Activation of P2X receptors for adenosine triphosphate evokes cardiorespiratory reflexes in anaesthetized rats

被引:65
作者
McQueen, DS
Bond, SM
Moores, C
Chessell, I
Humphrey, PPA
Dowd, E
机构
[1] Univ Edinburgh, Sch Med, Dept Pharmacol, Edinburgh EH8 9JZ, Midlothian, Scotland
[2] Univ Edinburgh, Sch Med, Dept Anaesthet, Edinburgh EH8 9JZ, Midlothian, Scotland
[3] Univ Cambridge, Dept Pharmacol, Glaxo Inst Appl Pharmacol, Cambridge CB2 1QJ, England
来源
JOURNAL OF PHYSIOLOGY-LONDON | 1998年 / 507卷 / 03期
关键词
D O I
10.1111/j.1469-7793.1998.843bs.x
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
1. We tested the hypothesis that activation of P2X receptors associated with vagal afferent nerves can evoke a Bezold-Jarisch (B-J) depressor reflex in anaesthetized rats. 2. Injection of alpha beta-methylene ATP (alpha beta-MeATP; 0.6-600 nmol I.V.) evoked a dose-dependent B-J reflex comprising bradycardia, hypotension and apnoea in rats anaesthetized with pentobarbitone. Apnoea was commonly preceded by hyperventilation. Bilateral vagotomy significantly reduced the bradycardia and most of the apnoeic response without affecting hyperventilation, and unmasked a vasopressor response. Hypotension and apnoea were subject to desensitization, and ATP Mras about 100 times less potent than alpha beta-MeATP in evoking the B-J reflex. 3. ED50 values for responses to alpha beta-MeATP were: bradycardia 14.6 +/- 3.8 nmol; apnoea 47.1 +/- 8.5 nmol; hyperventilation 23.3 +/- 6.0 nmol, n = 14. The ED50 for apnoea was significantly greater than that for bradycardia or hyperventilation (P < 0.05). Atropine (2.8 mu mol (kg body wt)(-1) I.V.) antagonized the reflex bradycardia and hypotension. 3. The P2 antagonists suramin (14 mu mol (kg body wt)(-1) I.V.) and PPADS (17 mu mol (kg body wt)(-1) I.V.) antagonized the bradycardic and apnoeic components of the reflex response to alpha beta-MeATP, without reducing the vasopressor or hyperventilatory responses to the agonist. 4. Recordings from vagal afferents showed that pulmonary inflation receptors were activated by alpha beta-MeATP in 62% of units recorded (ED50 22 +/- 5 nmol) and this was blocked by PPADS (17 mu mol (kg body wt)(-1) I.V.); unidentified vagal afferents were also activated. 5. alpha beta-MeATP activated carotid chemoreceptor afferents (ED50 23 +/- 9 nmol), an action that was unaffected by PPADS or suramin. 6. The results support the hypothesis that P2X receptor subtypes for ATP are associated with specific sensory nerves that form part of the homeostatic mechanism for cardiovascular and respiratory regulation and these receptors therefore have physiological, pathological and therapeutic significance.
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页码:843 / 855
页数:13
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