• 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

胃环境中铬的昼夜节律性减少。

Circadian reduction of chromium in the gastric environment.

作者信息

De Flora S, Badolati G S, Serra D, Picciotto A, Magnolia M R, Savarino V

机构信息

Institute of Hygiene, School of Medicine, University of Genoa, Italy.

出版信息

Mutat Res. 1987 Nov;192(3):169-74. doi: 10.1016/0165-7992(87)90051-0.

DOI:10.1016/0165-7992(87)90051-0
PMID:3683437
Abstract

Samples of gastric juice from variously treated subjects efficiently reduced hexavalent chromium and decreased its mutagenicity. Chromium reduction was due to thermostable components of gastric secretions and was favoured by the acidity of the intragastric environment. The circadian monitoring of pH and of chromium reduction, as assessed by colorimetric analysis at hourly intervals, showed a basal activity (less than 10 micrograms/ml gastric juice) during the night and interdigestive periods, and peaks (tens of micrograms/ml) during the 3-4-h periods after each meal. Assays in the Ames reversion test confirmed that the decrease in mutagenicity of sodium dichromate produced by gastric juice was significantly enhanced after meals. This physiological mechanism is expected to provide an important protective barrier against the oral toxicity of this metal, and may explain its lack of oral carcinogenicity.

摘要

来自不同处理对象的胃液样本能有效还原六价铬并降低其致突变性。铬的还原归因于胃分泌物中的热稳定成分,且胃内环境的酸性有利于此过程。通过每小时进行比色分析评估的pH值和铬还原的昼夜监测显示,夜间和消化间期有基础活性(胃液中低于10微克/毫升),而每餐饭后3 - 4小时出现峰值(数十微克/毫升)。艾姆斯回复突变试验证实,胃液使重铬酸钠致突变性降低的作用在饭后显著增强。这种生理机制有望为抵御这种金属的口服毒性提供重要的保护屏障,并且可能解释其缺乏口服致癌性的原因。

相似文献

1
Circadian reduction of chromium in the gastric environment.胃环境中铬的昼夜节律性减少。
Mutat Res. 1987 Nov;192(3):169-74. doi: 10.1016/0165-7992(87)90051-0.
2
Reduction of hexavalent chromium by fasted and fed human gastric fluid. I. Chemical reduction and mitigation of mutagenicity.禁食和进食状态下人体胃液对六价铬的还原作用。I. 化学还原及致突变性的减轻
Toxicol Appl Pharmacol. 2016 Sep 1;306:113-9. doi: 10.1016/j.taap.2016.07.004. Epub 2016 Jul 9.
3
Circadian monitoring of gastric juice mutagenicity.胃液诱变性的昼夜监测。
Mutagenesis. 1987 Mar;2(2):115-9. doi: 10.1093/mutage/2.2.115.
4
Interpretations on chromium mutagenicity and carcinogenicity.
Prog Clin Biol Res. 1982;109:453-64.
5
An evaluation of in vivo models for toxicokinetics of hexavalent chromium in the stomach.胃中六价铬毒代动力学的体内模型评估。
Toxicol Appl Pharmacol. 2015 Sep 15;287(3):293-8. doi: 10.1016/j.taap.2015.06.016. Epub 2015 Jun 27.
6
A revised model of ex-vivo reduction of hexavalent chromium in human and rodent gastric juices.一种人体和啮齿动物胃液中六价铬体外还原的修正模型。
Toxicol Appl Pharmacol. 2014 Oct 15;280(2):352-61. doi: 10.1016/j.taap.2014.08.010. Epub 2014 Aug 20.
7
Mutagenicity in gastric juice.胃液中的致突变性。
Gut. 1984 Jul;25(7):723-7. doi: 10.1136/gut.25.7.723.
8
[Continuous intragastric pH-metry].
Schweiz Med Wochenschr. 1985 Nov 16;115(46):1630-41.
9
Measurement of gastric functions during digestion of ordinary solid meals in man.人体在消化普通固体食物期间胃功能的测量。
Gastroenterology. 1976 Feb;70(2):203-10.
10
Estimates of the chromium(VI) reducing capacity in human body compartments as a mechanism for attenuating its potential toxicity and carcinogenicity.
Carcinogenesis. 1997 Mar;18(3):531-7. doi: 10.1093/carcin/18.3.531.

引用本文的文献

1
Acute Oral Chromium Exposure Resulting in Ulcerative Gastritis and Perforated Ulcers in Swine.猪急性经口接触铬导致溃疡性胃炎和溃疡穿孔
Animals (Basel). 2023 Dec 23;14(1):63. doi: 10.3390/ani14010063.
2
Hair, serum and urine chromium levels in children with cognitive defects: A systematic review and meta-analysis of case control studies.儿童认知缺陷患者的毛发、血清和尿液铬水平:病例对照研究的系统评价和荟萃分析。
Chemosphere. 2022 Mar;291(Pt 2):133017. doi: 10.1016/j.chemosphere.2021.133017. Epub 2021 Nov 20.
3
Melatonin protects against chromium (VI) induced hepatic oxidative stress and toxicity: Duration dependent study with realistic dosage.
褪黑素可抵御六价铬诱导的肝脏氧化应激和毒性:基于实际剂量的时间依赖性研究
Interdiscip Toxicol. 2017 Sep;10(1):20-29. doi: 10.1515/intox-2017-0003.
4
Chromium disrupts chromatin organization and CTCF access to its cognate sites in promoters of differentially expressed genes.铬扰乱染色质组织,影响差异表达基因启动子中 CTCF 与其同源结合位点的相互作用。
Epigenetics. 2018;13(4):363-375. doi: 10.1080/15592294.2018.1454243. Epub 2018 May 3.
5
A chronic oral reference dose for hexavalent chromium-induced intestinal cancer.六价铬诱发肠道癌的慢性口服参考剂量。
J Appl Toxicol. 2014 May;34(5):525-36. doi: 10.1002/jat.2907. Epub 2013 Aug 14.
6
Assessment of the mode of action underlying development of rodent small intestinal tumors following oral exposure to hexavalent chromium and relevance to humans.评估经口接触六价铬后诱发啮齿类动物小肠肿瘤的作用机制及其与人类的相关性。
Crit Rev Toxicol. 2013 Mar;43(3):244-74. doi: 10.3109/10408444.2013.768596.
7
Chromium in drinking water: sources, metabolism, and cancer risks.饮用水中的铬:来源、代谢和癌症风险。
Chem Res Toxicol. 2011 Oct 17;24(10):1617-29. doi: 10.1021/tx200251t. Epub 2011 Jul 28.
8
Metabolic reduction of chromium, as related to its carcinogenic properties.铬的代谢还原及其致癌特性
Biol Trace Elem Res. 1989 Jul-Sep;21:179-87. doi: 10.1007/BF02917250.