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

O Stücker, C Pons, J P Duverger, K Drieu, P D'Arbigny
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引用次数: 10

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.

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。
静脉注射银杏叶提取物(EGb 761)对血小板激活的血管痉挛反应的影响已经在麻醉小鼠的皮肤皮瓣制备中进行了评估。通过活体显微镜观察腋下动脉的小动脉,在常温(37℃)和低温(24℃)两种稳态条件下,局部应用ADP激活血小板。在静脉注射EGb 761或血栓素合成抑制剂(U63557)的动物中,还比较了局部应用血栓素激动剂(U46619)刺激皮肤小动脉的反应。ADP诱导对照动物小动脉收缩34%。然而,在血小板耗损动物(胶原诱导的血小板减少症)或egb761 (60 mg/kg,静脉注射)治疗的动物中,ADP没有引起小动脉收缩。在所有实验组动物中,将小动脉低温(24℃)暴露10分钟可引起7-12%的收缩。在这些低温条件下,EGb 761或血小板减少均能消除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可以抑制血小板激活引起的血管痉挛。由于局部应用U46619 (10(-5) M)诱导小动脉收缩(约22%),而静脉注射EGb 761可以消除这种收缩,因此该提取物似乎直接起作用,而不是作为血栓烷合成酶抑制剂。总的来说,这些发现表明血小板因子可以在皮肤血管痉挛中发挥重要作用,并且EGb 761通过对血栓素途径的作用,可以用于治疗雷诺现象和其他涉及血栓素产生增加的血管疾病。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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