Abstract
This chapter discusses an approach to control filariasis by the use of a new class of pharmacological agents, benzimidazoles. There are six species of human filariasis for which it is desirable to develop antifilarial agents: Wuchereria bancrofti , Brugia malayi , and Onchocerca volvulus are major human pathogens, responsible for practically all filaria-related deaths. Mansonella ozzardi , Dipetalonema perstans , and Loa Loa are less prevalent species. Benzimidazoles have been identified as antifilarial agents based on an extensive series of studies in jirds (a kind of gerbil) and cats. The mechanism of the action of benzimidazoles has been extensively studied in many laboratories, and, in general, three possible modes of action have been suggested for these drugs. It has been demonstrated by numerous workers that the majority of benzimidazoles inhibit the microtubulin of tegumental or intestinal cells of nematodes or cestodes through the degeneration of these cells. This mechanism is now well accepted as the mode of action for benzimidazole derivatives.
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