Ovotoxicity in female Fischer rats and B6 mice induced by low-dose exposure to three polycyclic aromatic hydrocarbons: Comparison through calculation of an ovotoxic index

被引:130
作者
Borman, SM [1 ]
Christian, PJ
Sipes, IG
Hoyer, PB
机构
[1] Univ Arizona, Dept Physiol, Tucson, AZ 85724 USA
[2] Univ Arizona, Dept Pharmacol Toxicol, Tucson, AZ 85724 USA
[3] Univ Arizona, SW Environm Hlth Sci Ctr, Tucson, AZ 85724 USA
关键词
ovotoxicity; PAHs; low-dose repeated exposures;
D O I
10.1006/taap.2000.9006
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Extensive destruction of primordial follicles by exposure to ovarian toxicants can cause early menopause in women. Primordial follicle destruction is known to result from dosing of mice and rats with three polycyclic aromatic hydrocarbons (PAHs), contaminants commonly found in cigarette smoke. Therefore, the purpose of this study was to compare relative ovotoxicity in mice and rats using the PAHs, 9,10-dimethylbenzanthracene (DMBA), 3-methylcholanthrene (3-MC), and benzo[a]pyrene (BaP). Female B6C3F(1) mice and Fischer 344 rats (age 28 days) were dosed daily tip) with vehicle control or a range of doses of the PAHs. Two groups were dosed with the occupational chemicals 4-vinylcyclohexene (VCH; 500 mg/kg ip) or its diepoxide metabolite (VCD; 80 mg/kg ip), other known ovotoxicants. After 15 days, ovaries were collected, histologically prepared, and follicles were microscopically classified (primordial, primary, or secondary) and counted. The dose of each chemical that produced 50% loss of primordial follicles (p < 0.05) was determined (ED50) and used to calculate an ovotoxic index (OI) in mice and rats (ED50 x 15 days). Thus, a chemical with a lower OI is more toxic. Primordial follicles in mice displayed a lower OI than rats to all chemicals tested (mouse: DMBA, 0.0012; 3-MC, 0.003; BaP, 0.18; VCD, 6.8; VCH, 69; rat: DMBA, 0.45; 3-MC, >3.4; BaP, >3.6; VCD, 8.6; VCH, >69). In mice, DMBA targeted primordial follicles at a 10-fold lower concentration than primary and secondary follicles, whereas 3-MC exposure targeted primordial and primary follicles to a similar degree. BaP exposure targeted primordial and primary follicles at a 100-fold higher concentration than DMBA or 3-MC. Although BaP and 3-MC did not target secondary follicles in mice, secondary follicles in rats were most susceptible to 3-MC. Furthermore, all three PAHs were more ovotoxic (lower OI) with repeated low-dose exposure compared with OIs calculated from other studies using single high-dose exposures. The earliest day of impending primordial follicle loss (increase in percentage of unhealthy follicles, p < 0.05) in mice was factored into the OI (ED50 x first day of damage, p < 0.05 x % healthy follicles remaining, relative to control). The revised OI became DMBA d15, 0.0006; 3-MC d12, 0.0008; BaP d15, 0.132; and VCD d8, 2.96. These results predict that DMBA is the most potent ovarian toxicant (lower OI) in both species but VCD damages primordial follicles after shorter exposures. Calculation of the OI in mice and rats represents a method for comparing the relative potential risk of a variety of chemicals that produce ovarian damage at low levels following repeated exposures. The results also demonstrate that low-dose repeated exposures are substantially more toxic to the ovary than a single high-dose exposure. This finding is particularly important in view of the implications for chronic low-dose exposures of women to environmental chemicals. a tow Academic Press.
引用
收藏
页码:191 / 198
页数:8
相关论文
共 26 条
[1]   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
[2]   A single dose of the ovotoxicant 4-vinylcyclohexene diepoxide is protective in rat primary ovarian follicles [J].
Borman, SM ;
VanDePol, BJ ;
Kao, S ;
Thompson, KE ;
Sipes, IG ;
Hoyer, PB .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1999, 158 (03) :244-252
[3]   Human T cells are highly sensitive to suppression of mitogenesis by polycyclic aromatic hydrocarbons and this effect is differentially reversed by alpha-naphthoflavone [J].
Davila, DR ;
Romero, DL ;
Burchiel, SW .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1996, 139 (02) :333-341
[4]   DESTRUCTION OF PREANTRAL FOLLICLES IN ADULT-RATS BY 4-VINYL-1-CYCLOHEXENE DIEPOXIDE [J].
FLAWS, JA ;
DOERR, JK ;
SIPES, IG ;
HOYER, PB .
REPRODUCTIVE TOXICOLOGY, 1994, 8 (06) :509-514
[5]   REDUCED ABILITY OF RAT PREANTRAL OVARIAN FOLLICLES TO METABOLIZE 4-VINYL-1-CYCLOHEXENE DIEPOXIDE IN-VITRO [J].
FLAWS, JA ;
SALYERS, KL ;
SIPES, IG ;
HOYER, PB .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1994, 126 (02) :286-294
[6]   HEPATIC SINUSOIDAL CELL DESTRUCTION IN THE DEVELOPMENT OF INTRAVASCULAR COAGULATION IN ACUTE LIVER-FAILURE OF RATS [J].
HIRATA, K ;
OGATA, I ;
OHTA, Y ;
FUJIWARA, K .
JOURNAL OF PATHOLOGY, 1989, 158 (02) :157-165
[7]  
HIRSHFIELD AN, 1991, INT REV CYTOL, V124, P43
[8]   Assessment of follicle destruction in chemical-induced ovarian toxicity [J].
Hoyer, PB ;
Sipes, IG .
ANNUAL REVIEW OF PHARMACOLOGY AND TOXICOLOGY, 1996, 36 :307-331
[9]   Early effects of ovotoxicity induced by 4-vinylcyclohexene diepoxide in rats and mice [J].
Kao, SW ;
Sipes, IG ;
Hoyer, PB .
REPRODUCTIVE TOXICOLOGY, 1999, 13 (01) :67-75
[10]   DIFFERENCE IN SENSITIVITY OF RAT AND MOUSE PRIMORDIAL OOCYTES TO DESTRUCTION BY POLYCYCLIC AROMATIC-HYDROCARBONS [J].
MATTISON, DR .
CHEMICO-BIOLOGICAL INTERACTIONS, 1979, 28 (01) :133-137