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Hypoxic cardiorespiratory reflexes in the facultative air-breathing fish jeju (Hoplerythrinus unitaeniatus): role of branchial O2 chemoreceptors
Authors:Jane Mello Lopes  Cheila de Lima Boijink  Luiz Henrique Florindo  Cleo Alcantara Costa Leite  Ana Lúcia Kalinin  William K Milsom  Francisco Tadeu Rantin
Institution:1. Department of Physiological Sciences, Federal University of S?o Carlos, Via Washington Luiz, km 235, S?o Carlos, SP, 13565-905, Brazil
2. Department of Zoology and Botany, Aquaculture Center (CAUNESP), S?o Paulo State University, UNESP, S?o José do Rio Preto, SP, 15054-000, Brazil
4. National Institute of Science and Technology in Comparative Physiology (INCT-FAPESP/CNPq), S?o Paulo, Brazil
3. Department of Zoology, University of British Columbia, Vancouver, BC, Canada
Abstract:In one series of experiments, heart frequency (f H), blood pressure (P a), gill ventilation frequency (f R ), ventilation amplitude (V AMP) and total gill ventilation (V TOT) were measured in intact jeju (Hoplerythrinus unitaeniatus) and jeju with progressive denervation of the branchial branches of cranial nerves IX (glossopharyngeal) and X (vagus) without access to air. When these fish were submitted to graded hypoxia (water PO2 ~140, normoxia to 17 mmHg, severe hypoxia), they increased f R , V AMP, V TOT and P a and decreased f H. In a second series of experiments, air-breathing frequency (f RA), measured in fish with access to the surface, increased with graded hypoxia. In both series, bilateral denervation of all gill arches eliminated the responses to graded hypoxia. Based on the effects of internal (caudal vein, 150 μg NaCN in 0.2 mL saline) and external (buccal) injections of NaCN (500 μg NaCN in 1.0 mL water) on f R , V AMP, V TOT, P a and f H we conclude that the O2 receptors involved in eliciting changes in gill ventilation and associated cardiovascular responses are present on all gill arches and monitor the O2 levels of both inspired water and blood perfusing the gills. We also conclude that air breathing arises solely from stimulation of branchial chemoreceptors and support the hypothesis that internal hypoxaemia is the primary drive to air breathing.
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