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ToxSci Advance Access published online on February 29, 2008

Toxicological Sciences, doi:10.1093/toxsci/kfn044
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© The Author 2008. Published by Oxford University Press on behalf of the Society of Toxicology. All rights reserved. For Permissions, please email: journals.permissions@oxfordjournals.org

Khat (Catha edulis) induces reactive oxygen species and apoptosis in normal human oral keratinocytes and fibroblasts

Ochiba M. Lukandu*,{dagger}, Daniela E. Costea*, Evelyn Neppelberg{ddagger}, Anne C. Johannessen*,§ and Olav K. Vintermyr§,*

* Section for Pathology, The Gade Institute, University of Bergen, Bergen, Norway {dagger} Centre for International Health, University of Bergen, Bergen, Norway {ddagger} Department of Clinical Dentistry, University of Bergen, Bergen, Norway § Department of Pathology, The Gade Institute, Haukeland University Hospital, University of Bergen, Bergen, Norway

Corresponding author: Olav K. Vintermyr, Department of Pathology, The Gade Institute, Haukeland University Hospital, University of Bergen, N-5021 Bergen, Norway, E-mail: Olav.Vintermyr{at}helse-bergen.no, Fax: 4755973158, Tel: 4755973164

Received November 12, 2007; revision received February 26, 2008; accepted February 26, 2008


   Abstract

Khat chewing is widely practised in Eastern Africa and the Middle East. Khat is genotoxic to cells within the oral mucosa, and several studies have suggested an association between khat use and oral lesions like hyperkeratosis and oral cancer. This study investigated the mechanism of khat induced cytotoxicity using primary normal human oral keratinocytes (NOK) and fibroblasts (NOF). Khat induced rounding up of cells, plasma membrane blebbing and condensation of nuclear chromatin within 3-6 h of exposure. The cells also showed externalisation of phosphatidylserine and fragmentation of DNA. Morphological and biochemical features were compatible with cell death by apoptosis. Khat also induced an increase in cytosolic reactive oxygen species (ROS) and a depletion of intracellular glutathione (GSH) within 1 h of exposure. Antioxidants reduced ROS generation, GSH depletion and delayed the onset of cytotoxicity in both cell types. Generally, NOF cells were more sensitive to khat-induced cytotoxicity than NOK cells. These effects were elicited at concentrations of khat expected to occur in the oral cavity during khat chewing. In summary, khat induced apoptotic cell death in primary normal oral keratinocytes and fibroblasts by an early effect on mechanisms that regulate oxidative stress

Key Words: khat; oral keratinocytes; oral fibroblasts; reactive oxygen species; apoptosis.


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