Suppr超能文献

阿片受体介导对大鼠中基底下丘脑切片中[3H]多巴胺释放的抑制,但对[3H]去甲肾上腺素释放无抑制作用。

Opioid-receptor-mediated inhibition of [3H]dopamine but not [3H]noradrenaline release from rat mediobasal hypothalamus slices.

作者信息

Heijna M H, Padt M, Hogenboom F, Schoffelmeer A N, Mulder A H

机构信息

Department of Pharmacology, Medical Faculty, Free University, Amsterdam, The Netherlands.

出版信息

Neuroendocrinology. 1991 Aug;54(2):118-26. doi: 10.1159/000125860.

Abstract

The modulation of the electrically evoked release of [3H]dopamine (DA) and [3H]noradrenaline (NA) by opioid receptor activation was examined in superfused slices of rat mediobasal hypothalamus (MBH). [3H]DA release was inhibited (maximally by 30-35%) by both the selective kappa-agonist U 50,488 (1 nM to 1 microM) and the selective mu-agonist DAGO (0.01-1 microM) but not by the delta-selective agonist DPDPE (1 microM). Naloxone partly antagonized the inhibitory effect of U 50,488 and completely that of DAGO, whereas the selective kappa-antagonist norbinaltorphimine (nor-BNI) only antagonized the inhibition caused by U 50,488. The dopamine D2 receptor agonist quinpirole as well as the alpha 2-adrenoceptor agonist oxymetazoline both decreased (by 25-30%) the evoked overflow of [3H]DA. The evoked release of [3H]NA was not modulated by any of the opioid agonists nor by quinpirole. However, the alpha 2-adrenoceptor agonist oxymetazoline inhibited the release of [3H]NA by 30-40%. Activation of alpha 2-adrenoceptors by oxymetazoline prevented the inhibitory effect of U 50,488, but not DAGO, on evoked [3H]DA release, whereas the selective kappa-antagonist nor-BNI antagonized the inhibition by oxymetazoline of [3H]DA, but not [3H]NA, release. In conclusion, activation of both kappa- and mu-opioid receptors results in an inhibition of evoked DA release from MBH slices but does not modulate NA release. Therefore, several of the reported effects of opioids on hormone secretion may be an (indirect) consequence of a reduction of DA release.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在大鼠中脑基底下丘脑(MBH)的灌流切片中,研究了阿片受体激活对电诱发的[3H]多巴胺(DA)和[3H]去甲肾上腺素(NA)释放的调节作用。选择性κ-激动剂U 50,488(1 nM至1 μM)和选择性μ-激动剂DAGO(0.01 - 1 μM)均可抑制[3H]DA的释放(最大抑制30 - 35%),但δ-选择性激动剂DPDPE(1 μM)则无此作用。纳洛酮可部分拮抗U 50,488的抑制作用,并完全拮抗DAGO的抑制作用,而选择性κ-拮抗剂诺宾那托啡(nor-BNI)仅拮抗U 50,488引起的抑制作用。多巴胺D2受体激动剂喹吡罗以及α2-肾上腺素能受体激动剂羟甲唑啉均可使[3H]DA的诱发溢出减少(25 - 30%)。[3H]NA的诱发释放不受任何阿片类激动剂或喹吡罗的调节。然而,α2-肾上腺素能受体激动剂羟甲唑啉可使[3H]NA的释放抑制30 - 40%。羟甲唑啉激活α2-肾上腺素能受体可阻止U 50,488而非DAGO对诱发的[3H]DA释放的抑制作用,而选择性κ-拮抗剂nor-BNI可拮抗羟甲唑啉对[3H]DA释放的抑制作用,但不拮抗[3H]NA的释放。总之,κ-和μ-阿片受体激活均导致MBH切片中诱发的DA释放受到抑制,但不调节NA释放。因此,阿片类药物对激素分泌的一些报道效应可能是DA释放减少的(间接)结果。(摘要截短于250字)

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验