单酰基甘油脂肪酶抑制大鼠脑突触体/线粒体部分和皮质切片的短期线粒体功能障碍和氧化损伤:大麻素受体的作用。

IF 2.9 3区 医学 Q2 NEUROSCIENCES Neurotoxicity Research Pub Date : 2023-12-01 Epub Date: 2023-07-17 DOI:10.1007/s12640-023-00661-4
Karen Jaqueline Paredes-Ruiz, Karla Chavira-Ramos, Sonia Galvan-Arzate, Edgar Rangel-López, Çimen Karasu, Isaac Túnez, Anatoly V Skalny, Tao Ke, Michael Aschner, Mario Orozco-Morales, Ana Laura Colín-González, Abel Santamaría
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引用次数: 0

摘要

抑制负责内源性大麻素水解的酶代表了神经退行性疾病潜在治疗的宝贵新兴工具。单酰基甘油脂肪酶(MAGL)是一种降解2-花生酰基甘油(2-AG)的酶,2-AG是中枢神经系统(CNS)中含量最多的内源性大麻素。在这里,我们测试了选择性MAGL抑制剂JZL184对3-硝基丙酸(3-NP)诱导的大鼠脑突触体/线粒体部分和皮质切片线粒体还原能力/活力短期丧失和氧化损伤的影响。在突触体中,虽然3-NP降低了线粒体功能并增加了脂质过氧化,但JZL184减弱了这两种标记。JZL184对3- np诱导的线粒体功能障碍的保护作用主要通过激活大麻素受体2 (cannabinoid receptor 2, CB2R)介导,CB2R选择性拮抗剂JTE907对其有抑制作用。大麻素受体1 (CB1R)也在较小程度上参与了这种作用,CB1R拮抗剂/逆激动剂AM281证明了这一点。相比之下,JZL184对3- np诱导的脂质过氧化的保护作用主要是激活CB1R,而不是CB2R。JZL184的保护作用在其他以兴奋性毒性和氧化损伤为内控的毒性模型中得到证实。在皮质切片中,JZL184改善了3- np诱导的线粒体功能丧失、脂质过氧化增加和琥珀酸脱氢酶(线粒体复合物II)活性的抑制,这些作用不依赖于CB1R和CB2R, AM281和JTE907分别缺乏作用。我们的新结果提供了实验证据,证明JZL184对脑突触体和皮质切片中3-NP诱导的早期毒性作用的差异保护作用涉及MAGL抑制,并可能随后积累2-AG。这些作用涉及促能量和氧化还原调节机制,可能依赖或独立于大麻素受体的激活。
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Monoacylglycerol Lipase Inhibition Prevents Short-Term Mitochondrial Dysfunction and Oxidative Damage in Rat Brain Synaptosomal/Mitochondrial Fractions and Cortical Slices: Role of Cannabinoid Receptors.

Inhibition of enzymes responsible for endocannabinoid hydrolysis represents an invaluable emerging tool for the potential treatment of neurodegenerative disorders. Monoacylglycerol lipase (MAGL) is the enzyme responsible for degrading 2-arachydonoylglycerol (2-AG), the most abundant endocannabinoid in the central nervous system (CNS). Here, we tested the effects of the selective MAGL inhibitor JZL184 on the 3-nitropropinic acid (3-NP)-induced short-term loss of mitochondrial reductive capacity/viability and oxidative damage in rat brain synaptosomal/mitochondrial fractions and cortical slices. In synaptosomes, while 3-NP decreased mitochondrial function and increased lipid peroxidation, JZL184 attenuated both markers. The protective effects evoked by JZL184 on the 3-NP-induced mitochondrial dysfunction were primarily mediated by activation of cannabinoid receptor 2 (CB2R), as evidenced by their inhibition by the selective CB2R inverse agonist JTE907. The cannabinoid receptor 1 (CB1R) also participated in this effect in a lesser extent, as evidenced by the CB1R antagonist/inverse agonist AM281. In contrast, activation of CB1R, but not CB2R, was responsible for the protective effects of JZL184 on the 3-NP-iduced lipid peroxidation. Protective effects of JZL184 were confirmed in other toxic models involving excitotoxicity and oxidative damage as internal controls. In cortical slices, JZL184 ameliorated the 3-NP-induced loss of mitochondrial function, the increase in lipid peroxidation, and the inhibition of succinate dehydrogenase (mitochondrial complex II) activity, and these effects were independent on CB1R and CB2R, as evidenced by the lack of effects of AM281 and JTE907, respectively. Our novel results provide experimental evidence that the differential protective effects exerted by JZL184 on the early toxic effects induced by 3-NP in brain synaptosomes and cortical slices involve MAGL inhibition, and possibly the subsequent accumulation of 2-AG. These effects involve pro-energetic and redox modulatory mechanisms that may be either dependent or independent of cannabinoid receptors' activation.

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来源期刊
Neurotoxicity Research
Neurotoxicity Research 医学-神经科学
CiteScore
7.70
自引率
5.40%
发文量
164
审稿时长
6-12 weeks
期刊介绍: Neurotoxicity Research is an international, interdisciplinary broad-based journal for reporting both basic and clinical research on classical neurotoxicity effects and mechanisms associated with neurodegeneration, necrosis, neuronal apoptosis, nerve regeneration, neurotrophin mechanisms, and topics related to these themes. Published papers have focused on: NEURODEGENERATION and INJURY Neuropathologies Neuronal apoptosis Neuronal necrosis Neural death processes (anatomical, histochemical, neurochemical) Neurodegenerative Disorders Neural Effects of Substances of Abuse NERVE REGENERATION and RESPONSES TO INJURY Neural Adaptations Neurotrophin mechanisms and actions NEURO(CYTO)TOXICITY PROCESSES and NEUROPROTECTION Excitatory amino acids Neurotoxins, endogenous and synthetic Reactive oxygen (nitrogen) species Neuroprotection by endogenous and exogenous agents Papers on related themes are welcome.
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