Effects of the Functional Elimination of Sarcoplasmic Reticulum on the Manganese-Dependent Norepinephrine-Induced Contractions of the Guinea Pig Vas Deferens
We investigated the effects of inhibitors of the sarcoplasmic reticulum (SR) functions on the tonic contractions induced by norepinephrine (NE) in the Ca2+-depleted Mn2+-loaded was deferens of the guinea pig in the absence of both Ca2+ and Mn2+ (Mn2+-dependent NE-contraction). In control preparation...
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Veröffentlicht in: | Journal of Smooth Muscle Research 1996, Vol.32(4), pp.135-144 |
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description | We investigated the effects of inhibitors of the sarcoplasmic reticulum (SR) functions on the tonic contractions induced by norepinephrine (NE) in the Ca2+-depleted Mn2+-loaded was deferens of the guinea pig in the absence of both Ca2+ and Mn2+ (Mn2+-dependent NE-contraction). In control preparations without Ca2+ depletion and Mn2+ loading, either cyclopiazonic acid (CPA, 10μM) or ryanodine (RYA, 3μM) inhibited the initial phasic and tonic components but not the large phasic component of NE-induced contraction in normal medium containing 2.2mM Ca2+. In contrast, CPA did not affect the Mn2+-dependent NE-contractions. The inhibitory effect of RYA slowly developed with each repetition of the Mn2+-dependent NE-contraction and the magnitude of the inhibition was slight. A23187 (10μM) inhibited the NE-induced contractions of the control preparations in the same manner as CPA and RYA. Although A23187 did not induce contractions in the Mn2+-loaded preparations, A23187 augmented the Mn2+-dependent NE-contractions. The augmented tonic contractions returned to the resting level by washing NE and A23187. The augmentation remained for 3 successive contractions in the absence of A23187. However, the 2nd application of A23187 did not augment the contraction. These results suggest that neither Mn2+-release from SR nor Mn2+-influx from the extracellular space contributes to the Mn2+-dependent NE-contractions. We concluded that NE induces Mn2+-dependent contractions by increasing Mn2+ sensitivity ofcontractile processes but not by increasing intracellular Mn2+ concentration. |
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In control preparations without Ca2+ depletion and Mn2+ loading, either cyclopiazonic acid (CPA, 10μM) or ryanodine (RYA, 3μM) inhibited the initial phasic and tonic components but not the large phasic component of NE-induced contraction in normal medium containing 2.2mM Ca2+. In contrast, CPA did not affect the Mn2+-dependent NE-contractions. The inhibitory effect of RYA slowly developed with each repetition of the Mn2+-dependent NE-contraction and the magnitude of the inhibition was slight. A23187 (10μM) inhibited the NE-induced contractions of the control preparations in the same manner as CPA and RYA. Although A23187 did not induce contractions in the Mn2+-loaded preparations, A23187 augmented the Mn2+-dependent NE-contractions. The augmented tonic contractions returned to the resting level by washing NE and A23187. The augmentation remained for 3 successive contractions in the absence of A23187. However, the 2nd application of A23187 did not augment the contraction. These results suggest that neither Mn2+-release from SR nor Mn2+-influx from the extracellular space contributes to the Mn2+-dependent NE-contractions. We concluded that NE induces Mn2+-dependent contractions by increasing Mn2+ sensitivity ofcontractile processes but not by increasing intracellular Mn2+ concentration.</description><identifier>ISSN: 0916-8737</identifier><identifier>EISSN: 1884-8796</identifier><identifier>DOI: 10.1540/jsmr.32.135</identifier><identifier>PMID: 8910251</identifier><language>eng</language><publisher>Japan: Japan Society of Smooth Muscle Research</publisher><subject>Animals ; Calcimycin - pharmacology ; Calcium - metabolism ; guinea pig ; Guinea Pigs ; In Vitro Techniques ; Indoles - pharmacology ; Male ; manganese ; Manganese - metabolism ; Manganese - physiology ; Muscle Contraction - drug effects ; Muscle, Smooth - drug effects ; norepinephrine ; Norepinephrine - pharmacology ; Ryanodine - pharmacology ; sarcoplasmic reticulum ; Sarcoplasmic Reticulum - metabolism ; Sarcoplasmic Reticulum - physiology ; vas deferens ; Vas Deferens - drug effects</subject><ispartof>Journal of Smooth Muscle Research, 1996, Vol.32(4), pp.135-144</ispartof><rights>Japan Society of Smooth Muscle Research</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4205-81a7806f441a7d5f54209ae6e93d288cdca7ef8fc25aaba5175226306f8a84df3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,860,1876,4009,27902,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/8910251$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>TSUNOBUCHI-USHIJIMA, Hiromi</creatorcontrib><creatorcontrib>KATO, Hiroshi</creatorcontrib><creatorcontrib>UENO, Hiroko</creatorcontrib><creatorcontrib>GOMI, Yasuo</creatorcontrib><title>Effects of the Functional Elimination of Sarcoplasmic Reticulum on the Manganese-Dependent Norepinephrine-Induced Contractions of the Guinea Pig Vas Deferens</title><title>Journal of Smooth Muscle Research</title><addtitle>Journal of Smooth Muscle Research</addtitle><description>We investigated the effects of inhibitors of the sarcoplasmic reticulum (SR) functions on the tonic contractions induced by norepinephrine (NE) in the Ca2+-depleted Mn2+-loaded was deferens of the guinea pig in the absence of both Ca2+ and Mn2+ (Mn2+-dependent NE-contraction). In control preparations without Ca2+ depletion and Mn2+ loading, either cyclopiazonic acid (CPA, 10μM) or ryanodine (RYA, 3μM) inhibited the initial phasic and tonic components but not the large phasic component of NE-induced contraction in normal medium containing 2.2mM Ca2+. In contrast, CPA did not affect the Mn2+-dependent NE-contractions. The inhibitory effect of RYA slowly developed with each repetition of the Mn2+-dependent NE-contraction and the magnitude of the inhibition was slight. A23187 (10μM) inhibited the NE-induced contractions of the control preparations in the same manner as CPA and RYA. Although A23187 did not induce contractions in the Mn2+-loaded preparations, A23187 augmented the Mn2+-dependent NE-contractions. The augmented tonic contractions returned to the resting level by washing NE and A23187. The augmentation remained for 3 successive contractions in the absence of A23187. However, the 2nd application of A23187 did not augment the contraction. These results suggest that neither Mn2+-release from SR nor Mn2+-influx from the extracellular space contributes to the Mn2+-dependent NE-contractions. We concluded that NE induces Mn2+-dependent contractions by increasing Mn2+ sensitivity ofcontractile processes but not by increasing intracellular Mn2+ concentration.</description><subject>Animals</subject><subject>Calcimycin - pharmacology</subject><subject>Calcium - metabolism</subject><subject>guinea pig</subject><subject>Guinea Pigs</subject><subject>In Vitro Techniques</subject><subject>Indoles - pharmacology</subject><subject>Male</subject><subject>manganese</subject><subject>Manganese - metabolism</subject><subject>Manganese - physiology</subject><subject>Muscle Contraction - drug effects</subject><subject>Muscle, Smooth - drug effects</subject><subject>norepinephrine</subject><subject>Norepinephrine - pharmacology</subject><subject>Ryanodine - pharmacology</subject><subject>sarcoplasmic reticulum</subject><subject>Sarcoplasmic Reticulum - metabolism</subject><subject>Sarcoplasmic Reticulum - physiology</subject><subject>vas deferens</subject><subject>Vas Deferens - drug effects</subject><issn>0916-8737</issn><issn>1884-8796</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1996</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo9kU2P0zAQhi0EWsrCiTOST1xQij_ixD6itrustHyIr2s064xbV4mTtZMDP4b_irOtehmP_bzzjjxDyFvO1lyV7OMx9XEtxZpL9YysuNZloWtTPScrZniVc1m_JK9SOjImtDLmilxpw5lQfEX-7ZxDOyU6ODodkN7MwU5-CNDRXed7H2C5LfQnRDuMHaTeW_oDJ2_nbu5phkvdFwh7CJiw2OKIocUw0a9DxNEHHA8xx-IutLPFlm6GMEV46nJpeztnBdDvfk__QKJbdBgxpNfkhYMu4ZvzeU1-3-x-bT4X999u7zaf7gtbCqYKzaHWrHJlmZNWOZVfDWCFRrZCa9taqNFpZ4UCeADFayVEJXOFBl22Tl6T9yffMQ6PM6ap6X2y2HX5S8OcmlorLqU2WfjhJLRxSCmia8boe4h_G86aZRnNsoxGiiYvI6vfnW3nhx7bi_Y8_cy3J35ME-zxwiHm6Xb45MWN4YtfeQrZ9oLtAWKDQf4H9Seg6g</recordid><startdate>1996</startdate><enddate>1996</enddate><creator>TSUNOBUCHI-USHIJIMA, Hiromi</creator><creator>KATO, Hiroshi</creator><creator>UENO, Hiroko</creator><creator>GOMI, Yasuo</creator><general>Japan Society of Smooth Muscle Research</general><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>7X8</scope></search><sort><creationdate>1996</creationdate><title>Effects of the Functional Elimination of Sarcoplasmic Reticulum on the Manganese-Dependent Norepinephrine-Induced Contractions of the Guinea Pig Vas Deferens</title><author>TSUNOBUCHI-USHIJIMA, Hiromi ; KATO, Hiroshi ; UENO, Hiroko ; GOMI, Yasuo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4205-81a7806f441a7d5f54209ae6e93d288cdca7ef8fc25aaba5175226306f8a84df3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1996</creationdate><topic>Animals</topic><topic>Calcimycin - pharmacology</topic><topic>Calcium - metabolism</topic><topic>guinea pig</topic><topic>Guinea Pigs</topic><topic>In Vitro Techniques</topic><topic>Indoles - pharmacology</topic><topic>Male</topic><topic>manganese</topic><topic>Manganese - metabolism</topic><topic>Manganese - physiology</topic><topic>Muscle Contraction - drug effects</topic><topic>Muscle, Smooth - drug effects</topic><topic>norepinephrine</topic><topic>Norepinephrine - pharmacology</topic><topic>Ryanodine - pharmacology</topic><topic>sarcoplasmic reticulum</topic><topic>Sarcoplasmic Reticulum - metabolism</topic><topic>Sarcoplasmic Reticulum - physiology</topic><topic>vas deferens</topic><topic>Vas Deferens - drug effects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>TSUNOBUCHI-USHIJIMA, Hiromi</creatorcontrib><creatorcontrib>KATO, Hiroshi</creatorcontrib><creatorcontrib>UENO, Hiroko</creatorcontrib><creatorcontrib>GOMI, Yasuo</creatorcontrib><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 Smooth Muscle Research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>TSUNOBUCHI-USHIJIMA, Hiromi</au><au>KATO, Hiroshi</au><au>UENO, Hiroko</au><au>GOMI, Yasuo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effects of the Functional Elimination of Sarcoplasmic Reticulum on the Manganese-Dependent Norepinephrine-Induced Contractions of the Guinea Pig Vas Deferens</atitle><jtitle>Journal of Smooth Muscle Research</jtitle><addtitle>Journal of Smooth Muscle Research</addtitle><date>1996</date><risdate>1996</risdate><volume>32</volume><issue>4</issue><spage>135</spage><epage>144</epage><pages>135-144</pages><issn>0916-8737</issn><eissn>1884-8796</eissn><abstract>We investigated the effects of inhibitors of the sarcoplasmic reticulum (SR) functions on the tonic contractions induced by norepinephrine (NE) in the Ca2+-depleted Mn2+-loaded was deferens of the guinea pig in the absence of both Ca2+ and Mn2+ (Mn2+-dependent NE-contraction). In control preparations without Ca2+ depletion and Mn2+ loading, either cyclopiazonic acid (CPA, 10μM) or ryanodine (RYA, 3μM) inhibited the initial phasic and tonic components but not the large phasic component of NE-induced contraction in normal medium containing 2.2mM Ca2+. In contrast, CPA did not affect the Mn2+-dependent NE-contractions. The inhibitory effect of RYA slowly developed with each repetition of the Mn2+-dependent NE-contraction and the magnitude of the inhibition was slight. A23187 (10μM) inhibited the NE-induced contractions of the control preparations in the same manner as CPA and RYA. Although A23187 did not induce contractions in the Mn2+-loaded preparations, A23187 augmented the Mn2+-dependent NE-contractions. The augmented tonic contractions returned to the resting level by washing NE and A23187. The augmentation remained for 3 successive contractions in the absence of A23187. However, the 2nd application of A23187 did not augment the contraction. These results suggest that neither Mn2+-release from SR nor Mn2+-influx from the extracellular space contributes to the Mn2+-dependent NE-contractions. We concluded that NE induces Mn2+-dependent contractions by increasing Mn2+ sensitivity ofcontractile processes but not by increasing intracellular Mn2+ concentration.</abstract><cop>Japan</cop><pub>Japan Society of Smooth Muscle Research</pub><pmid>8910251</pmid><doi>10.1540/jsmr.32.135</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Calcimycin - pharmacology Calcium - metabolism guinea pig Guinea Pigs In Vitro Techniques Indoles - pharmacology Male manganese Manganese - metabolism Manganese - physiology Muscle Contraction - drug effects Muscle, Smooth - drug effects norepinephrine Norepinephrine - pharmacology Ryanodine - pharmacology sarcoplasmic reticulum Sarcoplasmic Reticulum - metabolism Sarcoplasmic Reticulum - physiology vas deferens Vas Deferens - drug effects |
title | Effects of the Functional Elimination of Sarcoplasmic Reticulum on the Manganese-Dependent Norepinephrine-Induced Contractions of the Guinea Pig Vas Deferens |
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