Experimental amoebiasis and the development of anti-amoebic compounds
- 1 February 1983
- journal article
- trends and-perspectives
- Published by Cambridge University Press (CUP) in Parasitology
- Vol. 86 (1) , 175-191
- https://doi.org/10.1017/s0031182000057279
Abstract
In the ideal situation, the development of new amoebicides, or more accurately anti-amoebic compounds which are compounds with activity againstEntamoeba histolytica, should initially proceed with the study of parasite-specific metabolic pathways and their inhibition, followed by whole parasitein vitrostudies, experimentalin vivomodels and finally clinical trial. However, there are considerable gaps in our knowledge which will be discussed below, and consequently many investigators consider that empirically selected compounds should be tested experimentally in addition to specifically designed compounds. Before clinical trials can begin, extensive examination of the candidate amoebicide in experimental animals is required in order to investigate possible toxicological hazards.In addition to inhibiting the amoebic parasite, the drug has to reach the parasite in several different sites in the body, thus there is also a problem of pharmacokinetics and distribution. Prior to the discovery of the nitroimidazole class of amoebicides, the multi-site attack was solved by the use of several drugs, sometimes in sequence during the treatment of an individual case (Powell, 1972). The discovery of the nitroimidazole class of compound changed the situation dramatically and these have shown a clinical and parasitological effect against extra-intestinal and intestinal wall infections. The effect on intralumenal infection (that is mildly symptomatic or asymptomatic infections) of the large intestine is, however, less certain (Finegold, 1977; Spillman, Ayala & Sanchez, 1976).Although the treatment of amoebiasis appears to be satisfactory at the present time, it is difficult to predict problems which might arise in the future, and therefore it is valuable to continue the pre-clinical development, especially the investigation of parasite metabolism, in order to define parasite-specific points of chemotherapeutic attack.The chemotherapy of amoebiasis was reviewed comprehensively by Woolf (1963, 1965). The present account of the development of amoebicides therefore starts from the Woolfe reviews.Keywords
This publication has 67 references indexed in Scilit:
- Attachment and Short‐Term Maintenance of Motility and Viability of Entamoeba Histolytica In A Defined Medium*The Journal of Protozoology, 1980
- The effect of bisamidines of 2,6-diaminoanthraquinone onEntamoeba histolytica infections in rats and hamstersCellular and Molecular Life Sciences, 1979
- A new medium for the axenic cultivation of Entamoeba histolytica and other EntamoebaPublished by Oxford University Press (OUP) ,1978
- Clonal Growth of Entamoeba histolytica and other Species of Entamoeba in Agar*The Journal of Protozoology, 1978
- Synthèse et propriétés amœbicides d'analogues de l'émétine*. Analyse des composés nouveaux en 13C‐RMN. I. (±) Alkyl‐1‐déséthyl‐3‐émétine à jonction B/C cis ou trans*Helvetica Chimica Acta, 1977
- TinidazoleDrugs, 1976
- Inhibition of Protein Synthesis: A Mechanism of Amebicide Action of Emetine and Other Structurally Related Compounds*The Journal of Protozoology, 1973
- Entamoeba histolytica Infections in the Chimpanzee (Pan satyrus)Journal of Parasitology, 1966
- Experimental ChemotherapyThe Lancet Healthy Longevity, 1965
- Genetics of Entamoeba histolytica: Differences in Drug Sensitivity between Laredo and other Strains of Entamoeba histolytica*The Journal of Protozoology, 1962