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慢性注射吗啡和/或咪达唑仑期间大鼠体内甲硫氨酸脑啡肽的变化。

Met-enkephalin alteration in the rat during chronic injection of morphine and/or midazolam.

作者信息

Tejwani G A, Rattan A K

机构信息

Department of Pharmacology, Ohio State University, College of Medicine and Public Health, Columbus 43210-1239, USA.

出版信息

Brain Res. 1997 Nov 14;775(1-2):119-26. doi: 10.1016/s0006-8993(97)00875-5.

Abstract

We have recently reported that the short-acting anesthetic and analgesic drug midazolam can produce analgesia and decrease morphine tolerance and dependence in the rat by interacting with the opioid system. This study was designed to investigate the effect of midazolam, morphine, and both together on met-enkephalin levels in the rat. Male Sprague-Dawley rats were divided into four groups: (1) saline-saline; (2) saline-morphine; (3) midazolam-saline, and (4) midazolam-morphine groups. First, a saline or midazolam injection was given intraperitoneally and after 30 min a second injection of saline or morphine was given subcutaneously once daily for 11 days. Animals were sacrificed on the 11th day 60 min after the last injection to measure met-enkephalin by radioimmunoassay. Morphine tolerant animals showed a significant increase in met-enkephalin levels in the cortex (137%) and midbrain (89%), and a significant decrease in met-enkephalin levels in the pituitary (74%), cerebellum (34%) and medulla (72%). Midazolam treated animals showed a significant decrease in met-enkephalin levels in the pituitary (63%), cortex (39%), medulla (58%), kidneys (36%), heart (36%) and adrenals (43%), and a significant increase in met-enkephalin levels in the striatum (54%) and pons (51%). When morphine and midazolam were injected together, midazolam antagonized the increase in met-enkephalin levels in cortex and midbrain region and the decrease in met-enkephalin level in the medulla region observed in morphine tolerant animals. These results indicate that morphine tolerance and dependence is associated with changes in the concentration of met-enkephalin in the brain. Midazolam may inhibit morphine tolerance and dependence by reversing some of the changes induced in met-enkephalin levels in brain by morphine in morphine tolerant and dependent animals.

摘要

我们最近报道,短效麻醉和镇痛药咪达唑仑可通过与阿片系统相互作用,在大鼠中产生镇痛作用,并降低吗啡耐受性和依赖性。本研究旨在调查咪达唑仑、吗啡以及二者共同作用对大鼠甲硫氨酸脑啡肽水平的影响。将雄性Sprague-Dawley大鼠分为四组:(1) 生理盐水-生理盐水组;(2) 生理盐水-吗啡组;(3) 咪达唑仑-生理盐水组,以及(4) 咪达唑仑-吗啡组。首先,腹腔注射生理盐水或咪达唑仑,30分钟后,每天皮下注射一次生理盐水或吗啡,共11天。在最后一次注射后60分钟的第11天处死动物,通过放射免疫分析法测量甲硫氨酸脑啡肽。吗啡耐受的动物在皮质(137%)和中脑(89%)中甲硫氨酸脑啡肽水平显著升高,而在垂体(74%)、小脑(34%)和延髓(72%)中甲硫氨酸脑啡肽水平显著降低。咪达唑仑处理的动物在垂体(63%)、皮质(39%)、延髓(58%)、肾脏(36%)、心脏(36%)和肾上腺(43%)中甲硫氨酸脑啡肽水平显著降低,而在纹状体(54%)和脑桥(51%)中甲硫氨酸脑啡肽水平显著升高。当吗啡和咪达唑仑一起注射时,咪达唑仑拮抗了吗啡耐受动物中观察到的皮质和中脑区域甲硫氨酸脑啡肽水平升高以及延髓区域甲硫氨酸脑啡肽水平降低。这些结果表明,吗啡耐受性和依赖性与脑中甲硫氨酸脑啡肽浓度的变化有关。咪达唑仑可能通过逆转吗啡耐受和依赖动物中吗啡引起的脑中甲硫氨酸脑啡肽水平的一些变化来抑制吗啡耐受性和依赖性。

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