• 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

有限获取条件下P大鼠的乙醇和糖精摄入模式。

Patterns of ethanol and saccharin intake in P rats under limited-access conditions.

作者信息

Nowak K L, McKinzie D L, McBride W J, Murphy J M

机构信息

Department of Psychiatry, Institute of Psychiatric Research, Indiana University School of Medicine, Indianapolis, USA.

出版信息

Alcohol. 1999 Aug;19(1):85-96. doi: 10.1016/s0741-8329(99)00028-2.

DOI:10.1016/s0741-8329(99)00028-2
PMID:10487392
Abstract

Patterns of drinking and responding for ethanol (EtOH) and saccharin (SACC) were examined in the alcohol-preferring P rat using various limited-access paradigms. Adult female P rats (n = 10-20) were given 2-h access to EtOH (10-13% v/v) and SACC (0.0125% g/v) concurrently each day, or each solution individually on alternate days. Total 2-h SACC intake was significantly greater than EtOH under both concurrent (12+/-2 vs. 7+/-0.8 ml, p<0.05) and alternate-day access (18+/-1.6 vs. 10+/-0.5 ml) conditions. Under both conditions, however, EtOH intake (over 55% of the total) in the first 15 min was significantly greater than that of SACC (<25% of total). In an operant paradigm, total responding for EtOH (124+/-29) and SACC (114+/-7) under 2-h alternate-day conditions did not differ, but 65% of total EtOH responding occurred during the first 20 min versus less than 45% for SACC (p<0.05). Increasing response requirements (FR-1 to FR-5) did not significantly alter the total number of EtOH reinforcements, but decreased the total number of SACC reinforcements by approximately 50% (p<0.05). Increasing the EtOH concentration from 15% to 35% decreased the number of reinforcements approximately 50% but did not decrease the estimated g/kg EtOH intake. Increasing the SACC concentration from 0.0125% to 0.05%, however, nearly doubled the number of reinforcements. The greater preference for EtOH versus SACC during the initial part of the access period, together with the maintenance of EtOH intake in g/kg when the response requirements and the EtOH concentration were increased, suggests that EtOH intake is motivated by pharmacological consequences. Therefore, different motivational factors appear to underlie EtOH and SACC intake of the P rat. Furthermore, the pattern of EtOH intake and responding displayed by the P rat may be the result of a "bout-" or "binge-" like loss of control under restricted EtOH access conditions.

摘要

使用各种有限接触范式,在酒精偏好型P大鼠中研究了对乙醇(EtOH)和糖精(SACC)的饮用及反应模式。成年雌性P大鼠(n = 10 - 20)每天有2小时同时接触EtOH(10 - 13% v/v)和SACC(0.0125% g/v)的机会,或者隔天分别接触每种溶液。在同时接触(12±2对7±0.8毫升,p<0.05)和隔天接触(18±1.6对10±0.5毫升)条件下,2小时内SACC的总摄入量均显著高于EtOH。然而,在这两种条件下,最初15分钟内EtOH的摄入量(超过总量的55%)均显著高于SACC(<总量的25%)。在操作性范式中,在2小时隔天接触条件下,对EtOH(124±29)和SACC(114±7)的总反应量没有差异,但EtOH总反应量的65%发生在最初20分钟内,而SACC的这一比例不到45%(p<0.05)。增加反应要求(从FR - 1到FR - 5)并未显著改变EtOH强化的总数,但使SACC强化的总数减少了约50%(p<0.05)。将EtOH浓度从15%提高到35%,强化次数减少了约50%,但并未降低估计的g/kg EtOH摄入量。然而,将SACC浓度从0.0125%提高到0.05%,强化次数几乎增加了一倍。在接触期开始部分对EtOH的偏好高于SACC,以及当反应要求和EtOH浓度增加时g/kg EtOH摄入量的维持,表明EtOH摄入是由药理作用驱动的。因此,不同的动机因素似乎是P大鼠EtOH和SACC摄入的基础。此外,P大鼠表现出的EtOH摄入和反应模式可能是在有限EtOH接触条件下“发作性”或“暴饮性”失控的结果。

相似文献

1
Patterns of ethanol and saccharin intake in P rats under limited-access conditions.有限获取条件下P大鼠的乙醇和糖精摄入模式。
Alcohol. 1999 Aug;19(1):85-96. doi: 10.1016/s0741-8329(99)00028-2.
2
Involvement of dopamine D2 autoreceptors in the ventral tegmental area on alcohol and saccharin intake of the alcohol-preferring P rat.腹侧被盖区多巴胺D2自身受体对偏爱酒精的P大鼠酒精和糖精摄取的影响
Alcohol Clin Exp Res. 2000 Apr;24(4):476-83.
3
Effects of alcohol and saccharin deprivations on concurrent ethanol and saccharin operant self-administration by alcohol-preferring (P) rats.酒精和糖精剥夺对偏爱酒精(P)大鼠同时进行乙醇和糖精操作性自我给药的影响。
Alcohol. 2008 Jun;42(4):277-84. doi: 10.1016/j.alcohol.2008.01.011. Epub 2008 Apr 8.
4
Blocking GABA(A) receptors in the anterior ventral tegmental area attenuates ethanol intake of the alcohol-preferring P rat.阻断腹侧被盖区前部的GABA(A)受体可减少偏爱酒精的P大鼠的乙醇摄入量。
Psychopharmacology (Berl). 1998 Sep;139(1-2):108-16. doi: 10.1007/s002130050695.
5
The novel benzodiazepine inverse agonist RO19-4603 antagonizes ethanol motivated behaviors: neuropharmacological studies.新型苯二氮䓬反向激动剂RO19 - 4603拮抗乙醇诱导的行为:神经药理学研究。
Brain Res. 1998 Feb 16;784(1-2):256-75. doi: 10.1016/s0006-8993(97)01380-2.
6
The delta 2-opioid receptor antagonist naltriben reduces motivated responding for ethanol.δ2阿片受体拮抗剂纳曲苄可降低对乙醇的动机性反应。
Psychopharmacology (Berl). 1999 Nov;147(1):81-9. doi: 10.1007/s002130051145.
7
Central opioid receptors differentially regulate the nalmefene-induced suppression of ethanol- and saccharin-reinforced behaviors in alcohol-preferring (P) rats.中枢阿片受体对纳美芬诱导的酒精偏好(P)大鼠乙醇和糖精强化行为抑制的调节作用存在差异。
Neuropsychopharmacology. 2004 Feb;29(2):285-99. doi: 10.1038/sj.npp.1300338.
8
Impulsivity as a behavioral measure of withdrawal of orally delivered PCP and nondrug rewards in male and female monkeys.冲动作为雄性和雌性猴子停止口服 PCP 和非药物奖励的行为测量。
Psychopharmacology (Berl). 2009 Nov;207(1):85-98. doi: 10.1007/s00213-009-1636-y. Epub 2009 Aug 21.
9
Effects of the benzodiazepine inverse agonist RO19-4603 alone and in combination with the benzodiazepine receptor antagonists flumazenil, ZK 93426 and CGS 8216, on ethanol intake in alcohol-preferring (P) rats.苯二氮䓬反向激动剂RO19 - 4603单独使用以及与苯二氮䓬受体拮抗剂氟马西尼、ZK 93426和CGS 8216联合使用对嗜酒(P)大鼠乙醇摄入量的影响。
Brain Res. 1996 Sep 23;734(1-2):19-34.
10
High Alcohol-Preferring Mice Show Reaction to Loss of Ethanol Reward Following Repeated Binge Drinking.高酒精偏好小鼠在反复 binge 饮酒后对乙醇奖赏丧失的反应。
Alcohol Clin Exp Res. 2020 Sep;44(9):1717-1727. doi: 10.1111/acer.14419. Epub 2020 Aug 31.

引用本文的文献

1
Binge-Like, Naloxone-Sensitive, Voluntary Ethanol Intake at Adolescence Is Greater Than at Adulthood, but Does Not Exacerbate Subsequent Two-Bottle Choice Drinking.青春期类似暴饮暴食、对纳洛酮敏感的自愿乙醇摄入量高于成年期,但不会加剧随后的双瓶选择饮酒行为。
Front Behav Neurosci. 2020 Apr 9;14:50. doi: 10.3389/fnbeh.2020.00050. eCollection 2020.
2
The reinforcing properties of ethanol are quantitatively enhanced in adulthood by peri-adolescent ethanol, but not saccharin, consumption in female alcohol-preferring (P) rats.在成年期,围青春期摄入乙醇而非糖精,可使雌性嗜酒(P)大鼠体内乙醇的强化特性在数量上增强。
Alcohol. 2015 Aug;49(5):513-8. doi: 10.1016/j.alcohol.2015.04.007. Epub 2015 May 22.
3
Scheduled access alcohol drinking by alcohol-preferring (P) and high-alcohol-drinking (HAD) rats: modeling adolescent and adult binge-like drinking.
酒精偏好(P)和高酒精摄入(HAD)大鼠的定时饮酒:建模青少年和成年期 binge-like 样饮酒。
Alcohol. 2014 May;48(3):225-34. doi: 10.1016/j.alcohol.2013.10.004. Epub 2013 Oct 31.
4
The alcohol-preferring (P) and high-alcohol-drinking (HAD) rats--animal models of alcoholism.酒精偏爱(P)和高酒精摄入(HAD)大鼠——酒精中毒的动物模型。
Alcohol. 2014 May;48(3):209-15. doi: 10.1016/j.alcohol.2013.09.044. Epub 2013 Oct 30.
5
Environments predicting intermittent shortening access reduce operant performance but not home cage binge size in rats.环境预测间歇性缩短获取途径会降低操作性表现,但不会减少大鼠在自宅笼中的 binge 大小。
Physiol Behav. 2013 May 27;116-117:35-43. doi: 10.1016/j.physbeh.2013.03.015. Epub 2013 Mar 25.
6
Regulation of operant oral ethanol self-administration: a dose-response curve study in rats.操作性口服乙醇自我给药的调节:大鼠的剂量-反应曲线研究。
Alcohol Clin Exp Res. 2011 Jan;35(1):116-25. doi: 10.1111/j.1530-0277.2010.01328.x. Epub 2010 Oct 6.
7
Clozapine chronically suppresses alcohol drinking in Syrian golden hamsters.氯氮平慢性抑制叙利亚金黄地鼠的饮酒行为。
Neuropharmacology. 2010 Feb;58(2):351-6. doi: 10.1016/j.neuropharm.2009.10.006. Epub 2009 Nov 4.
8
Effects of alcohol and saccharin deprivations on concurrent ethanol and saccharin operant self-administration by alcohol-preferring (P) rats.酒精和糖精剥夺对偏爱酒精(P)大鼠同时进行乙醇和糖精操作性自我给药的影响。
Alcohol. 2008 Jun;42(4):277-84. doi: 10.1016/j.alcohol.2008.01.011. Epub 2008 Apr 8.