Age-related changes in adipose tissue metabolomics and inflammation, cardiolipin metabolism, and ferroptosis markers in female aged rat model.

Age-related changes in adipose tissue metabolomics and inflammation, cardiolipin metabolism, and ferroptosis markers in female aged rat model.
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DOI:
10.1016/j.bbrc.2023.06.027
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发表时间:
2023-06
影响因子:
3.1
通讯作者:
Zhuangzhuang Wang;Fanghui Li;Pinfei Ni;Lei Sun;Chen-Kai Zhang;Bo-Ming Li;Jia-Han He;Xiao-ming Yu;Yun-Qing Liu
Zhuangzhuang Wang;Fanghui Li;Pinfei Ni;Lei Sun;Chen-Kai Zhang;Bo-Ming Li;Jia-Han He;Xiao-ming Yu;Yun-Qing Liu
中科院分区:
生物学4区
文献类型:
--
作者:
Zhuangzhuang Wang;Fanghui Li;Pinfei Ni;Lei Sun;Chen-Kai Zhang;Bo-Ming Li;Jia-Han He;Xiao-ming Yu;Yun-Qing Liu

文献摘要

相似文献

Aging adipose tissue exhibits elevated inflammation and oxidative stress that are major sources of age-related metabolic dysfunction. However, the exact metabolic changes associated with inflammation and oxidative stress are unclear. To address this topic, we assessed variation in metabolic phenotypes of adipose tissue from 18 months adult sedentary (ASED), 26 months old sedentary (OSED), and 8 months young sedentary (YSED). The results of metabolomic analysis showed that ASED and OSED group had higher palmitic acid, elaidic acid, 1-heptadecanol, and α-tocopherol levels than YSED, but lower sarcosine levels. Furthermore, stearic acid was specifically elevated in ASED compared with YSED. Cholesterol was upregulated specifically in the OSED group compared with YSED, whereas linoleic acid was downregulated. In addition, ASED and OSED had more inflammatory cytokines, lower antioxidant capacity, and higher expression of ferroptosis-related genes than YSED. Moreover, mitochondrial dysfunction associated with abnormal cardiolipin synthesis was more pronounced in the OSED group. In conclusion, both ASED and OSED can affect the FA metabolism and increase oxidative stress in adipose tissue, leading to inflammation. In particular, linoleic acid content specifically decreases in OSED, which associated with abnormal cardiolipin synthesis and mitochondrial dysfunction in adipose tissue.