DIAZEPAM BINDING INHIBITOR (DBI) INCREASES AFTER ACUTE STRESS IN RAT

被引：55

作者：

FERRARESE, C ^{[1
]}

MENNINI, T ^{[1
]}

PECORA, N ^{[1
]}

PIERPAOLI, C ^{[1
]}

FRIGO, M ^{[1
]}

MARZORATI, C ^{[1
]}

GOBBI, M ^{[1
]}

BIZZI, A ^{[1
]}

CODEGONI, A ^{[1
]}

GARATTINI, S ^{[1
]}

FRATTOLA, L ^{[1
]}

机构：

[1] MARIO NEGRI INST PHARMACOL RES,I-20157 MILAN,ITALY

来源：

NEUROPHARMACOLOGY | 1991年 / 30卷 / 12B期

关键词：

DBI; STRESS; BENZODIAZEPINES; STEROIDOGENESIS;

D O I：

10.1016/S0028-3908(11)80015-8

中图分类号：

Q189 [神经科学];

学科分类号：

071006 ;

摘要：

Diazepam binding inhibitor (DBI) acts in brain by binding to GABA(A)/benzodiazepine receptors (GBR) and to mitochondrial benzodiazepine receptors (MBR). Because DBI acting at MBR, has been shown to be an effector of ACTH-induced steroidogenesis and stress is known to change the level of GBR and MBR, the model of acute noise stress in rats was used to study modifications of DBI and GRB or the content of MBR in various areas of the brain and adrenal gland. It was found that, in the brain of stressed rats, DBI and its processing products (ODN-like immunoreactivity), increased selectively in the hippocampus. This increase in the content of DBI was preceded and followed by a net decrease of GBR and an increase of MBR. Similarly, in adrenal cortex, the content of DBI and MBR increased during the first hour, following acute stress and this increase paralleled the increase in plasma corticosterone. These data suggest that DBI, acting on MBR may regulate steroidogenic function in stress.

引用

页码：1445 / 1452

页数：8

共 48 条

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