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从人腹水液中分离白细胞激肽-H和白细胞激肽原;它们的性质和作用。

The isolation of leukokinin-H and leukokininogen from human ascites fluid; their properties and role.

作者信息

Greenbaum L M, Semente G, Grebow P, Roffman S

出版信息

Adv Exp Med Biol. 1979;120B:205-14.

PMID:92880
Abstract

The leukokinin-leukokininogen system is a pathological kinin generating system which is catalyzed by acid proteases present in neoplastic cells, white cells and even normal tissues. The components of the human system including leukokinin-H and leukokininogen have now been isolated and characterized. Very specific protease inhibitors of the system such as pepstatin have been found and are now known to prevent "in vivo" the formation of pathological fluids such as neoplastic ascites. Strong evidence has been previously published and additional evidence has been presented here which indicates that pepstatin's actions are related to the inhibition of cathepsin-D in vivo and the inhibition of leukokinin formation. Both leukokinins and leukokininogens have been clearly defined and shown to differ from bradykinin and human bradykininogens. This clearly demonstrates the presence in pathological systems of a kinin-generating system which is separate and distinct from the bradykinin generating system. The importance of the leukokinin-leukokininogen system in disease would seem to be very great. The finding that pepstatin can inhibit the system in vivo opens the way for studies of pepstatin and related protease inhibitors as therapeutic agents in neoplastic disease and protease mediated inflammatory disorders.

摘要

白细胞激肽-白细胞激肽原系统是一种病理性激肽生成系统,由存在于肿瘤细胞、白细胞甚至正常组织中的酸性蛋白酶催化。包括白细胞激肽-H和白细胞激肽原在内的人类系统的组成成分现已被分离并鉴定。现已发现该系统非常特异的蛋白酶抑制剂,如胃酶抑素,并且已知其可在“体内”阻止病理性液体如肿瘤腹水的形成。先前已发表了有力证据,本文也提供了更多证据,表明胃酶抑素的作用与体内组织蛋白酶-D的抑制及白细胞激肽形成的抑制有关。白细胞激肽和白细胞激肽原均已得到明确界定,并显示与缓激肽和人缓激肽原不同。这清楚地证明在病理性系统中存在一个与缓激肽生成系统分开且不同的激肽生成系统。白细胞激肽-白细胞激肽原系统在疾病中的重要性似乎非常大。胃酶抑素可在体内抑制该系统这一发现为研究胃酶抑素及相关蛋白酶抑制剂作为肿瘤疾病和蛋白酶介导的炎症性疾病的治疗药物开辟了道路。

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