Kaineder K, Birngruber T, Rauter G, Obermüller B, Eichler J, Münzker J, Al-Zoughbi W, Mautner S I, Torekov S S, Hartmann B, Kotzbeck P, Pieber T R
Division of Endocrinology and Diabetology, Department of Internal Medicine, Medical University of Graz, Graz, Austria.
Joanneum Research, Health - Institute for Biomedicine and Health Sciences, Graz, Austria.
Int J Obes (Lond). 2017 Aug;41(8):1263-1270. doi: 10.1038/ijo.2017.98. Epub 2017 Apr 25.
The GLP-1 receptor agonist liraglutide is marketed for obesity treatment where it induces body weight reduction possibly via the hypothalamus, which regulates energy homeostasis. In animal studies, acute liraglutide treatment triggers satiety, weight loss and activates thermogenesis in adipose tissue. However, the precise mechanisms how liraglutide affects in particular chronic weight loss are still under investigation.
We aimed to evaluate whether chronic hypothalamic or chronic subcutaneous administration of liraglutide induces sustained weight loss through altered adipose tissue function and to what extent hypothalamic neuronal appetite regulators are involved in the liraglutide-induced weight loss in healthy lean rats on a normal diet.
MATERIALS/METHODS: We continuously administered liraglutide either intrahypothalamically (10 μg per day) or subcutaneously (200 μg kg per day) for 28 days to lean Sprague Dawley rats (n=8 each). We assessed changes in body weight, adipose tissue mass, adipocyte size and adipose tissue volume in the abdominal region by using micro-CT. We analyzed genetic expression patterns of browning, thermogenic and adipocyte differentiation regulators in adipose tissues as well as particular neuronal appetite regulators in the hypothalamus.
Intrahypothalamic liraglutide administration induced an 8% body weight reduction at day 9 compared with the control group (P<0.01) and a 7% body weight loss at day 9 compared with subcutaneous liraglutide treatment (P<0.01), supported by a significant reduction in adipose tissue mass and volume with intrahypothalamic liraglutide administration (P<0.05). Our data show that chronic intrahypothalamic liraglutide treatment triggered an 18-fold induction of the hypothalamic mc4r gene (P<0.01) accompanied by a significant increase in circulating thyroxine (T4) levels (P<0.05).
Chronic intrahypothalamic liraglutide administration resulted in a profound reduction in body weight and fat mass loss most likely mediated by the hypothalamic melanocortin system rather than by adipose tissue browning or improved thermogenesis.
胰高血糖素样肽-1(GLP-1)受体激动剂利拉鲁肽已上市用于肥胖治疗,它可能通过调节能量平衡的下丘脑诱导体重减轻。在动物研究中,急性利拉鲁肽治疗可引发饱腹感、体重减轻并激活脂肪组织的产热作用。然而,利拉鲁肽如何具体影响慢性体重减轻的确切机制仍在研究中。
我们旨在评估慢性下丘脑或慢性皮下注射利拉鲁肽是否通过改变脂肪组织功能诱导持续体重减轻,以及下丘脑神经元食欲调节因子在正常饮食的健康瘦大鼠利拉鲁肽诱导的体重减轻中参与的程度。
材料/方法:我们对瘦的斯普拉格-道利大鼠(每组n = 8)持续28天进行下丘脑内(每天10μg)或皮下(每天200μg/kg)注射利拉鲁肽。我们使用微型计算机断层扫描(micro-CT)评估体重、脂肪组织质量、脂肪细胞大小和腹部脂肪组织体积的变化。我们分析了脂肪组织中褐变、产热和脂肪细胞分化调节因子以及下丘脑中特定神经元食欲调节因子的基因表达模式。
与对照组相比,下丘脑内注射利拉鲁肽在第9天导致体重减轻8%(P < 0.01),与皮下注射利拉鲁肽治疗相比,在第9天体重减轻7%(P < 0.01),下丘脑内注射利拉鲁肽使脂肪组织质量和体积显著减少(P < 0.05)。我们的数据表明,慢性下丘脑内注射利拉鲁肽治疗引发下丘脑黑皮质素4受体(mc4r)基因诱导18倍(P < 0.01),同时循环甲状腺素(T4)水平显著升高(P < 0.05)。
慢性下丘脑内注射利拉鲁肽导致体重和脂肪量显著减少,最有可能是由下丘脑黑皮质素系统介导,而非通过脂肪组织褐变或改善产热作用。