H. Matsumoto, R. Takeuchi, M. Ono, Y. Akimoto, A. Fujii
{"title":"A possible therapeutic for gingival overgrowth caused by calcium channel blockers","authors":"H. Matsumoto, R. Takeuchi, M. Ono, Y. Akimoto, A. Fujii","doi":"10.11263/JSOTP1982.27.103","DOIUrl":null,"url":null,"abstract":"In the present study, the results of characters in nifedipine responders (NIFr) and nifedipine non-responders (NIFn) are summarized, and the possibility of using tenidap and 18ƒ¿ -glycyrrhetinic acid (18ƒ¿-GA) as a therapeutic for gingival overgrowth caused by calcium channel blockers is investigated. 18ƒ¿-GA inhibited cell proliferation and G1/S transition were induced in NIFr cells. It was also shown that cell cycle control proteins were down-stream targets in the growth-inhibition activity of 18ƒ¿-GA in NIFr cells. Tenidap discharges intracellular Ca2+ store, resulting in a depletion of intracellular Ca2+ store in NIFr cells. It also inhibits cell growth, DNA and collagen syntheses, lowered intracellular pH, and enhanced matrix metalloproteinase-1 formation in NIFr cells. These results suggest that 18ƒ¿-GA and tenidap might be effective for the prevention of gingival overgrowth caused by calcium channel blockers.","PeriodicalId":19590,"journal":{"name":"Oral Therapeutics and Pharmacology","volume":"27 1","pages":"103-108"},"PeriodicalIF":0.0000,"publicationDate":"2008-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Oral Therapeutics and Pharmacology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.11263/JSOTP1982.27.103","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"Pharmacology, Toxicology and Pharmaceutics","Score":null,"Total":0}
引用次数: 0
Abstract
In the present study, the results of characters in nifedipine responders (NIFr) and nifedipine non-responders (NIFn) are summarized, and the possibility of using tenidap and 18ƒ¿ -glycyrrhetinic acid (18ƒ¿-GA) as a therapeutic for gingival overgrowth caused by calcium channel blockers is investigated. 18ƒ¿-GA inhibited cell proliferation and G1/S transition were induced in NIFr cells. It was also shown that cell cycle control proteins were down-stream targets in the growth-inhibition activity of 18ƒ¿-GA in NIFr cells. Tenidap discharges intracellular Ca2+ store, resulting in a depletion of intracellular Ca2+ store in NIFr cells. It also inhibits cell growth, DNA and collagen syntheses, lowered intracellular pH, and enhanced matrix metalloproteinase-1 formation in NIFr cells. These results suggest that 18ƒ¿-GA and tenidap might be effective for the prevention of gingival overgrowth caused by calcium channel blockers.