Prapaharan Brinda, Lea Micah, Beaudry Jacqueline L
Temerty Faculty of Medicine, Department of Nutritional Sciences, University of Toronto, Toronto, ON, Canada.
J Pharm Pharm Sci. 2024 Jul 17;27:13157. doi: 10.3389/jpps.2024.13157. eCollection 2024.
Brown adipose tissue (BAT) activation is an emerging target for obesity treatments due to its thermogenic properties stemming from its ability to shuttle energy through uncoupling protein 1 (Ucp1). Recent rodent studies show how BAT and white adipose tissue (WAT) activity can be modulated to increase the expression of thermogenic proteins. Consequently, these alterations enable organisms to endure cold-temperatures and elevate energy expenditure, thereby promoting weight loss. In humans, BAT is less abundant in obese subjects and impacts of thermogenesis are less pronounced, bringing into question whether energy expending properties of BAT seen in rodents can be translated to human models. Our review will discuss pharmacological, hormonal, bioactive, sex-specific and environmental activators and inhibitors of BAT to determine the potential for BAT to act as a therapeutic strategy. We aim to address the feasibility of utilizing BAT modulators for weight reduction in obese individuals, as recent studies suggest that BAT's contributions to energy expenditure along with Ucp1-dependent and -independent pathways may or may not rectify energy imbalance characteristic of obesity.
棕色脂肪组织(BAT)的激活是肥胖治疗的一个新兴靶点,因为其产热特性源于其通过解偶联蛋白1(Ucp1)传递能量的能力。最近的啮齿动物研究表明,如何调节BAT和白色脂肪组织(WAT)的活性以增加产热蛋白的表达。因此,这些改变使生物体能够耐受低温并提高能量消耗,从而促进体重减轻。在人类中,肥胖受试者体内的BAT较少,产热的影响也不那么明显,这就引发了一个问题,即啮齿动物中所见的BAT的能量消耗特性是否可以转化为人类模型。我们的综述将讨论BAT的药理学、激素、生物活性、性别特异性和环境激活剂及抑制剂,以确定BAT作为一种治疗策略的潜力。我们旨在探讨利用BAT调节剂减轻肥胖个体体重的可行性,因为最近的研究表明,BAT对能量消耗的贡献以及Ucp1依赖性和非依赖性途径可能会也可能不会纠正肥胖的能量失衡特征。