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Carbon monoxide: a role in carotid body chemoreception.
Author(s) -
Nanduri R. Prabhakar,
Jay Dinerman,
Faton Agani,
Solomon H. Snyder
Publication year - 1995
Publication title -
proceedings of the national academy of sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.011
H-Index - 771
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.92.6.1994
Subject(s) - carotid body , glomus cell , heme oxygenase , heme , zinc protoporphyrin , brainstem , chemoreceptor , protoporphyrin , chemistry , carbon monoxide , biochemistry , endogeny , medicine , endocrinology , biology , enzyme , neuroscience , receptor , porphyrin , stimulation , catalysis
Carbon monoxide (CO), produced endogenously by heme oxygenase, has been implicated as a neuronal messenger. Carotid bodies are sensory organs that regulate ventilation by responding to alterations of blood oxygen, CO2, and pH. Changes in blood gases are sensed by glomus cells in the carotid body that synapse on afferent terminals of the carotid sinus nerve that projects to respiratory-related neurons in the brainstem. Using immunocytochemistry, we demonstrate that heme oxygenase 2 is localized to glomus cells in the cat and rat carotid bodies. Physiological studies show that zinc protoporphyrin IX, a potent heme oxygenase inhibitor, markedly increases carotid body sensory activity, while copper protoporphyrin IX, which does not inhibit the enzyme, is inactive. Exogenous CO reverses the stimulatory effects of zinc protoporphyrin IX. These results suggest that glomus cells are capable of synthesizing CO and endogenous CO appears to be a physiologic regulator of carotid body sensory activity.

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