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[Ac-D-NAL(2)1,4FD-Phe2,D-Trp3,D-Arg6]-LHRH,一种促性腺激素释放激素(LHRH)的强效拮抗剂,可在大鼠中引起短暂性水肿和行为变化。

[Ac-D-NAL(2)1,4FD-Phe2,D-Trp3,D-Arg6]-LHRH, a potent antagonist of LHRH, produces transient edema and behavioral changes in rats.

作者信息

Schmidt F, Sundaram K, Thau R B, Bardin C W

出版信息

Contraception. 1984 Mar;29(3):283-9. doi: 10.1016/s0010-7824(84)80008-6.

Abstract

Acute toxicity studies of [Ac-D-NAL(2)1,4FD-Phe2,D-Trp3,D-Arg6]-LHRH (LHRH-A), a potent antagonist of LHRH were performed. Subcutaneous administration of this peptide to rats induced transient edema of the face and extremities. This effect was maximal 3-5 h after peptide administration and subsided by 24 h. These effects were not seen with an LHRH agonist or two other antagonists. This side effects of LHRH-A was peculiar to rats and not observed in mice, rabbits and rhesus monkeys. Intravenous administration led within minutes to depression of spontaneous activity in rats and monkeys. We conclude that some LHRH antagonists produce species specific effects on vascular permeability and spontaneous activity.

摘要

对促性腺激素释放激素(LHRH)的强效拮抗剂[Ac-D-NAL(2)1,4FD-Phe2,D-Trp3,D-Arg6]-LHRH(LHRH-A)进行了急性毒性研究。给大鼠皮下注射该肽会引起面部和四肢的短暂水肿。这种效应在肽给药后3至5小时达到最大,并在24小时内消退。LHRH激动剂或其他两种拮抗剂未观察到这些效应。LHRH-A的这种副作用是大鼠特有的,在小鼠、兔子和恒河猴中未观察到。静脉注射在几分钟内导致大鼠和猴子的自发活动受到抑制。我们得出结论,一些LHRH拮抗剂对血管通透性和自发活动产生种属特异性影响。

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