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首页> 外文期刊>European review for medical and pharmacological sciences. >Purified Cannabidiol, the main non-psychotropic component of Cannabis sativa, alone, counteracts neuronal apoptosis in experimental multiple sclerosis
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Purified Cannabidiol, the main non-psychotropic component of Cannabis sativa, alone, counteracts neuronal apoptosis in experimental multiple sclerosis

机译:纯化的大麻二酚(大麻的主要非精神成分)可以单独抵抗实验性多发性硬化症中的神经元凋亡

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OBJECTIVE: Multiple Sclerosis (MS) is a global concern disease leading to a progressive, chronic and demyelinating condition, affecting the central nervous system (CNS). The pathology has an inflammatory/autoimmune origin; nevertheless, neuronal cell death mechanisms are not to be underestimated. The present study was designed to test the effects of intraperitoneal administration of cannabidiol (CBD), the main non-psychotropic cannabinoid of Cannabis sativa (CS), in an experimental model of MS. The aim is to evaluate the capability of CBD administration to thwart the cascade of mediators involved in MS-induced apoptosis. MATERIALS AND METHODS: Experimental Autoimmune Encephalomyelitis (EAE) was induced by immunization with myelin oligodendroglial glycoprotein (MOG)35-55 peptide in mice. After immunization, mice were observed daily for signs of EAE and weight loss. Disease signs were evaluated using a standardized scoring system. RESULTS: Immunohistochemical and Western blot assessments of key apoptotic markers reveal that CBD treatment is able to avoid Fas pathway activation, phospho-ERK p42/44 and cleaved caspase-3 triggering as well as alterations in mitochondrial permeability due to Bax/Bcl-2 unbalance. Moreover, CBD interferes with p53-p21 axis activation. As results, the absence of tissue apobody formation in spinal cord tissues of EAE-mice treated with CBD was established. Most of therapeutic properties of CS are currently ascribed to the psychotropic effects of phenylterpenoid delta-9 tetrahydrocannabinol. CONCLUSIONS: We have demonstrated that, alone, purified CBD possesses an anti-apoptotic power against the neurodegenerative processes underlying MS development. This represents an interesting new profile of CBD that could lead to its introduction in the clinical management of MS.
机译:目的:多发性硬化症(MS)是一种引起全球关注的疾病,可导致进行性,慢性和脱髓鞘疾病,影响中枢神经系统(CNS)。病理具有炎性/自身免疫起源。但是,神经细胞死亡机制不可低估。本研究旨在在MS实验模型中测试腹腔注射大麻二酚(CBD)的效果,大麻二酚是大麻的主要非精神大麻素(CS)。目的是评估施用CBD抑制与MS诱导的细胞凋亡有关的介质级联反应的能力。材料与方法:用髓磷脂少突胶质糖蛋白(MOG)35-55肽免疫小鼠,诱发实验性自身免疫性脑脊髓炎(EAE)。免疫后,每天观察小鼠的EAE和体重减轻的迹象。使用标准化评分系统评估疾病迹象。结果:关键凋亡标志物的免疫组织化学和蛋白质印迹评估表明,CBD处理能够避免Fas途径活化,磷酸化ERK p42 / 44和裂解的caspase-3触发以及由于Bax / Bcl-2不平衡导致的线粒体通透性改变。 。此外,CBD会干扰p53-p21轴激活。结果,证实了在用CBD处理的EAE小鼠的脊髓组织中不存在组织顶体形成。 CS的大多数治疗性质目前归因于苯基萜类δ9四氢大麻酚的精神作用。结论:我们已经证明,单独的纯化的CBD具有抗凋亡的能力,可抵抗MS发育背后的神经变性过程。这代表了一个有趣的CBD新特性,可能导致其被引入MS的临床管理中。

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