TY - JOUR
T1 - Gender and oral contraceptive steroids as determinants of drug glucuronidation
T2 - effects on clofibric acid elimination.
AU - Miners, JO
AU - Robson, RA
AU - Birkett, DJ
PY - 1984/8
Y1 - 1984/8
N2 - The disposition of clofibric acid, a drug metabolised largely by glucuronidation, was studied in eight males, eight females and eight females receiving oral contraceptive steroids (OCS). Clofibric acid plasma clearance was not significantly different in males compared to the control female group but was 48% greater (P less than 0.01) in women receiving OCS compared to non‐pill using females. This difference was due to an alteration in clofibric acid metabolic clearance as there were no differences between the groups in clofibric acid free fraction. Along with previous data the results suggest that induction of drug glucuronidation by OCS may be of clinical importance, although any sex‐ related differences are unlikely to be of clinical significance. 1984 The British Pharmacological Society
AB - The disposition of clofibric acid, a drug metabolised largely by glucuronidation, was studied in eight males, eight females and eight females receiving oral contraceptive steroids (OCS). Clofibric acid plasma clearance was not significantly different in males compared to the control female group but was 48% greater (P less than 0.01) in women receiving OCS compared to non‐pill using females. This difference was due to an alteration in clofibric acid metabolic clearance as there were no differences between the groups in clofibric acid free fraction. Along with previous data the results suggest that induction of drug glucuronidation by OCS may be of clinical importance, although any sex‐ related differences are unlikely to be of clinical significance. 1984 The British Pharmacological Society
UR - http://www.scopus.com/inward/record.url?scp=0021224495&partnerID=8YFLogxK
U2 - 10.1111/j.1365-2125.1984.tb02461.x
DO - 10.1111/j.1365-2125.1984.tb02461.x
M3 - Article
C2 - 6487463
AN - SCOPUS:0021224495
SN - 0306-5251
VL - 18
SP - 240
EP - 243
JO - British Journal of Clinical Pharmacology
JF - British Journal of Clinical Pharmacology
IS - 2
ER -