Department of Internal Medicine I, Luebeck University, Ratzeburger Allee 160, 23538 Luebeck, Germany.
Endocrinology. 2012 Jan;153(1):143-53. doi: 10.1210/en.2011-1586. Epub 2011 Nov 29.
Resistance to brain-mediated effects of leptin is a characteristic feature of obesity, resulting from alterations in leptin receptor signaling in hypothalamic neurons and/or transport across the blood-brain-barrier. We have shown previously, that the latter can be circumvented by intranasal (i.n.) application of leptin in lean rats. This prompted us to test i.n. leptin in animals with diet-induced obesity (DIO) as a basis for future human administration. DIO was induced in male Wistar rats by feeding a cafeteria diet for 25 or 32 wk, respectively. Consecutively, these DIO animals (seven to eight per treatment) and standard diet rats (lean) (14-15 per treatment, matched for age and diet duration) were treated with 0.1, 0.2 mg/kg leptin, or control solution i.n. daily for 4 wk before onset of dark period. Energy intake and body weight were measured daily; blood glucose, serum insulin, and leptin were measured before and after treatment. Expression of hypothalamic neuropeptides was assessed by quantitative real-time PCR. We demonstrate, for the first time, that i.n. leptin reduces appetite and induces weight loss in DIO to the same extent as in lean rats. Our findings are supported accordingly by an altered expression pattern of anorexigenic and orexigenic neuropeptides in the hypothalamus, e.g. proopiomelanocortin, cocaine and amphetamine-related transcript, neuropeptide Y, agouti-related protein. It now appears clear that i.n. leptin is effectively acting in obese animals in the same fashion as in their lean counterparts. These findings now clearly warrant studies in humans and may open new perspectives in the treatment of obesity.
抵抗瘦素对大脑的作用是肥胖的一个特征,这是由于下丘脑神经元中瘦素受体信号转导和/或血脑屏障转运的改变所致。我们之前已经表明,在瘦鼠中,通过鼻内(i.n.)给予瘦素可以绕过后者。这促使我们在饮食诱导肥胖(DIO)动物中测试鼻内瘦素,作为未来人类给药的基础。通过分别喂食自助餐饮食 25 或 32 周,在雄性 Wistar 大鼠中诱导 DIO。随后,这些 DIO 动物(每种处理七到八只)和标准饮食大鼠(瘦)(每种处理 14-15 只,年龄和饮食时间匹配)每天接受 0.1、0.2 mg/kg 瘦素或对照溶液 i.n.治疗,持续 4 周,在黑暗期开始前。每日测量能量摄入和体重;在治疗前后测量血糖、血清胰岛素和瘦素。通过定量实时 PCR 评估下丘脑神经肽的表达。我们首次证明,鼻内给予瘦素可降低 DIO 大鼠的食欲并诱导体重减轻,与瘦大鼠的效果相同。我们的发现得到了相应的支持,即下丘脑中厌食性和食欲刺激性神经肽的表达模式发生了改变,例如前阿黑皮素原、可卡因和安非他命相关转录物、神经肽 Y、肥胖相关蛋白。现在很明显,鼻内给予瘦素在肥胖动物中的作用与在其瘦鼠中的作用相同。这些发现现在显然需要在人类中进行研究,并可能为肥胖症的治疗开辟新的前景。