Diabetes, Endocrinology, and Obesity Branch, Intramural Research Program, National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK), NIH, Bethesda, Maryland, USA.
Liver Diseases Branch, NIDDK, NIH, Bethesda, Maryland, USA.
J Clin Invest. 2020 May 1;130(5):2209-2219. doi: 10.1172/JCI131126.
BACKGROUNDMirabegron is a β3-adrenergic receptor (β3-AR) agonist approved only for the treatment of overactive bladder. Encouraging preclinical results suggest that β3-AR agonists could also improve obesity-related metabolic disease by increasing brown adipose tissue (BAT) thermogenesis, white adipose tissue (WAT) lipolysis, and insulin sensitivity.METHODSWe treated 14 healthy women of diverse ethnicities (27.5 ± 1.1 years of age, BMI of 25.4 ± 1.2 kg/m2) with 100 mg mirabegron (Myrbetriq extended-release tablet, Astellas Pharma) for 4 weeks in an open-label study. The primary endpoint was the change in BAT metabolic activity as measured by [18F]-2-fluoro-d-2-deoxy-d-glucose (18F-FDG) PET/CT. Secondary endpoints included resting energy expenditure (REE), plasma metabolites, and glucose and insulin metabolism as assessed by a frequently sampled intravenous glucose tolerance test.RESULTSChronic mirabegron therapy increased BAT metabolic activity. Whole-body REE was higher, without changes in body weight or composition. Additionally, there were elevations in plasma levels of the beneficial lipoprotein biomarkers HDL and ApoA1, as well as total bile acids. Adiponectin, a WAT-derived hormone that has antidiabetic and antiinflammatory capabilities, increased with acute treatment and was 35% higher upon completion of the study. Finally, an intravenous glucose tolerance test revealed higher insulin sensitivity, glucose effectiveness, and insulin secretion.CONCLUSIONThese findings indicate that human BAT metabolic activity can be increased after chronic pharmacological stimulation with mirabegron and support the investigation of β3-AR agonists as a treatment for metabolic disease.TRIAL REGISTRATIONClinicaltrials.gov NCT03049462.FUNDINGThis work was supported by grants from the Intramural Research Program of the NIDDK, NIH (DK075112, DK075116, DK071013, and DK071014).
米拉贝隆是一种仅用于治疗膀胱过度活动症的β3 肾上腺素能受体(β3-AR)激动剂。令人鼓舞的临床前研究结果表明,β3-AR 激动剂还可以通过增加棕色脂肪组织(BAT)产热、白色脂肪组织(WAT)脂肪分解和胰岛素敏感性来改善肥胖相关代谢疾病。
我们在一项开放性研究中,用 100mg 米拉贝隆(Astellas Pharma 的米拉贝隆缓释片)治疗了 14 名不同种族的健康女性(年龄 27.5±1.1 岁,BMI 为 25.4±1.2kg/m2),为期 4 周。主要终点是通过 [18F]-2-氟-2-脱氧-d-葡萄糖(18F-FDG)PET/CT 测量的 BAT 代谢活性的变化。次要终点包括静息能量消耗(REE)、血浆代谢物以及通过频繁采样静脉葡萄糖耐量试验评估的葡萄糖和胰岛素代谢。
慢性米拉贝隆治疗可增加 BAT 代谢活性。全身 REE 升高,而体重或体成分无变化。此外,有益的脂蛋白生物标志物 HDL 和 ApoA1 以及总胆汁酸的血浆水平升高。脂联素是一种源自 WAT 的激素,具有抗糖尿病和抗炎作用,在急性治疗时升高,在研究结束时升高了 35%。最后,静脉葡萄糖耐量试验显示胰岛素敏感性、葡萄糖效能和胰岛素分泌增加。
这些发现表明,慢性药物刺激米拉贝隆后可增加人体 BAT 代谢活性,并支持β3-AR 激动剂作为治疗代谢疾病的研究。
Clinicaltrials.gov NCT03049462。
这项工作得到了美国国立卫生研究院(NIH)糖尿病、消化和肾脏疾病研究所(DK075112、DK075116、DK071013 和 DK071014)内部研究计划的支持。