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Δ9-四氢大麻酚可预防甲基苯丙胺引起的神经毒性。

Δ9-tetrahydrocannabinol prevents methamphetamine-induced neurotoxicity.

作者信息

Castelli M Paola, Madeddu Camilla, Casti Alberto, Casu Angelo, Casti Paola, Scherma Maria, Fattore Liana, Fadda Paola, Ennas M Grazia

机构信息

Department of Biomedical Sciences, University of Cagliari, Cagliari, Italy; Center of Excellence "Neurobiology of Addiction", University of Cagliari, Cagliari, Italy.

Department of Biomedical Sciences, University of Cagliari, Cagliari, Italy.

出版信息

PLoS One. 2014 May 20;9(5):e98079. doi: 10.1371/journal.pone.0098079. eCollection 2014.

Abstract

Methamphetamine (METH) is a potent psychostimulant with neurotoxic properties. Heavy use increases the activation of neuronal nitric oxide synthase (nNOS), production of peroxynitrites, microglia stimulation, and induces hyperthermia and anorectic effects. Most METH recreational users also consume cannabis. Preclinical studies have shown that natural (Δ9-tetrahydrocannabinol, Δ9-THC) and synthetic cannabinoid CB1 and CB2 receptor agonists exert neuroprotective effects on different models of cerebral damage. Here, we investigated the neuroprotective effect of Δ9-THC on METH-induced neurotoxicity by examining its ability to reduce astrocyte activation and nNOS overexpression in selected brain areas. Rats exposed to a METH neurotoxic regimen (4 × 10 mg/kg, 2 hours apart) were pre- or post-treated with Δ9-THC (1 or 3 mg/kg) and sacrificed 3 days after the last METH administration. Semi-quantitative immunohistochemistry was performed using antibodies against nNOS and Glial Fibrillary Acidic Protein (GFAP). Results showed that, as compared to corresponding controls (i) METH-induced nNOS overexpression in the caudate-putamen (CPu) was significantly attenuated by pre- and post-treatment with both doses of Δ9-THC (-19% and -28% for 1 mg/kg pre- and post-treated animals; -25% and -21% for 3 mg/kg pre- and post-treated animals); (ii) METH-induced GFAP-immunoreactivity (IR) was significantly reduced in the CPu by post-treatment with 1 mg/kg Δ9-THC1 (-50%) and by pre-treatment with 3 mg/kg Δ9-THC (-53%); (iii) METH-induced GFAP-IR was significantly decreased in the prefrontal cortex (PFC) by pre- and post-treatment with both doses of Δ9-THC (-34% and -47% for 1 mg/kg pre- and post-treated animals; -37% and -29% for 3 mg/kg pre- and post-treated animals). The cannabinoid CB1 receptor antagonist SR141716A attenuated METH-induced nNOS overexpression in the CPu, but failed to counteract the Δ9-THC-mediated reduction of METH-induced GFAP-IR both in the PFC and CPu. Our results indicate that Δ9-THC reduces METH-induced brain damage via inhibition of nNOS expression and astrocyte activation through CB1-dependent and independent mechanisms, respectively.

摘要

甲基苯丙胺(METH)是一种具有神经毒性的强效精神兴奋剂。大量使用会增加神经元型一氧化氮合酶(nNOS)的活性、过氧亚硝酸盐的产生、小胶质细胞的刺激,并诱发体温过高和食欲抑制作用。大多数甲基苯丙胺的娱乐性使用者也吸食大麻。临床前研究表明,天然的(Δ9-四氢大麻酚,Δ9-THC)和合成的大麻素CB1和CB2受体激动剂对不同的脑损伤模型具有神经保护作用。在此,我们通过检测Δ9-THC在选定脑区减少星形胶质细胞激活和nNOS过表达的能力,研究了其对甲基苯丙胺诱导的神经毒性的神经保护作用。将暴露于甲基苯丙胺神经毒性方案(4×10 mg/kg,间隔2小时)的大鼠在末次给予甲基苯丙胺前或后用Δ9-THC(1或3 mg/kg)进行处理,并在末次给予甲基苯丙胺3天后处死。使用针对nNOS和胶质纤维酸性蛋白(GFAP)的抗体进行半定量免疫组织化学分析。结果显示,与相应对照组相比:(i)在尾状核-壳核(CPu)中,两种剂量的Δ9-THC预处理和后处理均显著减轻了甲基苯丙胺诱导的nNOS过表达(1 mg/kg预处理和后处理的动物分别为-19%和-28%;3 mg/kg预处理和后处理的动物分别为-25%和-21%);(ii)在CPu中,1 mg/kg Δ9-THC后处理(-50%)和3 mg/kg Δ9-THC预处理(-53%)显著降低了甲基苯丙胺诱导的GFAP免疫反应性(IR);(iii)在额叶前皮质(PFC)中,两种剂量的Δ9-THC预处理和后处理均显著降低了甲基苯丙胺诱导的GFAP-IR(1 mg/kg预处理和后处理的动物分别为-34%和-47%;3 mg/kg预处理和后处理的动物分别为-37%和-29%)。大麻素CB1受体拮抗剂SR141716A减轻了CPu中甲基苯丙胺诱导的nNOS过表达,但未能抵消Δ9-THC介导的在PFC和CPu中甲基苯丙胺诱导的GFAP-IR的降低。我们的结果表明,Δ9-THC分别通过CB1依赖性和非依赖性机制抑制nNOS表达和星形胶质细胞激活,从而减轻甲基苯丙胺诱导的脑损伤。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d50/4028295/49b9f06ceb97/pone.0098079.g001.jpg

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