Chronic hypoxia differentially increases glutathione content and γ-glutamyl cysteine synthetase expression in fetal guinea pig organs

• Published in: Early human development 2008-02, Vol.84 (2), p.121-127
• Main Authors: Oh, Chien, Dong, Yafeng, Harman, Christopher, Mighty, Hugh E, Kopelman, Jerome, Thompson, Loren P
• Format: Article
• Language: English
• Subjects: Adaptation; Advanced Basic Science; Animals; Biological and medical sciences; Blotting, Western; Body Weight - physiology; Embryology: invertebrates and vertebrates. Teratology; Female; Fetal Hypoxia - blood; Fetal Hypoxia - enzymology; Fetal Hypoxia - metabolism; Fetus; Fundamental and applied biological sciences. Psychology; Glutamate-Cysteine Ligase - biosynthesis; Glutathione; Glutathione - metabolism; Guinea Pigs; Immunohistochemistry; Kidney; Kidney - enzymology; Kidney - metabolism; Lactic Acid - blood; Liver; Liver - embryology; Liver - enzymology; Liver - metabolism; Lung; Lung - enzymology; Lung - metabolism; Neonatal and Perinatal Medicine; Organ Size - physiology; Pregnancy; Pyruvic Acid - blood
• ISSN: 0378-3782; 1872-6232
• DOI: 10.1016/j.earlhumdev.2007.03.013

Abstract Objective: Glutathione is a natural antioxidant in the fetus and adult. We sought to determine whether maternal hypoxia alters glutathione levels in fetal organs as an adaptive response to the reduced oxygenation. Study design: Timed pregnant guinea pigs were housed in either a Plexiglas chamber containing 10.5% O2 from 46 to 60 days gestation (HPX, n = 6) or in room air, as the normoxic control (NMX, n = 5). Pregnant guinea pigs were anesthetized at near term (∼ 60 days, term = 65 days) and liver, lung and kidney were excised from anesthetized fetuses and stored frozen (− 80 °C) prior to sample processing. Using the hypoxia marker, pimonidazole, we measured a hypoxia-induced increase in stained cells of fetal liver compared to no change in either the lung or kidney. To measure the effect of hypoxia among different organs, total glutathione (GSH) content and protein levels of γ-glutamyl cysteine synthetase (γ-GCS) were measured from the same organs. Results: Maternal hypoxia increased ( P < 0.05) total glutathione levels by 121% in the fetal liver but had no effect in either fetal lung or kidney. Chronic hypoxia increased ( P < 0.05) γ-GCS protein levels in all three fetal organs studied. Conclusion: These results demonstrate that the fetal response to maternal hypoxia may be organ specific. The increase in fetal liver glutathione via upregulation of γ-GCS may be an important adaptive response to prolonged hypoxic stress.