Detection of hypoxia-evoked ATP release from chemoreceptor cells of the rat carotid body

被引:98
作者
Buttigieg, J [1 ]
Nurse, CA [1 ]
机构
[1] McMaster Univ, Dept Biol, Hamilton, ON L8S 4K1, Canada
基金
加拿大创新基金会; 加拿大健康研究院; 加拿大自然科学与工程研究理事会;
关键词
carotid body slice; hypoxia; ATP release; type I cells; bioluminescence; iberiotoxin; nifedipine; neurotransmitter;
D O I
10.1016/j.bbrc.2004.07.081
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The carotid body (CB) is a chemosensory organ that detects changes in chemical composition of arterial blood and maintains homeostasis via reflex control of ventilation. Thus, in response to a fall in arterial PO2 (hypoxia), CB chemoreceptors (type I cells) depolarize, and release neurotransmitters onto afferent sensory nerve endings. Recent studies implicate ATP as a key excitatory neurotransmitter released during CB chemoexcitation, but direct evidence is lacking. Here we use the luciferin-luciferase bioluminescence assay to detect ATP, released from rat chemoreceptors in CB cultures, fresh tissue slices, and whole CB. Hypoxia evoked an increase in extracellular ATP, that was inhibited by L-type Ca2+ channel blockers and reduced by the nucleoside hydrolase, apyrase. Additionally, iberiotoxin (IbTX; 100 nM), a blocker of O-2-sensitive Ca2+-dependent K+ (BK) channels, stimulated ATP release and largely occluded the effect of hypoxia. These data strongly support a neurotransmitter role for ATP in carotid body function. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:82 / 87
页数:6
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