Dopaminergic (DA) treatment of hyperprolactinemia caused by prolactin (Prl) secreting pituitary neoplasms is a striking example of successful medical management of human neoplasia. The treatment typically shrinks the tumor, reduces Prl levels and restores fertility. The cytoplasmic free calcium level has a critical role in regulating Prl secretion and that of other hormones. However, there is yet much to learn about how physiological agents like DA may regulate the cytoplasmic calcium concentration to control hormone secretion.
We aim to study calcium flux in normal and neoplastic pituitary cells under the direct influence of THREE agents with IMPORTANT effects on hormone secretion: DA, growth hormone releasing factor (GRF), and SOMATOSTATIN (SRIF). To satisfy these aims and expand our knowledge about the regulation of hormone secretion under normal and pathological conditions three important parameters of 45Ca2+ flux will be comprehensively analyzed. To study 1) 45Ca2+ uptake and 2) net flux at isotopic equilibrium, normal or neoplastic rat pituitary cells are dispersed into a single cell suspension and incubated in 45Ca2+ followed by rapid vacuum filtration and washing. Calcium flux as a function of 45Ca2+ specific activity is then calculated from the radioactivity within the cells trapped on each filter. The third parameter, 45Ca2+ efflux, is directly measured as the fractional loss from prelabeled cells using a perifusion apparatus. Regulation of calcium flux has been speculated to be the basis for DA control of Prl secretion yet this vital question has not been critically evaluated. We know that GRF is dependent in some manner on calcium to stimulate growth hormone secretion, but although important, specific details about this dependency are unknown. SRIF IS A NATURALLY OCCURRING PEPTIDE WHICH INHIBITS THE SECRETION OF GH, AS WELL AS MANY OTHER BIOLOGICALLY ACTIVE HORMONES. MODULATION OF CALCIUM FLUX BY SRIF HAS BEEN TENTATIVELY INFERRED AS ONE MECHANISM CONTRIBUTING TO ITS ACTION, BUT RIGOROUS INVESTIGATION IS LACKING. The preliminary studies are promising; the experiments are rationally organized; and the resources and environment suitable for the efficient execution of this three year program.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
1R01CA038228-01A2
Application #
3176312
Study Section
Biochemical Endocrinology Study Section (BCE)
Project Start
1985-12-01
Project End
1988-11-30
Budget Start
1985-12-01
Budget End
1986-11-30
Support Year
1
Fiscal Year
1986
Total Cost
Indirect Cost
Name
University of Virginia
Department
Type
Schools of Medicine
DUNS #
001910777
City
Charlottesville
State
VA
Country
United States
Zip Code
22904
Login, I S; Pal, S N; Adams, D T et al. (1998) Muscimol increases acetylcholine release by directly stimulating adult striatal cholinergic interneurons. Brain Res 779:33-40
Login, I S (1997) Carbachol inhibits basal and forskolin-evoked adult rat striatal acetylcholine release. Neuroreport 8:1863-6
Login, I S (1997) D2 dopamine receptor activation inhibits basal and forskolin-evoked acetylcholine release from dissociated striatal cholinergic interneurons. Brain Res 749:147-51
Login, I S; Harrison, M B (1996) A D1 dopamine agonist stimulates acetylcholine release from dissociated striatal cholinergic neurons. Brain Res 727:162-8
Login, I S; Hewlett, E L (1996) Adenylate cyclase in striatal cholinergic interneurons regulates acetylcholine release. Brain Res 735:330-4
Login, I S; Borland, K; Harrison, M B et al. (1995) Acetylcholine release from dissociated striatal cells. Brain Res 697:271-5
Login, I S; Borland, K; Harrison, M B (1995) Acute dopamine depletion potentiates independent stimulatory and inhibitory D1 DA receptor-mediated control of striatal acetylcholine release in vitro. Brain Res 681:209-12
Goger, M J; Login, I S; Fernandez, E J et al. (1994) 31P NMR investigation of energy metabolism in perifused MMQ cells. Magn Reson Med 32:584-91
Login, I S; Judd, A M; Kuan, S I et al. (1991) Role of calcium in dopaminergic regulation of TRH- and angiotensin II-stimulated prolactin release. Am J Physiol 260:E553-60
Kuan, S I; Login, I S; Judd, A M et al. (1990) A comparison of the concentration-dependent actions of thyrotropin-releasing hormone, angiotensin II, bradykinin, and Lys-bradykinin on cytosolic free calcium dynamics in rat anterior pituitary cells: selective effects of dopamine. Endocrinology 127:1841-8

Showing the most recent 10 out of 27 publications