Effect of a polymorphism in the ND1 mitochondrial gene on human skeletal muscle mitochondrial function

Obesity (Silver Spring). 2008 Feb;16(2):363-8. doi: 10.1038/oby.2007.40.

Abstract

Objective: A non-silent polymorphism in the mitochondrial coding region of the ND1 gene, a subunit of reduced nicotinamide adenine dinucleotide (NADH) dehydrogenase is associated with resting metabolic rate (RMR) in 245 non-diabetic Pima Indians. The purpose of this investigation was to determine the effect of the ND1 gene polymorphism on mitochondrial function in 14 male Pima Indians.

Methods and procedures: Seven subjects with an A at site 3547 of the ND1 gene (Ile at amino acid 81), and seven with a G at this site (Val) were studied. Mitochondria were isolated from 0.8 to 1.5 g of skeletal muscle obtained by needle biopsy of the lateral quadriceps muscle. In intact mitochondria, maximal (state-3) and resting (state-4) respiration rates were measured polarographically at 37 degrees C with a variety of single substrates or substrate combinations. Disrupted mitochondria were analyzed for maximal capacities through the entire electron transport chain (ETC) (NADH oxidase (NADHOX)), as well as through a segment of Complex I that is independent of the ND1 component (NADH-ferricyanide (NADH-FeCN) reductase).

Results: Mitochondria were well coupled and exhibited higher respiratory control ratios (RCRs) than rodent muscle. There were no differences between the two groups for any of the measured parameters.

Discussion: These results indicate that the cause of the observed association between RMR and the ND1 polymorphism is not related to in vitro mitochondrial function.

MeSH terms

  • Adult
  • Basal Metabolism / genetics
  • Basal Metabolism / physiology
  • Biopsy
  • Cohort Studies
  • Electron Transport Chain Complex Proteins / genetics
  • Electron Transport Chain Complex Proteins / physiology
  • Energy Metabolism / genetics
  • Energy Metabolism / physiology
  • Genes, Mitochondrial / genetics*
  • Humans
  • Indians, North American
  • Male
  • Mitochondria, Muscle / genetics
  • Mitochondria, Muscle / physiology*
  • Muscle, Skeletal / metabolism
  • Muscle, Skeletal / pathology
  • NADH Dehydrogenase / genetics*
  • NADH Dehydrogenase / metabolism
  • Polymorphism, Genetic / genetics*

Substances

  • Electron Transport Chain Complex Proteins
  • NADH Dehydrogenase
  • NADH dehydrogenase subunit 1, human