Impaired oxidative phosphorylation in hepatic mitochondria in growth-retarded rats

• Published in: American journal of physiology: endocrinology and metabolism Vol. 285; no. 6; pp. E1258 - E1266
• Main Authors: Peterside, Iyalla E, Selak, Mary A, Simmons, Rebecca A
• Format: Journal Article
• Language: English
• Published: United States 01.12.2003
• Subjects: Aging - metabolism; Animals; Animals, Newborn; Blood Glucose - analysis; Cell Respiration; Cells, Cultured; Diabetes Mellitus, Type 2 - etiology; Electron Transport Complex I - metabolism; Electron Transport Complex IV - metabolism; Female; Fetal Growth Retardation - complications; Fetal Growth Retardation - enzymology; Fetal Growth Retardation - metabolism; Fetal Growth Retardation - pathology; Insulin - blood; Mitochondria, Liver - enzymology; Mitochondria, Liver - metabolism; Organ Size; Oxidation-Reduction; Oxidative Phosphorylation; Oxygen - metabolism; Pregnancy; Rats
• ISSN: 0193-1849; 1522-1555
• DOI: 10.1152/ajpendo.00437.2002

Department of Pediatrics, Children's Hospital and University of Pennsylvania, Philadelphia, Pennsylvania 19104 Submitted 7 October 2002 ; accepted in final form 7 August 2003 Intrauterine growth retardation (IUGR) has been linked to the development of type 2 diabetes in adulthood. We have developed an IUGR model in the rat whereby the animals develop diabetes between 3 and 6 mo of age that is associated with insulin resistance. Alterations in hepatic glucose metabolism are known to contribute to the hyperglycemia of diabetes; however, the mechanisms underlying this phenomenon have not been fully explained. To address this issue, intact liver mitochondria were isolated from IUGR and control offspring at different ages to examine the nature and time course of possible defects in oxidative metabolism. Phospho enol pyruvate carboxykinase (PEPCK) expression was also measured in livers of IUGR and control offspring. Rates of ADP-stimulated (state 3) oxygen consumption were increased for succinate in the fetus and for -ketoglutarate and glutamate at day 1 , reflecting possible compensatory metabolic adaptations to acute hypoxia and acidosis in IUGR rats. By day 14 , oxidation of glutamate and -ketoglutarate had returned to normal, and by day 28 , oxidation rates of pyruvate, glutamate, succinate, and -ketoglutarate were significantly lower than those of controls. Rotenone-sensitive NADH-O 2 oxidoreductase activity was similar in control and IUGR mitochondria at all ages, showing that the defect responsible for decreased pyruvate, glutamate, and -ketoglutarate oxidation in IUGR liver precedes the electron transport chain and involves pyruvate and -ketoglutarate dehydrogenases. Increased levels of manganese superoxide dismutase suggest that an antioxidant response has been mounted, and hydroxynonenal (HNE) modification of pyruvate dehydrogenase E2-(catalytic) and E3-binding protein subunits suggests that HNE-induced inactivation of this key enzyme may play a role in the mechanism of injury. The level of PEPCK mRNA was increased 250% in day 28 IUGR liver, indicating altered gene expression of the gluconeogenic enzyme that precedes overt hyperglycemia. These results indicate that uteroplacental insufficiency impairs mitochondrial oxidative phosphorylation in the liver and that this derangement predisposes the IUGR rat to increased hepatic glucose production by suppressing pyruvate oxidation and increasing gluconeogenesis. liver; growth retardation; diabetes; gluconeogenesis Address for reprint requests and other correspondence: R. Simmons, Univ. of Pennsylvania, BRB II/III, Rm 1308, 421 Curie Blvd., Philadelphia, PA 19104 (E-mail: rsimmons{at}mail.med.upenn.edu ).