The Characteristics of Endothelin Receptor Subtypes on Muscle Contraction and Neuro-transmission in Rat Vas Deferens

We observed encothelin (ET)-induced contractile responses on prostatic and epididymal segments, as well as the facilitation of an electrically stimulated tone on prostatic segments of isolated rat vas deferens. In both segments, the selective ETB-receptor agonists, IRL 1620 and safafotoxin S6c, prod...

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Veröffentlicht in:Biological & pharmaceutical bulletin 1998/07/15, Vol.21(7), pp.718-722
Hauptverfasser: SATOH, Mitsutoshi, TAKADA, Mikiko, OHSHIMA, Noriko, TAKAYANAGI, Issei, KOIKE, Katsuo
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container_issue 7
container_start_page 718
container_title Biological & pharmaceutical bulletin
container_volume 21
creator SATOH, Mitsutoshi
TAKADA, Mikiko
OHSHIMA, Noriko
TAKAYANAGI, Issei
KOIKE, Katsuo
description We observed encothelin (ET)-induced contractile responses on prostatic and epididymal segments, as well as the facilitation of an electrically stimulated tone on prostatic segments of isolated rat vas deferens. In both segments, the selective ETB-receptor agonists, IRL 1620 and safafotoxin S6c, produced only a small contraction or no contraction at a concentration of 1 μM. The rank order of contraction potencies (pD2 value) was ET-1=ET-2>ET-3sarafotoxin S6c=IRL 1620. The maximum responses of ET-induced contractions in the prostatic segments were larger than those in the epididymal segments. The contractile response to ET-3 was antagonized by pretreatment for 30 min with BQ-123 (10 nM), a selective ETA receptor antagonist, and BQ-788 (1 μM), a selective ETB receptor antagonist. The contractile responses to ET-1 were antagonized by pretreatment with BQ-123 (10 μM), but not with BQ-788 (1 μM). The ET-3-induced facilitation on the twitch response to electrical stimulation in the prostatic segment of the vas deferens was antagonized by BQ-123 (0.1 μM) and BQ-788 (1 μM). The ET-1-induced facilitation was antagonized by pretreatment with BQ-123 (3 μM), but not with BQ-788 (10 μM). These results suggest that in rat vas deferens the ETA receptors are divided into BQ-123-sensitive ETA1 and BQ-123-insensitive ETA2 subtypes, and the production of a contractile response of smooth muscle as well as the facilitation of neurotransmission are accomplished through mediation by ETA1-and ETA2-subtypes.
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In both segments, the selective ETB-receptor agonists, IRL 1620 and safafotoxin S6c, produced only a small contraction or no contraction at a concentration of 1 μM. The rank order of contraction potencies (pD2 value) was ET-1=ET-2&gt;ET-3sarafotoxin S6c=IRL 1620. The maximum responses of ET-induced contractions in the prostatic segments were larger than those in the epididymal segments. The contractile response to ET-3 was antagonized by pretreatment for 30 min with BQ-123 (10 nM), a selective ETA receptor antagonist, and BQ-788 (1 μM), a selective ETB receptor antagonist. The contractile responses to ET-1 were antagonized by pretreatment with BQ-123 (10 μM), but not with BQ-788 (1 μM). The ET-3-induced facilitation on the twitch response to electrical stimulation in the prostatic segment of the vas deferens was antagonized by BQ-123 (0.1 μM) and BQ-788 (1 μM). The ET-1-induced facilitation was antagonized by pretreatment with BQ-123 (3 μM), but not with BQ-788 (10 μM). These results suggest that in rat vas deferens the ETA receptors are divided into BQ-123-sensitive ETA1 and BQ-123-insensitive ETA2 subtypes, and the production of a contractile response of smooth muscle as well as the facilitation of neurotransmission are accomplished through mediation by ETA1-and ETA2-subtypes.</description><identifier>ISSN: 0918-6158</identifier><identifier>EISSN: 1347-5215</identifier><identifier>DOI: 10.1248/bpb.21.718</identifier><identifier>PMID: 9703256</identifier><language>eng</language><publisher>Tokyo: The Pharmaceutical Society of Japan</publisher><subject>Animals ; Biological and medical sciences ; contraction ; Electric Stimulation ; endothelin ; Endothelin Receptor Antagonists ; Endothelins - pharmacology ; Endothelins - physiology ; Fundamental and applied biological sciences. Psychology ; In Vitro Techniques ; Male ; Muscle Contraction - drug effects ; Muscle Contraction - physiology ; Peptide Fragments - pharmacology ; Peripheral nervous system. Autonomic nervous system. Neuromuscular transmission. Ganglionic transmission. 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In both segments, the selective ETB-receptor agonists, IRL 1620 and safafotoxin S6c, produced only a small contraction or no contraction at a concentration of 1 μM. The rank order of contraction potencies (pD2 value) was ET-1=ET-2&gt;ET-3sarafotoxin S6c=IRL 1620. The maximum responses of ET-induced contractions in the prostatic segments were larger than those in the epididymal segments. The contractile response to ET-3 was antagonized by pretreatment for 30 min with BQ-123 (10 nM), a selective ETA receptor antagonist, and BQ-788 (1 μM), a selective ETB receptor antagonist. The contractile responses to ET-1 were antagonized by pretreatment with BQ-123 (10 μM), but not with BQ-788 (1 μM). The ET-3-induced facilitation on the twitch response to electrical stimulation in the prostatic segment of the vas deferens was antagonized by BQ-123 (0.1 μM) and BQ-788 (1 μM). The ET-1-induced facilitation was antagonized by pretreatment with BQ-123 (3 μM), but not with BQ-788 (10 μM). These results suggest that in rat vas deferens the ETA receptors are divided into BQ-123-sensitive ETA1 and BQ-123-insensitive ETA2 subtypes, and the production of a contractile response of smooth muscle as well as the facilitation of neurotransmission are accomplished through mediation by ETA1-and ETA2-subtypes.</description><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>contraction</subject><subject>Electric Stimulation</subject><subject>endothelin</subject><subject>Endothelin Receptor Antagonists</subject><subject>Endothelins - pharmacology</subject><subject>Endothelins - physiology</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>In Vitro Techniques</subject><subject>Male</subject><subject>Muscle Contraction - drug effects</subject><subject>Muscle Contraction - physiology</subject><subject>Peptide Fragments - pharmacology</subject><subject>Peripheral nervous system. Autonomic nervous system. 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Electric organ</subject><subject>Prostate - drug effects</subject><subject>Prostate - physiology</subject><subject>rat vas deferens</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Receptors, Endothelin - agonists</subject><subject>Receptors, Endothelin - classification</subject><subject>Receptors, Endothelin - physiology</subject><subject>smooth muscle</subject><subject>Synaptic Transmission - drug effects</subject><subject>Synaptic Transmission - physiology</subject><subject>Vas Deferens - drug effects</subject><subject>Vas Deferens - innervation</subject><subject>Vas Deferens - physiology</subject><subject>Vasoconstrictor Agents - pharmacology</subject><subject>Vertebrates: nervous system and sense organs</subject><subject>Viper Venoms - pharmacology</subject><issn>0918-6158</issn><issn>1347-5215</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkUFv1DAQhS1EVbaFC3ekSKAekLJ47CS2j2hboFIBCQpXy3HGbFZZJ7WdQ_99HXa1SFxsad7nN-N5hLwGugZWyQ_t1K4ZrAXIZ2QFvBJlzaB-TlZUgSwbqOULchHjjlIqKOPn5FwJylndrEi632Kx2ZpgbMLQx9TbWIyuuPHdmLY49L74gRanNIbi59ymxwmz7ouvc7RDfjn6tDztc8n4rviGcxjLXPJx38e4lBcHk4rfJhbX6DCgjy_JmTNDxFfH-5L8-nRzv_lS3n3_fLv5eFfaholUIrNoeWMc78AJKUTDXM1oa6lprG0kOOWgtlLQLn_XUYVSYatExzqJtZL8klwdfKcwPswYk85DWRwG43GcoxZccsGgyuDb_8DdOAefZ9NQVQoEANSZen-gbBhjDOj0FPq9CY8aqF6C0DkIzUDnIDL85mg5t3vsTuhx81l_d9RNtGZweWW2j_8ca1lxvmCbA7aLyfzBk25CTmrApSMoxf92PRy5-Um1OViNnj8B8tmoxA</recordid><startdate>19980701</startdate><enddate>19980701</enddate><creator>SATOH, Mitsutoshi</creator><creator>TAKADA, Mikiko</creator><creator>OHSHIMA, Noriko</creator><creator>TAKAYANAGI, Issei</creator><creator>KOIKE, Katsuo</creator><general>The Pharmaceutical Society of Japan</general><general>Maruzen</general><general>Japan Science and Technology Agency</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QP</scope><scope>7QR</scope><scope>7TK</scope><scope>7U9</scope><scope>8FD</scope><scope>FR3</scope><scope>H94</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>19980701</creationdate><title>The Characteristics of Endothelin Receptor Subtypes on Muscle Contraction and Neuro-transmission in Rat Vas Deferens</title><author>SATOH, Mitsutoshi ; TAKADA, Mikiko ; OHSHIMA, Noriko ; TAKAYANAGI, Issei ; KOIKE, Katsuo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c627t-e2cec36af3d1f787762f520bc0a6cc681f9f15c870d215f09e89eb97d2d8e5983</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>contraction</topic><topic>Electric Stimulation</topic><topic>endothelin</topic><topic>Endothelin Receptor Antagonists</topic><topic>Endothelins - pharmacology</topic><topic>Endothelins - physiology</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>In Vitro Techniques</topic><topic>Male</topic><topic>Muscle Contraction - drug effects</topic><topic>Muscle Contraction - physiology</topic><topic>Peptide Fragments - pharmacology</topic><topic>Peripheral nervous system. Autonomic nervous system. Neuromuscular transmission. Ganglionic transmission. 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In both segments, the selective ETB-receptor agonists, IRL 1620 and safafotoxin S6c, produced only a small contraction or no contraction at a concentration of 1 μM. The rank order of contraction potencies (pD2 value) was ET-1=ET-2&gt;ET-3sarafotoxin S6c=IRL 1620. The maximum responses of ET-induced contractions in the prostatic segments were larger than those in the epididymal segments. The contractile response to ET-3 was antagonized by pretreatment for 30 min with BQ-123 (10 nM), a selective ETA receptor antagonist, and BQ-788 (1 μM), a selective ETB receptor antagonist. The contractile responses to ET-1 were antagonized by pretreatment with BQ-123 (10 μM), but not with BQ-788 (1 μM). The ET-3-induced facilitation on the twitch response to electrical stimulation in the prostatic segment of the vas deferens was antagonized by BQ-123 (0.1 μM) and BQ-788 (1 μM). The ET-1-induced facilitation was antagonized by pretreatment with BQ-123 (3 μM), but not with BQ-788 (10 μM). These results suggest that in rat vas deferens the ETA receptors are divided into BQ-123-sensitive ETA1 and BQ-123-insensitive ETA2 subtypes, and the production of a contractile response of smooth muscle as well as the facilitation of neurotransmission are accomplished through mediation by ETA1-and ETA2-subtypes.</abstract><cop>Tokyo</cop><pub>The Pharmaceutical Society of Japan</pub><pmid>9703256</pmid><doi>10.1248/bpb.21.718</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record>
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subjects Animals
Biological and medical sciences
contraction
Electric Stimulation
endothelin
Endothelin Receptor Antagonists
Endothelins - pharmacology
Endothelins - physiology
Fundamental and applied biological sciences. Psychology
In Vitro Techniques
Male
Muscle Contraction - drug effects
Muscle Contraction - physiology
Peptide Fragments - pharmacology
Peripheral nervous system. Autonomic nervous system. Neuromuscular transmission. Ganglionic transmission. Electric organ
Prostate - drug effects
Prostate - physiology
rat vas deferens
Rats
Rats, Wistar
Receptors, Endothelin - agonists
Receptors, Endothelin - classification
Receptors, Endothelin - physiology
smooth muscle
Synaptic Transmission - drug effects
Synaptic Transmission - physiology
Vas Deferens - drug effects
Vas Deferens - innervation
Vas Deferens - physiology
Vasoconstrictor Agents - pharmacology
Vertebrates: nervous system and sense organs
Viper Venoms - pharmacology
title The Characteristics of Endothelin Receptor Subtypes on Muscle Contraction and Neuro-transmission in Rat Vas Deferens
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