INHIBITION OF N-ACETYLATION OF PROCAINAMIDE AND RENAL CLEARANCE OF N-ACETYLPROCAINAMIDE BY PARA-AMINOBENZOIC ACID IN HUMANS

被引:7
作者
TISDALE, JE
RUDIS, MI
PADHI, ID
SVENSSON, CK
WEBB, CR
BORZAK, S
WARE, JA
KREPOSTMAN, A
ZAROWITZ, BJ
机构
[1] HENRY FORD HOSP,DEPT PHARM SERV,DETROIT,MI 48202
[2] HENRY FORD HOSP,DIV CARDIOVASC MED,DETROIT,MI 48202
关键词
D O I
10.1002/j.1552-4604.1995.tb04135.x
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Procainamide administration often results in excessively high serum N-acetylprocainamide (NAPA) concentrations and subtherapeutic serum procainamide concentrations, Inhibition of N-acetylation of procainamide may prevent accumulation of excessive NAPA while maintaining therapeutic serum procainamide concentrations, The purpose of this randomized, two-way crossover study was to determine if para-aminobenzoic acid (PABA) inhibits N-acetylation of procainamide in healthy volunteers. Eleven (7 female, 4 male) fast acetylators of caffeine received, in random order, PABA 1.5 g orally every 6 hours for 5 days, with a single intravenous dose of procainamide 750 mg administered over 30 minutes on the third day, or intravenous procainamide alone. Blood samples were collected during a 48-hour period after initiation of the infusion. Urine was collected over a 72-hour period. Serum procainamide and NAPA concentrations were analyzed using fluorescence polarization immunoassay, Urine procainamide and NAPA concentrations were measured with high performance liquid chromatography, PABA did not significantly influence total or renal procainamide clearance, elimination rate constant, AUC(0-infinity), amount of procainamide excreted unchanged in the urine, or volume of distribution. However, concomitant PABA administration with procainamide resulted in increases in NAPA AUC(0-infinity) and t(1/2) and reductions in NAPA Ke, procainamide acetylation (NAPA formation) clearance, and NAPA renal clearance. Although PABA inhibits metabolic conversion of procainamide to NAPA, it also impairs the renal clearance of NAPA (but not procainamide) in healthy subjects. Therefore, PABA may not be useful for optimizing the safety or efficacy of procainamide in patients.
引用
收藏
页码:902 / 910
页数:9
相关论文
共 50 条
[31]   INVITRO AND INVIVO N-ACETYLATION OF CARCINOGENIC GLUTAMIC-ACID PYROLYSIS PRODUCTS IN HUMANS [J].
KANAI, Y ;
MANABE, S ;
WADA, O .
CARCINOGENESIS, 1988, 9 (12) :2179-2184
[32]   ANTIMUTAGENIC EFFECT OF PARA-AMINOBENZOIC ACID ON THE MUTAGENICITY OF N-METHYL-N'-NITRO-N-NITROSOGUANIDINE IN SALMONELLA-TYPHIMURIUM [J].
GICHNER, T ;
VELEMINSKY, J ;
RAPOPORT, IA ;
VASILIEVA, SV .
MUTATION RESEARCH, 1987, 192 (02) :95-98
[33]   REPAIR EFFECT OF GENETICALLY ACTIVE NATURAL COMPOUND PARA-AMINOBENZOIC ACID IN THE TEST WITH N-NITROSOMETHYLUREA [J].
VASILIEVA, SV ;
DAVNICHENKO, LS ;
LUTSKOVA, EV ;
RAPOPORT, IA .
DOKLADY AKADEMII NAUK SSSR, 1979, 247 (01) :226-230
[34]   INDIVIDUAL VARIABILITY IN P-AMINOBENZOIC ACID N-ACETYLATION BY HUMAN N-ACETYLTRANSFERASE (NAT1) OF PERIPHERAL-BLOOD [J].
WEBER, WW ;
VATSIS, KP .
PHARMACOGENETICS, 1993, 3 (04) :209-212
[35]   TRANSPORT OF PROCAINAMIDE AND N-ACETYLPROCAINAMIDE FROM BLOOD INTO THE INTESTINAL LUMEN AND INTESTINAL DIALYSIS BY ORAL ACTIVATED-CHARCOAL IN RATS WITH ACUTE RENAL-FAILURE [J].
ARIMORI, K ;
NAKANO, M .
JOURNAL OF PHARMACOBIO-DYNAMICS, 1988, 11 (07) :504-511
[36]   THE LIQUID-CRYSTALLINE MONOMER N-(PARA-METHACRYLOYLOXY-BENZYLIDENE)-PARA-AMINOBENZOIC ACID - ITS SYNTHESIS, CHARACTERIZATION AND POLYMERIZATION [J].
HAITJEMA, HJ ;
VANEKENSTEIN, GORA ;
TAN, YY .
EUROPEAN POLYMER JOURNAL, 1992, 28 (10) :1191-1200
[37]   SYNTHESIS OF POTENTIAL ANTI-CANCEROUS COMPOUNDS - N-MUSTARDS DERIVED FROM PARA-AMINOBENZOIC ACID AND PARA-NITROPHENOL [J].
CIUGUREANU, C ;
SUNEL, V ;
BUDEANU, C ;
DANET, D ;
DANET, R .
REVISTA DE CHIMIE, 1979, 30 (11) :1073-1076
[39]   Promotion of thyroid carcinogenesis by para-aminobenzoic acid in rats initiated with N-bis(2-hydroxypropyl)nitrosamine [J].
Hasumura, M ;
Imai, T ;
Takizawa, T ;
Ueda, M ;
Onose, J ;
Hirose, M .
TOXICOLOGICAL SCIENCES, 2005, 86 (01) :61-67