Adult-Onset CNS Sulfatide Deficiency Causes Sex-Dependent Metabolic Disruption in Aging

被引:2
|
作者
Qiu, Shulan [1 ,2 ]
He, Sijia [1 ]
Wang, Jianing [1 ,5 ]
Wang, Hu [1 ]
Bhattacharjee, Anindita [1 ]
Li, Xin [1 ]
Saeed, Moawiz [1 ]
Dupree, Jeffrey L. [3 ,4 ]
Han, Xianlin [1 ,2 ]
机构
[1] Univ Texas Hlth Sci Ctr San Antonio, Barshop Inst Longev & Aging Studies, San Antonio, TX 78229 USA
[2] Univ Texas Hlth Sci Ctr San Antonio, Dept Med, Div Diabet, San Antonio, TX 78229 USA
[3] Virginia Commonwealth Univ, Dept Anat & Neurobiol, Richmond, VA 23284 USA
[4] McGuire Vet Affairs Med Ctr, Res Div, Richmond, VA 23249 USA
[5] Hong Kong Baptist Univ, Dept Chem, State Key Lab Environm & Biol Anal, Hong Kong, Peoples R China
关键词
sulfatide; glucose metabolism; food intake; Alzheimer's disease; aging; ALZHEIMERS-DISEASE; HYPOTHALAMIC INFLAMMATION; RISK-FACTOR; OBESITY; MYELIN; HYPERGLYCEMIA;
D O I
10.3390/ijms241310483
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The interconnection between obesity and central nervous system (CNS) neurological dysfunction has been widely appreciated. Accumulating evidence demonstrates that obesity is a risk factor for CNS neuroinflammation and cognitive impairment. However, the extent to which CNS disruption influences peripheral metabolism remains to be elucidated. We previously reported that myelin-enriched sulfatide loss leads to CNS neuroinflammation and cognitive decline. In this study, we further investigated the impact of CNS sulfatide deficiency on peripheral metabolism while considering sex- and age-specific effects. We found that female sulfatide-deficient mice gained significantly more body weight, exhibited higher basal glucose levels, and were glucose-intolerant during glucose-tolerance test (GTT) compared to age-matched controls under a normal diet, whereas male sulfatide-deficient mice only displayed glucose intolerance at a much older age compared to female sulfatide-deficient mice. Mechanistically, we found that increased body weight was associated with increased food intake and elevated neuroinflammation, especially in the hypothalamus, in a sex-specific manner. Our results suggest that CNS sulfatide deficiency leads to sex-specific alterations in energy homeostasis via dysregulated hypothalamic control of food intake.
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页数:13
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