Oxygen chemoreceptor inhibition by dopamine D<sub>2</sub> receptors in isolated zebrafish gills

Dopamine is an essential modulator of oxygen sensing and control of ventilation and is the most well described and abundant neurotransmitter in the mammalian carotid body. Little is known of the evolutionary significance of dopamine in oxygen sensing, or whether it plays a similar role in anamniotes. In the model vertebrate, zebrafish (Danio rerio), presynaptic dopamine D<sub>2</sub> receptor (D<sub>2</sub>R) expression was demonstrated in gill neuroepithelial cells (NECs), analogues of mammalian oxygen chemoreceptors; however, a mechanism for dopamine and D<sub>2</sub>R in the gills had not been defined. The present study tested the hypothesis that presynaptic D<sub>2</sub>Rs provide a feedback mechanism attenuating the chemoreceptor response to hypoxia. Using an isolated gill preparation from Tg(elavl3:GCaMP6s) zebrafish, we measured hypoxia-induced changes in intracellular Ca<sup>2+</sup> concentration ([Ca<sup>2+</sup>]<sub>i</sub>) in NECs and postsynaptic neurons. Activation of D<sub>2</sub>R with dopamine or specific D<sub>2</sub>R agonist, quinpirole, decreased hypoxic responses in NECs; whereas D<sub>2</sub>R antagonist, domperidone, had the opposite effect. Addition of SQ22536, an adenylyl cyclase (AC) inhibitor, decreased the effect of hypoxia on [Ca<sup>2+</sup>]<sub>i</sub>, similar to dopamine. Activation of AC by forskolin partially recovered the suppressive effect of dopamine on the Ca<sup>2+</sup> response to hypoxia. Furthermore, we demonstrate that the response to hypoxia in postsynaptic neurons was dependent upon innervation with NECs, and was subject to modulation by activation of presynaptic D<sub>2</sub>R. Our results provide the first evidence of neurotransmission of the hypoxic signal at the NEC-nerve synapse in the gill and suggest that a presynaptic, modulatory role for dopamine in oxygen sensing arose early in vertebrate evolution. KEY POINTS: For the first time, we present an experimental model that permits imaging of intracellular Ca<sup>2+</sup> in identified oxygen chemoreceptors in zebrafish using GCaMP in a whole/intact sensing organ. The hypoxic response of zebrafish chemoreceptors is attenuated by dopamine through a mechanism involving D<sub>2</sub> receptors and adenylyl cyclase. Zebrafish oxygen chemoreceptors send a hypoxic signal to postsynaptic (sensory) neurons. Postsynaptic neuronal responses to hypoxia are modulated by presynaptic D<sub>2</sub> receptors, suggesting a link between chemoreceptor inhibition by dopamine and modulation of the hypoxic ventilatory response. Our results suggests that a modulatory role for dopamine in oxygen sensing arose early in vertebrate evolution.

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Publication Details

Journal
The Journal of Physiology
Published
2025-03-08
DOI
https://doi.org/10.1113/jp287824
Citations
5
Primary Topic
Neuroscience of respiration and sleep
Type
article
Field-Weighted Citation Impact
4.57
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article

Oxygen chemoreceptor inhibition by dopamine D2 receptors in isolated zebrafish gills

Maddison Reed, Michael G. Jonz
5 citations
The Journal of Physiology
Neuroscience of respiration and sleep
4.57
article

Oxygen chemoreceptor inhibition by dopamine D2 receptors in isolated zebrafish gills

Maddison Reed, Michael G. Jonz
article en
5 citations

Abstract

Dopamine is an essential modulator of oxygen sensing and control of ventilation and is the most well described and abundant neurotransmitter in the mammalian carotid body. Little is known of the evolutionary significance of dopamine in oxygen sensing, or whether it plays a similar role in anamniotes. In the model vertebrate, zebrafish (Danio rerio), presynaptic dopamine D<sub>2</sub> receptor (D<sub>2</sub>R) expression was demonstrated in gill neuroepithelial cells (NECs), analogues of mammalian oxygen chemoreceptors; however, a mechanism for dopamine and D<sub>2</sub>R in the gills had not been defined. The present study tested the hypothesis that presynaptic D<sub>2</sub>Rs provide a feedback mechanism attenuating the chemoreceptor response to hypoxia. Using an isolated gill preparation from Tg(elavl3:GCaMP6s) zebrafish, we measured hypoxia-induced changes in intracellular Ca<sup>2+</sup> concentration ([Ca<sup>2+</sup>]<sub>i</sub>) in NECs and postsynaptic neurons. Activation of D<sub>2</sub>R with dopamine or specific D<sub>2</sub>R agonist, quinpirole, decreased hypoxic responses in NECs; whereas D<sub>2</sub>R antagonist, domperidone, had the opposite effect. Addition of SQ22536, an adenylyl cyclase (AC) inhibitor, decreased the effect of hypoxia on [Ca<sup>2+</sup>]<sub>i</sub>, similar to dopamine. Activation of AC by forskolin partially recovered the suppressive effect of dopamine on the Ca<sup>2+</sup> response to hypoxia. Furthermore, we demonstrate that the response to hypoxia in postsynaptic neurons was dependent upon innervation with NECs, and was subject to modulation by activation of presynaptic D<sub>2</sub>R. Our results provide the first evidence of neurotransmission of the hypoxic signal at the NEC-nerve synapse in the gill and suggest that a presynaptic, modulatory role for dopamine in oxygen sensing arose early in vertebrate evolution. KEY POINTS: For the first time, we present an experimental model that permits imaging of intracellular Ca<sup>2+</sup> in identified oxygen chemoreceptors in zebrafish using GCaMP in a whole/intact sensing organ. The hypoxic response of zebrafish chemoreceptors is attenuated by dopamine through a mechanism involving D<sub>2</sub> receptors and adenylyl cyclase. Zebrafish oxygen chemoreceptors send a hypoxic signal to postsynaptic (sensory) neurons. Postsynaptic neuronal responses to hypoxia are modulated by presynaptic D<sub>2</sub> receptors, suggesting a link between chemoreceptor inhibition by dopamine and modulation of the hypoxic ventilatory response. Our results suggests that a modulatory role for dopamine in oxygen sensing arose early in vertebrate evolution.

The Journal of PhysiologyVol. 603(8)
University of Ottawa (CA)
Life below water
Openalex Percentile: Top 6%
Neuroscience of respiration and sleep
4.57
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