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本文引用的文献

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Pharmacologically targeting the P2rx4 gene on maintenance and reinstatement of alcohol self-administration in rats.药理学靶向 P2rx4 基因对大鼠酒精自我给药的维持和复吸的影响。
Pharmacol Biochem Behav. 2011 Jun;98(4):533-8. doi: 10.1016/j.pbb.2011.02.026. Epub 2011 Mar 21.
2
The effects of pre-pubertal gonadectomy and binge-like ethanol exposure during adolescence on ethanol drinking in adult male and female rats.青春期前性腺切除术和青春期 binge 样乙醇暴露对成年雄性和雌性大鼠乙醇饮用量的影响。
Behav Brain Res. 2011 Jan 20;216(2):569-75. doi: 10.1016/j.bbr.2010.08.048. Epub 2010 Sep 15.
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Effective prevention against risky underage drinking--the need for higher excise taxes on alcoholic beverages in Germany.有效预防危险的未成年人饮酒——德国需要提高酒精饮料的消费税。
Alcohol Alcohol. 2010 Jul-Aug;45(4):387-94. doi: 10.1093/alcalc/agq031. Epub 2010 Jun 16.
4
The effectiveness of brief interventions in the clinical setting in reducing alcohol misuse and binge drinking in adolescents: a critical review of the literature.临床环境中简短干预对减少青少年酒精滥用和狂饮的效果:文献综述。
J Clin Nurs. 2010 Mar;19(5-6):605-20. doi: 10.1111/j.1365-2702.2009.03060.x.
5
Ethanol consumption: how should we measure it? Achieving consilience between human and animal phenotypes.乙醇摄入:我们应该如何测量它?在人类和动物表型之间实现一致。
Addict Biol. 2010 Apr;15(2):109-24. doi: 10.1111/j.1369-1600.2009.00192.x.
6
Ontogeny of ethanol-induced motor impairment following acute ethanol: assessment via the negative geotaxis reflex in adolescent and adult rats.急性乙醇暴露后乙醇诱导运动障碍的个体发育:通过青少年和成年大鼠的负趋地性反射进行评估。
Pharmacol Biochem Behav. 2010 Apr;95(2):242-8. doi: 10.1016/j.pbb.2010.01.013. Epub 2010 Feb 4.
7
Changes in gene expression in regions of the extended amygdala of alcohol-preferring rats after binge-like alcohol drinking.酒精偏好大鼠 binge 样饮酒后延伸杏仁核区域基因表达的变化。
Alcohol. 2010 Mar;44(2):171-83. doi: 10.1016/j.alcohol.2009.12.001. Epub 2010 Jan 29.
8
Adolescent C57BL/6J (but not DBA/2J) mice consume greater amounts of limited-access ethanol compared to adults and display continued elevated ethanol intake into adulthood.青春期的 C57BL/6J(而非 DBA/2J)小鼠与成年鼠相比,消耗更多限量摄入的乙醇,并在成年期持续摄入更多乙醇。
Alcohol Clin Exp Res. 2010 Apr;34(4):734-42. doi: 10.1111/j.1530-0277.2009.01143.x. Epub 2010 Jan 26.
9
Causal links between binge drinking patterns, unsafe sex and HIV in South Africa: its time to intervene.南非酗酒模式、不安全性行为与艾滋病病毒之间的因果联系:是时候进行干预了。
Int J STD AIDS. 2010 Jan;21(1):2-7. doi: 10.1258/ijsa.2000.009432.
10
"Binge" drinking experience in adolescent mice shows sex differences and elevated ethanol intake in adulthood.青春期小鼠的“ binge ”饮酒经历表现出性别差异,并导致成年后乙醇摄入量增加。
Horm Behav. 2010 Jun;58(1):82-90. doi: 10.1016/j.yhbeh.2009.10.008. Epub 2009 Oct 23.

建立青少年和成年 P 大鼠 binge-like 乙醇饮用模型。

Modeling binge-like ethanol drinking by peri-adolescent and adult P rats.

机构信息

Department of Psychiatry, Institute of Psychiatric Research, Indiana University School of Medicine, Indianapolis, IN 46202-4887, USA.

出版信息

Pharmacol Biochem Behav. 2011 Nov;100(1):90-7. doi: 10.1016/j.pbb.2011.07.017. Epub 2011 Jul 29.

DOI:10.1016/j.pbb.2011.07.017
PMID:21824488
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3183250/
Abstract

Alcohol binge-drinking, especially among adolescents and young adults, is a serious public health concern. The present study examined ethanol binge-like drinking by peri-adolescent [postnatal days (PNDs 30-72)] and adult (PNDs 90-132) alcohol-preferring (P) rats with a drinking-in-the-dark-multiple-scheduled-access (DID-MSA) procedure used by our laboratory. Male and female P rats were provided concurrent access to 15% and 30% ethanol for three 1-h sessions across the dark cycle 5 days/week. For the 1st week, adolescent and adult female P rats consumed 3.4 and 1.6g/kg of ethanol, respectively, during the 1st hour of access, whereas for male rats the values were 3.5 and 1.1g/kg of ethanol, respectively. Adult intakes increased to ~2.0 g/kg/h and adolescent intakes decreased to ~2.5 g/kg/h across the 6 weeks of ethanol access. The daily ethanol intake of adult DID-MSA rats approximated or modestly exceeded that seen in continuous access (CA) rats or the selection criterion for P rats (≥5 g/kg/day). However, in general, the daily ethanol intake of DID-MSA peri-adolescent rats significantly exceeded that of their CA counterparts. BELs were assessed at 15-min intervals across the 3rd hour of access during the 4th week. Ethanol intake was 1.7 g/kg vs. 2.7 g/kg and BELs were 57 mg% vs. 100mg% at 15- and 60-min, respectively. Intoxication induced by DID-MSA in female P rats was assessed during the 1st vs. 4th week of ethanol access. Level of impairment did not differ between the 2 weeks (106 vs. 97 s latency to fall, 120 s criterion) and was significant (vs. naïve controls) only during the 4th week. Overall, these findings support the use of the DID-MSA procedure in rats, and underscore the presence of age- and sex-dependent effects mediating ethanol binge-like drinking in P rats.

摘要

酒精 binge 饮酒,尤其是在青少年和年轻人中,是一个严重的公共卫生问题。本研究通过我们实验室使用的暗时多相序进(DID-MSA)程序,检测了围青春期(出生后第 30-72 天)和成年(第 90-132 天)酒精偏好(P)大鼠的乙醇 binge 样饮酒。雄性和雌性 P 大鼠在暗周期内的 5 天/周内,同时提供 15%和 30%乙醇,进行 3 次 1 小时的访问。在第 1 周,青春期和成年雌性 P 大鼠在第 1 小时内分别摄入 3.4 和 1.6g/kg 的乙醇,而雄性大鼠的摄入量分别为 3.5 和 1.1g/kg 的乙醇。在 6 周的乙醇摄入期间,成年大鼠的摄入量增加到约 2.0g/kg/h,而青春期大鼠的摄入量减少到约 2.5g/kg/h。成年 DID-MSA 大鼠的每日乙醇摄入量接近或略高于连续摄入(CA)大鼠或 P 大鼠的选择标准(≥5g/kg/天)。然而,一般来说,DID-MSA 围青春期大鼠的每日乙醇摄入量明显高于 CA 对照大鼠。在第 4 周的第 3 小时访问期间,每隔 15 分钟评估 BEL。在 15 分钟和 60 分钟时,乙醇摄入量分别为 1.7g/kg 和 2.7g/kg,BEL 分别为 57mg%和 100mg%。在第 1 周和第 4 周的乙醇摄入期间评估 DID-MSA 在雌性 P 大鼠中引起的中毒。在这 2 周内,损伤程度没有差异(106 与 97 秒跌倒潜伏期,120 秒标准),仅在第 4 周时与未处理的对照相比具有显著性(106 与 97 秒跌倒潜伏期,120 秒标准)。总体而言,这些发现支持在大鼠中使用 DID-MSA 程序,并强调了年龄和性别依赖性效应在 P 大鼠乙醇 binge 样饮酒中的存在。