内科学
迷走神经切断术
内分泌学
医学
褐色脂肪组织
脂肪组织
脂肪变性
胰岛素
脂肪肝
脂肪细胞
肥胖
减肥
高胰岛素血症
白色脂肪组织
饮食性肥胖
抵抗素
摄入
脂肪垫
甘油三酯
胰岛素抵抗
传出的
假手术
糖尿病
作者
Antonio Machado Felisberto,Andresa Jesica Zamoner,Jean Franciesco Vettorazzi,Janaina de Oliveira Chaves,Vanessa Cristina de Souza Melo,Amanda Gotz Lopes,Joseane Morari,Paulo Roberto Ribeiro,Antônio C. Boschero,Rosane Aparecida Ribeiro,Maria Lúcia Bonfleur,Sandra Lucinei Balbo
标识
DOI:10.1139/apnm-2025-0190
摘要
The abolishment of vagal abdominal afferents and efferent inputs through vagotomy has been shown to prevent obesity. However, it is unknown whether such a strategy, performed after obesity installation, may treat or ameliorate obesity and its comorbidities. Here, we aimed to verify the effects of subdiaphragmatic vagotomy on obesity and metabolic dysfunction-associated steatotic liver disease (MASLD) in obese mice that continued to be fed an obesogenic diet after the operation. Obesity was induced in male C57Bl/6 mice by ingestion of a high-fat diet (HFD). Afterward, obese (OB) mice were randomly submitted to Sham (OB-Sham group) or subdiaphragmatic vagotomy (OB-Vag group) and continued to be fed a HFD for 8 weeks. Vagotomy led to reductions in body weight, without modifying food intake in OB-Vag mice. While these rodents showed no modifications in subcutaneous fat accumulation, they exhibited higher abdominal adiposity. In contrast, the weight of the interscapular brown adipose tissue (BAT) was lower in OB-Vag mice, with brown adipocytes in its parenchyma showing reduced size and fewer lipid vacuoles, resembling the high-thermogenic adipocyte type. This effect was partially explained by increased gene expressions of Prdm16, Pgc-1α, and Dio2, key factors maintaining BAT identity and function. Furthermore, subdiaphragmatic vagotomy enhanced glucose tolerance, insulin sensitivity, improved serum and hepatic lipids levels, and ameliorated MASLD in OB-Vag mice. Vagotomy performed after obesity induction improved BAT function and insulin sensitivity, which may partly contribute to alleviating MASLD in OB mice that continued to consume an obesogenic diet.
科研通智能强力驱动
Strongly Powered by AbleSci AI