Neuroscience Research Program, Garvan Institute of Medical Research, St Vincent's Hospital, Darlinghurst, Sydney, New South Wales, Australia.
Diabetes Obes Metab. 2012 Aug;14(8):727-36. doi: 10.1111/j.1463-1326.2012.01592.x. Epub 2012 Mar 21.
Both the neuronal-derived neuropeptide Y (NPY) and the gut hormone peptide YY (PYY) have been implicated in the regulation of energy balance and glucose homeostasis. However, despite similar affinities for the same Y receptors, the co-ordinated actions of these two peptides in energy and glucose homeostasis remain largely unknown.
To investigate the mechanisms and possible interactions between PYY with NPY in the regulation of these processes, we utilized NPY/PYY single and double mutant mouse models and examined parameters of energy balance and glucose homeostasis.
PYY(-/-) mice exhibited increased fasting-induced food intake, enhanced fasting and oral glucose-induced serum insulin levels, and an impaired insulin tolerance, - changes not observed in NPY(-/-) mice. Interestingly, whereas PYY deficiency-induced impairment in insulin tolerance remained in NPY(-/-) PYY(-/-) mice, effects of PYY deficiency on fasting-induced food intake and serum insulin concentrations at baseline and after the oral glucose bolus were absent in NPY(-/-) PYY(-/-) mice, suggesting that NPY signalling may be required for PYY's action on insulin secretion and fasting-induced hyperphagia. Moreover, NPY(-/-) PYY(-/-) , but not NPY(-/-) or PYY(-/-) mice had significantly decreased daily food intake, indicating interactive control by NPY and PYY on spontaneous food intake. Furthermore, both NPY(-/-) and PYY(-/-) mice showed significantly reduced respiratory exchange ratio during the light phase, with no additive effects observed in NPY(-/-) PYY(-/-) mice, indicating that NPY and PYY may regulate oxidative fuel selection via partly shared mechanisms. Overall, physical activity and energy expenditure, however, are not significantly altered by NPY and PYY single or double deficiencies.
These findings show significant and diverse interactions between NPY and PYY signalling in the regulation of different aspects of energy balance and glucose homeostasis.
神经元衍生的神经肽 Y(NPY)和肠激素肽 YY(PYY)都与能量平衡和葡萄糖稳态的调节有关。然而,尽管它们对相同的 Y 受体具有相似的亲和力,但这两种肽在能量和葡萄糖稳态中的协同作用在很大程度上仍不清楚。
为了研究 PYY 与 NPY 在这些过程调节中的相互作用机制,我们利用 NPY/PYY 单突变和双突变小鼠模型,检测了能量平衡和葡萄糖稳态的相关参数。
PYY(-/-)小鼠表现出空腹诱导的食物摄入增加、空腹和口服葡萄糖诱导的血清胰岛素水平升高以及胰岛素耐量受损,而 NPY(-/-)小鼠则没有这些变化。有趣的是,尽管 NPY 缺失导致的胰岛素耐量受损在 NPY(-/-)PYY(-/-)小鼠中仍然存在,但 PYY 缺失对空腹诱导的食物摄入和口服葡萄糖负荷后基础和血清胰岛素浓度的影响在 NPY(-/-)PYY(-/-)小鼠中消失,表明 NPY 信号可能是 PYY 对胰岛素分泌和空腹诱导的多食作用所必需的。此外,NPY(-/-)PYY(-/-)小鼠的日摄食量明显减少,而 NPY(-/-)或 PYY(-/-)小鼠则没有,这表明 NPY 和 PYY 可能通过相互作用来控制自发性摄食。此外,NPY(-/-)和 PYY(-/-)小鼠在光照期的呼吸交换率均显著降低,而在 NPY(-/-)PYY(-/-)小鼠中则没有观察到相加效应,这表明 NPY 和 PYY 可能通过部分共享机制调节氧化燃料选择。总的来说,NPY 和 PYY 的单或双缺失对体力活动和能量消耗没有显著影响。
这些发现表明 NPY 和 PYY 信号在能量平衡和葡萄糖稳态的不同方面的调节中存在显著而多样的相互作用。