Patch clamp technique and biophysical study of membrane channels

1986 ◽  
Vol 42 (6) ◽  
pp. 589-594 ◽  
Author(s):  
F. Franciolini
Keyword(s):  
Patch Clamp ◽  
Membrane Channels ◽  
Patch Clamp Technique ◽  
Clamp Technique ◽  
Biophysical Study

Ketamine blocks Ca2+-activated K+ channels in rabbit cerebral arterial smooth muscle cells

2003 ◽  
Vol 285 (3) ◽  
pp. H1347-H1355 ◽  
Author(s):  
Jin Han ◽  
Nari Kim ◽  
Hyun Joo ◽  
Euiyong Kim
Keyword(s):  
Smooth Muscle ◽  
Patch Clamp ◽  
Smooth Muscle Cells ◽  
Cerebral Arteries ◽  
Muscle Cells ◽  
Channel Activity ◽  
Patch Clamp Technique ◽  
Arterial Smooth Muscle ◽  
Clamp Technique ◽  
Arterial Smooth Muscle Cells

Although ketamine and Ca2+-activated K+ (KCa) channels have been implicated in the contractile activity regulation of cerebral arteries, no studies have addressed the specific interactions between ketamine and the KCa channels in cerebral arteries. The purpose of this study was to examine the direct effects of ketamine on KCa channel activities using the patch-clamp technique in single-cell preparations of rabbit middle cerebral arterial smooth muscle. We tested the hypothesis that ketamine modulates the KCa channel activity of the cerebral arterial smooth muscle cells of the rabbit. Vascular myocytes were isolated from rabbit middle cerebral arteries using enzymatic dissociation. Single KCa channel activities of smooth muscle cells from rabbit cerebral arteries were recorded using the patch-clamp technique. In the inside-out patches, ketamine in the micromolar range inhibited channel activity with a half-maximal inhibition of the ketamine conentration value of 83.8 ± 12.9 μM. The Hill coefficient was 1.2 ± 0.3. The slope conductance of the current-voltage relationship was 320.1 ± 2.0 pS between 0 and +60 mV in the presence of ketamine and symmetrical 145 mM K+. Ketamine had little effect on either the voltage-dependency or open- and closed-time histograms of KCa channel. The present study clearly demonstrates that ketamine inhibits KCa channel activities in rabbit middle cerebral arterial smooth muscle cells. This inhibition of KCa channels may represent a mechanism for ketamine-induced cerebral vasoconstriction.

Patch-clamp technique

1995 ◽  
pp. 527-555 ◽  
Author(s):  
Oscar Moran
Keyword(s):  
Patch Clamp ◽  
Patch Clamp Technique ◽  
Clamp Technique

Patch Clamp Technique and Applications

2017 ◽  
pp. 49-64
Author(s):  
Chao-Yin Chen
Keyword(s):  
Patch Clamp ◽  
Patch Clamp Technique ◽  
Clamp Technique

Patch-Clamp Technique

2008 ◽  
pp. 2268-2268
Keyword(s):  
Patch Clamp ◽  
Patch Clamp Technique ◽  
Clamp Technique

Molecular mechanisms of action for CFTR potentiators

2019 ◽  
Author(s):  
◽  
Han-I Yeh
Keyword(s):  
Cystic Fibrosis ◽  
Patch Clamp ◽  
Binding Site ◽  
Molecular Mechanisms ◽  
Mechanisms Of Action ◽  
Drug Binding ◽  
Patch Clamp Technique ◽  
Chemical Structures ◽  
Clamp Technique ◽  
Sites Of Action

[ACCESS RESTRICTED TO THE UNIVERSITY OF MISSOURI AT REQUEST OF AUTHOR.] As the culprit behind cystic fibrosis (CF) is the dysfunction of the chloride channel cystic fibrosis transmembrane conductance regulator (CFTR), pharmacological reagents targeting CFTR may hold the key to the ultimate cure of CF. In this thesis, we present the studies in the mechanisms of action for CFTR potentiators, the small molecules that enhance the functions of CFTR. Using the patch-clamp technique, we demonstrated that the permeant anion nitrate modulates CFTR gating through a mechanism similar to the FDA-approved CFTR potentiator VX-770 (ivacaftor). Via separate sites of action, VX-770 and nitrate stabilize the open channel conformation of CFTR in an energetically additive manner. Next, we investigated the action of a novel CFTR potentiator, GLPG1837, and showed that despite their different chemical structures, GLPG1837 and VX-770 share the same mechanisms of action on CFTR gating and compete for a common binding site in the transmembrane domains of CFTR. An allosteric modulation model is further proposed to explain how the affinity and efficacy of both potentiators are determined by the energetic coupling between drug binding and channel gating. Finally, we combined molecular docking and patch-clamp technique to identify the binding site(s) for GLPG1837 and VX-770.

Understanding Control of Exocytotic Secretion in Single Adenohypophysial Cells

Physiology ◽  
1994 ◽  
Vol 9 (5) ◽  
pp. 219-223
Author(s):  
Robert Zorec ◽  
G. Zupančič ◽  
M. Rupnik ◽  
L. Kocmur ◽  
S. Grilc ◽  
...  
Keyword(s):  
Patch Clamp ◽  
Cellular Level ◽  
Membrane Capacitance ◽  
Secretory Cells ◽  
Patch Clamp Technique ◽  
Clamp Technique ◽  
Stimulus Secretion Coupling ◽  
Insight Into

Stimulus-secretion coupling at the cellular level is studied by measuring changes in membrane capacitance in a variety of secretory cells. Attempts to gain new insight into the control of exocytosis in adenohypophysial cells by the patch-clamp technique are briefly outlined.

PKC regulation of cardiac CFTR Cl− channel function in guinea pig ventricular myocytes

1998 ◽  
Vol 275 (1) ◽  
pp. C293-C302 ◽  
Author(s):  
Lisa M. Middleton ◽  
Robert D. Harvey
Keyword(s):  
Protein Kinase ◽  
Patch Clamp ◽  
Guinea Pig ◽  
Ventricular Myocytes ◽  
Transmembrane Conductance Regulator ◽  
Transmembrane Conductance ◽  
Patch Clamp Technique ◽  
Clamp Technique ◽  
Whole Cell Patch Clamp ◽  
Perforated Patch Clamp

The role of protein kinase C (PKC) in regulating the protein kinase A (PKA)-activated Cl− current conducted by the cardiac isoform of the cystic fibrosis transmembrane conductance regulator (cCFTR) was studied in guinea pig ventricular myocytes using the whole cell patch-clamp technique. Although stimulation of endogenous PKC with phorbol 12,13-dibutyrate (PDBu) alone did not activate this Cl− current, even when intracellular dialysis was limited with the perforated patch-clamp technique, activation of PKC did elicit a significant response in the presence of PKA-dependent activation of the current by the β-adrenergic receptor agonist isoproterenol. PDBu increased the magnitude of the Cl− conductance activated by a supramaximally stimulating concentration of isoproterenol by 21 ± 3.3% ( n = 9) when added after isoproterenol and by 36 ± 16% ( n= 14) when introduced before isoproterenol. 4α-Phorbol 12,13-didecanoate, a phorbol ester that does not activate PKC, did not mimic these effects. Preexposure to chelerythrine or bisindolylmaleimide, two highly selective inhibitors of PKC, significantly reduced the magnitude of the isoproterenol-activated Cl− current by 79 ± 7.7% ( n = 11) and 52 ± 10% ( n = 8), respectively. Our results suggest that although acute activation of endogenous PKC alone does not significantly regulate cCFTR Cl− channel activity in native myocytes, it does potentiate PKA-dependent responses, perhaps most dramatically demonstrated by basal PKC activity, which may play a pivotal role in modulating the function of these channels.

Ca2+Channel Properties in Neuroendocrine Tumor Cell Cultures Investigated by Whole-Cell Patch-Clamp Technique

2004 ◽  
Vol 1014 (1) ◽  
pp. 137-139 ◽  
Author(s):  
STEFAN MERGLER ◽  
ADRIANA DROST ◽  
WOLF-OTTO BECHSTEIN ◽  
PETER NEUHAUS ◽  
BERTRAM WIEDENMANN
Keyword(s):  
Patch Clamp ◽  
Tumor Cell ◽  
Neuroendocrine Tumor ◽  
Cell Cultures ◽  
Patch Clamp Technique ◽  
Whole Cell ◽  
Clamp Technique ◽  
Cell Patch Clamp ◽  
Whole Cell Patch Clamp ◽  
Channel Properties

Patch-Clamp Technique in ESC-Derived Cardiomyocytes

2014 ◽  
pp. 203-214 ◽  
Author(s):  
Jie Liu ◽  
Peter H. Backx
Keyword(s):  
Patch Clamp ◽  
Patch Clamp Technique ◽  
Clamp Technique
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