• 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

Insulin and the paraventricular hypothalamus: modulation of energy balance.

作者信息

Menéndez J A, Atrens D M

机构信息

Department of Psychology, University of Sydney, NSW, Australia.

出版信息

Brain Res. 1991 Aug 2;555(2):193-201. doi: 10.1016/0006-8993(91)90342-s.

DOI:10.1016/0006-8993(91)90342-s
PMID:1933333
Abstract

The effects of insulin injections (0.1, 1, 10 and 40 mU) into the paraventricular hypothalamus (PVN) were investigated in an open-circuit calorimeter. Wistar rats were tested, with no food available during the tests. The 0.1 and 1 mU doses had no effects on either respiratory quotient or energy expenditure. The 10 mU dose increased respiratory quotient which indicates increased dependency on carbohydrates as an energy substrate. The same dose had no effects on thermogenesis. In contrast, the 40 mU dose decreased respiratory quotient which indicates increased dependency on fats as an energy substrate. The higher dose also increased thermogenesis. Since neither dose significantly affected locomotor activity, the metabolic data are not confounded with activity effects. These data indicate that insulin in the PVN produces a primary modulation of the metabolic parameters central to maintaining energy balance. In separate experiments, the 4 doses of insulin reduced food intake and body weight over a 24 h period. They also produced a dose-related increase in blood glucose concentration over a one hour period. Taken together, these findings are interpreted in a model in which insulin in the PVN acts as a signal indicating increased body fat. This increases thermogenesis, fat utilization and glycemic levels, and inhibits feeding. The net effect of this integrated metabolic-behavioural response is a regulatory reduction in body fat.

摘要

相似文献

1
Insulin and the paraventricular hypothalamus: modulation of energy balance.
Brain Res. 1991 Aug 2;555(2):193-201. doi: 10.1016/0006-8993(91)90342-s.
2
Somatostatin and the paraventricular hypothalamus: modulation of energy balance.生长抑素与下丘脑室旁核:对能量平衡的调节
Brain Res. 1993 Dec 10;630(1-2):238-44. doi: 10.1016/0006-8993(93)90662-7.
3
Glucagon and the paraventricular hypothalamus: modulation of energy balance.胰高血糖素与下丘脑室旁核:能量平衡的调节
Brain Res. 1993 Dec 10;630(1-2):245-51. doi: 10.1016/0006-8993(93)90663-8.
4
Metabolic modulation by amino acid stimulation of the paraventricular nucleus of the hypothalamus.下丘脑室旁核氨基酸刺激引起的代谢调节
Pharmacol Biochem Behav. 1993 Nov;46(3):617-22. doi: 10.1016/0091-3057(93)90552-5.
5
Metabolic effects of galanin injections into the paraventricular nucleus of the hypothalamus.向下丘脑室旁核注射甘丙肽的代谢效应。
Peptides. 1992 Mar-Apr;13(2):323-7. doi: 10.1016/0196-9781(92)90116-k.
6
Metabolic effects of neuropeptide Y injections into the paraventricular nucleus of the hypothalamus.向下丘脑室旁核注射神经肽Y的代谢效应。
Brain Res. 1990 May 14;516(1):8-14. doi: 10.1016/0006-8993(90)90890-n.
7
Effects of norepinephrine infused in the paraventricular hypothalamus on energy expenditure in the rat.下丘脑室旁核注入去甲肾上腺素对大鼠能量消耗的影响。
Brain Res. 1989 May 15;487(1):79-88. doi: 10.1016/0006-8993(89)90942-6.
8
Central effects of insulin detemir on feeding, body weight, and metabolism in rats.地特胰岛素对大鼠摄食、体重及代谢的中枢作用
Am J Physiol Endocrinol Metab. 2017 Nov 1;313(5):E613-E621. doi: 10.1152/ajpendo.00111.2016. Epub 2017 Jul 18.
9
Insulin increases energy expenditure and respiratory quotient in the rat.胰岛素可增加大鼠的能量消耗和呼吸商。
Pharmacol Biochem Behav. 1989 Dec;34(4):765-8. doi: 10.1016/0091-3057(89)90272-4.
10
Brain-derived neurotrophic factor in the hypothalamic paraventricular nucleus increases energy expenditure by elevating metabolic rate.下丘脑室旁核中的脑源性神经营养因子通过提高代谢率来增加能量消耗。
Am J Physiol Regul Integr Comp Physiol. 2007 Sep;293(3):R992-1002. doi: 10.1152/ajpregu.00516.2006. Epub 2007 Jun 13.

引用本文的文献

1
Insulin activates parasympathetic hepatic-related neurons of the paraventricular nucleus of the hypothalamus through mTOR signaling.胰岛素通过mTOR信号传导激活下丘脑室旁核中与肝脏相关的副交感神经元。
J Neurophysiol. 2025 Jan 1;133(1):320-332. doi: 10.1152/jn.00284.2024. Epub 2024 Dec 12.
2
Dual Regulation Mechanism of Obesity: DNA Methylation and Intestinal Flora.肥胖的双重调节机制:DNA甲基化与肠道菌群
Biomedicines. 2024 Jul 23;12(8):1633. doi: 10.3390/biomedicines12081633.
3
Intra-NAc insulin reduces the motivation for food and food intake without altering cue-triggered food-seeking.
内囊啡肽胰岛素可降低食物动机和食物摄入量,而不改变线索引发的觅食行为。
Physiol Behav. 2022 Oct 1;254:113892. doi: 10.1016/j.physbeh.2022.113892. Epub 2022 Jun 24.
4
Novel Noninvasive Approaches to the Treatment of Obesity: From Pharmacotherapy to Gene Therapy.新型非侵入性肥胖治疗方法:从药物治疗到基因治疗。
Endocr Rev. 2022 May 12;43(3):507-557. doi: 10.1210/endrev/bnab034.
5
Adiponectin is required for maintaining normal body temperature in a cold environment.脂联素是在寒冷环境中维持正常体温所必需的。
BMC Physiol. 2017 Oct 23;17(1):8. doi: 10.1186/s12899-017-0034-7.
6
Obesity: Current and potential pharmacotherapeutics and targets.肥胖症:当前及潜在的药物治疗方法与靶点
Pharmacol Ther. 2017 Feb;170:116-147. doi: 10.1016/j.pharmthera.2016.10.015. Epub 2016 Oct 20.
7
Hypothalamic control of brown adipose tissue thermogenesis.下丘脑对棕色脂肪组织产热的控制。
Front Syst Neurosci. 2015 Nov 3;9:150. doi: 10.3389/fnsys.2015.00150. eCollection 2015.
8
Distinct networks of leptin- and insulin-sensing neurons regulate thermogenic responses to nutritional and cold challenges.瘦素和胰岛素感知神经元的不同网络调节对营养和寒冷刺激的产热反应。
Diabetes. 2015 Jan;64(1):137-46. doi: 10.2337/db14-0567. Epub 2014 Aug 14.
9
Insulin and glucagon signaling in the central nervous system.中枢神经系统中的胰岛素和胰高血糖素信号转导。
Rev Endocr Metab Disord. 2013 Dec;14(4):365-75. doi: 10.1007/s11154-013-9258-4.
10
Molecules affecting hypothalamic control of core body temperature in response to calorie intake.影响摄入热量时下丘脑对核心体温控制的分子。
Front Genet. 2012 Oct 5;3:184. doi: 10.3389/fgene.2012.00184. eCollection 2012.