Protective effects of Ginkgo biloba extract EGb 761 on myocardium of experimentally diabetic rats - I: Ultrastructural and biochemical investigation on cardiomyocytes
G. Fitzl et al., Protective effects of Ginkgo biloba extract EGb 761 on myocardium of experimentally diabetic rats - I: Ultrastructural and biochemical investigation on cardiomyocytes, EXP TOX PAT, 51(3), 1999, pp. 189-198
Chronic diabetes in man and animal models develops cardiomyopathic alterati
ons which cannot be absolutely avoided by insuline therapy. Since diabetic
damage is part ly attributed to oxidative stress antioxidative treatment co
uld be able to reduce the alterations. Aim of this study was to investigate
the cardioprotective effects of EGb 761, Known as a radical scavenger, aga
inst diabetic alterations in rats.
The diabetes was induced by i.p. injection of 60 mg/kg body weight streptoz
otocin. Duration of diabetes was 4 months, the protected group received 100
mg/kg body weight EGb 761 with the drinking water over 3 months.
Electron and light microscopic morphometry of left-ventricular samples reve
aled typical diabetic alterations consisting in decrease of volume fraction
of myofibrils, SR and t-tubules and diminishing of cardiomyocyte diameter,
increase of interstitial volume, mitochondrial size and volume fraction, a
nd of vacuoles and of lipid drops. EGb treat ment could gradually prevent t
he loss of myofibrils and reduction of myocyte diameter but has only little
influence on interstitial and mitochondria volume. The diabetic-induced in
crease of lipid and vacuoles and the decrease of SR and t-tubules were not
influenced.
Biochemical parameters of oxidative stress: malondialdehyde (MDA) was only
insignificantly altered by diabetes and EGb. The superoxide dismutase (SOD)
activity was in creased by diabetes and more increased by EGb treatment. C
reatine kinase (CK) activity was diminished by diabetes but slightly increa
sed by EGb. The polymerase chain reaction (PCR) of i-NOS was not different
between the diabetic and protected diabetic groups.