Center for Metabolism and Obesity Research, Johns Hopkins University School of Medicine, 855 N. Wolfe St., Baltimore, MD 21205, USA.
Am J Physiol Regul Integr Comp Physiol. 2011 Jul;301(1):R116-30. doi: 10.1152/ajpregu.00147.2011. Epub 2011 Apr 13.
Storage of excess calories as triglycerides is central to obesity and its associated disorders. Glycerol-3-phosphate acyltransferases (GPATs) catalyze the initial step in acylglyceride syntheses, including triglyceride synthesis. We utilized a novel small-molecule GPAT inhibitor, FSG67, to investigate metabolic consequences of systemic pharmacological GPAT inhibition in lean and diet-induced obese (DIO) mice. FSG67 administered intraperitoneally decreased body weight and energy intake, without producing conditioned taste aversion. Daily FSG67 (5 mg/kg, 15.3 μmol/kg) produced gradual 12% weight loss in DIO mice beyond that due to transient 9- to 10-day hypophagia (6% weight loss in pair-fed controls). Continued FSG67 maintained the weight loss despite return to baseline energy intake. Weight was lost specifically from fat mass. Indirect calorimetry showed partial protection by FSG67 against decreased rates of oxygen consumption seen with hypophagia. Despite low respiratory exchange ratio due to a high-fat diet, FSG67-treated mice showed further decreased respiratory exchange ratio, beyond pair-fed controls, indicating enhanced fat oxidation. Chronic FSG67 increased glucose tolerance and insulin sensitivity in DIO mice. Chronic FSG67 decreased gene expression for lipogenic enzymes in white adipose tissue and liver and decreased lipid accumulation in white adipose, brown adipose, and liver tissues without signs of damage. RT-PCR showed decreased gene expression for orexigenic hypothalamic neuropeptides AgRP or NPY after acute and chronic systemic FSG67. FSG67 given intracerebroventricularly (100 and 320 nmol icv) produced 24-h weight loss and feeding suppression, indicating contributions from direct central nervous system sites of action. Together, these data point to GPAT as a new potential therapeutic target for the management of obesity and its comorbidities.
将多余的卡路里以甘油三酯的形式储存是肥胖及其相关疾病的核心。甘油-3-磷酸酰基转移酶 (GPAT) 催化酰甘油合成的初始步骤,包括甘油三酯合成。我们利用一种新型小分子 GPAT 抑制剂 FSG67,研究了全身性药理学 GPAT 抑制在瘦鼠和饮食诱导肥胖 (DIO) 小鼠中的代谢后果。FSG67 腹腔内给药可降低体重和能量摄入,而不会产生条件性味觉厌恶。每日 FSG67(5mg/kg,15.3μmol/kg)可使 DIO 小鼠逐渐减轻 12%的体重,而不是由于短暂的 9-10 天的食欲减退(配对喂养对照组减轻 6%的体重)。尽管恢复到基线能量摄入,但持续的 FSG67 仍保持体重减轻。体重是从脂肪质量中减轻的。间接测热法显示,FSG67 部分保护了由于食欲减退而导致的耗氧量降低。尽管由于高脂肪饮食导致呼吸交换率低,但 FSG67 处理的小鼠表现出进一步降低的呼吸交换率,超过了配对喂养对照组,表明脂肪氧化增强。慢性 FSG67 可提高 DIO 小鼠的葡萄糖耐量和胰岛素敏感性。慢性 FSG67 降低了白色脂肪组织和肝脏中脂肪生成酶的基因表达,并减少了白色脂肪、棕色脂肪和肝脏组织中的脂质积累,而没有损伤迹象。实时 PCR 显示,急性和慢性全身性 FSG67 后下丘脑食欲肽 AgRP 或 NPY 的基因表达减少。FSG67 脑室给药(100 和 320nmol icv)可产生 24 小时体重减轻和摄食抑制,表明与中枢神经系统直接作用部位有关。总之,这些数据表明 GPAT 是肥胖及其合并症管理的新的潜在治疗靶点。