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Insulin suppresses ghrelin-induced calcium signaling in neuropeptide Y neurons of the hypothalamic arcuate nucleus

机译:胰岛素抑制下丘脑弓状核神经肽Y神经元中生长素释放肽诱导的钙信号传导

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摘要

Neuropeptide Y (NPY) neurons in the hypothalamic arcuate nucleus (ARC) play an important role in feeding regulation. Plasma levels of ghrelin and insulin show reciprocal dynamics before and after meals. We hypothesized that ghrelin and insulin also exert reciprocal effects on ARC NPY neurons. Cytosolic Ca2+ concentration ([Ca2+]i) was measured by fura-2 microfluorometry in single neurons isolated from ARC of adult rats, followed by immunocytochemical identification of NPY neurons. Ghrelin at 10−10 M increased [Ca2+]i in isolated ARC neurons, and co-administration of insulin concentration-dependently suppressed the ghrelin-induced [Ca2+]i increases. Insulin at 10−16 M, 10−14 M, 10−12 M and 10−10 M counteracted ghrelin action in 26%, 41%, 61% and 53% of ghrelin-responsive neurons, respectively, showing a maximal effect at 10−12 M, the estimated postprandial concentration of insulin in the brain. The majority (>70%) of the ghrelin-activated insulin-inhibited neurons were shown to contain NPY. Double-immunohistochemistry revealed that 85% of NPY neurons in ARC express insulin receptors. These data demonstrate that insulin directly interacts with ARC NPY neurons and counteracts ghrelin action. Our results suggest that postprandial increase in plasma insulin/ghrelin ratio and insulin inhibition of ghrelin action on ARC NPY neurons cooperate to effectively inhibit the neuron activity and terminate feeding.
机译:下丘脑弓状核(ARC)中的神经肽Y(NPY)神经元在进食调节中起重要作用。生长素释放肽和胰岛素的血浆水平在进餐前后显示出相互的动态关系。我们假设生长素释放肽和胰岛素也对ARC NPY神经元产生相互影响。用呋喃2微量荧光法测定从成年大鼠ARC分离的单个神经元的胞浆Ca2 +浓度([Ca2 +] i),然后进行NPY神经元的免疫细胞化学鉴定。在10−10 M的Ghrelin增加了孤立的ARC神经元中的[Ca2 +] i,并且共同给药胰岛素可抑制Ghrelin诱导的[Ca2 +] i的增加。 10-16 M,10-14 M,10-12 M和10-10 M的胰岛素分别在26%,41%,61%和53%的ghrelin响应神经元中抵消了ghrelin的作用,在10时表现出最大的作用-12 M,即大脑中餐后胰岛素的估计浓度。 ghrelin激活的胰岛素抑制神经元的大多数(> 70%)显示含有NPY。双重免疫组织化学显示,ARC中NPY神经元的85%表达胰岛素受体。这些数据表明,胰岛素直接与ARC NPY神经元相互作用,并抵消ghrelin的作用。我们的研究结果表明,餐后血浆胰岛素/生长素释放肽比率的增加和胰岛素对ARC NPY神经元的生长素释放肽的抑制作用可以有效抑制神经元活性并终止进食。

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