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髓鞘碱性蛋白及其他碱性多肽引起的血小板形状改变。

Shape change of blood platelets brought about by myelin basic protein and other basic polypeptides.

作者信息

Laubscher A, Pletscher A, Honegger C G, Richards J G

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 1979 Dec;310(1):87-92. doi: 10.1007/BF00499878.

Abstract

Basic proteins and polypeptides (BPP) such as myelin basic protein (MBP), polyornithine (M.W. 40,000), polylysine and protamine, which are known to cause neuronal depolarization in the central nervous system, induced a shape change reaction in blood platelets of various species, including man. This reaction was not accompanied by platelet aggregation or marked alterations of 5-hydroxytryptamine release. Cyclic nucleotide levels were also unchanged. The shape change induced by polyornithine was inhibited by heparin but not by antagonists of 5HT, catecholamines or gamma-aminobutryic acid, substances which are known to have no effect on the MBP-induced neuronal depolarization. Other basic substances, e.g. low molecular weight polyornithine (M.W. 4,000), cytochrome c, spermine and spermidine, did not induce either platelet shape change or (as shown before) neuronal depolarization. It is concluded, that 1) the shape change reaction of platelets seems to be a sensitive and simple means of detecting those BPP which induce functional changes in mammalian cells and 2) the use of platelets as models for neurons can be extended to include the action of BPP on the plasma membranes.

摘要

诸如髓鞘碱性蛋白(MBP)、聚鸟氨酸(分子量40,000)、聚赖氨酸和鱼精蛋白等碱性蛋白质和多肽(BPP),已知它们会在中枢神经系统中引起神经元去极化,在包括人类在内的各种物种的血小板中诱导了形状变化反应。该反应不伴有血小板聚集或5-羟色胺释放的明显改变。环核苷酸水平也未改变。聚鸟氨酸诱导的形状变化被肝素抑制,但不被5-羟色胺、儿茶酚胺或γ-氨基丁酸的拮抗剂抑制,这些物质已知对MBP诱导的神经元去极化没有影响。其他碱性物质,例如低分子量聚鸟氨酸(分子量4,000)、细胞色素c、精胺和亚精胺,既不诱导血小板形状变化,也不(如之前所示)诱导神经元去极化。得出的结论是,1)血小板的形状变化反应似乎是检测那些在哺乳动物细胞中诱导功能变化的BPP的一种敏感且简单的方法,并且2)将血小板用作神经元模型可以扩展到包括BPP对质膜的作用。

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