Effects of substance P and its antagonist spantide on corticosterone secretion and cytosolic free calcium concentration of dispersed zona fasciculata-reticularis cells of the rat adrenal cortex

References

• Vinson G P, Hinson J P, Toth I E. The neuroendocrinology of the adrenal cortex. J Neuroendocrinol 1994; 6: 235–246
   PubMed Web of Science ®Google Scholar
• Toth I E, Hinson J P. Neuropeptides in the adrenal gland: distribution, localization of receptors, and effects on steroid hormone synthesis. Endocrine Res 1995; 21: 39–51
   PubMed Web of Science ®Google Scholar
• Malendowicz L K, Markowska A. Neuromedins and their involvement in the regulation of growth structure and function of the adrenal cortex. Histol Histopathol 1994; 9: 591–601
   PubMed Web of Science ®Google Scholar
• Maggio J E. Tachykinins. Annu Rev Neurosci 1988; 11: 13–28
   PubMed Web of Science ®Google Scholar
• Mazzocchi G, Malendowicz L K, Andreis P G, Meneghelli V, Markowska A, Belloni A S, Nussdorfer G G. Neuropeptide-K enhances glucocorticoid release by acting directly on the rat adrenal gland: the possible involvement of zona medullaris. Brain Res 1994; 661: 91–96
   PubMedGoogle Scholar
• Mazzocchi G, Malendowicz L K, Belloni A S, Nussdorfer G G. Adrenal medulla is involved in the aldosterone secretagogue effect of substance P. Peptides 1995; 16: 351–355
   PubMedGoogle Scholar
• Kodjo M K, Leboulenger F, Porcedda P, Lamacz M, Conlon J M, Pelletier G, Vaudry H. Evidence for the involvement of chromaffin cells in the stimulatory effect of tachykinins on corticosteroid secretion by the frog adrenal gland. Endocrinology 1995; 136: 3253–3259
   PubMed Web of Science ®Google Scholar
• Malendowicz L K, Warchol J B, Nussdorfer G G, Nowak M, Filipiak K. Effects of neurokinin-A on the rat hypothalamo-pituitary-adrenal axis. Endocrine Res 1995; 21: 757–767
   PubMed Web of Science ®Google Scholar
• Malendowicz L K, Nussdorfer G G, Warchol J B, Markowska A, Macchi C, Nowak K W, Butowska W. Effects of neuromedin-K on the rat hypothalamo-pituitary-adrenal axis. Neuropeptides 1995; 29: 337–341
   PubMedGoogle Scholar
• Neri G, Andreis P G, Nussdorfer G G. Effects of neuropeptide-Y and substance-P on the secretory activity of dispersed zona-glomerulosa cells of rat adrenal gland. Neuropeptides 1990; 17: 121–125
   PubMed Web of Science ®Google Scholar
• Yoshida T, Mio M, Tasaka K. Cortisol secretion induced by substance P from bovine adrenocortical cells and its inhibition by calmodulin inhibitors. Biochem Pharmacol 1992; 43: 513–517
   PubMedGoogle Scholar
• Hinson J P, Kapas S, Orford C D, Vinson G P. Vasoactive intestinal peptide stimulation of aldosterone secretion by the rat adrenal cortex may be mediated by the local release of catecholamines. J Endocrinol 1992; 133: 253–258
   PubMed Web of Science ®Google Scholar
• Hakanson R, Wang Z Y, Folkers K. Comparison of spantide-II and CP 96. 345 for blockade of tachykinin-evoked contractions of smooth muscle. Biochem Biophys Res Commun 1991; 178: 297–302
   PubMedGoogle Scholar
• Mason W T, Hoyland J, Rawling S R, Relf G T. Techniques and technology for dynamic video-imaging of cellular fluorescence. Methods in Neuroscience, vol. 3., P M Conn. Academic Press, San Diego 1990; pp 109–135
   Google Scholar
• Leboulenger F, Vaglini L, Conlon J M, Homo-Delarche F, Wang Y, Kerdelhue B, Pelletier G, Vaudry H. Immunohistochemical distribution biochemical characterization and biological action of tachykinins in the frog adrenal gland. Endocrinology 1993; 133: 1999–2008
   PubMed Web of Science ®Google Scholar
• Kocsis J F, Schimmel R J, MeIlroy P J, Carsia R V. Dissociation of increases in intracellular calcium and aldosterone production induced by angiotensin II (AH): evidence for regulation by distinct AII receptor subtypes or isomorphs. Endocrinology 1995; 136: 1626–1634
   Google Scholar
• Markowska A, Warchol J B, Neri G, Nussdorfer G G, Malendowicz L K. Effect of pneumadin (PNM) on the adrenal gland. 1. Evidence that PNM increases cytosolic free calcium concentration in dispersed rat adrenocortical cells without evoking a secretory response. Med Sci Res 1995; 23: 749–750
   Google Scholar
• Aguilera G, Harwood J P, Catt K J. Somatostatin modulates the effects of angiotensin II in adrenal glomerulosa zona. Nature 1981; 292: 262–263
   PubMed Web of Science ®Google Scholar
• Vinson G P, Whitehouse B J, Hinson J P. The Adrenal Cortex. Prentice Hall, Englewood Cliffs 1992; pp 65–139
   Google Scholar
• Garland A M, Grady E F, Payan D G, Bunnett N W. Mechanisms regulating the responsiveness of cells to substance P: cell-surface degradation of substance P and NK1 receptor endocytosis. Biomed Res 1994; 15((Suppl. 2))5–13
   Google Scholar
• Grady E F, Garland A M, Gamp P D, Lovett M, Payan D G, Bunnett N W. Delineation of the endocytic pathway of substance P and its seven-transmembrane domain NK1 receptor. Mol Biol Cell 1995; 6: 509–524
   Google Scholar
• Malendowicz L K, Macchi C, Nussdorfer G G, Warchol J B. Effects of bradykinin on the secretory activity of dispersed zona fasciculata/reticularis cells of the rat adrenal cortex. Biomed Res 1995; 16: 187–190
   Google Scholar
• Bucsics A, Saria A, Lembeck F. Substance P in the adrenal gland: origin and species distribution. Neuropeptides 1981; 1: 329–341
   Web of Science ®Google Scholar
• Basile S, Cheung N S, Livett B G. Chromatographic evidence for the presence of multiple tachykinins in the bovine adrenal medulla. J Neurochem 1992; 58: 1584–1586
   Google Scholar
• Cheung N S, Basile S, Livett B G. Identification of multiple tachykinins in bovine adrenal medulla using an improved chromatographic procedure. Neuropeptides 1993; 24: 91–97
   Google Scholar
• Kuramoto H, Kondo H, Fujita T. Substance P-like immunoreactivity in adrenal chromaffin cells and intra-adrenal nerve fibers of rats. Histochemistry 1985; 82: 507–512
   PubMedGoogle Scholar