Matsushita Hiroko, Ishihara Akane, Mashiko Satoshi, Tanaka Takeshi, Kanno Tetsuya, Iwaasa Hisashi, Ohta Hisashi, Kanatani Akio
Tsukuba Research Institute, Banyu Pharmaceutical Co Ltd, Tsukuba, Japan.
Endocrinology. 2009 Jun;150(6):2668-73. doi: 10.1210/en.2008-1515. Epub 2009 Feb 5.
Nociceptin/orphanin FQ (N/OFQ), an endogenous ligand for opioid receptor-like 1 (ORL1), is involved in various central functions, such as pain, psychological stress, locomotor activity, learning and memory, and feeding regulation. Of these functions, the role of N/OFQ in the regulation of feeding has been suggested by the fact that the central administration of N/OFQ leads to feeding behavior. However, the manner in which N/OFQ influences body weight control and subsequent obesity is unclear. To clarify the involvement of N/OFQ in the development of obesity, we evaluated the effects of intracerebroventricular infusion of N/OFQ on food intake and body weight in C57BL/6J mice that were fed a regular chow diet or moderately high-fat (MHF) diet (32.6% kcal fat). N/OFQ significantly increased food intake and body weight both in the regular diet- and MHF diet-fed mice, and these changes were more apparent in the MHF diet-fed mice. When we performed a pair-feeding study in N/OFQ intracerebroventricularly infused mice, N/OFQ did not cause body weight gain but increased white adipose tissue weight and plasma leptin, insulin, and cholesterol levels. N/OFQ reduced rectal temperature in pair-fed mice, in keeping with decreased UCP1 mRNA expression in brown adipose tissue. These results suggest that N/OFQ contributes to the development of obesity not only by inducing hyperphagia but also by decreasing energy expenditure.
孤啡肽/痛敏肽(N/OFQ)是阿片受体样1(ORL1)的内源性配体,参与多种中枢功能,如疼痛、心理应激、运动活动、学习和记忆以及进食调节。在这些功能中,N/OFQ在进食调节中的作用已通过向中枢给予N/OFQ会导致进食行为这一事实得到提示。然而,N/OFQ影响体重控制及随后肥胖的方式尚不清楚。为阐明N/OFQ在肥胖发生中的作用,我们评估了向C57BL/6J小鼠脑室内注射N/OFQ对其食物摄入量和体重的影响,这些小鼠分别喂食常规饲料或中度高脂肪(MHF)饲料(32.6%千卡脂肪)。N/OFQ显著增加了喂食常规饲料和MHF饲料小鼠的食物摄入量和体重,且这些变化在喂食MHF饲料的小鼠中更明显。当我们对脑室内注射N/OFQ的小鼠进行配对喂养研究时,N/OFQ并未导致体重增加,但增加了白色脂肪组织重量以及血浆瘦素、胰岛素和胆固醇水平。N/OFQ降低了配对喂养小鼠的直肠温度,这与棕色脂肪组织中解偶联蛋白1(UCP1)mRNA表达降低一致。这些结果表明,N/OFQ不仅通过诱导摄食过多,还通过降低能量消耗,促进了肥胖的发生。