Division of Endocrinology, Department of Medicine, Beth Israel Deaconess Medical Center and Harvard Medical School, 330 Brookline Avenue, EC/CLS717, Boston, MA 02215, USA.
Neuron. 2011 Jul 14;71(1):142-54. doi: 10.1016/j.neuron.2011.05.028.
Leptin acts in the brain to prevent obesity. The underlying neurocircuitry responsible for this is poorly understood, in part because of incomplete knowledge regarding first-order, leptin-responsive neurons. To address this, we and others have been removing leptin receptors from candidate first-order neurons. While functionally relevant neurons have been identified, the observed effects have been small, suggesting that most first-order neurons remain unidentified. Here we take an alternative approach and test whether first-order neurons are inhibitory (GABAergic, VGAT⁺) or excitatory (glutamatergic, VGLUT2⁺). Remarkably, the vast majority of leptin's antiobesity effects are mediated by GABAergic neurons; glutamatergic neurons play only a minor role. Leptin, working directly on presynaptic GABAergic neurons, many of which appear not to express AgRP, reduces inhibitory tone to postsynaptic POMC neurons. As POMC neurons prevent obesity, their disinhibition by leptin action on presynaptic GABAergic neurons probably mediates, at least in part, leptin's antiobesity effects.
瘦素在大脑中发挥作用以预防肥胖。负责这一过程的基本神经回路尚不清楚,部分原因是对一级、瘦素反应神经元的了解不完整。为了解决这个问题,我们和其他人一直在从候选一级神经元中去除瘦素受体。虽然已经确定了具有功能相关性的神经元,但观察到的效果很小,这表明大多数一级神经元仍未被识别。在这里,我们采用了一种替代方法,测试一级神经元是否是抑制性的(GABA 能的,VGAT⁺)或兴奋性的(谷氨酸能的,VGLUT2⁺)。值得注意的是,瘦素绝大多数的抗肥胖作用是由 GABA 能神经元介导的;谷氨酸能神经元只起次要作用。瘦素直接作用于大多数似乎不表达 AgRP 的突触前 GABA 能神经元,降低了对突触后 POMC 神经元的抑制性冲动。由于 POMC 神经元可以预防肥胖,因此瘦素作用于突触前 GABA 能神经元对其去抑制作用可能至少部分介导了瘦素的抗肥胖作用。