Physostigmine challenge before and after chronic cholinergic blockade in elderly volunteers

Background: As a test of possible muscarinic up-regulation, the cortisol response to intravenous (IV) physostigmine (an anticholinesterase) was measured in 9 elderly volunteers before and after chronic cholinergic blockade with the muscarinic cholinergic antagonist scopolamine. Methods: Each of the...

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Veröffentlicht in:Biological psychiatry (1969) 1999-07, Vol.46 (2), p.189-195
Hauptverfasser: Dukoff, Ruth, Wilkinson, Charles W, Lasser, Robert, Friz, Judy, Conway, Anne, Bahro, Marcel, Peskind, Elaine R, Sunderland, Trey
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container_end_page 195
container_issue 2
container_start_page 189
container_title Biological psychiatry (1969)
container_volume 46
creator Dukoff, Ruth
Wilkinson, Charles W
Lasser, Robert
Friz, Judy
Conway, Anne
Bahro, Marcel
Peskind, Elaine R
Sunderland, Trey
description Background: As a test of possible muscarinic up-regulation, the cortisol response to intravenous (IV) physostigmine (an anticholinesterase) was measured in 9 elderly volunteers before and after chronic cholinergic blockade with the muscarinic cholinergic antagonist scopolamine. Methods: Each of the 9 elderly control subjects was given two physostigmine (0.5 mg IV) infusions separated by 21 doses of nightly scopolamine (1.2 mg p.o.). No scopolamine was administered the night before infusions, and glycopyrrolate (0.2 mg IV) was administered prior to physostigmine to block its peripheral effects. Vital signs were monitored and blood samples were collected at six time points surrounding the physostigmine infusion (−10, +10, +20, +30, +50, and +70 min). Behavioral measures and cognitive tests were administered prior to and 30 min after the physostigmine. Results: The cortisol response to physostigmine was greater after the second (post-chronic scopolamine) infusion study compared to the first ( p < .05) as measured by an area under the curve analysis of all time points. When individual time points were compared, the mean cortisol response was significantly increased after the second physostigmine infusion at the +50- and +70-min time points ( p < .05). There were no significant changes in behavioral rating scales, cognitive tests, or vital signs between the two physostigmine infusion study days. Conclusions: This study demonstrates increased hypothalamic–pituitary–adrenocortical axis responsivity to a central nervous system cholinergic stimulus after chronic muscarinic blockade in 9 elderly control subjects. It also gives further evidence to support previous suggestions of muscarinic plasticity, specifically postsynaptic up-regulation, in the aging brain following exposure to chronic anticholinergic treatment.
doi_str_mv 10.1016/S0006-3223(98)00286-8
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Methods: Each of the 9 elderly control subjects was given two physostigmine (0.5 mg IV) infusions separated by 21 doses of nightly scopolamine (1.2 mg p.o.). No scopolamine was administered the night before infusions, and glycopyrrolate (0.2 mg IV) was administered prior to physostigmine to block its peripheral effects. Vital signs were monitored and blood samples were collected at six time points surrounding the physostigmine infusion (−10, +10, +20, +30, +50, and +70 min). Behavioral measures and cognitive tests were administered prior to and 30 min after the physostigmine. Results: The cortisol response to physostigmine was greater after the second (post-chronic scopolamine) infusion study compared to the first ( p &lt; .05) as measured by an area under the curve analysis of all time points. When individual time points were compared, the mean cortisol response was significantly increased after the second physostigmine infusion at the +50- and +70-min time points ( p &lt; .05). There were no significant changes in behavioral rating scales, cognitive tests, or vital signs between the two physostigmine infusion study days. Conclusions: This study demonstrates increased hypothalamic–pituitary–adrenocortical axis responsivity to a central nervous system cholinergic stimulus after chronic muscarinic blockade in 9 elderly control subjects. It also gives further evidence to support previous suggestions of muscarinic plasticity, specifically postsynaptic up-regulation, in the aging brain following exposure to chronic anticholinergic treatment.</description><identifier>ISSN: 0006-3223</identifier><identifier>EISSN: 1873-2402</identifier><identifier>DOI: 10.1016/S0006-3223(98)00286-8</identifier><identifier>PMID: 10418693</identifier><identifier>CODEN: BIPCBF</identifier><language>eng</language><publisher>New York, NY: Elsevier Inc</publisher><subject>Aged ; Aging ; Aging - physiology ; Alzheimer’s ; Biological and medical sciences ; Brief Psychiatric Rating Scale ; Cholinesterase Inhibitors - pharmacology ; Cognition Disorders - diagnosis ; cortisol ; Depressive Disorder - diagnosis ; Depressive Disorder - psychology ; Dose-Response Relationship, Drug ; Female ; Fundamental and applied biological sciences. Psychology ; General aspects. Models. Methods ; Glycopyrrolate - pharmacology ; Humans ; Hydrocortisone - blood ; Hypothalamo-Hypophyseal System - drug effects ; Injections, Intravenous ; Male ; Muscarinic Antagonists - pharmacology ; neuroendocrine ; Neuronal Plasticity - drug effects ; physostigmine ; Physostigmine - pharmacology ; Pituitary-Adrenal System - drug effects ; plasticity ; Presynaptic Terminals - drug effects ; Receptors, Muscarinic - drug effects ; scopolamine ; Scopolamine - pharmacology ; Severity of Illness Index ; Time Factors ; Up-Regulation - drug effects ; Vertebrates: nervous system and sense organs</subject><ispartof>Biological psychiatry (1969), 1999-07, Vol.46 (2), p.189-195</ispartof><rights>1999 Society of Biological Psychiatry</rights><rights>1999 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c390t-3bb4c5b078cd1a28e1f496811de8a4270a6f6e2c76cce481b1241ad86fda40e63</citedby><cites>FETCH-LOGICAL-c390t-3bb4c5b078cd1a28e1f496811de8a4270a6f6e2c76cce481b1241ad86fda40e63</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/S0006-3223(98)00286-8$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=1881238$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10418693$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Dukoff, Ruth</creatorcontrib><creatorcontrib>Wilkinson, Charles W</creatorcontrib><creatorcontrib>Lasser, Robert</creatorcontrib><creatorcontrib>Friz, Judy</creatorcontrib><creatorcontrib>Conway, Anne</creatorcontrib><creatorcontrib>Bahro, Marcel</creatorcontrib><creatorcontrib>Peskind, Elaine R</creatorcontrib><creatorcontrib>Sunderland, Trey</creatorcontrib><title>Physostigmine challenge before and after chronic cholinergic blockade in elderly volunteers</title><title>Biological psychiatry (1969)</title><addtitle>Biol Psychiatry</addtitle><description>Background: As a test of possible muscarinic up-regulation, the cortisol response to intravenous (IV) physostigmine (an anticholinesterase) was measured in 9 elderly volunteers before and after chronic cholinergic blockade with the muscarinic cholinergic antagonist scopolamine. Methods: Each of the 9 elderly control subjects was given two physostigmine (0.5 mg IV) infusions separated by 21 doses of nightly scopolamine (1.2 mg p.o.). No scopolamine was administered the night before infusions, and glycopyrrolate (0.2 mg IV) was administered prior to physostigmine to block its peripheral effects. Vital signs were monitored and blood samples were collected at six time points surrounding the physostigmine infusion (−10, +10, +20, +30, +50, and +70 min). Behavioral measures and cognitive tests were administered prior to and 30 min after the physostigmine. Results: The cortisol response to physostigmine was greater after the second (post-chronic scopolamine) infusion study compared to the first ( p &lt; .05) as measured by an area under the curve analysis of all time points. When individual time points were compared, the mean cortisol response was significantly increased after the second physostigmine infusion at the +50- and +70-min time points ( p &lt; .05). There were no significant changes in behavioral rating scales, cognitive tests, or vital signs between the two physostigmine infusion study days. Conclusions: This study demonstrates increased hypothalamic–pituitary–adrenocortical axis responsivity to a central nervous system cholinergic stimulus after chronic muscarinic blockade in 9 elderly control subjects. It also gives further evidence to support previous suggestions of muscarinic plasticity, specifically postsynaptic up-regulation, in the aging brain following exposure to chronic anticholinergic treatment.</description><subject>Aged</subject><subject>Aging</subject><subject>Aging - physiology</subject><subject>Alzheimer’s</subject><subject>Biological and medical sciences</subject><subject>Brief Psychiatric Rating Scale</subject><subject>Cholinesterase Inhibitors - pharmacology</subject><subject>Cognition Disorders - diagnosis</subject><subject>cortisol</subject><subject>Depressive Disorder - diagnosis</subject><subject>Depressive Disorder - psychology</subject><subject>Dose-Response Relationship, Drug</subject><subject>Female</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>General aspects. Models. Methods</subject><subject>Glycopyrrolate - pharmacology</subject><subject>Humans</subject><subject>Hydrocortisone - blood</subject><subject>Hypothalamo-Hypophyseal System - drug effects</subject><subject>Injections, Intravenous</subject><subject>Male</subject><subject>Muscarinic Antagonists - pharmacology</subject><subject>neuroendocrine</subject><subject>Neuronal Plasticity - drug effects</subject><subject>physostigmine</subject><subject>Physostigmine - pharmacology</subject><subject>Pituitary-Adrenal System - drug effects</subject><subject>plasticity</subject><subject>Presynaptic Terminals - drug effects</subject><subject>Receptors, Muscarinic - drug effects</subject><subject>scopolamine</subject><subject>Scopolamine - pharmacology</subject><subject>Severity of Illness Index</subject><subject>Time Factors</subject><subject>Up-Regulation - drug effects</subject><subject>Vertebrates: nervous system and sense organs</subject><issn>0006-3223</issn><issn>1873-2402</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkEtP3DAQgK0KVLbQn9AqB4TKIcXjeB3nhBBqAQmJStBTD5ZjT3bdem2ws0j77_E-VLhxmhnNNw99hHwB-h0oiLN7SqmoG8aab508pZRJUcsPZAKybWrGKdsjk__IAfmU899StozBR3IAlIMUXTMhf37NVznm0c0WLmBl5tp7DDOsehxiwkoHW-lhxFRaKQZnSoy-oGlW8t5H809brFyo0FtMflU9R78MI2LKR2R_0D7j5108JL9__ni4vK5v765uLi9ua9N0dKybvudm2tNWGguaSYSBd0ICWJSas5ZqMQhkphXGIJfQA-OgrRSD1ZyiaA7JyXbvY4pPS8yjWrhs0HsdMC6zEl0HU8FpAadb0KSYc8JBPSa30GmlgKq1VbWxqtbKVCfVxqqSZe7r7sCyX6B9M7XVWIDjHaCz0X5IOhiXXzkpgTXrPedbDIuNZ4dJZeMwGLQuoRmVje6dT14AcM-U-w</recordid><startdate>19990715</startdate><enddate>19990715</enddate><creator>Dukoff, Ruth</creator><creator>Wilkinson, Charles W</creator><creator>Lasser, Robert</creator><creator>Friz, Judy</creator><creator>Conway, Anne</creator><creator>Bahro, Marcel</creator><creator>Peskind, Elaine R</creator><creator>Sunderland, Trey</creator><general>Elsevier Inc</general><general>Elsevier Science</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></search><sort><creationdate>19990715</creationdate><title>Physostigmine challenge before and after chronic cholinergic blockade in elderly volunteers</title><author>Dukoff, Ruth ; Wilkinson, Charles W ; Lasser, Robert ; Friz, Judy ; Conway, Anne ; Bahro, Marcel ; Peskind, Elaine R ; Sunderland, Trey</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c390t-3bb4c5b078cd1a28e1f496811de8a4270a6f6e2c76cce481b1241ad86fda40e63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>Aged</topic><topic>Aging</topic><topic>Aging - physiology</topic><topic>Alzheimer’s</topic><topic>Biological and medical sciences</topic><topic>Brief Psychiatric Rating Scale</topic><topic>Cholinesterase Inhibitors - pharmacology</topic><topic>Cognition Disorders - diagnosis</topic><topic>cortisol</topic><topic>Depressive Disorder - diagnosis</topic><topic>Depressive Disorder - psychology</topic><topic>Dose-Response Relationship, Drug</topic><topic>Female</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>General aspects. Models. Methods</topic><topic>Glycopyrrolate - pharmacology</topic><topic>Humans</topic><topic>Hydrocortisone - blood</topic><topic>Hypothalamo-Hypophyseal System - drug effects</topic><topic>Injections, Intravenous</topic><topic>Male</topic><topic>Muscarinic Antagonists - pharmacology</topic><topic>neuroendocrine</topic><topic>Neuronal Plasticity - drug effects</topic><topic>physostigmine</topic><topic>Physostigmine - pharmacology</topic><topic>Pituitary-Adrenal System - drug effects</topic><topic>plasticity</topic><topic>Presynaptic Terminals - drug effects</topic><topic>Receptors, Muscarinic - drug effects</topic><topic>scopolamine</topic><topic>Scopolamine - pharmacology</topic><topic>Severity of Illness Index</topic><topic>Time Factors</topic><topic>Up-Regulation - drug effects</topic><topic>Vertebrates: nervous system and sense organs</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Dukoff, Ruth</creatorcontrib><creatorcontrib>Wilkinson, Charles W</creatorcontrib><creatorcontrib>Lasser, Robert</creatorcontrib><creatorcontrib>Friz, Judy</creatorcontrib><creatorcontrib>Conway, Anne</creatorcontrib><creatorcontrib>Bahro, Marcel</creatorcontrib><creatorcontrib>Peskind, Elaine R</creatorcontrib><creatorcontrib>Sunderland, Trey</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><jtitle>Biological psychiatry (1969)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Dukoff, Ruth</au><au>Wilkinson, Charles W</au><au>Lasser, Robert</au><au>Friz, Judy</au><au>Conway, Anne</au><au>Bahro, Marcel</au><au>Peskind, Elaine R</au><au>Sunderland, Trey</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Physostigmine challenge before and after chronic cholinergic blockade in elderly volunteers</atitle><jtitle>Biological psychiatry (1969)</jtitle><addtitle>Biol Psychiatry</addtitle><date>1999-07-15</date><risdate>1999</risdate><volume>46</volume><issue>2</issue><spage>189</spage><epage>195</epage><pages>189-195</pages><issn>0006-3223</issn><eissn>1873-2402</eissn><coden>BIPCBF</coden><abstract>Background: As a test of possible muscarinic up-regulation, the cortisol response to intravenous (IV) physostigmine (an anticholinesterase) was measured in 9 elderly volunteers before and after chronic cholinergic blockade with the muscarinic cholinergic antagonist scopolamine. Methods: Each of the 9 elderly control subjects was given two physostigmine (0.5 mg IV) infusions separated by 21 doses of nightly scopolamine (1.2 mg p.o.). No scopolamine was administered the night before infusions, and glycopyrrolate (0.2 mg IV) was administered prior to physostigmine to block its peripheral effects. Vital signs were monitored and blood samples were collected at six time points surrounding the physostigmine infusion (−10, +10, +20, +30, +50, and +70 min). Behavioral measures and cognitive tests were administered prior to and 30 min after the physostigmine. Results: The cortisol response to physostigmine was greater after the second (post-chronic scopolamine) infusion study compared to the first ( p &lt; .05) as measured by an area under the curve analysis of all time points. When individual time points were compared, the mean cortisol response was significantly increased after the second physostigmine infusion at the +50- and +70-min time points ( p &lt; .05). There were no significant changes in behavioral rating scales, cognitive tests, or vital signs between the two physostigmine infusion study days. Conclusions: This study demonstrates increased hypothalamic–pituitary–adrenocortical axis responsivity to a central nervous system cholinergic stimulus after chronic muscarinic blockade in 9 elderly control subjects. It also gives further evidence to support previous suggestions of muscarinic plasticity, specifically postsynaptic up-regulation, in the aging brain following exposure to chronic anticholinergic treatment.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>10418693</pmid><doi>10.1016/S0006-3223(98)00286-8</doi><tpages>7</tpages></addata></record>
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subjects Aged
Aging
Aging - physiology
Alzheimer’s
Biological and medical sciences
Brief Psychiatric Rating Scale
Cholinesterase Inhibitors - pharmacology
Cognition Disorders - diagnosis
cortisol
Depressive Disorder - diagnosis
Depressive Disorder - psychology
Dose-Response Relationship, Drug
Female
Fundamental and applied biological sciences. Psychology
General aspects. Models. Methods
Glycopyrrolate - pharmacology
Humans
Hydrocortisone - blood
Hypothalamo-Hypophyseal System - drug effects
Injections, Intravenous
Male
Muscarinic Antagonists - pharmacology
neuroendocrine
Neuronal Plasticity - drug effects
physostigmine
Physostigmine - pharmacology
Pituitary-Adrenal System - drug effects
plasticity
Presynaptic Terminals - drug effects
Receptors, Muscarinic - drug effects
scopolamine
Scopolamine - pharmacology
Severity of Illness Index
Time Factors
Up-Regulation - drug effects
Vertebrates: nervous system and sense organs
title Physostigmine challenge before and after chronic cholinergic blockade in elderly volunteers
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