Janina Borgonovo1,2,3
Patricio Ahumada-Galleguillos1,2
Alejandro Oñate-Ponce1,2,3
Camilo Allende-Castro1,2,3
Pablo Henny4
Miguel L. Concha1,2,3*- 1Laboratory of Experimental Ontogeny, Faculty of Medicine, Institute of Biomedical Sciences, Universidad de Chile, Santiago, Chile
- 2Biomedical Neuroscience Institute, Santiago, Chile
- 3Center for Geroscience, Brain Health and Metabolism, Santiago, Chile
- 4Department of Anatomy and Interdisciplinary Center of Neurosciences, School of Medicine, Pontificia Universidad Católica de Chile, Santiago, Chile
The catecholaminergic system has received much attention based on its regulatory role in a wide range of brain functions and its relevance in aging and neurodegenerative diseases. In the present study, we analyzed the neuroanatomical distribution of catecholaminergic neurons based on tyrosine hydroxylase (TH) immunoreactivity in the brain of adult Nothobranchius furzeri. In the telencephalon, numerous TH+ neurons were observed in the olfactory bulbs and the ventral telencephalic area, arranged as strips extending through the rostrocaudal axis. We found the largest TH+ groups in the diencephalon at the preoptic region level, the ventral thalamus, the pretectal region, the posterior tuberculum, and the caudal hypothalamus. In the dorsal mesencephalic tegmentum, we identified a particular catecholaminergic group. The rostral rhombencephalon housed TH+ cells in the locus coeruleus and the medulla oblongata, distributing in a region dorsal to the inferior reticular formation, the vagal lobe, and the area postrema. Finally, scattered TH+ neurons were present in the ventral spinal cord and the retina. From a comparative perspective, the overall organization of catecholaminergic neurons is consistent with the general pattern reported for other teleosts. However, N. furzeri shows some particular features, including the presence of catecholaminergic cells in the midbrain. This work provides a detailed neuroanatomical map of the catecholaminergic system of N. furzeri, a powerful aging model, also contributing to the phylogenetic understanding of one of the most ancient neurochemical systems.
Introduction
Historically, the catecholaminergic (CAergic) system has aroused particular interest due to its role in a variety of neural functions, including motor control, memory, learning, reward, motivation, sleep, temperature regulation, and reproduction (Crocker, 1997; Hurley et al., 2004; Salamone and Correa, 2012). The CAergic system has also attracted attention from the clinical perspective since imbalances in catecholamines or components of the CAergic system are present in neuropsychiatric disorders such as schizophrenia, depression, and anxiety (Joyce, 1993; Davis et al., 1994), and in neurodegenerative diseases with high prevalence as is the case of Parkinson’s disease (PD; Dawson and Dawson, 2003). In PD, the dopaminergic (DAergic) neurons of the substantia nigra (SN) are severely affected, and other CAergic cells also suffer changes during the disease’s development. For instance, TH+ neurons increase in the olfactory bulb of PD patients (Huisman et al., 2004, 2008) and the striatum of animal models of PD (Tashiro et al., 1989, 1990; Palfi et al., 2002; Tande et al., 2006; Huot et al., 2007; El Massri et al., 2017). Moreover, the CAergic system deteriorates in the course of physiological aging, showing an age-dependent loss of neuronal components in the locus coeruleus (LC; Manaye et al., 1995), striatum (Huot et al., 2007), and retina (Roufail and Rees, 1997). Together, these findings reveal that the CAergic system’s deterioration is a cross-cutting issue of normal and pathological aging.
The organization of the CAergic system has been reported in a wide range of vertebrates, from cyclostomes to mammals, since the first demonstration of catecholamines in the central nervous system (CNS; Montagu, 1956; Bertler and Rosengren, 1959; Carlsson, 1959; von, 1961). These studies have revealed an overtly conserved distribution of CAergic neuronal groups throughout evolution (Smeets and Gonzalez, 2000). Such conservation has especially been relevant for biomedical research since it allowed drawing parallels between humans and species of biomedical relevance, such as mouse and some teleost fish species, in the search for models of neurodegenerative disorders. Among the latter, zebrafish and medaka have gained space as key non-mammalian vertebrate models for studying neurological diseases and PD (Matsui et al., 2014; Wang et al., 2017; Matsui and Takahashi, 2018). These teleost species show a complex CAergic system, containing most of the CAergic groups found in mammals based on anatomical, molecular and connectivity criteria (Rink and Wullimann, 2001; Tay et al., 2011; Filippi et al., 2012). Furthermore, the TH+ cells found in the posterior tuberculum of these species have been considered analogous to the mammalian SN and, as seen in mammals, these neurons are especially vulnerable to toxic insults and the expression of mutant proteins linked to PD (Sallinen et al., 2009; Sheng et al., 2010; Soman et al., 2019).
In the last decade, the turquoise killifish (Nothobranchius furzeri) has reached popularity as a model organism for aging research (Genade et al., 2005; Terzibasi et al., 2009). N. furzeri belongs to the order Cyprinodontiformes and inhabits temporary puddles in the African savannah, showing a life cycle adapted to the temporary habitat in which fish live. In a short period of the year that coincides with the rainy season, fish hatch from the eggs, reach sexual maturity and reproduce. When the puddles dry, the adults die. Still, the eggs remain buried in the mud resisting desiccation until the environmental conditions are adequate to restart the life cycle (Reichard et al., 2009; Blazek et al., 2013). Since introducing the first individuals of the Gona Re Zhou (GRZ) strain into the laboratory, the use of N. furzeri has persistently grown due to their short lifespan and accelerated aging, in which fish express biological markers of aging common to other vertebrates, including humans (Genade et al., 2005; Valenzano et al., 2006; Terzibasi et al., 2009; Di Cicco et al., 2011; Baumgart et al., 2015). Recent work also showed that N. furzeri develops a PD-like pathology in an age-dependent manner with physiological loss of the TH+ cells in the posterior tuberculum, deposition of α-synuclein aggregates, and motor disability (Matsui et al., 2019). Together, the short lifespan, accelerated aging and age-related loss of CAergic neurons make N. furzeri a versatile and tractable model for longitudinal studies with a biomedical perspective, especially for pathologies associated with age like PD. However, although information of the CAergic system is available for zebrafish and many other teleosts (Parent and Northcutt, 1982; Roberts et al., 1989; Hornby and Piekut, 1990; Manso et al., 1993; Meek and Joosten, 1993; Brinon et al., 1998; Rodriguez-Gomez et al., 2000; Goebrecht et al., 2014; Bhat and Ganesh, 2017), a systematic description of the different neuronal groups that compose this system has not been performed in N. furzeri. This missing information is relevant since the CAergic system is heterogeneous in its composition, and knowledge of the diverse neuronal types is essential, considering that they are differentially affected during physiological aging and under pathological conditions (Manaye et al., 1995; Roufail and Rees, 1997; Huot et al., 2007).
The present study aims to provide a comprehensive analysis of the CAergic system’s anatomy in N. furzeri. For this, we used tyrosine hydroxylase (TH) immunofluorescence to locate the CAergic cells and fibers in the turquoise killifish brain. We focused on describing the spatial organization of the different neuronal groups and the morphological features of neurons immunoreactive for TH. Our results show that the overall organization of the CAergic system of N. furzeri is comparable to other teleosts. However, killifish shows a distinct TH+ group in the dorsal midbrain that resembles CAergic neuronal groups observed in some species of holosteans and cladistians. This work provides a detailed neuroanatomical framework for aging studies related to the CAergic system in N. furzeri, and contributes to our understanding of the evolution of the CAergic system in vertebrates, especially of the mesencephalic groups.
Materials and Methods
Fish Maintenance and Husbandry
Adult wild type N. furzeri of the Grz strain were raised and maintained in the fish facility of the Laboratory of Experimental Ontogeny, from the Faculty of Medicine, University of Chile. Fish were kept under 12/12 h light/dark cycle regime at 26°C, in a recirculating system. The conductivity of water was set to 400–500 μS and the pH to 7–7.5. Adult fish were kept at density of one male or 3 females per tank. The food was supplied 3 times a day with newly hatched brine shrimps and once with freshwater live food (Lumbriculus variegatus). Weekly, 50% of total water volume was replaced with fresh water to remove the waste produced by fish. All animal procedures were approved by the Bioethics Committee of the Faculty of Medicine, University of Chile (Cicua certificate number: 20385-Med-Uch).
Tissue Sampling
Experiments were performed on N. furzeri brains of both sexes from 2 to 4 months old. The total of animals used for the experiments were 14, from which 5 were male and 9 were female. Individuals were euthanized with a 0.1% solution of ethyl 3-aminobenzoate methane sulfonate (MS-222; Sigma, St. Louis, MO, United States; A-5040). The brains were removed and fixed by immersion in 4% w/v paraformaldehyde in 0.1 M phosphate buffer (PB, pH 7,2 at 4°C) for 24 h and subsequently were embedded in 2% low melting-agarose. The tissue was cut in coronal, sagittal or horizontal orientation at 150–200 μm of thick using the vibroslice (Campden MA752). The brain sections were collected in PBS 1X.
Immunofluorescence
The immunofluorescence was performed according to Matsui and Sugie (2017). In brief, the floating slices were incubated in 10 mM sodium citrate buffer, pH 8.5, at 80°C for 120 min, washed three times in wash buffer (PBS, Triton X-100 1%) and blocked for 30 min in blocking buffer (PBS, Triton X-100 1%, and 2% BSA). Then, the slices were incubated with anti-TH (Millipore Cat# AB152), anti-HuC/HuD (Thermo Fisher Scientific Cat# A-21271) or anti-acetylated α-tubulin (Sigma-Aldrich Cat# T6793) primary antibody overnight at 4°C, all at dilution of 1/200. After washing, the sections were incubated with the respective secondary antibody and counterstained with hoechst 33258 (1:1000, Thermo Fisher Scientific Cat# H3569) overnight at 4°C. The secondary antibodies used were anti-rabbit Alexa Fluor 488 (1:200, Molecular Probes Cat#A11070) and anti-mouse Alexa Fluor 568 (1:200, Invitrogen Cat#A11004). Lastly, the tissue was washed three times in washing buffer and the sections mounted with Vectashield (Vector Cat#VC-H-1400-L010) on glass slides for imaging.
The specificity of the TH antibody used in the present study was previously verified by Matsui et al. (2019). In this study, different controls were performed in brain tissue of adult N. furzeri, including western blot analysis and comparison of TH immunostaining with the expression pattern of the dopamine transporter (dat) and the noradrenaline transporter (net) obtained after in situ hybridization (Matsui et al., 2019). Most vertebrates, with the exception of placental mammals, have two paralog genes for the enzyme TH, the th1 and th2 genes. Commercially available TH antibodies only detect the product of th1, one of the two TH genes (th1 and th2) present in non-mammalian vertebrates. Previous studies have shown that in teleosts such as zebrafish, TH immunoreactivity using the same antibody as this study matches the neuronal groups expressing th1, which are widely distributed in the brain. On the other hand, neurons expressing th2 do not show TH immunoreactivity and have a more restricted distribution in the brain, being observed in the preoptic nucleus (PM) and in the cerebrospinal fluid-contacting cells (CSF-c) of the paraventricular organ (PVO), the intermediate and caudal hypothalamus (Hc; Yamamoto et al., 2010). Given the wide distribution of TH+ neuronal groups observed in N. furzeri and their similarity with the spatial organization observed in zebrafish, it is likely that the population of TH+ neurons detected in this study expresses the th1 gene, although future studies are needed to corroborate this possibility.
Imaging
The immunofluorescent images were acquired using a Leica TCS LSI macro zoom confocal microscope with a 5× objective. In addition, to obtain a cellular resolution, the slices were imaged with a Volocity ViewVox spinning disk (Perkin Elmer) coupled to a Zeiss Axiovert 200 inverted microscope using a Plan-Apochromat 40×/1.2W or 10×/0.3W objective with a laser 488/520 (excitation/emission wavelengths). The different neuronal groups were recognized on the basis of their anatomical position, their morphology and the intensity of TH immunostaining. To determine the cell size, only those neurons where the nucleus was clearly visible were selected and the largest diameter of the soma was measured. As the sagittal sections gave us a global view of the different TH+ groups (in the same section we could observe several groups distributed along the rostrocaudal axis), all measurements were made on sections with this orientation. We did not observe any difference in the distribution of CAergic neurons between the sexes. The processing and analysis of digital images including measurement of soma diameter were performed using ImageJ1 and Adobe Photoshop CS3 (Adobe).
Presentation of the Results
Figures (and panels within each figure) were arranged from cranial to caudal and in cases where there was partial or complete overlap of TH+ groups on the rostrocaudal axis, the groups were presented from dorsal to ventral position. The groups of CAergic neurons detected in the present study were summarized in Figure 1, in a schematic diagram of a latereal view of the brain. Also, in the same figure, an additional diagram indicated the number of the figures in which the different TH+ groups have been presented.
Figure 1. Summary diagram illustrating the localization of the catecholaminergic neuronal groups in a lateral view of the brain of Nothobranchius furzeri. The schematic drawing shown on the bottom right indicates the number of the figures where the different TH+ groups were presented. For abbreviations see list.
Results
The main subdivisions of the brain, the localization of brain nuclei, and the neuroanatomical terminology used in this paper is based on D’Angelo (2013), the only available brain atlas of adult N. furzeri. For the caudal sections of the rhombencephalon we included information from the brain atlas of zebrafish developed by Wullimann et al. (1996). We followed the classical forebrain subdivision into telencephalon and diencephalon consistent with D’Angelo (2013), where the diencephalon includes the pretectal area, thalamus, hypothalamus, and preoptic areas (PO). However, it is important to bear in mind that this classical paradigm differs from the prosomeric model proposed by Puelles and Rubenstein (2003), where the forebrain is divided into three caudorostral segments (p1, p2, and p3), and a secondary prosencephalon. Within this frame, the pretectum, thalamus (dorsal thalamus), and prethalamus (ventral thalamus) are the alar part of the p1, p2, and p3 prosomeres, respectively, while the hypothalamic and PO are part of the secondary prosencephalon together with the telencephalon (Puelles and Rubenstein, 2003).
Telencephalon
Olfactory Bulbs
The olfactory bulbs (OB) of N. furzeri are located in the ventral part of the rostralmost telencephalic hemispheres. These regions showed a large population of TH+ cells distributed predominantly at the outer zone, along the dorsal region of the external cell layer and less abundantly in the internal cell layer. Conspicuous TH+ fibers were present in the glomerular layer (Figures 2A, 3A,B and Supplementary Figures 1A, 3C). TH+ neurons were ovoid in shape varying in size from 10 to 12 μm. A single process emerged from the cell bodies and TH+ fibers were generally oriented toward the internal area (Figure 4A).
Figure 2. Summary of TH immunoreactivity in the brain of Nothobranchius furzeri. (A–N) Diagrams of transverse sections showing TH+ cells bodies (large red dots), fibers (wavy red lines), and nerve terminals (small blue dots). The rostrocaudal level of each section is indicated in the lower brain scheme. See list of abbreviations, which applies to all figures.
Figure 3. TH immunoreactive neurons and fibers in the telencephalon and anterior preoptic area of Nothobranchius furzeri. (A) Para-sagittal section showing a panoramic view of TH+ neuronal groups in the olfactory bulb, subpallium and in the anterior preoptic nucleus. (B) Para-sagittal section showing the TH+ groups in the olfactory bulb. (C–E) Ventral telencephalic areas showing TH+ groups in the ventral, dorsal, supracomissural, and posterior zones. (C) Transverse section showing local TH+ processes of ventral/dorsal zones (arrow) and intense immunoreactive innervation at the ventrolateral edge of the telencephalon (arrowhead). (D) Horizontal section showing the caudalward projections of the dorsal zone (arrows) and the TH+ fibers at the level of the anterior commissure (arrowhead). (E) Horizontal section showing the lateral processes of the posterior zone (arrows). (F) Transverse section showing the TH+ neurons at the anterior preoptic nucleus. Arrows and arrowheads indicate the TH+ dorsocaudal projections of the anterior preoptic neurons and the lateral intense neuropil seen at each side of this cell group, respectively. For abbreviations see list. The orientation/level of sections is shown at the bottom right corner of each panel. Dorsal is to the top in transverse sections. Rostral is to the top and left, in horizontal and para-sagittal sections, respectively. Scale bars, 250 μm (A) and 100 μm (B–F).
Figure 4. Morphology of the different types of TH+ neurons in the brain of Nothobranchius furzeri. The upper image illustrates the positions of TH+ cells in a para-sagittal section of the brain. (A–P) High resolution images of TH+ neurons present in the olfactory bulb (OB; A), subpallium (Sp; B), anterior preoptic nucleus (PPa; C), ventral periventricular pretectal nucleus (PPv; D), magnocellular preoptic nucleus (PM) and parvocellular portion of preoptic nucleus (PPp; E), ventral thalamus (VT; F), periventricular nucleus of posterior tuberculum (TPp; G), posterior tuberal nucleus (PTN; H), caudal hypothalamus (Hc; I), mesencephalic tegmentum (Tegm; J), locus coeruleus (LC; K), medulla oblongata (MO; L), vagal lobe (LX; M), area postrema (AP; N), and in the rostral (O) and caudal (P) clusters of the paraventricular organ-accompanying cells (PVOa). Arrowheads points to TH+ neuronal processes. For abbreviations see list. Scale bar, 500 μm (upper panel) and 10 μm (A–P).
Telencephalic Hemispheres
The telencephalic hemispheres of N. furzeri, as in other vertebrates, are subdivided into pallial (dorsal) and subpallial (ventral) regions. While the pallium was devoid of TH+ cells, the subpallium harbored populations of CAergic neurons in its ventral (Vv), dorsal (Vd), supracomissural (Vs), and posterior (Vp) nuclei (Figures 2B–D). These TH+ neurons were disposed as a continuous strip, extending rostrocaudally from the caudal end of the OB to the Vp (Figure 3A and Supplementary Figure 2A). The neurons of the rostral regions projected locally (Figure 3C) and also sent fibers in a rostroventral direction (Supplementary Figures 1B,C). The most caudal TH+ cells of the Vd also projected caudalward and some fibers crossed the anterior commissure (Figure 3D and Supplementary Figure 3B). In turn, TH+ neurons in the Vs and Vp presented long laterocaudal processes (Figure 3E and Supplementary Figures 1D, 3A). TH+ cells of all these areas shared a similar morphology being round in shape with medium immunoreactivity level and showing an average size of 11–15 μm (Figure 4B).
Diencephalon
The diencephalon of N. furzeri showed the largest number of TH+ groups, which were located in the following regions: PO, thalamus, pretectum, posterior tuberculum (TP) and hypothalamus.
Preoptic Area
A group of TH+ cells was present in the anterior parvocellular preoptic nucleus (PPa), caudal to the anterior commissure (Cant) and at the floor of the telencephalon (Figures 2D, 3A,F and Supplementary Figures 1D, 2A–C). These neurons elaborated lateral projections that ended in an intensely labeled neuropil at each side of the PPa (Figure 3F and Supplementary Figure 1D). In addition, PPa neurons emitted long processes dorsocaudally, which fasciculated to form the preopticohypothalamic tract (poht; Figure 3F and Supplementary Figures 2A–C). The PPa was constituted by small round cells with an average size of 8–10 μm and intense TH immunoreactivity (Figure 4C). In a position caudal to the PPa, the suprachiasmatic nucleus (SC) contained a few scattered TH+ cells (Figure 2E and Supplementary Figures 1E, 2B,C). The SC neurons showed a similar morphology to those of the PPa and their projections joined the poht (Supplementary Figures 2B,C). Further, two groups of TH+ cells were observed along the posterior parvocellular preoptic nucleus (PPp) and magnocellular PM (Figures 2E,F, 5A,B,E,F and Supplementary Figures 1E,F, 2B,C). The neurons of both nuclei were located against the ventricular surface and their round somas exhibited a diameter of 11–14 μm (Figure 4E). PM neurons showed intense TH immunoreactivity and displayed a radial arborization, which extended laterally to the adjacent PO regions. In contrast, PPp neurons were lightly immunostained and their processes were not discernible (Figure 4E).
Figure 5. TH immunoreactive neurons and fibers in the diencephalon of Nothobranchius furzeri at the preoptic, thalamic, and pretectal levels. (A) Para-sagittal section of the brain showing a panoramic distribution of TH+ groups. The dotted box delimits the neuronal groups analyzed in this figure. (B) Para-sagittal section showing the TH+ groups at the ventral periventricular pretectal nucleus, ventral thalamic nucleus, parvocellular portion of preoptic nucleus, magnocellular preoptic nucleus, and paraventricular organ-accompanying cells. (C) Horizontal section showing the densely packed TH+ neurons of the ventral periventricular pretectal nucleus sending projections toward to the optic tectum (arrows). (D) Transverse section showing TH+ neurons at the ventral thalamus with characteristic slightly stained somas (asterisks). (E) TH+ cells of the parvocellular portion of preoptic nucleus and the magnocellular preoptic nucleus with their lateral projections as seen in a transverse section (arrows). (F) Horizontal section showing TH+ neurons and their projections (arrow) at the magnocellular nucleus and its relative position with respect to the periventricular nucleus of the posterior tuberculum. For abbreviations see list. The orientation/level of sections is shown at the bottom right corner of each panel. Dorsal is to the top in transverse sections. Rostral is to the top and left in horizontal and para-sagittal sections, respectively. Scale bars, 500 μm (A) and 100 μm (B–F).
Epithalamus, Thalamus, and Pretectal Region
The epithalamus lacked CAergic cells, however, the habenula (Ha) showed discrete TH+ innervation (Supplementary Figure 3A). In the thalamus, at the ventral subdivision (VT; also called prethalamus), a few TH+ cells were found away from the ventricular zone (Figures 5A,B,D and Supplementary Figures 1E, 2B,C). Their lateral processes extended toward the lateral edge of the diencephalon. These neurons were weakly stained and measured less than 11 μm (Figure 4F).
A densely-packed population of TH+ neurons was observed at the pretectal nucleus, in the ventral periventricular subdivision (PPv; Figures 2G, 5A–C and Supplementary Figures 1G, 2A–C). Their TH+ fibers followed a dorso-lateral trajectory to reach the rostral region of the optic tectum (OT; Supplementary Figure 3A). The pretectal cells exhibited intense immunoreactivity and round cell bodies with an average some size of 8–12 μm (Figure 4D).
Posterior Tuberculum and Hypothalamus
Three groups of TH+ cells were present in the posterior tuberculum. The rostralmost group was localized in the periventricular nucleus of the posterior tuberculum (TPp), positioned ventral to the VT (Figures 2G, 6A and Supplementary Figures 2B,C, 3C). A tuft of processes emerged laterally from the nucleus and ended in the vicinity (Figure 6B and Supplementary Figure 1G). TPp neurons presented moderate TH immunostaining, were densely packed and showed round soma with a diameter of 10–13 μm (Figure 4G). The second group appeared in a more ventral and caudal position to the TPp. This group was not strictly associated with a specific nucleus, but rather it extended in the boundaries of the TPp and the PVO, and we decided to name it as paraventricular organ-accompanying cells of the posterior tuberculum (PVOa), as others authors (Figure 2H and Supplementary Figures 1H, 2A–C, 3C; Ma, 2003). The PVOa consisted of a few large, multipolar and intensely labeled neurons (Figures 6A,C,D). We could distinguish two neuronal subpopulations within the PVOa. The first adopted a more rostral position and the neurons showed a soma diameter of 20–25 μm (Figure 4O). These cells sent axonal projections in rostroventral and lateral directions toward the telencephalon and hypothalamus (Figure 6A and Supplementary Figures 2A–C, 3C). The second PVOa group appeared more caudally, their cells bodies were slightly smaller with a diameter of 14–18 μm and emitted thick processes with dorsal orientation (Figure 4P). These axons traveled large distances to reach the floor of the tectal ventricle (TeV) where they turned 90°caudalward to descend toward the medulla (Figures 6A, 7A,B and Supplementary Figures 2A–C, 3C). The third TH+ group of the posterior tuberculum was observed in the posterior tuberal nucleus (Figures 2I, 6A,E and Supplementary Figures 1I, 2B,C). It was composed of a few teardrop shape neurons scattered on each side of the ventricle with ascending processes that extended toward the PVOa (Figure 4H).
Figure 6. TH immunoreactive neurons and fibers in the diencephalon of Nothobranchius furzeri at the level of the posterior tuberculum and hypothalamus. (A) Para-sagittal section showing a panoramic view of the distribution of all TH+ groups in the diencephalon. Arrowheads indicate TH+ fibers traveling from the paraventricular organ-accompanying cells toward the telencephalon and hypothalamus (bottom left), and across the mesencephalon to turn posteriorly toward the medulla (top right). (B) Transverse section showing the TH+ group in the periventricular nucleus of the posterior tuberculum. Arrows show the lateral tuft of projections emerging from the nucleus. The asterisk indicates a soma of the paraventricular organ-accompanying cells. (C) Transverse section showing the large pear shape neurons of the TH+ paraventricular organ-accompanying cells group. Arrows indicate the ascending and descending processes. (D) Horizontal section showing the relative position of the periventricular nucleus of the posterior tuberculum and the paraventricular organ-accompanying cells. Arrows point to ascending/descending processes of the paraventricular organ-accompanying cells. (E) Transverse section showing TH+ neurons at the posterior tuberal nucleus. The few cells of this group are positioned at each side of the ventricle and send projections in the dorsal direction (arrows). (F) Transverse section showing the TH+ neurons at the caudal hypothalamus. The arrow indicates the orientation of processes. The asterisk indicates a cell of the posterior tuberal nucleus. For abbreviations see list. The orientation/level of sections is shown at the bottom right corner of each panel. Dorsal is to the top in transverse sections. Rostral is to the top and left, in horizontal and para-sagittal sections, respectively. Scale bars, 500 μm (A) and 100 μm (B–F).
Figure 7. TH immunoreactive neurons and fibers in the mesencephalon, rhombencephalon, and spinal cord of Nothobranchius furzeri. (A) Para-sagittal section showing the group of mesencephalic TH+ neurons at the level of the oculomotor nucleus (tegm; asterisks indicate their lightly stained somas) and the intense TH+ plexus (arrow). TH+ fibers traveling from the paraventricular organ-accompanying cells across the mesencephalon to turn posteriorly toward the medulla are indicated with arrowheads. (B) Para-sagittal section along the extension of the rhombencephalon showing the most rostral TH+ group at the locus coeruleus and the caudal group in the vagal lobe. Arrowheads point to the same TH+ projections as in (A). (C) Horizontal section showing the TH+ group of the locus coeruleus. (D) Para-sagittal section showing the distribution of caudal rhombencephalic TH+ groups (medulla oblongata, vagal lobe, and area postrema). (E,F) Horizontal sections showing the TH+ groups at the medulla oblongata and vagal lobe. Arrows indicate the lateral projections. (G) Transverse section showing the densely packed group of TH+ neurons at the area postrema. Arrows indicate the ventral processes. (H) Para-sagittal section showing scattered small TH+ neurons in the spinal cord. The arrowhead points to a TH+ fiber in the ventral region of the spinal cord. For abbreviations see list. The orientation/level of sections is shown at the bottom right corner of each panel. Dorsal is to the top in transverse sections. Rostral is to the top and left, in horizontal and para-sagittal sections, respectively. Scale bars, 500 μm (A,D), 250 μm (B,G), and 100 μm (C,E,F,H).
At the hypothalamus, TH+ neurons were observed in the caudal subdivision (Hc), dorsal to the posterior recess (rec; Figures 2I, 6A,F and Supplementary Figures 1I,J, 2A–C). The cell bodies were small and round with a size of 9–12 μm and showed dorsally and ventrolaterally oriented processes that projected locally in the adjacent brain regions (Figures 4I, 6F). The hypothalamus also showed a dense network of TH+ fibers on the ventral surface, originated from the PO and the ventral diencephalon (Supplementary Figures 2A–C).
Mesencephalon
The dorsal mesencephalon of N. furzeri is composed of two large OT and the torus longitudinalis. Both structures lacked CAergic cells, but the OT showed a dense innervation, with TH+ fibers splaying out along the tectal layers (Figures 2G–K and Supplementary Figures 1G–L, 3A–C).
In the midbrain tegmentum, the torus semicircularis also presented TH+ neuropil, especially in the periventricular and lateral zones (Figure 2J and Supplementary Figures 1K, 3A,B). In addition, intense and varicose CAergic fibers were observed in the tegmentum at the level of the oculomotor nucleus (NIII). Many of these fibers originated from the TP (Figures 2J, 7A,B and Supplementary Figures 1K, 2A–C). Interestingly, a small group of TH+ positive neurons were located close to the ventricle and dorsal to the oculomotor nucleus in the mesencephalic tegmentum (tegm), where a TH+ plexus was placed (Figures 2J, 7A and Supplementary Figure 2C). These cells showed weak TH immunofluorescence and presented a pear shape morphology (Figure 4J).
Rhombencephalon
Cerebellum and Rostral Rhombencephalon
The cerebellum of N. furzeri showed low density of TH+ fibers in the corpus of the cerebellumand in the granular eminence (Supplementary Figures 1L,M).
In the rostral rhombencephalon, a small group of TH+ cells were found dorsal to the superior reticular formation (SRF; Figures 2K,L, 7B,C and Supplementary Figures 1L,M, 2B, 3A). This group corresponded to the LC and was composed of large pear shape neurons with an average size of 25–30 μm, showing long branched processes directed ventrally (Figure 4K and Supplementary Figure 1M).
Medulla Oblongata
At the caudal rhomencephalic level, a longitudinal column of CAergic neurons was observed in rostrocaudal direction from the caudal end of LVII to the medullospinal junction (Supplementary Figures 2A,C). This column consisted of two neuronal populations distinguishable by their morphology. The rostral group (MO) was positioned in a position dorsomedial to the intermediate (IMRF) and inferior (IRF) reticular formation (Figures 2M, 7D,E). These cells showed a multipolar shape and presented lateroventral processes (Figure 4L). The second group was positioned more caudally, in the vagal lobe (LX) and consisted of teardrop shape neurons with an intense TH immunoreactivity and lateroventral processes that reached the lateral edge of the medulla (Figures 2M, 4M, 7B,D,F,G and Supplementary Figures 1O–Q, 2A–C). An additional TH+ group was present in the medulla oblongata, at the level of the area postrema (AP; Figures 2N, 7D,G and Supplementary Figures 1P,Q, 2C, 3A,B), where a densely packed group of the round cells formed a wedge in the midline (Figure 4N).
Many regions of the medulla oblongata showed CAergic innervation. The medial octavolateralis nucleus had an intense TH+ neuropil and the SRF/IMRF/IRF also presented a moderate innervation, which was more prominent in the ventral surface (Supplementary Figures 1M–P, 2A–C). Besides, a longitudinal tract, probably originated in the diencephalic area, spanned all the rostrocaudal extension of the rhombencephalon to reach the spinal cord (sc; Supplementary Figures 1O–Q, 2A,B).
Spinal Cord
The sc showed a reduced number of small lightly immunostained CAergic neurons in the ventral aspect (Figure 7H), away from the central canal. In addition, many TH+ fibers coursed in rostrocaudal direction, predominantly at the medial and ventral positions of the sc (Figure 7H).
Retina
At the retina, a sparse population of TH+ neurons was observed in the inner nuclear layer (INL) and characteristically sent single process to the inner plexiform layer (IPL; Figure 8). Based on their general morphology, localization and orientation we suggest these neurons correspond to amacrine cells.
Figure 8. TH+ cells in the retina of Nothobranchius furzeri. (A) Hoechst stain showing the basic organization of the retina into the ganglion cell layer, inner plexiform layer, inner nuclear layer, outer plexiform layer, outer nuclear layer, and outer segment. (B) HUC/TubAc immunohistochemistry (magenta) showing the spatial distribution of somas and axons within the retina layers. (C) TH immunohistochemistry (yellow). Asterisks indicate TH+ amacrine cells. (D) Merge of the staining in a-c showing the localization of TH+ cells in the inner nuclear layer. For abbreviations see list. Scale bar, 100 μm.
Discussion
The distribution of catecholamines appears to be highly conserved throughout evolution and constitutes one of the oldest neurochemical systems in the vertebrate brain (Carlberg and Anctil, 1993; Yamamoto and Vernier, 2011). Despite the variation in the morphology and complexity of the vertebrate brain, five main groups of CAergic cells can be identified in the CNS of all vertebrates. These conserved groups include the noradrenergic groups of the caudal and rostral/isthmic rhombencephalon and the DAergic groups located in the diencephalon, olfactory bulb and the retina, which suggests that certain essential functions have been preserved during evolution (Smeets and Gonzalez, 2000). However, other groups such as those located in the midbrain are more variable and while they are commonly found in the tetrapod lineage, they are unusual among actinopterygians. In contrast, the existence of DAergic groups in the subpallium and pretectum is abundant among actinopterygians but it is not a common feature of amniotes. Some of these inter-group differences has been attributed to brain function adaptations to the different types of vertebrate lifes (Yamamoto and Vernier, 2011).
Here, we show that the CAergic system of N. furzeri shares the general spatial organization observed among actinopterygians, in particular in the teleost group. However, the killifish shows some distinct features compared with other teleosts. Next, we discuss from a comparative perspective, the main conserved and divergent features of the organization of the CAergic system of N. furzeri.
Telencephalon
Olfactory Bulb
The rostralmost TH+ cells in the forebrain of N. furzeri are found in the OB. The presence of DAergic cells in the OB is a constant feature among vertebrates and in mammals, according to the classical nomenclature, they correspond to the group A16 (Björklund and Lindvall, 1984; Hökfelt et al., 1984). In mice, dopamine exerts a negative regulatory role on olfactory inputs, inhibiting the release of glutamate to favor discrimination between odorants (Kruzich and Grandy, 2004). This function seems to be conserved in different taxa and has been described in fish such as goldfish (Kawai et al., 2012). The density and distribution of CAergic neurons in the layers of the OB is variable among vertebrates. While in mammals DAergic cells are more abundant in the glomerular and external layers, in teleosts they predominate in the deeper layers (Alonso et al., 1989; Batten et al., 1993; Smeets and Gonzalez, 2000). The latter organization is considered a primitive condition in vertebrates and is the most widespread among teleosts. However, there are several exceptions where cells adopt more external locations, such as in the case of zebrafish (Byrd and Brunjes, 1995), the ovoviviparous fishes Poencilla reticulata and Gambusia affinis (Parafati et al., 2009; Bhat and Ganesh, 2017), and the electric fish Apteronotus leptorhynchus (Sas et al., 1990). The origin of these cytoarchitectonic variations is unknown, but it appears to be a derived condition present in a few teleosts and possibly related to the way CAergic neurons integrate the chemosensitive information in these species (Parafati et al., 2009). In our study, we found that killifish TH+ cells adopt a peripheral position in the OB, being located primarily in the outermost layers. The significance of this distribution in the OB and whether it responds to an adaptation to the particular ecological niche of N. furzeri remain to be investigated.
Telencephalic Hemispheres
Similar to other teleosts, the killifish brain does not contain TH+ neurons in the pallium but it does in the subpallium. The presence of DAergic cells in the subpallium is an ancestral feature and has been described in cyclostomes, chondrichthyans, and all actinopterygians (Yamamoto and Vernier, 2011). In contrast, these cells are absent in sarcopterygians such as lungfishes, and among tetrapods they have been only reported in monotremes and primates (Betarbet et al., 1997; Manger et al., 2002; Lopez and Gonzalez, 2017). The function of the subpallial CAergic neurons is unknown, but it has been proposed they project locally and provide DA to this region (Huot et al., 2007). Likewise, in the N. furzeri a substantial fraction of the subpallial TH+ neurons showed confined projections to the ventral telencephalic area.
Diencephalon
Preoptic Region
The distribution of CAergic neurons in the preoptic region of N. furzeri is similar to other fish, including cyclostomes, chondrichthyans, actinopterygians, and sarcopterygians (Meredith and Smeets, 1987; Reiner and Northcutt, 1992; Wicht and Northcutt, 1994; Ma, 2003; Bhat and Ganesh, 2017; Lopez and Gonzalez, 2017). In teleosts such as zebrafish, PO DAergic neurons send extensive projections to the pituitary resembling the tuberohypophyseal system of mammals (A14, A15; Kaslin and Panula, 2001; Filippi et al., 2010). At a functional level, the most anteroventral TH+ cells of the PO (PPa) regulate the release of luteinizing hormone from the adenohypophysis (Kah et al., 1984; Fontaine et al., 2015; Bryant et al., 2016). Likewise, the PPa TH+ neurons of killifish send long-range projections to the ventral hypothalamus and apparently reach the hypophysis (Supplementary Figures 2B,C). However, it remains to be determined whether these CAergic neurons also have a regulatory role in reproduction.
Ventral Thalamus and Pretectum
The thalamus of N. furzeri contains TH+ neurons in its VT. DAergic cells are commonly found in this brain region in elasmobranchs, chondrosteans, cladistians, holosteans, and teleosts (Adrio et al., 2002; Lopez et al., 2019; Lozano et al., 2019). In mammals, a comparable population of CAergic cells are located in the zona incerta and corresponds to the A13 group (Meister et al., 1987; Smeets and Gonzalez, 2000). Remarkably, DAergic neurons in the VT of zebrafish and the prethalamic groups described in mammals share the same transcription factors (Arx and Isl1) during development suggesting they are homologous groups. However, at the functional level such homology is less clear (Filippi et al., 2012).
In the pretectal region (PPv) of N. furzeri exists conspicuous group of CAergic neurons with dendritic extension to the OT. The pretectal DAergic cells are frequently found in bony fishes and amniotes, with the exception of mammals (Smeets and Gonzalez, 2000). These cells could be implicated in the modulation of the retino-tectal visual input (Yamamoto and Vernier, 2011).
Posterior Tuberculum and Hypothalamus
Nothobranchius furzeri exhibits different groups of CAergic neurons in the posterior tuberculum that are similar in terms of morphology and projection pattern to other teleosts (Kaslin and Panula, 2001; Rink and Wullimann, 2001; Forlano and Sisneros, 2016; Karoubi et al., 2016; Bhat and Ganesh, 2017) and other groups of fish such as cyclostomes (Pierre et al., 1997), elasmobranchs (Molist et al., 1993), holosteans (Lozano et al., 2019), chondrosteans (Adrio et al., 2002), and cladistians (Reiner and Northcutt, 1992; Lopez et al., 2019). Studies in zebrafish and in Polypterus senegalus demonstrated that some of these neurons project onto a region homologous to the mammalian striatum (Reiner and Northcutt, 1992; Rink and Wullimann, 2001; Tay et al., 2011) and degenerate in toxic-induced models of PD (Sallinen et al., 2009). Furthermore, zebrafish TP neurons require NR4A2/Nurr1 for their development, in the same way that DAergic neurons of the mammalian substantia nigra/ventral tegmental area (SN/VTA) do (Blin et al., 2008). These findings, added to the lack of DAergic groups in the mesencephalon of actinopterygians, have led to the proposal that part of the neurons of the TP correspond to the A9/A10 groups of mammals. On the other hand, a subgroup of large TH+ cells in the posterior tuberculum of zebrafish projects to the hindbrain and sc, and modulate motor and sensory activity (Tay et al., 2011; Reinig et al., 2017). In addition, these neurons require Nkx2.1 and Otp for their differentiation as also observed for the A11 neurons of mice (Ryu et al., 2007). Thereby, it has been suggested that different subpopulations of DAergic neurons that coexist in the posterior tuberculum of teleosts resemble the A9/A10 and A11 groups of mammals (Yamamoto and Vernier, 2011). Consistent with this proposal, we found that killifish contains different subgroups of TH+ neurons in the posterior tuberculum that either send ascending projections in direction to the telencephalon or descending projections to the medulla oblongata. Previously, Matsui et al. (2019) reported that the large TH+ neurons located in the TP suffer an age-dependent degeneration and accumulate α-synuclein aggregates, thus reinforcing the idea that this group shares similar properties to the DAergic neurons of the mammalian SN.
The distribution of TH+ cells in the hypothalamus of N. furzeri seems to be less conserved compared to other teleosts. The killifish lacks TH immunoreactivity in the PVO and only has positive neurons in the Hc. The presence of cerebrospinal CSF-c containing monoamine in the PVO occurs in most vertebrates, but is reduced in the tetrapod lineage and even absent in placental mammals (Xavier et al., 2017). In zebrafish, the PVO CSF-c mainly express the th2 transcript of the TH enzyme, however, a group of neurons located in the most rostral region of the PVO expresses th1 (Yamamoto et al., 2010). By contrast, the holosteans and sarcopterygians also contain DAergic cells in the PVO, but they use the th2 enzyme and thus lack immunoreactivity with common TH antibodies (Lopez and Gonzalez, 2017; Lozano et al., 2019). We found that the PVO of killifish is TH negative, but we cannot rule out the existence of th2 DAergic CSF-c in this region. The functional significance of DAergic neurons in the PVO is not clear, but they seem to play a role in deep brain photoreception in non-mammalian vertebrates (Vigh et al., 2002). Furthermore, unlike other teleosts that present a more extended TH labeling in the basal hypothalamus (Rink and Wullimann, 2001), the CAergic neurons of killifish are restricted to the Hc. Likewise as the PVO, the TH+ cells in the Hc are absent in mammals and only are observed in some groups of actinopterygians (Xavier et al., 2017). In zebrafish, two different population of CSF-c co-exist in this region, one that expresses th1 and the other th2 gene. The latter group seems to play a specific role in fishes associated with the initiation of swimming behavior (McPherson et al., 2016). Instead, the th1 cluster appears to have a functional correlate with the A14 group of mammals, based on their projections (Tay et al., 2011). The TH+ cells in the Hc of killifish also send local processes on the ventral hypothalamus as seen for the Hc cluster in zebrafish. Thus, it is possible that this group also corresponds to the A14 cells of the mammals.
Mesencephalon
Strikingly, a small group of lightly stained TH+ cells is detected in the rostral mesencephalic tegmentum of N. furzeri, near the ventricle and dorsal to the oculomotor nucleus. The absence of DAergic neurons in the mesencephalic tegmentum is a common trait of cyclostomes and most species of actinopterygians (Lopez et al., 2019), with a few exceptions that include the holostean Amia calva and Lepisosteus osseus (Parent and Northcutt, 1982; Lozano et al., 2019), the cladistia Polypterus senegalus (Lopez et al., 2019) and the teleost Anguilla Anguilla (Roberts et al., 1989). This mesencephalic group differs in terms of location and morphology from the SN/VTA found in the elasmobranchs, lungfish and tetrapods (Smeets and Gonzalez, 2000; Lopez and Gonzalez, 2017). The connectivity and functional significance of this CAergic cluster is still unknown.
Rhombencephalon
Dorsal Rhombencephalon
In the rostral rhombencephalon, N. furzeri shows a small population of large TH+ cells with ventral projections. These neurons belong to the LC. The CAergic cells of the LC constitute a conserved group among vertebrates and are the main source of noradrenaline (NA) in the CNS (Smeets and Gonzalez, 2000). In mammals, the LC is recognized as the A6 group and innervates widely the brain and the sc. Given the complex and vast projections of the LC, this nucleus is associated with a wide range of functions including cardiovascular control, olfactory and auditory information processing, endocrine control, nociception, arousal state and motor behavior, among others (Aston-Jones and Bloom, 1981). A similar connectivity has been described for the LC in teleosts (Ma, 1994a,b; Tay et al., 2011). Although the role of this noradrenergic (NAergic) group is less clear in fishes, a recent study in zebrafish shows that the LC mediates wakefulness through the hypocretin-induced arousal system (Singh et al., 2015).
Medulla Oblongata
Three groups of TH+ neurons are observed in the caudal rhombencephalon of N. furzeri, along the medulla oblongata spanning the vagal lobe and the AP. Comparable NAergic neurons have been described in the caudal hindbrain of other teleosts, holosteans, cladistians and lungfish (Ma, 1997; Kaslin and Panula, 2001; Lopez and Gonzalez, 2017; Lopez et al., 2019; Lozano et al., 2019). In mammals, the NAergic neurons of the medulla oblongata correspond to the A1-A2 group and are involved in sympathetic functions such as the control of arterial pressure, respiratory pacemaking and response to pH (Freiria-Oliveira et al., 2015). It has been proposed that the NAergic neurons in the caudal rombencephalon have a conserved function in vertebrates (Smeets and Gonzalez, 2000).
Spinal Cord
The ventral aspect of the sc in N. furzeri houses small TH+ neurons, located away from the central canal. Two types of sc DAergic cells have been described in vertebrates, one with CSF-c characteristics and the other lacking contacts with the central canal. The former type is widely distributed in fish and has been reported in cyclostomes (lampreys), elasmobranchs (rays), teleosts (not in zebrafish), holosteans, cladistians and lungfish, but are absent in mammals (Roberts and Meredith, 1987; Sueiro et al., 2004; Rodicio et al., 2008; Lopez and Gonzalez, 2017; Lopez et al., 2019; Lozano et al., 2019). The second type has only been detected in lampreys, the eel Anguilla anguilla and in a few mammals as rats and monkeys (Roberts et al., 1989; Smeets and Gonzalez, 2000; Rodicio et al., 2008). The significance of CAergic neurons in the sc is not fully understood, but could contribute to modulation of spinal reflexes, nociception and locomotion (Smeets and Gonzalez, 2000). The TH+ sc neurons in the killifish do not appear to contact the central canal and it remains to be determined whether they correspond to the second neuronal type described in other species.
Retina
The retina of N. furzeri displays a discrete number of TH+ neurons in the INL, which according to their morphology appear to correspond to amacrine cells (Gatta et al., 2014). The presence of TH+ amacrine cells has been described in almost all vertebrates studied to date and in mammals constitute the group A17. The DAergic amacrine cells play a conserved role in retinal adaptation to light through the regulation of retinomotor movements and changes in the size of the receptive field (Masland, 2001).
Concluding Remarks
Nothobranchius furzeri belongs to the teleosts, one of the largest taxa among vertebrates with large variability in brain neuroanatomical structure as a result of extreme specialized behaviors. Despite this variability, teleost fish have a common organization of the CArgic system that in turn is largely conserved with other vertebrates. In this context, killifish shares the same basic pattern seen in other teleosts. However, unlike other members of this group such as zebrafish, killifish shows a more limited number of TH+ groups in the hypothalamus and has CAergic neurons in the sc. Furthermore, the killifish shows a particular group of CAergic neurons in the mesencephalic tegmentum that is an unusual trait among actinopterygians. Future studies will provide a more detailed analysis of the ontogeny, neurotransmitter phenotype (DA, NA) and the afferent/efferent connections of the different TH+ groups of N. furzeri, to dissect the functional correlate with CAergic neuronal groups of other species.
Data Availability Statement
The original contributions presented in the study are included in the article/Supplementary Material, further inquiries can be directed to the corresponding author/s.
Ethics Statement
The animal study was reviewed and approved by Bioethics Committee of the Faculty of Medicine, University of Chile (CICUA certificate number: 20385-MED-UCH).
Author Contributions
MLC and JB conceived and designed the work. JB and AO-P performed the tissue processing and immunofluorescence assays. JB, PA-G, AO-P, CA-C, PH, and MLC contributed to the analysis of the data and created the figures. MLC supervised the work and provided funds. JB and MLC wrote the manuscript with critical revision from PA-G and PH. All authors contributed to the article and approved the submitted version.
Funding
This work was funded by the following projects of the Chilean National Agency for Research and Development (ANID): Millennium Institute ICN09_015 to MLC and PA-G; FONDAP 15150012 to MLC, JB, and CA-C; FONDEQUIP EQM130051 to MLC; and Ring PIA ACT-192015 to MLC.
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.
Publisher’s Note
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.
Acknowledgments
We thank the support of the annual killifish facility of the Faculty of Medicine, University of Chile, jointly funded by ICBM, GERO, and BNI.
Supplementary Material
The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fnana.2021.728720/full#supplementary-material
Abbreviations
AP, area postrema; Cant, commissura anterior; Cb, cerebellum; CC, cerebellar crest; CCe, corpus of cerebellum; Dc1-2-3-4, central zone of dorsal telencephalon 1–4; Dd, dorsal zone of dorsal telencephalon; Dien, diencephalon; DIL, diffuse nucleus of inferior lobe; Dld, dorso-lateral zone of dorsal telencephalon; Dll, laterol-lateral zone of dorsal telencephalon; Dlv, ventro-lateral zone of dorsal telencephalon; Dm1-2-3-4, medial zone of dorsal telencephalon 1–4; ECL, external cellular layer; Ed, dorsal entopeduncular nucleus; EG, granular eminence; gc, griseum centrale; GCL, ganglion cell layer; gl, glomerular layer; GL, glomerular layer of the olfactory bulb; Ha, habenular nucleus; Hc, caudal hypothalamus; Hv, ventral hypothalamus; ICL, internal cellular layer; IMRF, intermediate reticular formation; INL, inner nuclear layer; IPL, inner plexiform layer; IRF, inferior reticular formation; LC, locus coeruleus; lfb, lateral forebrain bundle; llf, lateral longitudinal fascicle; lt, longitudinal tract; LVII, facial lobe; LX, vagal lobe; Mes, mesencephalon; mlf, medial longitudinal fascicle; MO, medulla oblongata; MON, medial octavolateralis nucleus; NG, glomerular nucleus; NIII, oculomotor nucleus; nV, nerve V; OB, olfactory bulb; ON, optic nerve; ONL, outer nuclear layer; OPL, outer plexiform layer; OS, outer segment; OT, optic tectum; PGc, central preglomerular nucleus; PGZ, periglomerular gray zone; PM, magnocellular preoptic nucleus; PO, preoptic area; poht, preopticohypothalamic tract; PPa, anterior preoptic nucleus; PPp, parvocellular portion of preoptic nucleus; PPv, ventral periventricular pretectal nucleus; PTN, posterior tuberal nucleus; PVO, paraventricular organ; PVOa, paraventricular organ-accompanying cells; rec, posterior recess; Rh, rhomboenchephalon; sc, spinal cord; SC, suprachiasmatic nucleus; Sp, subpallium; SRF, superior reticular formation; tegm, mesencephalic tegmentum; Tel, telencephalon; Tl, torus longitudinalis; TPp, periventricular nucleus of posterior tuberculum; TS, torus semicircularis; V, ventricle; Va, valvula of cerebellum; Vd, dorsal zone of ventral telencephalon; Vp, posterior zone of ventral telencephalon; Vs, supracommissural zone of ventral telencephalon; VT, ventral thalamic nucleus; Vv, ventral zone of ventral telencephalon.
Footnotes
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Keywords: tyrosine hydroxylase, catecholaminergic system, aging, annual killifish, Nothobranchius furzeri, teleosts
Citation: Borgonovo J, Ahumada-Galleguillos P, Oñate-Ponce A, Allende-Castro C, Henny P and Concha ML (2021) Organization of the Catecholaminergic System in the Short-Lived Fish Nothobranchius furzeri. Front. Neuroanat. 15:728720. doi: 10.3389/fnana.2021.728720
Received: 21 June 2021; Accepted: 13 August 2021;
Published: 13 September 2021.
Edited by:
Mónica Folgueira, University of A Coruña, SpainReviewed by:
Livia D’Angelo, University of Naples Federico II, ItalyBusisiwe Constance Maseko, University of the Witwatersrand, South Africa
Copyright © 2021 Borgonovo, Ahumada-Galleguillos, Oñate-Ponce, Allende-Castro, Henny and Concha. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Miguel L. Concha, bWNvbmNoYUB1Y2hpbGUuY2w=