Kim Sang R, Lee Da Y, Chung Eun S, Oh Uh T, Kim Seung U, Jin Byung K
Brain Disease Research Center, Ajou University School of Medicine, Suwon 442-749, Korea.
J Neurosci. 2005 Jan 19;25(3):662-71. doi: 10.1523/JNEUROSCI.4166-04.2005.
Intranigral injection of the transient receptor potential vanilloid subtype 1 (TRPV1; also known as VR1) agonist capsaicin (CAP) into the rat brain, or treatment of rat mesencephalic cultures with CAP, resulted in cell death of dopaminergic (DA) neurons, as visualized by immunocytochemistry. This in vivo and in vitro effect was ameliorated by the TRPV1 antagonist capsazepine (CZP) or iodo-resiniferatoxin, suggesting the direct involvement of TRPV1 in neurotoxicity. In cultures, both CAP and anandamide (AEA), an endogenous ligand for both TRPV1 and cannabinoid type 1 (CB1) receptors, induced degeneration of DA neurons, increases in intracellular Ca2+ ([Ca2+]i), and mitochondrial damage, which were inhibited by CZP, the CB1 antagonist N-(piperidin-1-yl)-5-(4-iodophenyl)-1-(2,4-dichlorophenyl)-4-methyl-1H-pyrazole-3-carboxamide (AM251) or the intracellular Ca2+ chelator BAPTA/AM. We also found that CAP or AEA increased mitochondrial cytochrome c release as well as immunoreactivity to cleaved caspase-3 and that the caspase-3 inhibitor z-Asp-Glu-Val-Asp-fmk protected DA neurons from CAP- or AEA-induced neurotoxicity. Additional studies demonstrated that treatment of mesencephalic cultures with CB1 receptor agonist (6aR)-trans 3-(1,1-dimethylheptyl)-6a,7,10,10a-tetrahydro-1-hydroxy-6,6-dimethyl-6H-dibenzo[b,d] pyran-9-methanol (HU210) also produced degeneration of DA neurons and increases in [Ca2+]i, which were inhibited by AM251 and BAPTA/AM. The CAP-, AEA-, or HU210-induced increases in [Ca2+]i were dependent on extracellular Ca2+, with significantly different patterns of Ca2+ influx. Surprisingly, CZP and AM251 reversed HU210- or CAP-induced neurotoxicity by inhibiting Ca2+ influx, respectively, suggesting the existence of functional cross talk between TRPV1 and CB1 receptors. To our knowledge, this study is the first to demonstrate that the activation of TRPV1 and/or CB1 receptors mediates cell death of DA neurons. Our findings suggest that these two types of receptors, TRPV1 and CB1, may contribute to neurodegeneration in response to endogenous ligands such as AEA.
向大鼠脑内黑质注射瞬时受体电位香草酸亚型1(TRPV1;也称为VR1)激动剂辣椒素(CAP),或用CAP处理大鼠中脑培养物,免疫细胞化学显示多巴胺能(DA)神经元发生细胞死亡。TRPV1拮抗剂辣椒平(CZP)或碘树脂毒素可改善这种体内和体外效应,提示TRPV1直接参与神经毒性作用。在培养物中,CAP和花生四烯乙醇胺(AEA,TRPV1和大麻素1型(CB1)受体的内源性配体)均可诱导DA神经元变性、细胞内Ca2+([Ca2+]i)升高及线粒体损伤,这些均被CZP、CB1拮抗剂N-(哌啶-1-基)-5-(4-碘苯基)-1-(2,4-二氯苯基)-4-甲基-1H-吡唑-3-甲酰胺(AM251)或细胞内Ca2+螯合剂BAPTA/AM抑制。我们还发现,CAP或AEA可增加线粒体细胞色素c释放以及对裂解的半胱天冬酶-3的免疫反应性,并且半胱天冬酶-3抑制剂z-Asp-Glu-Val-Asp-fmk可保护DA神经元免受CAP或AEA诱导的神经毒性作用。进一步研究表明,用CB1受体激动剂(6aR)-反式-3-(1,1-二甲基庚基)-6a,7,10,10a-四氢-1-羟基-6,6-二甲基-6H-二苯并[b,d]吡喃-9-甲醇(HU210)处理中脑培养物也可导致DA神经元变性及[Ca2+]i升高,这些均被AM251和BAPTA/AM抑制。CAP、AEA或HU210诱导的[Ca2+]i升高依赖于细胞外Ca2+,Ca2+内流模式明显不同。令人惊讶的是,CZP和AM251分别通过抑制Ca2+内流逆转了HU210或CAP诱导的神经毒性作用,提示TRPV1和CB1受体之间存在功能性相互作用。据我们所知,本研究首次证明TRPV1和/或CB1受体的激活介导DA神经元的细胞死亡。我们的研究结果表明,TRPV1和CB1这两种受体可能在内源性配体如AEA的作用下参与神经退行性变。