항(抗) Histamine제(劑)와 Muscarinic Receptor와의 상호작용(相互作用)(I) -심장(心臟) muscarinic receptor에 대한 작용(作用)
$[^3H]$ Quinuclidinyl benzilate(QNB) binding assays were performed in the dog ventricular sarcolemma fraction enriched approx. 32-fold in sarcolemma compared to the starting homogenate to elucidate the effect of antihistaminics on cardiac muscarinic receptor. Chlorpheniramine(CHP) inhibited specific...
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Veröffentlicht in: | Yaghag-hoi-ji 1988, Vol.32 (2), p.101-111 |
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creator | 이신웅 박영주 이정수 하광원 진갑덕 Lee, Shin-Woong Park, Yeung-Joo Lee, Jeung-Soo Ha, Kwang-Won Jin, Kap-Duck |
description | $[^3H]$ Quinuclidinyl benzilate(QNB) binding assays were performed in the dog ventricular sarcolemma fraction enriched approx. 32-fold in sarcolemma compared to the starting homogenate to elucidate the effect of antihistaminics on cardiac muscarinic receptor. Chlorpheniramine(CHP) inhibited specific binding of $[^3H]$QNB and delayed the equilibrium binding. The rate constants at $37^{\circ}C$ for formation and dissociation of the QNB receptor complex were $0.38{\times}10^9\;M^{-1}$ and $1.6{\times}10^{-2}\;min^{-1}$, respectively. The mean value for the dissociation constant from the pairs of the rate constants was 43. 2 pM and this value was similar to the value(44.8pM) determined from Scatchard analysis. CHP decreased association rate constant, indicating increase in $K_D$ value. Decrease in affinity without affecting the binding site concentration$(B_{max})$ for $[^3H]$QNB binding by CHP was also demonstrated by Scatchard analysis. $K_i$ values for $H_i$-blockers that inhibited specific $[^3H]$QNB binding were $0.02{\sim}4.8{\mu}M$. Cimetidine with $K_i$ value of $230{\mu}M$, however, was ineffective in displacing $[^3H]$QNB binding at concentration of $50{\mu}M$. The Hill coefficient for $H_1$-blockers were about one. The results indicate that $H_1$-antihistaminics inhibit $[^3H]$ QNB binding by interaction with myocardiac muscarinic cholinergic receptor and anticholinergic side effects of these drugs are mainly due to this receptor blocking mechanism. |
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fullrecord | <record><control><sourceid>kisti</sourceid><recordid>TN_cdi_kisti_ndsl_JAKO198803038857451</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>JAKO198803038857451</sourcerecordid><originalsourceid>FETCH-kisti_ndsl_JAKO1988030388574513</originalsourceid><addsrcrecordid>eNpjYuA0MrYw1rU0MTVnYeA0MDY317U0NTXjYOAtLs5MMjAxMTczNTQx5WSY9HbqWo1nXdM1FTwyi0sSczPzUt8smKPxtGui5puZDQq-pcXJiUWZeZnJCkGpyakFJflFQOE3c2covGlufDtjx5t5E9_MWqnxfPaOJ7smPdk75_mUFZoanpoKum-617yZt1Tj6f7mF-3zNRVyEeYUwcyZPkHhdU_D26lzFKCmQPXzMLCmJeYUp_JCaW4GVTfXEGcP3WygCzPj81KKc-K9HL39DS0tLAyMDYwtLEzNTUwNjYlVBwChTG7p</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>항(抗) Histamine제(劑)와 Muscarinic Receptor와의 상호작용(相互作用)(I) -심장(心臟) muscarinic receptor에 대한 작용(作用)</title><source>Alma/SFX Local Collection</source><creator>이신웅 ; 박영주 ; 이정수 ; 하광원 ; 진갑덕 ; Lee, Shin-Woong ; Park, Yeung-Joo ; Lee, Jeung-Soo ; Ha, Kwang-Won ; Jin, Kap-Duck</creator><creatorcontrib>이신웅 ; 박영주 ; 이정수 ; 하광원 ; 진갑덕 ; Lee, Shin-Woong ; Park, Yeung-Joo ; Lee, Jeung-Soo ; Ha, Kwang-Won ; Jin, Kap-Duck</creatorcontrib><description>$[^3H]$ Quinuclidinyl benzilate(QNB) binding assays were performed in the dog ventricular sarcolemma fraction enriched approx. 32-fold in sarcolemma compared to the starting homogenate to elucidate the effect of antihistaminics on cardiac muscarinic receptor. Chlorpheniramine(CHP) inhibited specific binding of $[^3H]$QNB and delayed the equilibrium binding. The rate constants at $37^{\circ}C$ for formation and dissociation of the QNB receptor complex were $0.38{\times}10^9\;M^{-1}$ and $1.6{\times}10^{-2}\;min^{-1}$, respectively. The mean value for the dissociation constant from the pairs of the rate constants was 43. 2 pM and this value was similar to the value(44.8pM) determined from Scatchard analysis. CHP decreased association rate constant, indicating increase in $K_D$ value. Decrease in affinity without affecting the binding site concentration$(B_{max})$ for $[^3H]$QNB binding by CHP was also demonstrated by Scatchard analysis. $K_i$ values for $H_i$-blockers that inhibited specific $[^3H]$QNB binding were $0.02{\sim}4.8{\mu}M$. Cimetidine with $K_i$ value of $230{\mu}M$, however, was ineffective in displacing $[^3H]$QNB binding at concentration of $50{\mu}M$. The Hill coefficient for $H_1$-blockers were about one. The results indicate that $H_1$-antihistaminics inhibit $[^3H]$ QNB binding by interaction with myocardiac muscarinic cholinergic receptor and anticholinergic side effects of these drugs are mainly due to this receptor blocking mechanism.</description><identifier>ISSN: 0377-9556</identifier><identifier>EISSN: 2383-9457</identifier><language>kor</language><ispartof>Yaghag-hoi-ji, 1988, Vol.32 (2), p.101-111</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,4024</link.rule.ids></links><search><creatorcontrib>이신웅</creatorcontrib><creatorcontrib>박영주</creatorcontrib><creatorcontrib>이정수</creatorcontrib><creatorcontrib>하광원</creatorcontrib><creatorcontrib>진갑덕</creatorcontrib><creatorcontrib>Lee, Shin-Woong</creatorcontrib><creatorcontrib>Park, Yeung-Joo</creatorcontrib><creatorcontrib>Lee, Jeung-Soo</creatorcontrib><creatorcontrib>Ha, Kwang-Won</creatorcontrib><creatorcontrib>Jin, Kap-Duck</creatorcontrib><title>항(抗) Histamine제(劑)와 Muscarinic Receptor와의 상호작용(相互作用)(I) -심장(心臟) muscarinic receptor에 대한 작용(作用)</title><title>Yaghag-hoi-ji</title><addtitle>Yakhak hoeji</addtitle><description>$[^3H]$ Quinuclidinyl benzilate(QNB) binding assays were performed in the dog ventricular sarcolemma fraction enriched approx. 32-fold in sarcolemma compared to the starting homogenate to elucidate the effect of antihistaminics on cardiac muscarinic receptor. Chlorpheniramine(CHP) inhibited specific binding of $[^3H]$QNB and delayed the equilibrium binding. The rate constants at $37^{\circ}C$ for formation and dissociation of the QNB receptor complex were $0.38{\times}10^9\;M^{-1}$ and $1.6{\times}10^{-2}\;min^{-1}$, respectively. The mean value for the dissociation constant from the pairs of the rate constants was 43. 2 pM and this value was similar to the value(44.8pM) determined from Scatchard analysis. CHP decreased association rate constant, indicating increase in $K_D$ value. Decrease in affinity without affecting the binding site concentration$(B_{max})$ for $[^3H]$QNB binding by CHP was also demonstrated by Scatchard analysis. $K_i$ values for $H_i$-blockers that inhibited specific $[^3H]$QNB binding were $0.02{\sim}4.8{\mu}M$. Cimetidine with $K_i$ value of $230{\mu}M$, however, was ineffective in displacing $[^3H]$QNB binding at concentration of $50{\mu}M$. The Hill coefficient for $H_1$-blockers were about one. The results indicate that $H_1$-antihistaminics inhibit $[^3H]$ QNB binding by interaction with myocardiac muscarinic cholinergic receptor and anticholinergic side effects of these drugs are mainly due to this receptor blocking mechanism.</description><issn>0377-9556</issn><issn>2383-9457</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1988</creationdate><recordtype>article</recordtype><sourceid>JDI</sourceid><recordid>eNpjYuA0MrYw1rU0MTVnYeA0MDY317U0NTXjYOAtLs5MMjAxMTczNTQx5WSY9HbqWo1nXdM1FTwyi0sSczPzUt8smKPxtGui5puZDQq-pcXJiUWZeZnJCkGpyakFJflFQOE3c2covGlufDtjx5t5E9_MWqnxfPaOJ7smPdk75_mUFZoanpoKum-617yZt1Tj6f7mF-3zNRVyEeYUwcyZPkHhdU_D26lzFKCmQPXzMLCmJeYUp_JCaW4GVTfXEGcP3WygCzPj81KKc-K9HL39DS0tLAyMDYwtLEzNTUwNjYlVBwChTG7p</recordid><startdate>1988</startdate><enddate>1988</enddate><creator>이신웅</creator><creator>박영주</creator><creator>이정수</creator><creator>하광원</creator><creator>진갑덕</creator><creator>Lee, Shin-Woong</creator><creator>Park, Yeung-Joo</creator><creator>Lee, Jeung-Soo</creator><creator>Ha, Kwang-Won</creator><creator>Jin, Kap-Duck</creator><scope>JDI</scope></search><sort><creationdate>1988</creationdate><title>항(抗) Histamine제(劑)와 Muscarinic Receptor와의 상호작용(相互作用)(I) -심장(心臟) muscarinic receptor에 대한 작용(作用)</title><author>이신웅 ; 박영주 ; 이정수 ; 하광원 ; 진갑덕 ; Lee, Shin-Woong ; Park, Yeung-Joo ; Lee, Jeung-Soo ; Ha, Kwang-Won ; Jin, Kap-Duck</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-kisti_ndsl_JAKO1988030388574513</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>kor</language><creationdate>1988</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>이신웅</creatorcontrib><creatorcontrib>박영주</creatorcontrib><creatorcontrib>이정수</creatorcontrib><creatorcontrib>하광원</creatorcontrib><creatorcontrib>진갑덕</creatorcontrib><creatorcontrib>Lee, Shin-Woong</creatorcontrib><creatorcontrib>Park, Yeung-Joo</creatorcontrib><creatorcontrib>Lee, Jeung-Soo</creatorcontrib><creatorcontrib>Ha, Kwang-Won</creatorcontrib><creatorcontrib>Jin, Kap-Duck</creatorcontrib><collection>KoreaScience</collection><jtitle>Yaghag-hoi-ji</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>이신웅</au><au>박영주</au><au>이정수</au><au>하광원</au><au>진갑덕</au><au>Lee, Shin-Woong</au><au>Park, Yeung-Joo</au><au>Lee, Jeung-Soo</au><au>Ha, Kwang-Won</au><au>Jin, Kap-Duck</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>항(抗) Histamine제(劑)와 Muscarinic Receptor와의 상호작용(相互作用)(I) -심장(心臟) muscarinic receptor에 대한 작용(作用)</atitle><jtitle>Yaghag-hoi-ji</jtitle><addtitle>Yakhak hoeji</addtitle><date>1988</date><risdate>1988</risdate><volume>32</volume><issue>2</issue><spage>101</spage><epage>111</epage><pages>101-111</pages><issn>0377-9556</issn><eissn>2383-9457</eissn><abstract>$[^3H]$ Quinuclidinyl benzilate(QNB) binding assays were performed in the dog ventricular sarcolemma fraction enriched approx. 32-fold in sarcolemma compared to the starting homogenate to elucidate the effect of antihistaminics on cardiac muscarinic receptor. Chlorpheniramine(CHP) inhibited specific binding of $[^3H]$QNB and delayed the equilibrium binding. The rate constants at $37^{\circ}C$ for formation and dissociation of the QNB receptor complex were $0.38{\times}10^9\;M^{-1}$ and $1.6{\times}10^{-2}\;min^{-1}$, respectively. The mean value for the dissociation constant from the pairs of the rate constants was 43. 2 pM and this value was similar to the value(44.8pM) determined from Scatchard analysis. CHP decreased association rate constant, indicating increase in $K_D$ value. Decrease in affinity without affecting the binding site concentration$(B_{max})$ for $[^3H]$QNB binding by CHP was also demonstrated by Scatchard analysis. $K_i$ values for $H_i$-blockers that inhibited specific $[^3H]$QNB binding were $0.02{\sim}4.8{\mu}M$. Cimetidine with $K_i$ value of $230{\mu}M$, however, was ineffective in displacing $[^3H]$QNB binding at concentration of $50{\mu}M$. The Hill coefficient for $H_1$-blockers were about one. The results indicate that $H_1$-antihistaminics inhibit $[^3H]$ QNB binding by interaction with myocardiac muscarinic cholinergic receptor and anticholinergic side effects of these drugs are mainly due to this receptor blocking mechanism.</abstract><oa>free_for_read</oa></addata></record> |
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title | 항(抗) Histamine제(劑)와 Muscarinic Receptor와의 상호작용(相互作用)(I) -심장(心臟) muscarinic receptor에 대한 작용(作用) |
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