PLASMODIUM-CHABAUDI - INVIVO EFFECTS OF CA-2+ ANTAGONISTS ON CHLOROQUINE-RESISTANT AND CHLOROQUINE-SENSITIVE PARASITES

被引:41
作者
TANABE, K
KATO, M
IZUMO, A
HAGIWARA, A
DOI, S
机构
[1] OSAKA CITY UNIV,SCH MED,DEPT MED ZOOL,OSAKA 545,JAPAN
[2] KINKI UNIV,SCH MED,DEPT LEGAL MED,SAYAMA,OSAKA 589,JAPAN
关键词
Ca[!sup]2+[!/sup] antagonists; Chloroquine; Malaria; Plasmodium chabaudi;
D O I
10.1016/0014-4894(90)90126-W
中图分类号
R38 [医学寄生虫学]; Q [生物科学];
学科分类号
07 ; 0710 ; 09 ; 100103 ;
摘要
The effects of Ca2+ antagonists, verapamil, nicardipine, and diltiazem, on susceptibility to chloroquine were examined in mice infected with chloroquine-sensitive and chloroquine-resistant lines of Plasmodium chabaudi. In mice that received no chloroquine, daily injections of 50 mg/kg of verapamil, nicardipine, or diltiazem did not affect the growth of both sensitive and resistant parasites. When mice were injected daily with verapamil plus 2 to 3 mg/kg chloroquine, the chloroquine-sensitive parasite became more susceptible to chloroquine than the parasite in mice given chloroquine alone. On the other hand, in mice infected with chloroquine-resistant parasites, verapamil severely suppressed the growth of the parasite when accompanied by daily injections of 2 to 3 mg/kg of chloroquine, at which doses resistant parasites grew steadily in the absence of verapamil, indicating reversal of chloroquine resistance. This reversal was dose-dependent between 5 and 50 mg/kg of verapamil. Daily injections of nicardipine or diltiazem at 50 mg/kg also reversed resistance to chloroquine in resistant parasites. These results indicate that Ca2+ antagonists increase the susceptibility to chloroquine in a sensitive line of P. chabaudi and reverse chloroquine resistance in a resistant line. © 1990.
引用
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页码:419 / 426
页数:8
相关论文
共 37 条
[1]  
AKIYAMA S, 1986, J NATL CANCER I, V76, P839
[2]   REVERSAL OF CHLOROQUINE RESISTANCE IN MALARIA PARASITE PLASMODIUM-FALCIPARUM BY DESIPRAMINE [J].
BITONTI, AJ ;
SJOERDSMA, A ;
MCCANN, PP ;
KYLE, DE ;
ODUOLA, AMJ ;
ROSSAN, RN ;
MILHOUS, WK ;
DAVIDSON, DE .
SCIENCE, 1988, 242 (4883) :1301-1303
[3]   MEMBRANE-VESICLES FROM MULTIDRUG-RESISTANT HUMAN CANCER-CELLS CONTAIN A SPECIFIC 150-KDA TO 170-KDA PROTEIN DETECTED BY PHOTOAFFINITY-LABELING [J].
CORNWELL, MM ;
SAFA, AR ;
FELSTED, RL ;
GOTTESMAN, MM ;
PASTAN, I .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1986, 83 (11) :3847-3850
[4]  
CORNWELL MM, 1987, J BIOL CHEM, V262, P2166
[5]   PLASMODIUM FALCIPARUM IN OWL MONKEYS - DRUG RESISTANCE AND CHLOROQUINE BINDING CAPACITY [J].
FITCH, CD .
SCIENCE, 1970, 169 (3942) :289-+
[6]  
FOJO A, 1985, CANCER RES, V45, P3002
[7]  
FOOTE SJ, 1989, CELL, V57, P920
[8]  
GOTTESMAN MM, 1988, J BIOL CHEM, V263, P12163
[9]   CLONING AND CHARACTERIZATION OF A 2ND MEMBER OF THE MOUSE MDR GENE FAMILY [J].
GROS, P ;
RAYMOND, M ;
BELL, J ;
HOUSMAN, D .
MOLECULAR AND CELLULAR BIOLOGY, 1988, 8 (07) :2770-2778
[10]   FUNCTIONAL-ROLE FOR THE 170-KDA TO 180-KDA GLYCOPROTEIN SPECIFIC TO DRUG-RESISTANT TUMOR-CELLS AS REVEALED BY MONOCLONAL-ANTIBODIES [J].
HAMADA, H ;
TSURUO, T .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1986, 83 (20) :7785-7789