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
Hauptverfasser: TSUNOBUCHI-USHIJIMA, Hiromi, KATO, Hiroshi, UENO, Hiroko, GOMI, Yasuo
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creator TSUNOBUCHI-USHIJIMA, Hiromi
KATO, Hiroshi
UENO, Hiroko
GOMI, Yasuo
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. 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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><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 ; 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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.</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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