Metabolic remodeling of visceral and subcutaneous white adipose tissue during reacclimation of rats after cold

白色脂肪组织 内科学 内分泌学 脂肪甘油三酯脂肪酶 脂肪组织 脂质代谢 化学 乙酰辅酶A羧化酶 甘油三酯 生物 丙酮酸羧化酶 生物化学 脂解 医学 胆固醇
作者
Marta Marta Budnar Soskic,Tamara Zakić,Aleksandra Korać,Bato Korać,Aleksandra Janković
出处
期刊:Applied Physiology, Nutrition, and Metabolism [Canadian Science Publishing]
被引量:1
标识
DOI:10.1139/apnm-2023-0448
摘要

Deciphering lipid metabolism in white adipose tissue (WAT) depots during weight gain is important to understand the heterogeneity of WAT and its roles in obesity. Here, we examined the expression of key enzymes of lipid metabolism and changes in the morphology of representative visceral (epididymal) and subcutaneous (inguinal) WAT (eWAT and iWAT, respectively)-in adult male rats acclimated to cold (4 ± 1 °C) for 45 days and reacclimated to room temperature (RT, 22 ± 1 °C) for 1, 3, 7, 12, 21, or 45 days. The relative mass of both depots decreased to a similar extent after cold acclimation. However, fatty acid synthase (FAS), glucose-6-phosphate dehydrogenase (G6PDH), and medium-chain acyl-CoA dehydrogenase (ACADM) protein level increased only in eWAT, whereas adipose triglyceride lipase (ATGL) expression increased only in iWAT. During reacclimation, the relative mass of eWAT reached control values on day 12 and that of iWAT on day 45 of reacclimation. The faster recovery of eWAT mass is associated with higher expression of FAS, acetyl-CoA carboxylase (ACC), G6PDH, and ACADM during reacclimation and a delayed increase in ATGL. The absence of an increase in proliferating cell nuclear antigen suggests that the observed depot-specific mass increase is predominantly due to metabolic adjustments. In summary, this study shows a differential rate of visceral and subcutaneous adipose tissue weight regain during post-cold reacclimation of rats at RT. Faster recovery of the visceral WAT as compared to subcutaneous WAT during reacclimation at RT could be attributed to observed differences in the expression patterns of lipid metabolic enzymes.
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