Zhang Huina, Shi Yong-Gong, Woods James H, Watson Stanley J, Ko Mei-Chuan
Department of Pharmacology, University of Michigan Medical School, Ann Arbor, MI 48109, USA.
Eur J Pharmacol. 2007 Sep 10;570(1-3):89-96. doi: 10.1016/j.ejphar.2007.05.045. Epub 2007 Jun 9.
kappa-opioid receptor antagonists such as nor-Binaltorphimine (nor-BNI) have been shown to produce antidepressant-like behavioral effects in animal models of depression. The aim of this study was to investigate further the duration of centrally administered nor-BNI-induced antidepressant-like actions measured by both behavior and brain-derived neurotrophic factor (BDNF) gene expression. In addition, antagonist studies were conducted to determine the role of opioid receptor subtypes and the time course of nor-BNI's pharmacological actions. Antidepressant-like behavioral effects were measured by decreased immobility in the rat forced swim test and BDNF mRNA expression was determined by in situ hybridization. Centrally administered nor-BNI (20 microg, i.c.v.) decreased immobility and increased BDNF mRNA expression in the hippocampus on day 1, not on days 3-14, post-administration. Systemic administration of selective mu-, delta- and kappa-opioid receptor antagonists did not block nor-BNI-induced antidepressant-like effects. In contrast, i.c.v. administration of nor-BNI 7 or 14 days earlier significantly blocked subsequent nor-BNI-induced decreased immobility and upregulation of BDNF mRNA expression. Although the duration of nor-BNI's antidepressant-like effects did not synchronize with that of its kappa-opioid receptor antagonist effects, this study is the first to show that centrally administered nor-BNI, like most clinically used antidepressants, can upregulate BDNF mRNA expression in the rat hippocampus. These findings further demonstrate that central kappa-opioid receptor mediates antidepressant-like effects of nor-BNI measured by both behavior and BDNF gene expression.
κ-阿片受体拮抗剂,如去甲二丙诺啡(nor-BNI),已被证明在抑郁症动物模型中可产生类抗抑郁行为效应。本研究的目的是进一步探究通过行为和脑源性神经营养因子(BDNF)基因表达测量的中枢给予nor-BNI诱导的类抗抑郁作用的持续时间。此外,进行拮抗剂研究以确定阿片受体亚型的作用以及nor-BNI药理作用的时间进程。通过大鼠强迫游泳试验中不动时间的减少来测量类抗抑郁行为效应,并通过原位杂交确定BDNF mRNA表达。中枢给予nor-BNI(20微克,脑室内注射)在给药后第1天可减少不动时间并增加海马体中BDNF mRNA表达,而在第3 - 14天则无此作用。全身给予选择性μ-、δ-和κ-阿片受体拮抗剂并未阻断nor-BNI诱导的类抗抑郁效应。相反,提前7天或14天脑室内注射nor-BNI可显著阻断随后nor-BNI诱导的不动时间减少和BDNF mRNA表达上调。尽管nor-BNI的类抗抑郁效应持续时间与其κ-阿片受体拮抗剂效应的持续时间不同步,但本研究首次表明,与大多数临床使用的抗抑郁药一样,中枢给予nor-BNI可上调大鼠海马体中BDNF mRNA表达。这些发现进一步证明,中枢κ-阿片受体介导了通过行为和BDNF基因表达测量的nor-BNI的类抗抑郁效应。