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Sympathetic Neuro-adipose Connections Mediate Leptin-Driven Lipolysis

机译:交感神经-脂肪连接介导瘦素驱动的脂解

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摘要

Leptin is a hormone produced by the adipose tissue that acts in the brain, stimulating white fat breakdown. We find that the lipolytic effect of leptin is mediated through the action of sympathetic nerve fibers that innervate the adipose tissue. Using intravital two-photon microscopy, we observe that sympathetic nerve fibers establish neuro-adipose junctions, directly "enveloping'' adipocytes. Local optogenetic stimulation of sympathetic inputs induces a local lipolytic response and depletion of white adipose mass. Conversely, genetic ablation of sympathetic inputs onto fat pads blocks leptin-stimulated phosphorylation of hormone-sensitive lipase and consequent lipolysis, as do knockouts of dopamine beta-hydroxylase, an enzyme required for catecholamine synthesis. Thus, neuro-adipose junctions are necessary and sufficient for the induction of lipolysis in white adipose tissue and are an efferent effector of leptin action. Direct activation of sympathetic inputs to adipose tissues may represent an alternative approach to induce fat loss, circumventing central leptin resistance.
机译:瘦素是由脂肪组织产生的一种激素,作用于大脑,刺激白色脂肪分解。我们发现瘦素的脂解作用是通过支配脂肪组织的交感神经纤维的作用介导的。使用活体双光子显微镜,我们观察到交感神经纤维建立了神经-脂肪连接,直接“包裹”了脂肪细胞,交感神经输入的局部光遗传学刺激引起了局部脂肪分解反应和白色脂肪团的消耗。脂肪垫上的输入会阻止瘦素刺激的激素敏感性脂肪酶的磷酸化和随后的脂解作用,而多巴胺β-羟化酶(儿茶酚胺合成所需的酶)的敲除也是如此,因此,神经-脂肪连接对于诱导脂肪分解中的脂解是必要和充分的。脂肪组织是白色的脂肪组织,是瘦素作用的传出效应物,直接激活脂肪组织的交感神经输入可能是诱导脂肪减少,规避中央瘦素抵抗的另一种方法。

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