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Muscarinic Acetylcholine Receptor-2 in the Cerebellar Fastigial Nucleus is Involved in Acetylcholine-Mediated Blood Pressure Regulation in Rats
被引:1
|作者:
Zhou, Peiling
[1
,2
]
Liao, Ge
[1
,2
]
Zhong, Qiulin
[1
,2
]
Wen, Qingyun
[1
,2
]
Gao, Guowei
[1
,2
]
Zhang, Changzheng
[1
,2
]
机构:
[1] Lingnan Normal Univ, Dept Psychol, Cunjing Rd 29, Zhanjiang 524048, Guangdong, Peoples R China
[2] Lingnan Normal Univ, Key Lab Psychol Assessment & Rehabil Except Child, Cunjing Rd 29, Zhanjiang 524048, Guangdong, Peoples R China
关键词:
blood pressure;
depressor response;
acetylcholine;
muscarinic ACh receptor-2;
inward current;
CHOLINERGIC INNERVATION;
DEPRESSOR RESPONSE;
CORTEX;
BRAIN;
NEURONS;
REGION;
D O I:
10.1134/S1819712419020168
中图分类号:
Q189 [神经科学];
学科分类号:
071006 ;
摘要:
Our previous investigations have revealed that microinjection of acetylcholine (ACh) into the cerebellar fastigial nucleus (FN) induces a systemic blood pressure (BP) depressor response and that the muscarinic ACh (mACh) receptor contributes substantially to this process. This study was determined to explore the role of muscarinic ACh receptor-2 (M2 receptor) in ACh-mediated BP regulation and its underlying electrophysiological mechanism. ACh mixed with methoctramine hydrate (MCT, a selective M2 receptor antagonist) and normal saline (0.9% NaCl) were separately microinjected into the FN of anaesthetized rats, and the mean arterial pressure during the reactive time (the duration for BP to return to its basal level) was calculated; the responses of cholinergic reagents to the inward currents in FN neurons were also examined via patch-clamp recording in vitro; in addition, the receptor expression in the FN was confirmed by immunohistochemistry. The results demonstrated that MCT effectively blocked the ACh-mediated BP depressor response and the ACh-induced inward currents in FN neurons; moreover, M2 receptors were unequivocally distributed in the FN. Taken together, the results indicate that M2 receptors in the FN may be involved in ACh-mediated BP down-regulation by tuning neuronal excitation.
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页码:195 / 200
页数:6
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