Malonylation of Acetyl-CoA carboxylase 1 promotes hepatic steatosis and is attenuated by ketogenic diet in NAFLD

Cao, Huanyi; Cai, Qingxian; Guo, Wanrong; Qiao, Shan; Qin, Hancheng; Xian, Yingxin; Cai, Mengyin; Guan, Haixia; Chen, Sifan; Liang, Hua; Xu, Fen

doi:10.1016/j.celrep.2023.112319

Cited by 6 publications

(1 citation statement)

References 53 publications

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“…The immunofluorescence staining in adipose tissue was conducted as previously described [27]. Rabbit anti-cytochrome c (CytC) (#11940, 1:100, CST, USA) and mouse anti-cytochrome c oxidase subunit IV (COX IV) (# PTM-5908, 1:50, PTM Biolabs, China) were applied to fixed and embedded sections overnight at 4 °C, followed by incubation with secondary antibodies (1:500).…”

Section: Immunofluorescence Stainingmentioning

confidence: 99%

Pioglitazone-Enhanced Brown Fat Whitening Contributes to Weight Gain in Diet-Induced Obese Mice

Yu,

Wang,

Guo

et al. 2023

Exp Clin Endocrinol Diabetes

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Pioglitazone is an insulin sensitizer used for the treatment of type 2 diabetes mellitus (T2DM) by activating peroxisome proliferator-activated receptor gamma. This study aimed to investigate the effects of pioglitazone on white adipose tissue (WAT) and brown adipose tissue (BAT) in diet-induced obese (DIO) mice. C57BL/6 mice were treated with pioglitazone (30mg/kg/day) for four weeks after a sixteen-week high-fat diet (HFD) challenge. Body weight gain, body fat mass, energy intake and glucose homeostasis were measured during or after the treatment. Histopathology was observed by hematoxylin and eosin, oil red O, immunohistochemistry and immunofluorescence staining. The expression of thermogenic and mitochondrial biogenesis related genes was detected by quantitative real-time PCR and western blotting. After four-week pioglitazone treatment, the fasting blood glucose levels, glucose tolerance, and insulin sensitivity were significantly improved, but the body weight gain and fat mass were increased in DIO mice. Compared with the HFD group, pioglitazone did not significantly affect the weights of liver and WAT in both subcutaneous and epididymal regions. Unexpectedly, the weight of BAT was increased after pioglitazone treatment. Histological staining revealed that pioglitazone ameliorated hepatic steatosis, reduced the adipocyte size in WAT, but increased the adipocyte size in BAT. Though pioglitazone can promote lipolysis, thermogenesis and mitochondrial function in WAT, it also leads to the impaired thermogenesis and mitochondrial dysfunction in BAT. In conclusion, pioglitazone could promote the browning of WAT but lead to the BAT whitening, the latter might be a new potential mechanism of pioglitazone-induced weight gain during the treatment of T2DM.

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Section: Immunofluorescence Stainingmentioning

confidence: 99%