• 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

纳曲酮在孤束核中对神经肽Y诱导进食的阻断作用的区域效应

Regional effect of naltrexone in the nucleus of the solitary tract in blockade of NPY-induced feeding.

作者信息

Kotz C M, Glass M J, Levine A S, Billington C J

机构信息

Departments of Food Science and Nutrition, University of Minnesota, Saint Paul 55108, USA.

出版信息

Am J Physiol Regul Integr Comp Physiol. 2000 Feb;278(2):R499-503. doi: 10.1152/ajpregu.2000.278.2.R499.

DOI:10.1152/ajpregu.2000.278.2.R499
PMID:10666153
Abstract

Naltrexone (NLTX) in the nucleus of the solitary tract (NTS) decreases feeding induced by neuropeptide Y (NPY) in the paraventricular nucleus (PVN). We sought to determine the NTS region most sensitive to NLTX blockade of PVN NPY-induced feeding. Male Sprague-Dawley rats were fitted with two cannulas; one in the PVN and one in a hindbrain region: caudal, medial, or rostral NTS or 1 mm outside the NTS. Animals received NLTX (0, 1, 3, 10, and 30 microg in 0.3 microl) into the hindbrain region just prior to PVN NPY (0.5 microg, 0.3 microl) or artificial cerebrospinal fluid (0.3 microl). Food intake was measured at 2 h following injection. PVN NPY stimulated feeding, and NLTX in the medial NTS significantly decreased NPY-induced feeding at 2 h, whereas administration of NLTX in the other hindbrain regions did not significantly influence PVN NPY induced feeding. These data suggest that opioid receptors in the medial NTS are most responsive to feeding signals originating in the PVN after NPY stimulation.

摘要

孤束核(NTS)中的纳曲酮(NLTX)可减少室旁核(PVN)中神经肽Y(NPY)诱导的进食。我们试图确定对NLTX阻断PVN中NPY诱导的进食最敏感的NTS区域。雄性Sprague-Dawley大鼠植入两根套管,一根置于PVN,另一根置于后脑区域:尾侧、内侧或 Rostral NTS 或 NTS 外 1 毫米处。在向PVN注射NPY(0.5微克,0.3微升)或人工脑脊液(0.3微升)之前,动物向后脑区域注射NLTX(0、1、3、10和30微克,溶于0.3微升)。注射后2小时测量食物摄入量。PVN NPY刺激进食,内侧NTS中的NLTX在2小时时显著减少NPY诱导的进食,而在其他后脑区域注射NLTX对PVN NPY诱导的进食没有显著影响。这些数据表明,内侧NTS中的阿片受体对NPY刺激后源自PVN的进食信号反应最为敏感。

相似文献

1
Regional effect of naltrexone in the nucleus of the solitary tract in blockade of NPY-induced feeding.纳曲酮在孤束核中对神经肽Y诱导进食的阻断作用的区域效应
Am J Physiol Regul Integr Comp Physiol. 2000 Feb;278(2):R499-503. doi: 10.1152/ajpregu.2000.278.2.R499.
2
Evidence for a feeding related association between melanocortin in the NTS and Neuropeptide-Y in the PVN.证据表明,NTS 中的黑皮质素和 PVN 中的神经肽 Y 之间存在与进食相关的关联。
Appetite. 2023 Sep 1;188:106618. doi: 10.1016/j.appet.2023.106618. Epub 2023 May 29.
3
Divergence of the feeding and thermogenic pathways influenced by NPY in the hypothalamic PVN of the rat.大鼠下丘脑室旁核中受神经肽Y影响的进食和产热途径的分歧。
Am J Physiol. 1998 Aug;275(2):R471-7. doi: 10.1152/ajpregu.1998.275.2.R471.
4
Effects of the opioid antagonist naltrexone on feeding induced by DAMGO in the central nucleus of the amygdala and in the paraventricular nucleus in the rat.阿片类拮抗剂纳曲酮对大鼠杏仁核中央核和室旁核中由DAMGO诱导的进食的影响。
Brain Res. 1998 Jan 26;782(1-2):18-23. doi: 10.1016/s0006-8993(97)01140-2.
5
Interaction of the hypothalamic paraventricular nucleus and central nucleus of the amygdala in naloxone blockade of neuropeptide Y-induced feeding revealed by c-fos expression.通过c-fos表达揭示下丘脑室旁核与杏仁核中央核在纳洛酮阻断神经肽Y诱导进食中的相互作用。
J Neurosci. 1997 Jul 1;17(13):5175-82. doi: 10.1523/JNEUROSCI.17-13-05175.1997.
6
Naltrexone induces arcuate nucleus neuropeptide Y gene expression in the rat.纳曲酮可诱导大鼠弓状核神经肽Y基因表达。
Am J Physiol. 1996 Jul;271(1 Pt 2):R289-94. doi: 10.1152/ajpregu.1996.271.1.R289.
7
Galanin injection into the nucleus of the solitary tract stimulates feeding in rats with lesions of the paraventricular nucleus of the hypothalamus.向孤束核注射甘丙肽可刺激下丘脑室旁核损伤大鼠的进食行为。
Physiol Behav. 1998 Feb 15;63(4):521-7. doi: 10.1016/s0031-9384(97)00480-0.
8
The effect of norbinaltorphimine, beta-funaltrexamine and naltrindole on NPY-induced feeding.
Brain Res. 1993 Dec 24;631(2):325-8. doi: 10.1016/0006-8993(93)91552-4.
9
Feeding association between the nucleus of the solitary tract and the ventral tegmental area.孤束核与腹侧被盖区之间的摄食关联。
Appetite. 2009 Dec;53(3):457-60. doi: 10.1016/j.appet.2009.09.003. Epub 2009 Sep 11.
10
Opioid receptor blockade in rat nucleus tractus solitarius alters amygdala dynorphin gene expression.大鼠孤束核中的阿片受体阻断会改变杏仁核强啡肽基因的表达。
Am J Physiol Regul Integr Comp Physiol. 2002 Jul;283(1):R161-7. doi: 10.1152/ajpregu.00480.2001.

引用本文的文献

1
Regulation of body weight and food intake by AGRP neurons during opioid dependence and abstinence in mice.阿黑皮素原神经元在小鼠阿片类药物依赖和戒断期间对体重和摄食的调节。
Front Neural Circuits. 2022 Aug 30;16:977642. doi: 10.3389/fncir.2022.977642. eCollection 2022.
2
Promotion of Wakefulness and Energy Expenditure by Orexin-A in the Ventrolateral Preoptic Area.外侧视前区中食欲素A对觉醒和能量消耗的促进作用。
Sleep. 2015 Sep 1;38(9):1361-70. doi: 10.5665/sleep.4970.
3
Opioids inhibit visceral afferent activation of catecholamine neurons in the solitary tract nucleus.
阿片类药物抑制孤束核内脏传入激活儿茶酚胺神经元。
Neuroscience. 2012 Oct 11;222:181-90. doi: 10.1016/j.neuroscience.2012.07.010. Epub 2012 Jul 13.
4
Neuropeptides controlling energy balance: orexins and neuromedins.控制能量平衡的神经肽:食欲素和神经介素
Handb Exp Pharmacol. 2012(209):77-109. doi: 10.1007/978-3-642-24716-3_4.
5
μ-Opioid modulation in the rostral solitary nucleus and reticular formation alters taste reactivity: evidence for a suppressive effect on consummatory behavior.孤束核和网状结构中的 μ-阿片受体调制改变味觉反应:对摄食行为有抑制作用的证据。
Am J Physiol Regul Integr Comp Physiol. 2011 Sep;301(3):R690-700. doi: 10.1152/ajpregu.00142.2011. Epub 2011 Jun 22.
6
Opioidergic consequences of dietary-induced binge eating.饮食诱导暴食的阿片能后果。
Physiol Behav. 2011 Jul 25;104(1):98-104. doi: 10.1016/j.physbeh.2011.04.032. Epub 2011 Apr 28.
7
Leptin and the systems neuroscience of meal size control.瘦素与进食量控制的系统神经科学。
Front Neuroendocrinol. 2010 Jan;31(1):61-78. doi: 10.1016/j.yfrne.2009.10.005. Epub 2009 Oct 28.
8
Pharmacology of morphine in obese patients: clinical implications.肥胖患者中吗啡的药理学:临床意义
Clin Pharmacokinet. 2009;48(10):635-51. doi: 10.2165/11317150-000000000-00000.
9
Amygdalar opioids modulate hypothalamic melanocortin-induced anorexia.杏仁核阿片类物质调节下丘脑促黑素诱导的厌食症。
Physiol Behav. 2009 Mar 23;96(4-5):568-73. doi: 10.1016/j.physbeh.2008.12.007. Epub 2008 Dec 24.
10
Activation of delta-opioid receptors reduces excitatory input to putative gustatory cells within the nucleus of the solitary tract.δ-阿片受体的激活减少了孤束核内假定味觉细胞的兴奋性输入。
J Neurophysiol. 2009 Jan;101(1):258-68. doi: 10.1152/jn.90648.2008. Epub 2008 Nov 19.