Note to users. If you're seeing this message, it means that your browser cannot find this page's style/presentation instructions -- or possibly that you are using a browser that does not support current Web standards. Find out more about why this message is appearing, and what you can do to make your experience of our site the best it can be.


Science 21 April 1978:
Vol. 200. no. 4339, pp. 312 - 314
DOI: 10.1126/science.635586

Articles

Science, Vol 200, Issue 4339, 312-314
Copyright © 1978 by American Association for the Advancement of Science


articles

delta9-Tetrahydrocannabinol and 17beta-estradiol bind to different macromolecules in estrogen target tissues

AB Okey and GP Bondy

delta9-Tetrahydrocannabinol (delta9-THC), added to the limit of its solubility, did not compete with tritiated 17beta-estradiol for binding to estrogen receptor sites in mouse mammary or uterine cytosols. On sucrose density gradients of low-ionic strength, mammary cytosol labeled with [3H]estradiol exhibited a binding peak near the "8S" region typical of estrogen receptor whereas in cytosol labeled with delta9-[3H]THC binding was limited to the nonspecific 4- to 5S region. Differences in sedimentation properties and reciprocal competition studies strongly refute previous claims that delta-9-THC binds to estrogen receptor and that by so doing it directly acts as an estrogen.


THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES:
An Aryl Hydrocarbon Receptor Odyssey to the Shores of Toxicology: The Deichmann Lecture, International Congress of Toxicology-XI.
A. B. Okey (2007)
Toxicol. Sci. 98, 5-38
   Abstract »    Full Text »    PDF »



To Advertise     Find Products


Science. ISSN 0036-8075 (print), 1095-9203 (online)