AJP - Lung Fuel your research with LabChart
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Am J Physiol Lung Cell Mol Physiol 290: L1202-L1209, 2006. First published January 13, 2006; doi:10.1152/ajplung.00371.2005
1040-0605/06 $8.00
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
290/6/L1202    most recent
00371.2005v1
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 Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via ISI Web of Science (2)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Sarafian, T. A.
Right arrow Articles by Roth, M. D.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Sarafian, T. A.
Right arrow Articles by Roth, M. D.

Inhaled marijuana smoke disrupts mitochondrial energetics in pulmonary epithelial cells in vivo

Theodore A. Sarafian,1 Nancy Habib,1 Michael Oldham,3 Navindra Seeram,2 Ru-Po Lee,2 Laura Lin,1 Donald P. Tashkin,1 and Michael D. Roth1

1Division of Pulmonary and Critical Care and 2Center for Human Nutrition, Department of Medicine, David Geffen School of Medicine at UCLA, Los Angeles; and 3Department of Community and Environmental Medicine, University of California, Irvine, California

Submitted 24 August 2005 ; accepted in final form 6 January 2006

Habitual marijuana smoking is associated with inflammation and atypia of airway epithelium accompanied by symptoms of chronic bronchitis. We hypothesized that {Delta}9-tetrahydrocannabinol (THC), the primary psychoactive component of marijuana, might contribute to these findings by impairing cellular energetics and mitochondrial function. To test this hypothesis, we examined particulate smoke extracts from marijuana cigarettes, tobacco cigarettes, and placebo marijuana (0% THC) cigarettes for their effects on the mitochondrial function of A549 cells in vitro. Only extracts prepared from marijuana cigarettes altered mitochondrial staining by the potentiometric probe JC-1. With the use of a cross-flow, nose-only inhalation system, rats were then exposed for 20 min to whole marijuana smoke and examined for its effects on airway epithelial cells. Inhalation of marijuana smoke produced lung tissue concentrations of THC that were 8–10 times higher than those measured in blood (75 ± 38 ng/g wet wt tissue vs. 9.2 ± 2.0 ng/ml), suggesting high local exposure. Intratracheal infusion of JC-1 immediately following marijuana smoke exposure revealed a diffuse decrease in lung cell JC-1 red fluorescence compared with tissue from unexposed or placebo smoke-exposed rats. Exposure to marijuana smoke in vivo also decreased JC-1 red fluorescence (54% decrease, P < 0.01) and ATP levels (75% decrease, P < 0.01) in single-cell preparations of tracheal epithelial cells. These results suggest that inhalation of marijuana smoke has deleterious effects on airway epithelial cell energetics that may contribute to the adverse pulmonary consequences of marijuana smoking.

{Delta}9-tetrahydrocannabinol; JC-1; A549; adenosine 5'-triphosphate



Address for reprint requests and other correspondence: T. Sarafian, 37-131 Center for Health Sciences, Division of Pulmonary and Critical Care, Dept. of Medicine, David Geffen School of Medicine at UCLA, Los Angeles, CA 90095-1690 (e-mail: tsarafian{at}mednet.ucla.edu)




This article has been cited by other articles:


Home page
Eur Respir JHome page
A. S. Reece
Cannabis and lung cancer
Eur. Respir. J., July 1, 2008; 32(1): 238 - 239.
[Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Visit Other APS Journals Online
Copyright © 2006 by the American Physiological Society.