Depressed glutathione synthesis precedes oxidative stress and atherogenesis in Apo-E(-/-) mice

Saibal K Biswas, David E Newby, Irfan Rahman, Ian L Megson

Research output: Contribution to journalArticle

57 Citations (Scopus)

Abstract

Glutathione is a vital intracellular antioxidant. The enzymes involved in its synthesis and utilisation are tightly regulated, but the importance of glutathione regulation in atherogenesis is poorly understood. Here, we establish that glutathione is severely (approximately 80%) depleted very early (10 weeks) in the atheroma-prone aortic arch of male apoprotein E-deficient (Apo-E(-/-)) mice compared to age-matched wild-type controls. Importantly, this event pre-empts lipid peroxidation and detectable atheroma by several months. Depletion of glutathione was associated with excessive oxidant burden and reduced transcription and activity of the rate-limiting enzyme for glutathione synthesis, gamma-glutamylcysteine ligase, together with the glutathione-dependent antioxidant enzyme, glutathione peroxidase. Depletion via reduced synthesis of glutathione precedes lipid peroxidation and atherogenesis in Apo-E(-/-) mice. We suggest that glutathione deficiency is central to the failure of the intracellular antioxidant defences and is causally implicated in the pathogenesis of atherosclerosis. Modification of the glutathione pathway may present a novel and important therapeutic target in the prevention and treatment of atherosclerosis.
Original languageEnglish
Pages (from-to)1368-73
Number of pages6
JournalBiochemical and Biophysical Research Communications
Volume338
Issue number3
DOIs
Publication statusPublished - 2005

Fingerprint Dive into the research topics of 'Depressed glutathione synthesis precedes oxidative stress and atherogenesis in Apo-E(-/-) mice'. Together they form a unique fingerprint.

  • Cite this