谷氨酰胺合成酶
内科学
海马结构
内分泌学
海马体
谷氨酰胺
神经油
脂肪变性
免疫组织化学
生物
医学
中枢神经系统
生物化学
氨基酸
作者
Virawudh Soontornniyomkij,James P. Kesby,Benchawanna Soontornniyomkij,Jane J. Kim,Tatiana Kisseleva,Cristian L. Achim,Svetlana Semenova,Dilip V. Jeste
出处
期刊:Current Aging Science
[Bentham Science Publishers]
日期:2016-04-18
卷期号:9 (4): 301-309
被引量:16
标识
DOI:10.2174/1874609809666160413113311
摘要
Background: High-Fat Diet (HFD)-induced obesity may promote agerelated memory impairment via disturbances of ammonia-glutamine metabolism. Objective: We studied the effects of age and long-term HFD exposure on Glutamine Synthetase (GS) expression in the liver and hippocampus and recognition memory in mice. Methods: Adult (5-month-old) and aged (15-month-old) male C57BL/6 mice were exposed to control diet (CD, 14% calories from fat) or HFD (60% fat). Novel place recognition testing was conducted and tissue was collected after 4 and 5 months on HFD, respectively. Tissue GS expression levels were assessed using immunohistochemistry and image analysis. Results: The obese mice developed moderate/severe hepatic steatosis. GS immunoreactivity was observed in perivenous hepatocytes and in hippocampal astrocytes and neuropil. Hepatic GS immunoreactivity density was higher in aged mice on HFD (n = 8) than CD (n = 13, P = 0.004). In aged mice, hippocampal GS immunoreactivity density was higher with HFD than CD (P = 0.037). In the novel place recognition test, aged mice were classified into impaired (n = 7) and unimpaired (n = 12), relative to adult mice (n = 22). Hippocampal GS immunoreactivity density was higher in impaired than unimpaired aged mice (P < 0.05). Conclusion: Long-term exposure of aged mice to HFD was associated with increased GS expression in the liver and hippocampus. Novel place recognition impairment in aged mice was associated with increased hippocampal GS expression. These findings suggest that excess ammonia is involved in the age-related effects of HFD exposure and in neurotoxicity. Keywords: Aging, GLUL, glutamine synthetase, high-fat diet, hippocampus, liver.
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