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Highly selective σ receptor ligands elevate inositol 1,4,5-trisphosphate production in rat cardiac myocytes

Exposure of cardiac myocytes from adult rat ventricles to the highly selective, high affinity σ receptor ligands 1 S,2 R- cis- N-[2-(3,4-dichlorophenyl)ethyl]- N-methyl-2-(1-pyrrolidinyl)-cyclohexylamine (BD-737) (0.1–100 nM) and N-[2-(3,4-dichlorophenyl)ethyl]- N, N′, N′-trimethylethylenediamine (B...

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Published in:European journal of pharmacology 1998-07, Vol.353 (2), p.315-327
Main Authors: Novakova, Marie, Ela, Catherine, Bowen, Wayne D, Hasin, Yonathan, Eilam, Yael
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cited_by cdi_FETCH-LOGICAL-c389t-bda74b806e7e31eece0e8f0f0c4903e1dabaad0335101d24ce46232707ac3ddc3
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container_title European journal of pharmacology
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description Exposure of cardiac myocytes from adult rat ventricles to the highly selective, high affinity σ receptor ligands 1 S,2 R- cis- N-[2-(3,4-dichlorophenyl)ethyl]- N-methyl-2-(1-pyrrolidinyl)-cyclohexylamine (BD-737) (0.1–100 nM) and N-[2-(3,4-dichlorophenyl)ethyl]- N, N′, N′-trimethylethylenediamine (BD-1047) (0.01–10 nM), caused potentiation of electrically-evoked amplitudes of contraction and Ca 2+ transients, while exposure to 100 nM BD-1047 caused attenuation of these amplitudes. In addition, BD-737 (1–100 nM) and BD-1047 (10–100 nM) caused an increase in the incidence of spontaneous twitches. These effects were inhibited when the incubation with BD-737 was done in the presence of the phospholipase C inhibitor, neomycin, or after pre-incubation with thapsigargin or caffeine which deplete the sarcoplasmic reticulum Ca 2+ stores. Inositol 1,4,5-trisphosphate (IP 3) production in cardiac myocytes was determined by the IP 3 binding protein assay. Both substances caused an increase in the intracellular concentration of IP 3. BD-737 caused a rapid transient increase to 3.2-fold in 1 min and stabilization at 2.1-fold of control thereafter. BD-1047 caused a gradual increase reaching 4.4-fold after 5 min. The results suggest that the effects of these σ receptor ligands on contractility and spontaneous contractions are mediated by activation of phospholipase C and elevation of intracellular IP 3 level.
doi_str_mv 10.1016/S0014-2999(98)00398-7
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Psychology</topic><topic>Heart</topic><topic>Heart Ventricles - cytology</topic><topic>Heart Ventricles - drug effects</topic><topic>Heart Ventricles - metabolism</topic><topic>Inositol 1,4,5-trisphosphate</topic><topic>Inositol 1,4,5-Trisphosphate - biosynthesis</topic><topic>Ligands</topic><topic>Myocardial Contraction - drug effects</topic><topic>Phospholipase C</topic><topic>Pyrrolidines - pharmacology</topic><topic>Rats</topic><topic>Receptors, sigma - agonists</topic><topic>Receptors, sigma - metabolism</topic><topic>Vertebrates: cardiovascular system</topic><topic>σ Receptor</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Novakova, Marie</creatorcontrib><creatorcontrib>Ela, Catherine</creatorcontrib><creatorcontrib>Bowen, Wayne D</creatorcontrib><creatorcontrib>Hasin, Yonathan</creatorcontrib><creatorcontrib>Eilam, Yael</creatorcontrib><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>European journal of pharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Novakova, Marie</au><au>Ela, Catherine</au><au>Bowen, Wayne D</au><au>Hasin, Yonathan</au><au>Eilam, Yael</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Highly selective σ receptor ligands elevate inositol 1,4,5-trisphosphate production in rat cardiac myocytes</atitle><jtitle>European journal of pharmacology</jtitle><addtitle>Eur J Pharmacol</addtitle><date>1998-07-24</date><risdate>1998</risdate><volume>353</volume><issue>2</issue><spage>315</spage><epage>327</epage><pages>315-327</pages><issn>0014-2999</issn><eissn>1879-0712</eissn><coden>EJPHAZ</coden><abstract>Exposure of cardiac myocytes from adult rat ventricles to the highly selective, high affinity σ receptor ligands 1 S,2 R- cis- N-[2-(3,4-dichlorophenyl)ethyl]- N-methyl-2-(1-pyrrolidinyl)-cyclohexylamine (BD-737) (0.1–100 nM) and N-[2-(3,4-dichlorophenyl)ethyl]- N, N′, N′-trimethylethylenediamine (BD-1047) (0.01–10 nM), caused potentiation of electrically-evoked amplitudes of contraction and Ca 2+ transients, while exposure to 100 nM BD-1047 caused attenuation of these amplitudes. In addition, BD-737 (1–100 nM) and BD-1047 (10–100 nM) caused an increase in the incidence of spontaneous twitches. These effects were inhibited when the incubation with BD-737 was done in the presence of the phospholipase C inhibitor, neomycin, or after pre-incubation with thapsigargin or caffeine which deplete the sarcoplasmic reticulum Ca 2+ stores. Inositol 1,4,5-trisphosphate (IP 3) production in cardiac myocytes was determined by the IP 3 binding protein assay. Both substances caused an increase in the intracellular concentration of IP 3. BD-737 caused a rapid transient increase to 3.2-fold in 1 min and stabilization at 2.1-fold of control thereafter. BD-1047 caused a gradual increase reaching 4.4-fold after 5 min. The results suggest that the effects of these σ receptor ligands on contractility and spontaneous contractions are mediated by activation of phospholipase C and elevation of intracellular IP 3 level.</abstract><cop>Amsterdam</cop><pub>Elsevier B.V</pub><pmid>9726662</pmid><doi>10.1016/S0014-2999(98)00398-7</doi><tpages>13</tpages></addata></record>
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ispartof European journal of pharmacology, 1998-07, Vol.353 (2), p.315-327
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source ScienceDirect Journals
subjects Analgesics - pharmacology
Animals
Biological and medical sciences
Ca 2+, cytosolic
Calcium - metabolism
Cardiac myocyte
Contractility
Cyclohexylamines - pharmacology
Cytosol - drug effects
Cytosol - metabolism
Ethylenediamines - pharmacology
Fundamental and applied biological sciences. Psychology
Heart
Heart Ventricles - cytology
Heart Ventricles - drug effects
Heart Ventricles - metabolism
Inositol 1,4,5-trisphosphate
Inositol 1,4,5-Trisphosphate - biosynthesis
Ligands
Myocardial Contraction - drug effects
Phospholipase C
Pyrrolidines - pharmacology
Rats
Receptors, sigma - agonists
Receptors, sigma - metabolism
Vertebrates: cardiovascular system
σ Receptor
title Highly selective σ receptor ligands elevate inositol 1,4,5-trisphosphate production in rat cardiac myocytes
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