School of Chemistry, Chemical Engineering and Life Sciences, Wuhan University of Technology, Wuhan, 430070, China.
State Key Laboratory of Advanced Technology for Materials Synthesis and Processing, Wuhan University of Technology, Wuhan, 430070, China.
Sci Rep. 2022 Apr 1;12(1):5502. doi: 10.1038/s41598-022-09541-x.
Obesity induced by antipsychotics have plagued more than 20 million people worldwide. However, no drug is available to eliminate the obesity induced by antipsychotics. Here we examined the effect and potential mechanisms of a gold nanoclusters (AuNCs) modified by N-isobutyryl-L-cysteine on the obesity induced by olanzapine, the most prescribed but obesogenic antipsychotics, in a rat model. Our results showed that AuNCs completely prevented and reversed the obesity induced by olanzapine and improved glucose metabolism profile in rats. Further mechanism investigations revealed that AuNCs exert its anti-obesity function through inhibition of olanzapine-induced dysfunction of histamine H1 receptor and proopiomelanocortin signaling therefore reducing hyperphagia, and reversing olanzapine-induced inhibition of uncoupling-protein-1 signaling which increases thermogenesis. Together with AuNCs' good biocompatibility, these findings not only provide AuNCs as a promising nanodrug candidate for treating obesity induced by antipsychotics, but also open an avenue for the potential application of AuNCs-based nanodrugs in treating general obesity.
抗精神病药引起的肥胖困扰着全球超过 2000 万人。然而,目前尚无药物可消除抗精神病药引起的肥胖。在这里,我们研究了一种由 N-异丁酰-L-半胱氨酸修饰的金纳米簇(AuNCs)对奥氮平诱导的肥胖的作用及其潜在机制,奥氮平是处方量最大但致肥胖的抗精神病药之一,在大鼠模型中。我们的结果表明,AuNCs 完全预防和逆转了奥氮平诱导的肥胖,并改善了大鼠的葡萄糖代谢谱。进一步的机制研究表明,AuNCs 通过抑制奥氮平诱导的组氨酸 H1 受体和前阿黑皮素原信号的功能障碍发挥其抗肥胖作用,从而减少过度进食,并逆转奥氮平诱导的解偶联蛋白-1 信号的抑制,增加产热。结合 AuNCs 的良好生物相容性,这些发现不仅为治疗抗精神病药引起的肥胖提供了一种有前途的纳米药物候选物,也为基于 AuNCs 的纳米药物在治疗一般肥胖方面的潜在应用开辟了道路。