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银杏叶提取物(EGb 761)对小鼠皮肤小动脉对血小板活化的血管痉挛反应的影响。

Effect of Ginkgo biloba extract (EGb 761) on the vasospastic response of mouse cutaneous arterioles to platelet activation.

作者信息

Stücker O, Pons C, Duverger J P, Drieu K, D'Arbigny P

机构信息

CEROM, Paris, France.

出版信息

Int J Microcirc Clin Exp. 1997 Mar-Apr;17(2):61-6. doi: 10.1159/000179208.

Abstract

The effect of intravenously administered Ginkbo biloba extract (EGb 761) on the vasospastic response to platelet activation has been assessed using a cutaneous flap preparation in anaesthetized mice. Arterioles of the axillary artery were observed by intravital microscopy, and platelets were activated by topical application of ADP under two steady state conditions: normothermia (37 degrees C) and hypothermia (24 degrees C). Responses of the cutaneous arterioles to stimulation by topical application of a thromboxane agonist (U46619) were also compared in animals treated intravenously with EGb 761 or with a thromboxane synthesis inhibitor (U63557). ADP induced a 34% constriction of the arterioles in control animals. However, no arteriolar constriction occurred in response to ADP in platelet-depleted animals (collagen-induced thrombocytopenia) or in animals treated with EGb 761 (60 mg/kg, i.v.). Exposure of the arterioles to hypothermia (24 degrees C) for 10 min induced constriction of 7-12% in all experimental groups of animals. Under these hypothermic conditions, either EGb 761 or thrombocytopenia abolished ADP-induced arteriolar constriction which was substituted by arteriolar dilation, indicating that EGb 761 can inhibit the vasospasm that is produced by platelet activation. As topically applied U46619 (10(-5) M) induced arterioles constriction (about 22%) that was abolished by intravenous treatment with EGb 761, the extract appears to act directly rather than as a thromboxane synthase inhibitor. Collectively, these findings indicate that platelet factors can play a significant role in cutaneous vasospasm, and that EGb 761, via an action on the thromboxane pathway, could be useful in treating Raynaud's phenomenon and other vascular disorders which involve increased thromboxane production.

摘要

在麻醉小鼠身上,通过皮瓣制备评估了静脉注射银杏叶提取物(EGb 761)对血小板激活所致血管痉挛反应的影响。利用活体显微镜观察腋动脉的小动脉,并在两种稳态条件下通过局部应用ADP激活血小板:正常体温(37摄氏度)和低温(24摄氏度)。还比较了静脉注射EGb 761或血栓素合成抑制剂(U63557)的动物中,皮动脉对局部应用血栓素激动剂(U46619)刺激的反应。在对照动物中,ADP可使小动脉收缩34%。然而,在血小板减少的动物(胶原诱导的血小板减少症)或接受EGb 761(60毫克/千克,静脉注射)治疗的动物中,ADP刺激未引起小动脉收缩。将小动脉暴露于低温(24摄氏度)10分钟,在所有实验组动物中均诱导7%-12%的收缩。在这些低温条件下,EGb 761或血小板减少症均消除了ADP诱导的小动脉收缩,取而代之的是小动脉扩张,这表明EGb 761可抑制血小板激活产生的血管痉挛。由于局部应用U46619(10^-5 M)可诱导小动脉收缩(约22%),而静脉注射EGb 761可消除该收缩,因此该提取物似乎是直接发挥作用,而非作为血栓素合酶抑制剂。总体而言,这些发现表明血小板因子在皮肤血管痉挛中可发挥重要作用,并且EGb 761通过作用于血栓素途径,可能有助于治疗雷诺现象和其他涉及血栓素产生增加的血管疾病。

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