Prenatal effects on reproductive capacity during aging in female mice.

The production of live young during successive pregnancies was investigated in female CF-1 house mice (Mus musculus) identified at cesarean delivery as having developed in utero between 2 male fetuses (2M females) or not next to a male fetus (0M females). 2M female mice have previously been found to be exposed to higher concentrations of testosterone than 0M females during fetal life, presumably as a result of the transport of steroids between contiguous fetuses. 0M and 2M females were paired with stud males. The males were removed prior to delivery of a litter and replaced by other males when the litter was weaned. This process was repeated until: 1) a female did not become pregnant within 2.5 mo or 2) two successive litters were produced in which all of the pups were dead. In Experiment 1 females were first mated when 25 days old, and 2M females ceased producing litters containing live pups at a younger age and after fewer litters than did 0M females; however, many females were terminated from the study as a result of producing 2 successive litters of dead young rather than failing to become pregnant during a 2.5-mo period. There was a gradual decline in the number of live young produced by 0M females as a function of age and parity, but 2M females abruptly ceased producing any live young after producing a litter of normal size. For the last live litter, there were thus significantly fewer live young produced by 0M females than by 2M females. None of these differences were observed in Experiment 2, in which 0M and 2M females were mated for the first time beginning at 7 mo of age. The 2M females in this experiment ceased producing live young at a significantly older age than did the 2M females first mated at puberty. In contrast, there was no effect of age at initial mating on the age at which 0M females ceased producing live young. This finding suggests that exposure of 2M females to elevated titers of testosterone during fetal life results in a reduction in reproductive life span if they first become pregnant during the pubertal period.

[1]  C. Finch,et al.  Ovarian and steroidal influences on neuroendocrine aging processes in female rodents. , 1984, Endocrine reviews.

[2]  F. S. Saal,et al.  Fetal effects on sexual behavior and aggression in young and old female mice treated with estrogen and testosterone , 1984, Hormones and Behavior.

[3]  C. Finch,et al.  Estradiol-induced adult anovulatory syndrome in female C57BL/6J mice: age-like neuroendocrine, but not ovarian, impairments. , 1984, Biology of reproduction.

[4]  F. S. Saal Models of Early Hormonal Effects on Intrasex Aggression in Mice , 1983 .

[5]  F. S. Saal The Interaction of Circulating Oestrogens and Androgens in Regulating Mammalian Sexual Differentiation , 1983 .

[6]  B. Robaire,et al.  Effects of long term androgen and estradiol exposure on the hypothalamus. , 1983, Endocrinology.

[7]  C. Finch,et al.  Efficiency of mating in C57BL/6J female mice as a function of age and previous parity , 1981, Experimental Gerontology.

[8]  C. Finch,et al.  The distribution of fetal mortality in ageing C57BL/6J mice: A statistical analysis , 1981, Experimental Gerontology.

[9]  F. S. Saal Variation in phenotype due to random intrauterine positioning of male and female fetuses in rodents. , 1981 .

[10]  F. V. vom Saal,et al.  Effects of prior intrauterine position and housing on oestrous cycle length in adolescent mice. , 1981, Journal of reproduction and fertility.

[11]  C. Finch,et al.  Studies on ovarian-hypothalamic-pituitary interactions during reproductive aging in C57BL/6J mice , 1980, Peptides.

[12]  C. D. Jacobson,et al.  Ontogeny of the sexually dimorphic nucleus of the preoptic area , 1980, The Journal of comparative neurology.

[13]  F. V. vom Saal,et al.  Sexual characteristics of adult female mice are correlated with their blood testosterone levels during prenatal development. , 1980, Science.

[14]  F. V. vom Saal,et al.  Variation in length of the estrous cycle in mice due to former intrauterine proximity to male fetuses. , 1980, Biology of reproduction.

[15]  R. Gorski The neuroendocrinology of reproduction: an overview. , 1979, Biology of reproduction.

[16]  C. Finch,et al.  Prolonged gestation, elevated preparturitional plasma progesterone and reproductive aging in C57BL/6J mice. , 1978, Biology of reproduction.

[17]  F. V. vom Saal,et al.  In utero proximity of female mouse fetuses to males: effect on reproductive performance during later life. , 1978, Biology of reproduction.

[18]  B. Goldman,et al.  Testosterone-induced aggression in adult female mice , 1977, Hormones and Behavior.

[19]  D. A. Edwards Post-neonatal androgenization and adult aggressive behavior in female mice. , 1970, Physiology & behavior.

[20]  R. Rugh,et al.  The mouse; its reproduction and development , 1968 .

[21]  N. Russo,et al.  Structural changes in the fetal gonads and gonaducts during maturation of an enzyme, steroid 3-beta-ol-dehydrogenase, in the gonads, adrenal cortex and placenta of fetal rats. , 1967, Endocrinology.

[22]  K. Fox,et al.  Oestrous synchronization and pregnancy blocking in wild house mice (Mus musculus). , 1966, Journal of reproduction and fertility.

[23]  H. E. Swanson,et al.  THE "EARLY-ANDROGEN" SYNDROME; DIFFERENCES IN RESPONSE TO PRE-NATAL AND POST-NATAL ADMINISTRATION OF VARIOUS DOSES OF TESTOSTERONE PROPIONATE IN FEMALE AND MALE RATS. , 1964, Acta endocrinologica.

[24]  D. Michie,et al.  Foetal growth in the mouse , 1961, Proceedings of the Royal Society of London. Series B. Biological Sciences.

[25]  D. Michie,et al.  Control of Pre-Natal Growth in Mammals , 1960, Nature.

[26]  C. Barraclough,et al.  Infertility Induced in Mice by a Single Injection of Testosterone Propionate.∗ , 1954, Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine.

[27]  Carroll A. Pfeiffer,et al.  Sexual differences of the hypophyses and their determination by the gonads , 1936 .