|Year : 2006 | Volume
| Issue : 1 | Page : 24-27
Altered pituitary hormone secretion in male rats exposed to bisphenol A
AM Gharravi1, R Ghorbani2, M Khazaei2, Pour A Motabbad3, M Al Agha4, J Ghasemi5, P Sayadi6
1 Department of Anatomy, School of Medicine, Gorgan University of Medical Sciences, Department of Anatomy, School of Medicine, Kerman Shah University of Medical Science, Kerman Shah, Iran
2 Department of Anatomy, School of Medicine, Kerman Shah University of Medical Science, Kerman Shah, Iran
3 Department of Physiology, School of Medicine, Kerman Shah University of Medical Science, Kerman Shah, Iran
4 Department of Pathology, School of Medicine, Kerman Shah University of Medical Science, Kerman Shah, Iran
5 Department of Chemistry, School of Sciences, Razi University, Kerman Shah, Iran
6 Department of Biophysics, School of Medicine, Kerman Shah University of Medical Science, Kerman Shah, Iran
A M Gharravi
Department of Anatomy, Gorgan University of Medical Sciences, Gorgan
Source of Support: None, Conflict of Interest: None
Bisphenol A (BPA) is a xenobiotic estrogenic compound. This compound has been suspected to have estrogenic effects on reproductive system of males and females. In this present study we investigated possible low-dose effects of BPA on Luteinizing Hormone in rats. Male Wistar rats (12-13 weeks old) were administrated a daily intra peritoneal 10 µg/kgbw/day, 50 µg/kgbw/day, 100 µg/kgbw/day dose of BPA for 6, 6, and 12 days, and one day after last injection, serum level of Luteinizing Hormone was examined by ELISA method. All data were expressed as means ± SE. Two-way ANOVA was performed. Analysis of data showed that in all dose groups, plasma level of Luteinizing Hormone significantly decreased compared to control group. The present study showed that BPA at low doses affects Luteinizing Hormone, one of main hormones in spermatogenesis in the adult Wistar rats, and subsequently alters the steroidgenesis in testicular Leydig cells.
Keywords: Bisphenol A, luteinizing hormone, spermatogenesis
|How to cite this article:|
Gharravi A M, Ghorbani R, Khazaei M, Motabbad PA, Al Agha M, Ghasemi J, Sayadi P. Altered pituitary hormone secretion in male rats exposed to bisphenol A. Indian J Occup Environ Med 2006;10:24-7
|How to cite this URL:|
Gharravi A M, Ghorbani R, Khazaei M, Motabbad PA, Al Agha M, Ghasemi J, Sayadi P. Altered pituitary hormone secretion in male rats exposed to bisphenol A. Indian J Occup Environ Med [serial online] 2006 [cited 2021 Jul 26];10:24-7. Available from: https://www.ijoem.com/text.asp?2006/10/1/24/22891
| Introduction|| |
The substance 2, 2- bis (4-hydroxyphenyl) propane, more commonly known as bisphenol A (BPA), is used as a monomer in the manufacture of polycarbonates and epoxy resins, as an antioxidant in PVC plastics and as an inhibitor of end polymerisation in PVC. Polycarbonates are used in food-contact materials such as returnable beverage bottles, infant-feeding bottles, tableware (plates and mugs) and storage containers. Epoxy resins are used in protective linings for food and beverage cans and vats.
Much of the current focus in the endocrine disruption field surrounds the estrogenic action of various manmade chemicals. The ability of a chemical to bind to the estrogen receptor, either in vivo or in vitro , has been used as a definition of estrogenicity. Of concern is whether exposure to chemicals with steroid-like activity can disrupt normal endocrine function, leading to altered reproductive capacity, infertility, endometriosis, and cancers of the breast, uterus, and prostate. ,,
The xenoestrogens are a structurally diverse group of naturally occurring and manmade chemicals thtat mimic the actions of the female sex hormone estradiol. In the last decade, an increasing effort has been made to investigate the interactions between these chemicals (including various phenolic compounds, phthalate esters, phytoestrogens and certain pesticides) and the endocrine system of humans as well as several wild life species. A causative link between the exposure to environmental xenoestrogens and deterioration in male reproductive health and function has been proposed. Furthermore, an increased human exposure to these compounds and an apparent increase in prevalence of a range of hormone-dependent human cancers of the reproductive tissue (breast, prostate, endometrium, testis and ovary) has been observed., One of the first chemicals discovered to mimic estrogen was the bicyclic aromatic compound bisphenol A (BPA). In 1936 BPA was found to stimulate growth of the rodent uterus, an indication of estrogenic action that has recently been confirmed by several in vitro and in vivo assays., Presently, BPA is widely used in the production of polycarbonate, epoxy resins (i.e., dental sealants and lacquer coatings of food cans), flame retarders and other products.
Male factor contributes to 40% of infertility cases worldwide.
Androgen biosynthesis by Leydig cell is under the control of the gonadotropin. LH, FSH release from the pituitary is regulated by hypothalamic GnRH, which signals through its receptors in pituitary gonadtropes. Effect of BPA on hypothalamus-pituitary-gonadal axis has not been clearly determined. Therefore, an objective of the present study was to determine whether exposure to environmentally relevant BPA levels affect pituitary LH secretion; we saw that BPA has inhibitory effect on pituitary LH secretion at low-dose exposure levels.
| Materials and Methods|| |
In order to establish a dose-response relationship of the in vivo estrogenicity of BPA, albino rats were exposed to several concentrations of the compound. The goal of this study was to observe changes in hormone levels of LH following exposure to BPA.
Animals, 40 Wistar-derived strain adult male rats (12-13 weeks old and 200-250 g weight) were purchased from Razi Institute, Iran, and were housed in standard stainless-steel cages in animal lab of Kerman shah Medical College of Kerman shah University of Medical Science and exposed to a 12:12 h light:dark photoperiod at ~20°C and ~40% humidity and had free access to laboratory chow and tap water supplied from glass bottles. All rats were handled in accordance with the principles and procedures outlined in the Guide for the Care and Use of Laboratory Animals issued by the U.S. National Academy of Sciences.
Animals were placed into eight experimental groups (5 rats in every group): vehicle-treated (control), 10 µg/kg body weight/day of BPA (10-BPA), and 50 µg/kg body weight/day of BPA (50-BPA), 10 µg/kg body weight/day of BPA (100-BPA) for 6 and 12 days [Table - 1]. Before and after study all rats were weighed.
BPA or its vehicle was administered continuously intraperitoneal [IP]. Dose levels for BPA 10 µg/kg/day, 50 µg/kg/day or 100 µg/kg/day were injected in 00:09 in morning by insulin syringe
Appropriate amount of BPA was dissolved in 1 ml ethanol and then diluted with distilled water. The final concentration of ethanol was 0.0001% in distilled water. Control rats received distilled water containing 0.0001% ethanol.
After one day, last-injection animals were anesthetized deeply by chloroform. About 2-3 ml of blood sample from ventricles of heart were collected in lab tubes and prepared for examination. After centrifuge serum detached and storage until hormone assay. Serum LH was quantified by ELISA method in Razi lab, Kerman shah, Iran. The assay was performed using the following materials supplied by Monobind and IBL Company. Assay was performed according to order of LH kits of Monobind and IBL Company. In summary, these steps were performed: washing buffer, specimen collection, assay procedure (incubation, enzyme conjugation, incubation, washing, substrate solution and reading at 450 nm within 30 min). ELISA reader for this study was stat fax 2100.
All data were collected and were expressed as means±SE. Data for each attribute were subjected to two-way analysis of variance . For determining of difference between groups, post-hoc (tukey test) was performed by spss statistical software (version 11.5). P <0.05 was significant. [Table - 1]
| Results|| |
Effects of various treatments on serum LH concentrations one day after dosing on adult rats are shown in [Table - 2], [Figure - 1]. Serum level of LH in treatment groups was recorded and assessed. Statistically, difference in LH concentration was observed between the control and BPA groups. Analysis of data showed no difference between 6 and 12 days groups, but there was a difference between dosage groups. Interaction of days and dosage showed no difference. Analysis of data by post-hoc (tukey test) showed that the BPA-exposed groups had a significantly decreased mean concentration of serum LH when compared to the injected controls ( P <0.005). [Table - 2], [Figure - 1]
| Discussion|| |
The present study shows that a very low dose of BPA affects serum level of LH in adult rats. Exposure to substances that can mimic or disrupt the normal functioning of reproductive hormones has been linked to effects such as a reduction in fertility. Furthermore, numerous morphological effects have been noted in the offspring of rats exposed to sex-hormone-disrupting substances, including deformities of the reproductive tract, such as undescended testicles and hypospadias, alterations in bone mass, as well as the other effects, which are not so immediately apparent, such as reduced sperm counts in males. Estrogen and androgen generally act by binding at receptor sites, and synthetic chemicals may disrupt this action in a number of ways. For example, a chemical may mimic the action of the natural ligand by being able to act on this receptor site, or it may interfere with the receptor in some other way, and be able to block the action of the hormone. Some chemicals can also perturb the normal functioning of the sex hormones by inhibiting the enzymes responsible for steroid hormone biosynthesis and/or inducing enzymes responsible for steroid metabolism.
Tohei showed that BPA increased LH concentration. He used high doses of BPA. It has been showed that BPA decreased LH concentrations. The present study was consistent with the observation of Chahoud, Liaw and Akingbemi. Chahoud showed that BPA in low doses affect LH concentration but this effect was not in high doses of BPA. Also, Liaw showed administration of BPA in utero decreased LH concentration. In another study, Akingbemi revealed that decreasing LH concentration after BPA exposition is a result of decreasing induction effect of LH synthesis in pituitary gland.
The present study demonstrated that exposure of rats to environmentally relevant BPA levels has adverse effects on pituitary LH secretion. Exposure of adult rats [12-13 weeks old] to 10 µg/kgbw/day, 50 µg/kgbw /day or 100 µg/kgbw /day for 6 and 12 days, intra peritoneal, decreased serum level of LH. Decreasing serum level of LH was thought to be due to disruption of normal synthesis of LH in pituitary gland. These results support the hypothesis that exposure of adult rats to environmental doses of BPA induces alterations in the male reproductive axis, hormone secretion at different levels.
| Acknowledgments|| |
We are extremely grateful to a number of Razi pathology lab at Kerman shah, particularly Rezvani, who developed the hormone assays we have used. We also thank Salimeh Gharravi, M. Zhaleh, M. Yadegari, G. H. Rajabi, and histology and pathology department of medical college, Kerman shah for their help. We are also grateful to the Kerman shah University of Medical Science, Iran.
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[Figure - 1]
[Table - 1], [Table - 2]