Can Drosophila metanogaster represent a model system for the detection of reproductive adverse drug reactions?

被引:25
作者
Avanesian, Agnesa [1 ]
Semnani, Sahar [1 ]
Jafari, Mahtab [1 ]
机构
[1] Univ Calif Irvine, Dept Pharmaceut Sci, Irvine, CA 92697 USA
关键词
VERTEBRATE-TYPE STEROIDS; SEX DETERMINATION; CELLULAR-DAMAGE; GENE; METHOTREXATE; MELANOGASTER; DISCOVERY; CHLORPYRIFOS; EXPRESSION; TISSUES;
D O I
10.1016/j.drudis.2009.05.010
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Once a molecule is identified as a potential drug, the detection of adverse drug reactions is one of the key components of its development and the FDA approval process. We propose using Drosophila melanogaster to screen for reproductive adverse drug reactions in the early stages of drug development. Compared with other non-mammalian models, D. melanogaster has many similarities to the mammalian reproductive system, including putative sex hormones and conserved proteins involved in genitourinary development. Furthermore, the D. melanogaster model would present significant advantages in time efficiency and cost-effectiveness compared with mammalian models. We present data on methotrexate (MTX) reproductive adverse events in multiple animal models, including fruit flies, as proof-of-concept for the use of the D. melanogaster model.
引用
收藏
页码:761 / 766
页数:6
相关论文
共 55 条
[1]   The effects of methotrexate on Drosophila development, female fecundity, and gene expression [J].
Affleck, JG ;
Neumann, K ;
Wong, LL ;
Walker, VK .
TOXICOLOGICAL SCIENCES, 2006, 89 (02) :495-503
[2]   A role for Drosophila in understanding drug-induced cytotoxicity and teratogenesis [J].
Affleck, Joslynn G. ;
Walker, Virginia K. .
CYTOTECHNOLOGY, 2008, 57 (01) :1-9
[3]   Transgenic rescue of methotrexate-induced teratogenicity in Drosophila melanogaster [J].
Affleck, Joslynn G. ;
Walker, Virginia K. .
TOXICOLOGICAL SCIENCES, 2007, 99 (02) :522-531
[4]   The Sf1-related nuclear hormone receptor Hr39 regulates Drosophila female reproductive tract development and function [J].
Allen, Anna K. ;
Spradling, Allan C. .
DEVELOPMENT, 2008, 135 (02) :311-321
[5]  
Baier A, 2002, J EXP BIOL, V205, P1233
[6]   Differential follicle counts as a screen for chemically induced ovarian toxicity in mice: Results from continuous breeding bioassays [J].
Bolon, B ;
Bucci, TJ ;
Warbritton, AR ;
Chen, JJ ;
Mattison, DR ;
Heindel, JJ .
FUNDAMENTAL AND APPLIED TOXICOLOGY, 1997, 39 (01) :1-10
[7]   Regulation of the human menstrual cycle [J].
Buffet, NC ;
Djakoure, C ;
Maitre, SC ;
Bouchard, P .
FRONTIERS IN NEUROENDOCRINOLOGY, 1998, 19 (03) :151-186
[8]   The regulation of sex determination and sexually dimorphic differentiation in Drosophila [J].
Burtis, Kenneth C. .
CURRENT OPINION IN CELL BIOLOGY, 1993, 5 (06) :1006-1014
[9]  
Carney GE, 2000, GENETICS, V154, P1203
[10]   Neurodevelopmental toxicity of methylmercury: Laboratory animal data and their contribution to human risk assessment [J].
Castoldi, Anna F. ;
Onishchenko, Natalia ;
Johansson, Carolina ;
Coccini, Teresa ;
Roda, Elisa ;
Vahter, Marie ;
Ceccatelli, Sandra ;
Manzo, Luigi .
REGULATORY TOXICOLOGY AND PHARMACOLOGY, 2008, 51 (02) :215-229