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吗啡耐受大鼠和小鼠脑及脊髓中细胞内游离钙水平[(Ca++)i]的调节

Modulation of free intracellular calcium levels [(Ca++)i] in brain and spinal cord of morphine-tolerant rats and mice.

作者信息

Welch S P, Bass P P

机构信息

Department of Pharmacology and Toxicology, Medical College of Virginia/Virginia Commonwealth University, Richmond 23298-0613, USA.

出版信息

Pharmacol Biochem Behav. 1995 May;51(1):57-63. doi: 10.1016/0091-3057(94)00356-n.

Abstract

Evaluation of the effects of tolerance to morphine in vivo on free intracellular calcium levels [(Ca++)i] in whole brain synaptosomes from rats and synaptosomes from brain regions and spinal cords of both rats and mice indicated that in whole brain and spinal cord synaptosomes, [Ca++]i levels are significantly higher in morphine-tolerant mice. Although levels do not differ between nontolerant and tolerant preparations from the rat spinal cord, [Ca++]i brain levels are significantly higher in morphine-tolerant rats. Evaluation of three brain regions from both nontolerant and tolerant rats and two brain regions from mice indicated no significant differences in basal [Ca++]i, with the exception that lower basal levels of calcium were observed in the midbrain of the tolerant rat. In vivo, mice tolerant to morphine (SC) were cross tolerant to DAMGO (IT and ICV). Cross tolerance between morphine and DAMGO was observed in vitro. No cross-tolerance was observed between morphine (SC) and the delta-agonist, DPDPE (IT or ICV), or the kappa-agonist, U50,488H (U50, IT or ICV) in vivo. Similarly, no cross tolerance was observed between morphine (SC) and DPDPE or U50 in vitro. These data indicate that tolerance in vivo induced a change in synaptosomal calcium modulation such that tolerance could be observed in vitro. Thus, a membrane component may be altered by the development of tolerance to morphine leading to an alteration in [Ca++]i in both the brain and spinal cord.

摘要

对大鼠全脑突触体以及大鼠和小鼠脑区及脊髓突触体中体内吗啡耐受性对游离细胞内钙水平[Ca++]i的影响进行评估,结果表明,在全脑和脊髓突触体中,吗啡耐受小鼠的[Ca++]i水平显著更高。虽然大鼠脊髓中未耐受和耐受制剂之间的水平没有差异,但吗啡耐受大鼠的脑内[Ca++]i水平显著更高。对未耐受和耐受大鼠的三个脑区以及小鼠的两个脑区进行评估,结果表明基础[Ca++]i没有显著差异,不过在耐受大鼠的中脑观察到较低的基础钙水平。在体内,对吗啡(皮下注射)耐受的小鼠对DAMGO(鞘内注射和脑室内注射)产生交叉耐受。在体外也观察到吗啡和DAMGO之间的交叉耐受。在体内,未观察到吗啡(皮下注射)与δ激动剂DPDPE(鞘内注射或脑室内注射)或κ激动剂U50,488H(U50,鞘内注射或脑室内注射)之间的交叉耐受。同样,在体外也未观察到吗啡(皮下注射)与DPDPE或U50之间的交叉耐受。这些数据表明,体内耐受性引起了突触体钙调节的变化,从而在体外也能观察到耐受性。因此,对吗啡耐受性的发展可能会改变膜成分,导致脑和脊髓中[Ca++]i发生改变。

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