Advanced Search

Journal Navigation

Journal Home

Subscriptions

Archive

Contact Us

Table of Contents

CiteULike is a free service for managing and discovering scholarly references - click here to get started.

Sign In to gain access to subscriptions and/or personal tools.
Journal of Dental Research
This Article
Right arrow Full Text (PDF)
Right arrow References
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to Saved Citations
Right arrow Download to citation manager
Right arrowRequest Permissions
Right arrow Request Reprints
Right arrow Add to My Marked Citations
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Right arrow Citing Articles via Scopus
Google Scholar
Right arrow Articles by Jeng, J.H.
Right arrow Articles by Kuo, M.Y.P.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Jeng, J.H.
Right arrow Articles by Kuo, M.Y.P.
Social Bookmarking
 Add to CiteULike   Add to Complore   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Reddit   Add to Technorati   Add to Twitter  
What's this?

Eugenol Triggers Different Pathobiological Effects on Human Oral Mucosal Fibroblasts 1

J.H. Jeng

School of Dentistry, National Taiwan University, 1 Chang-Te Street, Taipei, Taiwan 10016, ROC

L.J. Hahn

School of Dentistry, National Taiwan University, 1 Chang-Te Street, Taipei, Taiwan 10016, ROC

EJ Lu

Graduate Institute of Biochemistry, College of Medicine, National Taiwan University, 1 Chang-Te Street, Taipei, Taiwan 10016, ROC

YJ Wang

Graduate Institute of Biochemistry, College of Medicine, National Taiwan University, 1 Chang-Te Street, Taipei, Taiwan 10016, ROC

M.Y.P. Kuo

School of Dentistry, National Taiwan University, 1 Chang-Te Street, Taipei, Taiwan 10016, ROC

Pathobiological effects of eugenol (4-allyl-2-methoxyphenol), a major constituent of betel quid (BQ), were studied on oral mucosal fibroblasts. At a concentration higher than 3 mmol/L, eugenol was cytotoxic to oral mucosal fibroblasts in a concentration-and time-dependent manner. Cell death was associated with intracellular depletion of glutathione (GSH). Most of the GSH was depleted prior to the onset of cell death. At concentrations of 3 mmol/L and 4 mmol/L, eugenol depleted about 45% and 77% of GSH after one-hour incubation. In addition, eugenol decreased cellular ATP level in a concentration- and time-dependent manner. Eugenol also inhibited lipid peroxidation. Inhibition of lipid peroxidation was partially explained by its dose-dependent inhibition of xanthine oxidase activity. The IC50 of eugenol on xanthine oxidase activity was about 0.3 mmol/L. No DNA strand break activity for eugenol was found at concentrations between 0.5 and 3 mmol/L. Taken together, frequent exposure of oral mucosa to a high concentration of eugenol during the chewing of BQ might be involved in the pathogenesis of oral submucous fibrosis and oral cancer via its cytotoxicity. In contrast, eugenol at a concentration less than 1 mmol/L might protect cells from the genetic attack of reactive oxygen species via inhibition of xanthine oxidase activity and lipid peroxidation.

Key Words: Eugenol • Betel Quid Chewing • Cytotoxicity • Glutathione Depletion • Fibroblast.

Journal of Dental Research, Vol. 73, No. 5, 1050-1055 (1994)
DOI: 10.1177/00220345940730050601


Add to CiteULike CiteULike   Add to Complore Complore   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati   Add to Twitter Twitter    What's this?


This article has been cited by other articles:


Home page
Exp. Biol. Med.Home page
B. B. Aggarwal, M. E. Van Kuiken, L. H. Iyer, K. B. Harikumar, and B. Sung
Molecular Targets of Nutraceuticals Derived from Dietary Spices: Potential Role in Suppression of Inflammation and Tumorigenesis
Experimental Biology and Medicine, August 1, 2009; 234(8): 825 - 849.
[Abstract] [Full Text] [PDF]


Home page
Hum Exp ToxicolHome page
J. Usta, S. Kreydiyyeh, P. Barnabe, Y. Bou-Moughlabay, and H. Nakkash-Chmaisse
Comparative study on the effect of cinnamon and clove extracts and their main components on different types of ATPases
Human and Experimental Toxicology, July 1, 2003; 22(7): 355 - 362.
[Abstract] [PDF]


Home page
JDRHome page
M.Y.P. Kuo, H.M. Chen, L.J. Hahn, C.C. Hsieh, and C.P. Chiang
Collagen Biosynthesis in Human Oral Submucous Fibrosis Fibroblast Cultures
Journal of Dental Research, November 1, 1995; 74(11): 1783 - 1788.
[Abstract] [PDF]