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过敏毒素诱导的血小板聚集及其抑制作用。

Platelet aggregation induced by anaphylatoxin and its inhibition.

作者信息

Benner K U, Schumacher K A, Classen H G

出版信息

Arzneimittelforschung. 1975 Oct;25(10):1635-8.

PMID:812506
Abstract

Anaphylatoxin (AT), a splitting product of the fifth component of the complement system can be prepared by incubation of rat plasma with low-molecular weight dextran (MW 2000) at 37 degrees C, or by treatment with cobra venom factor. Using the turbidimetric method of Born the effect of AT was studied on platelets from man, dog, rabbit, cat, guinea pig, and rat. AT was found to induce aggregation only in platelet rich plasma from cat and guinea pig. This aggregation could be reduced by several known inhibitors of aggregation and platelet function, such as phentolamine, tosylarginine-methylester (TAMe), p-chloromercuribenzoate (PCMB), and ethylenediamine-tetraacetic acid (EDTA) whereas adenosine, methysergide-bimaleinate, and mepyramine-maleate proved to be ineffective. Experiments with PCMB and TAMe suggest a release reaction induced by AT. Further more, there is evidence that with platelets from guinea pigs AT produces some tachyphylactic state.

摘要

过敏毒素(AT)是补体系统第五成分的裂解产物,可通过将大鼠血浆与低分子量葡聚糖(分子量2000)在37℃孵育,或用眼镜蛇毒因子处理来制备。采用博恩比浊法研究了AT对人、狗、兔、猫、豚鼠和大鼠血小板的作用。发现AT仅能诱导猫和豚鼠富含血小板血浆中的血小板聚集。这种聚集可被几种已知的聚集和血小板功能抑制剂所抑制,如酚妥拉明、甲苯磺酰精氨酸甲酯(TAMe)、对氯汞苯甲酸(PCMB)和乙二胺四乙酸(EDTA),而腺苷、马来酸麦角新碱和马来酸美吡拉敏则无效。PCMB和TAMe的实验提示AT诱导了一种释放反应。此外,有证据表明,对于豚鼠血小板,AT会产生某种快速耐受状态。

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