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血小板活化因子的分子异质性:病理生物学意义

PAF molecular heterogeneity: pathobiological implications.

作者信息

McManus L M, Woodard D S, Deavers S I, Pinckard R N

机构信息

Department of Pathology, University of Texas Health Science Center, San Antonio.

出版信息

Lab Invest. 1993 Dec;69(6):639-50.

PMID:8264227
Abstract

The existence and potential (patho)physiologic significance of PAF molecular heterogeneity can no longer be summarily dismissed or ignored. While significant advances in the chemistry of PAF have been made, the (patho)physiologic behaviors of most of the PAF molecular species of biologic origin await further study. This is because to date, investigators have studied the biologic activities of what was previously thought to be PAF, i.e., only 16:0- and 18:0-AGEPC. In view of the evidence presented in this review, a comprehensive investigation of the possible biologic relevance and significance of PAF molecular heterogeneity is warranted. Hopefully, such studies will be designed to elucidate the extent to which the various molecular species of PAF differ in their intrinsic in vitro and in vivo (patho)physiologic behaviors (agonistic, synergistic, and possibly antagonistic) and modes of action. Once this additional information has been derived, the pathobiologic relevance of this class of phospholipid autacoid may be better understood.

摘要

血小板活化因子(PAF)分子异质性的存在及其潜在的(病理)生理意义再也不能被一概而论地忽视或忽略了。虽然PAF化学方面已取得重大进展,但大多数生物来源的PAF分子种类的(病理)生理行为仍有待进一步研究。这是因为迄今为止,研究人员研究的是以前被认为是PAF的生物活性,即仅16:0 - 和18:0 - 乙酰基甘油醚磷酸胆碱(AGEPC)。鉴于本综述中提供的证据,有必要对PAF分子异质性可能的生物学相关性和意义进行全面研究。希望此类研究将旨在阐明PAF的各种分子种类在其内在体外和体内(病理)生理行为(激动、协同以及可能的拮抗)和作用方式上的差异程度。一旦获得这些额外信息,这类磷脂自分泌调节因子的病理生物学相关性可能会得到更好的理解。

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