Perez-Leighton Claudio E, Billington Charles J, Kotz Catherine M
Veterans Health Care System, GRECC, One Veterans Drive, Minneapolis, MN 55417, USA; University of Minnesota, MN Obesity Center, 1334 Eckles Avenue, St Paul, MN 55108, USA; Center for Integrative Medicine and Innovative Sciences, Facultad de Medicina, Universidad Andres Bello, Echaurren 183, Santiago, 8370071, Chile.
Veterans Health Care System, Endocrinology, One Veterans Drive, Minneapolis, MN 55417, USA; University of Minnesota, MN Obesity Center, 1334 Eckles Avenue, St Paul, MN 55108, USA; University of Minnesota, Graduate Program in Nutrition, 1334 Eckles Avenue, St Paul, MN 55108, USA.
Biochim Biophys Acta. 2014 Mar;1842(3):440-5. doi: 10.1016/j.bbadis.2013.06.007. Epub 2013 Jun 18.
The orexins are neuropeptides with critical functions in the central nervous system. These neuropeptides have important roles in energy balance and obesity, and therefore on the accumulation of adipose tissue. Rodents lacking orexins, typically through genetic knockouts, experience increased weight gain and accumulation of adipose tissue. Evidence indicates that the lack of the orexins increase adiposity as a result of decreased energy expenditure, principally through a reduction of physical activity. Different lines of evidence suggest that other mechanisms are likely also in play, and neural influences on both white and brown adipose tissues remain to be fully and functionally defined. In addition, the orexin peptides and their receptors are expressed in adipose tissue, with little available information as to their significance. This review summarizes our current understanding of how the orexin peptides affect adipose tissue. We provide a brief introduction to the physiology of orexins and their effects on white and brown adipose tissues in the context of energy balance. We conclude this review by integrating this information in the context of the known physiology of the orexins. This article is part of a Special Issue entitled: Modulation of Adipose Tissue in Health and Disease.
食欲素是在中枢神经系统中具有关键功能的神经肽。这些神经肽在能量平衡和肥胖症中发挥重要作用,进而影响脂肪组织的积累。缺乏食欲素的啮齿动物(通常是通过基因敲除)体重增加,脂肪组织积累增多。有证据表明,缺乏食欲素会导致能量消耗减少,主要是通过减少身体活动,从而增加肥胖。不同的证据表明,其他机制可能也在起作用,对白色和棕色脂肪组织的神经影响仍有待全面和功能性地界定。此外,食欲素肽及其受体在脂肪组织中表达,但其意义的相关信息较少。本综述总结了我们目前对食欲素肽如何影响脂肪组织的理解。我们简要介绍了食欲素的生理学及其在能量平衡背景下对白色和棕色脂肪组织的影响。我们通过将这些信息整合到食欲素已知的生理学背景中来结束本综述。本文是名为:健康与疾病中脂肪组织的调节的特刊的一部分。