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Influence of the AT1 Receptor Antagonists Telmisartan and Losartan on Reproduction and Offspring After Paternal Exposure to Ionizing Radiation.
Cavalim Vale, Ana Paula; Dos Santos, Guilherme; da Silva, Teresa Prado; Mansano, Naira da Silva; Chies, Agnaldo Bruno; Chagas, Eduardo Federighi Baisi; Spadella, Maria Angélica.
Affiliation
  • Cavalim Vale AP; 1 Marília Medical School, Marília, São Paulo, Brazil.
  • Dos Santos G; 1 Marília Medical School, Marília, São Paulo, Brazil.
  • da Silva TP; 2 Human Anatomy Laboratory, Marília Medical School, Marília, São Paulo, Brazil.
  • Mansano NDS; 3 Department of Anatomy, Institute of Biomedical Sciences, University of São Paulo, São Paulo, Brazil.
  • Chies AB; 4 Laboratory of Pharmacology, Marília Medical School, Marília, São Paulo, Brazil.
  • Chagas EFB; 5 Human Development and Technology, University of Marília, São Paulo, Brazil.
  • Spadella MA; 6 Human Embryology Laboratory, Marília Medical School, Marília, São Paulo, Brazil.
Reprod Sci ; 26(5): 639-648, 2019 05.
Article in En | MEDLINE | ID: mdl-29938606
ABSTRACT
This study evaluated the repercussions of paternal exposure to radiation on reproduction and offspring in rats, as well as whether treatment with the angiotensin II type 1 (AT1) receptor antagonists telmisartan and losartan has a mitigating effect. Rats were randomly divided into 6 groups control, radiation, telmisartan, losartan, radiation + telmisartan, and radiation + losartan. A single 5 Gy dose of radiation was administered directly into the scrotum, followed by treatment with telmisartan (12 mg/kg/d) or losartan (34 mg/kg/2 times per day) for 60 days in the groups receiving these medications. The reproductive ability of the test animals was assessed before and after exposure to radiation via fertility tests. The resulting offspring were analyzed for the presence of external and internal anomalies. Ionizing radiation significantly affected the rates of fertility, pre- and postimplantation losses, and implantation. Telmisartan and losartan did not significantly prevent this radiation-induced damage. The frequency of fetal anomalies was similar in offspring produced before and after paternal radiation exposure. Moreover, irradiated rats that received treatments and were able to generate offspring did not produce fetuses with morphological changes; this may represent a possible radioprotective effect AT1 antagonists have on offspring development, although few fetuses survived and were evaluated for malformations. Although the study findings indicate that these medications have a positive effect, further studies with longer treatment periods (extending beyond 1 rat spermatogenic cycle) are needed to determine whether these drugs significantly improve reproductive rates after paternal exposure to radiation, which may also reflect an increase in the number of viable fetuses.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Reproduction / Paternal Exposure / Radiation Exposure / Losartan / Angiotensin II Type 1 Receptor Blockers / Fetal Viability / Telmisartan Limits: Animals / Pregnancy Language: En Journal: Reprod Sci Journal subject: MEDICINA REPRODUTIVA Year: 2019 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Reproduction / Paternal Exposure / Radiation Exposure / Losartan / Angiotensin II Type 1 Receptor Blockers / Fetal Viability / Telmisartan Limits: Animals / Pregnancy Language: En Journal: Reprod Sci Journal subject: MEDICINA REPRODUTIVA Year: 2019 Document type: Article Affiliation country:
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