Y. Korystov, A. Korystova, L. Kublik, M. Levitman, T. Samochvalova, V. Shaposhnikova
{"title":"Green Tea Suppresses the Radiation-Induced Increase of the AngiotensinConverting Enzyme & Reactive Oxygen Species in the Aorta of Rats","authors":"Y. Korystov, A. Korystova, L. Kublik, M. Levitman, T. Samochvalova, V. Shaposhnikova","doi":"10.31487/j.jicoa.2021.01.02","DOIUrl":null,"url":null,"abstract":"The consumption of green tea reduces the risk of cardiovascular diseases and suppresses the development\nof atherosclerosis. The main factor for the initiation and progression of atherosclerosis is an increase in the\nproduction of reactive oxygen species (ROS) in vessels. A significant contribution to the increase in ROS\nproduction is made by increased concentration of angiotensin II, a product of the angiotensin-converting\nenzyme (ACE). The effect of green tea on the level of ROS and ACE activity in blood vessels in vivo has\nnot yet been studied. The activity of ACE in aorta sections of rat was determined by measuring the\nhydrolysis of hippuryl-L-histidyl-L-leucine, and the production of ROS was estimated from the oxidation\nof dichlorodihydrofluorescein. Green tea inhibited the radiation-induced activation of the ACE in the aorta\nof rats on intraperitoneal (i.p.) and peroral administration. Six hours after the administration of tea, the\nactivity of ACE in irradiated rats decreased to the control level, and by 24 h after administration, the tea did\nnot almost affect the ACE activity. On i.p. administration, effective doses were lower than on peroral\nadministration. The concentration of orally administered tea that inhibited the ACE activation in irradiated\nrats by 50% (IC50) was 1 ml of an extract of 2.1 g of tea brewed per 100 ml of water. One milliliter of i.p.\nadministered green tea (1 g per 100 ml of water) completely suppressed the increased ROS production in\nthe aorta of irradiated rats.","PeriodicalId":93027,"journal":{"name":"Journal of integrative cardiology open access","volume":" ","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2021-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of integrative cardiology open access","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.31487/j.jicoa.2021.01.02","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
The consumption of green tea reduces the risk of cardiovascular diseases and suppresses the development
of atherosclerosis. The main factor for the initiation and progression of atherosclerosis is an increase in the
production of reactive oxygen species (ROS) in vessels. A significant contribution to the increase in ROS
production is made by increased concentration of angiotensin II, a product of the angiotensin-converting
enzyme (ACE). The effect of green tea on the level of ROS and ACE activity in blood vessels in vivo has
not yet been studied. The activity of ACE in aorta sections of rat was determined by measuring the
hydrolysis of hippuryl-L-histidyl-L-leucine, and the production of ROS was estimated from the oxidation
of dichlorodihydrofluorescein. Green tea inhibited the radiation-induced activation of the ACE in the aorta
of rats on intraperitoneal (i.p.) and peroral administration. Six hours after the administration of tea, the
activity of ACE in irradiated rats decreased to the control level, and by 24 h after administration, the tea did
not almost affect the ACE activity. On i.p. administration, effective doses were lower than on peroral
administration. The concentration of orally administered tea that inhibited the ACE activation in irradiated
rats by 50% (IC50) was 1 ml of an extract of 2.1 g of tea brewed per 100 ml of water. One milliliter of i.p.
administered green tea (1 g per 100 ml of water) completely suppressed the increased ROS production in
the aorta of irradiated rats.