Literature DB >> 2181211

Reproductive toxicity: male and female reproductive systems as targets for chemical injury.

D R Mattison1, D R Plowchalk, M J Meadows, A Z al-Juburi, J Gandy, A Malek.   

Abstract

On the basis of current knowledge of reproductive biology and toxicology, it is apparent that chemicals affecting reproduction may elicit their effects at a number of sites in both the male and the female reproductive system. This multiplicity of targets is attributable to the dynamic nature of the reproductive system, in which the hypothalamic-pituitary-gonadal axis is controlled by precise positive and negative feedback mechanisms among its components. Interference by a xenobiotic at any level in either the male or the female reproductive system may ultimately impair hypothalamic or pituitary function. Normal gonadal processes such as spermatogenesis or oogenesis, ejaculation or ovulation, hormone production by Leydig or granulosa cells, and the structure or function of the accessory reproductive structures (e.g., epididymis, fallopian tube) also appear vulnerable to xenobiotics. The reproductive system is a complex one that requires local and circulating hormones for control. This brief review illustrates a system for characterizing the mechanism of action of reproductive toxicants, as well as for defining the sites available for disruption of reproduction. Unfortunately, at present, data addressing the actual vulnerability of reproduction are sorely lacking. However, when experiments have been conducted and combined with epidemiologic data or clinical observation, it has been possible to demonstrate impairment of reproductive processes by xenobiotics. The role of environmental exposure to xenobiotics in the increase in infertility that has been observed remains to be defined.

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Year:  1990        PMID: 2181211     DOI: 10.1016/s0025-7125(16)30569-7

Source DB:  PubMed          Journal:  Med Clin North Am        ISSN: 0025-7125            Impact factor:   5.456


  5 in total

Review 1.  Environmental endocrine disruption: an effects assessment and analysis.

Authors:  T M Crisp; E D Clegg; R L Cooper; W P Wood; D G Anderson; K P Baetcke; J L Hoffmann; M S Morrow; D J Rodier; J E Schaeffer; L W Touart; M G Zeeman; Y M Patel
Journal:  Environ Health Perspect       Date:  1998-02       Impact factor: 9.031

Review 2.  Effects of nanotoxicity on female reproductivity and fetal development in animal models.

Authors:  Jianling Sun; Qiu Zhang; Zhiping Wang; Bing Yan
Journal:  Int J Mol Sci       Date:  2013-04-29       Impact factor: 5.923

3.  Benzo[a]pyrene reduces testosterone production in rat Leydig cells via a direct disturbance of testicular steroidogenic machinery.

Authors:  Jin-Yong Chung; Yoon-Jae Kim; Ji Young Kim; Seung Gee Lee; Ji-Eun Park; Won Rok Kim; Yong-Dal Yoon; Ki Soo Yoo; Young Hyun Yoo; Jong-Min Kim
Journal:  Environ Health Perspect       Date:  2011-07-07       Impact factor: 9.031

Review 4.  Toxicity of Nanoparticles on the Reproductive System in Animal Models: A Review.

Authors:  Rahim Dad Brohi; Li Wang; Hira Sajjad Talpur; Di Wu; Farhan Anwar Khan; Dinesh Bhattarai; Zia-Ur Rehman; F Farmanullah; Li-Jun Huo
Journal:  Front Pharmacol       Date:  2017-09-05       Impact factor: 5.810

5.  Worldwide trend analysis of primary and secondary infertility rates over past decades: A cross-sectional study.

Authors:  Nasrin Borumandnia; Hamid Alavi Majd; Naghmeh Khadembashi; Hojat Alaii
Journal:  Int J Reprod Biomed       Date:  2022-02-18
  5 in total

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