Efeitos da exposição ao cloreto de mercúrio durante a gestação e lactação em ratas wistar e sua prole: parâmetros bioquímicos e distribuição de mercúrio

• Ano de defesa: 2015
• Autor(a) principal: Oliveira, Cláudia Sirlene de
• Tipo de documento: Tese
• Tipo de acesso: Acesso aberto
• Idioma: por
• Instituição de defesa: Universidade Federal de Santa Maria; BR; Bioquímica; UFSM; Programa de Pós-Graduação em Ciências Biológicas: Bioquímica Toxicológica
• Palavras-chave em Português: Água de beber; Intravenoso; Dano renal; Metais essenciais; Porfobilinogênio sintase; Metalotioneínas; Ureia; Creatinina; Tarefas comportamentais; Drinking water; Intravenous; Renal damage; Essential metals; Porfobilinogen-synthase; Metallothionein; Urea; Creatinine; Behavioral tasks; CNPQ::CIENCIAS BIOLOGICAS::BIOQUIMICA
• Link de acesso: http://repositorio.ufsm.br/handle/1/4492

The objective of this work was to evaluate the effects of HgCl2 exposure in drinking water in pregnant and/or lactating rats and their offspring. Still, it evaluated if the HgCl2 intravenous exposure as well as the renal damage induced by this exposure altered the offspring mercury content. The drinking water (v.o.) HgCl2 exposure protocol was as follows: Female Wistar rats were exposed to HgCl2 (0, 0.2, 0.5, 10 and 50 μg Hg2+/mL) from gestation day 0 until 20 or until the last day of lactation. Every two days, the mercury solutions were changed, food and water intake and rats weight were analyzed. The offspring was killed on gestation day 20 and on the post-natal days 10, 20, 30 and 40. Tissues weight, essential metal homeostasis, mercury content and biochemical parameters were evaluated. Behavioral tasks were carried out on post-natal days 3, 5, 7, 9 and 11 (negative geotaxis test) and 17, 18, 19 and 20 (beaker test). The intravenous (i.v.) HgCl2 exposure protocol was as follows: Female Wistar rats were exposed to HgCl2 (0.5 and 2.5 μmol HgCl2/kg/2 mL) on gestation day 20 and killed 6 h later or on gestation day 18 and killed 48 h later. Hg maternal and fetal distribution and renal damage through histology and biochemical and molecular markers were evaluated. Dams exposed to HgCl2 v.o. presented water intake decreased. The exposure to 50 μg Hg2+/mL caused an increase in relative renal weight. Animals exposed to 10 and 50 μg Hg2+/mL presented an increase in renal and hepatic Cu and Zn levels, respectively, and mercury accumulation (pregnant rats); and, an increase in total thiol and metallothionein renal levels (lactating rats). The offspring only presented an increase in hepatic porfobilinogensynthase activity (fetuses) and in relative renal weight (post-natal day 20). The pregnant rats exposed i.v. to HgCl2 presented the greater mercury accumulation in kidney in both periods analyzed; although 48 h after the exposure the Hg levels were lower than at 6 h. The exposure to 2.5 μmol HgCl2/kg/2 mL caused an increase in serum creatinine levels and in Kim-1 renal expression as well as renal histology alterations. The placental and fetal Hg did not change in both periods analyzed; the increase in fetal organs Hg levels were dose and time dependent. In conclusion, the exposure to low doses of HgCl2 in drinking water caused mild alterations in dams; also the dam organism was able to handle the Hg avoiding offspring damages; probably, this protection is related with the increase on scavenger molecules (metallothionein, for example) during the pregnancy and lactation. Besides, we verified that when dams were exposed intravenously to HgCl2, the developing organisms (fetuses) were unable to excrete/depurate the Hg.