Critical windows of exposure for children's health: The reproductive system in animals and humans

被引:122
作者
Pryor, JL
Hughes, C
Foster, W
Hales, BF
Robaire, B
机构
[1] McGill Univ, Dept Pharmacol & Therapeut, Montreal, PQ H3G 1Y6, Canada
[2] Univ Minnesota, Sch Med, Minneapolis, MN 55455 USA
[3] Cedars Sinai Med Ctr, Ctr Womens Hlth, Los Angeles, CA 90048 USA
关键词
development; germ cell; oogenesis; reproductive system; spermatogenesis; toxicant;
D O I
10.2307/3454541
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Drugs and environmental chemicals can adversely affect the reproductive system. Currently, available data indicate that the consequences of exposure depend on the nature of the chemical, its target, and the timing of exposure relative to critical windows in development of the reproductive system. The reproductive system is designed to produce gametes in far greater excess than would seem to be necessary for the survival of species. Ten to hundreds of millions of spermatozoa are generated daily by most adult male mammals, yet Very few of these germ cells succeed in transmitting their genetic material to the next generation. Although the number of oocytes produced in mammalian females is more limited, and their production occurs only during fetal life, most ovaries contain several orders of magnitude more oocytes than ever will be fertilized. Toxicant exposures may affect critical events in the development of the reproductive system, ranging from early primordial germ cell determination to gonadal differentiation, gametogenesis, external genitalia, or signaling events regulating sexual behavior. Although there are differences between the human reproductive system and that of the usual animal models, such models have been extremely useful in assessing risks for key human reproductive and developmental processes. The objectives for future studies should include the elucidation of the specific cellular and molecular targets of known toxicants; the design of a systematic approach to the identification of reproductive toxicants; and the development of sensitive, specific, and predictive animal models, minimally invasive surrogate markers, or in vitro tests to assess reproductive system function during embryonic, postnatal, and adult life.
引用
收藏
页码:491 / 503
页数:13
相关论文
共 146 条
[71]   Abdominal B (AbdB) Hoxa genes: Regulation in adult uterus by estrogen and progesterone and repression in Mullerian duct by the synthetic estrogen diethylstilbestrol (DES) [J].
Ma, L ;
Benson, GV ;
Lim, HJ ;
Dey, SK ;
Maas, RL .
DEVELOPMENTAL BIOLOGY, 1998, 197 (02) :141-154
[72]   BLOCKADE OF NEONATAL ACTIVATION OF THE PITUITARY-TESTICULAR AXIS - EFFECT ON PERIPUBERTAL LUTEINIZING-HORMONE AND TESTOSTERONE SECRETION AND ON TESTICULAR DEVELOPMENT IN MALE MONKEYS [J].
MANN, DR ;
GOULD, KG ;
COLLINS, DC ;
WALLEN, K .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1989, 68 (03) :600-607
[73]   NEONATAL TREATMENT WITH LUTEINIZING-HORMONE-RELEASING HORMONE ANALOGS ALTERS PERIPHERAL LYMPHOCYTE SUBSETS AND CELLULAR AND HUMORALLY MEDIATED IMMUNE-RESPONSES IN JUVENILE AND ADULT MALE MONKEYS [J].
MANN, DR ;
ANSARI, AA ;
AKINBAMI, MA ;
WALLEN, K ;
GOULD, KG ;
MCCLURE, HM .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1994, 78 (02) :292-298
[74]   Sexual maturation in male rhesus monkeys: importance of neonatal testosterone exposure and social rank [J].
Mann, DR ;
Akinbami, MA ;
Gould, KG ;
Paul, K ;
Wallen, K .
JOURNAL OF ENDOCRINOLOGY, 1998, 156 (03) :493-501
[75]   BLOCKADE OF NEONATAL ACTIVATION OF THE PITUITARY-TESTICULAR AXIS WITH CONTINUOUS ADMINISTRATION OF A GONADOTROPIN-RELEASING HORMONE AGONIST IN MALE RHESUS-MONKEYS [J].
MANN, DR ;
DAVISDASILVA, M ;
WALLEN, K ;
COAN, P ;
EVANS, DE ;
COLLINS, DC .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1984, 59 (02) :207-211
[76]   NEONATAL TREATMENT OF MALE MONKEYS WITH A GONADOTROPIN-RELEASING-HORMONE AGONIST ALTERS DIFFERENTIATION OF CENTRAL-NERVOUS-SYSTEM CENTERS THAT REGULATE SEXUAL AND SKELETAL DEVELOPMENT [J].
MANN, DR ;
AKINBAMI, MA ;
GOULD, KG ;
TANNER, JM ;
WALLEN, K .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1993, 76 (05) :1319-1324
[77]   SEXUAL DIMORPHISM IN WIRING PATTERN IN THE HYPOTHALAMIC ARCUATE NUCLEUS AND ITS MODIFICATION BY NEONATAL HORMONAL ENVIRONMENT [J].
MATSUMOTO, A ;
ARAI, Y .
BRAIN RESEARCH, 1980, 190 (01) :238-242
[78]   OOCYTE DESTRUCTION BY POLYCYCLIC AROMATIC-HYDROCARBONS [J].
MATTISON, DR ;
SHIROMIZU, K ;
NIGHTINGALE, MS .
AMERICAN JOURNAL OF INDUSTRIAL MEDICINE, 1983, 4 (1-2) :191-202
[79]   MENSTRUAL SYNCHRONY AND SUPPRESSION [J].
MCCLINTOCK, MK .
NATURE, 1971, 229 (5282) :244-+