Norepinephrine causes a biphasic change in mammalian pinealocye membrane potential: role of alpha1B-adrenoreceptors, phospholipase C, and Ca2+
Language English Country United States Media print-electronic
Document type Journal Article, Research Support, N.I.H., Intramural, Research Support, Non-U.S. Gov't
Grant support
Intramural NIH HHS - United States
PubMed
21828176
PubMed Central
PMC3176642
DOI
10.1210/en.2011-1180
PII: en.2011-1180
Knihovny.cz E-resources
- MeSH
- Receptors, Adrenergic, alpha-1 physiology MeSH
- Pineal Gland cytology drug effects physiology MeSH
- Type C Phospholipases physiology MeSH
- Rats MeSH
- Membrane Potentials drug effects MeSH
- Norepinephrine pharmacology MeSH
- Rats, Sprague-Dawley MeSH
- Calcium metabolism MeSH
- Animals MeSH
- Check Tag
- Rats MeSH
- Male MeSH
- Female MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Research Support, N.I.H., Intramural MeSH
- Names of Substances
- Receptors, Adrenergic, alpha-1 MeSH
- Type C Phospholipases MeSH
- Norepinephrine MeSH
- Calcium MeSH
Perforated patch clamp recording was used to study the control of membrane potential (V(m)) and spontaneous electrical activity in the rat pinealocyte by norepinephrine. Norepinephrine did not alter spiking frequency. However, it was found to act through α(1B)-adrenoreceptors in a concentration-dependent manner (0.1-10 μM) to produce a biphasic change in V(m). The initial response was a hyperpolarization (∼13 mV from a resting potential of -46 mV) due to a transient (∼5 sec) outward K(+) current (∼50 pA). This current appears to be triggered by Ca(2+) released from intracellular stores, based on the observation that it was also seen in cells bathed in Ca(2+)-deficient medium. In addition, pharmacological studies indicate that this current was dependent on phospholipase C (PLC) activation and was in part mediated by bicuculline methiodide and apamin-sensitive Ca(2+)-controlled K(+) channels. The initial transient hyperpolarization was followed by a sustained depolarization (∼4 mV) due to an inward current (∼10 pA). This response was dependent on PLC-dependent activation of Na(+)/Ca(2+) influx but did not involve nifedipine-sensitive voltage-gated Ca(2+) channels. Together, these results indicate for the first time that activation of α(1B)-adrenoreceptors initiates a PLC-dependent biphasic change in pinealocyte V(m) characterized by an initial transient hyperpolarization mediated by a mixture of Ca(2+)-activated K(+) channels followed by a sustained depolarization mediated by a Ca(2+)-conducting nonselective cation channel. These observations indicate that both continuous elevation of intracellular Ca(2+) and sustained depolarization at approximately -40 mV are associated with and are likely to be required for activation of the pinealocyte.
See more in PubMed
Harrison NL, Zatz M. 1989. Voltage-dependent calcium channels regulate melatonin output from cultured chick pineal cells. J Neurosci 9:2462–2467 PubMed PMC
Reuss S, Vollrath L. 1984. Electrophysiological properties of rat pinealocytes: evidence for circadian and ultradian rhythms. Exp Brain Res 55:455–461 PubMed
Klein DC. 1985. Photoneural regulation of the mammalian pineal gland. Ciba Found Symp 117:38–56 PubMed
Klein DC. 2007. Arylalkylamine N-acetyltransferase: “the Timezyme.” J Biol Chem 282:4233–4237 PubMed
Kappers JA. 1960. The development, topographical relations and innervation of the epiphysis cerebri in the albino rat. Z Zellforsch Mikrosk Anat 52:163–215 PubMed
Sugden LA, Sugden D, Klein DC. 1987. α 1-adrenoceptor activation elevates cytosolic calcium in rat pinealocytes by increasing net influx. J Biol Chem 262:741–745 PubMed
Bailey MJ, Coon SL, Carter DA, Humphries A, Kim JS, Shi Q, Gaildrat P, Morin F, Ganguly S, Hogenesch JB, Weller JL, Rath MF, Møller M, Baler R, Sugden D, Rangel ZG, Munson PJ, Klein DC. 2009. Night/day changes in pineal expression of >600 genes: central role of adrenergic/cAMP signaling. J Biol Chem 284:7606–7622 PubMed PMC
Vanecek J, Sugden D, Weller J, Klein DC. 1985. Atypical synergistic α 1- and β-adrenergic regulation of adenosine 3′,5′-monophosphate and guanosine 3′,5′-monophosphate in rat pinealocytes. Endocrinology 116:2167–2173 PubMed
Berg GR, Klein DC. 1972. Norepinephrine increases the (32P)labelling of a specific phospholipid frac tion of post-synaptic pineal membranes. J Neurochem 19:2519–2532 PubMed
Sugden D, Vanecek J, Klein DC, Thomas TP, Anderson WB. 1985. Activation of protein kinase C potentiates isoprenaline-induced cyclic AMP accumulation in rat pinealocytes. Nature 314:359–361 PubMed
Ho AK, Chik CL, Klein DC. 1988. Permissive role of calcium in α 1-adrenergic stimulation of pineal phosphatidylinositol phosphodiesterase (phospholipase C) activity. J Pineal Res 5:553–564 PubMed
Ho AK, Klein DC. 1987. Activation of α 1-adrenoceptors, protein kinase C, or treatment with intracellular free Ca2+ elevating agents increases pineal phospholipase A2 activity. Evidence that protein kinase C may participate in Ca2+-dependent α 1-adrenergic stimulation of pineal phospholipase A2 activity. J Biol Chem 262:11764–11770 PubMed
Klein D, Weller JL. 1973. Adrenergic-adenosine 3′,5′-monophosphate regulation of serotonin N-acetyltransferase activity and the temporal relationship of serotonin N-acetyltransferase activity synthesis of 3H-N-acetylserotonin and 3H-melatonin in the cultured rat pineal gland. J Pharmacol Exp Ther 186:516–527 PubMed
Yu L, Schaad NC, Klein DC. 1993. Calcium potentiates cyclic AMP stimulation of pineal arylalkylamine N-acetyltransferase. J Neurochem 60:1436–1443 PubMed
Schaad NC, Parfitt A, Russell JT, Schaffner AE, Korf HW, Klein DC. 1993. Single-cell [Ca2+]i analysis and biochemical characterization of pinealocytes immobilized with novel attachment peptide preparation. Brain Res 614:251–256 PubMed
Darvish N, Russell JT. 1998. Neurotransmitter-induced novel modulation of a nonselective cation channel by a cAMP-dependent mechanism in rat pineal cells. J Neurophysiol 79:2546–2556 PubMed
Henderson D, Dryer SE. 1992. Voltage- and Ca(2+)-activated ionic currents in acutely dissociated cells of the chick pineal gland. Brain Res 572:182–189 PubMed
Afeche SC, Barbosa R, Scialfa JH, Terra IM, Cassola AC, Cipolla-Neto J. 2006. Effects of the blockade of high voltage-activated calcium channels on in vitro pineal melatonin synthesis. Cell Biochem Funct 24:499–505 PubMed
Castellano A, López-Barneo J, Armstrong CM. 1989. Potassium currents in dissociated cells of the rat pineal gland. Pflugers Arch 413:644–650 PubMed
Chik CL, Li B, Karpinski E, Ho AK. 1999. Regulation of the L-type Ca2+ channel current in rat pinealocytes: role of basal phosphorylation. J Neurochem 72:73–80 PubMed
Ceña V, Halperin JI, Yeandle S, Klein DC. 1991. Norepinephrine stimulates potassium efflux from pinealocytes: evidence for involvement of biochemical “AND” gate operated by calcium and adenosine 3′,5′-monophosphate. Endocrinology 128:559–569 PubMed
Reuss S, Semm P, Vollrath L. 1985. Changes in the electrical activity of the rat pineal gland following stimulation of the cervical sympathetic ganglia. J Auton Nerv Syst 12:281–288 PubMed
Semm P, Demaine C, Vollrath L. 1981. Electrical responses of pineal cells to melatonin and putative transmitters. Evidence for circadian changes in sensitivity. Exp Brain Res 43:361–370 PubMed
Schenda J, Vollrath L. 1998. Demonstration of action-potential-producing cells in the rat pineal gland in vitro and their regulation by norepinephrine and nitric oxide. J Comp Physiol A 183:573–581 PubMed
Schenda J, Vollrath L. 1999. An intrinsic neuronal-like network in the rat pineal gland. Brain Res 823:231–233 PubMed
Stojilkovic SS, Tabak J, Bertram R. 2010. Ion channels and signaling in the pituitary gland. Endocr Rev 31:845–915 PubMed PMC
Freschi JE, Parfitt AG. 1986. Intracellular recordings from pineal cells in tissue culture: membrane properties and response to norepinephrine. Brain Res 368:366–370 PubMed
Parfitt A, Weller JL, Klein DC, Sakai KK, Marks BH. 1975. Blockade by ouabain or elevated potassium ion concentration of the adrenergic and adenosine cyclic 3′,5′-monophosphate-induced stimulation of pineal serotonin N-acetyltransferase activity. Mol Pharmacol 11:241–255 PubMed
Sakai KK, Marks BH. 1972. Adrenergic effects on pineal cell membrane potential. Life Sci I 11:285–291 PubMed
Horn R, Marty A. 1988. Muscarinic activation of ionic currents measured by a new whole-cell recording method. J Gen Physiol 92:145–159 PubMed PMC
Schomerus C, Laedtke E, Korf HW. 1995. Calcium responses of isolated, immunocytochemically identified rat pinealocytes to noradrenergic, cholinergic and vasopressinergic stimulations. Neurochem Int 27:163–175 PubMed
Berridge MJ. 2009. Inositol trisphosphate and calcium signalling mechanisms. Biochim Biophys Acta 1793:933–940 PubMed
Lee SY, Choi BH, Hur EM, Lee JH, Lee SJ, Lee CO, Kim KT. 2006. Norepinephrine activates store-operated Ca2+ entry coupled to large-conductance Ca2+-activated K+ channels in rat pinealocytes. Am J Physiol Cell Physiol 290:C1060–C1066 PubMed
Letz B, Schomerus C, Maronde E, Korf HW, Korbmacher C. 1997. Stimulation of a nicotinic ACh receptor causes depolarization and activation of L-type Ca2+ channels in rat pinealocytes. J Physiol 499(Pt 2):329–340 PubMed PMC
Chik CL, Liu QY, Li B, Klein DC, Zylka M, Kim DS, Chin H, Karpinski E, Ho AK. 1997. α 1D L-type Ca(2+)-channel currents: inhibition by a β-adrenergic agonist and pituitary adenylate cyclase-activating polypeptide (PACAP) in rat pinealocytes. J Neurochem 68:1078–1087 PubMed
Chin H, Smith MA, Kim HL, Kim H. 1992. Expression of dihydropyridine-sensitive brain calcium channels in the rat central nervous system. FEBS Lett 299:69–74 PubMed
Chik CL, Liu QY, Li B, Karpinski E, Ho AK. 1995. cGMP inhibits L-type Ca2+ channel currents through protein phosphorylation in rat pinealocytes. J Neurosci 15:3104–3109 PubMed PMC
Poling JS, Karanian JW, Salem N, Jr, Vicini S. 1995. Time- and voltage-dependent block of delayed rectifier potassium channels by docosahexaenoic acid. Mol Pharmacol 47:381–390 PubMed
Kucka M, Kretschmannova K, Murano T, Wu CP, Zemkova H, Ambudkar SV, Stojilkovic SS. 2010. Dependence of multidrug resistance protein-mediated cyclic nucleotide efflux on the background sodium conductance. Mol Pharmacol 77:270–279 PubMed PMC
Sankaranarayanan S, Simasko SM. 1996. A role for a background sodium current in spontaneous action potentials and secretion from rat lactotrophs. Am J Physiol 271:C1927–C1934 PubMed
Schaad NC, Vanecek J, Rodriguez IR, Klein DC, Holtzclaw L, Russell JT. 1995. Vasoactive intestinal peptide elevates pinealocyte intracellular calcium concentrations by enhancing influx: evidence for involvement of a cyclic GMP-dependent mechanism. Mol Pharmacol 47:923–933 PubMed
Yue C, Yaari Y. 2004. KCNQ/M channels control spike afterdepolarization and burst generation in hippocampal neurons. J Neurosci 24:4614–4624 PubMed PMC
Putney JW. 2009. Capacitative calcium entry: from concept to molecules. Immunol Rev 231:10–22 PubMed
Smyth JT, Hwang SY, Tomita T, DeHaven WI, Mercer JC, Putney JW. 2010. Activation and regulation of store-operated calcium entry. J Cell Mol Med 14:2337–2349 PubMed PMC
Clapham DE, Julius D, Montell C, Schultz G. 2005. International union of pharmacology. XLIX. Nomenclature and structure-function relationships of transient receptor potential channels. Pharmacol Rev 57:427–450 PubMed
Sáez JC, Berthoud VM, Kadle R, Traub O, Nicholson BJ, Bennett MV, Dermietzel R. 1991. Pinealocytes in rats: connexin identification and increase in coupling caused by norepinephrine. Brain Res 568:265–275 PubMed
Parkington HC, McCance I, Coleman HA. 1987. Two types of cells with central innervation in pineal gland of guinea pigs. Am J Physiol 252:C369–C377 PubMed
Ceña V, González-García C, Svoboda P, Weller JL, Klein DC. 1987. Developmental study of ouabain inhibition of adrenergic induction of rat pineal serotonin N-acetyltransferase (EC 2.3.1.87). J Biol Chem 262:14467–14471 PubMed
Stojilkovic SS, Zemkova H, Van Goor F. 2005. Biophysical basis of pituitary cell type-specific Ca2+ signaling-secretion coupling. Trends Endocrinol Metab 16:152–159 PubMed