Journal of Periodontal and Implant Science
- Volume 31 Issue 1
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- Pages.123-135
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- 2001
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- 2093-2278(pISSN)
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- 2093-2286(eISSN)
Effects of Extracts of Natural Products on Alkaline Phosphatase Activity of MC3T3 - E1 Cells
수종의 생약추출물이 MC3T3-E1 세포의 염기성 인산분해 효소 활성에 미치는 영향
- Park, Sang-Kee (Department of Periodontology, College of Dentistry, Wonkwang University) ;
- Kim, Dae-Kyum (Department of Periodontology, College of Dentistry, Wonkwang University) ;
- You, Seung-Han (Department of Periodontology, College of Dentistry, Wonkwang University) ;
- Kim, Hyun-A (Department of Periodontology, College of Dentistry, Wonkwang University) ;
- Kim, Myoung-Dong (Department of Periodontology, College of Dentistry, Wonkwang University) ;
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You, Hyung-Keun
(Department of Periodontology, College of Dentistry, Wonkwang University) ;
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Shin, Hyung-Shik
(Department of Periodontology, College of Dentistry, Wonkwang University)
- 박상기 (원광대학교 치과대학 치주과학교실) ;
- 김대겸 (원광대학교 치과대학 치주과학교실) ;
- 유승한 (원광대학교 치과대학 치주과학교실) ;
- 김현아 (원광대학교 치과대학 치주과학교실) ;
- 김명동 (원광대학교 치과대학 치주과학교실) ;
-
유형근
(원광대학교 치과대학 치주과학교실) ;
-
신형식
(원광대학교 치과대학 치주과학교실)
- Published : 2001.03.30
Abstract
Several growth factors and polypeptides were studied for the regeneration of periodontal supporting tissues which had been lost due to periodontal disease. But these are not commonly used for regenerators of bone tissue or alveolar bone, because of the insufficiency of studies on their side effects, genetic engineering for mass production and stability for clinical application. Recently, many natural products, which have advantage of less side effects and possibility of long-term use, have been studied for their capacity and effects of anti-bacterial, anti-inflammatory and regenerative potential or periodontal tissues. Cnidii Rhizoma, Rhinocerotis Cornu and Drynariae Rhizoma have been traditionally used as a drug for treatment of bone disease in oriental medicine. The purpose of this study was to examine the ability of alkaline phosphatase synthesis of MC3T3-E1 cells when above medicines were supplimented. MC3T3-E1 cells were cultured with
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