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大鼠脑内多巴胺能和去甲肾上腺素能损伤后儿茶酚-O-甲基转移酶(COMT)蛋白表达和活性的变化。

Catechol-O-methyltransferase (COMT) protein expression and activity after dopaminergic and noradrenergic lesions of the rat brain.

机构信息

Division of Pharmacology & Toxicology, Faculty of Pharmacy, University of Helsinki, Helsinki, Finland.

出版信息

PLoS One. 2013 Apr 16;8(4):e61392. doi: 10.1371/journal.pone.0061392. Print 2013.

DOI:10.1371/journal.pone.0061392
PMID:23613844
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3628796/
Abstract

The occurrence of catechol-O-methyltransferase (COMT) in presynaptic neurons remains controversial. This study utilized dopaminergic and noradrenergic toxins to assess the presence of COMT in the presynaptic neurons originating from the substantia nigra, ventral tegmental area or locus coeruleus. Destruction of dopaminergic and noradrenergic neurons was assessed by measuring the dopamine and noradrenaline content in the projection areas of these neurons. Additionally, COMT protein expression and activity were examined in several projection areas to determine whether there are any changes in COMT values. Colocalization studies were done to identify COMT-containing postsynaptic neurons. Despite successful lesioning of dopaminergic and noradrenergic neurons, no changes in COMT protein expression or activity could be noted. These results strongly suggest that COMT is not present in presynaptic dopaminergic and noradrenergic neurons. There was a high colocalization of COMT with the GABAergic marker of short neurons both in the striatum and cortex but only a weak, if any, with the cholinergic marker in the cortex.

摘要

儿茶酚-O-甲基转移酶(COMT)是否存在于突触前神经元中一直存在争议。本研究利用多巴胺能和去甲肾上腺素能毒素来评估源自黑质、腹侧被盖区或蓝斑的突触前神经元中 COMT 的存在。通过测量这些神经元投射区的多巴胺和去甲肾上腺素含量来评估多巴胺能和去甲肾上腺素能神经元的破坏情况。此外,还在几个投射区检查了 COMT 蛋白表达和活性,以确定 COMT 值是否有任何变化。进行共定位研究以鉴定含有 COMT 的突触后神经元。尽管多巴胺能和去甲肾上腺素能神经元的损伤成功,但未观察到 COMT 蛋白表达或活性的变化。这些结果强烈表明 COMT 不存在于突触前多巴胺能和去甲肾上腺素能神经元中。COMT 与纹状体和皮质中的短神经元的 GABA 标记物高度共定位,但与皮质中的胆碱能标记物的共定位仅为弱共定位(如果有)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/117a/3628796/b2286ab9bd04/pone.0061392.g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/117a/3628796/70b7a9a41348/pone.0061392.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/117a/3628796/8be749a02ca7/pone.0061392.g002.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/117a/3628796/cb2cc4bac893/pone.0061392.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/117a/3628796/3fdad5d7026a/pone.0061392.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/117a/3628796/adfcd68d7e99/pone.0061392.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/117a/3628796/b2286ab9bd04/pone.0061392.g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/117a/3628796/70b7a9a41348/pone.0061392.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/117a/3628796/8be749a02ca7/pone.0061392.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/117a/3628796/cfb322a11aa8/pone.0061392.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/117a/3628796/cb2cc4bac893/pone.0061392.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/117a/3628796/3fdad5d7026a/pone.0061392.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/117a/3628796/adfcd68d7e99/pone.0061392.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/117a/3628796/b2286ab9bd04/pone.0061392.g007.jpg

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