肾上腺素能神经元阻滞剂对肾上腺素诱导血小板反应的影响。

Acta biologica et medica Germanica Pub Date : 1982-01-01
E Glusa, F Markwardt
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引用次数: 0

摘要

肾上腺素通过刺激类似于α 2型的α -肾上腺素受体而引起人类血小板聚集。-肾上腺素受体阻滞剂可特异性抑制肾上腺素诱导的血小板反应。肾上腺素能神经元阻滞剂如guanoxan、guanclofine和guanethidine可特异性抑制肾上腺素诱导的人血小板聚集。Guanoxan (I50 = 0.6 mu mol/l)的有效性比guanethidiine高约3个数量级,guanclofine处于中位。所测试的化合物在相对高浓度下抑制ADP和胶原诱导的聚集。这可能是由于非特异性膜效应。已知的guanoxan的α -肾上腺素溶解作用主要是由α - 2肾上腺素受体介导的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Influence of adrenergic neuron blocking agents on the adrenaline-induced platelet reactions.

Adrenaline causes aggregation of human blood platelets through stimulation of alpha-adrenoceptors resembling the alpha 2-type. Alpha-adrenoceptor blocking agents inhibit specifically the adrenaline-induced platelet reactions. The adrenaline-induced aggregation of human blood platelets was inhibited specifically by adrenergic neuron blocking agents such as guanoxan, guanclofine and guanethidine. Guanoxan (I50 = 0.6 mu mol/l) was about three orders of magnitude more effective than guanethidine, guanclofine occupied a median position. The compounds tested inhibited the ADP- and collagen-induced aggregation at relatively high concentrations. This is probably due to non-specific membrane effects. The known alpha-adrenolytic effect of guanoxan is believed to be mediated mainly by alpha 2-adrenoceptors.

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