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Early Functional Changes in Rat Arteries and Microcirculatory Vessels while Modeling Metabolic Syndrome
Early changes in the cardiovascular system of young Wistar rats were studied in modeling metabolic syndrome by a fructose load. It was found that despite some weight loss in rats fed a fructose diet, as compared to control animals, these animals showed the signs of metabolic syndrome: hyperglycemia,...
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Published in: | Journal of evolutionary biochemistry and physiology 2022-09, Vol.58 (5), p.1471-1481 |
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Main Authors: | , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Early changes in the cardiovascular system of young Wistar rats were studied in modeling metabolic syndrome by a fructose load. It was found that despite some weight loss in rats fed a fructose diet, as compared to control animals, these animals showed the signs of metabolic syndrome: hyperglycemia, insulin resistance, dyslipidemia, increased activity of the sympathetic nervous system, arterial hypertension. Changes in the mesenteric arteries included an increase in the reactivity to phenylephrine and a decrease in acetylcholine-induced dilation due to decreased NO production by the endothelium, which is to a certain extent compensated by an increased production of the endothelium-derived hyperpolarizing factor realizing its effects through the activation of intermediate-conductance Ca
2+
-activated K
+
-channels. Fructose load led to the inhibition of soluble guanylate cyclase in arterial smooth muscle cells. In the skin microcirculatory bed of fructose-loaded rats, perfusion remained at the level typical for control animals, while skin microvessels showed an increase in neurogenic tone and an attenuation of endothelium-dependent tone. A decreased endothelial NO production was found in microcirculatory vessels, which was compensated by the synthesis of other endothelium-derived vasodilating factors. |
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ISSN: | 0022-0930 1608-3202 |
DOI: | 10.1134/S0022093022050179 |