Protection against radiation-induced chromosome damage in mouse bone marrow by Ocimum sanctum

被引:66
作者
Ganasoundari, A
Devi, PU
Rao, MNA
机构
[1] KASTURBA MED COLL & HOSP,DR TMA PAI RES CTR,MANIPAL 576119,INDIA
[2] COLL PHARM,MANIPAL 576119,INDIA
关键词
chromosome damage; radiation; bone marrow; Ocimum sanctum;
D O I
10.1016/S0027-5107(96)00208-4
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The radioprotective effect of the leaf extract of Ocimum sanctum (Ocimum extract, OE) was investigated by taking chromosome aberrations as the end point. Adult Swiss mice were whole-body exposed to 1-6 Gy of gamma radiation with/without pretreatment with 10 mg/kg b.wt. of OE intraperitoneally for 5 consecutive days. Radiation was given 30 min after the last injection. Metaphase plates were prepared from femur marrow on days 1, 2, 7 and 14 post-treatment and the frequency of aberrant cells and individual aberrations were scored. OE alone did not have any significant effect on the chromosomes. Maximum percent of aberrant cells was observed at 24 h in all the exposed groups. The percent aberrant cells showed a linear quadratic increase with radiation dose, in both radiation alone (RT) and OE + RT-treated groups. Exchange (dicentrics and rings) and multiple (pulverized and severely damaged cells) aberrations also showed a similar response. However, the slopes of OE + RT was significantly shallower than RT groups (p < 0.05). A dose-modifying factor of 2.63 was obtained taking percent aberrant cells for 2 Gy as the base. Progressive decline in the percent aberrant cells as well as the number of aberrations with time after irradiation was observed in both RT and OE + RT groups. OE treatment resulted in a faster recovery compared to RT alone group. At doses below 3 Gy, OE pretreatment almost completely eliminated the exchange aberrations from the cell population by day 2. Studies on a chemical system demonstrated that OE significantly reduced the generation of hydroxyl radical; a lower dose of OE (1 mg/ml) was more effective than 5 mg/ml and this effect was more pronounced than that produced by DMSO. These results show that OE affords in vivo protection against radiation-induced cytogenetic damage. Free radical scavenging is a likely mechanism of OE protection.
引用
收藏
页码:271 / 276
页数:6
相关论文
共 16 条
[1]  
[Anonymous], INT J PHARM
[2]  
BHARGAVA KP, 1981, INDIAN J MED RES, V73, P443
[3]   MODIFICATION OF RADIATION-INDUCED CHROMOSOME-DAMAGE AND MICRONUCLEUS INDUCTION IN MOUSE BONE-MARROW BY MISONIDAZOLE AND HYPERTHERMIA [J].
BISHT, KS ;
DEVI, PU .
ACTA ONCOLOGICA, 1995, 34 (07) :913-918
[4]  
BRAUGHLER JM, 1986, J BIOL CHEM, V261, P282
[5]  
Chattopadhyay R. R., 1992, Indian Journal of Pharmacology, V24, P163
[6]   RADIOPROTECTIVE EFFECT OF COMBINATIONS OF WR-2721 AND MERCAPTOPROPIONYLGLYCINE ON MOUSE BONE-MARROW CHROMOSOMES [J].
DEVI, PU ;
PRASANNA, PGS .
RADIATION RESEARCH, 1990, 124 (02) :165-170
[7]  
DEVI PU, 1995, J EXP BIOL, V33, P205
[8]  
GANASOUNDARI A, 1996, UNPUB BR J RADIOL
[9]   OCIMUM-SANCTUM - AN EXPERIMENTAL-STUDY EVALUATING ITS ANTIINFLAMMATORY, ANALGESIC AND ANTIPYRETIC ACTIVITY IN ANIMALS [J].
GODHWANI, S ;
GODHWANI, JL ;
VYAS, DS .
JOURNAL OF ETHNOPHARMACOLOGY, 1987, 21 (02) :153-163
[10]   HOW TO CHARACTERIZE A BIOLOGICAL ANTIOXIDANT [J].
HALLIWELL, B .
FREE RADICAL RESEARCH COMMUNICATIONS, 1990, 9 (01) :1-32