科研成果详情

题名Elevated intracranial dopamine impairs the glutamate-nitric oxide-cyclic guanosine monophosphate pathway in cortical astrocytes in rats with minimal hepatic encephalopathy
作者
发表日期2014-09
发表期刊MOLECULAR MEDICINE REPORTS   影响因子和分区
语种英语
原始文献类型Article
关键词dopamine primary cortical astrocytes glutamate-nitric oxide-cyclic guanosine monophosphate minimal hepatic encephalopathy
其他关键词WORKING-MEMORY ; RECEPTOR ; MICE ; STRIATUM ; PROTEIN ; CELLS ; TRANSMISSION ; MODULATION ; ACTIVATION ; INHIBITION
摘要In a previous study by our group memory impairment in rats with minimal hepatic encephalopathy (MHE) was associated with the inhibition of the glutamate-nitric oxide-cyclic guanosine monophosphate (Glu-NO-cGMP) pathway due to elevated dopamine (DA). However, the effects of DA on the Glu-NO-cGMP pathway localized in primary cortical astrocytes (PCAs) had not been elucidated in rats with MHE. In the present study, it was identified that when the levels of DA in the cerebral cortex of rats with MHE and high-dose DA (3 mg/kg)-treated rats were increased, the co-localization of N-methyl-D-aspartate receptors subunit 1 (NMDAR1), calmodulin (CaM), nitric oxide synthase (nNOS), soluble guanylyl cyclase (sGC) and cyclic guanine monophosphate (cGMP) with the glial fibrillary acidic protein (GFAP), a marker protein of astrocytes, all significantly decreased, in both the MHE and high-dose DA-treated rats (P<0.01). Furthermore, NMDA-induced augmentation of the expression of NMDAR1, CaM, nNOS, sGC and cGMP localized in PCAs was decreased in MHE and DA-treated rats, as compared with the controls. Chronic exposure of cultured cerebral cortex PCAs to DA treatment induced a dose-dependent decrease in the concentration of intracellular calcium, nitrites and nitrates, the formation of cGMP and the expression of NMDAR1, CaM, nNOS and sGC/cGMP. High doses of DA (50 mu M) significantly reduced NMDA-induced augmentation of the formation of cGMP and the contents of NMDAR1,CaM, nNOS, sGC and cGMP (P<0.01). These results suggest that the suppression of DA on the Glu-NO-cGMP pathway localized in PCAs contributes to memory impairment in rats with MHE.
资助项目Natural Science Foundation of ChinaNational Natural Science Foundation of China (NSFC) [81300308, 81301014]
出版者SPANDIDOS PUBL LTD
出版地ATHENS
ISSN1791-2997
EISSN1791-3004
卷号10期号:3页码:1215-1224
DOI10.3892/mmr.2014.2386
页数10
WOS类目Oncology ; Medicine, Research & Experimental
WOS研究方向Oncology ; Research & Experimental Medicine
WOS记录号WOS:000340854500005
收录类别SCIE ; PUBMED ; SCOPUS
URL查看原文
PubMed ID25059564
PMC记录号PMC4121426
SCOPUSEID2-s2.0-84905440077
通讯作者地址[Lin, Yuanshao]First Department of Neurology, Wenzhou Medical University,China
Scopus学科分类Biochemistry;Molecular Medicine;Molecular Biology;Genetics;Oncology;Cancer Research
引用统计
被引频次:8[WOS]   [WOS记录]     [WOS相关记录]
文献类型期刊论文
条目标识符https://kms.wmu.edu.cn/handle/3ETUA0LF/12729
专题附属第一医院
第一临床医学院(信息与工程学院)、附属第一医院_计算机与信息管理系
第一临床医学院(信息与工程学院)、附属第一医院_内科学_神经内科
通讯作者Lin, Yuanshao
作者单位
1.Zhejiang Provincial Key Laboratory of Aging and Neurological Disease Research, Department of Surgery Laboratory, Wenzhou Medical University,China;
2.Neurosurgery Department, Wenzhou Medical University,China;
3.Department of Computer, Wenzhou Medical University,China;
4.First Department of Neurology, Wenzhou Medical University,China
第一作者单位温州医科大学
通讯作者单位温州医科大学
第一作者的第一单位温州医科大学
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GB/T 7714
Ding, Saidan,Huang, Weilong,Ye, Yiru,et al. Elevated intracranial dopamine impairs the glutamate-nitric oxide-cyclic guanosine monophosphate pathway in cortical astrocytes in rats with minimal hepatic encephalopathy[J]. MOLECULAR MEDICINE REPORTS,2014,10(3):1215-1224.
APA Ding, Saidan., Huang, Weilong., Ye, Yiru., Yang, Jianjing., Hu, Jiangnan., ... & Lin, Yuanshao. (2014). Elevated intracranial dopamine impairs the glutamate-nitric oxide-cyclic guanosine monophosphate pathway in cortical astrocytes in rats with minimal hepatic encephalopathy. MOLECULAR MEDICINE REPORTS, 10(3), 1215-1224.
MLA Ding, Saidan,et al."Elevated intracranial dopamine impairs the glutamate-nitric oxide-cyclic guanosine monophosphate pathway in cortical astrocytes in rats with minimal hepatic encephalopathy".MOLECULAR MEDICINE REPORTS 10.3(2014):1215-1224.

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