Jaime Eugenín
George B. Richerson- 1Departamento de Biología, Facultad de Química y Biología, Universidad de Santiago de Chile, USACH, Santiago, Chile
- 2Departments of Neurology and Molecular Physiology and Biophysics, University of Iowa, Iowa City, IA, United States
Editorial on the Research Topic
Alternative and expanding views on central respiratory chemoreception in health and disease
Central respiratory chemoreception is a fundamental brain function for adjusting breathing to physiological demands and for systemic CO2 and H+ homeostasis. Hence, failure in central chemoreception is a known feature of life-threatening human conditions such as Congenital Central Hypoventilation Syndrome (CCHS), Sudden Infant Death Syndrome (SIDS), and Rett Syndrome (RS) (Feldman et al., 2003; Kinney et al., 2009; Nattie and Li, 2012; Guyenet and Bayliss, 2022).
Several decades ago, pioneering work established that the ventral medullary surface contains three regions showing chemosensitivity to topical acidification, which were implied in the control of breathing (Severinghaus, 1998). These areas were named: M for the rostral area (after Robert Mitchell), S for the intermediate area (after Marianne Schläfke) and L for the caudal area (after Hans Loeschcke) (Severinghaus, 1998). In later studies, it was shown that acidification of other brainstem areas also triggered hyperventilation, suggesting that central respiratory chemoreceptors are widely distributed along the brain stem (Coates et al., 1993; Feldman et al., 2003; Nattie and Li, 2012). It was once believed central chemoreception involves only a limited number of specialized neurons in specific regions, but recently more varied hypotheses have been proposed. Thus, much of the recent experimental effort has been devoted to determining the type of cell and the molecular mechanisms that endows these cells with chemosensitivity. Although not exempt of controversies and, sometimes, in absence of definitive evidence, it seems that neurons and astrocytes play a crucial role as central chemoreceptors (Richerson et al.; Gourine et al., 2010; Beltran-Castillo et al.; Guyenet and Bayliss, 2022)
That a type of cell is a true respiratory chemoreceptor, implies that this cell intrinsically senses hypercapnia/acidosis and, because of this, activates the respiratory network. Accordingly, a set of five experimental criteria have been proposed to be necessary and sufficient for a particular type of cell to be a central respiratory chemoreceptor (Guyenet and Bayliss, 2022). These criteria are: “1) Cell-specific activation and inhibition have opposite effects on breathing; 2) Cell-specific inhibition blunts effects of CO2 on breathing; 3) Cell activity is CO2/H+-modulated in vivo; 4) Cell modulation by CO2/H+ is at least partly a direct effect; 5) Disrupting the mechanism for direct CO2/H+ sensing selectively in the presumptive chemoreceptor cell interferes with CO2-stimulated breathing” (Guyenet and Bayliss, 2022).
In the minireview by Gonye and Bayliss, the authors analyze the available evidence for retrotrapezoid nucleus (RTN), serotonergic raphe nucleus (RN), medullary astrocytes, locus coeruleus, and lateral hypothalamus to satisfy the five criteria for chemoreceptors. This is an interesting work that revealed that in all of the cases, despite great advances in their study, evidence is still lacking to assure unequivocally that each of these types of cell are true chemoreceptors. Although the criteria are reasonable and exacting, they are linked to the assumption that respiratory chemoreception resides on a single type of cell. Whether central respiratory chemoreception in a particular brainstem area emerges from interactions between different types of cells is an open question. For example, recent work suggests that serotonergic raphe neurons are essential for expression of chemosensory responses of other chemosensory neurons, like those in the RTN (Wu et al., 2019). Other chemoreceptor neurons may depend on interaction with astrocytes to fully express chemosensitivity.
Nowadays it is clear that central CO2/H+ -sensitive areas are not restricted to the brainstem (Nattie and Li, 2012; Vollmer et al., 2016). In fact, in the hypothalamus, one can find CO2-sensitive neurons that have been associated with panic disorder (Nattie and Li, 2012; Vollmer et al., 2016). As part of this Topic Research, Kinkead et al. reviewed how panic disorder can disrupt respiratory control and how stress, biological sex, and neuroendocrine mechanisms influence respiratory control underlying pathophysiology of panic disorder. This minireview implicitly embraces the idea that the function of structures generating central chemoreception also depends on and is modulated by other systems, like the neuroendocrine system. Furthermore, ventilatory effects and fear and escape behaviors seem intimately connected, since despite CO2 being able to increase ventilation at a lower threshold than panic associated-behaviors, in patients with panic disorder, CO2-thresholds for inducing hyperventilation, fear, and escape are lower, and the intensity of reactions is greater than that observed in controls.
The Topic Research also includes two experimental articles. The manuscript by Marciante et al. shows that during presumptive sleep, rTg4510 mice, that develop tauopathy initially in the hippocampus and cortex which then progresses to the brainstem, show disruption of the respiratory rhythm (sighs and apneas) and blunting of O2- and CO2-chemoreflexes. Breathing dysregulation was observed even before neurodegeneration was declared and the severity of breathing irregularity and impaired ventilatory chemoreflexes were age-dependent and strongly associated with the accumulation of hyperphosphorylated tau protein in respiratory-related brainstem areas. These results have translational implications, since human tauopathy patients present unstable breathing during sleep, and therefore these rTg4510 mice could be a relevant model for studying the biological mechanisms involved in respiratory dysfunction due to tauopathy.
The other experimental work reported by Eugenín et al. is focused on the phenotypical effects of prolonged hypercapnia upon microglia in brainstem and hippocampus. The authors show that 30 min of 10% CO2 in air induces the transformation of homeostatic microglia into reactive microglia in specific brainstem respiratory nuclei of C57BL/6 and CF-1 mice, but not in Sp5 and hippocampal microglia. Immunofluorescence detection of surface inflammatory or regulatory markers to recognize functional states of reactive microglia, as well as ELISA detection of inflammatory (IL1β) and regulatory (TGFβ) cytokines by microglia, revealed that, likely, hypercapnia-induced microglia acquire an inflammatory phenotype. These results, also have translational implications given that the high levels of CO2 selected for the experiments mimics conditions of hypercapnia found in several human breathing disorders, such as Obesity Hypoventilation Syndrome (Shah et al., 2021), Congenital Central Hypoventilation Syndrome (Schafer et al., 1999; Lamon et al., 2012), and Sleep Apnea Hypopnea Syndrome (Wu et al., 2019). Whether microglia could play either a role in human hypoventilation syndromes or they simply exacerbate inflammatory damage in hypoventilation syndromes, are open questions.
Thus, this Research Topic of papers emphasizes new evidence that points to a more complex set of mechanisms for respiratory chemoreception than has been favored in the field in the past and indicates that much more work needs to be done to understand this vital function in health and disease.
Author contributions
JE: Conceptualization, Funding acquisition, Writing–original draft, Writing–review and editing. GBR: Conceptualization, Funding acquisition, Investigation, Writing–original draft, Writing–review and editing.
Funding
The author(s) declare financial support was received for the research, authorship, and/or publication of this article. This work was supported by grant from the ANID-Programa Fondecyt Regular folio 1211359 (JE) and U01NS090414 and R01NS113764 (GBR).
Acknowledgments
We are grateful to all contributors, in particular the authors for generating an interesting and high-quality Research Topic. We also want to thank the reviewers for their comments and suggestions, which were constructive and useful for the clarity of the accepted works.
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
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References
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Keywords: central chemoreception, estrogen, panic disorder, hypercapnia, taupathy, alzheimer disease, reactive microglia, hypoventilation syndromes
Citation: Eugenín J and Richerson GB (2024) Editorial: Alternative and expanding views on central respiratory chemoreception in health and disease. Front. Physiol. 15:1403768. doi: 10.3389/fphys.2024.1403768
Received: 19 March 2024; Accepted: 26 March 2024;
Published: 05 April 2024.
Edited and reviewed by:
Andrew John Halayko, University of Manitoba, CanadaCopyright © 2024 Eugenín and Richerson. 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: Jaime Eugenín, amFpbWUuZXVnZW5pbkB1c2FjaC5jbA==