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


     


Am J Physiol Endocrinol Metab (July 22, 2003). doi:10.1152/ajpendo.00238.2003
This Article
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
285/5/E1039    most recent
00238.2003v1
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 Google Scholar
Google Scholar
Right arrow Articles by Vazquez-Martinez, R.
Right arrow Articles by Malagon, M. M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Vazquez-Martinez, R.
Right arrow Articles by Malagon, M. M.
Submitted on May 23, 2003
Accepted on July 16, 2003

Melanotrope Secretory Cycle is Regulated by Physiological Inputs via the Hypothalamus

Rafael Vazquez-Martinez1, Justo P. Castano1, Marie Christine Tonon2, Hubert Vaudry2, Francisco Gracia-Navarro1, and Maria M. Malagon1*

1 Department of Cell Biology, University of Cordoba, Cordoba, Spain
2 European Institute for Peptide Research, Laboratory of Cellular and Molecular Neuroendocrinology, University of Rouen, Rouen, France

* To whom correspondence should be addressed. E-mail: bc1mapom{at}uco.es.

Previously, it has been shown that background color conditions regulate the overall activity of the frog intermediate lobe by varying the proportions of the two subtypes of melanotropes existing in the gland, the highly active or secretory melanotropes and hormone-storage melanotropes, depending on melanocyte-stimulating hormone ({alpha}-MSH) requirements. However, the factors and mechanisms underlying these background-induced changes are still unknown. In the present study, we investigated whether hypothalamic factors known to regulate melanotrope cell function can induce changes in vitro similar to those caused by background adaptation in vivo. We found that the inhibitors apomorphine (a dopamine receptor agonist) and NPY decreased the number of active melanotropes and increased simultaneously that of storage melanotropes. On the other hand, the stimulator TRH increased the number of active cells and concomitantly reduced that of storage cells. Inasmuch as none of these treatments modified the apoptotic and proliferation rates in melanotrope cells, it appears that these hypothalamic factors caused actual interconversions of cells from a subpopulation to its counterpart. When taken together, these findings suggest that the hypothalamus would control melanotrope activity not only through short-term regulation of hormone synthesis and release, but also through a long-term regulation of the secretory phenotype of these cells whereby the activity of the intermediate lobe would be adjusted to fulfill the hormonal requirements imposed by background conditions.







HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH
Visit Other APS Journals Online
Copyright © 2003 by the American Physiological Society.