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长期给予Δ⁹-四氢大麻酚会导致大鼠脑中大麻素受体和大麻素受体激活的G蛋白随时间推移而减少。

Chronic delta9-tetrahydrocannabinol treatment produces a time-dependent loss of cannabinoid receptors and cannabinoid receptor-activated G proteins in rat brain.

作者信息

Breivogel C S, Childers S R, Deadwyler S A, Hampson R E, Vogt L J, Sim-Selley L J

机构信息

Department of Physiology and Pharmacology, Center for the Neurobiological Investigation of Drug Abuse, Wake Forest University School of Medicine, Winston-Salem, North Carolina, USA.

出版信息

J Neurochem. 1999 Dec;73(6):2447-59. doi: 10.1046/j.1471-4159.1999.0732447.x.

Abstract

Chronic treatment of rats with delta9-tetrahydrocannabinol (delta9-THC) results in tolerance to its acute behavioral effects. In a previous study, 21-day delta9-THC treatment in rats decreased cannabinoid activation of G proteins in brain, as measured by in vitro autoradiography of guanosine-5'-O-(3-[35S]thiotriphosphate) ([35S]GTPgammaS) binding. The present study investigated the time course of changes in cannabinoid-stimulated [35S]GTPgammaS binding and cannabinoid receptor binding in both brain sections and membranes, following daily delta9-THC treatments for 3, 7, 14, and 21 days. Autoradiographic results showed time-dependent decreases in WIN 55212-2-stimulated [35S]GTPgammaS and [3H]WIN 55212-2 binding in cerebellum, hippocampus, caudate-putamen, and globus pallidus, with regional differences in the rate and magnitude of down-regulation and desensitization. Membrane binding assays in these regions showed qualitatively similar decreases in WIN 55212-2-stimulated [35S]GTPgammaS binding and cannabinoid receptor binding (using [3H]SR141716A), and demonstrated that decreases in ligand binding were due to decreases in maximal binding values, and not ligand affinities. These results demonstrated that chronic exposure to delta9-THC produced time-dependent and region-specific down-regulation and desensitization of brain cannabinoid receptors, which may represent underlying biochemical mechanisms of tolerance to cannabinoids.

摘要

用Δ⁹-四氢大麻酚(Δ⁹-THC)对大鼠进行长期治疗会导致对其急性行为效应产生耐受性。在先前的一项研究中,通过鸟苷-5'-O-(3-[³⁵S]硫代三磷酸)([³⁵S]GTPγS)结合的体外放射自显影法测量,大鼠接受21天的Δ⁹-THC治疗会降低大脑中大麻素对G蛋白的激活作用。本研究调查了在每天给予Δ⁹-THC治疗3、7、14和21天后,大脑切片和膜中大麻素刺激的[³⁵S]GTPγS结合以及大麻素受体结合的变化时间进程。放射自显影结果显示,在小脑、海马体、尾状核-壳核和苍白球中,WIN 55212-2刺激的[³⁵S]GTPγS和[³H]WIN 55212-2结合呈时间依赖性下降,下调和脱敏的速率和程度存在区域差异。这些区域的膜结合试验显示,WIN 55212-2刺激的[³⁵S]GTPγS结合和大麻素受体结合(使用[³H]SR141716A)在质量上有类似的下降,并表明配体结合的下降是由于最大结合值的降低,而不是配体亲和力的降低。这些结果表明,长期暴露于Δ⁹-THC会导致大脑大麻素受体出现时间依赖性和区域特异性的下调和脱敏,这可能代表了对大麻素耐受性的潜在生化机制。

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