E. H. Juárez, F. Ochoa-Cortés, M. Miranda-Morales, R. Espinosa-Luna, L. M. Montaño, C. Barajas-López
{"title":"Selectivity of antagonists for the Cys-loop native receptors for ACh, 5-HT and GABA in guinea-pig myenteric neurons","authors":"E. H. Juárez, F. Ochoa-Cortés, M. Miranda-Morales, R. Espinosa-Luna, L. M. Montaño, C. Barajas-López","doi":"10.1111/aap.12016","DOIUrl":null,"url":null,"abstract":"<div>\n \n <p>\n \n </p><ol>\n \n \n <li>The three most common <i>Cys-loop</i> receptors expressed by myenteric neurons are nACh, 5-HT<sub>3</sub> and GABA<sub>A</sub>. To investigate the function of these proteins researchers have used channel inhibitors such as hexamethonium (antagonist of nACh receptors), ondansetron (antagonist of 5-HT<sub>3</sub> receptors), picrotoxin and bicuculline (both antagonists of GABA<sub>A</sub> receptors). The aim of this study was to investigate the specificity of these inhibitors on <i>Cys-loop</i> receptors of primary cultured neurons obtained from the guinea-pig small intestine. The whole-cell configuration of the patch clamp techniques was used to record membrane currents induced by ACh (I<sub>ACh</sub>), 5-HT (I<sub>5-HT</sub>) and GABA (I<sub>GABA</sub>) in the absence and the presence of various concentrations of hexamethonium, ondansetron, picrotoxin or bicuculline.</li>\n \n \n <li>The three <i>Cys-loop</i> receptors present in enteric neurons are expressed independently and they do not cross-desensitized. Hexamethonium inhibited I<sub>ACh</sub> without affecting I<sub>5-HT</sub> and I<sub>GABA</sub>. Ondansetron inhibited I<sub>5-HT</sub> and also I<sub>ACh</sub> but did not affect I<sub>GABA</sub>. Picrotoxin and bicuculline inhibited I<sub>5-HT</sub>, I<sub>ACh</sub> and I<sub>GABA</sub> with different potency, being the lowest potency on 5-HT<sub>3</sub> receptors. All these inhibitory effects were concentration dependent and reversible.</li>\n \n \n <li>Our observations showed that except for hexamethonium, all other inhibitors used here show different degrees of selectivity, which has to be considered when these antagonists are used in experimental studies aimed to investigate the functions of these receptors. In particular, in tissues expressing nACh receptors because these are the targets of all other inhibitors used here. The low potency of picrotoxin and bicuculline to inhibit 5-HT<sub>3</sub> receptors suggests that these receptors are heteromeric proteins.</li>\n </ol>\n \n </div>","PeriodicalId":100151,"journal":{"name":"Autonomic and Autacoid Pharmacology","volume":"34 1-2","pages":"1-8"},"PeriodicalIF":0.0000,"publicationDate":"2013-10-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1111/aap.12016","citationCount":"8","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Autonomic and Autacoid Pharmacology","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1111/aap.12016","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 8
Abstract
The three most common Cys-loop receptors expressed by myenteric neurons are nACh, 5-HT3 and GABAA. To investigate the function of these proteins researchers have used channel inhibitors such as hexamethonium (antagonist of nACh receptors), ondansetron (antagonist of 5-HT3 receptors), picrotoxin and bicuculline (both antagonists of GABAA receptors). The aim of this study was to investigate the specificity of these inhibitors on Cys-loop receptors of primary cultured neurons obtained from the guinea-pig small intestine. The whole-cell configuration of the patch clamp techniques was used to record membrane currents induced by ACh (IACh), 5-HT (I5-HT) and GABA (IGABA) in the absence and the presence of various concentrations of hexamethonium, ondansetron, picrotoxin or bicuculline.
The three Cys-loop receptors present in enteric neurons are expressed independently and they do not cross-desensitized. Hexamethonium inhibited IACh without affecting I5-HT and IGABA. Ondansetron inhibited I5-HT and also IACh but did not affect IGABA. Picrotoxin and bicuculline inhibited I5-HT, IACh and IGABA with different potency, being the lowest potency on 5-HT3 receptors. All these inhibitory effects were concentration dependent and reversible.
Our observations showed that except for hexamethonium, all other inhibitors used here show different degrees of selectivity, which has to be considered when these antagonists are used in experimental studies aimed to investigate the functions of these receptors. In particular, in tissues expressing nACh receptors because these are the targets of all other inhibitors used here. The low potency of picrotoxin and bicuculline to inhibit 5-HT3 receptors suggests that these receptors are heteromeric proteins.