INVOLVEMENT OF MUSCARINIC M1 RECEPTOR IN THE CENTRAL PATHWAY OF THE SEROTONIN-INDUCED BEZOLD-JARISCH REFLEX IN RATS

被引:13
作者
SAITO, K [1 ]
YOSHIOKA, M [1 ]
KOHYA, T [1 ]
KITABATAKE, A [1 ]
机构
[1] HOKKAIDO UNIV, SCH MED, DEPT PHARMACOL 1, SAPPORO 060, JAPAN
来源
JOURNAL OF THE AUTONOMIC NERVOUS SYSTEM | 1994年 / 49卷 / 01期
关键词
BEZOLD-JARISCH REFLEX; VAGUS NERVE ACTIVITY; 5-HYDROXYTRYPTAMINE (SEROTONIN); MUSCARINIC RECEPTOR; PIRENZEPINE;
D O I
10.1016/0165-1838(94)90021-3
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The involvement of central muscarinic receptors in mediating the Bezold-Jarisch reflex elicited by injection of 5-hydroxytryptamine (5-HT) was studied in urethane/chloralose-anesthetized rats. Intravenous bolus injection of 5-HT (3.1 to 50 mu g/kg) evoked a short-lasting dose-related bradycardia and hypotension, the Bezold-Jarisch reflex, accompanied with bursts of the efferent cervical vagus nerve. Systemic administration of atropine (0.1 and 1 mg/kg) blocked not only the cardiac responses but also the efferent cervical vagus nerve activity changes. Although the afferent cervical vagus nerve was also activated by an intravenous bolus injection of 5-HT, these responses were not altered by the systemic administration of even a high dose of atropine (1 mg/kg). Intracerebroventricular (i.c.v.) administration of pirenzepine (1 and 10 mu g/10 mu l), a selective M, receptor antagonist, caused a rightward shift of the 5-HT dose-response curve for efferent vagus nerve activity. In contrast, i.c.v. administration of muscarinic type 2 receptor antagonist, gallamine, and type 3 receptor antagonist, p-fluorohexahydrosiladifenidol, failed to alter the response in nerve activity to 5-HT. These results suggest that the activation of central nervous muscarinic receptors might be involved in mediating the Bezold-Jarisch reflex and that the subtype might belong to type 1.
引用
收藏
页码:61 / 68
页数:8
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