• 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

多次口服吗啡效力的解释?

Explanation for potency of repeated oral doses of morphine?

作者信息

Hanks G W, Hoskin P J, Aherne G W, Turner P, Poulain P

机构信息

Royal Marsden Hospital, Sutton.

出版信息

Lancet. 1987 Sep 26;2(8561):723-5. doi: 10.1016/s0140-6736(87)91083-x.

DOI:10.1016/s0140-6736(87)91083-x
PMID:2888950
Abstract

Morphine given by injection is the standard by which all other strong analgesics are measured, but when given orally in single doses it is a poor analgesic. With repeated oral administration it becomes very effective and it may be that on repeated dosage active metabolites, particularly morphine-6-glucuronide, account for much of the analgesic activity. Enterohepatic circulation may also contribute to the maintenance of blood and tissue levels of morphine and its metabolites in chronic use.

摘要

注射用吗啡是衡量所有其他强效镇痛药的标准,但单次口服时它却是一种低效镇痛药。反复口服给药后它会变得非常有效,可能是反复给药时活性代谢产物,尤其是吗啡 -6- 葡萄糖醛酸苷,发挥了大部分镇痛活性。肝肠循环也可能有助于长期使用吗啡时维持其血液和组织中的水平及其代谢产物的水平。

相似文献

1
Explanation for potency of repeated oral doses of morphine?多次口服吗啡效力的解释?
Lancet. 1987 Sep 26;2(8561):723-5. doi: 10.1016/s0140-6736(87)91083-x.
2
The intravenous to oral relative milligram potency ratio of morphine during chronic dosing in cancer pain.吗啡在癌症疼痛慢性给药期间的静脉到口服相对毫克效价比。
Palliat Med. 2010 Jan;24(1):9-16. doi: 10.1177/0269216309346595. Epub 2009 Nov 12.
3
Morphine-6-glucuronide is responsible for the analgesic effect after morphine administration: a quantitative review of morphine, morphine-6-glucuronide, and morphine-3-glucuronide.吗啡-6-葡萄糖醛酸是吗啡给药后镇痛作用的原因:对吗啡、吗啡-6-葡萄糖醛酸和吗啡-3-葡萄糖醛酸的定量综述。
Br J Anaesth. 2014 Dec;113(6):935-44. doi: 10.1093/bja/aeu186. Epub 2014 Jul 1.
4
The oral-to-intravenous equianalgesic ratio of morphine based on plasma concentrations of morphine and metabolites in advanced cancer patients receiving chronic morphine treatment.基于接受慢性吗啡治疗的晚期癌症患者血浆中吗啡及其代谢物浓度的吗啡口服至静脉注射等效镇痛比。
Palliat Med. 2003 Dec;17(8):673-8. doi: 10.1191/0269216303pm824oa.
5
A Compartmental Analysis for Morphine and Its Metabolites in Young Children After a Single Oral Dose.单次口服剂量后幼儿体内吗啡及其代谢物的房室分析
Clin Pharmacokinet. 2015 Oct;54(10):1083-90. doi: 10.1007/s40262-015-0256-4.
6
Morphine pharmacokinetics and metabolism in humans. Enterohepatic cycling and relative contribution of metabolites to active opioid concentrations.吗啡在人体内的药代动力学与代谢。肠肝循环及代谢产物对活性阿片类药物浓度的相对贡献。
Clin Pharmacokinet. 1993 Apr;24(4):344-54. doi: 10.2165/00003088-199324040-00007.
7
[Treatment of severe non-cancer pain by oral morphine].口服吗啡治疗重度非癌性疼痛
Masui. 2008 Nov;57(11):1343-50.
8
Efficacy and safety of sublingual fentanyl orally disintegrating tablet at doses determined from oral morphine rescue doses in the treatment of breakthrough cancer pain.舌下芬太尼口崩片治疗爆发性癌痛时,根据口服吗啡解救剂量确定的剂量的疗效和安全性。
Jpn J Clin Oncol. 2015 Feb;45(2):189-96. doi: 10.1093/jjco/hyu182. Epub 2014 Nov 6.
9
Sustained relief of chronic pain. Pharmacokinetics of sustained release morphine.慢性疼痛的持续缓解。缓释吗啡的药代动力学。
Clin Pharmacokinet. 1998 Sep;35(3):173-90. doi: 10.2165/00003088-199835030-00002.
10
Lack of effect of ondansetron on the pharmacokinetics and analgesic effects of morphine and metabolites after single-dose morphine administration in healthy volunteers.在健康志愿者单次给予吗啡后,昂丹司琼对吗啡及其代谢产物的药代动力学和镇痛效果无影响。
Br J Clin Pharmacol. 2001 Apr;51(4):309-16. doi: 10.1046/j.1365-2125.2001.01369.x.

引用本文的文献

1
Pharmacokinetics and thermal anti-nociceptive effects of oral morphine in horses.口服吗啡在马体内的药代动力学及热镇痛作用
Front Vet Sci. 2024 Sep 17;11:1461648. doi: 10.3389/fvets.2024.1461648. eCollection 2024.
2
Pharmacokinetics, adverse effects and effects on thermal nociception following administration of three doses of codeine to horses.给马给予三剂可待因后的药代动力学、不良反应和对热伤害感受的影响。
BMC Vet Res. 2022 May 25;18(1):196. doi: 10.1186/s12917-022-03299-0.
3
Metabolism of Carfentanil, an Ultra-Potent Opioid, in Human Liver Microsomes and Human Hepatocytes by High-Resolution Mass Spectrometry.
用高分辨率质谱法研究超高效阿片类药物卡芬太尼在人肝微粒体和人肝细胞中的代谢
AAPS J. 2016 Nov;18(6):1489-1499. doi: 10.1208/s12248-016-9963-5. Epub 2016 Aug 5.
4
Strong opioids in pediatric palliative medicine.儿科姑息医学中的强效阿片类药物。
Paediatr Drugs. 2005;7(1):1-9. doi: 10.2165/00148581-200507010-00001.
5
Contribution to variability in response to opioids.对阿片类药物反应变异性的贡献。
Support Care Cancer. 2005 Mar;13(3):145-52. doi: 10.1007/s00520-004-0730-2. Epub 2004 Dec 10.
6
The bioavailability and pharmacokinetics of subcutaneous, nebulized and oral morphine-6-glucuronide.皮下注射、雾化吸入及口服吗啡 -6- 葡萄糖醛酸苷的生物利用度和药代动力学。
Br J Clin Pharmacol. 2002 Apr;53(4):347-54. doi: 10.1046/j.1365-2125.2002.01554.x.
7
Morphine-6-glucuronide: an analgesic of the future?吗啡-6-葡萄糖醛酸:未来的镇痛药?
Clin Pharmacokinet. 2001;40(7):485-99. doi: 10.2165/00003088-200140070-00001.
8
Morphine and alternative opioids in cancer pain: the EAPC recommendations.吗啡及其他阿片类药物用于癌症疼痛治疗:欧洲姑息治疗学会(EAPC)的建议
Br J Cancer. 2001 Mar 2;84(5):587-93. doi: 10.1054/bjoc.2001.1680.
9
Pharmacokinetics of opioids in liver disease.阿片类药物在肝脏疾病中的药代动力学。
Clin Pharmacokinet. 1999 Jul;37(1):17-40. doi: 10.2165/00003088-199937010-00002.
10
Morphine and morphine-6-glucuronide in the plasma and cerebrospinal fluid of children.儿童血浆和脑脊液中的吗啡及吗啡-6-葡萄糖醛酸苷
Br J Clin Pharmacol. 1999 Jul;48(1):37-42. doi: 10.1046/j.1365-2125.1999.00948.x.