Effects of graded oral doses of meptazinol and pentazocine in comparison with placebo on experimentally induced pain in healthy humans

The opioid agonist/antagonist meptazinol has proven to exert significant analgesia in a series of painful conditions. This study investigated the effects of single oral doses of meptazinol 100, 200, and 400 mg in comparison with pentazocine 50 and 100 mg and with placebo on experimentally induced pa...

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Veröffentlicht in:British journal of clinical pharmacology 1983-08, Vol.16 (2), p.149-156
Hauptverfasser: Stacher, G., Steinringer, H., Winklehner, S., Mittelbach, G., Schneider, C.
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container_issue 2
container_start_page 149
container_title British journal of clinical pharmacology
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creator Stacher, G.
Steinringer, H.
Winklehner, S.
Mittelbach, G.
Schneider, C.
description The opioid agonist/antagonist meptazinol has proven to exert significant analgesia in a series of painful conditions. This study investigated the effects of single oral doses of meptazinol 100, 200, and 400 mg in comparison with pentazocine 50 and 100 mg and with placebo on experimentally induced pain. In addition, the side effect profiles were assessed. Twenty‐four healthy subjects participated each in six experiments in which they received, in random double‐blind fashion, each of the treatments. Every experiment comprised 10 series of measurements, two before and eight after drug administration, carried out at 30 min intervals. Meptazinol produced significant dose‐ related increases of threshold and tolerance to electrically and thermally induced pain. Meptazinol 400 mg was significantly superior to placebo in all pain measures and proved as effective as pentazocine 50 and 100 mg, which yielded about equal effects. Meptazinol 200 mg was significantly weaker than pentazocine 50 mg and differed significantly from placebo only in its effects on pain tolerance. Meptazinol did not cause any severe side effects or systematic alterations of respiration, blood pressure, heart rate and central nervous functions. Pentazocine caused a higher number and more severe side effects, one subject reporting severe dysphoria after pentazocine 100 mg. The results give further evidence that meptazinol is well suited to replace other opioid analgesics compromised by a high incidence of adverse effects.
doi_str_mv 10.1111/j.1365-2125.1983.tb04979.x
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This study investigated the effects of single oral doses of meptazinol 100, 200, and 400 mg in comparison with pentazocine 50 and 100 mg and with placebo on experimentally induced pain. In addition, the side effect profiles were assessed. Twenty‐four healthy subjects participated each in six experiments in which they received, in random double‐blind fashion, each of the treatments. Every experiment comprised 10 series of measurements, two before and eight after drug administration, carried out at 30 min intervals. Meptazinol produced significant dose‐ related increases of threshold and tolerance to electrically and thermally induced pain. Meptazinol 400 mg was significantly superior to placebo in all pain measures and proved as effective as pentazocine 50 and 100 mg, which yielded about equal effects. Meptazinol 200 mg was significantly weaker than pentazocine 50 mg and differed significantly from placebo only in its effects on pain tolerance. Meptazinol did not cause any severe side effects or systematic alterations of respiration, blood pressure, heart rate and central nervous functions. Pentazocine caused a higher number and more severe side effects, one subject reporting severe dysphoria after pentazocine 100 mg. The results give further evidence that meptazinol is well suited to replace other opioid analgesics compromised by a high incidence of adverse effects.</description><identifier>ISSN: 0306-5251</identifier><identifier>EISSN: 1365-2125</identifier><identifier>DOI: 10.1111/j.1365-2125.1983.tb04979.x</identifier><identifier>PMID: 6615689</identifier><identifier>CODEN: BCPHBM</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Adult ; Analgesics ; Arousal - drug effects ; Azepines - therapeutic use ; Biological and medical sciences ; Dose-Response Relationship, Drug ; Double-Blind Method ; Drug Evaluation ; Electric Stimulation ; Electroencephalography ; Female ; Flicker Fusion - drug effects ; Hemodynamics - drug effects ; Hot Temperature ; Humans ; Male ; Medical sciences ; Meptazinol - adverse effects ; Meptazinol - therapeutic use ; Neuropharmacology ; Pain - drug therapy ; Pentazocine - adverse effects ; Pentazocine - therapeutic use ; Pharmacology. 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This study investigated the effects of single oral doses of meptazinol 100, 200, and 400 mg in comparison with pentazocine 50 and 100 mg and with placebo on experimentally induced pain. In addition, the side effect profiles were assessed. Twenty‐four healthy subjects participated each in six experiments in which they received, in random double‐blind fashion, each of the treatments. Every experiment comprised 10 series of measurements, two before and eight after drug administration, carried out at 30 min intervals. Meptazinol produced significant dose‐ related increases of threshold and tolerance to electrically and thermally induced pain. Meptazinol 400 mg was significantly superior to placebo in all pain measures and proved as effective as pentazocine 50 and 100 mg, which yielded about equal effects. Meptazinol 200 mg was significantly weaker than pentazocine 50 mg and differed significantly from placebo only in its effects on pain tolerance. Meptazinol did not cause any severe side effects or systematic alterations of respiration, blood pressure, heart rate and central nervous functions. Pentazocine caused a higher number and more severe side effects, one subject reporting severe dysphoria after pentazocine 100 mg. The results give further evidence that meptazinol is well suited to replace other opioid analgesics compromised by a high incidence of adverse effects.</description><subject>Adult</subject><subject>Analgesics</subject><subject>Arousal - drug effects</subject><subject>Azepines - therapeutic use</subject><subject>Biological and medical sciences</subject><subject>Dose-Response Relationship, Drug</subject><subject>Double-Blind Method</subject><subject>Drug Evaluation</subject><subject>Electric Stimulation</subject><subject>Electroencephalography</subject><subject>Female</subject><subject>Flicker Fusion - drug effects</subject><subject>Hemodynamics - drug effects</subject><subject>Hot Temperature</subject><subject>Humans</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Meptazinol - adverse effects</subject><subject>Meptazinol - therapeutic use</subject><subject>Neuropharmacology</subject><subject>Pain - drug therapy</subject><subject>Pentazocine - adverse effects</subject><subject>Pentazocine - therapeutic use</subject><subject>Pharmacology. 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Drug treatments</topic><topic>Reaction Time - drug effects</topic><topic>Respiration - drug effects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Stacher, G.</creatorcontrib><creatorcontrib>Steinringer, H.</creatorcontrib><creatorcontrib>Winklehner, S.</creatorcontrib><creatorcontrib>Mittelbach, G.</creatorcontrib><creatorcontrib>Schneider, C.</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>PubMed Central (Full Participant titles)</collection><jtitle>British journal of clinical pharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Stacher, G.</au><au>Steinringer, H.</au><au>Winklehner, S.</au><au>Mittelbach, G.</au><au>Schneider, C.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effects of graded oral doses of meptazinol and pentazocine in comparison with placebo on experimentally induced pain in healthy humans</atitle><jtitle>British journal of clinical pharmacology</jtitle><addtitle>Br J Clin Pharmacol</addtitle><date>1983-08</date><risdate>1983</risdate><volume>16</volume><issue>2</issue><spage>149</spage><epage>156</epage><pages>149-156</pages><issn>0306-5251</issn><eissn>1365-2125</eissn><coden>BCPHBM</coden><abstract>The opioid agonist/antagonist meptazinol has proven to exert significant analgesia in a series of painful conditions. 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Meptazinol did not cause any severe side effects or systematic alterations of respiration, blood pressure, heart rate and central nervous functions. Pentazocine caused a higher number and more severe side effects, one subject reporting severe dysphoria after pentazocine 100 mg. The results give further evidence that meptazinol is well suited to replace other opioid analgesics compromised by a high incidence of adverse effects.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>6615689</pmid><doi>10.1111/j.1365-2125.1983.tb04979.x</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record>
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subjects Adult
Analgesics
Arousal - drug effects
Azepines - therapeutic use
Biological and medical sciences
Dose-Response Relationship, Drug
Double-Blind Method
Drug Evaluation
Electric Stimulation
Electroencephalography
Female
Flicker Fusion - drug effects
Hemodynamics - drug effects
Hot Temperature
Humans
Male
Medical sciences
Meptazinol - adverse effects
Meptazinol - therapeutic use
Neuropharmacology
Pain - drug therapy
Pentazocine - adverse effects
Pentazocine - therapeutic use
Pharmacology. Drug treatments
Reaction Time - drug effects
Respiration - drug effects
title Effects of graded oral doses of meptazinol and pentazocine in comparison with placebo on experimentally induced pain in healthy humans
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