Gizem Gemikonakli, John Mach, Trang Tran, Harry Wu, Sarah N. Hilmer
{"title":"使用不同的测试探究多种药物、老龄化和性别对身体功能的影响。","authors":"Gizem Gemikonakli, John Mach, Trang Tran, Harry Wu, Sarah N. Hilmer","doi":"10.1111/fcp.12978","DOIUrl":null,"url":null,"abstract":"<div>\n \n \n <section>\n \n <h3> Background</h3>\n \n <p>Ageing, sex and polypharmacy affect physical function.</p>\n </section>\n \n <section>\n \n <h3> Objectives</h3>\n \n <p>This mouse study investigates how ageing, sex and polypharmacy interact and affect grip strength, balance beam and wire hang, correlating and comparing the different test results between and within subgroups.</p>\n </section>\n \n <section>\n \n <h3> Methods</h3>\n \n <p>Young (2.5 months) and old (21.5 months) C57BL/6 J male and female mice (<i>n =</i> 10–6/group) were assessed for physical function at baseline on grip strength, balance beam and wire hang with three trials of 60 s (WH60s) and one trial of 300 s (WH300s). Mice were randomised to control or diet containing a high Drug Burden Index (DBI, total anticholinergic and sedative drug exposure) polypharmacy regimen (metoprolol, simvastatin, citalopram, oxycodone and oxybutynin at therapeutic oral doses). Following 6–8 weeks of treatment, mice were reassessed.</p>\n </section>\n \n <section>\n \n <h3> Results</h3>\n \n <p>High DBI polypharmacy and control mice both showed age group differences on all tests (<i>p <</i> 0.05). Only control mice showed sex differences, with females outperforming males on the WH60s and balance beam for old mice, WH300s for young mice (<i>p <</i> 0.05). Polypharmacy reduced grip strength in all subgroups (<i>p <</i> 0.05) and only in old females reduced wire hang time and cumulative behaviour and balance beam time and %walked (<i>p <</i> 0.05). Physical function assessments were all correlated with each other, with differences between subgroups (<i>p <</i> 0.05), and mice within subgroups showed interindividual variability in performance.</p>\n </section>\n \n <section>\n \n <h3> Conclusion</h3>\n \n <p>Age, sex and polypharmacy have variable effects on different tests, and behavioural measures are useful adjuvants to assessing performance. There was considerable within-group variability in change in measures over time. These findings can inform design and sample size of future studies.</p>\n </section>\n </div>","PeriodicalId":12657,"journal":{"name":"Fundamental & Clinical Pharmacology","volume":null,"pages":null},"PeriodicalIF":2.1000,"publicationDate":"2024-01-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/fcp.12978","citationCount":"0","resultStr":"{\"title\":\"Probing polypharmacy, ageing and sex effects on physical function using different tests\",\"authors\":\"Gizem Gemikonakli, John Mach, Trang Tran, Harry Wu, Sarah N. 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Mice were randomised to control or diet containing a high Drug Burden Index (DBI, total anticholinergic and sedative drug exposure) polypharmacy regimen (metoprolol, simvastatin, citalopram, oxycodone and oxybutynin at therapeutic oral doses). Following 6–8 weeks of treatment, mice were reassessed.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Results</h3>\\n \\n <p>High DBI polypharmacy and control mice both showed age group differences on all tests (<i>p <</i> 0.05). Only control mice showed sex differences, with females outperforming males on the WH60s and balance beam for old mice, WH300s for young mice (<i>p <</i> 0.05). Polypharmacy reduced grip strength in all subgroups (<i>p <</i> 0.05) and only in old females reduced wire hang time and cumulative behaviour and balance beam time and %walked (<i>p <</i> 0.05). Physical function assessments were all correlated with each other, with differences between subgroups (<i>p <</i> 0.05), and mice within subgroups showed interindividual variability in performance.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Conclusion</h3>\\n \\n <p>Age, sex and polypharmacy have variable effects on different tests, and behavioural measures are useful adjuvants to assessing performance. There was considerable within-group variability in change in measures over time. 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Probing polypharmacy, ageing and sex effects on physical function using different tests
Background
Ageing, sex and polypharmacy affect physical function.
Objectives
This mouse study investigates how ageing, sex and polypharmacy interact and affect grip strength, balance beam and wire hang, correlating and comparing the different test results between and within subgroups.
Methods
Young (2.5 months) and old (21.5 months) C57BL/6 J male and female mice (n = 10–6/group) were assessed for physical function at baseline on grip strength, balance beam and wire hang with three trials of 60 s (WH60s) and one trial of 300 s (WH300s). Mice were randomised to control or diet containing a high Drug Burden Index (DBI, total anticholinergic and sedative drug exposure) polypharmacy regimen (metoprolol, simvastatin, citalopram, oxycodone and oxybutynin at therapeutic oral doses). Following 6–8 weeks of treatment, mice were reassessed.
Results
High DBI polypharmacy and control mice both showed age group differences on all tests (p < 0.05). Only control mice showed sex differences, with females outperforming males on the WH60s and balance beam for old mice, WH300s for young mice (p < 0.05). Polypharmacy reduced grip strength in all subgroups (p < 0.05) and only in old females reduced wire hang time and cumulative behaviour and balance beam time and %walked (p < 0.05). Physical function assessments were all correlated with each other, with differences between subgroups (p < 0.05), and mice within subgroups showed interindividual variability in performance.
Conclusion
Age, sex and polypharmacy have variable effects on different tests, and behavioural measures are useful adjuvants to assessing performance. There was considerable within-group variability in change in measures over time. These findings can inform design and sample size of future studies.
期刊介绍:
Fundamental & Clinical Pharmacology publishes reports describing important and novel developments in fundamental as well as clinical research relevant to drug therapy. Original articles, short communications and reviews are published on all aspects of experimental and clinical pharmacology including:
Antimicrobial, Antiviral Agents
Autonomic Pharmacology
Cardiovascular Pharmacology
Cellular Pharmacology
Clinical Trials
Endocrinopharmacology
Gene Therapy
Inflammation, Immunopharmacology
Lipids, Atherosclerosis
Liver and G-I Tract Pharmacology
Metabolism, Pharmacokinetics
Neuropharmacology
Neuropsychopharmacology
Oncopharmacology
Pediatric Pharmacology Development
Pharmacoeconomics
Pharmacoepidemiology
Pharmacogenetics, Pharmacogenomics
Pharmacovigilance
Pulmonary Pharmacology
Receptors, Signal Transduction
Renal Pharmacology
Thrombosis and Hemostasis
Toxicopharmacology
Clinical research, including clinical studies and clinical trials, may cover disciplines such as pharmacokinetics, pharmacodynamics, pharmacovigilance, pharmacoepidemiology, pharmacogenomics and pharmacoeconomics. Basic research articles from fields such as physiology and molecular biology which contribute to an understanding of drug therapy are also welcomed.