Salivation after Single-Doses of the New Antidepressants Femoxetine, Mianserin and Citalopram. A Cross-Over Study
Abstract Twelve healthy volunteers were given oral single doses of a reference drug (nortriptyline), test drugs, and placebo on a randomised single-blind basis at weekly intervals. The doses corresponded to average daily patient medication. Spontaneous whole mouth salivation was measured before (at...
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Veröffentlicht in: | Pharmacopsychiatry 1984-07, Vol.17 (4), p.126-132 |
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creator | Clemmesen, L. Jensen, E. Min, S. K. Bolwig, T. G. Rafaelsen, O. J. |
description | Abstract
Twelve healthy volunteers were given oral single doses of a reference drug (nortriptyline), test drugs, and placebo on a randomised single-blind basis at weekly intervals. The doses corresponded to average daily patient medication. Spontaneous whole mouth salivation was measured before (at 10 p.m.) and 10 hours after drug administration (at 8 a.m.). Drug plasma levels were determined after 4 and 10 hours.
When analysing the salivations 10 hours after drug administration adjusted for the effects of the pre-treatment salivations, statistically significant inhibition of salivation was found after nortriptyline (56%), femoxetine (34%), and mianserin (29%) when compared with placebo, while for citalopram and cis- and trans-flupenthixol no significant inhibition of salivation was demonstrated (Fig. 1, Table 5).
From the estimated log linear regression coefficients, relating adjusted salivation rates and drug plasma levels 10 hours after drug administration (Table 6), and reported average steady-state plasma drug levels (Table 7), semiquantitative predictions of the average level of anticholinergic activity during long-term treatment may be made: For femoxetine and mianserin, moderate anticholinergic activity, less pronounced than with nortriptyline, are predicted, while for citalopram no such activity can be predicted (Table 7). |
doi_str_mv | 10.1055/s-2007-1017422 |
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Twelve healthy volunteers were given oral single doses of a reference drug (nortriptyline), test drugs, and placebo on a randomised single-blind basis at weekly intervals. The doses corresponded to average daily patient medication. Spontaneous whole mouth salivation was measured before (at 10 p.m.) and 10 hours after drug administration (at 8 a.m.). Drug plasma levels were determined after 4 and 10 hours.
When analysing the salivations 10 hours after drug administration adjusted for the effects of the pre-treatment salivations, statistically significant inhibition of salivation was found after nortriptyline (56%), femoxetine (34%), and mianserin (29%) when compared with placebo, while for citalopram and cis- and trans-flupenthixol no significant inhibition of salivation was demonstrated (Fig. 1, Table 5).
From the estimated log linear regression coefficients, relating adjusted salivation rates and drug plasma levels 10 hours after drug administration (Table 6), and reported average steady-state plasma drug levels (Table 7), semiquantitative predictions of the average level of anticholinergic activity during long-term treatment may be made: For femoxetine and mianserin, moderate anticholinergic activity, less pronounced than with nortriptyline, are predicted, while for citalopram no such activity can be predicted (Table 7).</description><identifier>ISSN: 0176-3679</identifier><identifier>EISSN: 1439-0795</identifier><identifier>DOI: 10.1055/s-2007-1017422</identifier><identifier>PMID: 6591216</identifier><language>eng</language><publisher>Germany</publisher><subject>Adolescent ; Adult ; Antidepressive Agents - blood ; Antidepressive Agents - pharmacology ; Citalopram ; Dibenzazepines - pharmacology ; Female ; Flupenthixol - blood ; Flupenthixol - pharmacology ; Humans ; Male ; Mianserin - blood ; Mianserin - pharmacology ; Nortriptyline - blood ; Nortriptyline - pharmacology ; Piperidines - blood ; Piperidines - pharmacology ; Propylamines - blood ; Propylamines - pharmacology ; Random Allocation ; Salivation - drug effects ; Serotonin Antagonists - blood ; Serotonin Antagonists - pharmacology</subject><ispartof>Pharmacopsychiatry, 1984-07, Vol.17 (4), p.126-132</ispartof><rights>Georg Thieme Verlag KG Stuttgart · New York</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c2432-2fc98a7b0910ecf662a024ae30dd02aa414478dab35672fe80996a81664e3bc63</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.thieme-connect.de/products/ejournals/pdf/10.1055/s-2007-1017422.pdf$$EPDF$$P50$$Gthieme$$H</linktopdf><link.rule.ids>314,780,784,3015,3016,27923,27924,54558</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/6591216$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Clemmesen, L.</creatorcontrib><creatorcontrib>Jensen, E.</creatorcontrib><creatorcontrib>Min, S. K.</creatorcontrib><creatorcontrib>Bolwig, T. G.</creatorcontrib><creatorcontrib>Rafaelsen, O. J.</creatorcontrib><title>Salivation after Single-Doses of the New Antidepressants Femoxetine, Mianserin and Citalopram. A Cross-Over Study</title><title>Pharmacopsychiatry</title><addtitle>Pharmacopsychiatry</addtitle><description>Abstract
Twelve healthy volunteers were given oral single doses of a reference drug (nortriptyline), test drugs, and placebo on a randomised single-blind basis at weekly intervals. The doses corresponded to average daily patient medication. Spontaneous whole mouth salivation was measured before (at 10 p.m.) and 10 hours after drug administration (at 8 a.m.). Drug plasma levels were determined after 4 and 10 hours.
When analysing the salivations 10 hours after drug administration adjusted for the effects of the pre-treatment salivations, statistically significant inhibition of salivation was found after nortriptyline (56%), femoxetine (34%), and mianserin (29%) when compared with placebo, while for citalopram and cis- and trans-flupenthixol no significant inhibition of salivation was demonstrated (Fig. 1, Table 5).
From the estimated log linear regression coefficients, relating adjusted salivation rates and drug plasma levels 10 hours after drug administration (Table 6), and reported average steady-state plasma drug levels (Table 7), semiquantitative predictions of the average level of anticholinergic activity during long-term treatment may be made: For femoxetine and mianserin, moderate anticholinergic activity, less pronounced than with nortriptyline, are predicted, while for citalopram no such activity can be predicted (Table 7).</description><subject>Adolescent</subject><subject>Adult</subject><subject>Antidepressive Agents - blood</subject><subject>Antidepressive Agents - pharmacology</subject><subject>Citalopram</subject><subject>Dibenzazepines - pharmacology</subject><subject>Female</subject><subject>Flupenthixol - blood</subject><subject>Flupenthixol - pharmacology</subject><subject>Humans</subject><subject>Male</subject><subject>Mianserin - blood</subject><subject>Mianserin - pharmacology</subject><subject>Nortriptyline - blood</subject><subject>Nortriptyline - pharmacology</subject><subject>Piperidines - blood</subject><subject>Piperidines - pharmacology</subject><subject>Propylamines - blood</subject><subject>Propylamines - pharmacology</subject><subject>Random Allocation</subject><subject>Salivation - drug effects</subject><subject>Serotonin Antagonists - blood</subject><subject>Serotonin Antagonists - pharmacology</subject><issn>0176-3679</issn><issn>1439-0795</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1984</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kE1P3DAQhq2qFV2gV26VfOqp3vorTnxcLeVDouVAOVuzyQSMEnuxHSj_vlntiltPI82882jmIeRM8KXgVfUjM8l5zQQXtZbyA1kIrSzjta0-ksXcNEyZ2n4mxzk_cS605eqIHJnKCinMgjzfweBfoPgYKPQFE73z4WFAdh4zZhp7Wh6R_sZXugrFd7hNmDOEkukFjvEvFh_wO_3lIWRMfmaEjq59gSFuE4xLuqLrFHNmty87dJm6t1PyqYch45dDPSH3Fz__rK_Yze3l9Xp1w1qplWSyb20D9YZbwbHtjZHApQZUvOu4BNBC67rpYKMqU8seG26tgUYYo1FtWqNOyLc9d5vi84S5uNHnFocBAsYpu0ZIWUmj5uByH2x3lybs3Tb5EdKbE9ztHLvsdo7dwfG88PVAnjYjdu_xg9R5zvbz8uhxRPcUpxTmV__H-wdMcITc</recordid><startdate>198407</startdate><enddate>198407</enddate><creator>Clemmesen, L.</creator><creator>Jensen, E.</creator><creator>Min, S. K.</creator><creator>Bolwig, T. G.</creator><creator>Rafaelsen, O. J.</creator><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>198407</creationdate><title>Salivation after Single-Doses of the New Antidepressants Femoxetine, Mianserin and Citalopram. A Cross-Over Study</title><author>Clemmesen, L. ; Jensen, E. ; Min, S. K. ; Bolwig, T. G. ; Rafaelsen, O. J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2432-2fc98a7b0910ecf662a024ae30dd02aa414478dab35672fe80996a81664e3bc63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1984</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Antidepressive Agents - blood</topic><topic>Antidepressive Agents - pharmacology</topic><topic>Citalopram</topic><topic>Dibenzazepines - pharmacology</topic><topic>Female</topic><topic>Flupenthixol - blood</topic><topic>Flupenthixol - pharmacology</topic><topic>Humans</topic><topic>Male</topic><topic>Mianserin - blood</topic><topic>Mianserin - pharmacology</topic><topic>Nortriptyline - blood</topic><topic>Nortriptyline - pharmacology</topic><topic>Piperidines - blood</topic><topic>Piperidines - pharmacology</topic><topic>Propylamines - blood</topic><topic>Propylamines - pharmacology</topic><topic>Random Allocation</topic><topic>Salivation - drug effects</topic><topic>Serotonin Antagonists - blood</topic><topic>Serotonin Antagonists - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Clemmesen, L.</creatorcontrib><creatorcontrib>Jensen, E.</creatorcontrib><creatorcontrib>Min, S. K.</creatorcontrib><creatorcontrib>Bolwig, T. G.</creatorcontrib><creatorcontrib>Rafaelsen, O. J.</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><jtitle>Pharmacopsychiatry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Clemmesen, L.</au><au>Jensen, E.</au><au>Min, S. K.</au><au>Bolwig, T. G.</au><au>Rafaelsen, O. J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Salivation after Single-Doses of the New Antidepressants Femoxetine, Mianserin and Citalopram. A Cross-Over Study</atitle><jtitle>Pharmacopsychiatry</jtitle><addtitle>Pharmacopsychiatry</addtitle><date>1984-07</date><risdate>1984</risdate><volume>17</volume><issue>4</issue><spage>126</spage><epage>132</epage><pages>126-132</pages><issn>0176-3679</issn><eissn>1439-0795</eissn><abstract>Abstract
Twelve healthy volunteers were given oral single doses of a reference drug (nortriptyline), test drugs, and placebo on a randomised single-blind basis at weekly intervals. The doses corresponded to average daily patient medication. Spontaneous whole mouth salivation was measured before (at 10 p.m.) and 10 hours after drug administration (at 8 a.m.). Drug plasma levels were determined after 4 and 10 hours.
When analysing the salivations 10 hours after drug administration adjusted for the effects of the pre-treatment salivations, statistically significant inhibition of salivation was found after nortriptyline (56%), femoxetine (34%), and mianserin (29%) when compared with placebo, while for citalopram and cis- and trans-flupenthixol no significant inhibition of salivation was demonstrated (Fig. 1, Table 5).
From the estimated log linear regression coefficients, relating adjusted salivation rates and drug plasma levels 10 hours after drug administration (Table 6), and reported average steady-state plasma drug levels (Table 7), semiquantitative predictions of the average level of anticholinergic activity during long-term treatment may be made: For femoxetine and mianserin, moderate anticholinergic activity, less pronounced than with nortriptyline, are predicted, while for citalopram no such activity can be predicted (Table 7).</abstract><cop>Germany</cop><pmid>6591216</pmid><doi>10.1055/s-2007-1017422</doi><tpages>7</tpages></addata></record> |
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subjects | Adolescent Adult Antidepressive Agents - blood Antidepressive Agents - pharmacology Citalopram Dibenzazepines - pharmacology Female Flupenthixol - blood Flupenthixol - pharmacology Humans Male Mianserin - blood Mianserin - pharmacology Nortriptyline - blood Nortriptyline - pharmacology Piperidines - blood Piperidines - pharmacology Propylamines - blood Propylamines - pharmacology Random Allocation Salivation - drug effects Serotonin Antagonists - blood Serotonin Antagonists - pharmacology |
title | Salivation after Single-Doses of the New Antidepressants Femoxetine, Mianserin and Citalopram. A Cross-Over Study |
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