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The effect of Ginkgo biloba extract on mitochondrial oxidative phosphorylation in the normal and ischemic rat heart.

Abstract
Free radical-induced myocardial damage and impairment of vascular endothelium-dependent relaxation are amongst the most important mechanisms responsible for ischemic heart injury. Ginkgo biloba leaf extract (GE) has been reported to improve blood circulation in the brain and have a beneficial impact on the cardiovascular system but its cardioprotective effects have not been elucidated yet. Therefore, this study investigated the influence of GE in 70% ethanol (1:5) administered orally to rats on the functions of isolated heart mitochondria under normal and ischemic conditions. Wistar rats were given GE or ethanol (solvent control) at a dosage of 0.32 mL/kg in drinking water for 10 and 18 days, while the control animals received untreated drinking water. Mitochondrial respiration rates were determined oxygraphically. Pyruvate and malate, succinate or palmitoyl-L-carnitine and malate were used as substrates. The GE treatment partially uncoupled mitochondrial oxidation from phosphorylation, reduced the generation of free radicals in the mitochondria, diminished the ischemia-induced V₃ decrease and the degree of respiration stimulation by exogenous cytochrome c. Thus, these results indicate that GE exerts cardioprotective effects reducing ischemia-caused impairment of the functions of heart mitochondria.
AuthorsJurga Bernatoniene, Daiva Majiene, Rimantas Peciura, Ale Laukeviciene, Ruta Bernatoniene, Tauras Mekas, Arturas Kasauskas, Dalia Kopustinskiene
JournalPhytotherapy research : PTR (Phytother Res) Vol. 25 Issue 7 Pg. 1054-60 (Jul 2011) ISSN: 1099-1573 [Electronic] England
PMID21259351 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
CopyrightCopyright © 2011 John Wiley & Sons, Ltd.
Chemical References
  • Plant Extracts
  • Reactive Oxygen Species
Topics
  • Animals
  • Ginkgo biloba (chemistry)
  • Ischemia (drug therapy)
  • Male
  • Mitochondria, Heart (drug effects, metabolism)
  • Oxidation-Reduction
  • Oxidative Phosphorylation
  • Plant Extracts (pharmacology)
  • Rats
  • Rats, Wistar
  • Reactive Oxygen Species (metabolism)

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