• 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

体外对人血液及骨髓细胞由乙醇生成乙酸盐的研究。

Investigations into the production of acetate from ethanol by human blood and bone marrow cells in vitro.

作者信息

Bond A N, Wickramasinghe S N

出版信息

Acta Haematol. 1983;69(5):303-13. doi: 10.1159/000206911.

DOI:10.1159/000206911
PMID:6404112
Abstract

The metabolism of ethanol to acetate and CO2 by suspension cultures of human blood and marrow cells has been investigated. The average rate of metabolism of ethanol by relatively pure preparations of monocytes plus lymphocytes, neutrophils and erythrocytes obtained from normal peripheral blood were, respectively, 12.58, 5.44 and 0.32 nmol/10(7) cells/h, when the concentration of ethanol in the culture was 2.63 mM. Under similar culture conditions, the average rate of metabolism of ethanol by suspension cultures of human marrow cells was 19.0 nmol/10(7) nucleated marrow cells/h. The metabolism of ethanol by nucleated marrow cells was only slightly inhibited by pyrazole and 3-amino-1,2,4-triazole indicating that it was largely independent of pyrazole-sensitive alcohol dehydrogenase and catalase. By contrast, the oxidation of ethanol by isolated rat hepatocytes was markedly inhibited by pyrazole and therefore appeared to be mainly dependent on alcohol dehydrogenase. It is concluded that bone marrow cells have a considerable capacity to metabolize ethanol and that the predominant biochemical pathway involved in this metabolism is different from that involved in rat hepatocytes.

摘要

已对人血细胞和骨髓细胞悬浮培养物将乙醇代谢为乙酸盐和二氧化碳的过程进行了研究。当培养物中乙醇浓度为2.63 mM时,从正常外周血获得的相对纯的单核细胞加淋巴细胞、中性粒细胞和红细胞制剂对乙醇的平均代谢速率分别为12.58、5.44和0.32 nmol/10⁷细胞/小时。在相似的培养条件下,人骨髓细胞悬浮培养物对乙醇的平均代谢速率为19.0 nmol/10⁷有核骨髓细胞/小时。有核骨髓细胞对乙醇的代谢仅受到吡唑和3-氨基-1,2,4-三唑的轻微抑制,这表明该代谢在很大程度上不依赖于对吡唑敏感的乙醇脱氢酶和过氧化氢酶。相比之下,分离的大鼠肝细胞对乙醇的氧化受到吡唑的显著抑制,因此似乎主要依赖于乙醇脱氢酶。得出的结论是,骨髓细胞具有相当大的乙醇代谢能力,并且参与这种代谢的主要生化途径与大鼠肝细胞中的不同。

相似文献

1
Investigations into the production of acetate from ethanol by human blood and bone marrow cells in vitro.体外对人血液及骨髓细胞由乙醇生成乙酸盐的研究。
Acta Haematol. 1983;69(5):303-13. doi: 10.1159/000206911.
2
Observations on the biochemical basis of ethanol metabolism by human macrophages.
Alcohol Alcohol. 1986;21(1):57-63.
3
Effect of ethanol concentration on rates of ethanol elimination in normal rats in vivo.
Curr Alcohol. 1979;5:81-9.
4
The capacity of macrophages from different murine tissues to metabolise ethanol and generate an ethanol-dependent non-dialysable cytotoxic activity in vitro.来自不同小鼠组织的巨噬细胞在体外代谢乙醇并产生乙醇依赖性非透析性细胞毒性活性的能力。
Alcohol Alcohol. 1987;22(1):31-9.
5
Evidence that catalase is a major pathway of ethanol oxidation in vivo: dose-response studies in deer mice using methanol as a selective substrate.过氧化氢酶是体内乙醇氧化主要途径的证据:以甲醇作为选择性底物对鹿鼠进行剂量反应研究。
Arch Biochem Biophys. 1993 May 15;303(1):172-6. doi: 10.1006/abbi.1993.1269.
6
Increased alcohol dehydrogenase independent ethanol oxidation at high ethanol concentrations in isolated rat hepatocytes: the effect of chronic ethanol feeding.高乙醇浓度下分离的大鼠肝细胞中酒精脱氢酶非依赖性乙醇氧化增加:长期乙醇喂养的影响
J Pharmacol Exp Ther. 1981 Apr;217(1):133-7.
7
Rates of metabolism of ethanol to acetate by human neutrophil precursors and macrophages.人类中性粒细胞前体和巨噬细胞将乙醇代谢为乙酸盐的速率。
Alcohol Alcohol. 1985;20(3):299-303.
8
Inhibition of methanol and ethanol oxidation by pyrazole in the rat and monkey in vivo.
Mol Pharmacol. 1970 Sep;6(5):567-72.
9
Significant pathways of hepatic ethanol metabolism.肝脏乙醇代谢的重要途径。
Fed Proc. 1975 Oct;34(11):2075-81.
10
Effect of 3-amino-1,2,4-triazole on narcosis time and lethality of ethanol in UChA rats.
Alcohol. 1988 Jan-Feb;5(1):5-8. doi: 10.1016/0741-8329(88)90035-3.

引用本文的文献

1
Changes of Exhaled Volatile Organic Compounds in Postoperative Patients Undergoing Analgesic Treatment: A Prospective Observational Study.接受镇痛治疗的术后患者呼出挥发性有机化合物的变化:一项前瞻性观察研究。
Metabolites. 2020 Aug 7;10(8):321. doi: 10.3390/metabo10080321.
2
Digging deeper into volatile organic compounds associated with cancer.深入探究与癌症相关的挥发性有机化合物。
Biol Methods Protoc. 2019 Nov 27;4(1):bpz014. doi: 10.1093/biomethods/bpz014. eCollection 2019.
3
Alcohol abuse and disorder of granulopoiesis.酒精滥用与粒细胞生成障碍。
Pharmacol Ther. 2019 Jun;198:206-219. doi: 10.1016/j.pharmthera.2019.03.001. Epub 2019 Mar 1.
4
Alcohol dehydrogenase- and rat liver cytosol-dependent bioactivation of 1-chloro-2-hydroxy-3-butene to 1-chloro-3-buten-2-one, a bifunctional alkylating agent.乙醇脱氢酶和大鼠肝胞液依赖的 1-氯-2-羟基-3-丁烯转化为 1-氯-3-丁烯-2-酮,一种双功能烷化剂。
Chem Res Toxicol. 2012 Nov 19;25(11):2600-7. doi: 10.1021/tx300369b. Epub 2012 Nov 7.
5
Alcohol suppresses the granulopoietic response to pulmonary Streptococcus pneumoniae infection with enhancement of STAT3 signaling.酒精抑制肺肺炎链球菌感染的粒状细胞生成反应,增强 STAT3 信号传导。
J Immunol. 2011 Apr 1;186(7):4306-13. doi: 10.4049/jimmunol.1002885. Epub 2011 Feb 28.
6
Acetaldehyde and hexanaldehyde from cultured white cells.来自培养白细胞的乙醛和己醛。
J Transl Med. 2009 Apr 29;7:31. doi: 10.1186/1479-5876-7-31.
7
Gastric metabolism of ethanol in Syrian golden hamster.
Dig Dis Sci. 1995 Dec;40(12):2712-6. doi: 10.1007/BF02220464.
8
Role of macrophages in the pathogenesis of alcohol induced tissue damage.巨噬细胞在酒精诱导的组织损伤发病机制中的作用。
Br Med J (Clin Res Ed). 1987 May 2;294(6580):1137-9. doi: 10.1136/bmj.294.6580.1137.
9
Role of superoxide anion radicals in ethanol metabolism by blood monocyte-derived human macrophages.超氧阴离子自由基在血液单核细胞衍生的人巨噬细胞乙醇代谢中的作用。
J Exp Med. 1989 Mar 1;169(3):755-63. doi: 10.1084/jem.169.3.755.