Hyperglycemia Impairs Acetylcholine-Induced Vasodilation of Retinal Arterioles Through Polyol Pathway–Independent Mechanisms in Rats

• Published in: Journal of Pharmacological Sciences 2010, Vol.112(3), pp.336-342
• Main Authors: Mori, Asami, Saigo, Orie, Sakamoto, Kenji, Nakahara, Tsutomu, Ishii, Kunio
• Format: Article
• Language: English
• Subjects: Acetylcholine - pharmacology; aldose reductase; Animals; Arterioles - drug effects; Arterioles - physiology; diabetes; Diabetes Mellitus, Experimental - drug therapy; Diabetes Mellitus, Experimental - physiopathology; endothelium; Hyperglycemia - drug therapy; Hyperglycemia - physiopathology; L-Iditol 2-Dehydrogenase - antagonists & inhibitors; L-Iditol 2-Dehydrogenase - physiology; Male; Phenylacetates - pharmacology; Phenylacetates - therapeutic use; polyol pathway; Rats; Rats, Wistar; retinal circulation; Retinal Vessels - drug effects; Retinal Vessels - physiology; Signal Transduction - drug effects; Signal Transduction - physiology; Thiazoles - pharmacology; Thiazoles - therapeutic use; Vasodilation - drug effects; Vasodilation - physiology
• ISSN: 1347-8613; 1347-8648
• DOI: 10.1254/jphs.09312FP

We previously reported that acetylcholine (ACh)–induced vasodilation of retinal arterioles is diminished in diabetic rats; however, the underlying mechanism(s) of this phenomenon has not been fully elucidated. To determine the role of the polyol pathway in the diabetes-induced retinal vascular dysfunction, we investigated the effect of GP-1447, an inhibitor of aldose reductase, on the attenuation of ACh-induced vasodilation of retinal arterioles seen in diabetic rats. Male Wistar rats were treated with streptozotocin (STZ) and experiments were performed 2 weeks later. The STZ-treated animals were given drinking water containing 5% d-glucose to shorten the term for the development of retinal vascular dysfunction. Treatment with GP-1447 was initiated immediately after STZ treatment and continued throughout the 2-week experimental period. The attenuation of retinal vascular responses to ACh were not modified by treatment with GP-1447, whereas the aldose reductase inhibitor completely prevented diabetes-induced thinning of the retina and sorbitol accumulation in the retina and the lens. These results suggest that mechanisms that are independent of the polyol pathway may contribute to the onset of retinal endothelial dysfunction, although the pathway plays an important role in morphological changes of retina and formation of cataracts in diabetic rats.