Abstract:
:Human cysticercosis caused by Taenia crassiceps is unusual; however, it is an useful experimental model for cysticercosis studies. Benzimidazole derivatives are important antihelminthic drugs widely used against helminths. A novel compound 6-chloro-5-(1-naphthyloxy) -2-(trifluoromethyl)-1H-benzimidazole (RCB20) is a benzimidazole derivative less polar and more lipophilic. The aim of this study was to detect the effect of the RCB20 on the in vitro energetic metabolism of T. crassiceps cysticerci. For this, products of the metabolism both produced and secreted/excreted (S/E) by the parasite were detected through spectrophotometry and high performance liquid chromatography after exposure to 6.5 and 13 μM of RCB20 and albendazole sulfoxide (ABZSO). There was a gradual increase in the concentrations of glucose not uptaken by parasites exposed to both concentrations RCB20 and ABZSO. There was a higher concentration of all the organic acids related to the tricarboxilic acid cycle int the parasites exposed to RCB20. The structural differences between RCB20 and ABZSO result in different targets within the parasite and in a greater induction of the energetic pathways, such as the glycolysis and the TCA cycle. RCB20 is a good candidate as a substitute for anthelminthic benzimidazoles due to a differentiated site of action with similar outcome.
journal_name
Exp Parasitoljournal_title
Experimental parasitologyauthors
Fraga CM,da Costa TL,de Castro AM,Reynoso-Ducoing O,Ambrosio J,Hernández-Campos A,Castillo R,Vinaud MCdoi
10.1016/j.exppara.2016.11.002subject
Has Abstractpub_date
2017-01-01 00:00:00pages
12-17eissn
0014-4894issn
1090-2449pii
S0014-4894(16)30326-5journal_volume
172pub_type
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journal_title:Experimental parasitology
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