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[前列腺素与血栓素]

[Prostaglandins and thromboxanes].

作者信息

Falardeau P, Martineau A, Gagnon D

出版信息

Sem Hop. 1984 Apr 12;60(16):1117-36.

PMID:6326304
Abstract

Prostaglandins and thromboxanes are 20-carbon-atom-chain fatty acids which contain a cyclopentane or oxane nucleus respectively. They belong to a family of icosanoids whose main intracellular precursor is arachidonic acid. These icosanoids are synthetized in all tissues (except red cells). Enzymatic hydrolysis of the arachidonic acid of lipids is the first step of their biosynthesis. This step, which is limitative, is usually catalyzed by phospholipase A2 and may be indirectly inhibited by glucocorticoids. Once released, arachidonic acid is promptly transformed into an endoperoxide intermediary through the action of an enzymatic complex called "cyclooxygenase". This intermediary is the precursor of both prostaglandins and thromboxane. Non-steroidal antiinflammatory agents such as acetylsalicylic acid and indomethacin have an inhibitory action on cyclooxygenase. The mechanisms of action of prostaglandins and thromboxane are still poorly understood. In certain tissues (platelets, adipose cells) their effect seems to involve stimulation of adenyl-cyclase and/or guanyl-cyclase. In other tissues (smooth muscle) their biological action is associated with changes in transcellular flows of calcium. Prostaglandins and thromboxane have many biological properties. Their effects are local, as they are produced in small quantities and promptly metabolized. They act more often as cell function modulators than as essential mediators. The often conflicting biological actions of these icosanoids involve: a) smooth muscles (stimulation or relaxation of blood vessel, respiratory tract, digestive tract and genitourinary tract musculatures); b) platelets (induction or inhibition of aggregation); c) the inflammatory reaction; d) the cellular fluid and electrolyte transports; e) and certain metabolic functions (lipolysis, insulin release, renin release, mobilization of bone calcium...). The advances achieved over the last decade now provide some insight into the significance of the physiologic role of icosanoids. Several prostaglandins, as well as some of their analogues, are already being used as therapeutic agents. In the future, rational manipulation of dietary fatty acids and development of selective inhibitors can be expected to provide the necessary tools for better controlling the icosanoid system in medicine.

摘要

前列腺素和血栓素是分别含有环戊烷或氧杂环核的20个碳原子链的脂肪酸。它们属于类二十烷酸家族,其主要细胞内前体是花生四烯酸。这些类二十烷酸在所有组织(红细胞除外)中合成。脂质中花生四烯酸的酶促水解是其生物合成的第一步。这一步是限速步骤,通常由磷脂酶A2催化,并且可能被糖皮质激素间接抑制。一旦释放,花生四烯酸通过一种称为“环氧化酶”的酶复合物的作用迅速转化为内过氧化物中间体。这种中间体是前列腺素和血栓素的前体。非甾体抗炎药如乙酰水杨酸和吲哚美辛对环氧化酶有抑制作用。前列腺素和血栓素的作用机制仍知之甚少。在某些组织(血小板、脂肪细胞)中,它们的作用似乎涉及刺激腺苷酸环化酶和/或鸟苷酸环化酶。在其他组织(平滑肌)中,它们的生物学作用与钙的跨细胞流动变化有关。前列腺素和血栓素有许多生物学特性。它们的作用是局部的,因为它们少量产生并迅速代谢。它们更多地作为细胞功能调节剂而不是必需介质起作用。这些类二十烷酸经常相互矛盾的生物学作用包括:a)平滑肌(血管、呼吸道、消化道和泌尿生殖道肌肉组织的刺激或松弛);b)血小板(诱导或抑制聚集);c)炎症反应;d)细胞液和电解质转运;e)以及某些代谢功能(脂肪分解、胰岛素释放、肾素释放、骨钙动员……)。过去十年取得的进展现在为了解类二十烷酸生理作用的重要性提供了一些见解。几种前列腺素及其一些类似物已经被用作治疗剂。未来,合理控制膳食脂肪酸和开发选择性抑制剂有望为更好地控制医学中的类二十烷酸系统提供必要的工具。

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