Perinatal exposure to 2,2′,4′4′ −Tetrabromodiphenyl ether induces testicular toxicity in adult rats

Toxicology ◽  
2017 ◽  
Vol 389 ◽  
pp. 21-30 ◽  
Author(s):  
Ahmed Khalil ◽  
Mikhail Parker ◽  
Sarah E. Brown ◽  
Sebnem E. Cevik ◽  
Lian W. Guo ◽  
...  
Author(s):  
Yasmina M. Abd-Elhakim ◽  
Nabela I. El Sharkawy ◽  
Khlood M. El Bohy ◽  
Mona A. Hassan ◽  
Heba S. A. Gharib ◽  
...  

1990 ◽  
Vol 47 (3) ◽  
pp. 507-512 ◽  
Author(s):  
Robert J. Contreras ◽  
Kelly W. Ryan

Epigenomics ◽  
2020 ◽  
Vol 12 (3) ◽  
pp. 235-249 ◽  
Author(s):  
Alexander Suvorov ◽  
Vladimir Naumov ◽  
Victoria Shtratnikova ◽  
Maria Logacheva ◽  
Alex Shershebnev ◽  
...  

Perinatal exposures to polybrominated diphenyl ethers permanently reprogram liver metabolism and induce a nonalcoholic fatty liver disease-like phenotype and insulin resistance in rodents. Aim: To test if these changes are associated with altered liver epigenome. Materials & methods: Expression of small RNA and changes in DNA methylation in livers of adult rats were analyzed following perinatal exposure to 2,2′,4,4′-tetrabromodiphenyl ether, the polybrominated diphenyl ether congener most prevalent in human tissues. Results: We identified 33 differentially methylated DNA regions and 15 differentially expressed miRNAs. These changes were enriched for terms related to lipid and carbohydrate metabolism, insulin signaling, Type-2 diabetes and nonalcoholic fatty liver disease. Conclusion: Changes in the liver epigenome are a likely candidate mechanism of long-term maintenance of an aberrant metabolic phenotype.


2010 ◽  
Vol 48 (2) ◽  
pp. 572-578 ◽  
Author(s):  
Hamdy A.A. Aly ◽  
Ahmed M. Mansour ◽  
Osama M. Abo-Salem ◽  
Hala F. Abd-Ellah ◽  
Ashraf B. Abdel-Naim

Endocrinology ◽  
2011 ◽  
Vol 152 (8) ◽  
pp. 3049-3061 ◽  
Author(s):  
Jie Wei ◽  
Yi Lin ◽  
Yuanyuan Li ◽  
Chenjiang Ying ◽  
Jun Chen ◽  
...  

2019 ◽  
Vol 38 (11) ◽  
pp. 1302-1313 ◽  
Author(s):  
HAA Aly

The current study was aimed to investigate the ameliorative effect of lycopene against gentamicin-induced testicular toxicity in adult rat testes. Pretreatment with lycopene (4 mg/kg/day) significantly prevented the decrease in the absolute testes weight and relative testes weight and the reduction in sperm count, motility, viability, and daily sperm production in gentamicin (100 mg/kg/day)-treated rats. Gentamicin significantly decreased the level of serum testosterone and testicular lactate dehydrogenase-X and G6PDH activities but a marked increase was observed upon pretreatment with lycopene. Testicular caspase-3 and -9 activities were significantly increased but lycopene showed significant protection from gentamicin-induced apoptosis. Oxidative stress was induced by gentamicin treatment as evidenced by increased hydrogen peroxide level and lipid peroxidation and decreased the antioxidant enzymes superoxide dismutase, catalase, glutathione peroxidase, and glutathione reductase activities and glutathione content. These alterations were effectively prevented by lycopene pretreatment. Histopathological examination showed loss of spermatogenesis and morphological abnormalities of the testis after treatment with gentamycin. These abnormalities were effectively normalized by pretreatment with lycopene. In conclusion, gentamicin decreases rat testes weight and inhibits spermatogenesis. It induces oxidative stress and apoptosis by possible mitochondrial dysfunction. These data provide insight into the mode of action of gentamicin-induced testicular toxicity and the beneficial role provided by lycopene to restore the suppressed spermatogenesis.


2017 ◽  
Vol 329 ◽  
pp. 173-189 ◽  
Author(s):  
Samuel Mucio-Ramírez ◽  
Eduardo Sánchez-Islas ◽  
Edith Sánchez-Jaramillo ◽  
Margarita Currás-Collazo ◽  
Victor R. Juárez-González ◽  
...  

2020 ◽  
Vol 391 ◽  
pp. 114914
Author(s):  
Mhar Y. Alvarez-Gonzalez ◽  
Eduardo Sánchez-Islas ◽  
Samuel Mucio-Ramirez ◽  
Patricia de Gortari ◽  
María I. Amaya ◽  
...  

2008 ◽  
Vol 22 (S1) ◽  
Author(s):  
Ashini Shah ◽  
Mark Gaertner ◽  
Cary Coburn ◽  
Prasada Rao Kodavanti ◽  
Abeena Watson‐Siroboe ◽  
...  

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