Amitriptyline has a dual effect on the conductive properties of the epithelial Na channel

This study was undertaken with the aim of testing the action of amitriptyline on the epithelial Na channel (ENaC), which belongs to the same family (Deg/ENaC) as ASICs (acid‐sensing ion channels) and many other putative members in the brain. We assumed that, having a common protein structure, charac...

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Veröffentlicht in:Journal of pharmacy and pharmacology 2002-10, Vol.54 (10), p.1393-1398
Hauptverfasser: Pena, Florentina, Neaga, Emil, Amuzescu, Bogdan, Nitu, Alina, Flonta, Maria-Luisa
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container_issue 10
container_start_page 1393
container_title Journal of pharmacy and pharmacology
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creator Pena, Florentina
Neaga, Emil
Amuzescu, Bogdan
Nitu, Alina
Flonta, Maria-Luisa
description This study was undertaken with the aim of testing the action of amitriptyline on the epithelial Na channel (ENaC), which belongs to the same family (Deg/ENaC) as ASICs (acid‐sensing ion channels) and many other putative members in the brain. We assumed that, having a common protein structure, characterization of the amitriptyline‐ENaC interaction could help to elucidate the analgesic mechanism of this tricyclic antidepressant. Na‐channel characteristics were derived from the analysis of blocker‐induced lorentzian noise produced by amiloride. The effect of amitriptyline, present in the mucosal bathing solution, on the transepithelial short‐circuit current (1sc) and conductance (Gt), and on the blocker‐induced noise of apical Na channels, was studied on isolated ventral skin of the frog Rana ridibunda. Amitriptyline exerted a dual effect on the macroscopic short‐circuit current and conductance of the epithelia, increasing these two parameters in the concentration range 0.1–50 μM, while at higher concentrations (100–1000 μM) it showed an inhibitory action. The decrease in the association rate (k01) of amiloride to the apical Na channels from 15.6 ± 4.2 μM−1 S−1 in control Cl‐Ringer to 7.4 ± 1.7 μM−1 S−1 at 200 μM amitriptyline in a concentration‐dependent manner suggests a competitive binding of amitriptyline to the pyrazine ring binding site for amiloride.
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We assumed that, having a common protein structure, characterization of the amitriptyline‐ENaC interaction could help to elucidate the analgesic mechanism of this tricyclic antidepressant. Na‐channel characteristics were derived from the analysis of blocker‐induced lorentzian noise produced by amiloride. The effect of amitriptyline, present in the mucosal bathing solution, on the transepithelial short‐circuit current (1sc) and conductance (Gt), and on the blocker‐induced noise of apical Na channels, was studied on isolated ventral skin of the frog Rana ridibunda. Amitriptyline exerted a dual effect on the macroscopic short‐circuit current and conductance of the epithelia, increasing these two parameters in the concentration range 0.1–50 μM, while at higher concentrations (100–1000 μM) it showed an inhibitory action. The decrease in the association rate (k01) of amiloride to the apical Na channels from 15.6 ± 4.2 μM−1 S−1 in control Cl‐Ringer to 7.4 ± 1.7 μM−1 S−1 at 200 μM amitriptyline in a concentration‐dependent manner suggests a competitive binding of amitriptyline to the pyrazine ring binding site for amiloride.</description><identifier>ISSN: 0022-3573</identifier><identifier>EISSN: 2042-7158</identifier><identifier>DOI: 10.1211/002235702760345482</identifier><identifier>PMID: 12396302</identifier><identifier>CODEN: JPPMAB</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Algorithms ; Amiloride - metabolism ; Amitriptyline - pharmacology ; Animals ; Antidepressive Agents, Tricyclic - pharmacology ; Biological and medical sciences ; Electrophysiology ; Epithelium - drug effects ; Epithelium - metabolism ; In Vitro Techniques ; Medical sciences ; Neuropharmacology ; Pharmacology. 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The decrease in the association rate (k01) of amiloride to the apical Na channels from 15.6 ± 4.2 μM−1 S−1 in control Cl‐Ringer to 7.4 ± 1.7 μM−1 S−1 at 200 μM amitriptyline in a concentration‐dependent manner suggests a competitive binding of amitriptyline to the pyrazine ring binding site for amiloride.</description><subject>Algorithms</subject><subject>Amiloride - metabolism</subject><subject>Amitriptyline - pharmacology</subject><subject>Animals</subject><subject>Antidepressive Agents, Tricyclic - pharmacology</subject><subject>Biological and medical sciences</subject><subject>Electrophysiology</subject><subject>Epithelium - drug effects</subject><subject>Epithelium - metabolism</subject><subject>In Vitro Techniques</subject><subject>Medical sciences</subject><subject>Neuropharmacology</subject><subject>Pharmacology. Drug treatments</subject><subject>Psychoanaleptics: cns stimulant, antidepressant agent, nootropic agent, mood stabilizer..., (alzheimer disease)</subject><subject>Psychology. Psychoanalysis. 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Drug treatments</topic><topic>Psychoanaleptics: cns stimulant, antidepressant agent, nootropic agent, mood stabilizer..., (alzheimer disease)</topic><topic>Psychology. Psychoanalysis. Psychiatry</topic><topic>Psychopharmacology</topic><topic>Rana ridibunda</topic><topic>Sodium Channels - drug effects</topic><topic>Sodium Channels - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pena, Florentina</creatorcontrib><creatorcontrib>Neaga, Emil</creatorcontrib><creatorcontrib>Amuzescu, Bogdan</creatorcontrib><creatorcontrib>Nitu, Alina</creatorcontrib><creatorcontrib>Flonta, Maria-Luisa</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of pharmacy and pharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pena, Florentina</au><au>Neaga, Emil</au><au>Amuzescu, Bogdan</au><au>Nitu, Alina</au><au>Flonta, Maria-Luisa</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Amitriptyline has a dual effect on the conductive properties of the epithelial Na channel</atitle><jtitle>Journal of pharmacy and pharmacology</jtitle><addtitle>J Pharm Pharmacol</addtitle><date>2002-10</date><risdate>2002</risdate><volume>54</volume><issue>10</issue><spage>1393</spage><epage>1398</epage><pages>1393-1398</pages><issn>0022-3573</issn><eissn>2042-7158</eissn><coden>JPPMAB</coden><abstract>This study was undertaken with the aim of testing the action of amitriptyline on the epithelial Na channel (ENaC), which belongs to the same family (Deg/ENaC) as ASICs (acid‐sensing ion channels) and many other putative members in the brain. 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source MEDLINE; Wiley Online Library Journals Frontfile Complete; Oxford University Press Journals All Titles (1996-Current)
subjects Algorithms
Amiloride - metabolism
Amitriptyline - pharmacology
Animals
Antidepressive Agents, Tricyclic - pharmacology
Biological and medical sciences
Electrophysiology
Epithelium - drug effects
Epithelium - metabolism
In Vitro Techniques
Medical sciences
Neuropharmacology
Pharmacology. Drug treatments
Psychoanaleptics: cns stimulant, antidepressant agent, nootropic agent, mood stabilizer..., (alzheimer disease)
Psychology. Psychoanalysis. Psychiatry
Psychopharmacology
Rana ridibunda
Sodium Channels - drug effects
Sodium Channels - metabolism
title Amitriptyline has a dual effect on the conductive properties of the epithelial Na channel
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