Teniposide (VM-26) treatment enhances the radiation-induced micronuclei in the bone marrow of mouse

被引:8
|
作者
Jagetia, GC [1 ]
Aruna, R [1 ]
机构
[1] Kasturba Med Coll & Hosp, Dept Radiobiol, Manipal 576119, India
关键词
irradiation; teniposide; micronucleus; polychromatic erythrocyte normochromatic erythrocyte ratio; mouse; bone marrow;
D O I
10.1016/S0027-5107(99)00003-2
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 effect of Teniposide (VM-26) pretreatment was studied on the micronuclei induction in the bone marrow of mice exposed to 0, 0.5, 1, 2 and 3 Gy of gamma radiation at 12, 24 and 36 h post-irradiation. Administration of 0.05 mg/kg body weight of VM-26 to mice before irradiation resulted in the significant enhancement of micronucleated polychromatic erythrocytes (MPCE) at 12, 24 and 36 h post-it-radiation. Highest elevation in the frequency of MPCE was observed in VM-26 + irradiation group after exposure to 0.5 Gy when compared to concurrent DDW + irradiation group. This increase was two fold higher in VM-26 + irradiation group at 12 and 24 h, while it was 3 fold higher at 36 h post-irradiation compared to DDW + irradiation group. The peak frequency of MPCE was observed at 24 h post-irradiation in both groups, which declined thereafter. The frequency of micronucleated normochromatic erythrocytes (MNCE) increased in a dose dependent manner in both DDW + irradiation and VW-26 + irradiation groups. However, the frequency of MNCE was significantly higher in the latter when compared to the former group. The frequency of MNCE exhibited a continuous elevation up to 36 h post-irradiation in both DDW + irradiation and VM-26 + irradiation groups. Treatment of mice with teniposide before irradiation resulted in a significant decline in the PCE/NCE ratio compared to DDW + irradiation group. The PCE/NCE ratio continued to decline up to 36 h post-irradiation in both the groups. The dose response for MPCE and PCE/NCE ratio was linear quadratic, while it was linear for MNCE. (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:87 / 98
页数:12
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