• 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

对氧磷酶-1基因Q192R多态性与活性氧代谢产物

Paraoxonase-1 gene Q192R polymorphism and reactive oxygen metabolites.

作者信息

Kotani K, Tsuzaki K, Sakane N

机构信息

Division of Preventive Medicine, Clinical Research Institute, National Hospital Organization Kyoto Medical Centre, 1-1 Fukakusa mukaihata, Fushimi-ku, Kyoto 612-8555, Japan.

出版信息

J Int Med Res. 2012;40(4):1513-8. doi: 10.1177/147323001204000431.

DOI:10.1177/147323001204000431
PMID:22971504
Abstract

OBJECTIVE

Paraoxonase-1 (PON1) is a high-density lipoprotein-associated antioxidant enzyme. The Q192R polymorphism of the PON1 gene can protect against oxidative conditions, but the relationship between Q192R polymorphism and oxidative stress-related markers remains controversial. In this study, the diacron reactive oxygen metabolites (d-ROMs) test was used to investigate the relationship between Q192R polymorphism and oxidative stress-related markers in Japanese subjects.

METHODS

Patients without a history of overt cardiovascular disease who were not receiving antioxidant medication were enrolled in a cross-sectional clinic-based study. An allele-specific polymerase chain reaction method was used to assess the PON1 Q192R polymorphism and compare the level of d-ROMs between genotypes.

RESULTS

A total of 103 subjects were analysed. The RR genotype was associated with a significantly lower level of d-ROMs than the RQ and QQ genotypes. After multivariate analysis the relationship between the genotypes and level of d-ROMs remained independently significant.

CONCLUSIONS

The RR genotype may be protective against oxidative stress in cardiovascular diseasefree Japanese subjects. In addition, the d-ROMs test can be useful for examining the role of the PON1 Q192R polymorphism under oxidative conditions.

摘要

目的

对氧磷酶-1(PON1)是一种与高密度脂蛋白相关的抗氧化酶。PON1基因的Q192R多态性可抵御氧化状态,但Q192R多态性与氧化应激相关标志物之间的关系仍存在争议。在本研究中,采用戴克隆活性氧代谢产物(d-ROMs)检测来研究日本受试者中Q192R多态性与氧化应激相关标志物之间的关系。

方法

将无明显心血管疾病病史且未接受抗氧化药物治疗的患者纳入一项基于门诊的横断面研究。采用等位基因特异性聚合酶链反应方法评估PON1 Q192R多态性,并比较各基因型之间的d-ROMs水平。

结果

共分析了103名受试者。RR基因型与d-ROMs水平显著低于RQ和QQ基因型相关。多变量分析后,基因型与d-ROMs水平之间的关系仍具有独立显著性。

结论

RR基因型可能对无心血管疾病的日本受试者的氧化应激具有保护作用。此外,d-ROMs检测对于研究氧化条件下PON1 Q192R多态性的作用可能有用。

相似文献

1
Paraoxonase-1 gene Q192R polymorphism and reactive oxygen metabolites.对氧磷酶-1基因Q192R多态性与活性氧代谢产物
J Int Med Res. 2012;40(4):1513-8. doi: 10.1177/147323001204000431.
2
Association of paraoxonase-1(Q192R and L55M) gene polymorphisms and activity with colorectal cancer and effect of surgical intervention.对氧磷酶-1(Q192R和L55M)基因多态性及活性与结直肠癌的关联以及手术干预的影响
Asian Pac J Cancer Prev. 2015;16(2):803-9. doi: 10.7314/apjcp.2015.16.2.803.
3
Paraoxonase (PON)1 Q192R functional genotypes and PON1 Q192R genotype by smoking interactions are risk factors for the metabolic syndrome, but not overweight or obesity.对氧磷酶(PON)1 Q192R功能基因型以及吸烟相互作用导致的PON1 Q192R基因型是代谢综合征的危险因素,但不是超重或肥胖的危险因素。
Redox Rep. 2014 Nov;19(6):232-41. doi: 10.1179/1351000214Y.0000000093. Epub 2014 Jul 18.
4
The Q192R polymorphism of the paraoxonase-1 (PON1) gene is associated with susceptibility to gestational diabetes mellitus in the Greek population.对氧磷酶-1(PON1)基因的Q192R多态性与希腊人群患妊娠糖尿病的易感性相关。
Gynecol Endocrinol. 2017 Aug;33(8):617-620. doi: 10.1080/09513590.2017.1302419. Epub 2017 Mar 28.
5
Lowered plasma paraoxonase (PON)1 activity is a trait marker of major depression and PON1 Q192R gene polymorphism-smoking interactions differentially predict the odds of major depression and bipolar disorder.血浆对氧磷酶 1(PON1)活性降低是重度抑郁症的特征性标志物,PON1 Q192R 基因多态性-吸烟相互作用可不同程度地预测重度抑郁症和双相情感障碍的发病风险。
J Affect Disord. 2014 Apr;159:23-30. doi: 10.1016/j.jad.2014.02.018. Epub 2014 Feb 19.
6
Q192R polymorphism in the PON1 gene and familial hypercholesterolemia in a Saudi population.沙特人群中对氧磷酶1(PON1)基因的Q192R多态性与家族性高胆固醇血症
Ann Saudi Med. 2017 Nov-Dec;37(6):425-432. doi: 10.5144/0256-4947.2017.425.
7
The Association of the Cholesterol Efflux Capacity with the Paraoxonase 1 Q192R Genotype and the Paraoxonase Activity.胆固醇外排能力与对氧磷酶 1 Q192R 基因型和对氧磷酶活性的关系。
J Atheroscler Thromb. 2024 Sep 1;31(9):1263-1276. doi: 10.5551/jat.64711. Epub 2024 Mar 19.
8
Q192R polymorphism in the PON1 gene and nasal polyp in a Turkish population.土耳其人群中 PON1 基因 Q192R 多态性与鼻息肉的关系。
J Biochem Mol Toxicol. 2021 Jan;35(1):e22628. doi: 10.1002/jbt.22628. Epub 2020 Sep 9.
9
The Q192R polymorphism of the paraoxonase 1 gene is a risk factor for coronary artery disease in Saudi subjects.载脂蛋白 1 基因的 Q192R 多态性是沙特人群冠心病的一个危险因素。
Mol Cell Biochem. 2013 Aug;380(1-2):121-8. doi: 10.1007/s11010-013-1665-z. Epub 2013 Apr 27.
10
A Genetic Biomarker of Oxidative Stress, the Paraoxonase-1 Q192R Gene Variant, Associates with Cardiomyopathy in CKD: A Longitudinal Study.氧化应激的一种遗传生物标志物——对氧磷酶-1 Q192R基因变异与慢性肾脏病中的心肌病相关:一项纵向研究
Oxid Med Cell Longev. 2016;2016:1507270. doi: 10.1155/2016/1507270. Epub 2016 May 30.

引用本文的文献

1
Paraoxonase 1 and Non-Alcoholic Fatty Liver Disease: A Meta-Analysis.对氧磷酶 1 与非酒精性脂肪性肝病:一项荟萃分析。
Molecules. 2021 Apr 16;26(8):2323. doi: 10.3390/molecules26082323.
2
Paraoxonases (PON) 1, 2, and 3 Polymorphisms and PON-1 Activities in Patients with Sickle Cell Disease.镰状细胞病患者对氧磷酶(PON)1、2和3的多态性及PON-1活性
Antioxidants (Basel). 2019 Jul 30;8(8):252. doi: 10.3390/antiox8080252.
3
Paraoxonases: metabolic role and pharmacological projection.对氧磷酶:代谢作用和药物研发前景。
Naunyn Schmiedebergs Arch Pharmacol. 2018 Apr;391(4):349-359. doi: 10.1007/s00210-018-1473-9. Epub 2018 Feb 6.
4
Associations between PON1 enzyme activities in human ovarian follicular fluid and serum specimens.人卵巢卵泡液和血清样本中对氧磷酶1(PON1)酶活性之间的关联。
PLoS One. 2017 Feb 14;12(2):e0172193. doi: 10.1371/journal.pone.0172193. eCollection 2017.
5
Genome-wide SNP analysis of the Systemic Capillary Leak Syndrome (Clarkson disease).系统性毛细血管渗漏综合征(克拉克森病)的全基因组单核苷酸多态性分析。
Rare Dis. 2013 Dec 12;1(1). doi: 10.4161/rdis.27445.