Lack of evidence for an antischistosomal activity of myrrh in experimental animals

被引:41
作者
Botros, S [1 ]
William, S
Ebeid, F
Cioli, D
Katz, N
Day, TA
Bennett, JL
机构
[1] Theodor Bilharz Res Inst, Giza, Egypt
[2] Inst Cell Biol, Rome, Italy
[3] Fiocruz MS, Ctr Pesquisas Rene Rachou, Minist Saude, Belo Horizonte, MG, Brazil
[4] Michigan State Univ, Dept Pharmacol & Toxicol, E Lansing, MI 48824 USA
关键词
D O I
10.4269/ajtmh.2004.71.206
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
In a multicenter investigation of the potential antischistosomal activity of myrrh, a resin obtained from an African plant, different derivatives of the resin, including the commercial preparation Mirazid, were tested at different doses in mice and hamsters infected with Schistosoma mansoni. In mice infected with the Egyptian (CD) strain of S. mansoni, four of six groups treated with Mirazid did not show significant worm reduction, while the remaining groups showed significant but trivial reductions. In mice infected with the Puerto Rican (Mill Hill) strain of S. mansoni, a Mirazid solution was toxic for mice at high doses and produced modest or no worm reduction at lower doses. In hamsters and mice infected with Puerto Rican (NMRI) and Brazilian (LE) strains of S. mansoni and treated with the crude extract of myrrh in doses ranging from 180 to 10,000 mg/kg, no signs of antibilharzial activity were observed. Total tissue egg load and egg developmental stages were not affected by any of the treatment regimens. These results were in contrast to those obtained in praziquantel-treated animals in which 94% worm reduction and 100% egg reduction was observed. Based on the findings of this work, we cannot recommend the use of Mirazid in human cases of schistosomiasis.
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页码:206 / 210
页数:5
相关论文
共 16 条
[1]  
ALAWADI F, 1991, DIABETES RES CLIN EX, V18, P163
[2]   Mirazid: A new schistosomicidal drug [J].
Badria, F ;
Abou-Mohamed, G ;
El-Mowafy, A ;
Masoud, A ;
Salama, O .
PHARMACEUTICAL BIOLOGY, 2001, 39 (02) :127-131
[3]   T-CADINOL - A PHARMACOLOGICALLY ACTIVE CONSTITUENT OF SCENTED MYRRH - INTRODUCTORY PHARMACOLOGICAL CHARACTERIZATION AND HIGH-FIELD H-1-NMR AND C-13-NMR DATA [J].
CLAESON, P ;
ANDERSSON, R ;
SAMUELSSON, G .
PLANTA MEDICA, 1991, 57 (04) :352-356
[4]   AN IMPROVED PERFUSION TECHNIQUE FOR RECOVERING ADULT SCHISTOSOMES FROM LABORATORY ANIMALS [J].
DUVALL, RH ;
DEWITT, WB .
AMERICAN JOURNAL OF TROPICAL MEDICINE AND HYGIENE, 1967, 16 (04) :483-&
[5]   DRUG-RESISTANT SCHISTOSOMIASIS - RESISTANCE TO PRAZIQUANTEL AND OXAMNIQUINE INDUCED IN SCHISTOSOMA-MANSONI IN MICE IS DRUG-SPECIFIC [J].
FALLON, PG ;
DOENHOFF, MJ .
AMERICAN JOURNAL OF TROPICAL MEDICINE AND HYGIENE, 1994, 51 (01) :83-88
[6]  
Greene D A, 1993, N C Med J, V54, P620
[7]   Are poor responses to praziquantel for the treatment of Schistosoma mansoni infections in Senegal due to resistance?: An overview of the evidence [J].
Gryseels, B ;
Mbaye, A ;
De Vlas, SJ ;
Stelma, FF ;
Guissé, F ;
Van Lieshout, L ;
Faye, D ;
Diop, M ;
Ly, A ;
Tchuem-Tchuenté, LA ;
Engels, D ;
Polman, K .
TROPICAL MEDICINE & INTERNATIONAL HEALTH, 2001, 6 (11) :864-873
[8]   Resistance to praziquantel:: Direct evidence from Schistosoma mansoni isolated from Egyptian villagers [J].
Ismail, M ;
Botros, S ;
Metwally, A ;
William, S ;
Farghally, A ;
Tao, LF ;
Day, TA ;
Bennett, JL .
AMERICAN JOURNAL OF TROPICAL MEDICINE AND HYGIENE, 1999, 60 (06) :932-935
[9]   Characterization of isolates of Schistosoma mansoni from Egyptian villagers that tolerate high doses of praziquantel [J].
Ismail, M ;
Metwally, A ;
Farghaly, A ;
Bruce, J ;
Tao, LF ;
Bennett, JL .
AMERICAN JOURNAL OF TROPICAL MEDICINE AND HYGIENE, 1996, 55 (02) :214-218
[10]  
KLOETZEL K, 1967, B WORLD HEALTH ORGAN, V37, P686