Rahardjo Gita L, Huang Xu-Feng, Tan Yean Yeow, Deng Chao
School of Health Sciences, University of Wollongong, Wollongong, New South Wales 2500, Australia.
Endocrinology. 2007 Oct;148(10):4704-10. doi: 10.1210/en.2007-0107. Epub 2007 Jul 5.
It is well known that the peripheral peptide YY (PYY)-central neuropeptide Y (NPY) Y2 receptor axis plays an important role in promoting negative energy balance regulation. Both the hypothalamus and medulla oblongata express a high level of Y2 receptors; however, the functional role of this receptor in chronic high-fat diet-induced obesity has not been fully examined. Using quantitative autoradiography, this study measured binding densities of total [(125)I]PYY and Y2 receptors in the hypothalamus and medulla of chronic high-fat diet-induced obese (DIO), obese-resistant, and low-fat-fed mice. Plasma PYY was also measured using RIA after 22 wk of dietary intervention. The results revealed that body weight gain was significantly higher in the obese mice, compared with the lean mice. Furthermore, PYY and NPY Y2 receptor binding densities in the medulla of the obese mice were significantly higher, compared with the lean mice, whereas the level of plasma PYY was significantly lower in the DIO mice than the low-fat-fed mice. In conclusion, this study showed that the DIO mice had low plasma PYY, which may have caused a compensatory up-regulation of PYY and Y2 receptor densities in the medulla. A low-level response of PYY-medullary regulation to positive energy balance may have contributed to the development of high-fat diet-induced obesity in DIO mice; conversely, a normal response of this regulatory axis in the obese-resistant mice may have contributed to the maintenance of body weight while on a high-fat diet.
众所周知,外周肽YY(PYY)-中枢神经肽Y(NPY)Y2受体轴在促进负能量平衡调节中发挥重要作用。下丘脑和延髓均高表达Y2受体;然而,该受体在慢性高脂饮食诱导的肥胖中的功能作用尚未得到充分研究。本研究采用定量放射自显影技术,测量了慢性高脂饮食诱导的肥胖(DIO)小鼠、肥胖抵抗小鼠和低脂喂养小鼠下丘脑和延髓中总[(125)I]PYY及Y2受体的结合密度。在进行22周饮食干预后,还采用放射免疫分析法测定了血浆PYY水平。结果显示,与瘦小鼠相比,肥胖小鼠的体重增加显著更高。此外,与瘦小鼠相比,肥胖小鼠延髓中PYY和NPY Y2受体的结合密度显著更高,而DIO小鼠的血浆PYY水平显著低于低脂喂养小鼠。总之,本研究表明DIO小鼠血浆PYY水平较低,这可能导致延髓中PYY和Y2受体密度的代偿性上调。PYY-延髓调节对正能量平衡的低水平反应可能促成了DIO小鼠高脂饮食诱导的肥胖的发生;相反,肥胖抵抗小鼠中该调节轴的正常反应可能有助于其在高脂饮食时维持体重。