NDLI: Functional link between muscarinic receptors and large-conductance $Ca^{2+}-activated$ $K^{+}$ channels in freshly-isolated human detrusor smooth muscle cells

Content Provider	World Health Organization (WHO)-Global Index Medicus
Author	Parajuli, Shankar P. Hristov, Kiril L. Cheng, Qiuping Malysz, John Rovner, Eric S. Petkov, Georgi V.
Description	Country affiliation: United States Author Affiliation: Parajuli SP ( Department of Drug Discovery and Biomedical Sciences, South Carolina College of Pharmacy, University of South Carolina, Coker Life Sciences Building, Room 609D, 715 Sumter St, Columbia, SC, 29208, USA.)
Abstract	Activation of muscarinic acetylcholine receptors (mAChRs) constitutes the primary mechanism for enhancing excitability and contractility of human detrusor smooth muscle (DSM). Since the large-conductance Ca(2+)-activated K(+) (KCa1.1) channels are key regulators of human DSM function, we investigated whether mAChR activation increases human DSM excitability by inhibiting KCa1.1 channels. We used the mAChR agonist, carbachol, to determine the changes in KCa1.1 channel activity upon mAChR activation in freshly isolated human DSM cells obtained from open bladder surgeries using the perforated whole cell and single KCa1.1 channel patch-clamp recordings. Human DSM cells were collected from 29 patients (23 males and 6 females, average age of 65.9 ± 1.5 years). Carbachol inhibited the amplitude and frequency of KCa1.1 channel-mediated spontaneous transient outward currents and spontaneous transient hyperpolarizations, which are triggered by the release of Ca(2+) from ryanodine receptors. Carbachol also caused membrane potential depolarization, which was not observed in the presence of iberiotoxin, a KCa1.1 channel inhibitor, indicating the critical role of the KCa1.1 channels. The potential direct carbachol effects on KCa1.1 channels were examined under conditions of removing the major cellular Ca(2+) sources for KCa1.1 channel activation with pharmacological inhibitors (thapsigargin, ryanodine, and nifedipine). In the presence of these inhibitors, carbachol did not affect the single KCa1.1 channel open probability and mean KCa1.1 channel conductance (cell-attached configuration) or depolarization-induced whole cell steady-state KCa1.1 currents. The data support the concept that mAChR activation triggers indirect functional KCa1.1 channel inhibition mediated by intracellular Ca(2+), thus increasing the excitability in human DSM cells.
File Format	HTM / HTML
ISSN	00316768
e-ISSN	14322013
DOI	10.1007/s00424-014-1537-8
Journal	Pflügers Archiv - European Journal of Physiology
Issue Number	4
Volume Number	467
Language	English
Publisher	Springer
Publisher Date	2015-04-01
Publisher Place	Germany
Access Restriction	Open
Subject Keyword	Discipline Physiology Large-conductance Calcium-activated Potassium Channel Alpha Subunits Metabolism Myocytes, Smooth Muscle Receptors, Muscarinic Urinary Bladder Action Potentials Calcium Carbachol Pharmacology Cholinergic Agonists Drug Effects Physiology Peptides Potassium Channel Blockers Ryanodine Receptor Calcium Release Channel Cytology Research Support, N.i.h., Extramural Research Support, Non-u.s. Gov't
Content Type	Text
Resource Type	Article
Subject	Physiology Physiology (medical) Clinical Biochemistry

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4	Project PI / Joint PI	Principal Investigator and Joint Principal Investigators of the project	Dr. B. Sutradhar bsutra@ndl.gov.in Prof. Saswat Chakrabarti will be added soon
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