• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

中枢促食欲素-1神经元在大鼠催产素诱导的摄食抑制中的作用。

Involvement of central nesfatin-1 neurons on oxytocin-induced feeding suppression in rats.

作者信息

Saito Reiko, Sonoda Satomi, Ueno Hiromichi, Motojima Yasuhito, Yoshimura Mitsuhiro, Maruyama Takashi, Hashimoto Hirofumi, Tanaka Kentaro, Yamamoto Yukiyo, Kusuhara Koichi, Ueta Yoichi

机构信息

Department of Physiology, School of Medicine, University of Occupational and Environmental Health, 1-1 Iseigaoka, Yahatanishi-ku, Kitakyushu, Fukuoka, 807-8555, Japan; Department of Pediatrics, School of Medicine, University of Occupational and Environmental Health, Kitakyushu, Fukuoka 807-8555, Japan.

Department of Physiology, School of Medicine, University of Occupational and Environmental Health, 1-1 Iseigaoka, Yahatanishi-ku, Kitakyushu, Fukuoka, 807-8555, Japan.

出版信息

Neurosci Lett. 2017 Aug 10;655:54-60. doi: 10.1016/j.neulet.2017.06.049. Epub 2017 Jul 3.

DOI:10.1016/j.neulet.2017.06.049
PMID:28684238
Abstract

Peripheral anorectic hormones, such as peptide YY (PYY) and oxytocin (OXT), suppress food intake. A newly identified anorectic neuropeptide, nesfatin-1, is synthesized in both peripheral tissue and the central nervous system, particularly by various nuclei in the hypothalamus and brainstem. Here, we examined the effects of intraperitoneal (ip) administration of PYY, OXT, and OXT analog, on nesfatin-1-immunoreactive (ir) neurons in the rat hypothalamus and brainstem, using Fos double fluorescence-immunohistochemistry. The ip administration of OXT and OXT analog significantly increased the number of nesfatin-1-ir neurons expressing Fos-ir in the paraventricular nucleus, the arcuate nucleus, and the nucleus tractus solitarius, but not in the supraoptic nucleus, the lateral hypothalamic area, and the area postrema. No differences in the percentage of nesfatin-1-ir neurons expressing Fos in the nuclei of the hypothalamus and brainstem were observed, between rats treated with vehicle or those treated with PYY. The decreased food intake, induced by OXT and OXT analog, was attenuated significantly by pretreatment with intracerebroventricular administration of antisense nesfatin-1. These results suggested that nesfatin-1-expressing neurons in the hypothalamus and brainstem may play a role in sensing the peripheral level of OXT and its suppression of feeding in rats.

摘要

外周食欲调节激素,如肽YY(PYY)和催产素(OXT),可抑制食物摄入。一种新发现的食欲调节神经肽——内脂素-1,在外周组织和中枢神经系统中均有合成,尤其是在下丘脑和脑干的各个核团中。在此,我们使用Fos双荧光免疫组织化学方法,研究了腹腔注射PYY、OXT和OXT类似物对大鼠下丘脑和脑干中内脂素-1免疫反应性(ir)神经元的影响。腹腔注射OXT和OXT类似物显著增加了室旁核、弓状核和孤束核中表达Fos-ir的内脂素-1-ir神经元数量,但在视上核、下丘脑外侧区和最后区中未增加。在用载体处理的大鼠和用PYY处理的大鼠之间,未观察到下丘脑和脑干核团中表达Fos的内脂素-1-ir神经元百分比的差异。脑室注射反义内脂素-1预处理可显著减弱由OXT和OXT类似物诱导的食物摄入量减少。这些结果表明,下丘脑和脑干中表达内脂素-1的神经元可能在感知大鼠外周OXT水平及其对进食的抑制作用中发挥作用。

相似文献

1
Involvement of central nesfatin-1 neurons on oxytocin-induced feeding suppression in rats.中枢促食欲素-1神经元在大鼠催产素诱导的摄食抑制中的作用。
Neurosci Lett. 2017 Aug 10;655:54-60. doi: 10.1016/j.neulet.2017.06.049. Epub 2017 Jul 3.
2
Activation of Nesfatin-1-Containing Neurones in the Hypothalamus and Brainstem by Peripheral Administration of Anorectic Hormones and Suppression of Feeding via Central Nesfatin-1 in Rats.外周给予厌食激素激活大鼠下丘脑和脑干中含Nesfatin-1的神经元并通过中枢Nesfatin-1抑制进食
J Neuroendocrinol. 2016 Sep;28(9). doi: 10.1111/jne.12400.
3
Centrally administered kisspeptin suppresses feeding via nesfatin-1 and oxytocin in male rats.中枢给予 kisspeptin 通过 nesfatin-1 和催产素抑制雄性大鼠摄食。
Peptides. 2019 Feb;112:114-124. doi: 10.1016/j.peptides.2018.12.003. Epub 2018 Dec 16.
4
Peripheral injection of bombesin induces c-Fos in NUCB2/nesfatin-1 neurons.外周注射蛙皮素可诱导NUCB2/nesfatin-1神经元中c-Fos的表达。
Brain Res. 2016 Oct 1;1648(Pt A):46-53. doi: 10.1016/j.brainres.2016.07.006. Epub 2016 Jul 7.
5
CCK-8S activates c-Fos in a dose-dependent manner in nesfatin-1 immunoreactive neurons in the paraventricular nucleus of the hypothalamus and in the nucleus of the solitary tract of the brainstem.胆囊收缩素八肽(CCK-8S)以下丘脑室旁核和脑干孤束核中神经肽N表达免疫反应性神经元呈剂量依赖性的方式激活c-Fos。
Regul Pept. 2009 Oct 9;157(1-3):84-91. doi: 10.1016/j.regpep.2009.06.009. Epub 2009 Jun 21.
6
Central NUCB2/Nesfatin-1-expressing neurones belong to the hypothalamic-brainstem circuitry activated by hypoglycaemia.表达中央 NUCB2/Nesfatin-1 的神经元属于在下丘脑-脑干回路中被低血糖激活的神经元。
J Neuroendocrinol. 2013 Jan;25(1):1-13. doi: 10.1111/j.1365-2826.2012.02375.x.
7
Intracerebroventricular injection of phoenixin alters feeding behavior and activates nesfatin-1 immunoreactive neurons in rats.脑室注射凤凰素可改变摄食行为并激活大鼠 nesfatin-1 免疫反应神经元。
Brain Res. 2019 Jul 15;1715:188-195. doi: 10.1016/j.brainres.2019.03.034. Epub 2019 Mar 28.
8
Nesfatin-1 neurons in paraventricular and supraoptic nuclei of the rat hypothalamus coexpress oxytocin and vasopressin and are activated by refeeding.大鼠下丘脑室旁核和视上核中的促食欲素-1神经元共同表达催产素和加压素,并在再进食时被激活。
Endocrinology. 2008 Mar;149(3):1295-301. doi: 10.1210/en.2007-1276. Epub 2007 Nov 29.
9
Activity-based anorexia activates nesfatin-1 immunoreactive neurons in distinct brain nuclei of female rats.基于活动的厌食症激活了雌性大鼠不同脑核中表达核仁组织区相关蛋白-1的免疫反应性神经元。
Brain Res. 2017 Dec 15;1677:33-46. doi: 10.1016/j.brainres.2017.09.024. Epub 2017 Sep 23.
10
Nasal oxytocin administration reduces food intake without affecting locomotor activity and glycemia with c-Fos induction in limited brain areas.经鼻腔给予催产素可减少食物摄入量,而不影响运动活性和血糖水平,且在有限的脑区诱导c-Fos表达。
Neuroendocrinology. 2015;101(1):35-44. doi: 10.1159/000371636. Epub 2015 Jan 5.

引用本文的文献

1
Current Understanding of the Role of Nesfatin-1.对Nesfatin-1作用的当前认识。
J Endocr Soc. 2018 Sep 10;2(10):1188-1206. doi: 10.1210/js.2018-00246. eCollection 2018 Oct 1.
2
A Systematic Review and Quantitative Meta-Analysis of Oxytocin's Effects on Feeding.催产素对进食影响的系统评价与定量荟萃分析
J Neuroendocrinol. 2018 Feb 26. doi: 10.1111/jne.12584.