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Toxicity of oxidized fish oil in pregnancy: a dose-response study in rats.
Satokar, Vidit V; Vickers, Mark H; Reynolds, Clare M; Ponnampalam, Anna P; Firth, Elwyn C; Garg, Manohar L; Bridge-Comer, Pania E; Cutfield, Wayne S; Albert, Benjamin B.
Afiliação
  • Satokar VV; Liggins Institute, University of Auckland, Auckland, New Zealand.
  • Vickers MH; Liggins Institute, University of Auckland, Auckland, New Zealand.
  • Reynolds CM; Liggins Institute, University of Auckland, Auckland, New Zealand.
  • Ponnampalam AP; University College Dublin Conway Institute of Biomolecular and Biomedical Research, Dublin, Ireland.
  • Firth EC; Department of Physiology, University of Auckland, Auckland, New Zealand.
  • Garg ML; Department of Obstetrics and Gynaecology, University of Auckland, Auckland, New Zealand.
  • Bridge-Comer PE; Liggins Institute, University of Auckland, Auckland, New Zealand.
  • Cutfield WS; Nutraceuticals Research Program, School of Biomedical Sciences and Pharmacy, University of Newcastle, Newcastle, New South Wales, Australia.
  • Albert BB; Liggins Institute, University of Auckland, Auckland, New Zealand.
Am J Physiol Regul Integr Comp Physiol ; 323(2): R244-R254, 2022 08 01.
Article em En | MEDLINE | ID: mdl-35726870
ABSTRACT
Fish oil (FO) supplements are consumed during pregnancy to increase dietary omega-3. However, FO is often oxidized past recommended limits. In rats, a large dose of highly oxidized FO substantially increased newborn mortality, but the effects of human-relevant doses of less oxidized oil are unknown. A dose-response study in rats was conducted to estimate the safe level of oxidation during pregnancy. Sprague-Dawley rat dams were mated, then individually housed and provided with a gel treatment on each day of pregnancy. Treatment groups differed only in the FO content of the gel; control (no oil), PV5, PV10, and PV40 [0.05 mL of FO oxidized to a peroxide value (PV) of 5, 10, or 40 meq/kg], or PV40(1 mL) (1 mL of PV40). A subset of dams was culled on gestational day 20 to enable sampling, and the remainder were allowed to give birth. Newborn mortality was recorded. Offspring were sampled on postnatal days 2 and 21, and dams on day 21. There were no signs of unwellness during pregnancy. However, there was markedly increased neonatal mortality affecting the PV40(1 mL) (12.8%) and PV40 (6.3%) groups, but not the control, PV5, or PV10 groups (1%-1.4%). Dietary-oxidized FO altered the expression of placental genes involved in antioxidant pathways and the production of free radicals. Highly oxidized FO was toxic in rat pregnancy leading to a marked increase in mortality even at a human-relevant dose. We observed no toxic effects of FOs with PV ≤10 meq/kg, suggesting that this is an appropriate maximum limit.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Placenta / Óleos de Peixe Limite: Animals / Female / Humans / Pregnancy Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Placenta / Óleos de Peixe Limite: Animals / Female / Humans / Pregnancy Idioma: En Ano de publicação: 2022 Tipo de documento: Article