scholarly journals Effects of Chronic Exposure to an Environmentally Relevant Mixture of Brominated Flame Retardants on the Reproductive and Thyroid System in Adult Male Rats

2012 ◽  
Vol 127 (2) ◽  
pp. 496-507 ◽  
Author(s):  
Sheila R. Ernest ◽  
Michael G. Wade ◽  
Claudia Lalancette ◽  
Yi-Qian Ma ◽  
Robert G. Berger ◽  
...  
2019 ◽  
Vol 212 ◽  
pp. 112694
Author(s):  
Faezeh Shafiei ◽  
Mohammad Reza Afarinesh ◽  
Fatemeh Golshan ◽  
Tahereh Haghpanah ◽  
Mansoureh Sabzalizadeh ◽  
...  

2007 ◽  
Vol 45 (5) ◽  
pp. 859-862 ◽  
Author(s):  
Alexandre Marafon Favero ◽  
Simone Nardin Weis ◽  
Eluza Curte Stangherlin ◽  
Joao Batista Teixeira Rocha ◽  
Cristina Wayne Nogueira

2015 ◽  
Vol 29 (S1) ◽  
Author(s):  
G Gonzalez ◽  
M Valdez ◽  
R Gutierrez ◽  
J Valdez ◽  
T McLaughlin ◽  
...  

2014 ◽  
Vol 221 (1) ◽  
pp. 167-179 ◽  
Author(s):  
Shibin Ding ◽  
Ying Fan ◽  
Nana Zhao ◽  
Huiqin Yang ◽  
Xiaolei Ye ◽  
...  

Epidemiological findings on the association between bisphenol A (BPA, 2,2-bis-(4-hydroxyphenyl)propane) exposure and type 2 diabetes mellitus (T2DM) are paradoxical. In animal studies, BPA has been shown to disrupt pancreatic function and blood glucose homeostasis even at a reference ‘safe’ level during perinatal period. In this study, we explored the effects of long-term paternal exposure to a ‘safe’ level of BPA on parents themselves and their offspring. Adult male genitor rats fed with either standard chow diet (STD) or high-fat diet (HFD) were treated respectively with either vehicle or BPA (50 μg/kg per day) for 35 weeks. The male rats treated with vehicle or BPA for 21 weeks were then used as sires, and the adult female rats were fed with STD during the gestation and lactation. Offspring rats were weaned on postnatal day 21 and fed with STD in later life. Metabolic parameters were recorded on the adult male rats and their adult offspring. BPA exposure disrupted glucose homeostasis and pancreatic function, and HFD aggravated these adverse effects. However, BPA exposure did not alter body weight, body fat percentage, or serum lipid. In addition, the paternal BPA exposure did not cause adverse reproductive consequence or metabolic disorder in the adult offspring. Our findings indicate that chronic exposure to a predicted ‘safe’ dose of BPA contributes to glucose metabolic disorders, and that HFD aggravates these adverse effects in paternal rats.


2017 ◽  
Vol 108 ◽  
pp. 93-103 ◽  
Author(s):  
Blanka Tariba Lovaković ◽  
Alica Pizent ◽  
Vilena Kašuba ◽  
Nevenka Kopjar ◽  
Vedran Micek ◽  
...  

2020 ◽  
Vol 54 (1) ◽  
pp. 14-21 ◽  
Author(s):  
Samuel Gbadebo Olukole ◽  
Eunice Olufunke Ola-Davies ◽  
Damilare Olaniyi Lanipekun ◽  
Bankole Olusiji Oke

AbstractObjectives. Bisphenol A (BPA) has been reported that among other male reproductive dys-functions, it can cause marked estrogenic effects including alteration in serum hormones as well as testicular lesions in exposed animals. This work sought to study the role of gallic acid (GA), a known antioxidant, on the BPA-induced testicular oxidative stress in adult male Wistar rats using serum hormone analysis, histopathology, and biochemical assays.Methods. Adult male rats were divided into four groups (n=10) including control (0.2 ml of corn oil), GA (20 mg/kg/day), BPA (10 mg/kg/day), BPA+GA (BPA, 10 mg/kg/day + GA, 20 mg/kg/day). All medications were given by oral gavage for 45 consecutive days. The body and testicular weights were measured. Blood and organ samples were collected for the serum hormonal assay: testosterone (T), luteinizing hormone (LH), follicle stimulating hormone (FSH) and prolactin (PRL), and tissue biochemistry analysis: superoxide dismutase (SOD), reduced glutathione (GSH), glutathione-S-transferase (GST), malondialdehyde (MDA), hydrogen peroxide (H2O2), respectively.Results. The BPA-treated rats showed significant reduction in the gonadosomatic index. BPA also caused significant decrease in the levels of the serum testosterone and prolactin. Furthermore, BPA induced testicular oxidative stress by decreasing the activities of antioxidant enzymes and increasing reactive oxygen species. However, co-treatment with GA protected against these alterations.Conclusion. Findings from the present study confirmed the previously reported data and show that the ability of GA, as a potent antioxidant, may protect against BPA-induced alterations in the male reproductive function. Hence, GA protects against testicular oxidative stress in adult male Wistar rats following chronic exposure to BPA.


2016 ◽  
Vol 33 (02) ◽  
pp. 103-107
Author(s):  
SH. Ahmadpour ◽  
K. Foghi ◽  
A. Behrad

Abstract Introduction: Studies have shown that even acute single dose of ketamine is associated with neurodegeneration in hippocampus. The aim of this study was to examine the effects of chronic exposure to ketamine on hippocampus proper in young adult male rats. Materials and Method: Twenty young adult male wistar rats weighing 120-150 g were randomly divided into two groups. Experimental group received ketamine intraperitoneally at the dose of 10mg/kg for one week. The control animals only received saline. At the end ofweek animals were anesthetized and the hippocampus and adrenal were harvested for further study. Results: Cytological examination of cresyl violet stained sections of ketamine group showed dark neurons in CA4 region. The number of dark neurons in CA4 (15±3) showed meaningful difference with control (P<0.001). The weight ofwet brain in ketamine group (1.34±0.04 gr) showed significant level of difference in comparison with those of control (1.6±.2gr) (P<0.05). The presence of oligodendrocytes aggregation around degenerating and healthy looking neurons was only recognized in ketamine group. Also in ketamine exposed animals, hypertrophic astrocytes especially in white matter hilar region, were observed. Conclusion: According to our findings it could be concluded repeated or chronic ketamine use is associated neurodegeneration in CA4region of hippocampus and sever glial reaction.


2016 ◽  
Vol 30 (S1) ◽  
Author(s):  
Matt Valdez ◽  
Gwen Gonzalez ◽  
Roberto Gutierrez ◽  
Joseph Valdez ◽  
John Lindner ◽  
...  

Author(s):  
Samira Ezi ◽  
Mahdi Eskandarian Boroujeni ◽  
Aysan Khatmi ◽  
Kimia Vakili ◽  
Mobina Fathi ◽  
...  

2020 ◽  
Author(s):  
Vivian Biancardi ◽  
Jashan Saini ◽  
Anileen Pageni ◽  
M. Hema Prashaad ◽  
Gregory D. Funk ◽  
...  

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