Journal Article

Dietary choline restriction causes complex I dysfunction and increased H<sub>2</sub>O<sub>2</sub> generation in liver mitochondria

Kenneth Hensley, Yashige Kotake, Hong Sang, Quentin N. Pye, Gemma L. Wallis, Lisa M. Kolker, Tahereh Tabatabaie, Charles A. Stewart, Yoichi Konishi, Dai Nakae and Robert A. Floyd

in Carcinogenesis

Volume 21, issue 5, pages 983-989
Published in print May 2000 | ISSN: 0143-3334
Published online May 2000 | e-ISSN: 1460-2180 | DOI:
Dietary choline restriction causes complex I dysfunction and increased H2O2 generation in liver mitochondria

More Like This

Show all results sharing this subject:

  • Clinical Cytogenetics and Molecular Genetics


Show Summary Details


Removal of choline from the diet results in accumulation of triglycerides in the liver, and chronic dietary deficiency produces a non-genotoxic model of hepatocellular carcinoma. An early event in choline deficiency is the appearance of oxidized lipid, DNA and protein, suggesting that increased oxidative stress may facilitate neoplasia in the choline deficient liver. In this study, we find that mitochondria isolated from rats fed a choline-deficient, l-amino acid defined diet (CDAA) demonstrate impaired respiratory function, particularly in regard to complex I-linked (NADH-dependent) respiration. This impairment in mitochondrial electron transport occurs coincidentally with alterations in phosphatidylcholine metabolism as indicated by an increased ratio of long-chain to short-chain mitochondrial phosphatidylcholine. Moreover, hydrogen peroxide (H2O2) generation is significantly increased in mitochondria isolated from CDAA rats compared with mitochondrial from normal rats, and the NADH-specific yield of H2O2 is increased by at least 2.5-fold. These findings suggest an explanation for the rapid onset of oxidative stress and energy compromise in the choline deficiency model of hepatocellular carcinoma and indicate that dietary choline withdrawal may be a useful paradigm for the study of mitochondrial pathophysiology in carcinogenesis.

Keywords: CDAA, choline-deficient l-amino acid defined; CSAA, choline-sufficient l-amino acid defined diet; MS, mass spectrometry; NADH, nicotinamide adenine dinucleotide (reduced); PC, phosphatidyl choline.

Journal Article.  5773 words.  Illustrated.

Subjects: Clinical Cytogenetics and Molecular Genetics

Full text: subscription required

How to subscribe Recommend to my Librarian

Users without a subscription are not able to see the full content. Please, subscribe or login to access all content.