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促肾上腺皮质激素释放因子对大鼠爪皮肤热损伤的保护作用。

Protective actions of corticotropin-releasing factor on thermal injury to rat pawskin.

作者信息

Wei E T, Serda S, Tian J Q

机构信息

School of Public Health, University of California, Berkeley.

出版信息

J Pharmacol Exp Ther. 1988 Dec;247(3):1082-5.

PMID:3264573
Abstract

Corticotropin-releasing factor (CRF), a 41-residue peptide, inhibits the edema and protein extravasation produced by heat applied to the rat pawskin. Here, the time course of CRFs actions against heat-induced swelling was investigated. The paws of pentobarbital-anesthetized rats were immersed in 58 degrees C water for 30 sec and the resultant swelling was measured by the fluid displacement method. Human/rat CRF, 28 micrograms/kg s.c., injected 0.5 to 2 hr before heat exposure reduced swelling by over 50%. Pretreatment at 4 hr before heat was also effective, but not at 12 or 24 hr. CRF, injected 28 micrograms/kg i.v. 0, 10 or 20 min after heat exposure, inhibited the progressive development of swelling immediately. Histological examination of skin showed that CRF, given before or after heat, reduced vesication, edema, epidermal necrosis and the disruption of tissue architecture produced by thermal injury. The alpha-helical CRF(9-41) antagonist administered alone, 92 micrograms/kg i.v., before or after heat did not affect heat injury. The antagonist, however, both prevented and reversed the inhibitory effects of CRF on the swelling produced by heat. The antagonist-induced reversal occurred as late as 2 hr after CRF, 28 micrograms/kg s.c. Overall, these results suggested that CRF is a potent and efficacious agent in protecting skin against experimental thermal injury.

摘要

促肾上腺皮质激素释放因子(CRF)是一种由41个氨基酸残基组成的肽,它能抑制热刺激大鼠爪皮肤所产生的水肿和蛋白质外渗。在此,对CRF抗热诱导肿胀作用的时间进程进行了研究。将戊巴比妥麻醉大鼠的爪子浸入58摄氏度的水中30秒,并用液体置换法测量由此产生的肿胀。在热暴露前0.5至2小时皮下注射28微克/千克的人/大鼠CRF,可使肿胀减少超过50%。在热暴露前4小时进行预处理也有效,但在12或24小时则无效。在热暴露后0、10或20分钟静脉注射28微克/千克的CRF,可立即抑制肿胀的进行性发展。皮肤的组织学检查表明,在热暴露之前或之后给予CRF,可减少水疱形成、水肿、表皮坏死以及热损伤所导致的组织结构破坏。单独静脉注射92微克/千克的α-螺旋CRF(9-41)拮抗剂,无论在热暴露之前还是之后,均不影响热损伤。然而,该拮抗剂既能预防又能逆转CRF对热诱导肿胀的抑制作用。拮抗剂诱导的逆转作用在皮下注射28微克/千克CRF后2小时仍会出现。总体而言,这些结果表明CRF是一种有效且高效的保护皮肤免受实验性热损伤的药物。

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