Tetrandrine, an alkaloid from S. tetrandra exhibits anti-hypertensive and sleep-enhancing effects in SHR via different mechanisms
Tetrandrine, an alkaloid from S. tetrandra exhibits anti-hypertensive and sleep-enhancing effects in SHR via different mechanisms
复制标题
粉防己碱是一种来自粉防己的生物碱，通过不同的机制在 SHR 中表现出抗高血压和促进睡眠的作用。
DOI：
10.1016/j.phymed.2016.10.021
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发表时间：
2016-12-15
期刊：
影响因子：
7.9
通讯作者：
Zhang, Yong-He
中科院分区：
文献类型：
--
作者：
Huang, Yuan-Li;Cui, Su-Ying;Zhang, Yong-He
Background: Sleep disorders have been found to be associated with hypertension in both cross- sectional and longitudinal epidemiological studies. Tetrandrine, a major component of Stephania tetrandra, is well known as an antihypertensive agent. The anti- hypertension mechanism mainly relies on its L- type calcium channel blocking property. In the previous study, tetrandrine revealed both anti- hypertension and hypnotic effects in spontaneously hypertensive rats (SHRs).Purpose: This study aims to elucidate whether the antihypertensive mechanism of tetrandrine in SHRs is relevant to its hypnotic effect. Design/Methods: Sleep- wake behavior of the SHRs was detected by electroencephalography (EEG) and electromyography (EMG) recordings. Blood pressure was measured by noninvasive blood pressure tail cufftest. Immunohistochemistry was performed to evaluate the noradrenergic neuronal activity. The level of norepinephrine (NE) was detected by HPLC- ECD.Results: Amlodipine (100 mg/kg, i.g.), the well- known L- type Ca2+ channel blockers (CCBs) exhibited remarkable antihypertensive activities in SHRs, but did not show effects on sleep of SHRs. Tetrandrine (30 and 60 mg/kg/day, i.g.) significantly suppressed blood pressure of SHRs. Meanwhile, tetrandrine (60 mg/kg/day, i.g.) remarkably increased non- rapid eye movement sleep (NREMS) time, bouts and mean duration. The hypnotic effect of tetrandrine was potentiated by prazosin (0.5 mg/kg, i. p.) but attenuated by yohimbine (2 mg/kg, i.p.). Administration of tetrandrine (60 mg/kg/day, i.g.) not only significantly decreased c- Fos positive ratio of noradrenergic neurons in the locus coeruleus (LC), but also significantly decrease NE in the endogenous sleep- wake regulating pathways including LC, hypothalamus and ventrolateral preoptic nucleus (VLPO).Conclusion: In spite of a good potency in blocking L-type Ca2+ channel, the hypnotic effects of tetrandrine may be related to its suppressing effects on the noradrenergic system other than to block calcium channels. As a multi- targets drug, tetrandrine might be favorable to the hypertension patients who suffered poor sleep. (C) 2016 Elsevier GmbH. All rights reserved.
