter systems (e.g., in neurological disorders), but also to detect acute changes in neurotransmission in relation to pharmacological challenges. In an extension of this latter rationale, the current study intended to investigate how varying intensities of acute exercise affect fALFF changes in brain regions linked to representative PET and SPECT neurotransmitter maps (Dukart et al., 2021; Hansen et al., 2022), thereby providing indirect markers for their involvement in acute exercise. Following up on previous work suggesting intensity-dependent effects on rs-fMRI measures (Schmitt et al., 2019, 2020), the current study examined fALFF map changes as means to investigate associated neurotransmitter effects in trained male athletes after performing a control, low-intensity (LIIE), and high-intensity (HIIE) interval exercise session. Complementing a traditional voxel-wise analysis to identify individual brain regions showing exercise-related differences in brain activity (as indicated by fALFF), we tested the spatial correlation between the observed changes across regions and the distribution of neurotransmitter systems to make inferences about the exercise-induced activation of the latter. We hypothesized specific involvement of dopaminergic, μ-opioidergic, and endocannabinoid neurotransmission, in particular for the high-intensity condition (Hiura et al., 2017; Saanijoki et al., 2018a), although a possible inverse U-curve relationship was suggested for the endocannabinoid system (i.e., changes only appearing after moderate, not heavy exercise challenges: Raichlen et al., 2013). Similar curvilinear associations were discussed for mood changes (Reed and Ones, 2006): Accordingly, increases in positive mood were already anticipated for the LIIE condition (see also Schmitt et al., 2019), while it remained open whether further increase (or even decrease) would be observed in the HIIE condition. Meanwhile, we also examined potential relationships with other neurotransmitter systems provided by the JuSpace toolbox (Dukart et al., 2021) in an exploratory manner. Considering previous human exercise studies which indicated exercise-induced effects in reward- (Bothe et al., 2013; Saanijoki et al., 2018b) and affect- (Boecker et al., 2008; Maurer et al., 2022) related brain networks, we also performed separate analyses focusing on those regions which overlap with meta-analytically defined “emotion” and “reward” networks.

Methods

General study design

This study, referred to as BEACON (“Bicycling Effects on Affect and COgnition in Neuroscience”), was conceptualized as a within-subject design to investigate the acute effects of exercise bouts of differing exercise intensities on brain functional networks as well as affect and cognition (Figure 1). Some of the reported measures will also be included in other manuscripts derived from this study with different research questions.

Figure 1

Figure 1. General study design (Created with Biorender.com).

All participants were informed about the study protocol, examinations, potential discomforts, risks and a written informed consent was obtained. Ethical approval was given by Ethics Committee at the Medical Faculty of the Rheinische Friedrich-Wilhelms-Universität Bonn (Nr. 358/19), conferring to national legislation and the Declaration of Helsinki.

Each participant completed three distinct intervention conditions—aerobic cycling (low intensity; LIIE), anaerobic cycling (high intensity; HIIE), and rest (control) condition—in a randomized order (further information below). The interventions were allowed to take place within a maximum of 8 weeks and at least 7 days apart. The night before the test, the subjects were instructed to obtain enough sleep, refrain from drinking alcohol for the preceding 24 h, and hold off on caffeine 2 h before the test. Additionally, subjects were told not to exercise 24 h beforehand. To prevent measurement differences owing to anxiety on the first exam day, subjects experienced a mock scanner session before the actual MRI. Other than that, the processes were carried out in a uniform manner on each examination day. First, subjects completed general and mood-related questionnaires as well as cognitive tests [a condensed version of the Attention Network Test (ANT) (Weaver et al., 2013) and Mnemonic Similarity Task (MST) (Stark et al., 2019) were gathered, but were not subject of the current analyses]. Then, rs-fMRI was acquired. Subsequently, one of the three interventions was performed. After the intervention, mood questionnaires, cognitive tests as well as fMRI were repeated in the same order as pre-intervention.

Participants

Well-trained right-handed male athletes aged between 20–35 years were recruited via flier distribution at local cycling and triathlon clubs as well as the university hospital and social media. Subject enrollment was restricted to male participants in order to minimize variance due to hormonal fluctuations during the menstrual cycle. Individuals with current and/or previous severe psychiatric, neurologic or cardiovascular diseases in addition to the typical MRI-specific exclusion criteria i.e., claustrophobia, non-removable metal/implants, tattoos exceeding a critical size or other prohibiting reasons were excluded. Additionally, in order to ensure a high fitness level of participants, individuals with a relative maximum oxygen uptake (relVO_2max) below 55 ml/min/kg were excluded (De Pauw et al., 2013).

Experimental procedures

Preparation phase

General screening

Selection was performed prior to the study phase: It included the recording of sociodemographic characteristics, a sports medical examination and performance diagnostics. A sociodemographic questionnaire and vocabulary test were administered to obtain descriptive characteristics such as age, educational level, and estimated verbal intelligence. The International Physical Activity Questionnaire (IPAQ) (Booth, 2000) was carried out to assess the physical activities of participants in everyday life. Edinburgh-Handedness-Inventory (Oldfield, 1971) was used to assess handedness. Further, participants were screened for psychiatric symptoms using several questionnaires such as the Mini International Neuropsychiatric Interview (Sheehan et al., 1998), the Beck Depression Inventory (BDI) (Hautzinger et al., 1994), and the trait anxiety of the State-Trait-Anxiety Inventory (STAI) (Spielberger, 1983). Moreover, a substance abuse questionnaire excluded possible substance use disorders.

The medical sports examination included an anamnestic questionnaire, lung and cardiac auscultation, and a 12-lead resting ECG. Where necessary, an additional transthoracic echocardiogram was carried out.

Performance diagnostics

Performance diagnostics, which included a maximal incremental step test on a cycling ergometer (Cyclus2, RBM Elektronik-Automation GmbH, Leipzig, Germany), were carried out to ascertain physical fitness and, consequently, individual training intensities. The Cyclus2 made it possible to mount each participant's own bike, guaranteeing that each subject would cycle in the same unique position throughout the study. The initial workload for the incremental step test was 100 Watts (W), followed by 20 W increases every 3 min at a cadence of 80 revolutions per min (rpm) until volitional exhaustion. Power was digitally controlled with direct drive throughout the performance diagnostics and the ensuing exercise modifications. When the cadence dropped to < 65 rpm, the test was stopped.

Throughout the test, measurements of oxygen uptake (VO₂), the metabolic respiratory quotient (RER), heart rate (HR) (Cortex meta-analyzer 3B, Leipzig, Germany, and Polar Electro Oy, Kempele, Finland), and the electrocardiogram (ECG) (Cardio 100 USB, Ergoline GmbH, Bitz, Germany) were continually recorded. A validated H10 chest strap was used to continually measure HR variability. Additionally, blood pressure was checked at each step. The final 15 seconds of each procedure were used to draw 20 μl of capillary blood from the earlobe, mix it immediately with 1 mL hemolysis solution, and analyze the sample amperometrically and enzymatically using an EBIOplus system (EKF Diagnostic Sales, Magdeburg, Germany). Within the last 15 seconds of each increment, the rating of perceived exertion (RPE) was measured using the Borg scale (6 to 20 points: 6 - no exertion at all, 20 - maximal exertion) (Borg, 1998).

Exhaustion was considered when at least two of the following criteria were met: plateauing in VO₂, RER ≥ 1.05, high levels of blood lactate (≥8 mmol/L), a RPE of ≥18. The greatest 30-second moving average of VO₂ divided by body mass (mL/min/kg) was used to calculate relVO_2max. Those who had a relVO_2max of < 55 mL/min/kg were not included in the study.

Study phase

Intervention

Following the first MRI examination, volunteers completed the supervised intervention on a bicycle ergometer. Depending on the treatment condition, subjects performed one of the two alternative exercise intensities (low and high) or the control condition (without load) in randomized order. An adapted Latin Square was used for randomization: ABC, ACB, BCA, BAC, CBA, CAB; order of these combinations additionally randomized within blocks of 6 subjects. A 4^*4-min load was alternated with 3 min of active recovery during the exercise interventions. Individual exercise intensities were established using the incremental step test. In the exercise interventions, subjects began with a 10-min warm-up at 1,5 Watts per kilogram of body weight (W/kg BW) followed by interval training and a final cooldown of 5 min < 1,5 W/kg BW. The intervention intensities were established as follows: (i) LIIE: 4 ^* 4 minutes' load at 100% first rise (W) with 3 min active recovery at 90% of first rise; (ii) HIIE: 4 ^* 4 min' load at 110% D_max (W) with 3 min active recovery at 60% of D_max; and (iii) control: no load while sitting on the cycling ergometer for 43 min.

The modified D_max approach of Zwingmann et al. (2019) was used to calculate lactate thresholds. The first rise was defined as the moment at which the lactate concentration increased by >4% from the previous value. The last 30 seconds of each load and recovery period were used to measure blood lactate, HR_int (during the intervention), and RPE. Blood pressure was tested both before and after the treatment.

Physiological and psychological testing

Each study day began with the subjects filling out a special questionnaire that measured their current levels of exhaustion, discomfort, previous night's sleep quantity and quality, and recent caffeine and alcohol intake.

To account for physiological effects due to exhaustion, the corresponding MoodMeter (Kleinert, 2006; Wollseiffen et al., 2016) subscale (consisting of the items “feeble” and “drowsy” from psychological strain), was included in the statistical analyses as this may influence mood and fMRI outcomes.

The Positive And Negative Affect Schedule (PANAS) was one of the questionnaires used to gauge mood in general (Krohne et al., 1996), which served as the primary affect measure in the presented analysis. Participants had to rate their current mood state based on a total of 20 adjectives, 10 of which are assigned to the dimension of positive affect and 10 to the dimension of negative affect (scoring with 5-point Likert scale ranging from 1 “not at all” to 5 “very much”). This way, the questionnaire allowed for a separate dimensional assessment of pleasure and displeasure effects which are assumed to be partially dissociable on the brain system level (Norris et al., 2010), and may therefore show differential susceptibility to acute exercise. To examine potential anxiolytic effects of exercise more specifically, the STAI-State scale was also collected (Spielberger, 1983).

MRI acquisition

On each study day, participants completed two identical MR sessions. To account for potential influences of circadian rhythms on the behavioral/imaging data, measurements of each subject were always performed at the same time of the day, either from 08:00–11:00, 11:00–14:00, or 14:00–17:00. The respective MRI scans (in total six scans) were acquired on a Philips Ingenia Elition 3.0T scanner with a 32-channel head coil at the Parent-Child Center of the University Hospital Bonn.

A regular session consisted of a T1-weighted (T1w), a fieldmap and a rs-fMRI sequence. For rs-fMRI, the light in the examination room was switched off and participants were instructed to close their eyes, not to think of anything in particular, and to stay awake during the whole scan. An echo-planar imaging (EPI) protocol with blood-oxygen-level-dependent (BOLD) contrast and 3D acquisition was performed with the following specifications: TR = 1,020 ms, TE = 30 ms, acquired voxel size = 2.5 × 2.5 × 2.5 mm, reconstructed voxel size = 2.17 × 2.17 × 2.5 mm, FoV = 208 × 208 mm, flip angle = 52°, SENSE: 2, MB factor: 3, EPI factor: 41, matrix: 84 × 82, slices: 51, scan order: FH (ascending). Over a total duration of 10:04 min, 585 dynamic scans were acquired. The anatomical T1w sequences were acquired with the following specifications: TR = 10 ms, TE = 4.7 ms, acquired voxel size = 0.7 × 0.7 × 0.7 mm, reconstructed voxel size: 0.49 × 0.49 × 0.57 mm, FoV = 250 × 250 mm, flip angle = 8°. The total duration of this sequence was 6:19 min. Field mapping was performed with the following parameters: TR = 650 ms, TE = 7 ms, voxel size: 3.75 × 3.75 × 4 mm, flip angle 80°.

During all fMRI scans, HR was continuously recorded (HR_rest) by a pulsoxymetry sensor on the index finger.

Physiological and psychological data analysis

The analysis of the behavioral and the physiological data was performed using IBM SPSS (Statistics Version 27.0. IBM Corp. Armonk, NY).

Exercise intervention

To evaluate whether exercise intensity between the low and high condition differed significantly, paired t-tests with Bonferroni correction were performed for the variables HR_int, lactate concentration and RPE. Significance was considered at p < 0.05 and the effect size is reported as Cohen's d.

HR_rest and exhaustion

Values above or below the mean ± 2.5 standard deviations (SD) were removed from the data set as outliers for HR_rest. Statistical analysis of the outlier-corrected means of HR_rest and raw exhaustion scores was performed using a 2 (timepoint: pre/post) × 3 (condition: control, low, high) repeated measures ANOVA, separately. Post-hoc paired t-tests with Bonferroni correction were also performed. Significance was considered at p < 0.008 (0.05/6), and the effect size was reported as partial eta square and Cohen's d.

Mood questionnaires

A repeated measures 2 (timepoint: pre-intervention/post-intervention) × 3 (condition: control/low/high) ANOVA was performed to assess the changes in PANAS and STAI-State according to the conditions. Post-hoc paired t-tests with Bonferroni correction were also performed. Significance was considered at p < 0.008 (0.05/6), and the effect size was reported as partial eta square and Cohen's d.

MRI data analysis

Quality control and image preprocessing

Resting-state fMRI data underwent a well-recognized MRIQC (Esteban et al., 2017) pipeline for visual quality check regarding acquisition artifacts. No datasets with substantial quality issues were identified.

Resting-state fMRI data were pre-processed using the fmriprep pipeline (https://fmriprep.org/en/stable/) (Esteban et al., 2019). Preprocessing started with skull stripping the fMRI data using a custom fmriprep methodology. Furthermore, fieldmaps were used to correct for susceptibility distortions by applying the FSL 6.0 (Jenkinson et al., 2012) fugue (https://fsl.fmrib.ox.ac.uk/fsl/fslwiki/FUGUE) and SDCflows tools (Wang et al., 2017). The estimated susceptibility distortion was used to create a corrected BOLD EPI reference in order to accurately register the functional data to the anatomical reference. The BOLD EPI reference was registered to the T1-weighted reference using a boundary-based registration approach. Before spatiotemporal filtering, head motion parameters with respect to BOLD EPI reference were estimated using mcflirt (Jenkinson et al., 2002). A single composite transform was applied to the BOLD time-series to correct for head motion and susceptibility distortions, and resampled to their original native space. Thereafter, BOLD time series were normalized to standard MNI152NLin2009cAsym space (Fonov et al., 2011). A detailed description of the fmriprep pipeline can be found in the Supplementary material [“Detailed Description of the fMRIPrep Pipeline (Boilerplate)”].

After preprocessing, data quality was further determined on the basis of the fmriprep DVARS and framewise displacement (FD) metrices. Both DVARS and FD reflect the rate of change of the BOLD signal across the whole brain at each frame of data and the head movement of the specific frames, respectively. In the case of more than 60% of the 585 volumes with FD larger than 0.2 mm, subjects were removed from the final analysis (Parkes et al., 2018).

Then, output functional maps were used to calculate fALFF for all six sessions (pre- and post-intervention in each condition). The 3dRSFC function in AFNI (https://afni.nimh.nih.gov/pub/dist/doc/program_help/3dRSFC.html) was applied, including quadratic detrending, band-pass filtering (0.01–0.08 Hz), 4 mm smoothing and regressing out white matter and cerebrospinal fluid signal as well as the 24 motion parameter time courses in a single step (Taylor and Saad, 2013). Normalized fALFF (zfALFF) maps were created by dividing the map through its mean.

Voxel-wise analyses of zfALFF maps

In a basic analysis, we compared the zfALFF maps from the pre- and post sessions of the three conditions using a voxel-wise approach, performing a 2 (timepoint: pre/post) × 3 (condition: control, low, high) repeated measures analysis of variance (ANOVA) for whole brain in SPM12 (https://www.fil.ion.ucl.ac.uk/spm/software/spm12/).

To exclude a direct effect of HR_Rest and Exhaustion on the zfALFF, regression analyses were performed with the zfALFF maps within each condition (HIIE, LIIE, and control) for the post-pre changes. Masks were created by saving significant clusters found at a lenient threshold of p < 0.01 (uncorrected). These masks from each condition were merged to one mask indicating brain regions influences by HR_Rest and Exhaustion. Later, the merged mask was used for exclusive masking in the repeated measure ANOVA for zfALFF.

We applied a voxel-wise cluster-defining threshold of p < 0.001 (uncorrected) and reported significant clusters at p < 0.05 after implementing a cluster-wise extent threshold (≥k) for different contrasts using the family-wise error (FWE) method for multiple comparisons correction.

Associations between fALFF changes and PANAS

To examine possible associations between the observed intervention-related fALFF changes and corresponding affective changes, we performed follow-up regression analyses within those brain areas which showed significant fALFF effects in the ANOVA analyses, using the questionnaire pre-to-post difference scores as the independent variable, and the corresponding pre-to-post differences of fALFF scores as the dependent variable.

Spatial correlations of fALFF changes with neurotransmitter maps

The JuSpace toolbox (https://github.com/juryxy/JuSpace; version 1.4) was used to compute spatial cross-correlations between the zfALFF changes per exercise condition (within-subject pairwise zfALFF differences between the pre- and post-intervention fMRI scans; computing option 6 of the toolbox) and neurotransmitter maps.

First, we tested for spatial correlations of the zfALFF changes induced by either of the three conditions (LIIE, HIIE, or control) with different neurotransmitter systems using a whole brain approach, using 14 neurotransmitter maps included in the JuSpace toolbox. In case of multiple maps per neurotransmitter system, the ones with highest reliability based on sample size and/or signal-to-noise ratio were chosen. We included the following neurotransmitter maps: dopamine synthesis, storage and transport [Fluorodopa (García-Gómez et al., 2018); DAT (Dukart et al., 2018)] and receptors [D1 (Kaller et al., 2017); D2 (Sandiego et al., 2015; Hansen et al., 2022)], GABA (gamma-aminobutyric acid) receptor (Dukart et al., 2018), endocannabinoid receptor (CB1) (Laurikainen et al., 2019; Hansen et al., 2022), μ-opioidergic receptor (MOR) (Kantonen et al., 2020; Hansen et al., 2022), serotonin receptors [5-hydroxytryptamine (5-HT1a, 5-HT1b, and 5-HT2a)] and transporter (SERT) (Savli et al., 2012), noradrenaline transporter (NET) (Hesse et al., 2017), vesicular acetyl choline transporter (VAChT) (Aghourian et al., 2017; Hansen et al., 2022), and the metabotropic glutamate receptor type 5 (mGluR₅) (Smart et al., 2019; Hansen et al., 2022).

Second, we tested for spatial correlations of the zfALFF changes in those regions of the neurotransmitter maps which overlapped with a priori defined “reward” and “emotion” networks. For this hypothesis-driven approach, we focused on three pre-informed neurotransmitter systems (i.e., D2, Mu and CB1) already known to be involved in affect and reward modulation in general (Schott et al., 2008; Mechoulam and Parker, 2013; Kantonen et al., 2021), or in the exercise context more specifically (Boecker et al., 2008; Saanijoki et al., 2018b; Forteza et al., 2021; Gorrell et al., 2022; Kantonen et al., 2022). For these analyses, spatial correlations were restricted to brain regions within the neurotransmitter-specific maps which are also linked with emotion and reward processing, respectively, based on independent neuroscientific evidence: A “reward network” mask was created using a term-based meta-analysis of functional neuroimaging studies implemented in Neurosynth (https://neurosynth.org) including the ventral striatum, thalamus, cingulate, orbitofrontal cortex. An “emotion network” mask was applied in an identical manner as in our previous study (Schmitt et al., 2020) and included anterior/middle/posterior cingulate cortex, inferior/medial/middle/superior orbitofrontal cortex, dorsolateral prefrontal cortex, hypothalamus, insula, amygdala, nucleus accumbens, and pallidum. Both masks are displayed in the Supplementary Figure S1.

Spearman correlation coefficients were calculated between the single subject pairwise zfALFF difference maps and the respective neurotransmitter maps, after parcellation according to the Neuromorphometric atlas (Landman and Warfield, 2012). Exact permutation-based p-values (with 10.000 permutations) were computed for all comparisons to test for significance of the mean correlation coefficients observed across participants from the null distribution. Finally, we reported the spatial cross-correlations at p < 0.05, false discovery rate (FDR) corrected for multiple comparisons.

fALFF-neurotransmitters correlations with mood questionnaires

Finally, we used Spearman correlations to assess the relationships between the outputs of JuSpace (significant zfALFF-neurotransmitters correlation, Fisher's Z-transformed) and the PANAS and the STAI-State, respectively. Significant results were reported at p < 0.05 after correcting for multiple comparisons using Bonferroni correction.

Results

Demographic measures

Among twenty-nine recruited participants only twenty (age: 27.3 ± 3.55 years) were included in the present analyses. Reasons for exclusion were: injury during private exercise or illness (N = 4), failure to reach the specified VO_2max limit of 55 mL/min/kg (N = 3), and motion artifact in MRI (N = 2). An overview of demographic and physiological characteristics of the sample is provided in Table 1 and in other manuscripts from this work. According to the IPAQ, N = 19 subjects could be categorized as highly active and N = 1 as moderately active.

Table 1

Table 1. Demographic and physiological characteristics.

Physiological data

Results of the HR_int and HR_rest are also reported in other manuscripts from this study (in preparation/parallel submission) with different research questions. Since the intervention is a key component of the study, overlapping reporting is inevitable.

Exercise intervention

All included participants were able to train within the desired power output in the LIIE and the HIIE interventions. Statistical analysis revealed significant differences between the two exercise conditions. Values and statistics of HR_int (Supplementary Table S1), lactate concentration (Supplementary Table S2), RPE (Supplementary Table S3), and the actual power values during the intervention (Supplementary Table S4) are summarized in the Supplementary material.

Heart rate during fMRI (HR_rest)

The results of the repeated measures ANOVA following Greenhouse-Geisser method for sphericity correction showed a significant main effect of condition [F_{(2, 32.36)} = 6.80, p = 0.005, η² = 0.26], a main effect of time [F_{(1, 19)} = 7.02, p = 0.016, η² = 0.27], and a significant time × condition interaction [F_{(2, 26.06)} = 18.01, p < 0.001, η² = 0.49] for the variable HR_rest.

Post-hoc tests showed significantly increased HR_rest during the scan from pre to post HIIE [t₍₁₉₎ = 4.71, p < 0.001, d = 1. 054; high pre: 52.03 ± 6.64 bpm; high post: 58.99 ± 6.95 bpm] and a significantly decreased HR_rest from pre to post of the control condition [t₍₁₉₎ = −5.38, p < 0.001, d = −1.20; control pre: 52.49 ± 8.37 bpm; control post: 48.73 ± 9.01 bpm]. No significant HR_rest changes were detected from pre to post LIIE [t₍₁₉₎ = 1.65, p = 0.116, d = −0.37; low pre: 52.44 ± 7.71 bpm; low post: 54.76 ± 9.49 bpm]. Comparing the conditions with each other, significant results were found comparing the HIIE vs. the control condition [“high post minus pre” vs. “control post minus pre”; t₍₁₉₎ = 6.85, p < 0.001, d = 1.531; delta high: 6.96 ± 6.60 bpm; delta control: −3.75 ± 3.12 bpm] and comparing the LIIE vs. the control condition (“low post minus pre” vs. “control post minus pre”; t₍₁₉₎ = 4.50, p < 0.001, d = 1.01; delta low: 2.32 ± 6.30 bpm; delta control: −3.75 ± 3.12 bpm). Results were not significant comparing the HIIE vs. LIIE condition [“high post minus pre” vs. “low post minus pre”; t₍₁₉₎ = 2.01, p = 0.059, d = 0.45; delta high: 6.96 ± 6.60 bpm; delta low: 2.32 ± 6.30 bpm].

Exhaustion

Repeated measures ANOVA showed a significant main effect of time [F_{(1, 19)} = 4.61, p = 0.045, η² = 0.19], and main effect of condition [F_{(2, 38)} = 3.42, p = 0.043, η² = 0.153], but no significant time × condition interaction [F_{(2, 38)} = 1.05, p = 0.361, η² = 0.052] for the variable exhaustion. Post-hoc analysis revealed no significant effects after Bonferroni correction: HIIE condition [t₍₁₉₎ = 2.13, p = 0.046, d = 0.48; high pre: 1.65 ± 1.33; high post: 1.07 ± 1.02]; LIIE condition [t₍₁₉₎ = 1.453, p = 0.163, d = 0.32; low pre: 1.02 ± 1.21; low post: 0.62 ± 0.76]; control condition [t₍₁₉₎ = 0.322, p = 0.751, d = 0.072; control pre: 1.27 ± 1.22; control post: 1.20 ± 1.13].

Behavioral data

PANAS

A 2 × 3 repeated measures ANOVA for PANAS Positive Affect found significant main effects of condition [F_{(2, 38)} = 17.29, p < 0.001, η² = 0.48] and time [F_{(1, 19)} = 28.17, p < 0.001, η² = 0.60], as well as a time × condition interaction [F_{(2, 38)} = 17.08, p < 0.001, η² = 0.47]. Post hoc comparisons showed significant increases after HIIE [t₍₁₉₎ = 6.42, p < 0.001, Cohen's d = 1.43; high pre: 30.30 ± 6.67; high post: 38.20 ± 5.21] and after LIIE [t₍₁₉₎ = 5.67, p < 0.001, Cohen's d = 1.27; low pre: 31.25 ± 6.97; low post: 36.25 ± 6.76]. No significant differences were observed from pre to post control conditions. Comparing the conditions with each other, significant results were found when testing HIIE vs. the control condition [“high post minus pre” vs. “control post minus pre”; t₍₁₉₎ = 7.12, p < 0.001, Cohen's d = 1.59; delta high: 7.90 ± 5.50; delta control: −0.45 ± 5.73] and testing LIIE vs. the control condition [“low post minus pre” vs. “control post minus pre”; t₍₁₉₎ = 3.38, p = 0.003, Cohen's d = 0.756; delta low: 5.0 ± 3.95; delta control: −0.45 ± 5.73]. Testing HIIE vs. the LIIE condition showed no significant differences [“high post minus pre” vs. “low post minus pre”; t₍₁₉₎ = 1.89, p = 0.073, Cohen's d = 0.42; delta high: 7.90 ± 5.50; delta low: 5.0 ± 3.95] (see Figure 2A).

Figure 2

Figure 2. Representation of the PANAS (A) positive and (B) negative scales pre- and post conditions. Whiskers represent the standard deviation. *p < 0.008 (Bonferroni-corrected); **p < 0.001.

On the other hand, the 2 × 3 repeated measures ANOVA for the PANAS Negative Affect scale showed a significant main effect of time [F_{(1, 19)} = 9.68, p = 0.006, η² = 0.34] and a significant time x condition interaction [F_{(2, 38)} = 5.11, p = 0.011, η² = 0.21] but no significant main effect of condition [F_{(2, 38)} = 0.099, p = 0.906, η² < 0.01]. Post-hoc tests showed significantly decreased PANAS Negative from pre to post control condition [t₍₁₉₎ = −3.94, p = 0.001, d = −0.882; control pre: 12.20 ± 2.62; control post: 10.85 ± 2.03]. No significant differences were observed from pre to post of the LIIE condition [t₍₁₉₎ = −2.43, p = 0.025, d = −0.544; low pre: 12.10 ± 3.09; low post: 10.65 ± 1.14] or from pre to post HIIE [t₍₁₉₎ = −0.37, p = 0.716, d = −0.083; high pre: 11.40 ± 1.93; high post: 11.50 ± 2.33]. Comparing the conditions with each other, significant results were found only comparing the high-intensity vs. the control condition [“high post minus pre” vs. “control post minus pre”; t₍₁₉₎ = 3.45, p = 0.003, d = 0.7721; delta high: 0.10 ± 1.21; delta control: −1.35 ± 1.531]. No significant changes were detected when testing the LIIE vs. the control condition [“low post minus pre” vs. “control post minus pre”; t₍₁₉₎ = 0.177, p = 0.862, Cohen's d = 0.039; delta low: −1.45 ± 2.67; delta control: −1.35 ± 1.531] or the HIIE vs. the LIIE [“high post minus pre” vs. “low post minus pre”; t₍₁₉₎ = 2.49, p = 0.022, Cohen's d = 0.56; delta high: 0.10± 1.21; delta low: −1.45 ± 2.67] (see Figure 2B).

STAI-state

A 2 × 3 repeated measures ANOVA for the STAI-State found no significant main effect of condition [F_{(2, 38)} = 0.055, p = 0.947, η² < 0.01] and time [F_{(1, 19)} = 3.99, p < 0.060, η² = 0.17], as well as no time × condition interaction [F_{(2, 38)} = 1.67, p = 0.20, η² = 0.008].

MR data

Voxelwise changes in zfALFF

When comparing the pre-to-post session changes within and between conditions using a 2 × 3 repeated measures ANOVA, we observed no significant main effects of time (pre vs. post), condition (low, high and control), or time × condition interaction effect. However, exploratory post hoc comparisons revealed significant decreases in zfALFF after the HIIE intervention (p < 0.05, k ≥ 101) in several brain regions including precuneus, orbitofrontal cortex, inferior temporal gyrus, thalamus, and cerebellum. For details see Figure 3A and Table 2A. Moreover, we found decreased (p < 0.05, k ≥ 90) and increased (p < 0.05, k ≥ 148) zfALFF after the HIIE compared to the control condition. The reported regions partially overlap with the pre-post changes in the HIIE condition (including precuneus, cerebellum, hippocampus, inferior temporal gyrus, middle cingulate, and precentral gyrus), along with additional regions, including thalamus, middle temporal gyrus, fusiform/parahippocampal gyrus, and frontal operculum (see Figure 3B, Table 2B). Conversely, zfALFF increases were found in hypothalamus, periaqueductal gray as well as in the pituitary (see Figure 3C, Table 2C). We did not observe any significant time effect within LIIE and control conditions, as well as between conditions (LIIE vs. control, and vice versa as well as HIIE vs. LIIE and vice versa).

Figure 3

Figure 3. Represents a 2 × 3 repeated measures ANOVA to compare time and condition effects on zfALFF: (A) Results from within condition showing clusters where zfALFF was reduced after the HIIE (p < 0.05, k = 101), (B) Results from between condition showing clusters where zfALFF was reduced after the HIIE condition compared to control (p < 0.05, k ≥ 90), and (C) Results from between condition showing clusters where zfALFF increased after the HIIE condition compared to control (p < 0.05, k ≥ 148). zfALFF, normalized fractional amplitude of low frequency fluctuations; k = cluster size. The color bars represent the t-statistics of corresponding test.

Table 2

Table 2. Significant clusters obtained from different post-hoc contrasts of 2 × 3 repeated measures ANOVA.

Associations between fALFF changes and PANAS

Follow-up regression analyses examined potential associations between the observed fALFF changes corresponding pre-to-post changes in the affective questionnaires. No significant associations were observed.

Spatial correlations of fALFF changes with neurotransmitter maps

In the exploratory whole-brain analysis for 14 neurotransmitter systems, no significant spatial correlations were observed between the pairwise differences in zfALFF and any of the neurotransmitter maps in the LIIE and the control condition. For the HIIE condition, only a marginal effect for the endocannabinoid map emerged (Fisher's z = −0.12, exact p = 0.029, Supplementary Figure S2), but this did not survive multiple comparison correction.

The hypothesis-driven analysis focusing on the “reward network” showed a significant spatial correlation of the pairwise zfALFF differences and the Mu-opiodergic receptor distribution (Fisher's z = 0.16, p = 0.027, corrected) after HIIE (Figure 4A). Additionally, we observed a significant effect (Fisher's z = 0.22, p = 0.037, corrected) with the dopamine (D2) receptor distribution after the HIIE condition (Figure 4A). Again, no significant correlation was observed within the reward network at the LIIE condition or the control condition.

Figure 4

Figure 4. Fisher's z distribution of the Spearman correlation between the fALFF changes from pre to post in the HIIE condition and neurotransmitters (included in JuSpace toolbox) (A) within the “reward network,” and (B) within the “emotion network” in trained athletes. *significant; (*)trend.

The hypothesis-driven analysis focusing on the “emotion network” revealed a trend spatial correlation (Fisher's z = −0.16, p = 0.064, corrected) between the pairwise zfALFF differences and the CB1 receptor distribution after the HIIE condition (Figure 4B).

fALFF-neurotransmitters correlations with mood changes

No significant correlations were observed between the changes in affective scores and the changes in spatial correlations between fALFF and the investigated neurotransmitter maps.

Discussion

This study examined acute exercise-induced changes in resting-state zfALFF and their spatial cross-correlations with representative PET neurotransmitter distribution maps using the JuSpace toolbox (Dukart et al., 2021) to make indirect inferences about exercise-related acute neurotransmission changes. The within-subject design with three acute training sessions at different activity levels (Control, LIEE, HIIE) in a group of 20 highly trained athletes allowed determining dose-dependent influences of training intensity on resting-state zfALFF changes and their relationship with respective neurotransmitter distributions in the human brain. While both exercise conditions showed the expected positive mood effects (PANAS Positive Affect scale), no robust exercise related changes of resting-state activation levels could be observed, although exploratory analyses revealed post-acute effects in the HIIE condition. Associated with these activity changes, results of spatial cross-correlations with representative PET neurotransmitter distribution maps suggest potential involvement of opioidergic (via mu-opioid receptors) and dopaminergic (via D2 receptors) neurotransmission after HIIE, with weak evidence for an additional involvement of the endocannabinoid system (via CB1 receptors).

Exercise had the anticipated mood-improving impact, as evidenced by the higher PANAS Positive Affect following LIIE and HIIE bouts (Reed and Ones, 2006; Schmitt et al., 2019, 2020). Meanwhile, no significant increases of PANAS Negative Affect were observed for LIIE and HIIE, indicating that these exercise bouts did not induce post-acute aversive mood states. Indeed, previous evidence suggests that HIIE bouts may induce negative affect during performance (if homeostasis is disrupted to a significant extent) that is followed by a positive affective rebound immediately after exercise (Dierkes et al., 2021). The fact that PANAS Negative Affect only decreased significantly in the control condition is unexpected, given that the participants generally scored in the low range. We can only speculate whether this indicates the athletes' relieve from passively sitting on the bicycle for an extended time period.

To the best of our knowledge, zfALFF changes have not yet been studied in acute exercise intervention settings, as reported here. We did not find significant condition-by-time interaction effects, i.e., no robust proof for differential zfALFF changes in the control relative to (or between) the exercise conditions. Exploratory post-hoc analyses revealed preliminary evidence for zfALFF changes after the HIIE condition: Decreases in zfALFF (pre- > post-intervention) were mainly found in precuneus, orbitofrontal cortex, thalamus, and cerebellum. Compared to the control condition, HIIE was associated with differential zfALFF decreases in precuneus, temporo-occipital, midcingulate and frontal regions, thalamus, and cerebellum, whereas differential zfALFF increases were identified in hypothalamus, pituitary, and periaqueductal gray. Comparing these findings with studies using related neuroimaging techniques, we did not replicate previous ASL studies that point toward post-exercise CBF increases in the hippocampus (Steventon et al., 2020) and posterior insula (Thackray et al., 2023). Yet, the available literature is not consistent, as there were also observations of hippocampal (MacIntosh et al., 2014; Alfini et al., 2020) and mesial orbitofrontal CBF decreases (Thackray et al., 2023), the latter being in line with the present result patterns, and also with previous models that suggested transient frontal activity reductions, at least during acute exercise (Dietrich and Audiffren, 2011). The significant clusters also show limited overlap with previous rs-fMRI studies which found increased FC in sensorimotor networks (Rajab et al., 2014), or affect-reward, hippocampal, cingulo-opercular, and executive control networks (Steventon et al., 2017), although again, conflicting FC reductions were also observed (Alfini et al., 2020). Partially consistent with our earlier FC analyses (Schmitt et al., 2019, 2020), results patterns suggested intensity-dependent effects, although in the present case, only the HIIE (not the LIIE) condition showed significant differences from the control condition, and there was no significant difference between the exercise conditions. Limited statistical power may have disguised weaker exercise-related changes in the LIIE condition. At least, the result pattern argues against a curvilinear, inverted U-shape relationship with exercise intensity (as discussed in other contexts, e.g., Reed and Ones, 2006; Raichlen et al., 2013). The lack of spatial consistency between our zALFF and previous FC analyses of rs-fMRI data may relate to the fact that the FC methods capture the functional integration between brain regions, and only allow indirect assumptions about the underlying levels. In general, it should be noted that the available neuroimaging studies show substantial methodological variations, e.g., regarding age and fitness level of the participants, duration and intensity of the acute exercise, which may to some degree explain the variable or even contradictory observations. In fact, the relatively intense, but short exercise bouts during HIIE may trigger somewhat different adaptational processes than continuous trainings used in earlier studies.

Interestingly, zfALFF increases were found after HIIE in regions belonging to the hypothalamic-pituitary-adrenal (HPA) axis. One previous study examined hypothalamic CBF, and found no exercise-related effects, but using a continuous, moderate intensity training instead of HIIE (Thackray et al., 2023). The hypothalamus integrates signals from other brain nuclei as well as environmental, hormonal, metabolic, and neuronal signals from the periphery (Taouis, 2016). Thereby, vital functions such as energy homeostasis, water balance, and stress are controlled (Taouis, 2016), which are essential for adequate responses to exercise, both acutely and chronically (Cano Sokoloff and Misra, 2016). For example, in order to appropriately respond to the rise in body temperature during strenuous exercise, effector responses are triggered by the hypothalamus (Gleeson, 1998). Differential zfALFF changes also occurred in the PAG, which is an integral hub region of the opioidergic descending antinociceptive system (Bagley and Ingram, 2020). Given that pain is a prominent symptom in exercise of high intensity and/or duration it is well conceivable that exercise triggers antinociceptive responses via the PAG (Scheef et al., 2012). Beyond its role in antinociception, the PAG also fulfills many requirements of a command center for the control of breathing during exercise (Paterson, 2014). It has functional connections to higher brain areas, receives sensory input from contracting muscles, and sends efferent information to brainstem nuclei involved in cardiorespiratory control (Paterson, 2014). In conclusion, the observed zfALFF increases may reflect enhanced regulation of neurohumoral processes, as an adaption to the acute stress during the exercise bouts (see also below).

A particular innovative aspect of the current study is the parallel examination of multiple neurotransmitter effects using rsfMRI after acute exercise bouts with varying intensity. Although the JuSpace approach (Dukart et al., 2021) is per se indirect (i.e., spatial cross-correlations of zfALFF changes with representative neurotransmitter maps) and does not allow quantification of endogenous transmitter release (as in PET displacement studies), this MRI-based approach has the unique advantage that several neurotransmitter systems can be tested at the same time in parallel, thereby providing novel insights that help generating hypotheses for future, more transmitter-specific studies. The present results were consistent with the a priori proposed roles of the dopaminergic, opioidergic and, less clearly, endocannabinoid neurotransmitter systems in high-intensity exercise, as suggested by previous research (Raichlen et al., 2013; Hiura et al., 2017; Saanijoki et al., 2018a).

At whole-brain level, unconstrained analyses found no robust evidence for pre-post changes for the 14 available neurotransmitter maps after correcting for multiple comparisons, even though there was marginal evidence for the CB1 receptor map at uncorrected p-values, which were moreover restricted to the high-intensity condition. Even in the constrained analysis for a priori-defined emotion-related networks, this spatial correlation only approached significance. While it was shown in humans that exercise increases circulating endocannabinoid levels in an intensity-dependent manner (Raichlen et al., 2013; Saanijoki et al., 2018b), the current observation must be interpreted with caution. Here, it should also be noted that the overall spatial correlation between the zfALFF changes and the CB1 map was negative, suggesting a trend for activity decreases across endocannabinoid-rich regions: While CB1 receptors are located presynaptically, and their activation by endocannabinoids generally inhibits the release of other transmitters from these synapses (Mechoulam and Parker, 2013), CB1 receptors are expressed on both excitatory and inhibitory synapses which can have complex net effects on signal transmission at system level. Ultimately, direct proof for exercise-induced changes in brain endocannabinoid transmission will depend on future ligand PET studies, although it would be especially interesting here to examine their relationship with concomitant zfALFF (and other rs-fMRI parameter) changes in combined PET/MRI studies.

The analysis restricted to the “reward network” revealed significant spatial correlations of zFALFF changes with the dopaminergic and μ-opiodergic transmitter maps after the high-intensity exercise condition, confirming our a priori hypotheses. For the dopaminergic system, results showed a positive association, suggesting higher brain activity (as indicated by zfALFF) in the D2-rich regions of the reward network. This positive correlation parallels findings from the original JuSpace study, which validated the toolbox with data from an acute risperidone challenge study (Dukart et al., 2021). Human evidence on dopamine transmission changes after exercise generally remains scarce. There are earlier observations of increased peripheral dopamine metabolite levels after exercise (Marques et al., 2021), but they provide no insight into central dopamine transmission. This is currently only possible with molecular imaging methods. An early PET study already demonstrated that a gait challenge significantly increased endogenous dopaminergic release in Parkinson patients, but did not examine possible relationships with motivational behavior (Ouchi et al., 2001), which is also a limitation of the present study. While a recent study in healthy individuals reported striatal dopamine release during acute exercise that also correlated with speeded reaction times in a cognitive task (Ando et al., 2024), this does not necessarily reflect motivational changes. Another PET ligand displacement study in Parkinson patients reported that ventral striatal dopamine release after steady-state cycling was more pronounced in habitual exercisers than in sedentary subjects with Parkinson's disease (Sacheli et al., 2018), suggesting an influence of training status. Interestingly, the patient groups also showed differential ventral striatal brain activation during an fMRI reward paradigm. While not acquired in the context of the exercise session, this sort of fMRI paradigm may be an interesting addition to generate more specific information about motivational changes. In fact, an earlier study observed blunted ventral striatal responses during monetary reward anticipation and receipt after treadmill exercise, which may reflect higher levels of baseline brain activity immediately after exercise bouts (Bothe et al., 2013): this would concur with our observation, assuming that the increased spatial correlation with the D2 map within the reward network reflects higher brain activity.

There was also a positive spatial correlation between the zfALFF and the mu-opioid distribution map within the reward network regions. Both neurotransmitter systems are assumed to play complementary roles in reward processing, with dopamine being more closely related to motivational-energetic (“wanting”) aspects, and opioids being more closely related to hedonic-consummatory aspects (“liking”) of reward (Berridge and Robinson, 2003). Indeed, joint opioidergic and dopaminergic neurotransmission was detected in the ventral striatum of rats: A rostro-dorsally located “opioid hedonic hotspot” in the nucleus accumbens, mediating behavioral “liking” reactions via endorphinergic transmission (Castro and Berridge, 2014). This “liking” hotspot could be distinguished from a separate, more caudally located hotspot for “wanting” behavior mediated via dopaminergic transmission (Castro and Berridge, 2014). Interestingly, one human study observed that the individual strength of opioid release after moderate exercise training correlated positively with the brain response of reward network areas (including ventral striatum) while viewing palatable, as compared to non-palatable food pictures, which would be consistent with an opioidergic mechanisms to hedonic aspects of reward processing (Saanijoki et al., 2018b). Although we do not have behavioral results to distinguish the representations of “liking” and “wanting” in the ventral striatum, it is noteworthy that our analyses indicate a common representation of these two neurotransmitter systems and an effect of HIIE on both. This finding is also consistent with observations that central opioid release appears to be dependent on the intensity of exercise (Hiura et al., 2017; Saanijoki et al., 2018a). Previous work from our group identified exercise-induced opioidergic transmitter release, as measured with 6-O-(2-[18F]fluoroethyl)-6-O-desmethyldiprenor-phine ([18F]DPN) PET (Boecker et al., 2008). Importantly, [18F]DPN binding changes correlated with VAS euphoria change scores (Boecker et al., 2008). Why such a relationship was not found with the current indirect analysis approach remains a matter of speculation and should be addressed in future studies. Another study reported that increased opioid release was correlated with increased euphoria after a moderate intensity continuous exercise, but increased negative affect after high-intensity interval training (Saanijoki et al., 2018a), which may indicate that at very high levels of exercise strain the stress-reducing effects of opioidergic neurotransmission become more important. In this context it is interesting to revisit an abovementioned observation from the present study: It is intriguing that zfALFF changes were found in the hypothalamus and the PAG, both of which are known as core regions of the central opioidergic neurotransmitter system, but not covered by the JuSpace maps. The hypothalamus is the region where β-endorphins are produced and released, in particular in the pro-opio-melano-cortin (POMC) neurons located in the arcuate hypothalamic nucleus (ARH) and, to a lesser extent, in the nucleus of the solitary tract (Veening et al., 2012). B-endorphins from the hypothalamic POMC neurons in the ARH are released inside the central nervous system, notably to limbic structures, hypothalamic and thalamic sites, and several brainstem nuclei (Veening et al., 2012). On the other hand, β-endorphins produced in the nucleus solitarius project axons to the spinal cord. In addition to these central acting β-endorphins, those from the pituitary are released into the peripheral systemic circulation (Veening et al., 2012). Activation of the hypothalamic-pituitary-adrenal (HPA) axis by physical exercise has been demonstrated by increased endorphin levels in the pituitary (Tendzegolskis et al., 1991; Goldfarb and Jamurtas, 1997) and elevated plasma immunoreactive β-endorphin/β-lipotropin levels (Kelso et al., 1984; Mastorakos et al., 2005). Differential zfALFF changes in the PAG are equally interesting as the region is a crucial hub region of the descending antinociceptive system which is opoidergically mediated and modulated by exercise, as shown by our group in human athletes after strenuous exercise (Scheef et al., 2012). In line with our observations, it was demonstrated in mice after exposure to forced walking stress that β-endorphin levels are increased in PAG and/or medial basal hypothalamus and may be involved in stress-induced analgesia (Nakagawasai et al., 1999). Meanwhile, extensive expression of CB1 and CB2 receptors of the endocannabinoid system has been found in limbic regions and also in the hypothalamus (Ferber et al., 2021). Furthermore, CB1 receptor signaling has been shown to have an effect on the activation of the HPA axis (Hillard et al., 2016). One thus needs to consider that there are mutual interactions between the endocannabinoid systems and the opioidergic (Crombie et al., 2018; Wenzel and Cheer, 2018) and dopaminergic (Wenzel and Cheer, 2018) systems in the human brain, with indications that the opioid system is involved in the increase of endocannabinoids following exercise (Crombie et al., 2018). Yet, with the currently available technical approaches, these complex interrelationships are difficult to disentangle in humans.

In general, both ligand PET studies of exercise-induced neurotransmission changes and the proposed JuSpace-based fMRI approach only provide correlational data by design, and even if these measures show associations with the subjective and behavioral effects of acute exercise, they do not allow inferences about causal relationships. Here, selective modulation of specific transmitter functions by means of pharmacological blocking or enhancement could provide important complementary insights. Meanwhile, the available literature is small (Marques et al., 2021; Hirschbeck et al., 2022), and gives few specific insights with regard to emotional/motivational changes after exercise (e.g., Siebers et al., 2021). Ideally, both methodological approaches would be combined, although this affords even more repeated scanning, which is probably more feasible with fMRI (due to radiation exposure regulations for PET). At least, imaging studies may provide a useful starting point for the selection of pharmacological manipulations (where JuSpace would allow to screen multiple transmitter systems in parallel).

This study is not without limitations: We constrained our analyses of the “emotion network” and the “reward network” to three transmitter systems described in the context of affect and reward processing. The reported effects were only detectable in the high-intensity condition and effect sizes were too weak to survive corrections for multiple testing of all available PET transmitter maps. Therefore, future studies of this kind should attempt to measure larger samples in order to detect further neurotransmitter involvement related to exercise. Moreover, future examinations should enroll all sexes, which was not the case in this pilot study. While we decided to examine cycling as a common form of training, we cannot make direct inferences for other types of endurance exercise, e.g., running: even if general fitness levels are comparable, varying demands of the exercise modes (e.g., regarding active muscle mass, motor unit recruitment patterns) can alter physiological responses like oxygen uptake (Kilding and Jones, 2008). Accordingly, generalizability should be scrutinized by examining additional (or mixed) athlete groups. We can only speculate on the association with neurotransmitter effects in those regions like the hypothalamus and the PAG which were not covered by the PET tracer distribution maps. Finally, we must acknowledge that although the study design controlled for the influence of examination time by keeping it the same for each participant throughout the study (i.e., reducing the influence of circadian rhythms as a confounding factor at the individual level), examination took place during normal working hours (08:00 to 17:00), and the sample size did not allow for a systematic analysis of possible moderator effects of the time of day.

In summary, this is the first attempt to study exercise-induced neurotransmission non-invasively and in a rather holistic manner using rs-fMRI in humans. Our approach of studying zfALFF changes in the context of acute exercise bouts differing in intensity has provided novel information on the neurobiology of exercise, extending previous evidence on the particular relevance of the opioidergic, the dopaminergic and the endocannabinoid systems in high-intensity physical activity. Interactions between these transmitter systems have been described and should be studied further in vivo, e.g., between endocannabinoid signaling and endorphin (Parolaro et al., 2010; Wenzel and Cheer, 2018) or dopamine release (Covey et al., 2017; Wenzel and Cheer, 2018), in the specific context of exercise physiology. Yet, this necessitates future studies in larger samples which also provide more statistical power to discover additional relationships for other neurotransmitter systems, and also to detect correlations with the behavioral effects of acute exercise. A deeper understanding of the neuropharmacological underpinning of acute exercise effects is not only interesting from the perspective of basic science, but may ultimately also help to further consolidate the role of exercise trainings in clinical populations with dysregulated transmitter function.

Data availability statement

The datasets presented in this article are not readily available because volunteers will need to provide consent possibly restricting deliverable data sets. Requests to access the datasets should be directed to aGVubmluZy5ib2Vja2VyJiN4MDAwNDA7dWtib25uLmRl.

Ethics statement

The studies involving humans were approved by Ethics Committee at the Medical Faculty of the Rheinische Friedrich-Wilhelms-Universität Bonn. The studies were conducted in accordance with the local legislation and institutional requirements. The participants provided their written informed consent to participate in this study.

Author contributions

HB: Conceptualization, Investigation, Resources, Supervision, Validation, Writing—original draft, Writing—review & editing. MD: Conceptualization, Methodology, Supervision, Visualization, Writing—review & editing. AM: Conceptualization, Data curation, Formal analysis, Investigation, Methodology, Project administration, Supervision, Validation, Writing—original draft, Writing—review & editing. LB: Data curation, Formal analysis, Investigation, Writing—original draft, Writing—review & editing. JW: Data curation, Investigation, Writing—review & editing. ML: Data curation, Investigation, Writing—review & editing. CM: Data curation, Formal analysis, Investigation, Methodology, Resources, Supervision, Writing—review & editing. UM: Data curation, Investigation, Resources, Writing—review & editing. AR: Funding acquisition, Resources, Writing—review & editing. UA: Funding acquisition, Resources, Writing—review & editing. JD: Methodology, Software, Supervision, Writing—review & editing. NU: Conceptualization, Data curation, Formal analysis, Investigation, Methodology, Software, Validation, Writing—original draft, Writing—review & editing.

Funding

The author(s) declare financial support was received for the research, authorship, and/or publication of this article. The study was financed exclusively by in-house funds. ML received an in-house grant in support of his thesis (SciMed-Promotionsstipendium O-141.0023). This work was supported by the Open Access Publication Fund of the University of Bonn.

Conflict of interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

The author(s) declared that they were an editorial board member of Frontiers, at the time of submission. This had no impact on the peer review process and the final decision.

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Supplementary material

The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fnimg.2024.1332384/full#supplementary-material

Abbreviations

BOLD, Blood oxygenation level-dependent; MRI, Magnetic resonance imaging; rs-fMRI, Resting-state functional MRI; PET, Positron emission tomography; fALFF, fractional amplitude of low frequency fluctuations; PANAS, Positive and negative affect scale; FDR, False discovery rate; PE, Physical exercise; HR, Heart rate; HR_int, Heart rate during exercise intervention; HR_rest, Heart rate during resting state functional MRI; PE, Physical exercise; RER, Respiratory exchange ratio; ROI, Region of interest; VO₂, Oxygen uptake; VO_2max, Maximal oxygen uptake (mL/min/kg).

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