• 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

重、轻度大麻使用者中氘标记的δ1-四氢大麻酚的单剂量动力学

Single dose kinetics of deuterium labelled delta 1-tetrahydrocannabinol in heavy and light cannabis users.

作者信息

Ohlsson A, Lindgren J E, Wahlén A, Agurell S, Hollister L E, Gillespie H K

出版信息

Biomed Mass Spectrom. 1982 Jan;9(1):6-10. doi: 10.1002/bms.1200090103.

DOI:10.1002/bms.1200090103
PMID:6277407
Abstract

Deuterium labelled delta 1-tetrahydrocannabinol was administered intravenously (5.0 mg) and by smoking (10.0 mg) to five heavy and four light marihuana users. All subjects smoked an estimated amount of 8.6-9.9 mg delta 1-tetrahydrocannabinol. The plasma levels of delta 1-tetrahydrocannabinol were followed for 48 hours and in two subjects fof 72 hours after administration. The systemic availability after inhalation calculated from the area under curve values was in the range of 27 +/- 10% for the heavy users and 14 +/- 1% for the light users. There was little difference between the groups with regard to the amount of smoked delta 1-tetrahydrocannabinol or plasma levels and area under curve values obtained after i.v. administration. Thus, it seems likely that the statistically significant difference in systemic availability of smoked delta 1-tetrahydrocannabinol was due to a more efficient smoking by the heavy users. It is also indicated that heavy users prefer slightly higher delta 1-tetrahydrocannabinol plasma levels than light users. Based on the area under curve values after i.v. administration, a plasma clearance of 760-1190 ml min-1 was calculated. The elimination half-life of delta 1-tetrahydrocannabinol is more than 20 hours. The present results do not suggest that tolerance or sensitivity to delta 1-tetrahydrocannabinol in heavy users is readily achieved.

摘要

将氘标记的δ1-四氢大麻酚以静脉注射(5.0毫克)和吸烟(10.0毫克)的方式给予5名重度大麻使用者和4名轻度大麻使用者。所有受试者吸食的δ1-四氢大麻酚估计量为8.6 - 9.9毫克。给药后对δ1-四氢大麻酚的血浆水平进行了48小时的跟踪,两名受试者跟踪了72小时。根据曲线下面积值计算,重度使用者吸入后的全身可用性范围为27±10%,轻度使用者为14±1%。在吸食的δ1-四氢大麻酚量、血浆水平以及静脉给药后获得的曲线下面积值方面,两组之间几乎没有差异。因此,吸食的δ1-四氢大麻酚在全身可用性上的统计学显著差异似乎是由于重度使用者吸烟效率更高。研究还表明,重度使用者比轻度使用者更喜欢略高的δ1-四氢大麻酚血浆水平。根据静脉给药后的曲线下面积值,计算出血浆清除率为760 - 1190毫升/分钟。δ1-四氢大麻酚的消除半衰期超过20小时。目前的结果并不表明重度使用者对δ1-四氢大麻酚容易产生耐受性或敏感性。

相似文献

1
Single dose kinetics of deuterium labelled delta 1-tetrahydrocannabinol in heavy and light cannabis users.重、轻度大麻使用者中氘标记的δ1-四氢大麻酚的单剂量动力学
Biomed Mass Spectrom. 1982 Jan;9(1):6-10. doi: 10.1002/bms.1200090103.
2
[Serum cannabinoid levels 24 to 48 hours after cannabis smoking].吸食大麻后24至48小时的血清大麻素水平
Arch Kriminol. 2003 Sep-Oct;212(3-4):83-95.
3
Validation of Large White Pig as an animal model for the study of cannabinoids metabolism: application to the study of THC distribution in tissues.大白猪作为大麻素代谢研究动物模型的验证:应用于四氢大麻酚在组织中分布的研究
Forensic Sci Int. 2006 Sep 12;161(2-3):169-74. doi: 10.1016/j.forsciint.2006.04.018. Epub 2006 Jul 21.
4
Clinical effects and plasma levels of delta 9-tetrahydrocannabinol (delta 9-THC) in heavy and light users of cannabis.大麻重度和轻度使用者中Δ9-四氢大麻酚(Δ9-THC)的临床效果及血浆水平
Psychopharmacology (Berl). 1981;74(3):208-12. doi: 10.1007/BF00427095.
5
Single-dose kinetics of deuterium-labelled cannabinol in man after intravenous administration and smoking.静脉注射和吸食后人体内氘标记大麻酚的单剂量动力学。
Biomed Environ Mass Spectrom. 1987 Sep;14(9):495-9. doi: 10.1002/bms.1200140904.
6
Comparative pharmacology of Delta9-tetrahydrocannabinol and its metabolite, 11-OH-Delta9-tetrahydrocannabinol.Δ9-四氢大麻酚及其代谢物11-羟基-Δ9-四氢大麻酚的比较药理学
J Clin Invest. 1973 Oct;52(10):2411-7. doi: 10.1172/JCI107431.
7
Pharmacokinetics of delta 9-tetrahydrocannabinol in rabbits following single or multiple intravenous doses.
Drug Metab Dispos. 1986 Mar-Apr;14(2):230-8.
8
Dose-dependent effects of smoked cannabis on capsaicin-induced pain and hyperalgesia in healthy volunteers.吸食大麻对健康志愿者辣椒素诱发的疼痛和痛觉过敏的剂量依赖性效应。
Anesthesiology. 2007 Nov;107(5):785-96. doi: 10.1097/01.anes.0000286986.92475.b7.
9
Metabolism and disposition of delta-9-tetrahydrocannabinol in man.人体内 Δ⁹-四氢大麻酚的代谢与处置
Pharmacol Rev. 1971 Dec;23(4):371-80.
10
Neurocognitive performance during acute THC intoxication in heavy and occasional cannabis users.重度和偶尔使用大麻者在急性四氢大麻酚中毒期间的神经认知表现。
J Psychopharmacol. 2009 May;23(3):266-77. doi: 10.1177/0269881108092393. Epub 2008 Aug 21.

引用本文的文献

1
Quantification and prediction of human fetal (-)-Δ-tetrahydrocannabinol/(±)-11-OH-Δ-tetrahydrocannabinol exposure during pregnancy to inform fetal cannabis toxicity.孕期人体胎儿暴露于(-)-Δ-四氢大麻酚/(±)-11-羟基-Δ-四氢大麻酚的定量与预测,以了解胎儿大麻毒性。
Nat Commun. 2025 Jan 18;16(1):824. doi: 10.1038/s41467-025-55863-5.
2
The impact of pregnancy and associated hormones on the pharmacokinetics of Δ-tetrahydrocannabinol.妊娠及相关激素对Δ-四氢大麻酚药代动力学的影响。
Expert Opin Drug Metab Toxicol. 2024 Jan-Feb;20(1-2):73-93. doi: 10.1080/17425255.2024.2309213. Epub 2024 Mar 4.
3
Medicinal Cannabis and Central Nervous System Disorders.
药用大麻与中枢神经系统疾病
Front Pharmacol. 2022 Apr 21;13:881810. doi: 10.3389/fphar.2022.881810. eCollection 2022.
4
Characterizing and Quantifying Extrahepatic Metabolism of (-)-Δ-Tetrahydrocannabinol (THC) and Its Psychoactive Metabolite, (±)-11-Hydroxy-Δ-THC (11-OH-THC).表征和量化 (-)-Δ-四氢大麻酚 (THC) 和其精神活性代谢物 (±)-11-羟基-Δ-THC (11-OH-THC) 的肝外代谢。
Drug Metab Dispos. 2022 Jun;50(6):734-740. doi: 10.1124/dmd.122.000868. Epub 2022 Apr 3.
5
The Transdermal Delivery of Therapeutic Cannabinoids.治疗性大麻素的透皮给药
Pharmaceutics. 2022 Feb 18;14(2):438. doi: 10.3390/pharmaceutics14020438.
6
The Neuroprotective Effects of Cannabis-Derived Phytocannabinoids and Resveratrol in Parkinson's Disease: A Systematic Literature Review of Pre-Clinical Studies.大麻衍生的植物大麻素和白藜芦醇对帕金森病的神经保护作用:临床前研究的系统文献综述
Brain Sci. 2021 Nov 28;11(12):1573. doi: 10.3390/brainsci11121573.
7
Objective Identification of Cannabis Use Levels in Clinical Populations Is Critical for Detecting Pharmacological Outcomes.目标 确定临床人群中大麻的使用水平对于检测药理学结果至关重要。
Cannabis Cannabinoid Res. 2022 Dec;7(6):852-864. doi: 10.1089/can.2021.0068. Epub 2021 Nov 18.
8
Development and Verification of a Linked -THC/11-OH-THC Physiologically Based Pharmacokinetic Model in Healthy, Nonpregnant Population and Extrapolation to Pregnant Women.建立并验证健康非妊娠人群中 THC/11-OH-THC 的连接性生理药代动力学模型,并外推至妊娠妇女。
Drug Metab Dispos. 2021 Jul;49(7):509-520. doi: 10.1124/dmd.120.000322. Epub 2021 May 5.
9
Potential of Plant Bioactive Compounds as SARS-CoV-2 Main Protease (M) and Spike (S) Glycoprotein Inhibitors: A Molecular Docking Study.植物生物活性化合物作为严重急性呼吸综合征冠状病毒2型(SARS-CoV-2)主要蛋白酶(M)和刺突(S)糖蛋白抑制剂的潜力:一项分子对接研究。
Scientifica (Cairo). 2020 Dec 23;2020:6307457. doi: 10.1155/2020/6307457. eCollection 2020.
10
Human Pharmacokinetic Parameters of Orally Administered Δ-Tetrahydrocannabinol Capsules Are Altered by Fed Versus Fasted Conditions and Sex Differences.口服Δ-四氢大麻酚胶囊的人体药代动力学参数受进食与空腹状态及性别差异的影响。
Cannabis Cannabinoid Res. 2019 Dec 6;4(4):255-264. doi: 10.1089/can.2019.0037. eCollection 2019.