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

Journal of clinical and medical sciences Pub Date : 2023-01-01 Epub Date: 2023-07-28
Komal Sodhi, Kyle Maxwell, Yanling Yan, Jiang Liu, Muhammad A Chaudhry, Zijian Xie, Joseph I Shapiro
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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 in vitro 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.

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pNaKtide抑制Na/K-ATP酶信号传导并减轻肥胖症
肥胖症是全球日益严重的公共健康危机,已被公认为代谢综合征的潜在风险因素。越来越多的证据表明,氧化应激在肥胖和相关代谢功能障碍的病理生理机制中起着至关重要的作用。由于我们之前已经证实 Na/K-ATPase 可以放大氧化应激信号,因此我们旨在利用多肽拮抗剂 pNaKtide 探索抑制该通路对肥胖表型的影响。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。此外,这些体外实验结果在以高脂肪饮食喂养的 C57Bl6 小鼠身上得到了证实。有趣的是,pNaKtide 能显著降低肥胖小鼠的体重,改善全身氧化和炎症环境,提高胰岛素敏感性。因此,这项研究证明了 pNaKtide 作为 Na/K-ATPase 氧化剂放大信号抑制剂对减轻肥胖症及相关合并症的治疗作用。
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