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首页> 外文期刊>Toxicology and Applied Pharmacology >Cytotoxicity of synthetic cannabinoids on primary neuronal cells of the forebrain: The involvement of cannabinoid CB1 receptors and apoptotic cell death
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Cytotoxicity of synthetic cannabinoids on primary neuronal cells of the forebrain: The involvement of cannabinoid CB1 receptors and apoptotic cell death

机译:合成大麻素对前脑原代神经元细胞的细胞毒性:大麻素CB1受体的参与和凋亡细胞的死亡

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The abuse of herbal products containing synthetic cannabinoids has become an issue of public concern. The purpose of this paper was to evaluate the acute cytotoxicity of synthetic cannabinoids on mouse brain neuronal cells. Cytotoxicity induced by synthetic cannabinoid (CP-55,940, CP-47,497, CP-47,497-C8, HU-210, JWH-018, JWH-210, AM-2201, and MAM-2201) was examined using forebrain neuronal cultures. These synthetic cannabinoids induced cytotoxicity in the forebrain cultures in a concentration-dependent manner. The cytotoxicity was suppressed by preincubation with the selective CB1 receptor antagonist AM251, but not with the selective CB2 receptor antagonist AM630. Furthermore, annexin-V-positive cells were found among the treated forebrain cells. Synthetic cannabinoid treatment induced the activation of caspase-3, and preincubation with a caspase-3 inhibitor significantly suppressed the cytotoxicity. These synthetic cannabinoids induced apoptosis through a caspase-3-dependent mechanism in the forebrain cultures. Our results indicate that the cytotoxicity of synthetic cannabinoids towards primary neuronal cells is mediated by the CB1 receptor, but not by the CB2 receptor, and further suggest that caspase cascades may play an important role in the apoptosis induced by these synthetic cannabinoids. In conclusion, excessive synthetic cannabinoid abuse may present a serious acute health concern due to neuronal damage or deficits in the brain.
机译:含有合成大麻素的草药产品的滥用已成为公众关注的问题。本文的目的是评估合成大麻素对小鼠大脑神经元细胞的急性细胞毒性。使用前脑神经元培养物检查了合成大麻素(CP-55,940,CP-47,497,CP-47,497-C8,HU-210,JWH-018,JWH-210,AM-2201和MAM-2201)诱导的细胞毒性。这些合成的大麻素以浓度依赖的方式在前脑培养物中诱导细胞毒性。通过与选择性CB1受体拮抗剂AM251进行预孵育抑制了细胞毒性,但与选择性CB2受体拮抗剂AM630进行了预孵育抑制了细胞毒性。此外,在处理过的前脑细胞中发现了膜联蛋白-V阳性细胞。合成大麻素处理诱导了caspase-3的激活,并且与caspase-3抑制剂一起预温育可显着抑制细胞毒性。这些合成的大麻素在前脑培养物中通过caspase-3依赖性机制诱导凋亡。我们的结果表明,合成大麻素对原代神经元细胞的细胞毒性是由CB1受体介导的,而不是由CB2受体介导的,并且进一步表明,胱天蛋白酶级联反应可能在这些合成大麻素诱导的凋亡中发挥重要作用。总之,由于神经元损伤或大脑缺陷,过度滥用合成大麻素可能会引起严重的急性健康问题。

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