[Prostaglandins and thromboxanes].

P Falardeau, A Martineau, D Gagnon
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引用次数: 0

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.

[前列腺素和凝血烷]。
前列腺素和血栓烷是20碳原子链脂肪酸,分别含有环戊烷或氧烷核。它们属于类二十烷酸家族,其主要的细胞内前体是花生四烯酸。这些类二十烷酸可以在所有组织中合成(红细胞除外)。脂质花生四烯酸的酶解是其生物合成的第一步。这一步骤是限制性的,通常由磷脂酶A2催化,并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“环加氧酶”的酶复合物的作用迅速转化为内过氧化物中间体。这种中间物是前列腺素和凝血素的前体。非甾体类抗炎药如乙酰水杨酸和吲哚美辛对环氧合酶有抑制作用。前列腺素和凝血素的作用机制尚不清楚。在某些组织(血小板、脂肪细胞)中,其作用似乎涉及刺激腺苷环化酶和/或鸟苷环化酶。在其他组织(平滑肌)中,它们的生物作用与钙的跨细胞流动变化有关。前列腺素和凝血素具有许多生物学特性。它们的作用是局部的,因为它们产生的量很少,而且能迅速代谢。它们更多的是作为细胞功能调节剂而不是必不可少的介质。这些类二十烷酸经常相互冲突的生物作用包括:a)平滑肌(刺激或放松血管、呼吸道、消化道和泌尿生殖系统肌肉组织);B)血小板(诱导或抑制聚集);C)炎症反应;D)细胞液体和电解质的运输;E)和某些代谢功能(脂肪分解、胰岛素释放、肾素释放、骨钙动员……)。在过去的十年中取得的进展,现在提供了一些见解的重要性的生理作用的类二十烷酸。几种前列腺素及其类似物已经被用作治疗药物。未来,膳食脂肪酸的合理调控和选择性抑制剂的开发有望为医学上更好地控制类二十烷酸系统提供必要的工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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