The Association of Age and Frailty with the Pharmacokinetics and Pharmacodynamics of Metoclopramide

• Published in: Age and ageing Vol. 22; no. 5; pp. 354 - 359
• Main Authors: WYNNE, H. A., YELLAND, C., COPE, L. H., BODDY, A., WOODHOUSE, K. W., BATEMAN, D. N.
• Format: Journal Article
• Language: English
• Published: Oxford Oxford University Press 01.09.1993; Oxford Publishing Limited (England)
• Subjects: Administration, Oral; Adult; Aged; Aging - physiology; Biological and medical sciences; Digestive system; Drug metabolism; Drug therapy; Drugs; Female; Frail Elderly; Geriatrics; Humans; Infusions, Intravenous; Male; Medical sciences; Metabolic Clearance Rate; Metoclopramide; Metoclopramide - administration & dosage; Metoclopramide - adverse effects; Metoclopramide - pharmacokinetics; Neurologic Examination - drug effects; Pharmacology; Pharmacology. Drug treatments; Reference Values; Human; Intravenous administration; Dopamine antagonist; Treatment efficiency; Oral administration; Sedation; Bolus injection; D2 Dopamine receptor; Pharmacokinetics; Elderly; Age; Antiemetic; Comparative study
• ISSN: 0002-0729; 1468-2834
• DOI: 10.1093/ageing/22.5.354

We have investigated the association of age and frailty with the pharmacokinetics and pharmacodynamics of the conjugated drug, metoclopramide. Six healthy young, six healthy elderly (>65 years), and six frail elderly (>65 years) subjects were studied on two occasions, receiving 10 mg metoclopramide by intravenous bolus and orally, in random order. Blood and urine were collected for measurement of pharmacokinetic parameters. Liver volume was measured by ultrasound. Sedation and contentment were self-recorded on visual analogue scales. Liver volume was not significantly different in the three groups, nor was bio-availability of metoclopramide. Clearance was similar in the young and fit elderly but reduced in the frail elderly subjects when compared with the young (p<0.05), both when expressed in absolute terms and per unit liver volume. There were no differences in percentages cleared as the free drug or as the sulphate or glucuronide metabolite within or between groups, suggesting that frailty can produce a general impairment of conjugation pathways. The frail elderly subjects reported more sedation after intravenous dosage than the other subjects, whilst only young subjects reported akathisia. This did not relate to pharmacokinetic differences and seemed therefore to reflect associated pharmacodynamic changes in specific receptor or target sites.