Selective inhibition of K+ ‐stimulation of Na,K‐ATPase by bretylium
1 The effects of bretylium were investigated on purified Na,K‐ATPase from guinea‐pig heart and on the Na/K pump in trout erythrocytes, with a view to further identifying the mechanism(s) associated with its antiarrhythmic effects. 2 Na,K‐ATPase activity of the thiocyanate‐dispersed enzyme was determ...
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Veröffentlicht in: | British journal of pharmacology 1991-12, Vol.104 (4), p.895-900 |
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description | 1
The effects of bretylium were investigated on purified Na,K‐ATPase from guinea‐pig heart and on the Na/K pump in trout erythrocytes, with a view to further identifying the mechanism(s) associated with its antiarrhythmic effects.
2
Na,K‐ATPase activity of the thiocyanate‐dispersed enzyme was determined by the measurement of inorganic phosphate produced by ATP hydrolysis.
3
When the concentrations of each of the Na,K‐ATPase activating components were varied in turn, bretylium (1–5 mmol l−1) exhibited competitive‐type effects against K+ with a Ki of 1.4 mmol l−1 and noncompetitive‐type effects against Na+, Mg2+ and ATP.
4
In K+ influx studies in trout erythrocytes with 86Rb+ used as the marker, the inhibition of total influx observed with bretylium (5 and 10 mmol l−1) was attributable to the bretylium cation selectively inhibiting the Na/K pump‐mediated influx with the associated tosylate anion inhibiting Na/K cotransport.
5
The observed inhibition kinetics indicated that the bretylium cation (2–15 mmol l−1) competitively inhibited K+ stimulation of the Na/K pump at 6 and 1.25 mmol l−1 external K+ with a mean K1 of 2.3 mmol l−1.
6
The effects demonstrated on the functioning Na/K pump in erythrocytes confirmed the Na,K‐ATPase findings, with bretylium selectively inhibiting K+ stimulation of the pump mechanism in both cases.
7
It is suggested that Na,K‐ATPase inhibition may contribute to the antiarrhythmic and positive inotropic effects of bretylium with the cardiac accumulation of bretylium also possibly being a further important factor. |
doi_str_mv | 10.1111/j.1476-5381.1991.tb12523.x |
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The effects of bretylium were investigated on purified Na,K‐ATPase from guinea‐pig heart and on the Na/K pump in trout erythrocytes, with a view to further identifying the mechanism(s) associated with its antiarrhythmic effects.
2
Na,K‐ATPase activity of the thiocyanate‐dispersed enzyme was determined by the measurement of inorganic phosphate produced by ATP hydrolysis.
3
When the concentrations of each of the Na,K‐ATPase activating components were varied in turn, bretylium (1–5 mmol l−1) exhibited competitive‐type effects against K+ with a Ki of 1.4 mmol l−1 and noncompetitive‐type effects against Na+, Mg2+ and ATP.
4
In K+ influx studies in trout erythrocytes with 86Rb+ used as the marker, the inhibition of total influx observed with bretylium (5 and 10 mmol l−1) was attributable to the bretylium cation selectively inhibiting the Na/K pump‐mediated influx with the associated tosylate anion inhibiting Na/K cotransport.
5
The observed inhibition kinetics indicated that the bretylium cation (2–15 mmol l−1) competitively inhibited K+ stimulation of the Na/K pump at 6 and 1.25 mmol l−1 external K+ with a mean K1 of 2.3 mmol l−1.
6
The effects demonstrated on the functioning Na/K pump in erythrocytes confirmed the Na,K‐ATPase findings, with bretylium selectively inhibiting K+ stimulation of the pump mechanism in both cases.
7
It is suggested that Na,K‐ATPase inhibition may contribute to the antiarrhythmic and positive inotropic effects of bretylium with the cardiac accumulation of bretylium also possibly being a further important factor.</description><identifier>ISSN: 0007-1188</identifier><identifier>EISSN: 1476-5381</identifier><identifier>DOI: 10.1111/j.1476-5381.1991.tb12523.x</identifier><identifier>PMID: 1667290</identifier><identifier>CODEN: BJPCBM</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Animals ; antiarrhythmic agents ; Antiarythmic agents ; Biological and medical sciences ; Bretylium ; Bretylium Compounds - pharmacology ; Cardiovascular system ; Enzyme Activation - drug effects ; Erythrocytes - drug effects ; Erythrocytes - enzymology ; Guinea Pigs ; guinea‐pig heart ; Heart - drug effects ; In Vitro Techniques ; Kinetics ; Magnesium - pharmacology ; Male ; Medical sciences ; Myocardium - enzymology ; Na,K‐ATPase ; Pharmacology. Drug treatments ; Phosphates - metabolism ; Potassium - antagonists & inhibitors ; Potassium - metabolism ; Potassium - pharmacology ; Rubidium Radioisotopes ; Sodium-Potassium-Exchanging ATPase - drug effects ; Sodium-Potassium-Exchanging ATPase - metabolism ; Thiocyanates - pharmacology ; Trout ; trout erythrocytes</subject><ispartof>British journal of pharmacology, 1991-12, Vol.104 (4), p.895-900</ispartof><rights>1991 British Pharmacological Society</rights><rights>1992 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5073-803ddad918ddc3b4564cc023aa68541f2151490ecb900e7aa605830f17d2abec3</citedby><cites>FETCH-LOGICAL-c5073-803ddad918ddc3b4564cc023aa68541f2151490ecb900e7aa605830f17d2abec3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1908819/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1908819/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,27903,27904,53770,53772</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=5046934$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/1667290$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Tiku, Patience E.</creatorcontrib><creatorcontrib>Nowell, Peter T.</creatorcontrib><title>Selective inhibition of K+ ‐stimulation of Na,K‐ATPase by bretylium</title><title>British journal of pharmacology</title><addtitle>Br J Pharmacol</addtitle><description>1
The effects of bretylium were investigated on purified Na,K‐ATPase from guinea‐pig heart and on the Na/K pump in trout erythrocytes, with a view to further identifying the mechanism(s) associated with its antiarrhythmic effects.
2
Na,K‐ATPase activity of the thiocyanate‐dispersed enzyme was determined by the measurement of inorganic phosphate produced by ATP hydrolysis.
3
When the concentrations of each of the Na,K‐ATPase activating components were varied in turn, bretylium (1–5 mmol l−1) exhibited competitive‐type effects against K+ with a Ki of 1.4 mmol l−1 and noncompetitive‐type effects against Na+, Mg2+ and ATP.
4
In K+ influx studies in trout erythrocytes with 86Rb+ used as the marker, the inhibition of total influx observed with bretylium (5 and 10 mmol l−1) was attributable to the bretylium cation selectively inhibiting the Na/K pump‐mediated influx with the associated tosylate anion inhibiting Na/K cotransport.
5
The observed inhibition kinetics indicated that the bretylium cation (2–15 mmol l−1) competitively inhibited K+ stimulation of the Na/K pump at 6 and 1.25 mmol l−1 external K+ with a mean K1 of 2.3 mmol l−1.
6
The effects demonstrated on the functioning Na/K pump in erythrocytes confirmed the Na,K‐ATPase findings, with bretylium selectively inhibiting K+ stimulation of the pump mechanism in both cases.
7
It is suggested that Na,K‐ATPase inhibition may contribute to the antiarrhythmic and positive inotropic effects of bretylium with the cardiac accumulation of bretylium also possibly being a further important factor.</description><subject>Animals</subject><subject>antiarrhythmic agents</subject><subject>Antiarythmic agents</subject><subject>Biological and medical sciences</subject><subject>Bretylium</subject><subject>Bretylium Compounds - pharmacology</subject><subject>Cardiovascular system</subject><subject>Enzyme Activation - drug effects</subject><subject>Erythrocytes - drug effects</subject><subject>Erythrocytes - enzymology</subject><subject>Guinea Pigs</subject><subject>guinea‐pig heart</subject><subject>Heart - drug effects</subject><subject>In Vitro Techniques</subject><subject>Kinetics</subject><subject>Magnesium - pharmacology</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Myocardium - enzymology</subject><subject>Na,K‐ATPase</subject><subject>Pharmacology. Drug treatments</subject><subject>Phosphates - metabolism</subject><subject>Potassium - antagonists & inhibitors</subject><subject>Potassium - metabolism</subject><subject>Potassium - pharmacology</subject><subject>Rubidium Radioisotopes</subject><subject>Sodium-Potassium-Exchanging ATPase - drug effects</subject><subject>Sodium-Potassium-Exchanging ATPase - metabolism</subject><subject>Thiocyanates - pharmacology</subject><subject>Trout</subject><subject>trout erythrocytes</subject><issn>0007-1188</issn><issn>1476-5381</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1991</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqVUcFu1DAUtCpQ2ZZ-AlJUIS6Q8J4dJzYHRKlKi1pBpZaz5ThO65WTlDhpuzc-gW_sl-Bltwsc8cXWzLzx0wwh-wgZxvN2nmFeFilnAjOUErOxQsopy-63yGxDPSEzAChTRCGekZ0Q5gCRLPk22caiKKmEGTm-sN6a0d3axHXXrnKj67ukb5LT18nDj59hdO3k9SP4Rb85jejB5bkONqkWSTXYceHd1D4nTxvtg91b37vk26ejy8OT9Ozr8efDg7PUcChZKoDVta4liro2rMp5kRsDlGldCJ5jQ5FjLsGaSgLYMsLABYMGy5rqyhq2S96vfG-mqrW1sd04aK9uBtfqYaF67dS_TOeu1VV_q1CCECijwau1wdB_n2wYVeuCsd7rzvZTUCUtJJVUROG7ldAMfQiDbTafIKhlDWqullmrZdZqWYNa16Du4_CLv9f8M7rKPfIv17wORvtm0J1xYSPjkBeS5VH2YSW7c94u_mMB9fH85PeT_QLFJacc</recordid><startdate>199112</startdate><enddate>199112</enddate><creator>Tiku, Patience E.</creator><creator>Nowell, Peter T.</creator><general>Blackwell Publishing Ltd</general><general>Nature Publishing</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>7X8</scope><scope>5PM</scope></search><sort><creationdate>199112</creationdate><title>Selective inhibition of K+ ‐stimulation of Na,K‐ATPase by bretylium</title><author>Tiku, Patience E. ; Nowell, Peter T.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5073-803ddad918ddc3b4564cc023aa68541f2151490ecb900e7aa605830f17d2abec3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1991</creationdate><topic>Animals</topic><topic>antiarrhythmic agents</topic><topic>Antiarythmic agents</topic><topic>Biological and medical sciences</topic><topic>Bretylium</topic><topic>Bretylium Compounds - pharmacology</topic><topic>Cardiovascular system</topic><topic>Enzyme Activation - drug effects</topic><topic>Erythrocytes - drug effects</topic><topic>Erythrocytes - enzymology</topic><topic>Guinea Pigs</topic><topic>guinea‐pig heart</topic><topic>Heart - drug effects</topic><topic>In Vitro Techniques</topic><topic>Kinetics</topic><topic>Magnesium - pharmacology</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Myocardium - enzymology</topic><topic>Na,K‐ATPase</topic><topic>Pharmacology. Drug treatments</topic><topic>Phosphates - metabolism</topic><topic>Potassium - antagonists & inhibitors</topic><topic>Potassium - metabolism</topic><topic>Potassium - pharmacology</topic><topic>Rubidium Radioisotopes</topic><topic>Sodium-Potassium-Exchanging ATPase - drug effects</topic><topic>Sodium-Potassium-Exchanging ATPase - metabolism</topic><topic>Thiocyanates - pharmacology</topic><topic>Trout</topic><topic>trout erythrocytes</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tiku, Patience E.</creatorcontrib><creatorcontrib>Nowell, Peter T.</creatorcontrib><collection>Pascal-Francis</collection><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><collection>PubMed Central (Full Participant titles)</collection><jtitle>British journal of pharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tiku, Patience E.</au><au>Nowell, Peter T.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Selective inhibition of K+ ‐stimulation of Na,K‐ATPase by bretylium</atitle><jtitle>British journal of pharmacology</jtitle><addtitle>Br J Pharmacol</addtitle><date>1991-12</date><risdate>1991</risdate><volume>104</volume><issue>4</issue><spage>895</spage><epage>900</epage><pages>895-900</pages><issn>0007-1188</issn><eissn>1476-5381</eissn><coden>BJPCBM</coden><abstract>1
The effects of bretylium were investigated on purified Na,K‐ATPase from guinea‐pig heart and on the Na/K pump in trout erythrocytes, with a view to further identifying the mechanism(s) associated with its antiarrhythmic effects.
2
Na,K‐ATPase activity of the thiocyanate‐dispersed enzyme was determined by the measurement of inorganic phosphate produced by ATP hydrolysis.
3
When the concentrations of each of the Na,K‐ATPase activating components were varied in turn, bretylium (1–5 mmol l−1) exhibited competitive‐type effects against K+ with a Ki of 1.4 mmol l−1 and noncompetitive‐type effects against Na+, Mg2+ and ATP.
4
In K+ influx studies in trout erythrocytes with 86Rb+ used as the marker, the inhibition of total influx observed with bretylium (5 and 10 mmol l−1) was attributable to the bretylium cation selectively inhibiting the Na/K pump‐mediated influx with the associated tosylate anion inhibiting Na/K cotransport.
5
The observed inhibition kinetics indicated that the bretylium cation (2–15 mmol l−1) competitively inhibited K+ stimulation of the Na/K pump at 6 and 1.25 mmol l−1 external K+ with a mean K1 of 2.3 mmol l−1.
6
The effects demonstrated on the functioning Na/K pump in erythrocytes confirmed the Na,K‐ATPase findings, with bretylium selectively inhibiting K+ stimulation of the pump mechanism in both cases.
7
It is suggested that Na,K‐ATPase inhibition may contribute to the antiarrhythmic and positive inotropic effects of bretylium with the cardiac accumulation of bretylium also possibly being a further important factor.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>1667290</pmid><doi>10.1111/j.1476-5381.1991.tb12523.x</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals antiarrhythmic agents Antiarythmic agents Biological and medical sciences Bretylium Bretylium Compounds - pharmacology Cardiovascular system Enzyme Activation - drug effects Erythrocytes - drug effects Erythrocytes - enzymology Guinea Pigs guinea‐pig heart Heart - drug effects In Vitro Techniques Kinetics Magnesium - pharmacology Male Medical sciences Myocardium - enzymology Na,K‐ATPase Pharmacology. Drug treatments Phosphates - metabolism Potassium - antagonists & inhibitors Potassium - metabolism Potassium - pharmacology Rubidium Radioisotopes Sodium-Potassium-Exchanging ATPase - drug effects Sodium-Potassium-Exchanging ATPase - metabolism Thiocyanates - pharmacology Trout trout erythrocytes |
title | Selective inhibition of K+ ‐stimulation of Na,K‐ATPase by bretylium |
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