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L-组氨酸在体内对人血小板功能及花生四烯酸代谢的影响。

Effect of L-histidine in vivo on human platelet function and arachidonic acid metabolism.

作者信息

Steinhauer H B, Kluthe R, Lubrich I, Schollmeyer P

出版信息

Prostaglandins Leukot Med. 1985 May;18(2):245-54. doi: 10.1016/0262-1746(85)90024-1.

Abstract

The effect of the amino acid l-histidine on human platelet function and arachidonic acid metabolism was studied in 18 healthy subjects with increased spontaneous platelet aggregation. The participants received placebo or l-histidine 3g/day for 7 days. The intake of l-histidine reduced the degree of spontaneous platelet aggregation (p less than 0.05) and inhibited the generation of platelet TXB2 by 47% (p less than 0.001) whereas platelet PGE2 synthesis was not affected. The mean l-histidine plasma concentration increased from 83.1 +/- 2.4 to 108 +/- 8.1 mumol/l (p less than 0.01) during the study. L-histidine was found to be an effective inhibitor of spontaneous platelet aggregation and platelet TXB2 generation. The present data verify interactions of histidine with human platelet function, probably mediated by arachidonic acid metabolites.

摘要

在18名自发性血小板聚集增加的健康受试者中,研究了氨基酸L-组氨酸对人血小板功能和花生四烯酸代谢的影响。参与者接受安慰剂或每日3克L-组氨酸,持续7天。摄入L-组氨酸降低了自发性血小板聚集程度(p<0.05),并抑制血小板TXB2生成达47%(p<0.001),而血小板PGE2合成未受影响。研究期间,L-组氨酸血浆平均浓度从83.1±2.4微摩尔/升增加至108±8.1微摩尔/升(p<0.01)。发现L-组氨酸是自发性血小板聚集和血小板TXB2生成的有效抑制剂。目前的数据证实了组氨酸与人血小板功能之间的相互作用,可能由花生四烯酸代谢产物介导。

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