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本文引用的文献

1
The anorexigenic and hypertensive effects of nesfatin-1 are reversed by pretreatment with an oxytocin receptor antagonist.nesfatin-1 的厌食和升压作用可被催产素受体拮抗剂预处理所逆转。
Am J Physiol Regul Integr Comp Physiol. 2010 Jun;298(6):R1642-7. doi: 10.1152/ajpregu.00804.2009. Epub 2010 Mar 24.
2
Restraint stress alters the secretory activity of neurons co-expressing urocortin-1, cocaine- and amphetamine-regulated transcript peptide and nesfatin-1 in the mouse Edinger-Westphal nucleus.束缚应激改变了在小鼠 Edinger-Westphal 核中共表达 Ucn-1、可卡因和安非他命调节转录肽和 nesfatin-1 的神经元的分泌活性。
Brain Res. 2010 Mar 4;1317:92-9. doi: 10.1016/j.brainres.2009.12.053. Epub 2010 Jan 4.
3
Nucleobindin-2/nesfatin in the endocrine pancreas: distribution and relationship to glycaemic state.胰岛内分泌中的核连蛋白 2/nesfatin:分布与糖状态的关系。
J Endocrinol. 2010 Mar;204(3):255-63. doi: 10.1677/JOE-09-0254. Epub 2009 Dec 23.
4
The novel function of nesfatin-1: anti-hyperglycemia.nesfatin-1 的新功能:抗高血糖。
Biochem Biophys Res Commun. 2010 Jan 1;391(1):1039-42. doi: 10.1016/j.bbrc.2009.12.014. Epub 2009 Dec 6.
5
Novel insight in distribution of nesfatin-1 and phospho-mTOR in the arcuate nucleus of the hypothalamus of rats.新型 nesfatin-1 和磷酸化 mTOR 在大鼠下丘脑弓状核中的分布研究。
Peptides. 2010 Feb;31(2):257-62. doi: 10.1016/j.peptides.2009.11.024. Epub 2009 Dec 2.
6
Abdominal surgery activates nesfatin-1 immunoreactive brain nuclei in rats.腹部手术激活大鼠脑中 nesfatin-1 免疫反应性核。
Peptides. 2010 Feb;31(2):263-70. doi: 10.1016/j.peptides.2009.11.015. Epub 2009 Nov 26.
7
Fasting plasma levels of nesfatin-1 in patients with type 1 and type 2 diabetes mellitus and the nutrient-related fluctuation of nesfatin-1 level in normal humans.1型和2型糖尿病患者的空腹血浆内脂素-1水平以及正常人内脂素-1水平与营养相关的波动情况。
Regul Pept. 2010 Jan 8;159(1-3):72-7. doi: 10.1016/j.regpep.2009.11.003.
8
Nesfatin-1-regulated oxytocinergic signaling in the paraventricular nucleus causes anorexia through a leptin-independent melanocortin pathway.室旁核中 nesfatin-1 调节的催产素能信号通过瘦素非依赖的黑皮质素途径引起厌食。
Cell Metab. 2009 Nov;10(5):355-65. doi: 10.1016/j.cmet.2009.09.002.
9
Nesfatin-1 evokes Ca2+ signaling in isolated vagal afferent neurons via Ca2+ influx through N-type channels.内脂素-1通过N型通道的钙离子内流在离体迷走神经传入神经元中引发钙离子信号。
Biochem Biophys Res Commun. 2009 Dec 18;390(3):958-62. doi: 10.1016/j.bbrc.2009.10.085. Epub 2009 Oct 21.
10
Glucocorticoids increase NPY gene expression in the arcuate nucleus by inhibiting mTOR signaling in rat hypothalamic organotypic cultures.糖皮质激素通过抑制大鼠下丘脑器官培养物中的 mTOR 信号传导增加弓状核中的 NPY 基因表达。
Peptides. 2010 Jan;31(1):145-9. doi: 10.1016/j.peptides.2009.09.036. Epub 2009 Oct 8.

内脂素-1:一种新型的抑制食欲和体重的调节因子。

Nesfatin-1: a novel inhibitory regulator of food intake and body weight.

机构信息

Department of Medicine, CURE Digestive Diseases Research Center and Center for Neurobiology of Stress, Digestive Diseases Division UCLA, and VA Greater Los Angeles Healthcare System, Los Angeles, CA 90073, USA.

出版信息

Obes Rev. 2011 Apr;12(4):261-71. doi: 10.1111/j.1467-789X.2010.00770.x.

DOI:10.1111/j.1467-789X.2010.00770.x
PMID:20546141
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4079085/
Abstract

The protein nucleobindin 2 (NUCB2) or NEFA (DNA binding/EF-hand/acidic amino acid rich region) was identified over a decade ago and implicated in intracellular processes. New developments came with the report that post-translational processing of hypothalamic NUCB2 may result in nesfatin-1, nesfatin-2 and nesfatin-3 and convergent studies showing that nesfatin-1 and full length NUCB2 injected in the brain potently inhibit the dark phase food intake in rodents including leptin receptor deficient Zucker rats. Nesfatin-1 also reduces body weight gain, suggesting a role as a new anorexigenic factor and modulator of energy balance. In light of the obesity epidemic and its associated diseases, underlying new mechanisms regulating food intake may be promising targets in the drug treatment of obese patients particularly as the vast majority of them display reduced leptin sensitivity or leptin resistance while nesfatin-1's mechanism of action is leptin independent. Although much progress on the localization of NUCB2/nesfatin-1 in the brain and periphery as well as on the understanding of nesfatin-1's anorexic effect have been achieved during the past three years, several important mechanisms have yet to be unraveled such as the identification of the nesfatin-1 receptor and the regulation of NUCB2 processing and nesfatin-1 release.

摘要

十多年前,人们发现了核结合蛋白 2(NUCB2)或 NEFA(DNA 结合/EF 手/酸性氨基酸丰富区),并认为其与细胞内过程有关。新的发展是由于报告表明,下丘脑 NUCB2 的翻译后加工可能导致 nesfatin-1、nesfatin-2 和 nesfatin-3,而趋同研究表明,nesfatin-1 和全长 NUCB2 注射到大脑中可有效抑制包括瘦素受体缺乏型 Zucker 大鼠在内的啮齿动物的暗期摄食。nesfatin-1 还可降低体重增加,表明其作为一种新的厌食因子和能量平衡调节剂的作用。鉴于肥胖症的流行及其相关疾病,调节食物摄入的潜在新机制可能成为肥胖患者药物治疗的有希望的靶点,特别是因为绝大多数肥胖患者表现出瘦素敏感性降低或瘦素抵抗,而 nesfatin-1 的作用机制与瘦素无关。尽管在过去三年中,人们在脑和外周组织中 NUCB2/nesfatin-1 的定位以及 nesfatin-1 的厌食作用方面取得了许多进展,但仍有几个重要的机制尚未阐明,例如 nesfatin-1 受体的鉴定以及 NUCB2 加工和 nesfatin-1 释放的调节。