Elevated customary alcohol consumption attenuates opioid effects
Regular alcohol consumption is on the rise among older adults and has the potential of altering the subjective experience of pain and response to pain medications. This study examined the cognitive, analgesic and side effect response to oxycodone in middle age and older adults with elevated levels o...
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Published in | Pharmacology, biochemistry and behavior Vol. 211; p. 173295 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
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Elsevier Inc
01.12.2021
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Abstract | Regular alcohol consumption is on the rise among older adults and has the potential of altering the subjective experience of pain and response to pain medications. This study examined the cognitive, analgesic and side effect response to oxycodone in middle age and older adults with elevated levels of customary alcohol consumption in a human laboratory setting.
After refraining from alcohol for one day, eligible participants underwent baseline assessment cognition and side effects by means of questionnaires that were repeated at three time points (90 min, 5 and 8 h) following administration of a 10 mg oral dose of oxycodone. Response to pain stimulus (Cold Pressor Test (CPT)), pupil size, and plasma oxycodone were also measured.
One hundred twenty-eight adults (age 35–85) completed the study day. Compared to those with lower customary alcohol consumption, participants with elevated alcohol consumption showed attenuated opioid-induced pupil constriction and cognitive decline on objective measures of working memory, sustained attention, inhibitory control, coordination on a simulated driving task, and subjective dysphoric effects with enhanced subjective euphoric effects. Oxycodone pharmacokinetics, pain tolerance to CPT, and Berg balance were impacted comparably between alcohol consumption groups. Women endorsed greater negative drug effects, whereas men endorsed positive drug effects.
Independent of subject's age, elevated customary alcohol consumption attenuates opioid central effects (i.e., pupil miosis, impaired cognition) and gender influences subjective drug effects. Clinicians should consider alcohol consumption and gender when prescribing opioid medications.
•Oxycodone impact on the central nervous system (CNS) as indicated by pupil constriction (miosis) is reduced or attenuated in middle age persons who consume heavier amounts of alcohol (average 3.3 drinks per day/ 25 drinks per week).•Oxycodone typically impairs cognition around 90 minutes following consumption of a 10mg dose, however, for middle age persons with customary alcohol consumption habits in the heavier range (average 3.3 drinks per day/ 25 drinks per week) there is reduced or minimal impairment of attention, working memory, declarative memory, inhibitory control, and performance on a simulated driving task.•Women in comparison to men, particularly women with elevated levels of customary alcohol consumption, did not demonstrate the typical increase in analgesia from oxycodone (10mg) in response to an experimental pain stimulus.•Male gender, prior experience of drug use and heavier customary alcohol consumption were all associated with stronger endorsement of positive or good drug effects from oxycodone. |
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AbstractList | Regular alcohol consumption is on the rise among older adults and has the potential of altering the subjective experience of pain and response to pain medications. This study examined the cognitive, analgesic and side effect response to oxycodone in middle age and older adults with elevated levels of customary alcohol consumption in a human laboratory setting.
After refraining from alcohol for one day, eligible participants underwent baseline assessment cognition and side effects by means of questionnaires that were repeated at three time points (90 min, 5 and 8 h) following administration of a 10 mg oral dose of oxycodone. Response to pain stimulus (Cold Pressor Test (CPT)), pupil size, and plasma oxycodone were also measured.
One hundred twenty-eight adults (age 35-85) completed the study day. Compared to those with lower customary alcohol consumption, participants with elevated alcohol consumption showed attenuated opioid-induced pupil constriction and cognitive decline on objective measures of working memory, sustained attention, inhibitory control, coordination on a simulated driving task, and subjective dysphoric effects with enhanced subjective euphoric effects. Oxycodone pharmacokinetics, pain tolerance to CPT, and Berg balance were impacted comparably between alcohol consumption groups. Women endorsed greater negative drug effects, whereas men endorsed positive drug effects.
Independent of subject's age, elevated customary alcohol consumption attenuates opioid central effects (i.e., pupil miosis, impaired cognition) and gender influences subjective drug effects. Clinicians should consider alcohol consumption and gender when prescribing opioid medications. Regular alcohol consumption is on the rise among older adults and has the potential of altering the subjective experience of pain and response to pain medications. This study examined the cognitive, analgesic and side effect response to oxycodone in middle age and older adults with elevated levels of customary alcohol consumption in a human laboratory setting. After refraining from alcohol for one day, eligible participants underwent baseline assessment cognition and side effects by means of questionnaires that were repeated at three time points (90 min, 5 and 8 h) following administration of a 10 mg oral dose of oxycodone. Response to pain stimulus (Cold Pressor Test (CPT)), pupil size, and plasma oxycodone were also measured. One hundred twenty-eight adults (age 35–85) completed the study day. Compared to those with lower customary alcohol consumption, participants with elevated alcohol consumption showed attenuated opioid-induced pupil constriction and cognitive decline on objective measures of working memory, sustained attention, inhibitory control, coordination on a simulated driving task, and subjective dysphoric effects with enhanced subjective euphoric effects. Oxycodone pharmacokinetics, pain tolerance to CPT, and Berg balance were impacted comparably between alcohol consumption groups. Women endorsed greater negative drug effects, whereas men endorsed positive drug effects. Independent of subject's age, elevated customary alcohol consumption attenuates opioid central effects (i.e., pupil miosis, impaired cognition) and gender influences subjective drug effects. Clinicians should consider alcohol consumption and gender when prescribing opioid medications. •Oxycodone impact on the central nervous system (CNS) as indicated by pupil constriction (miosis) is reduced or attenuated in middle age persons who consume heavier amounts of alcohol (average 3.3 drinks per day/ 25 drinks per week).•Oxycodone typically impairs cognition around 90 minutes following consumption of a 10mg dose, however, for middle age persons with customary alcohol consumption habits in the heavier range (average 3.3 drinks per day/ 25 drinks per week) there is reduced or minimal impairment of attention, working memory, declarative memory, inhibitory control, and performance on a simulated driving task.•Women in comparison to men, particularly women with elevated levels of customary alcohol consumption, did not demonstrate the typical increase in analgesia from oxycodone (10mg) in response to an experimental pain stimulus.•Male gender, prior experience of drug use and heavier customary alcohol consumption were all associated with stronger endorsement of positive or good drug effects from oxycodone. Regular alcohol consumption is on the rise among older adults and has the potential of altering the subjective experience of pain and response to pain medications. This study examined the cognitive, analgesic and side effect response to oxycodone in middle age and older adults with elevated levels of customary alcohol consumption in a human laboratory setting.BACKGROUNDRegular alcohol consumption is on the rise among older adults and has the potential of altering the subjective experience of pain and response to pain medications. This study examined the cognitive, analgesic and side effect response to oxycodone in middle age and older adults with elevated levels of customary alcohol consumption in a human laboratory setting.After refraining from alcohol for one day, eligible participants underwent baseline assessment cognition and side effects by means of questionnaires that were repeated at three time points (90 min, 5 and 8 h) following administration of a 10 mg oral dose of oxycodone. Response to pain stimulus (Cold Pressor Test (CPT)), pupil size, and plasma oxycodone were also measured.METHODSAfter refraining from alcohol for one day, eligible participants underwent baseline assessment cognition and side effects by means of questionnaires that were repeated at three time points (90 min, 5 and 8 h) following administration of a 10 mg oral dose of oxycodone. Response to pain stimulus (Cold Pressor Test (CPT)), pupil size, and plasma oxycodone were also measured.One hundred twenty-eight adults (age 35-85) completed the study day. Compared to those with lower customary alcohol consumption, participants with elevated alcohol consumption showed attenuated opioid-induced pupil constriction and cognitive decline on objective measures of working memory, sustained attention, inhibitory control, coordination on a simulated driving task, and subjective dysphoric effects with enhanced subjective euphoric effects. Oxycodone pharmacokinetics, pain tolerance to CPT, and Berg balance were impacted comparably between alcohol consumption groups. Women endorsed greater negative drug effects, whereas men endorsed positive drug effects.RESULTSOne hundred twenty-eight adults (age 35-85) completed the study day. Compared to those with lower customary alcohol consumption, participants with elevated alcohol consumption showed attenuated opioid-induced pupil constriction and cognitive decline on objective measures of working memory, sustained attention, inhibitory control, coordination on a simulated driving task, and subjective dysphoric effects with enhanced subjective euphoric effects. Oxycodone pharmacokinetics, pain tolerance to CPT, and Berg balance were impacted comparably between alcohol consumption groups. Women endorsed greater negative drug effects, whereas men endorsed positive drug effects.Independent of subject's age, elevated customary alcohol consumption attenuates opioid central effects (i.e., pupil miosis, impaired cognition) and gender influences subjective drug effects. Clinicians should consider alcohol consumption and gender when prescribing opioid medications.CONCLUSIONIndependent of subject's age, elevated customary alcohol consumption attenuates opioid central effects (i.e., pupil miosis, impaired cognition) and gender influences subjective drug effects. Clinicians should consider alcohol consumption and gender when prescribing opioid medications. |
ArticleNumber | 173295 |
Author | Cherrier, Monique M. Shen, Danny D. Shireman, Laura Men, Alex Simpson, Tracy Kooner, Preetma Terman, Gregory W. Saxon, Andrew J. |
AuthorAffiliation | 3. Department of Anesthesiology and Pain Medicine, School of Medicine; University of Washington, Seattle, WA 98195 2. Department of Pharmaceutics, School of Pharmacy 4. Center of Excellence in Substance Addiction Treatment and Education VA Puget Sound Health Care System, Seattle, WA 98108 1. Department of Psychiatry and Behavioral Sciences, School of Medicine |
AuthorAffiliation_xml | – name: 2. Department of Pharmaceutics, School of Pharmacy – name: 4. Center of Excellence in Substance Addiction Treatment and Education VA Puget Sound Health Care System, Seattle, WA 98108 – name: 3. Department of Anesthesiology and Pain Medicine, School of Medicine; University of Washington, Seattle, WA 98195 – name: 1. Department of Psychiatry and Behavioral Sciences, School of Medicine |
Author_xml | – sequence: 1 givenname: Monique M. surname: Cherrier fullname: Cherrier, Monique M. email: cherrier@uw.edu organization: Department of Psychiatry and Behavioral Sciences, School of Medicine, University of Washington, Seattle, WA 98195, United States of America – sequence: 2 givenname: Danny D. surname: Shen fullname: Shen, Danny D. organization: Department of Pharmaceutics, School of Pharmacy, University of Washington, Seattle, WA 98195, United States of America – sequence: 3 givenname: Laura surname: Shireman fullname: Shireman, Laura organization: Department of Pharmaceutics, School of Pharmacy, University of Washington, Seattle, WA 98195, United States of America – sequence: 4 givenname: Andrew J. surname: Saxon fullname: Saxon, Andrew J. organization: Department of Psychiatry and Behavioral Sciences, School of Medicine, University of Washington, Seattle, WA 98195, United States of America – sequence: 5 givenname: Tracy surname: Simpson fullname: Simpson, Tracy organization: Department of Psychiatry and Behavioral Sciences, School of Medicine, University of Washington, Seattle, WA 98195, United States of America – sequence: 6 givenname: Alex surname: Men fullname: Men, Alex organization: Department of Pharmaceutics, School of Pharmacy, University of Washington, Seattle, WA 98195, United States of America – sequence: 7 givenname: Preetma surname: Kooner fullname: Kooner, Preetma organization: Department of Anesthesiology and Pain Medicine, School of Medicine; University of Washington, Seattle, WA 98195, United States of America – sequence: 8 givenname: Gregory W. surname: Terman fullname: Terman, Gregory W. organization: Department of Anesthesiology and Pain Medicine, School of Medicine; University of Washington, Seattle, WA 98195, United States of America |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/34742948$$D View this record in MEDLINE/PubMed |
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Keywords | Pain Oxycodone Opioid Aging Alcohol Attenuation Cognition Miosis Elderly |
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Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Authorship contributions: Monique Cherrier participated in all aspects of the project including study design, primary oversight, regulatory approval and adherence, staff training and management, participant recruitment, data monitoring integrity and analysis, manuscript preparation and submission; Danny Shen participated in study design, ongoing participant enrollment, oversight of biologic specimen accrual, handling storage, integrity and assay process and related staff, data analysis, manuscript preparation and submission; Laura Shireman participated in oversight of biologic specimen accrual, handling, storage, assay process and data integrity, analysis and manuscript preparation; Andrew Saxon participated in study design, medical monitoring and oversight of study procedures and participants, regulatory approval and adherence, data analysis and manuscript preparation; Tracy Simpson participated in manuscript preparation, instrument selection and scoring; Alex Men participated in biologic sample assay process and data integrity; Preetma Kooner participated in medical oversight; Greg Terman participated in medical screening, monitoring and oversight of study participants and procedures, manuscript preparation and institutional support. |
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SubjectTerms | Adult Age Factors Aged Aged, 80 and over Aging Alcohol Alcohol Drinking Analgesics, Opioid - administration & dosage Attention - drug effects Attenuation Automobile Driving Cognition Cognition - drug effects Elderly Ethanol - administration & dosage Female Humans Male Memory, Short-Term - drug effects Middle Aged Miosis Miosis - etiology Opioid Oxycodone Oxycodone - administration & dosage Oxycodone - adverse effects Pain Pain - drug therapy Sex Factors Surveys and Questionnaires |
Title | Elevated customary alcohol consumption attenuates opioid effects |
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