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体外实验中糖皮质激素对脂肪组织前列腺素释放的抑制作用。

Inhibition by glucocorticoids of prostaglandin release from adipose tissue in vitro.

作者信息

Chang J, Lewis G P, Piper P J

出版信息

Br J Pharmacol. 1977 Mar;59(3):425-32. doi: 10.1111/j.1476-5381.1977.tb08396.x.

Abstract

1 When rabbit chopped adipose tissue was incubated with a lipolytic agent (adrenocorticotrophic hormone, ACTH1-24, 0.1 microng/ml) in Krebs solution, prostaglandin E2 was formed in the tissue and about the same amount was found in the medium. 2 In the presence of indomethacin (1 microng/ml) the appearance of prostaglandin E2 was almost abolished both in the tissue and in the medium. 3 When the incubation was carried out in the presence of hydrocortisone or betamethasone (1-10 microng)ml) the concentration of prostaglandin E2 leaking or carried into the medium was significantly reduced, whereas that remaining in the tissue was significantly increased. This action of the steroids was not reversed by increasing substrate (arachidonic acid) concentration in the medium. 4 The steroids did not affect lipolysis, nor did they influence prostaglandin metabolism since such activity was not detectable in the adipose tissue. 5 Anti-inflammatory steroids therefore did not reduce prostaglandin formation but increased the tissue/medium ratio, which supports the view that they inhibit the release of prostaglandins after these have been synthesized.

摘要
  1. 当将兔的切碎脂肪组织与一种脂解剂(促肾上腺皮质激素,促肾上腺皮质激素1 - 24,0.1微克/毫升)在 Krebs 溶液中孵育时,组织中会形成前列腺素 E2,并且在培养基中也发现了大致相同的量。2. 在吲哚美辛(1微克/毫升)存在的情况下,组织和培养基中前列腺素 E2 的出现几乎被消除。3. 当在氢化可的松或倍他米松(1 - 10微克/毫升)存在的情况下进行孵育时,泄漏到培养基中或被带入培养基中的前列腺素 E2 浓度显著降低,而留在组织中的浓度则显著增加。增加培养基中底物(花生四烯酸)的浓度并不能逆转类固醇的这种作用。4. 类固醇不影响脂解作用,也不影响前列腺素代谢,因为在脂肪组织中未检测到这种活性。5. 因此,抗炎类固醇不会减少前列腺素的形成,而是增加了组织/培养基的比例,这支持了这样一种观点,即它们在前列腺素合成后抑制其释放。

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2
Glucocorticoid effect on the prostaglandin system in fat tissue.
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Inhibition of prostaglandin release by antiinflammatory steroids.
Adv Prostaglandin Thromboxane Res. 1976;1:121-4.

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Br Med J. 1972 Aug 19;3(5824):452-3. doi: 10.1136/bmj.3.5824.452.

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