| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
Endocrinology, Vol 131, 1936-1941, Copyright © 1992 by Endocrine Society
ARTICLES |
I Shibuya and WW Douglas
Department of Pharmacology, Yale University School of Medicine, New Haven, Connecticut 06510.
Cobalt (Co), nickel (Ni), manganese (Mn), cadmium (Cd), and lanthanum (La) are commonly used as calcium (Ca) channel blockers, but some of them, besides reducing Ca entry, also traverse Ca channels and can exert effects intracellularly that confound interpretation of functional responses. Because of this and our need to use Ca channel blockers in an ongoing analysis of Ca channel activity in the regulation of the cytosolic free Ca concentration ([Ca2+]i) and secretion in melanotrophs, we assessed whether the cations mentioned enter these cells. This was done by incorporating the fluorescence for changes that would signal the presence of the cations in the cytosol. In cell-free solution, where the probe and cations can interact freely, Mn, Co, and Ni all quench fluorescence, whereas Cd and La act in a Ca- like manner. When tested on fura-2-loaded melanotrophs in basal (unstimulated) conditions, Mn, Co, and Cd each yielded corresponding signals, thereby showing that they had penetrated the cells. By contrast, Ni caused no quenching of fluorescence even in melanotrophs exposed to 100 mM K+ to recruit additional Ca channels. Ni, therefore, did not penetrate the cells. However, as expected, Ni quenched fluorescence when given artificial access to the cytoplasm by ionomycin. Ni blocked spontaneous entry of Mn, Co, and Cd. It also lowered [Ca2+]i in unstimulated melanotrophs, consistent with blockade of spontaneous Ca entry. Like Ni, La lowered basal [Ca2+]i in unstimulated melanotrophs without penetrating the cells; however, unlike Ni, it penetrated when the melanotrophs were exposed to high potassium. We conclude that Ni is the most specific of the Ca channel blockers tested and that results obtained with Mn, Co, Cd, and La must be interpreted with reserve.
This article has been cited by other articles:
![]() |
B. L. Prosser, E. O. Hernández-Ochoa, D. B. Zimmer, and M. F. Schneider Simultaneous recording of intramembrane charge movement components and calcium release in wild-type and S100A1\#8722;/\#8722; muscle fibres J. Physiol., September 15, 2009; 587(18): 4543 - 4559. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Asai, K. Takeuchi, M. Saotome, T. Urushida, H. Katoh, H. Satoh, H. Hayashi, and H. Watanabe Extracellular acidosis suppresses endothelial function by inhibiting store-operated Ca2+ entry via non-selective cation channels Cardiovasc Res, July 1, 2009; 83(1): 97 - 105. [Abstract] [Full Text] [PDF] |
||||
![]() |
K. Girijashanker, L. He, M. Soleimani, J. M. Reed, H. Li, Z. Liu, B. Wang, T. P. Dalton, and D. W. Nebert Slc39a14 Gene Encodes ZIP14, A Metal/Bicarbonate Symporter: Similarities to the ZIP8 Transporter Mol. Pharmacol., May 1, 2008; 73(5): 1413 - 1423. [Abstract] [Full Text] [PDF] |
||||
![]() |
V. A Fitsanakis, G. Piccola, A. P. Marreilha dos Santos, J. L Aschner, and M. Aschner Putative proteins involved in manganese transport across the blood-brain barr 1ier Human and Experimental Toxicology, April 1, 2007; 26(4): 295 - 302. [Abstract] [PDF] |
||||
![]() |
F. Xu, J. Xu, F. W. Tse, and A. Tse Adenosine stimulates depolarization and rise in cytoplasmic [Ca2+] in type I cells of rat carotid bodies Am J Physiol Cell Physiol, June 1, 2006; 290(6): C1592 - C1598. [Abstract] [Full Text] [PDF] |
||||
![]() |
P.-M. Yang, S.-J. Chiu, and L.-Y. Lin Differential Effects of Salen and Manganese-Salen Complex (EUK-8) on the Regulation of Cellular Cadmium Uptake and Toxicity Toxicol. Sci., May 1, 2005; 85(1): 551 - 559. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. K. Monteilh-Zoller, M. C. Hermosura, M. J.S. Nadler, A. M. Scharenberg, R. Penner, and A. Fleig TRPM7 Provides an Ion Channel Mechanism for Cellular Entry of Trace Metal Ions J. Gen. Physiol., December 30, 2002; 121(1): 49 - 60. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. I. Ivanov and R. L. Calabrese Intracellular Ca2+ Dynamics During Spontaneous and Evoked Activity of Leech Heart Interneurons: Low-Threshold Ca Currents and Graded Synaptic Transmission J. Neurosci., July 1, 2000; 20(13): 4930 - 4943. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. Yanagiya, N. Imura, S. Enomoto, Y. Kondo, and S. Himeno Suppression of a High-Affinity Transport System for Manganese in Cadmium-Resistant Metallothionein-Null Cells J. Pharmacol. Exp. Ther., March 1, 2000; 292(3): 1080 - 1086. [Abstract] [Full Text] |
||||
![]() |
M. Wartenberg, H. Diedershagen, J. Hescheler, and H. Sauer Growth Stimulation Versus Induction of Cell Quiescence by Hydrogen Peroxide in Prostate Tumor Spheroids Is Encoded by the Duration of the Ca2+ Response J. Biol. Chem., September 24, 1999; 274(39): 27759 - 27767. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. B. McFarlane and W. F. Gilly State-Dependent Nickel Block of a High-Voltage-Activated Neuronal Calcium Channel J Neurophysiol, October 1, 1998; 80(4): 1678 - 1685. [Abstract] [Full Text] [PDF] |
||||
![]() |
J.-R. Nofer, M. Tepel, M. Walter, U. Seedorf, G. Assmann, and W. Zidek Phosphatidylcholine-specific Phospholipase C Regulates Thapsigargin-induced Calcium Influx in Human Lymphocytes J. Biol. Chem., December 26, 1997; 272(52): 32861 - 32868. [Abstract] [Full Text] [PDF] |
||||
![]() |
K. Tanaka, I. Shibuya, N. Harayama, M. Nomura, N. Kabashima, Y. Ueta, and H. Yamashita Pituitary Adenylate Cyclase-Activating Polypeptide Potentiation of Ca2+ Entry via Protein Kinase C and A Pathways in Melanotrophs of the Pituitary Pars Intermedia of Rats Endocrinology, October 1, 1997; 138(10): 4086 - 4095. [Abstract] [Full Text] [PDF] |
||||
![]() |
X.-J. Du, A. Bobik, P. J. Little, M. D. Esler, and A. M. Dart Role of Ca2+ in Metabolic Inhibition–Induced Norepinephrine Release in Rat Brain Synaptosomes Circ. Res., February 1, 1997; 80(2): 179 - 188. [Abstract] [Full Text] |
||||
![]() |
O. McGuinness, R. Moreton, M. Johnson, and M. Berridge A direct measurement of increased divalent cation influx in fertilised mouse oocytes Development, July 1, 1996; 122(7): 2199 - 2206. [Abstract] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
| Endocrinology | Endocrine Reviews | J. Clin. End. & Metab. |
| Molecular Endocrinology | Recent Prog. Horm. Res. | All Endocrine Journals |