首页> 外文期刊>Neuroscience: An International Journal under the Editorial Direction of IBRO >Co-localization of P450 enzymes in the rat substantia nigra with tyrosine hydroxylase.
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Co-localization of P450 enzymes in the rat substantia nigra with tyrosine hydroxylase.

机译:P450酶在大鼠黑质中与酪氨酸羟化酶共定位。

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摘要

Susceptibility to develop Parkinson's disease has been linked to abnormalities of P450 enzyme function. Multiple P450 enzymes are expressed in brain but the relationship of these to Parkinson's disease is unknown. We have investigated the expression of P450 enzymes in the rat substantia nigra and their co-localization in tyrosine hydroxylase-positive neurons and astrocytes. Immunohistochemistry was performed using anti-peptide antisera against the following P450 enzymes: CYP1A1, CYP1A2, CYP2B1/2, CYP2C12, CYP2C13/2C6, CYP2D1, CYP2D4, CYP2E1, CYP3A1, CYP3A2 and NADPH-P450 oxidoreductase. Immunoreactivity in nigral cells was found only for CYP2E1 and CYP2C13/2C6. CYP2E1 immunoreactivity was localized to many midbrain nuclei including the substantia nigra pars compacta but not the substantia nigra pars reticulata while immunoreactivity to CYP2C13/2C6 was found in the substantia nigra pars compacta, substantia nigra pars reticulata and many other midbrain nuclei. Sections of rat midbrain double labelled for either CYP2E1 or CYP2C13/2C6 and tyrosine hydroxylase or glial fibrillary acidic protein were examined for co-localization by confocal laser scanning microscopy. CYP2E1 and CYP2C13/2C6 immunoreactivity was found in tyrosine hydroxylase-positive neurons in the substantia nigra pars compacta but not in glial cells. CYP2C13/2C6, but not CYP2E1, was also found in non-glial, non-tyrosine hydroxylase-expressing cells in the substantia nigra pars reticulata. Isoniazid induction increased CYP2E1 fluorescence signal intensity from nigral dopaminergic neurons. At least two P450 enzymes are found in nigral dopamine containing cells and one, namely CYP2E1, is selectively localized to this cell population. CYP2E1 is a potent generator of free radicals which may contribute to nigral pathology in Parkinson's disease. The expression of CYP2E1 in dopaminergic neurons in substantia nigra raises the possibility of a causal association with Parkinson's disease.
机译:帕金森氏病易感性与P450酶功能异常有关。多种P450酶在大脑中表达,但与帕金森氏病的关系尚不清楚。我们研究了大鼠黑质中P450酶的表达及其在酪氨酸羟化酶阳性神经元和星形胶质细胞中的共定位。使用针对以下P450酶的抗肽抗血清进行免疫组织化学:CYP1A1,CYP1A2,CYP2B1 / 2,CYP2C12,CYP2C13 / 2C6,CYP2D1,CYP2D4,CYP2E1,CYP3A1和CYP3A2450。仅针对CYP2E1和CYP2C13 / 2C6在黑细胞中发现了免疫反应性。 CYP2E1免疫反应性定位于许多中脑核,包括黑质致密部,而不是黑质网状组织,而对CYP2C13 / 2C6的免疫反应性则发现于黑质致密部,黑质网状组织和许多其他中脑核。通过共聚焦激光扫描显微镜检查了被CYP2E1或CYP2C13 / 2C6和酪氨酸羟化酶或神经胶质原纤维酸性蛋白双重标记的大鼠中脑切片的共定位。 CYP2E1和CYP2C13 / 2C6免疫反应性在黑质致密部的酪氨酸羟化酶阳性神经元中发现,但在神经胶质细胞中未发现。在黑质网中的非胶质,非酪氨酸羟化酶表达细胞中也发现了CYP2C13 / 2C6,而不是CYP2E1。异烟肼诱导增加了来自多巴胺能神经元的CYP2E1荧光信号强度。在含有多巴胺的黑色素细胞中发现至少两种P450酶,其中一种,即CYP2E1,选择性地定位于该细胞群。 CYP2E1是自由基的强力产生剂,可能有助于帕金森氏病的黑色病变。 CYP2E1在黑质的多巴胺能神经元中的表达增加了与帕金森氏病因果关系的可能性。

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