Inhibitory effect of tea catechins on collagenase activity

• Published in: Journal of periodontology (1970) Vol. 64; no. 7; p. 630
• Main Authors: Makimura, M, Hirasawa, M, Kobayashi, K, Indo, J, Sakanaka, S, Taguchi, T, Otake, S
• Format: Journal Article
• Language: English
• Published: United States 01.07.1993
• Subjects: Adult; Catechin - chemistry; Catechin - metabolism; Catechin - therapeutic use; Female; Gingival Crevicular Fluid - enzymology; Humans; Male; Matrix Metalloproteinase Inhibitors; Microbial Collagenase - antagonists & inhibitors; Middle Aged; Periodontitis - drug therapy; Periodontitis - enzymology; Porphyromonas gingivalis - enzymology; Tea - chemistry
• DOI: 10.1902/jop.1993.64.7.630
• ISSN: 0022-3492

A major purpose of this study was to examine inhibitory effect of the catechin derivatives from Japanese green tea Camellia sinensis on collagenase activity. The crude tea catechins, which contain (+)-catechin (C), (-)-epicatechin (EC), (+)-gallocatechin (GC), (-)-epigallocatechin (EGC), (-)-epicatechin gallate (ECg), and (-)-epigallocatechin gallate (EGCg), were tested for their ability to inhibit the prokaryotic and eukaryotic cell derived collagenase activities. Among the tea catechins tested, ECg and EGCg showed the most potent inhibitory effect on collagenase activity when an optimal concentration of tea catechins (100 micrograms/ml) was added to reaction mixture containing collagenase and collagen. Preincubation of collagenase with tea catechins reduced the collagenase activity as well. In contrast to ECg and EGCg, the other four tea catechins (C, EC, EGC, and GC) did not show any collagenase inhibitory effect. Our results suggest that the steric structure of 3-galloyl radical is important for the inhibition of collagenase activity. The collagenase activity in the gingival crevicular fluid from highly progressive adult periodontitis was completely inhibited by the addition of tea catechins. These results demonstrated that tea catechins containing galloyl radical possess the ability to inhibit both eukaryotic and prokaryotic cell derived collagenase.