Inflammatory pain affects alcohol intake in a dose-dependent manner in male rats in the intermittent access model.

IF 3.4 Q2 NEUROSCIENCES Pain Reports Pub Date : 2023-06-27 eCollection Date: 2023-07-01 DOI:10.1097/PR9.0000000000001082
Yolanda Campos-Jurado, Jose A Morón
{"title":"Inflammatory pain affects alcohol intake in a dose-dependent manner in male rats in the intermittent access model.","authors":"Yolanda Campos-Jurado, Jose A Morón","doi":"10.1097/PR9.0000000000001082","DOIUrl":null,"url":null,"abstract":"<p><strong>Introduction: </strong>Epidemiological studies have shown that there is a relation between pain and alcohol use disorder (AUD). Persistent pain is directly correlated with an increment in alcohol consumption and an increased risk of developing an AUD. Greater levels of pain intensity and unpleasantness are associated with higher levels of relapse, an increase in alcohol consumption, rates of hazardous drinking, and delay to seek for treatment. However, this interaction has not been deeply studied in the preclinical setting.</p><p><strong>Methods: </strong>Here, we aim to evaluate how inflammatory pain affects levels of alcohol drinking in male and female rats with a history of alcohol. For that, we used an intermittent access 2-bottle choice paradigm combined with the complete Freund Adjuvant (CFA) model of inflammatory pain.</p><p><strong>Results: </strong>Our results show that CFA-induced inflammatory pain does not alter total intake of 20% alcohol in male or female rats. Interestingly, in males, the presence of CFA-induced inflammatory pain blunts the decrease of alcohol intake when higher concentrations of alcohol are available, whereas it does not have an effect on intake at any concentration in female rats.</p><p><strong>Conclusion: </strong>Altogether, this study provides relevant data and constitutes an important contribution to the study of pain and AUD and it highlights the necessity to design better behavioral paradigms in animal models that are more translational and reflect current epidemiological findings.</p>","PeriodicalId":52189,"journal":{"name":"Pain Reports","volume":"8 4","pages":"e1082"},"PeriodicalIF":3.4000,"publicationDate":"2023-06-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/98/82/painreports-8-e1082.PMC10306431.pdf","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Pain Reports","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1097/PR9.0000000000001082","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2023/7/1 0:00:00","PubModel":"eCollection","JCR":"Q2","JCRName":"NEUROSCIENCES","Score":null,"Total":0}
引用次数: 0

Abstract

Introduction: Epidemiological studies have shown that there is a relation between pain and alcohol use disorder (AUD). Persistent pain is directly correlated with an increment in alcohol consumption and an increased risk of developing an AUD. Greater levels of pain intensity and unpleasantness are associated with higher levels of relapse, an increase in alcohol consumption, rates of hazardous drinking, and delay to seek for treatment. However, this interaction has not been deeply studied in the preclinical setting.

Methods: Here, we aim to evaluate how inflammatory pain affects levels of alcohol drinking in male and female rats with a history of alcohol. For that, we used an intermittent access 2-bottle choice paradigm combined with the complete Freund Adjuvant (CFA) model of inflammatory pain.

Results: Our results show that CFA-induced inflammatory pain does not alter total intake of 20% alcohol in male or female rats. Interestingly, in males, the presence of CFA-induced inflammatory pain blunts the decrease of alcohol intake when higher concentrations of alcohol are available, whereas it does not have an effect on intake at any concentration in female rats.

Conclusion: Altogether, this study provides relevant data and constitutes an important contribution to the study of pain and AUD and it highlights the necessity to design better behavioral paradigms in animal models that are more translational and reflect current epidemiological findings.

Abstract Image

Abstract Image

Abstract Image

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
在间歇性接触模型中,炎性疼痛会以剂量依赖的方式影响雄性大鼠的酒精摄入量。
简介流行病学研究表明,疼痛与饮酒障碍(AUD)之间存在一定关系。持续性疼痛与饮酒量增加和罹患 AUD 的风险增加直接相关。疼痛强度和难受程度越大,复发率越高,饮酒量越大,危险饮酒率越高,寻求治疗的时间越晚。方法:在此,我们旨在评估炎性疼痛如何影响有酗酒史的雄性和雌性大鼠的饮酒水平。为此,我们采用了间歇性两瓶选择范式,并结合完全弗罗因德佐剂(CFA)炎性疼痛模型:结果:我们的研究结果表明,CFA 引起的炎症性疼痛不会改变雄性或雌性大鼠对 20% 酒精的总摄入量。有趣的是,对于雄性大鼠,当酒精浓度较高时,CFA 引起的炎性疼痛会减弱酒精摄入量的减少,而对于雌性大鼠,任何浓度的酒精都不会影响其摄入量:总之,这项研究提供了相关数据,是对疼痛和 AUD 研究的重要贡献,它强调了在动物模型中设计更好的行为范例的必要性,这些范例更具转化性并反映了当前的流行病学发现。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Pain Reports
Pain Reports Medicine-Anesthesiology and Pain Medicine
CiteScore
7.50
自引率
2.10%
发文量
93
审稿时长
8 weeks
期刊最新文献
Preexisting chronic pain is not associated with moderate-to-severe acute pain after laparoscopic cholecystectomy: a prospective cohort study. Why might fears and worries persist after a pain education-grounded multimodal intervention for chronic back pain? A qualitative study. Pain and small fiber pathology in men with fibromyalgia syndrome. Upregulated spinal histone deacetylases induce nociceptive sensitization by inhibiting the GABA system in chronic constriction injury-induced neuropathy in rats. Integrated manual therapies: IASP taskforce viewpoint.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1