• 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

大麻二酚对人中性粒细胞中1型和2型环氧化酶表达及功能的影响。

Effect of Cannabidiol on Cyclooxygenase Type 1 and 2 Expression and Function in Human Neutrophils.

作者信息

Cosentino Marco, Legnaro Massimiliano, Luini Alessandra, Ferrari Marco, Sodergren Mikael, Pacchetti Barbara, Marino Franca

机构信息

Center for Research in Medical Pharmacology, University of Insubria, Varese, Italy.

Curaleaf International, London, United Kingdom.

出版信息

Cannabis Cannabinoid Res. 2023 Dec;8(6):999-1007. doi: 10.1089/can.2022.0008. Epub 2022 Aug 5.

DOI:10.1089/can.2022.0008
PMID:35930236
Abstract

In this study, the effects of the cannabinoid CBD were assessed on cyclooxygenase (COX)-1 and COX-2 expression and activity in resting and activated human neutrophils (polymorphonuclear [PMN] leukocytes). COX expression was measured at the mRNA levels, whereas COX activity was assessed by enzyme-linked immunosorbent assay measurement of prostaglandin (PG)E. experiments in a standard commercial acellular assay of COX-1/COX-2 activity completed the study. Results show that CBD profoundly inhibits expression of COX-1 and COX-2 mRNA in activated PMN, however, without any significant consequences for PGE production. CBD, however, was able to induce a slight but significant direct inhibition of COX-2 in the acellular model. The effects of CBD occur in the μM concentration range, which is attained in humans with therapeutic doses of the drug, suggesting the clinical relevance of these findings.

摘要

在本研究中,评估了大麻素CBD对静息和活化的人中性粒细胞(多形核[PMN]白细胞)中环氧化酶(COX)-1和COX-2表达及活性的影响。在mRNA水平上测量COX表达,而通过酶联免疫吸附测定法测量前列腺素(PG)E来评估COX活性。在标准的商业性COX-1/COX-2活性无细胞测定实验中完成了该研究。结果表明,CBD可显著抑制活化的PMN中COX-1和COX-2 mRNA的表达,然而,对PGE的产生没有任何显著影响。不过,在无细胞模型中,CBD能够对COX-2产生轻微但显著的直接抑制作用。CBD的作用发生在μM浓度范围内,这在人类使用该药物的治疗剂量时能够达到,表明这些发现具有临床相关性。

相似文献

1
Effect of Cannabidiol on Cyclooxygenase Type 1 and 2 Expression and Function in Human Neutrophils.大麻二酚对人中性粒细胞中1型和2型环氧化酶表达及功能的影响。
Cannabis Cannabinoid Res. 2023 Dec;8(6):999-1007. doi: 10.1089/can.2022.0008. Epub 2022 Aug 5.
2
A Novel Standardized L. Extract and Its Constituent Cannabidiol Inhibit Human Polymorphonuclear Leukocyte Functions.一种新型标准化 L. 提取物及其成分大麻二酚可抑制人多形核白细胞的功能。
Int J Mol Sci. 2019 Apr 13;20(8):1833. doi: 10.3390/ijms20081833.
3
5-Lipoxygenase and anandamide hydrolase (FAAH) mediate the antitumor activity of cannabidiol, a non-psychoactive cannabinoid.5-脂氧合酶和花生四烯乙醇胺水解酶(FAAH)介导了大麻二酚(一种非精神活性大麻素)的抗肿瘤活性。
J Neurochem. 2008 Feb;104(4):1091-100. doi: 10.1111/j.1471-4159.2007.05073.x. Epub 2007 Nov 17.
4
Interleukin-13 increases prostaglandin E2 (PGE2) production by normal human polymorphonuclear neutrophils by enhancing cyclooxygenase 2 (COX-2) gene expression.白细胞介素-13通过增强环氧化酶2(COX-2)基因表达,增加正常人多形核中性粒细胞中前列腺素E2(PGE2)的产生。
Inflamm Res. 1998 Apr;47(4):167-73. doi: 10.1007/s000110050312.
5
Anti-CD45 antibody enhances lipoxygenase pathway of human naïve mononuclear cells and cyclooxygenase pathway of neutrophils.抗CD45抗体增强人初始单核细胞的脂氧合酶途径和中性粒细胞的环氧化酶途径。
Inflamm Res. 2006 Mar;55(3):92-8. doi: 10.1007/s00011-005-0058-5.
6
Cannabidiol and other cannabinoids reduce microglial activation in vitro and in vivo: relevance to Alzheimer's disease.大麻二酚和其他大麻素可减少体外和体内小胶质细胞的激活:与阿尔茨海默病相关。
Mol Pharmacol. 2011 Jun;79(6):964-73. doi: 10.1124/mol.111.071290. Epub 2011 Feb 24.
7
Mannan and peptidoglycan induce COX-2 protein in human PMN via the mammalian target of rapamycin.甘露聚糖和肽聚糖通过雷帕霉素的哺乳动物靶点诱导人中性粒细胞中的COX-2蛋白。
Eur J Immunol. 2007 Sep;37(9):2572-82. doi: 10.1002/eji.200737262.
8
Macrolide antibiotics inhibit prostaglandin E2 synthesis and mRNA expression of prostaglandin synthetic enzymes in human leukocytes.大环内酯类抗生素可抑制人白细胞中前列腺素E2的合成以及前列腺素合成酶的mRNA表达。
Prostaglandins Leukot Essent Fatty Acids. 2003 Oct;69(4):229-35. doi: 10.1016/s0952-3278(03)00089-9.
9
Influence of Inhibition of COX-2-Dependent Lipid Metabolism on Regulation of UVB-Induced Keratinocytes Apoptosis by Cannabinoids.大麻素抑制 COX-2 依赖性脂代谢对 UVB 诱导的角质形成细胞凋亡的调控作用。
Biomolecules. 2022 Jun 17;12(6):842. doi: 10.3390/biom12060842.
10
R(+)-methanandamide and other cannabinoids induce the expression of cyclooxygenase-2 and matrix metalloproteinases in human nonpigmented ciliary epithelial cells.R(+)-花生四烯酸乙醇胺及其他大麻素可诱导人非色素睫状上皮细胞中环氧化酶-2和基质金属蛋白酶的表达。
J Pharmacol Exp Ther. 2006 Mar;316(3):1219-28. doi: 10.1124/jpet.105.092858. Epub 2005 Dec 5.

引用本文的文献

1
Molecular Mechanisms of the Endocannabinoid System with a Focus on Reproductive Physiology and the Cannabinoid Impact on Fertility.以生殖生理学为重点的内源性大麻素系统的分子机制以及大麻素对生育能力的影响。
Int J Mol Sci. 2025 Jul 23;26(15):7095. doi: 10.3390/ijms26157095.
2
Considering Long-Acting Synthetic Cannabidiol for Chronic Pain: A Narrative Review.考虑使用长效合成大麻二酚治疗慢性疼痛:一项叙述性综述。
Cureus. 2025 Apr 1;17(4):e81577. doi: 10.7759/cureus.81577. eCollection 2025 Apr.
3
Cannabis use associated with lower mortality among hospitalized Covid-19 patients using the national inpatient sample: an epidemiological study.
使用全国住院患者样本的研究表明,新冠病毒肺炎住院患者中,使用大麻与较低死亡率相关:一项流行病学研究。
J Cannabis Res. 2024 Apr 6;6(1):18. doi: 10.1186/s42238-024-00228-w.
4
Effect of Cannabidiol on Human Peripheral Blood Mononuclear Cells and CD4+ T Cells.大麻二酚对人外周血单核细胞和 CD4+T 细胞的影响。
Int J Mol Sci. 2023 Oct 4;24(19):14880. doi: 10.3390/ijms241914880.
5
Molecular and Cellular Mechanisms of Action of Cannabidiol.大麻素的分子和细胞作用机制。
Molecules. 2023 Aug 9;28(16):5980. doi: 10.3390/molecules28165980.
6
Effects of Cannabidiol on Innate Immunity: Experimental Evidence and Clinical Relevance.大麻二酚对固有免疫的影响:实验证据和临床相关性。
Int J Mol Sci. 2023 Feb 4;24(4):3125. doi: 10.3390/ijms24043125.
7
Role of Cannabidiol for Improvement of the Quality of Life in Cancer Patients: Potential and Challenges.大麻二酚改善癌症患者生活质量的作用:潜力与挑战。
Int J Mol Sci. 2022 Oct 26;23(21):12956. doi: 10.3390/ijms232112956.