详细信息
Theragra chalcogramma Hydrolysates, Rich of Fragment Gly-Leu- Pro-Ser-Tyr-Thr, Ameliorate Alcohol-Induced Cognitive Impairment via Attenuating Neuroinflammation and Enhancing Neuronal Plasticity in Sprague-Dawley Rats ( SCI-EXPANDED收录 EI收录) 被引量:3
文献类型:期刊文献
英文题名:Theragra chalcogramma Hydrolysates, Rich of Fragment Gly-Leu- Pro-Ser-Tyr-Thr, Ameliorate Alcohol-Induced Cognitive Impairment via Attenuating Neuroinflammation and Enhancing Neuronal Plasticity in Sprague-Dawley Rats
作者:Xu, Defeng[1,2];Zhao, Mouming[3]
机构:[1]Guangdong Ocean Univ, Coll Food Sci & Technol, Zhanjiang, 524088, Peoples R China;[2]Guangdong Prov Engn Technol Res Ctr Marine Food, Guangdong Prov Key Lab Aquat Prod Proc & Safety, Zhanjiang 524088, Peoples R China;[3]South China Univ Technol, Sch Food Sci & Engn, Guangzhou 510640, Peoples R China
年份:2022
卷号:70
期号:39
起止页码:12513
外文期刊名:JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY
收录:SCI-EXPANDED(收录号:WOS:000862788100001)、、EI(收录号:20224012842163)、Scopus(收录号:2-s2.0-85139206405)、WOS
基金:Funding This investigation was financially supported by the State Key Research and Development Plan (no. 2017YFD0400200) and the China Postdoctoral Science Foundation (no. 2014M552208) .
语种:英文
外文关键词:alcohol-induced cognitive impairment; neuroinflammation; Theragra chalcogramma hydrolysates; hippocampal histopathology; synaptic plasticity
外文摘要:Chronic alcohol abuse induces the cognitive deficits and is associated with low-grade inflammation and neurodegeneration. Currently, by virtue of the immunomodulatory and neuroprotective properties, nutrients represent a promising strategy to attenuate cognitive impairments. We previously prepared the hydrolysates from Theragra chalcogramma skin (TCH), and this study aims to evaluate the neuroprotection of TCH on alcohol-induced cognitive impairment (AICI) and to elucidate the associated mechanism. Behavioral results showed that TCH effectively ameliorated AICI and this amelioration was highly associated with the decrease of IL-1 beta and the increase of BDNF, CREB, and PSD95 in AICI rats (P < 0.05). Furthermore, TCH restored the histopathological impairment in hippocampus by reactivating extracellular signal-regulated kinase and suppressing Caspase-3 apoptosis signal pathways and modulating the abnormality of neurotransmitters acetylcholine and gamma-aminobutyric acid(P < 0.05 or 0.01). Therefore, TCH exhibits potent attenuation of neuroinflammation and represents a potential ingredient for prevention of AICI.
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