AJP - Regu Fuel your research with LabChart
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH
 QUICK SEARCH:   [advanced]


     


Am J Physiol Regul Integr Comp Physiol (January 26, 2006). doi:10.1152/ajpregu.00043.2005
This Article
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
290/6/R1736    most recent
00043.2005v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
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 Google Scholar
Google Scholar
Right arrow Articles by Tsushima, H.
Right arrow Articles by Mori, M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Tsushima, H.
Right arrow Articles by Mori, M.
Submitted on January 21, 2005
Accepted on January 23, 2006

Antidipsogenic effects of a TRPV4 agonist, 4{alpha}-phorbol 12, 13-didecanoate, injected into the cerebroventricle

Hiromi Tsushima1* and Mayumi Mori1

1 Cellular and Molecular Pharmacology, Nagoya City University Graduate School of Medical Sciences, Nagoya, Aichi, Japan

* To whom correspondence should be addressed. E-mail: tsushima{at}kinjo-u.ac.jp.

Transient receptor potential vanilloid 4 (TRPV4) is one member of the TRP superfamily of non-selective cation channels. Recently, the possibility has been raised that TRPV4 is an osmoreceptor, because it is found in the circumventricular organs where osmoreceptors are supposed to be distributed, and because it is sensitive to osmotic pressure in in vitro experiments. In addition, TRPV4 knockout mice have abnormal osmosensitivity. In this study, effects of 4{alpha}-phorbol 12, 13-didecanoate (4{alpha}-PDD), a TRPV4 agonist, on drinking behavior were examined to investigate roles for TRPV4 as an osmoreceptor in vivo in wild-type animals. Intracerebroventricular injections of 4{alpha}-PDD inhibited water intake under normal conditions in both light and dark periods of the day, after food deprivation, and after administration of angiotensin II. However, this drug did not influence increased water intake after administration of a hypertonic solution or after water deprivation that significantly increased plasma osmolality. Locomotor activity of the 4{alpha}-PDD-injected group decreased slightly compared with that of the vehicle-injected group; however, sweet taste, food intake, and body temperature were not different between the two groups. The antidipsogenic effects of 4{alpha}-PDD were blocked by pre-injection into the ventricle of TRPV4 antagonists such as ruthenium red or gadolinium. These findings suggest that TRPV4 regulates drinking behavior under certain conditions, and the regulation interacts with the angiotensin II pathway.




This article has been cited by other articles:


Home page
Am. J. Physiol. Regul. Integr. Comp. Physiol.Home page
A. C. Taylor, J. J. McCarthy, and S. D. Stocker
Mice lacking the transient receptor vanilloid potential 1 channel display normal thirst responses and central Fos activation to hypernatremia
Am J Physiol Regulatory Integrative Comp Physiol, April 1, 2008; 294(4): R1285 - R1293.
[Abstract] [Full Text] [PDF]


Home page
Exp PhysiolHome page
W. Liedtke
Hydromineral Neuroendocrinology: Role of TRPV ion channels in sensory transduction of osmotic stimuli in mammals
Exp Physiol, May 1, 2007; 92(3): 507 - 512.
[Abstract] [Full Text] [PDF]




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