Hostname: page-component-848d4c4894-ndmmz Total loading time: 0 Render date: 2024-05-13T00:21:30.163Z Has data issue: false hasContentIssue false

Brugia pahangi in the BALB/C mouse: a model for testing filaricidal compounds

Published online by Cambridge University Press:  18 November 2009

E. Devaney
Affiliation:
Department of Parasitology, Liverpool School of Tropical Medicine, Pembroke Place, Liverpool L3 5QA, UK
R.E. Howells
Affiliation:
Department of Parasitology, Liverpool School of Tropical Medicine, Pembroke Place, Liverpool L3 5QA, UK
G. Smith
Affiliation:
Department of Parasitology, Liverpool School of Tropical Medicine, Pembroke Place, Liverpool L3 5QA, UK

Abstract

The BALB/C mouse infected with Brugia pahangi has been evaluated as a model for the selection of filaricidal compounds with activity against immature worms. Mice were infected by the intraperitoneal inoculation of 50 infective larvae and candidate compounds were administered by the intraperitoneal (i.p.), subcutaneous or oral route once daily from day 4 to day 8 post infection. Animals were examined on days 29 to 32 post infection. Variation in the larval recoveries from undrugged mice within and between experimental groups limited the value of drug assessments based upon percentage worm recoveries. The infection rate of undrugged mice was 85% over-all, range 60 to 100%. Using the infection rate of drugged v. undrugged animals as the criterion of activity the test has been evaluated with a series of standard nematicidal compounds.. Lcvamisolc and the benzimidazole carbamatcs, mebendazole, flubendazole and fenbendazole given i.p. at lOmg/kg daily were active in this screen whilst DEC, DEC-N-oxidc, ivcrmcctin, amoscanatc, mctrifonatc and suramin were inactive at the dosages tested. No retardation of growth or morphological abnormalities were observed in worms from the drugged mice.

Type
Research Article
Copyright
Copyright © Cambridge University Press 1985

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

REFERENCES

Court, J. P. (1981) A new in vitro test for detecting antifilarial agents utilising the developing stages of Brugia pahangi, WHO Cyclostyled Report, WHO/FIL/81. 167.Google Scholar
Court, J. P. (1982) A diffusion chamber technique for detecting compounds with clinical prophylactic activity against Brugia pahangi. Tropenmedizin and Parasitologie, 33, 8286.Google Scholar
Denham, D. A. (1979) A review of methods for testing compounds for filaricidal activity. Journal of Helminthology, 53, 175187.Google Scholar
Denham, D. A. (1982) The effects of some avermectins on the growth of Brugla pahangi. Methods and Findings in Experimental Clinical Pharmacology, 4, 347350.Google Scholar
Denham, D. A., Ponnudurai, T, Nelson, G.S., Guy, F & Rogers, R (1971) The effect of metrifonate on Brugia pahangi infections in domestic cats. Bulletin of the World Health Organization, 45, 423429.Google Scholar
Denham, D. A., Samad, R, Cho, S. Y., Suswillo, R. R. & Skippins, S. C. (1979) The anthelminthic effects of flubendazole on Brugia pahangi. Transactions of the Royal Society of Tropical Medicine and Hygiene, 73, 673676.CrossRefGoogle Scholar
Howells, R. E., Devaney, E, Smith, G & Hedges, T (1983 a) The susceptibility of BALB/C and other inbred mouse strains to Brugia pahangi. Acta Tropica, 40, 341350.Google Scholar
Howells, R. E., Mendis, A. M. & Bray, P.G. (1983 b) The mode of action of suramin on the filarial worm Brugia pahangi. Parasitology, 87, 2948.CrossRefGoogle Scholar
Lammler, G, Herzog, H & Schutze, N.K. (1971 a) Chemotherapeutic studies on Litomosoides carinii infection of Mastomys natalenis. 2. The activity of drugs against microfilariac. Bulletin of the World Health Organization, 44, 757763.Google Scholar
Lammler, G, Herzog, H & Schutze, H.R. (1971 b) Chemotherapeutic studies on Litotnosoides carinii infection of Mastomys natalensis. 3. The activity of drugs against adult parasites. Bulletin of the World Health Organization, 44, 765770.Google Scholar
Saz, H.J., Dunbar, G. A. & Bueding, E (1977) Chemotherapeutic effects of a nitrodiphcnylaminoiso thiocyanate (C9333-GO/CGP 4540) on jirds injected with Brugia pahangi. American Journal of Tropical Medicine and hygiene, 26, 574575.CrossRefGoogle Scholar
Suswillo, R. R. & Denham, D. A. (1977) A new system for testing filaricidal activity using transplanted adult Brugia pahangi in the jird. Journal of Parasitology, 63, 591592.CrossRefGoogle Scholar
Suswillo, R. R., Owen, D. G. & Denham, D. A.(1980) infections of Brugia pahangi in conventional and nude (athymic) mice. Acta Tropica, 37, 327335.Google Scholar
Suswillo, R. R., DoenHoff, M. J. & Denham, D. A. (1981) Successful development of Brugia pahangi in T-cell deprived CBA mice. Acta Tropica, 38, 305308.Google Scholar
Vincent, A. L., Sodeman, W. A. & Winters, A (1980) Development of Brugia pahangi in normal and nude mice. Journal of Parasitology, 66, 448.Google Scholar
Wharton, R. H. (1959) A simple method of mounting and preserving filarial larvae. Bulletin of the World Health Organization, 20, 729730.Google Scholar
Wong, M. M., O'rourke, M. & Ling, S (1982) Experimental infection of Brugia pahangi in inbred mice. WHO Cyclostyled Report WHO/FIL/82. 170.Google Scholar
World Health Organization (1978) Second Annual Report of the Scientific Working Group on Filariasis. TDR/AR(2)/78.5.Google Scholar
World Health Organization (1979) Report of the Fourth Meeting of the Scicntific Working group on Filariasis. Progress in the Immunology of Filariasis. TDR/FIL-SWG(4) 79.3.Google Scholar