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An investigation of sodium transport in barnacle muscle fibres by means of the microsyringe technique
1. The cation composition of single barnacle muscle fibres following damage by axial insertion of a microsyringe has been measured. The Na and Ca contents of these fibres were raised. 2. Electronmicroscopic studies of fibres following insertion of a microsyringe indicated that the damage done result...
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Published in: | The Journal of physiology 1972-03, Vol.221 (2), p.389-414 |
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creator | Bittar, E. Edward Chen, Stephen Danielson, Bo G. Hartmann, Henrik A. Tong, Edmund Y. |
description | 1. The cation composition of single barnacle muscle fibres following damage by axial insertion of a microsyringe has been
measured. The Na and Ca contents of these fibres were raised.
2. Electronmicroscopic studies of fibres following insertion of a microsyringe indicated that the damage done resulted in
tubular obstruction of the T-system.
3. Fibres loaded with radiosodium by micro-injection showed that the Na * efflux declined exponentially with time, but that in most fibres the slope ratio of d/d t ln [Na * ] 1 to d/d t (ln d[Na * ] i /d t ) was less than unity. Injections of distilled water deep in the fibre failed to influence the course of the Na * efflux.
4. K removal reduced the Na efflux by 47%. However, a few fibres displayed very little K-dependence.
5. When measured in fibres already soaked in a K-free medium for long periods the sodium efflux consisted of a brief rapid
phase, followed by a slow phase of Na loss.
6. In the presence of 30 m M -K, there was little or no rise in the Na efflux. Raising the external K to 50 or 100 m M caused a marked rise in the Na efflux. Raising the external K to 30 m M in the absence of external Ca 2+ led to a rise in the Na efflux. A high K solution always caused shortening of these fibres.
7. Internal application of 1 M or 1 m M -CaCl 2 often caused a significant rise in the Na efflux.
8. Internal application of 2·5 or 5 M saline caused a prompt and large fall in the Na efflux. In the presence of high K saline-loaded fibres failed to contract.
9. Internal application of 0·5 M -ATP stimulated the Na efflux. A larger effect was not observed in fibres pre-treated with 2 M -MgCl 2 . Internal application of 0·5 M -ArP was without effect.
10. The results indicate that the barnacle fibre is a suitable preparation for the study of Na fluxes by means of the micro-injection
technique. They also indicate that the mechanism regulating the Na efflux is not quite the same as that found in squid axon
or frog muscle. |
doi_str_mv | 10.1113/jphysiol.1972.sp009757 |
format | article |
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measured. The Na and Ca contents of these fibres were raised.
2. Electronmicroscopic studies of fibres following insertion of a microsyringe indicated that the damage done resulted in
tubular obstruction of the T-system.
3. Fibres loaded with radiosodium by micro-injection showed that the Na * efflux declined exponentially with time, but that in most fibres the slope ratio of d/d t ln [Na * ] 1 to d/d t (ln d[Na * ] i /d t ) was less than unity. Injections of distilled water deep in the fibre failed to influence the course of the Na * efflux.
4. K removal reduced the Na efflux by 47%. However, a few fibres displayed very little K-dependence.
5. When measured in fibres already soaked in a K-free medium for long periods the sodium efflux consisted of a brief rapid
phase, followed by a slow phase of Na loss.
6. In the presence of 30 m M -K, there was little or no rise in the Na efflux. Raising the external K to 50 or 100 m M caused a marked rise in the Na efflux. Raising the external K to 30 m M in the absence of external Ca 2+ led to a rise in the Na efflux. A high K solution always caused shortening of these fibres.
7. Internal application of 1 M or 1 m M -CaCl 2 often caused a significant rise in the Na efflux.
8. Internal application of 2·5 or 5 M saline caused a prompt and large fall in the Na efflux. In the presence of high K saline-loaded fibres failed to contract.
9. Internal application of 0·5 M -ATP stimulated the Na efflux. A larger effect was not observed in fibres pre-treated with 2 M -MgCl 2 . Internal application of 0·5 M -ArP was without effect.
10. The results indicate that the barnacle fibre is a suitable preparation for the study of Na fluxes by means of the micro-injection
technique. They also indicate that the mechanism regulating the Na efflux is not quite the same as that found in squid axon
or frog muscle.</description><identifier>ISSN: 0022-3751</identifier><identifier>EISSN: 1469-7793</identifier><identifier>DOI: 10.1113/jphysiol.1972.sp009757</identifier><identifier>PMID: 5020983</identifier><language>eng</language><publisher>England: The Physiological Society</publisher><subject>Adenosine Triphosphate - pharmacology ; Animals ; Anura ; Biological Transport, Active ; Calcium - metabolism ; Calcium Chloride - pharmacology ; Injections ; Membrane Potentials ; Methods ; Microscopy, Electron ; Muscles - metabolism ; Myofibrils - cytology ; Myofibrils - metabolism ; Phosphates - pharmacology ; Potassium - metabolism ; Sodium - metabolism ; Sodium Isotopes ; Thoracica ; Time Factors</subject><ispartof>The Journal of physiology, 1972-03, Vol.221 (2), p.389-414</ispartof><rights>1972 The Physiological Society</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5339-48917bedf3948b5effea4e1341acb00e67cbeae83459f9e8b38b04378e64fc5d3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1331339/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1331339/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/5020983$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bittar, E. Edward</creatorcontrib><creatorcontrib>Chen, Stephen</creatorcontrib><creatorcontrib>Danielson, Bo G.</creatorcontrib><creatorcontrib>Hartmann, Henrik A.</creatorcontrib><creatorcontrib>Tong, Edmund Y.</creatorcontrib><title>An investigation of sodium transport in barnacle muscle fibres by means of the microsyringe technique</title><title>The Journal of physiology</title><addtitle>J Physiol</addtitle><description>1. The cation composition of single barnacle muscle fibres following damage by axial insertion of a microsyringe has been
measured. The Na and Ca contents of these fibres were raised.
2. Electronmicroscopic studies of fibres following insertion of a microsyringe indicated that the damage done resulted in
tubular obstruction of the T-system.
3. Fibres loaded with radiosodium by micro-injection showed that the Na * efflux declined exponentially with time, but that in most fibres the slope ratio of d/d t ln [Na * ] 1 to d/d t (ln d[Na * ] i /d t ) was less than unity. Injections of distilled water deep in the fibre failed to influence the course of the Na * efflux.
4. K removal reduced the Na efflux by 47%. However, a few fibres displayed very little K-dependence.
5. When measured in fibres already soaked in a K-free medium for long periods the sodium efflux consisted of a brief rapid
phase, followed by a slow phase of Na loss.
6. In the presence of 30 m M -K, there was little or no rise in the Na efflux. Raising the external K to 50 or 100 m M caused a marked rise in the Na efflux. Raising the external K to 30 m M in the absence of external Ca 2+ led to a rise in the Na efflux. A high K solution always caused shortening of these fibres.
7. Internal application of 1 M or 1 m M -CaCl 2 often caused a significant rise in the Na efflux.
8. Internal application of 2·5 or 5 M saline caused a prompt and large fall in the Na efflux. In the presence of high K saline-loaded fibres failed to contract.
9. Internal application of 0·5 M -ATP stimulated the Na efflux. A larger effect was not observed in fibres pre-treated with 2 M -MgCl 2 . Internal application of 0·5 M -ArP was without effect.
10. The results indicate that the barnacle fibre is a suitable preparation for the study of Na fluxes by means of the micro-injection
technique. They also indicate that the mechanism regulating the Na efflux is not quite the same as that found in squid axon
or frog muscle.</description><subject>Adenosine Triphosphate - pharmacology</subject><subject>Animals</subject><subject>Anura</subject><subject>Biological Transport, Active</subject><subject>Calcium - metabolism</subject><subject>Calcium Chloride - pharmacology</subject><subject>Injections</subject><subject>Membrane Potentials</subject><subject>Methods</subject><subject>Microscopy, Electron</subject><subject>Muscles - metabolism</subject><subject>Myofibrils - cytology</subject><subject>Myofibrils - metabolism</subject><subject>Phosphates - pharmacology</subject><subject>Potassium - metabolism</subject><subject>Sodium - metabolism</subject><subject>Sodium Isotopes</subject><subject>Thoracica</subject><subject>Time Factors</subject><issn>0022-3751</issn><issn>1469-7793</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1972</creationdate><recordtype>article</recordtype><recordid>eNqNkU-L1TAUxYMo43P0IyhZqZs-k6Ztko0wDv5lQBfjOiR5t68Z2qQm7Qz99qb0zaAbEQKBnN853JuD0CtK9pRS9u5m7JbkQr-nkpf7NBIiec0foR2tGllwLtljtCOkLAvGa_oUPUvphhDKiJRn6KwmJZGC7RBceOz8LaTJHfXkgsehxSkc3DzgKWqfxhCnTGCjo9e2BzzMab1aZyIkbBY8QMZW29Rl1dkY0hKdPwKewHbe_ZrhOXrS6j7Bi9N9jn5--nh9-aW4-v756-XFVWFrxmRRCUm5gUPLZCVMDW0LugLKKqqtIQQabg1oEKyqZStBGCYMqRgX0FStrQ_sHL3fcsfZDHCw4PMOvRqjG3RcVNBO_a1416ljuFWUsXxkDnh9Coghz50mNbhkoe-1hzAnJWjFGG9IBt_-E6SN4I1gdc0z2mzo-jMpQvswDyVq7VLdd6nWLtV9l9n48s9tHmyn8rL-YdPvXA_Lf6aq628_1oeypCUT68ZvtpDOHbs7F0FtthSsg2lRmVOlWsnfz97D9Q</recordid><startdate>19720301</startdate><enddate>19720301</enddate><creator>Bittar, E. Edward</creator><creator>Chen, Stephen</creator><creator>Danielson, Bo G.</creator><creator>Hartmann, Henrik A.</creator><creator>Tong, Edmund Y.</creator><general>The Physiological Society</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>7TN</scope><scope>F1W</scope><scope>H95</scope><scope>L.G</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>19720301</creationdate><title>An investigation of sodium transport in barnacle muscle fibres by means of the microsyringe technique</title><author>Bittar, E. Edward ; Chen, Stephen ; Danielson, Bo G. ; Hartmann, Henrik A. ; Tong, Edmund Y.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5339-48917bedf3948b5effea4e1341acb00e67cbeae83459f9e8b38b04378e64fc5d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1972</creationdate><topic>Adenosine Triphosphate - pharmacology</topic><topic>Animals</topic><topic>Anura</topic><topic>Biological Transport, Active</topic><topic>Calcium - metabolism</topic><topic>Calcium Chloride - pharmacology</topic><topic>Injections</topic><topic>Membrane Potentials</topic><topic>Methods</topic><topic>Microscopy, Electron</topic><topic>Muscles - metabolism</topic><topic>Myofibrils - cytology</topic><topic>Myofibrils - metabolism</topic><topic>Phosphates - pharmacology</topic><topic>Potassium - metabolism</topic><topic>Sodium - metabolism</topic><topic>Sodium Isotopes</topic><topic>Thoracica</topic><topic>Time Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bittar, E. Edward</creatorcontrib><creatorcontrib>Chen, Stephen</creatorcontrib><creatorcontrib>Danielson, Bo G.</creatorcontrib><creatorcontrib>Hartmann, Henrik A.</creatorcontrib><creatorcontrib>Tong, Edmund Y.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Oceanic Abstracts</collection><collection>ASFA: Aquatic Sciences and Fisheries Abstracts</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 1: Biological Sciences & Living Resources</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Professional</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>The Journal of physiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bittar, E. Edward</au><au>Chen, Stephen</au><au>Danielson, Bo G.</au><au>Hartmann, Henrik A.</au><au>Tong, Edmund Y.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>An investigation of sodium transport in barnacle muscle fibres by means of the microsyringe technique</atitle><jtitle>The Journal of physiology</jtitle><addtitle>J Physiol</addtitle><date>1972-03-01</date><risdate>1972</risdate><volume>221</volume><issue>2</issue><spage>389</spage><epage>414</epage><pages>389-414</pages><issn>0022-3751</issn><eissn>1469-7793</eissn><abstract>1. The cation composition of single barnacle muscle fibres following damage by axial insertion of a microsyringe has been
measured. The Na and Ca contents of these fibres were raised.
2. Electronmicroscopic studies of fibres following insertion of a microsyringe indicated that the damage done resulted in
tubular obstruction of the T-system.
3. Fibres loaded with radiosodium by micro-injection showed that the Na * efflux declined exponentially with time, but that in most fibres the slope ratio of d/d t ln [Na * ] 1 to d/d t (ln d[Na * ] i /d t ) was less than unity. Injections of distilled water deep in the fibre failed to influence the course of the Na * efflux.
4. K removal reduced the Na efflux by 47%. However, a few fibres displayed very little K-dependence.
5. When measured in fibres already soaked in a K-free medium for long periods the sodium efflux consisted of a brief rapid
phase, followed by a slow phase of Na loss.
6. In the presence of 30 m M -K, there was little or no rise in the Na efflux. Raising the external K to 50 or 100 m M caused a marked rise in the Na efflux. Raising the external K to 30 m M in the absence of external Ca 2+ led to a rise in the Na efflux. A high K solution always caused shortening of these fibres.
7. Internal application of 1 M or 1 m M -CaCl 2 often caused a significant rise in the Na efflux.
8. Internal application of 2·5 or 5 M saline caused a prompt and large fall in the Na efflux. In the presence of high K saline-loaded fibres failed to contract.
9. Internal application of 0·5 M -ATP stimulated the Na efflux. A larger effect was not observed in fibres pre-treated with 2 M -MgCl 2 . Internal application of 0·5 M -ArP was without effect.
10. The results indicate that the barnacle fibre is a suitable preparation for the study of Na fluxes by means of the micro-injection
technique. They also indicate that the mechanism regulating the Na efflux is not quite the same as that found in squid axon
or frog muscle.</abstract><cop>England</cop><pub>The Physiological Society</pub><pmid>5020983</pmid><doi>10.1113/jphysiol.1972.sp009757</doi><tpages>26</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adenosine Triphosphate - pharmacology Animals Anura Biological Transport, Active Calcium - metabolism Calcium Chloride - pharmacology Injections Membrane Potentials Methods Microscopy, Electron Muscles - metabolism Myofibrils - cytology Myofibrils - metabolism Phosphates - pharmacology Potassium - metabolism Sodium - metabolism Sodium Isotopes Thoracica Time Factors |
title | An investigation of sodium transport in barnacle muscle fibres by means of the microsyringe technique |
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