5-甲氧基-2-氨基茚满能逆转饮食诱发的肥胖症并改善小鼠的代谢参数:一类潜在的抗肥胖症新疗法

Saja Baraghithy, Asaad Gammal, Anna Permyakova, Sharleen Hamad, Radka Kočvarová, Yael Calles and Joseph Tam*, 
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引用次数: 0

摘要

肥胖症及其相关疾病的发病率不断攀升,对全球健康构成了严峻的挑战。遗憾的是,目前针对肥胖症的药物干预措施仍然有限,而且往往伴有使人衰弱的副作用。在此背景下,精神活性氨基茚满衍生物 5-甲氧基-2-氨基茚满(MEAI)因其在抑制酒精消费的同时还能诱发类似酒精的愉悦感觉而备受关注。鉴于 MEAI 对食物成瘾和能量平衡的潜在影响,我们利用饮食诱导肥胖(DIO)小鼠模型,研究了它在急性和慢性情况下对食欲调节、肥胖和相关合并症的代谢功效。我们的研究结果表明,MEAI治疗可通过保持瘦肉量和减少脂肪量来显著减轻DIO诱导的超重和肥胖。此外,MEAI治疗还通过减轻DIO诱发的高血糖、葡萄糖不耐受和高胰岛素血症,对血糖控制产生了积极影响。此外,MEAI 还能减少肝脏脂质积累,降低肝脏甘油三酯和胆固醇水平,主要是通过抑制脂质的新生合成,从而减轻 DIO 引起的肝脏脂肪变性。代谢表型分析表明,MEAI 增加了能量消耗和脂肪利用率,同时保持了与车辆处理组相似的食物消耗量。最后,MEAI 使自主运动正常化,而没有任何过度刺激作用。这些发现为 MEAI 治疗的抗肥胖效果提供了令人信服的证据,需要进一步进行临床前试验。总之,我们的研究凸显了 MEAI 作为一种新型治疗方法治疗肥胖症及其相关代谢紊乱的潜力,为开发新的治疗方案以应对这一全球性健康挑战带来了希望。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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5-Methoxy-2-aminoindane Reverses Diet-Induced Obesity and Improves Metabolic Parameters in Mice: A Potential New Class of Antiobesity Therapeutics

The escalating prevalence of obesity and its related disorders represents a daunting global health challenge. Unfortunately, current pharmacological interventions for obesity remain limited and are often associated with debilitating side effects. Against this backdrop, the psychoactive aminoindane derivative 5-methoxy-2-aminoindane (MEAI) has gained considerable attention for its ability to induce a pleasurable, alcohol-like sensation while curbing alcohol consumption. Given the potential impact of MEAI on food addiction and energy homeostasis, we examined its metabolic efficacy on appetite regulation, obesity, and related comorbidities under acute and chronic settings, utilizing a mouse model of diet-induced obesity (DIO). Our results demonstrated that MEAI treatment significantly reduced DIO-induced overweight and adiposity by preserving lean mass and decreasing fat mass. Additionally, MEAI treatment exhibited positive effects on glycemic control by attenuating DIO-induced hyperglycemia, glucose intolerance, and hyperinsulinemia. Furthermore, MEAI reduced DIO-induced hepatic steatosis by decreasing hepatic lipid accumulation and lowering liver triglyceride and cholesterol levels, primarily by inhibiting de novo lipid synthesis. Metabolic phenotyping revealed that MEAI increased energy expenditure and fat utilization while maintaining food consumption similar to that of the vehicle-treated group. Lastly, MEAI normalized voluntary locomotion actions without any overstimulatory effects. These findings provide compelling evidence for the antiobesity effects of MEAI treatment and call for further preclinical testing. In conclusion, our study highlights the potential of MEAI as a novel therapeutic approach for treating obesity and its associated metabolic disorders, offering hope for the development of new treatment options for this global health challenge.

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来源期刊
ACS Pharmacology and Translational Science
ACS Pharmacology and Translational Science Medicine-Pharmacology (medical)
CiteScore
10.00
自引率
3.30%
发文量
133
期刊介绍: ACS Pharmacology & Translational Science publishes high quality, innovative, and impactful research across the broad spectrum of biological sciences, covering basic and molecular sciences through to translational preclinical studies. Clinical studies that address novel mechanisms of action, and methodological papers that provide innovation, and advance translation, will also be considered. We give priority to studies that fully integrate basic pharmacological and/or biochemical findings into physiological processes that have translational potential in a broad range of biomedical disciplines. Therefore, studies that employ a complementary blend of in vitro and in vivo systems are of particular interest to the journal. Nonetheless, all innovative and impactful research that has an articulated translational relevance will be considered. ACS Pharmacology & Translational Science does not publish research on biological extracts that have unknown concentration or unknown chemical composition. Authors are encouraged to use the pre-submission inquiry mechanism to ensure relevance and appropriateness of research.
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