J Physiol Wellcome Trust-funded researchers
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


J Physiol Vol 404 pp 557-573
Copyright © 1988 by The Physiological Society
This Article
Right arrow Full Text (PDF)
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 HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Byrne, N G
Right arrow Articles by Large, W A
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Byrne, N G
Right arrow Articles by Large, W A

Membrane ionic mechanisms activated by noradrenaline in cells isolated from the rabbit portal vein.

N G Byrne and W A Large

Department of Pharmacology, St George's Hospital Medical School, London.

1. Membrane currents were recorded in cells freshly dispersed from the rabbit portal vein with patch pipette techniques in the whole-cell configuration of recording. In potassium-containing solutions at a holding potential of -50 mV noradrenaline usually evoked an inward current and enhanced greatly the outward current evoked by depolarizing voltage steps. 2. The ionic mechanism of the inward current was investigated in potassium-free solutions in which the inward current elicited by noradrenaline was produced by an increase in membrane conductance. 3. In the first series of experiments NaCl was the main salt in the patch pipette solution (representing the intracellular milieu) and the ionic composition of the bathing solution was altered. In these conditions the reversal potential of the noradrenaline-induced current was close to the chloride equilibrium potential (ECl). 4. When sodium glutamate was the major salt in the pipette solution the reversal potential of the noradrenaline-evoked current was influenced by the cation rather than the anion gradient. 5. With 89 mM-BaCl2 in the external solution (and sodium glutamate in the pipette) noradrenaline produced a membrane current with a reversal potential which was much more positive than ECl or ENa. These results indicate that noradrenaline opens a chloride-selective channel and a cation channel which is permeable to monovalent and divalent cations. 6. Bath application of 10 mM-caffeine evoked a membrane current with a reversal potential close to ECl with either NaCl or sodium glutamate in the pipette. This is interpreted to mean that the increase in membrane chloride conductance can occur as a consequence of a rise in intracellular calcium concentration. It is less evident that the cation channel is calcium activated.




This article has been cited by other articles:


Home page
J. Physiol.Home page
A. P. Albert and W. A. Large
Signal transduction pathways and gating mechanisms of native TRP-like cation channels in vascular myocytes
J. Physiol., January 1, 2006; 570(1): 45 - 51.
[Abstract] [Full Text] [PDF]


Home page
J. Physiol.Home page
M Liu, A. P Albert, and W. A Large
Facilitatory effect of Ins(1,4,5)P3 on store-operated Ca2+-permeable cation channels in rabbit portal vein myocytes
J. Physiol., July 1, 2005; 566(1): 161 - 171.
[Abstract] [Full Text] [PDF]


Home page
J. Physiol.Home page
D. J. Beech, K. Muraki, and R. Flemming
Non-selective cationic channels of smooth muscle and the mammalian homologues of Drosophila TRP
J. Physiol., September 15, 2004; 559(3): 685 - 706.
[Abstract] [Full Text] [PDF]


Home page
CirculationHome page
S. Samii, M. H. Khan, D. A. MacLean, N. King, M. D. Herr, and L. I. Sinoway
Muscle Interstitial Calcium During Head-Up Tilt in Humans
Circulation, January 20, 2004; 109(2): 215 - 219.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Heart Circ. Physiol.Home page
R. P. Burt
Phasic contractions of the rat portal vein depend on intracellular Ca2+ release stimulated by depolarization
Am J Physiol Heart Circ Physiol, May 1, 2003; 284(5): H1808 - H1817.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
R. C. Elble, G. Ji, K. Nehrke, J. DeBiasio, P. D. Kingsley, M. I. Kotlikoff, and B. U. Pauli
Molecular and Functional Characterization of a Murine Calcium-activated Chloride Channel Expressed in Smooth Muscle
J. Biol. Chem., May 17, 2002; 277(21): 18586 - 18591.
[Abstract] [Full Text] [PDF]


Home page
Physiol. Rev.Home page
T. J. Jentsch, V. Stein, F. Weinreich, and A. A. Zdebik
Molecular Structure and Physiological Function of Chloride Channels
Physiol Rev, April 1, 2002; 82(2): 503 - 568.
[Abstract] [Full Text] [PDF]


Home page
Circ. Res.Home page
R. Inoue, T. Okada, H. Onoue, Y. Hara, S. Shimizu, S. Naitoh, Y. Ito, and Y. Mori
The Transient Receptor Potential Protein Homologue TRP6 Is the Essential Component of Vascular {{alpha}}1-Adrenoceptor-Activated Ca2+-Permeable Cation Channel
Circ. Res., February 16, 2001; 88(3): 325 - 332.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Heart Circ. Physiol.Home page
J. E. Graves, I. A. Greenwood, and W. A. Large
Tonic regulation of vascular tone by nitric oxide and chloride ions in rat isolated small coronary arteries
Am J Physiol Heart Circ Physiol, December 1, 2000; 279(6): H2604 - H2611.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Respir. Cell Mol. Bio.Home page
H. Oonuma, T. Nakajima, T. Nagata, K. Iwasawa, Y. Wang, H. Hazama, Y. Morita, Y. Wang, K. Yamamoto, R. Nagai, et al.
Endothelin-1 Is a Potent Activator of Nonselective Cation Currents in Human Bronchial Smooth Muscle Cells
Am. J. Respir. Cell Mol. Biol., August 1, 2000; 23(2): 213 - 221.
[Abstract] [Full Text]


Home page
Am. J. Physiol. Heart Circ. Physiol.Home page
F. S. Lamb and T. J. Barna
Endothelium modulates anion channel-dependent aortic contractions to iodide
Am J Physiol Heart Circ Physiol, May 1, 2000; 278(5): H1527 - H1536.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Cell Physiol.Home page
J. H. Jaggar, V. A. Porter, W. J. Lederer, and M. T. Nelson
Calcium sparks in smooth muscle
Am J Physiol Cell Physiol, February 1, 2000; 278(2): C235 - C256.
[Abstract] [Full Text] [PDF]


Home page
Physiol. Rev.Home page
H. KURIYAMA, K. KITAMURA, T. ITOH, and R. INOUE
Physiological Features of Visceral Smooth Muscle Cells, With Special Reference to Receptors and Ion Channels
Physiol Rev, July 1, 1998; 78(3): 811 - 920.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Heart Circ. Physiol.Home page
F. S. Lamb and T. J. Barna
Chloride ion currents contribute functionally to norepinephrine-induced vascular contraction
Am J Physiol Heart Circ Physiol, July 1, 1998; 275(1): H151 - H160.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Heart Circ. Physiol.Home page
D. G. Welsh and S. S. Segal
Endothelial and smooth muscle cell conduction in arterioles controlling blood flow
Am J Physiol Heart Circ Physiol, January 1, 1998; 274(1): H178 - H186.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Heart Circ. Physiol.Home page
J. Xia and B. R. Duling
Patterns of excitation-contraction coupling in arterioles: dependence on time and concentration
Am J Physiol Heart Circ Physiol, January 1, 1998; 274(1): H323 - H330.
[Abstract] [Full Text] [PDF]


Home page
Circ. Res.Home page
C. H. Gelband and J. R. Hume
[Ca2+]i Inhibition of K+ Channels in Canine Renal Artery : Novel Mechanism for Agonist-Induced Membrane Depolarization
Circ. Res., July 1, 1995; 77(1): 121 - 130.
[Abstract] [Full Text]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 1988 The Physiological Society.