Oliveira Tadeu P D, Gonçalves Bruno D C, Oliveira Bruna S, de Oliveira Antonio Carlos P, Reis Helton J, Ferreira Claudia N, Aguiar Daniele C, de Miranda Aline S, Ribeiro Fabiola M, Vieira Erica M L, Palotás András, Vieira Luciene B
Departamento de Farmacologia, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.
Departamento de Morfologia, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.
Front Neurosci. 2021 Feb 10;15:631311. doi: 10.3389/fnins.2021.631311. eCollection 2021.
Obesity is a multifactorial disease, which in turn contributes to the onset of comorbidities, such as diabetes and atherosclerosis. Moreover, there are only few options available for treating obesity, and most current pharmacotherapy causes severe adverse effects, while offering minimal weight loss. Literature shows that metabotropic glutamate receptor 5 (mGluR5) modulates central reward pathways. Herein, we evaluated the effect of VU0409106, a negative allosteric modulator (NAM) of mGluR5 in regulating feeding and obesity parameters. Diet-induced obese C57BL/6 mice were treated for 14 days with VU0409106, and food intake, body weight, inflammatory/hormonal levels, and behavioral tests were performed. Our data suggest reduction of feeding, body weight, and adipose tissue inflammation in mice treated with high-fat diet (HFD) after chronic treatment with VU0409106. Furthermore, a negative modulation of mGluR5 also reduces binge-like eating, the most common type of eating disorder. Altogether, our results pointed out mGluR5 as a potential target for treating obesity, as well as related disorders.
肥胖是一种多因素疾病,反过来又会导致糖尿病和动脉粥样硬化等合并症的发生。此外,治疗肥胖的方法有限,目前大多数药物治疗会产生严重的不良反应,且减重效果甚微。文献表明,代谢型谷氨酸受体5(mGluR5)调节中枢奖赏通路。在此,我们评估了mGluR5的负变构调节剂(NAM)VU0409106在调节进食和肥胖参数方面的作用。用VU0409106对饮食诱导的肥胖C57BL/6小鼠进行14天治疗,并进行食物摄入量、体重、炎症/激素水平和行为测试。我们的数据表明,在用高脂饮食(HFD)喂养的小鼠中,经VU0409106长期治疗后,进食量、体重和脂肪组织炎症有所减少。此外,对mGluR5的负调节还可减少暴饮暴食,这是最常见的饮食失调类型。总之,我们的结果指出mGluR5是治疗肥胖及相关疾病的潜在靶点。