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交感胆碱能通路在组织型纤溶酶原激活物释放至血液的神经源性控制中的作用。

Role of sympathetic cholinergic pathway in the neurogenous control of tissue-type plasminogen activator release into the blood.

作者信息

Bashkov G V, Medvedeva N A

机构信息

National Haematological Scientific Centre, Moscow, Russia.

出版信息

Blood Coagul Fibrinolysis. 1993 Dec;4(6):993-8.

PMID:7908542
Abstract

The changes in conductivity of skeletal muscle vessels of the hind leg and tissue-type plasminogen activator (t-PA) activity in outflowing blood after electrostimulation (5 V, 0.5 ms, 20 Hz, 30 s) at the L4-L5 level of the peripheral end of the transected isolated sympathetic chain were studied in experiments on anaesthetized cats. Stimulation of the sympathetic chain induced vasoconstriction and release of t-PA from the vascular wall into the blood. Pretreatment with the beta-adrenoblocker propranolol neither changed the character of vascular reactions nor blocked t-PA secretion. Efferent stimulation of the sympathetic chain against a background of alpha-adrenoceptor blockade by dihydroergotoxin increased blood flow and was accompanied by a rise in t-PA activity. The M-cholinergic blocker atropine suppressed both vascular relaxation and release of t-PA into the blood. Vasodilatation accompanied by t-PA secretion could be induced by intraarterial infusion of acetylcholine and blocked by atropine. The existence of a neurogenic mechanism controlling t-PA release from the vascular wall involving a sympathetic cholinergic pathway and connected with excitation of vascular M-cholinoceptors by acetylcholine is suggested.

摘要

在麻醉猫的实验中,研究了在横断的孤立交感神经链外周端的L4-L5水平进行电刺激(5V,0.5ms,20Hz,30s)后,后腿骨骼肌血管的电导率变化以及流出血液中的组织型纤溶酶原激活物(t-PA)活性。刺激交感神经链可引起血管收缩以及t-PA从血管壁释放到血液中。用β-肾上腺素能阻滞剂普萘洛尔预处理既不改变血管反应的特征,也不阻断t-PA的分泌。在二氢麦角毒素对α-肾上腺素能受体进行阻断的背景下,对交感神经链进行传出刺激可增加血流量,并伴有t-PA活性升高。M胆碱能阻滞剂阿托品可抑制血管舒张以及t-PA释放到血液中。动脉内注入乙酰胆碱可诱导伴有t-PA分泌的血管舒张,并被阿托品阻断。提示存在一种神经源性机制,该机制通过交感胆碱能途径控制t-PA从血管壁的释放,并与乙酰胆碱对血管M胆碱受体的兴奋有关。

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