RENAL CLEARANCE OF PYRIDOSTIGMINE IN MYASTHENIC PATIENTS AND VOLUNTEERS UNDER THE INFLUENCE OF RANITIDINE AND PIRENZEPINE

被引:5
作者
EIERMANN, B
SOMMER, N
WINNE, D
SCHUMM, F
MAIER, U
BREYERPFAFF, U
机构
[1] UNIV TUBINGEN,INST TOXICOL,WILHELMSTR 56,D-72074 TUBINGEN,GERMANY
[2] UNIV TUBINGEN,NEUROL CLIN,D-72076 TUBINGEN,GERMANY
[3] CLIN NEUROL & PSYCHIAT CHRISTOPHSBAD,D-73035 GOPPINGEN,GERMANY
[4] UNIV TUBINGEN,INST PHARMACOL,D-72074 TUBINGEN,GERMANY
关键词
D O I
10.3109/00498259309059437
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
1. To assess the contribution of tubular secretion to the renal excretion of pyridostigmine, and its modification by other cationic drugs, six volunteers were given single oral doses of 60-mg pyridostigmine bromide with and without co-administration of ranitidine or pirenzepine. Renal clearances were determined by h.p.l.c. analysis of pyridostigmine and enzymic measurement of endogenous creatinine in plasma and urine. 2. In patients with myasthenia receiving continuous pyridostigmine therapy, renal clearance values were obtained in the same manner with and without ranitidine (10 patients) or pirenzepine (nine patients) co-medication. 3. Pyridostigmine was not bound to plasma proteins. Its renal clearance averaged 6.65 ml/min per kg (350% of the creatinine clearance) in all subjects, 74% being due to net tubular secretion. 4. Mean values for pyridostigmine renal clearance and for clearance by secretion were decreased in the presence of pirenzepine, but plasma concentrations were not affected significantly. Ranitidine caused a small non-significant decrease of the pyridostigmine clearance in patients. 5. Pyridostigmine had a higher elimination (2 h-1) than the absorption rate constant (0.23 h-1) when administered orally as a non-retarded preparation. 6. The renal clearance of creatinine was slightly increased by pyridostigmine in volunteers and slightly decreased by pirenzepine in the total group of subjects.
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页码:1263 / 1275
页数:13
相关论文
共 33 条
[11]  
HAVARD CWH, 1990, DRUGS, V39, P1
[12]   PYRIDOSTIGMINE USED AS A NERVE AGENT PRETREATMENT UNDER WARTIME CONDITIONS [J].
KEELER, JR ;
HURST, CG ;
DUNN, MA .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1991, 266 (05) :693-695
[13]  
KINSELLA JL, 1979, J PHARMACOL EXP THER, V209, P443
[14]   THE DRUG-INTERACTION POTENTIAL OF RANITIDINE - AN UPDATE [J].
KLOTZ, U ;
KROEMER, HK .
PHARMACOLOGY & THERAPEUTICS, 1991, 50 (02) :233-244
[15]   EFFECT OF CHRONIC PYRIDOSTIGMINE ADMINISTRATION ON PYRIDOSTIGMINE-C-14 METABOLISM IN MYASTHENIA GRAVIS [J].
KORNFELD, P ;
WOLF, RL ;
SAMUELS, AJ ;
OSSERMAN, KE .
NEUROLOGY, 1971, 21 (05) :550-&
[16]   METABOLISM OF C-14-LABELED PYRIDOSTIGMINE IN MYASTHENIA GRAVIS - EVIDENCE FOR MULTIPLE METABOLITES [J].
KORNFELD, P ;
SAMUELS, AJ ;
WOLF, RL ;
OSSERMAN, KE .
NEUROLOGY, 1970, 20 (07) :634-&
[17]   STEADY-STATE INTRAVENOUS PHARMACOKINETICS OF PIRENZEPINE IN PATIENTS WITH DIFFERING DEGREES OF RENAL DYSFUNCTION [J].
KRAKAMP, B ;
TANSWELL, P ;
VOGEL, H ;
BOZLER, G .
EUROPEAN JOURNAL OF CLINICAL PHARMACOLOGY, 1989, 36 (01) :75-78
[18]  
LIN JH, 1988, DRUG METAB DISPOS, V16, P52
[19]   VALIDITY OF CREATININE CLEARANCE ESTIMATES IN THE ASSESSMENT OF RENAL-FUNCTION [J].
LUKE, DR ;
HALSTENSON, CE ;
OPSAHL, JA ;
MATZKE, GR .
CLINICAL PHARMACOLOGY & THERAPEUTICS, 1990, 48 (05) :503-508
[20]  
MAIER U, 1985, THESIS U TOBINGEN GE