• 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

衰老与乙醇代谢

Aging and ethanol metabolism.

作者信息

Vestal R E, McGuire E A, Tobin J D, Andres R, Norris A H, Mezey E

出版信息

Clin Pharmacol Ther. 1977 Mar;21(3):343-54. doi: 10.1002/cpt1977213343.

DOI:10.1002/cpt1977213343
PMID:837653
Abstract

The effect of aging on the distribution and elimination of ethanol was studied in a group of 50 healthy subjects ranging in age from 21 to 81 yr (mean, 53.3). Ethanol was administered in a continuous 1-hr infusion at a mean rate of 375 mg/m2 body surface area/min (equivalent to a mean dose of 0.57 gm/kg body weight). Serial blood samples for the determination of ethanol concentration was obtained at 15- to 30-min intervals for up to 4 hr post infusion. Ethanol elimination and distribution were evaluated with the aid of a two-compartment model. Rates of ethanol elimination were not affected by age. Peak ethanol concentration in blood water at the end of the infusion period was correlated with age (r= 0.55, p less than 0.001). Lean body mass and total volume of distirbution fo the ethanol were negatively correlated with age. The smaller volume of distirbution, in association with the decreased lean body mass, most likely explains the higher peak ethanol concentration found in the blood after administration of an ethanol does on the basis of surface area in the old as compared with the young subjects. This study demonstrates that age-related changes in body composition are important factors in the study of ethanol metabolism and its pharmacologic effects.

摘要

在一组年龄从21岁至81岁(平均53.3岁)的50名健康受试者中,研究了衰老对乙醇分布和消除的影响。乙醇以平均速率375毫克/平方米体表面积/分钟(相当于平均剂量0.57克/千克体重)进行连续1小时输注。在输注后长达4小时内,每隔15至30分钟采集系列血样以测定乙醇浓度。借助二室模型评估乙醇的消除和分布。乙醇消除速率不受年龄影响。输注期结束时血水中乙醇的峰值浓度与年龄相关(r = 0.55,p < 0.001)。瘦体重和乙醇分布总体积与年龄呈负相关。与年轻受试者相比,老年受试者分布体积较小,加上瘦体重减少,很可能解释了按体表面积给予乙醇剂量后血液中较高的乙醇峰值浓度。本研究表明,身体组成的年龄相关变化是乙醇代谢及其药理作用研究中的重要因素。

相似文献

1
Aging and ethanol metabolism.衰老与乙醇代谢
Clin Pharmacol Ther. 1977 Mar;21(3):343-54. doi: 10.1002/cpt1977213343.
2
Blood ethanol concentrations during and following constant-rate intravenous infusion of alcohol.酒精恒速静脉输注期间及之后的血液乙醇浓度
Clin Pharmacol Ther. 1976 Feb;19(2):213-23. doi: 10.1002/cpt1976192213.
3
Interindividual variations in the disposition and metabolism of ethanol in healthy men.健康男性乙醇处置和代谢的个体间差异。
Alcohol. 1984 Sep-Oct;1(5):385-91. doi: 10.1016/0741-8329(84)90008-9.
4
Ethanol elimination in males and females: relationship to menstrual cycle and body composition.男性和女性的乙醇消除:与月经周期和身体组成的关系。
Hepatology. 1983 Sep-Oct;3(5):701-6. doi: 10.1002/hep.1840030513.
5
Nonlinear pharmacokinetics of ethanol: the disproportionate AUC-dose relationship.
Alcohol Clin Exp Res. 1980 Oct;4(4):384-90. doi: 10.1111/j.1530-0277.1980.tb04836.x.
6
[Pharmacokinetics of alcohol after 3-hour intravenous infusion with and without cimetidine in 10 healthy non-alcoholic subjects].[10名健康非酒精依赖受试者在静脉输注3小时酒精时联用与未联用西咪替丁后的酒精药代动力学]
Gastroenterol Clin Biol. 1984 Feb;8(2):103-8.
7
The effect of hypermetabolism induced by burn trauma on the ethanol-oxidizing capacity of the liver.烧伤创伤诱导的高代谢对肝脏乙醇氧化能力的影响。
Crit Care Med. 1999 Dec;27(12):2622-5. doi: 10.1097/00003246-199912000-00003.
8
Hepatic and extrahepatic elimination of ethanol in cirrhosis. With estimates of intrahepatic shunts and Km for ethanol elimination.肝硬化患者乙醇的肝内和肝外消除。伴有肝内分流及乙醇消除米氏常数的估计值。
Scand J Gastroenterol. 1980;15(3):297-304. doi: 10.3109/00365528009181473.
9
Metabolic effects and pharmacokinetics of a growth hormone pulse in healthy adults: relation to age, sex, and body composition.健康成年人中生长激素脉冲的代谢效应和药代动力学:与年龄、性别和身体成分的关系。
J Clin Endocrinol Metab. 1997 Nov;82(11):3612-8. doi: 10.1210/jcem.82.11.4388.
10
Comparison of ethanol metabolism in male and female cynomolgus macaques (Macaca fascicularis).雄性和雌性食蟹猴(猕猴)乙醇代谢的比较。
Alcohol Clin Exp Res. 1999 Apr;23(4):611-6.

引用本文的文献

1
Adolescent Alcohol and the Spectrum of Cognitive Dysfunction in Aging.青少年饮酒与衰老过程中的认知功能障碍谱系
Adv Exp Med Biol. 2025;1473:257-298. doi: 10.1007/978-3-031-81908-7_12.
2
Experimental Evidence on Age-related Differential Outcomes Associated With Substance Abuse.与药物滥用相关的年龄差异结果的实验证据。
Basic Clin Neurosci. 2024 Jan-Feb;15(1):27-36. doi: 10.32598/bcn.2023.587.1. Epub 2024 Jan 1.
3
Influence of age and sex on alcohol pharmacokinetics and subjective pharmacodynamic responses following intravenous alcohol exposure in humans.
年龄和性别对人类静脉酒精暴露后酒精药代动力学和主观药效反应的影响。
Alcohol. 2023 Mar;107:144-152. doi: 10.1016/j.alcohol.2022.08.010. Epub 2022 Sep 22.
4
The impact of heavy alcohol consumption on cognitive impairment in young old and middle old persons.大量饮酒对年轻老年人和中老年认知障碍的影响。
J Transl Med. 2022 Apr 5;20(1):155. doi: 10.1186/s12967-022-03353-3.
5
Consideration of an upper-bound continuous maximum drinks measure for adolescent binge and high-intensity drinking prevalence.考虑一个上限连续最大饮酒量来衡量青少年狂饮和高度饮酒的流行率。
Alcohol Clin Exp Res. 2021 Sep;45(9):1821-1828. doi: 10.1111/acer.14676. Epub 2021 Aug 18.
6
Relationship of Phosphatidylethanol Biomarker to Self-Reported Alcohol Drinking Patterns in Older and Middle-Age Adults.磷脂酰乙醇生物标志物与中老年人群自我报告饮酒模式的关系。
Alcohol Clin Exp Res. 2020 Dec;44(12):2449-2456. doi: 10.1111/acer.14475. Epub 2020 Nov 9.
7
Canadian Guidelines on Alcohol Use Disorder Among Older Adults.加拿大老年人酒精使用障碍指南。
Can Geriatr J. 2020 Mar 30;23(1):143-148. doi: 10.5770/cgj.23.425. eCollection 2020 Mar.
8
Determinants of harmful use of alcohol among urban slum dwelling adults in Kenya.肯尼亚城市贫民窟成年居民酒精有害使用的决定因素。
Afr Health Sci. 2019 Dec;19(4):2906-2925. doi: 10.4314/ahs.v19i4.12.
9
From adolescence to late aging: A comprehensive review of social behavior, alcohol, and neuroinflammation across the lifespan.从青春期到老年晚期:终生的社会行为、酒精和神经炎症的综合综述。
Int Rev Neurobiol. 2019;148:231-303. doi: 10.1016/bs.irn.2019.08.001. Epub 2019 Aug 24.
10
Physiologically Based Pharmacokinetic Modelling to Identify Pharmacokinetic Parameters Driving Drug Exposure Changes in the Elderly.基于生理学的药代动力学模型识别导致老年人药物暴露变化的药代动力学参数。
Clin Pharmacokinet. 2020 Mar;59(3):383-401. doi: 10.1007/s40262-019-00822-9.