DIFFERENCES IN STEREOSELECTIVE DISPOSITION OF PROPRANOLOL DO NOT EXPLAIN SENSITIVITY DIFFERENCES BETWEEN WHITE AND CHINESE SUBJECTS - CORRELATION BETWEEN THE CLEARANCE OF (-)-PROPRANOLOL AND (+)-PROPRANOLOL

被引:15
作者
ZHOU, HH
WOOD, AJJ
机构
[1] VANDERBILT UNIV,MED CTR,SCH MED,DEPT PHARMACOL,DIV CLIN PHARMACOL,NASHVILLE,TN 37232
[2] VANDERBILT UNIV,MED CTR,SCH MED,DEPT MED,NASHVILLE,TN 37232
关键词
D O I
10.1038/clpt.1990.98
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
We have previously demonstrated that Chinese subjects are more sensitive than white subjects to (β-blockade produced by propranolol. To determine if this difference was because a greater proportion of the total propranolol was the more active (-)-isomer of propranolol in the Chinese subjects than in the white subjects, the relative pharmacokinetics of (+)- and (-)-isomers of propranolol after administration of a single, 80 mg oral dose of racemic propranolol was studied in 10 Chinese male and in 9 white male healthy subjects. The plasma concentrations of both (+)- and (-)-propranolol were lower in Chinese than in white subjects, resulting in significantly lower peak plasma concentrations and areas under the concentration-time curve (AUC) in Chinese subjects, the half-life of elimination did not differ significantly between Chinese and white subjects or between the two isomers. The concentrations of the active (-)-propranolol were higher in both groups of subjects because of the lower clearance of the (-)-propranolol compared with the (+)-propranolol. An excellent correlation between the clearance of (+)- and (-)-propranolol was seen in the same individual. The ratio of AUC of (-)- and (+)-propranolol did not differ between Chinese subjects (0.64 ± 0.03) and white subjects (0.71 ± 0.09). The data suggest that the proportion of the two isomers found in Chinese and white subjects did not differ, and therefore differences in stereoselective disposition of propranolol cannot explain the increased sensitivity seen in Chinese individuals. © 1990.
引用
收藏
页码:719 / 723
页数:5
相关论文
共 13 条
[1]   NO STEREOSELECTIVE 1ST-PASS HEPATIC EXTRACTION OF PROPRANOLOL [J].
JACKMAN, GP ;
MCLEAN, AJ ;
JENNINGS, GL ;
BOBIK, A .
CLINICAL PHARMACOLOGY & THERAPEUTICS, 1981, 30 (03) :291-296
[2]   GENETICALLY-DETERMINED POLYMORPHISMS IN DRUG OXIDATION [J].
JACQZ, E ;
HALL, SD ;
BRANCH, RA .
HEPATOLOGY, 1986, 6 (05) :1020-1032
[3]   IMPROVED HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHIC METHOD FOR THE SIMULTANEOUS DETERMINATION OF PROPRANOLOL AND 4-HYDROXYPROPRANOLOL IN PLASMA WITH FLUORESCENCE DETECTION [J].
KOSHAKJI, RP ;
WOOD, AJJ .
JOURNAL OF CHROMATOGRAPHY-BIOMEDICAL APPLICATIONS, 1987, 422 :294-300
[4]   SUPPRESSION OF VENTRICULAR ARRHYTHMIAS IN MAN BY D-PROPRANOLOL INDEPENDENT OF BETA-ADRENERGIC-RECEPTOR BLOCKADE [J].
MURRAY, KT ;
REILLY, C ;
KOSHAKJI, RP ;
RODEN, DM ;
LINEBERRY, MD ;
WOOD, AJJ ;
SIDDOWAY, LA ;
BARBEY, JT ;
WOOSLEY, RL .
JOURNAL OF CLINICAL INVESTIGATION, 1990, 85 (03) :836-842
[5]   STEREOSELECTIVE CLEARANCE AND DISTRIBUTION OF INTRAVENOUS PROPRANOLOL [J].
OLANOFF, LS ;
WALLE, T ;
WALLE, UK ;
COWART, TD ;
GAFFNEY, TE .
CLINICAL PHARMACOLOGY & THERAPEUTICS, 1984, 35 (06) :755-761
[6]   SIMULTANEOUS DETERMINATION OF PROPRANOLOL ENANTIOMERS IN PLASMA BY HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY WITH FLUORESCENCE DETECTION [J].
PRAKASH, C ;
KOSHAKJI, RP ;
WOOD, AJJ ;
BLAIR, IA .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1989, 78 (09) :771-775
[7]   STEREOSELECTIVE DISPOSITION AND GLUCURONIDATION OF PROPRANOLOL IN HUMANS [J].
SILBER, B ;
HOLFORD, NHG ;
RIEGELMAN, S .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1982, 71 (06) :699-704
[8]   PHARMACOKINETICS AND PHARMACODYNAMICS OF PROPRANOLOL STEREOISOMERS IN HYPER-THYROID PATIENTS [J].
TAWARA, K ;
KAWASHIMA, K ;
ISHIKAWA, H ;
YAMAMOTO, K ;
SAITO, K ;
EBIHARA, A ;
YOSHIDA, S .
EUROPEAN JOURNAL OF CLINICAL PHARMACOLOGY, 1981, 19 (03) :197-203
[9]  
VONBAHR C, 1982, BRIT J CLIN PHARMACO, V14, P79
[10]   STEREOSELECTIVE BINDING OF PROPRANOLOL TO HUMAN-PLASMA, ALPHA-1-ACID GLYCOPROTEIN, AND ALBUMIN [J].
WALLE, UK ;
WALLE, T ;
BAI, SA ;
OLANOFF, LS .
CLINICAL PHARMACOLOGY & THERAPEUTICS, 1983, 34 (06) :718-723