Role of peripheral adenosine A1 receptors in the regulation of sleep apneas in rats

被引:7
作者
Carley, DW
Radulovacki, M
机构
[1] Univ Illinois, Coll Med, Dept Med, Chicago, IL 60612 USA
[2] Univ Illinois, Coll Med, Dept Pharmacol, Chicago, IL 60612 USA
关键词
N-6-p-sulfophenyladenosine (p-SPA); 8-(p-sulfophenyl)theophylline (p-SPT); central sleep apneas; rats;
D O I
10.1006/exnr.1999.7167
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The effects of administration of N-6-p-sulfophenyladenosine (p-SPA), a peripheral adenosine A(1) receptor agonist, and 8-(p-sulfophenyl)theophylline (p-SPT), a peripheral adenosine A(1) receptor blocker, on spontaneous apneas were studied in 10 adult Sprague-Dawley rats by monitoring respiration, sleep, and blood pressure for 6 h. Intraperitoneal injection of p-SPA (1 mg/kg) to rats suppressed spontaneous central apneas during non-rapid eye movement sleep by 50% in comparison to control recordings (p = 0.03). This effect was blocked by pretreatment with an equimolar dose of p-SPT (0.67 mg/kg) indicating that p-SPA suppression of apneas was receptor mediated in the peripheral nervous system. Administration of p-SPA did not affect apnea expression in rapid eye movement sleep and had no effect on sleep or blood pressure at the dose tested. Administration of p-SPT (0.67, 6.7, and 30 mg/kg) to rats had no effect on apneas, sleep, or blood pressure. The lack of p-SPT effect on sleep apneas argues against a physiologic role for endogenous adenosine in the peripheral nervous system as a modulator of sleep apnea expression under baseline conditions. (C) 1999 Academic Press.
引用
收藏
页码:545 / 550
页数:6
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