Nomegestrol acetate ameliorated adipose atrophy in a rat model of cisplatin‑induced cachexia

• Published in: Experimental and therapeutic medicine 2023-01, Vol.25 (1), Article 24
• Main Authors: Zhong, Ruihua, Yang, Wenjie, Li, Guoting, Xie, Shuwu, Guo, Xiangjie, Zhou, Jieyun, Ren, Bingtao, Zhu, Yan
• Format: Article
• Language: English
• Subjects: Adipose tissues; Animals; Anorexia; Antibodies; Body fat; Cachexia; Cancer; Chemotherapy; Cisplatin; Complications and side effects; Development and progression; Drug dosages; Drug therapy; Experiments; Health aspects; Megestrol acetate; Metabolism; Mortality; Patient outcomes; Pharmaceuticals; Proteins; Sodium; Tumor necrosis factor-TNF
• ISSN: 1792-0981; 1792-1015
• DOI: 10.3892/etm.2022.11723

Cachexia, a complex disorder that results in depletion of adipose tissue and skeletal muscle, is driven by anorexia, metabolic abnormalities and inflammation. There are limited therapeutic options for this syndrome. Previous evidence has demonstrated that increasing adipose tissue may improve quality of life and survival outcomes in cachexia. Cisplatin, as a chemotherapy drug, also causes cachexia during antitumor therapy due to its adverse effects. To establish a rat model of cachexia, the animals were intraperitoneally treated with cisplatin at doses of 1, 2 and 3 mg/kg, and the rats that responded to cisplatin at the optimal dose were used to test the effect of nomegestrol acetate (NOMAc). Rats that were assessed to be sensitive to cisplatin were randomly grouped and intragastrically administered vehicle, 5 or 10 mg/kg megestrol acetate (MA) or 2.5, 5 or 10 mg/kg NOMAc. The body weights and food consumption of the rats were assessed. Serum IL-6 and TNF-a levels were assessed using ELISA. The protein expression levels of adipose triglyceride lipase (ATGL), hormone-sensitive lipase (HSL), peroxisome proliferator activated receptor y (PPARy), fatty acid synthase (FASN) and sterol regulatory element-binding protein-1 (SREBP-1) from inguinal white adipose tissue (iWAT) and epididymal white adipose tissue (eWAT) were evaluated using western blotting. The optimal way to establish a chemotherapy-induced rat model of cachexia demonstrated in the present study was to intraperitoneally administer the rats with 2 mg/kg cisplatin for 3 consecutive days. NOMAc (2.5, 5 mg/kg) and MA (10 mg/kg) were able to significantly ameliorate the loss of body weight in the cisplatin-induced cachectic rats. NOMAc significantly reduced the serum levels of TNF-[alpha] at 10 mg/kg. Morphologically, iWAT atrophy, with a remarkable reduction in adipocyte volume, was observed in the cisplatin-induced cachectic rats, but the effects were reversed by administering 5, 10 mg/kg NOMAc or 10 mg/kg MA. Furthermore, 2.5 mg/kg NOMAc markedly reduced the protein expression levels of the lipolysis genes HSL and ATGL, and 5 mg/kg NOMAc markedly enhanced the protein expression levels of adipogenesis genes, including FASN, SREBP-1 and PPAR[gamma] in iWAT but not in eWAT. NOMAc was demonstrated to improve cachexia at lower doses compared with MA. Overall, NOMAc is likely to be a promising candidate drug for ameliorating cancer cachexia induced by cisplatin. Key words: cancer cachexia, megestrol acetat