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衰老细胞耗竭可缓解肥胖相关的代谢和心脏疾病。

Senescent cell depletion alleviates obesity-related metabolic and cardiac disorders.

作者信息

de Oliveira Silva Tábatha, Lunardon Guilherme, Lino Caroline A, de Almeida Silva Amanda, Zhang Shiju, Irigoyen Maria Cláudia Costa, Lu Yao Wei, Mably John D, Barreto-Chaves Maria Luiza M, Wang Da-Zhi, Diniz Gabriela P

机构信息

Department of Anatomy, Institute of Biomedical Sciences, University of Sao Paulo, Sao Paulo, SP, Brazil; Center for Regenerative Medicine, USF Health Heart Institute, University of South Florida, Tampa, FL, USA.

Department of Anatomy, Institute of Biomedical Sciences, University of Sao Paulo, Sao Paulo, SP, Brazil.

出版信息

Mol Metab. 2025 Jan;91:102065. doi: 10.1016/j.molmet.2024.102065. Epub 2024 Nov 16.

Abstract

UNLABELLED

Obesity is a major contributor to metabolic and cardiovascular disease. Although senescent cells have been shown to accumulate in adipose tissue, the role of senescence in obesity-induced metabolic disorders and in cardiac dysfunction is not yet clear; therefore, the therapeutic potential of managing senescence in obesity-related metabolic and cardiac disorders remains to be fully defined.

OBJECTIVE

We investigated the beneficial effects of a senolytic cocktail (dasatinib and quercetin) on senescence and its influence on obesity-related parameters.

METHODS AND RESULTS

We found that the increase in body weight and adiposity, glucose intolerance, insulin resistance, dyslipidemia, hyperleptinemia, and hepatic disorders which were induced by an obesogenic diet were alleviated by senolytic cocktail treatment in mice. Treatment with senolytic compounds eliminated senescent cells, counteracting the activation of the senescence program and DNA damage in white adipose tissue (WAT) observed with an obesogenic diet. Moreover, the senolytic cocktail prevented the brown adipose tissue (BAT) whitening and increased the expression of the thermogenic gene profile in BAT and pWAT. In the hearts of obese mice, senolytic combination abolished myocardial maladaptation, reducing the senescence-associated secretory phenotype (SASP) and DNA damage, repressing cardiac hypertrophy, and improving diastolic dysfunction. Additionally, we showed that treatment with the senolytic cocktail corrected gene expression programs associated with fatty acid metabolism, oxidative phosphorylation, the P53 pathway, and DNA repair, which were all downregulated in obese mice.

CONCLUSIONS

Collectively, these data suggest that a senolytic cocktail can prevent the activation of the senescence program in the heart and WAT and activate the thermogenic program in BAT. Our results suggest that targeting senescent cells may be a novel therapeutic strategy for alleviating obesity-related metabolic and cardiac disorders.

摘要

未标注

肥胖是代谢和心血管疾病的主要促成因素。尽管衰老细胞已被证明会在脂肪组织中积累,但衰老在肥胖诱导的代谢紊乱和心脏功能障碍中的作用尚不清楚;因此,在肥胖相关的代谢和心脏疾病中管理衰老的治疗潜力仍有待充分明确。

目的

我们研究了一种衰老细胞溶解鸡尾酒(达沙替尼和槲皮素)对衰老的有益作用及其对肥胖相关参数的影响。

方法与结果

我们发现,致肥胖饮食诱导的体重增加、肥胖、葡萄糖不耐受、胰岛素抵抗、血脂异常、高瘦素血症和肝脏疾病,在小鼠中通过衰老细胞溶解鸡尾酒治疗得到缓解。用衰老细胞溶解化合物治疗可消除衰老细胞,抵消致肥胖饮食观察到的白色脂肪组织(WAT)中衰老程序的激活和DNA损伤。此外,衰老细胞溶解鸡尾酒可防止棕色脂肪组织(BAT)变白,并增加BAT和pWAT中产热基因谱的表达。在肥胖小鼠的心脏中,衰老细胞溶解组合消除了心肌适应不良,减少了衰老相关分泌表型(SASP)和DNA损伤,抑制了心脏肥大,并改善了舒张功能障碍。此外,我们表明,用衰老细胞溶解鸡尾酒治疗可纠正与脂肪酸代谢、氧化磷酸化、P53途径和DNA修复相关的基因表达程序,这些程序在肥胖小鼠中均下调。

结论

总体而言,这些数据表明,衰老细胞溶解鸡尾酒可防止心脏和WAT中衰老程序的激活,并激活BAT中的产热程序。我们的结果表明,靶向衰老细胞可能是缓解肥胖相关代谢和心脏疾病的一种新的治疗策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/304b/11636344/7a931a0033a9/gr1.jpg

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