Key result
KB-R7943 preserves endothelium-dependent relaxation impaired by high glucose in rat aorta.
Why the study?
The effects of the Na+/Ca2+ exchanger inhibitor KB-R7943 on impaired endothelium-dependent relaxation induced by high glucose in rat aorta were investigated.
Does KB-R7943 improve impaired endothelium-dependent relaxation induced by high glucose in rat isolated aorta?
Does KB-R7943 improve impaired endothelium-dependent relaxation induced by high glucose in rat isolated aorta?
Inhibition of the Na+/Ca2+ exchanger with KB-R7943 ameliorates high glucose-induced endothelial dysfunction in rat aorta by reducing oxidative stress and enhancing NO production.
Hypothesis-generating for Na+/Ca2+ exchanger inhibition in diabetic endothelial dysfunction; human studies required before any clinical consideration.
The present study was designed to investigate the effects of KB-R7943, an inhibitor of the Na+/Ca2+ exchanger, on impaired endothelium-dependent relaxation (EDR) induced by high glucose in rat isolated aorta. Both acetylcholine (ACh)-induced EDR and sodium nitroprusside (SNP)-induced endothelium-independent relaxation (EIR) were measured after aortic rings had been exposed to high glucose in the absence and presence of KB-R7943. Coincubation of aortic rings with high glucose (25 mmol/L) for 24 h resulted in a significant inhibition of EDR, but had no effect on EIR. After incubation of aortic rings in the presence of both KB-R7943 (0.1-10 micromol/L) and high glucose for 24 h, significantly attenuation of impaired EDR was observed. This protective effect of KB-R7943 (10 micromol/L) was abolished by superoxide dismutase (SOD; 200 U/mL) and l-arginine (3 mmol/L), whereas d-arginine (3 mmol/L) had no effect. Similarly, high glucose decreased SOD activity and the release of nitric oxide (NO) and increased superoxide anion (O2(-)) production in aortic tissue. KB-R7943 significantly decreased O2(-) production and increased SOD activity and NO release. These results suggest that KB-R7943 can restore impaired EDR induced by high glucose in rat isolated aorta, which may be related to the scavenging of oxygen free radicals and enhanced NO production.
No takes yet. Share an insight, caveat, or question.
Su et al. (2008) studied High glucose-induced endothelial dysfunction. KB-R7943 vs. High glucose alone was evaluated on Endothelium-dependent relaxation (EDR). KB-R7943 (0.1-10 micromol/L) significantly attenuated impaired endothelium-dependent relaxation induced by high glucose (25 mmol/L) in rat isolated aorta.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: