Sedbazar Udval, Ayush Enkh-Amar, Maejima Yuko, Yada Toshihiko
aDepartment of Physiology, Division of Integrative Physiology, Jichi Medical University School of Medicine, Shimotsuke, Tochigi bDepartment of Development Physiology, Division of Adaptation Development, National Institute for Physiological Sciences, Okazaki, Aichi, Japan.
Neuroreport. 2014 Dec 17;25(18):1453-8. doi: 10.1097/WNR.0000000000000293.
Nesfatin-1 is an 82 amino acids peptide processed from its precursor nucleobindin-2 (NUCB2). Accumulating evidences have shown that the nesfatin-1/NUCB2 localized in the paraventricular nucleus (PVN) of the hypothalamus regulates food intake and energy metabolism. However, the factors that regulate nesfatin-1/NUCB2 neurons in PVN are less defined. In the hypothalamic feeding center, the second-order neurons in PVN are extensively projected by the first-order neurons in the arcuate nucleus (ARC), the representatives of which are orexigenic neuropeptide Y (NPY) and anorexigenic α-melanocyte-stimulating hormone (α-MSH) neurons. The present study explored whether NPY and α-MSH regulate the PVN nesfatin-1/NUCB2 neurons. This was achieved by cytosolic Ca ([Ca]i) imaging, followed by nesfatin-1/NUCB2 immunostaining in single neurons isolated from PVN. The moderate increase in [Ca]i with 5 mM glucose was suppressed by NPY, but further increased by α-MSH in the PVN neurons that were shown to be immunoreactive to nesfatin-1/NUCB2. The majority (60%) of nesfatin-1/NUCB2 neurons in PVN responded to NPY and/or α-MSH. Confocal immunohistochemical images showed that both NPY and α-MSH neuronal terminals contacted nesfatin-1/NUCB2 neurons in PVN. These data show that NPY inhibits and α-MSH activates PVN nesfatin-1/NUCB2 neurons, presenting dual and reciprocal neuro-circuits from ARC to PVN, possibly contributing toward the balanced regulation of feeding.
Nesfatin-1是一种由其前体核结合蛋白-2(NUCB2)加工而成的含82个氨基酸的肽。越来越多的证据表明,位于下丘脑室旁核(PVN)的nesfatin-1/NUCB2可调节食物摄入和能量代谢。然而,调节PVN中nesfatin-1/NUCB2神经元的因素尚不清楚。在下丘脑进食中枢,PVN中的二级神经元由弓状核(ARC)中的一级神经元广泛投射,其中的代表是促食欲神经肽Y(NPY)和抑食欲α-黑素细胞刺激激素(α-MSH)神经元。本研究探讨了NPY和α-MSH是否调节PVN中的nesfatin-1/NUCB2神经元。这是通过胞质钙([Ca]i)成像实现的,随后对从PVN分离的单个神经元进行nesfatin-1/NUCB2免疫染色。在显示对nesfatin-1/NUCB2有免疫反应的PVN神经元中,5 mM葡萄糖引起的[Ca]i适度增加被NPY抑制,但被α-MSH进一步增加。PVN中大多数(60%)nesfatin-1/NUCB2神经元对NPY和/或α-MSH有反应。共聚焦免疫组化图像显示,NPY和α-MSH神经元终末均与PVN中的nesfatin-1/NUCB2神经元接触。这些数据表明,NPY抑制而α-MSH激活PVN中的nesfatin-1/NUCB2神经元,呈现从ARC到PVN的双重和相互的神经回路,可能有助于进食的平衡调节。
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