SAGE Journals Online
Advertisement
Sign In to gain access to subscriptions and/or personal tools.

 

Advanced Search

Journal Navigation

Journal Home

Subscriptions

Archive

Contact Us

Table of Contents

Advertisement

Sign In to gain access to subscriptions and/or personal tools.
Journal of Psychopharmacology
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 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 Zarrindast, M.R.
Right arrow Articles by Heidari, M.R.
Right arrow Search for Related Content
PubMed
Right arrow Articles by Zarrindast, M.R.
Right arrow Articles by Heidari, M.R.
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?

Involvement of adenosine receptors in mouse thermoregulation

M.R. Zarrindast

Department of Pharmacology, School of Medicine, University of Tehran, P.O. Box 13145-784, Tehran, Iran

M.R. Heidari

Department of Pharmacology, School of Medicine, University of Tehran, P.O. Box 13145-784, Tehran, Iran

The effects of the activation of adenosine receptors on core body temperature of mice have been studied in the present investigation. Intraperitoneal (i.p.) injection of non-selective adenosine agonists 5'-N ethyl- carboxamide adenosine (NECA; 0.001, 0.01 and 0.05 mg/kg), R-(N6-phenylisopropyl)-adenosine (R-PIA; 0.01, 0.1 and 0.25 mg/kg) and selective A1 adenosine agonist N6-cyclohexyladenosine (CHA; 0.1, 0.25 and 0.4 mg/kg) reduced core body temperature. However, R-PIA and CHA were less potent than NECA in reducing the core body temperature. Theophylline (12.5, 25 and 50 mg/kg) blocked the hypothermia of the adenosine agonists. Pre-treatment of animals with selective A1 adenosine antagonist 8-phenyltheophylline (8-PT; 0.5, 1 and 2 mg/kg) decreased the hypothermic response of CHA but not of NECA and R-PIA. 8-PT potentiated the hypothermia induced by R-PIA. These results suggest that activation of both A1 and A2 adenosine receptors decreases core body temperature in mice.

Key Words: adenosine agonists and antagonists • body temperature • mice

Journal of Psychopharmacology, Vol. 7, No. 4, 365-370 (1993)
DOI: 10.1177/026988119300700408


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
J PsychopharmacolHome page
M.R. Zarrindast, A. Vahedy, M.R. Heidari, and M. Ghazi Khansari
On the mechanism(s) of morphine-induced hypothermia
J Psychopharmacol, January 1, 1994; 8(4): 222 - 226.
[Abstract] [PDF]



Advertisement