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胆碱能通路在去窦神经大鼠中的参与情况。

Participation of cholinergic pathways in sinoaortic denervated rats.

作者信息

Taira C A, Enero M A

出版信息

Gen Pharmacol. 1985;16(2):145-8. doi: 10.1016/0306-3623(85)90053-9.

Abstract

Seven days after sinoaortic denervation (SAD), mean blood pressure (MBP) and heart rate measured in conscious rats were not significantly different from sham-operated animals. A high dose of atropine, 8 mg kg-1, reduced MBP only in SAD rats. Atropine, 0.08-0.8 mg kg-1, or methylatropine, 0.8 mg kg-1, induced tachycardia in sham rats. This effect was reduced after sinoaortic denervation and it involves peripheral muscarinic receptors. The hypertension and tachycardia provoked by physostigmine were more marked in SAD than in sham rats. The cardiovascular responses induced by physostigmine were abolished by atropine and were not affected by methylatropine. The hypertension caused by physostigmine in SAD animals was more sensitive to the antagonism of atropine than in sham rats. Our results show that baroreceptor deafferentation affects peripheral parasympathetic tone to the heart and changes the cholinergic pathways involved in the modulation of cardiovascular response.

摘要

在进行去窦主动脉神经支配(SAD)七天后,清醒大鼠的平均血压(MBP)和心率与假手术动物相比无显著差异。高剂量阿托品(8毫克/千克)仅使SAD大鼠的MBP降低。0.08 - 0.8毫克/千克的阿托品或0.8毫克/千克的甲基阿托品可使假手术大鼠出现心动过速。这种效应在去窦主动脉神经支配后减弱,且涉及外周毒蕈碱受体。毒扁豆碱引发的高血压和心动过速在SAD大鼠中比在假手术大鼠中更明显。毒扁豆碱诱导的心血管反应可被阿托品消除,且不受甲基阿托品影响。毒扁豆碱在SAD动物中引起的高血压比在假手术大鼠中对阿托品拮抗作用更敏感。我们的结果表明,压力感受器去传入会影响心脏的外周副交感神经张力,并改变参与心血管反应调节的胆碱能途径。

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