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pNaKtide抑制钠钾ATP酶信号传导并减轻肥胖。

pNaKtide Inhibits Na/K-ATPase Signaling and Attenuates Obesity.

作者信息

Sodhi Komal, Maxwell Kyle, Yan Yanling, Liu Jiang, Chaudhry Muhammad A, Xie Zijian, Shapiro Joseph I

机构信息

Department of Medicine, Biomedical Science, and Surgery, Joan C. Edwards School of Medicine, Marshall University, Huntington, United States of America.

出版信息

J Clin Med Sci. 2023;7(4). Epub 2023 Jul 28.

Abstract

Obesity is a growing public health crisis across the world and has been recognized as an underlying risk factor for metabolic syndrome. Growing evidence demonstrates the critical role of oxidative stress in the pathophysiological mechanisms of obesity and related metabolic dysfunction. As we have established previously that Na/K-ATPase can amplify oxidative stress signaling, we aimed to explore the effect of inhibition of this pathway on obesity phenotype using the peptide antagonist, pNaKtide. The experiments performed in murine preadipocytes showed the dose-dependent effect of pNaKtide in attenuating oxidant stress and lipid accumulation. Furthermore, these findings were confirmed in C57Bl6 mice fed a high-fat diet. Interestingly, pNaKtide could significantly reduce body weight, ameliorate systemic oxidative and inflammatory milieu and improve insulin sensitivity in obese mice. Hence the study demonstrates the therapeutic utility of pNaKtide as an inhibitor of Na/K-ATPase oxidant amplification signaling to alleviate obesity and associated comorbidities.

摘要

肥胖是全球日益严重的公共卫生危机,已被公认为代谢综合征的潜在危险因素。越来越多的证据表明氧化应激在肥胖及相关代谢功能障碍的病理生理机制中起关键作用。由于我们之前已经确定钠钾ATP酶可以放大氧化应激信号,因此我们旨在使用肽拮抗剂pNaKtide探索抑制该途径对肥胖表型的影响。在小鼠前脂肪细胞中进行的实验表明,pNaKtide在减轻氧化应激和脂质积累方面具有剂量依赖性作用。此外,这些发现在用高脂饮食喂养的C57Bl6小鼠中得到了证实。有趣的是,pNaKtide可以显著降低肥胖小鼠的体重,改善全身氧化和炎症环境,并提高胰岛素敏感性。因此,该研究证明了pNaKtide作为钠钾ATP酶氧化放大信号抑制剂在减轻肥胖及相关合并症方面的治疗效用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6983/10812088/4a2ca380d915/nihms-1917373-f0001.jpg

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