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THE RELEASE OF LABELLED ACETYLCHOLINE AND CHOLINE FROM CEREBRAL CORTICAL SLICES STIMULATED ELECTRICALLY
1 In order to establish the origin of the increased efflux of radioactivity caused by electrical stimulation of cerebral cortical slices which had been incubated with [3H]‐choline, labelled choline and acetylcholine (ACh) collected by superfusion were separated by gold precipitation. 2 In the presen...
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Published in: | British journal of pharmacology 1974-12, Vol.52 (4), p.499-507 |
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creator | RICHARDSON, I.W. SZERB, J.C. |
description | 1
In order to establish the origin of the increased efflux of radioactivity caused by electrical stimulation of cerebral cortical slices which had been incubated with [3H]‐choline, labelled choline and acetylcholine (ACh) collected by superfusion were separated by gold precipitation.
2
In the presence of physostigmine electrical stimulation (1 Hz, 10 min) increased the release of only [3H]‐ACh which was greatly enhanced by the addition of atropine.
3
Continuous stimulation in the presence of physostigmine resulted in an evoked release of [3H]‐ACh which declined asymptotically. This evoked release appeared to follow first‐order kinetics with a rate constant which remained stable over the course of prolonged stimulation.
4
The rate constant for the evoked release of [3H]‐ACh with 1 Hz stimulation was three times greater in the presence of physostigmine and atropine than in the presence of physostigmine alone, while the size of the store from which [3H]‐ACh was released was nearly identical under these two conditions.
5
In the absence of physostigmine and atropine, stimulation caused the appearance of only [3H]‐choline in the samples.
6
Reduction of [3H]‐ACh stores before the application of physostigmine resulted in a reduced evoked release of total radioactivity, both in the absence or presence of physostigmine and atropine, and decreased the evoked release of [3H]‐ACh without affecting the release of [3H]‐choline.
7
Results suggest that electrical stimulation of cortical slices which had been incubated with [3H]‐choline causes the release of only [3H]‐ACh, both in the presence or absence of an anticholinesterase. The evoked increase in the efflux of total radioactivity is therefore a good measure of the release of [3H]‐ACh. |
doi_str_mv | 10.1111/j.1476-5381.1974.tb09717.x |
format | article |
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In order to establish the origin of the increased efflux of radioactivity caused by electrical stimulation of cerebral cortical slices which had been incubated with [3H]‐choline, labelled choline and acetylcholine (ACh) collected by superfusion were separated by gold precipitation.
2
In the presence of physostigmine electrical stimulation (1 Hz, 10 min) increased the release of only [3H]‐ACh which was greatly enhanced by the addition of atropine.
3
Continuous stimulation in the presence of physostigmine resulted in an evoked release of [3H]‐ACh which declined asymptotically. This evoked release appeared to follow first‐order kinetics with a rate constant which remained stable over the course of prolonged stimulation.
4
The rate constant for the evoked release of [3H]‐ACh with 1 Hz stimulation was three times greater in the presence of physostigmine and atropine than in the presence of physostigmine alone, while the size of the store from which [3H]‐ACh was released was nearly identical under these two conditions.
5
In the absence of physostigmine and atropine, stimulation caused the appearance of only [3H]‐choline in the samples.
6
Reduction of [3H]‐ACh stores before the application of physostigmine resulted in a reduced evoked release of total radioactivity, both in the absence or presence of physostigmine and atropine, and decreased the evoked release of [3H]‐ACh without affecting the release of [3H]‐choline.
7
Results suggest that electrical stimulation of cortical slices which had been incubated with [3H]‐choline causes the release of only [3H]‐ACh, both in the presence or absence of an anticholinesterase. The evoked increase in the efflux of total radioactivity is therefore a good measure of the release of [3H]‐ACh.</description><identifier>ISSN: 0007-1188</identifier><identifier>EISSN: 1476-5381</identifier><identifier>DOI: 10.1111/j.1476-5381.1974.tb09717.x</identifier><identifier>PMID: 4455326</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Acetylcholine - metabolism ; Animals ; Atropine - pharmacology ; Cerebral Cortex - metabolism ; Cerebral Cortex - physiology ; Choline - metabolism ; Cholinesterase Inhibitors - pharmacology ; Electric Stimulation ; In Vitro Techniques ; Physostigmine - pharmacology ; Rats ; Systematic Pharmacology ; Time Factors</subject><ispartof>British journal of pharmacology, 1974-12, Vol.52 (4), p.499-507</ispartof><rights>1974 British Pharmacological Society</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4777-4bce88c83ab41272bc0707d8c2cba4e26fdb24d001982fba122a012fe41263703</citedby><cites>FETCH-LOGICAL-c4777-4bce88c83ab41272bc0707d8c2cba4e26fdb24d001982fba122a012fe41263703</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/PMC1776885/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1776885/$$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/4455326$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>RICHARDSON, I.W.</creatorcontrib><creatorcontrib>SZERB, J.C.</creatorcontrib><title>THE RELEASE OF LABELLED ACETYLCHOLINE AND CHOLINE FROM CEREBRAL CORTICAL SLICES STIMULATED ELECTRICALLY</title><title>British journal of pharmacology</title><addtitle>Br J Pharmacol</addtitle><description>1
In order to establish the origin of the increased efflux of radioactivity caused by electrical stimulation of cerebral cortical slices which had been incubated with [3H]‐choline, labelled choline and acetylcholine (ACh) collected by superfusion were separated by gold precipitation.
2
In the presence of physostigmine electrical stimulation (1 Hz, 10 min) increased the release of only [3H]‐ACh which was greatly enhanced by the addition of atropine.
3
Continuous stimulation in the presence of physostigmine resulted in an evoked release of [3H]‐ACh which declined asymptotically. This evoked release appeared to follow first‐order kinetics with a rate constant which remained stable over the course of prolonged stimulation.
4
The rate constant for the evoked release of [3H]‐ACh with 1 Hz stimulation was three times greater in the presence of physostigmine and atropine than in the presence of physostigmine alone, while the size of the store from which [3H]‐ACh was released was nearly identical under these two conditions.
5
In the absence of physostigmine and atropine, stimulation caused the appearance of only [3H]‐choline in the samples.
6
Reduction of [3H]‐ACh stores before the application of physostigmine resulted in a reduced evoked release of total radioactivity, both in the absence or presence of physostigmine and atropine, and decreased the evoked release of [3H]‐ACh without affecting the release of [3H]‐choline.
7
Results suggest that electrical stimulation of cortical slices which had been incubated with [3H]‐choline causes the release of only [3H]‐ACh, both in the presence or absence of an anticholinesterase. The evoked increase in the efflux of total radioactivity is therefore a good measure of the release of [3H]‐ACh.</description><subject>Acetylcholine - metabolism</subject><subject>Animals</subject><subject>Atropine - pharmacology</subject><subject>Cerebral Cortex - metabolism</subject><subject>Cerebral Cortex - physiology</subject><subject>Choline - metabolism</subject><subject>Cholinesterase Inhibitors - pharmacology</subject><subject>Electric Stimulation</subject><subject>In Vitro Techniques</subject><subject>Physostigmine - pharmacology</subject><subject>Rats</subject><subject>Systematic Pharmacology</subject><subject>Time Factors</subject><issn>0007-1188</issn><issn>1476-5381</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1974</creationdate><recordtype>article</recordtype><recordid>eNqVkcFv2jAUxq1qU8e6_gmVrB12S2Y7Tmx22BSCKUhuU4X0wMlyjMOCAqEJbO1_X0cw1B7ni5_0fe977-kHwFeMfOze97WPKYu8MODYx0NG_X2Bhgwz__kCDM7SBzBACDEPY84_gc9dt0bIiSy8BJeUhmFAogFY5VMBMyFFPBcwnUAZj4SUYgzjROQLmUxTObsXML4fw3_1JEvvYCIyMcpiCZM0y2eJK-Zylog5nOezu0cZ5y7CpSZ51oty8QV8LHXd2evTfwUeJyJPpp5Mb3uHZ9xmzKOFsZwbHuiCYsJIYRBDbMkNMYWmlkTlsiB06Q4ZclIWGhOiESalde4oYCi4Aj-PubtDsbFLY7f7Vtdq11Yb3b6oRlfqvbKtfqtV80dhxiLOQxfw7RTQNk8H2-3VpuqMrWu9tc2hU5xEjA9pP-nH0WjaputaW56HYKR6TGqtehaqZ6F6TOqEST275pu3a55bT1yc_uuo_61q-_IfyWr0MO2r4BWJ8ZrB</recordid><startdate>197412</startdate><enddate>197412</enddate><creator>RICHARDSON, I.W.</creator><creator>SZERB, J.C.</creator><general>Blackwell Publishing Ltd</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><scope>5PM</scope></search><sort><creationdate>197412</creationdate><title>THE RELEASE OF LABELLED ACETYLCHOLINE AND CHOLINE FROM CEREBRAL CORTICAL SLICES STIMULATED ELECTRICALLY</title><author>RICHARDSON, I.W. ; SZERB, J.C.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4777-4bce88c83ab41272bc0707d8c2cba4e26fdb24d001982fba122a012fe41263703</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1974</creationdate><topic>Acetylcholine - metabolism</topic><topic>Animals</topic><topic>Atropine - pharmacology</topic><topic>Cerebral Cortex - metabolism</topic><topic>Cerebral Cortex - physiology</topic><topic>Choline - metabolism</topic><topic>Cholinesterase Inhibitors - pharmacology</topic><topic>Electric Stimulation</topic><topic>In Vitro Techniques</topic><topic>Physostigmine - pharmacology</topic><topic>Rats</topic><topic>Systematic Pharmacology</topic><topic>Time Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>RICHARDSON, I.W.</creatorcontrib><creatorcontrib>SZERB, J.C.</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><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>RICHARDSON, I.W.</au><au>SZERB, J.C.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>THE RELEASE OF LABELLED ACETYLCHOLINE AND CHOLINE FROM CEREBRAL CORTICAL SLICES STIMULATED ELECTRICALLY</atitle><jtitle>British journal of pharmacology</jtitle><addtitle>Br J Pharmacol</addtitle><date>1974-12</date><risdate>1974</risdate><volume>52</volume><issue>4</issue><spage>499</spage><epage>507</epage><pages>499-507</pages><issn>0007-1188</issn><eissn>1476-5381</eissn><abstract>1
In order to establish the origin of the increased efflux of radioactivity caused by electrical stimulation of cerebral cortical slices which had been incubated with [3H]‐choline, labelled choline and acetylcholine (ACh) collected by superfusion were separated by gold precipitation.
2
In the presence of physostigmine electrical stimulation (1 Hz, 10 min) increased the release of only [3H]‐ACh which was greatly enhanced by the addition of atropine.
3
Continuous stimulation in the presence of physostigmine resulted in an evoked release of [3H]‐ACh which declined asymptotically. This evoked release appeared to follow first‐order kinetics with a rate constant which remained stable over the course of prolonged stimulation.
4
The rate constant for the evoked release of [3H]‐ACh with 1 Hz stimulation was three times greater in the presence of physostigmine and atropine than in the presence of physostigmine alone, while the size of the store from which [3H]‐ACh was released was nearly identical under these two conditions.
5
In the absence of physostigmine and atropine, stimulation caused the appearance of only [3H]‐choline in the samples.
6
Reduction of [3H]‐ACh stores before the application of physostigmine resulted in a reduced evoked release of total radioactivity, both in the absence or presence of physostigmine and atropine, and decreased the evoked release of [3H]‐ACh without affecting the release of [3H]‐choline.
7
Results suggest that electrical stimulation of cortical slices which had been incubated with [3H]‐choline causes the release of only [3H]‐ACh, both in the presence or absence of an anticholinesterase. The evoked increase in the efflux of total radioactivity is therefore a good measure of the release of [3H]‐ACh.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>4455326</pmid><doi>10.1111/j.1476-5381.1974.tb09717.x</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Acetylcholine - metabolism Animals Atropine - pharmacology Cerebral Cortex - metabolism Cerebral Cortex - physiology Choline - metabolism Cholinesterase Inhibitors - pharmacology Electric Stimulation In Vitro Techniques Physostigmine - pharmacology Rats Systematic Pharmacology Time Factors |
title | THE RELEASE OF LABELLED ACETYLCHOLINE AND CHOLINE FROM CEREBRAL CORTICAL SLICES STIMULATED ELECTRICALLY |
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