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糖皮质激素受体拮抗剂Org 34850对皮质酮释放快速和延迟反馈的影响。

Effect of the glucocorticoid receptor antagonist Org 34850 on fast and delayed feedback of corticosterone release.

作者信息

Spiga Francesca, Harrison Louise R, Wood Susan A, MacSweeney Cliona P, Thomson Fiona J, Craighead Mark, Grassie Morag, Lightman Stafford L

机构信息

Henry Wellcome Laboratories for Integrative Neuroscience and Endocrinology, University of Bristol, Whitson Street, Bristol BS1 3NY, UK.

出版信息

J Endocrinol. 2008 Feb;196(2):323-30. doi: 10.1677/JOE-07-0503.

Abstract

We investigated the effect of the glucocorticoid receptor (GR) antagonist Org 34850 on fast and delayed inhibition of corticosterone secretion in response to the synthetic glucocorticoid methylprednisolone (MPL). Male rats were implanted with a catheter in the right jugular vein, for blood sampling and MPL administration, and with an s.c. cannula for Org 34850 administration. All experiments were conducted at the diurnal hormonal peak in the late afternoon. Rats were connected to an automated sampling system and blood samples were collected every 5 or 10 min. Org 34850 (10 mg/kg, s.c.) or vehicle (5% mulgofen in saline) was injected at 1630 h; 30 min later, rats received an injection of MPL (500 microg/rat, i.v.) or saline (0.1 ml/rat). We found that an acute administration of MPL rapidly decreased the basal corticosterone secretion and this effect was not prevented by acute pretreatment with Org 34850. However, blockade of GR with Org 34850 prevented delayed inhibition of MPL on corticosterone secretion measured between 4 and 12 h after MPL administration. Our data suggest an involvement of GR in modulating delayed, but not fast, inhibition induced by MPL on basal corticosterone secretion.

摘要

我们研究了糖皮质激素受体(GR)拮抗剂Org 34850对合成糖皮质激素甲泼尼龙(MPL)刺激下皮质酮分泌快速和延迟抑制的影响。雄性大鼠在右颈静脉植入导管用于采血和注射MPL,并在皮下植入套管用于注射Org 34850。所有实验均在下午晚些时候的昼夜激素高峰时段进行。大鼠连接至自动采样系统,每5或10分钟采集一次血样。在1630时皮下注射Org 34850(10 mg/kg)或溶剂(5%吐温80生理盐水溶液);30分钟后,大鼠静脉注射MPL(500 μg/只)或生理盐水(0.1 ml/只)。我们发现,急性注射MPL可迅速降低基础皮质酮分泌,且Org 34850急性预处理不能阻止这种作用。然而,Org 34850阻断GR可防止MPL给药后4至12小时测量的皮质酮分泌延迟抑制。我们的数据表明,GR参与调节MPL诱导的基础皮质酮分泌的延迟抑制,但不参与快速抑制。

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