Department of Neurobiology, Harvard Medical School, 200 Longwood Avenue, Goldenson 542, Boston, MA 02215, USA; Department of Medicine, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA 02215, USA.
Department of Medicine, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA 02215, USA.
Cell Metab. 2017 Jul 5;26(1):24-26. doi: 10.1016/j.cmet.2017.05.013. Epub 2017 Jun 22.
The discovery of the obese gene and the demonstration that its encoded protein leptin can reverse obesity due to genetic deficiency of the hormone were landmark discoveries in endocrinology and metabolism. Regarding leptin's role in physiology, it is now established that falling leptin levels are a key signal of the starved state in mice and humans. Repleting leptin reverses the starvation signal both in physiologic starvation and in obesity resulting from genetic leptin deficiency. Since its discovery, it has also been hypothesized that rising leptin levels caused by overfeeding provide a physiologic signal that orchestrates resistance to obesity. Although still widely believed, and possibly true in some circumstances, this aspect of leptin physiology has not been experimentally demonstrated. It will be important to determine whether leptin or as yet undiscovered factors are responsible for the well-documented capacity for physiologic resistance to overfeeding.
肥胖基因的发现以及证明其编码的蛋白瘦素可以逆转由于激素遗传缺乏引起的肥胖,是内分泌学和代谢领域的里程碑式发现。关于瘦素在生理学中的作用,现在已经确定,瘦素水平下降是小鼠和人类饥饿状态的关键信号。补充瘦素可以逆转生理性饥饿和由遗传瘦素缺乏引起的肥胖引起的饥饿信号。自发现以来,人们还假设,过度喂养引起的瘦素水平升高提供了一种生理信号,协调对肥胖的抵抗力。尽管这一观点仍然被广泛接受,并且在某些情况下可能是正确的,但瘦素生理学的这一方面尚未得到实验证实。重要的是要确定是瘦素还是尚未发现的因素导致了众所周知的对过度喂养的生理抵抗能力。