Baicalin promoted the repair of DNA single strand breakage caused by H2O2 in cultured NIH3T3 fibroblasts

被引:20
作者
Chen, X [1 ]
Nishida, H [1 ]
Konishi, T [1 ]
机构
[1] Niigata Univ Pharm & Appl Life Sci, Dept Radiochem Biophys & Funct Food Sci, Niigata 9502081, Japan
关键词
DNA damage repair; NIH3T3; fibroblast; baicalin; comet assay; DNA SSB (single strand break);
D O I
10.1248/bpb.26.282
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The protective effect of Baicalin, a flavonoid isolated from the root of Scutellaria baicalensis G., on H2O2-induced DNA single strand break (SSB) was examined in NIH3T3 mouse fibroblasts by Comet assay (single cell gel electrophoresis technique). When the cells were pulse-chased with H2O2 (0.1-0.5 mm) for 15 min in fetal bovine serum (FBS)-free Dulbecco's Modified Eagle's Medium (DMEM), SSB occurred in the DNA as reported elsewhere in dose-dependent manner. Baicalin (50, 100,mum) which was incubated with the cells for 24 h before the H2O2 chase did not give rise to significant protection against the SSB formation. However, when the time required to cause a change in the DNA damage histogram obtained by the Comet assay was precisely examined after the H2O2 chase, it was found that the H2O2 induced SSB was more promptly repaired in the cells pretreated with Baicalin prior to the H2O2 chase, compared to untreated control cells. At the same time, the cell viability examined by 3-(4,5-dimethylthiazol-2-yl) 2,5-diphenyltetrazolium bromide (MTT) assay after the H2O2 abuse was moderately recovered in the Baicalin increased by the Baicalin treatment. It was thus concluded that Baicalin that was known as an antioxidant flavonoid in vitro also functions as a biological response modifier, improving the cellular repair potential of oxidatively damaged DNA.
引用
收藏
页码:282 / 284
页数:3
相关论文
共 23 条
  • [1] BIOENERGETIC AND OXIDATIVE STRESS IN NEURODEGENERATIVE DISEASES
    BOWLING, AC
    BEAL, MF
    [J]. LIFE SCIENCES, 1995, 56 (14) : 1151 - 1171
  • [2] DEMPLE B, 1994, ANNU REV BIOCHEM, V63, P915, DOI 10.1146/annurev.biochem.63.1.915
  • [3] OXIDATIVE DAMAGE TO DNA IN MAMMALIAN CHROMATIN
    DIZDAROGLU, M
    [J]. MUTATION RESEARCH, 1992, 275 (3-6): : 331 - 342
  • [4] Review of the biology of quercetin and related bioflavonoids
    Formica, JV
    Regelson, W
    [J]. FOOD AND CHEMICAL TOXICOLOGY, 1995, 33 (12) : 1061 - 1080
  • [5] Regulation of antioxidant enzyme gene expression in response to oxidative stress and during differentiation of mouse skeletal muscle
    Franco, AA
    Odom, RS
    Rando, TA
    [J]. FREE RADICAL BIOLOGY AND MEDICINE, 1999, 27 (9-10) : 1122 - 1132
  • [6] Free radical scavenging and antioxidant activities of flavonoids extracted from the radix of Scutellaria baicalensis Georgi
    Gao, ZH
    Huang, KX
    Yang, XL
    Xu, HB
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS, 1999, 1472 (03): : 643 - 650
  • [7] HALLIWELL B, 1990, METHOD ENZYMOL, V186, P1
  • [8] ANTIOXIDANT RESPONSE ELEMENT
    JAISWAL, AK
    [J]. BIOCHEMICAL PHARMACOLOGY, 1994, 48 (03) : 439 - 444
  • [9] Repair of products of oxidative DNA base damage in human cells
    Jaruga, P
    Dizdaroglu, M
    [J]. NUCLEIC ACIDS RESEARCH, 1996, 24 (08) : 1389 - 1394
  • [10] The nitric oxide-producing activities of Scutellaria baicalensis
    Kim, HM
    Moon, EJ
    Li, E
    Kim, KM
    Nam, SY
    Chung, CK
    [J]. TOXICOLOGY, 1999, 135 (2-3) : 109 - 115