• 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

Chronic cholestasis in rats induces anhedonia and a loss of social interest.

作者信息

Swain M G, Le T

机构信息

Gastroenterology Research Group, Health Sciences Center, University of Calgary, Alberta, Canada.

出版信息

Hepatology. 1998 Jul;28(1):6-10. doi: 10.1002/hep.510280102.

DOI:10.1002/hep.510280102
PMID:9657089
Abstract

Central fatigue commonly occurs in patients with primary biliary cirrhosis (PBC) and correlates closely with depression, and cholestatic rats exhibit central fatigue. Therefore, we undertook a series of experiments in both rats with cholestasis caused by bile duct resection (BDR) and sham-resected controls (15 days after surgery) to determine if experimental cholestasis is associated with symptoms of depression that can be modeled in rats, namely anhedonia (loss of pleasure) and the loss of social interest. BDR rats exhibited significant anhedonia compared with sham controls as indicated by a loss in their preference for consuming a saccharin solution, a highly desirable drink for rats. Furthermore, social interest was examined by determining the time BDR or sham rats spent investigating a juvenile rat in an open-field apparatus compared with the time spent on nonsocial behaviors. BDR rats exhibited significantly reduced time spent in social investigation and significantly more time in nonsocial behaviors than did sham rats. Major depression in humans is often associated with elevated circulating glucocorticoid levels and impaired glucocorticoid feedback. Therefore, we measured these parameters in BDR and sham rats and found a striking elevation in circulating glucocorticoid levels in BDR compared with sham animals. However, elevated circulating glucocorticoid levels in BDR rats suppressed normally in response to exogenous dexamethasone, indicating intact glucocorticoid feedback control at the pituitary level in BDR rats. In summary, we have identified behaviors in cholestatic rats that are consistent with those seen in depression.

摘要

相似文献

1
Chronic cholestasis in rats induces anhedonia and a loss of social interest.
Hepatology. 1998 Jul;28(1):6-10. doi: 10.1002/hep.510280102.
2
Defective corticotropin-releasing hormone mediated neuroendocrine and behavioral responses in cholestatic rats: implications for cholestatic liver disease-related sickness behaviors.
Hepatology. 1995 Nov;22(5):1560-4.
3
Downregulated hypothalamic 5-HT3 receptor expression and enhanced 5-HT3 receptor antagonist-mediated improvement in fatigue-like behaviour in cholestatic rats.
Neurogastroenterol Motil. 2008 Mar;20(3):228-35. doi: 10.1111/j.1365-2982.2007.01016.x. Epub 2007 Sep 27.
4
5-hydroxytryptamine release in the anterior hypothalamic and the hippocampal areas of cholestatic rats.胆汁淤积性大鼠下丘脑前部和海马区5-羟色胺的释放
Life Sci. 2006 Feb 2;78(10):1078-83. doi: 10.1016/j.lfs.2005.06.025. Epub 2005 Sep 26.
5
Augmented interleukin-1beta-induced depression of locomotor activity in cholestatic rats.胆汁淤积大鼠中白细胞介素-1β增强诱导的运动活动抑制
Hepatology. 1998 Dec;28(6):1561-5. doi: 10.1002/hep.510280616.
6
Prevention of immune-mediated arthritis in cholestatic rats: involvement of endogenous glucocorticoids.
Gastroenterology. 1994 Nov;107(5):1469-74. doi: 10.1016/0016-5085(94)90551-7.
7
Differential leptin responses to acute and chronic biliary obstruction in rats.大鼠对急性和慢性胆道梗阻的瘦素反应差异
J Hepatol. 2000 Jul;33(1):19-25. doi: 10.1016/s0168-8278(00)80154-3.
8
Fatigue of cholestasis and the serotoninergic neurotransmitter system in the rat.大鼠胆汁淤积的疲劳与血清素能神经递质系统
Hepatology. 2005 Apr;41(4):731-7. doi: 10.1002/hep.20617.
9
Chronic glucocorticoid deficiency-induced abnormal aggression, autonomic hypoarousal, and social deficit in rats.慢性糖皮质激素缺乏诱导大鼠出现异常攻击行为、自主神经低唤醒及社交缺陷。
J Neuroendocrinol. 2004 Jun;16(6):550-7. doi: 10.1111/j.1365-2826.2004.01201.x.
10
Endogenous glucocorticoids inhibit neutrophil recruitment to inflammatory sites in cholestatic rats.
Am J Physiol. 1996 May;270(5 Pt 1):G821-5. doi: 10.1152/ajpgi.1996.270.5.G821.

引用本文的文献

1
Inflammation is increased with anxiety- and depression-like signs in a rat model of spinal cord injury.在脊髓损伤大鼠模型中,炎症反应随着焦虑样和抑郁样症状而增加。
Brain Behav Immun. 2016 Jan;51:176-195. doi: 10.1016/j.bbi.2015.08.009. Epub 2015 Aug 18.
2
Assessment of depression in a rodent model of spinal cord injury.脊髓损伤啮齿动物模型中抑郁的评估。
J Neurotrauma. 2014 Jun 15;31(12):1107-21. doi: 10.1089/neu.2013.3204. Epub 2014 May 8.
3
Fatigue in primary biliary cirrhosis.原发性胆汁性肝硬化的疲劳。
Nat Rev Gastroenterol Hepatol. 2010 Jun;7(6):313-9. doi: 10.1038/nrgastro.2010.62. Epub 2010 May 11.
4
Fatigue and autonomic dysfunction in non-alcoholic fatty liver disease.非酒精性脂肪性肝病中的疲劳和自主神经功能障碍。
Clin Auton Res. 2009 Dec;19(6):319-26. doi: 10.1007/s10286-009-0031-4.
5
Cerebral microglia recruit monocytes into the brain in response to tumor necrosis factoralpha signaling during peripheral organ inflammation.在外周器官炎症期间,脑小胶质细胞会响应肿瘤坏死因子α信号,将单核细胞招募到大脑中。
J Neurosci. 2009 Feb 18;29(7):2089-102. doi: 10.1523/JNEUROSCI.3567-08.2009.
6
Fluoxetine for the treatment of fatigue in primary biliary cirrhosis: a randomized, double-blind controlled trial.
Dig Dis Sci. 2006 Nov;51(11):1985-91. doi: 10.1007/s10620-006-9397-5. Epub 2006 Oct 20.
7
Four year follow up of fatigue in a geographically defined primary biliary cirrhosis patient cohort.对某一地理区域界定的原发性胆汁性肝硬化患者队列疲劳情况的四年随访
Gut. 2006 Apr;55(4):536-41. doi: 10.1136/gut.2005.080317. Epub 2005 Nov 18.
8
Liver Transplantation for Cholestatic Liver Disease.胆汁淤积性肝病的肝移植
Curr Treat Options Gastroenterol. 2003 Apr;6(2):113-121. doi: 10.1007/s11938-003-0012-y.
9
Primary biliary cirrhosis: new perspectives in diagnosis and treatment.原发性胆汁性肝硬化:诊断与治疗的新视角
Postgrad Med J. 2000 Apr;76(894):199-206. doi: 10.1136/pmj.76.894.199.