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Isradipine and lacidipine: effects in vivo and in vitro on Trypanosoma cruzi epimastigotes.
Núñez-Vergara, L J; Squella, J A; Bollo-Dragnic, S; Marín-Catalán, R; Pino, L; Díaz-Araya, G; Letelier, M E.
Affiliation
  • Núñez-Vergara LJ; Facultad De Ciencias Químicas y Farmacéuticas, Universidad de Chile, Santiago, Chile.
Gen Pharmacol ; 30(1): 85-7, 1998 Jan.
Article in En | MEDLINE | ID: mdl-9457486
1. Isradipine and lacidipine, two new drugs that are members of the nitro-aryl-1,4-dihydropyridine family, produced inhibition of both growth cultures and oxygen consumption on epimastigotes of Trypanosoma cruzi Tulahuen strain, at micromolar concentrations. 2. Isradipine was found to be the most potent derivative in both, in growth cultures (I50 = 20.8 microM) and in vivo oxygen uptake (I50 = 31.1 microM). 3. Diltiazem and verapamil, two well-known calcium channel antagonists, lacked inhibitory activity, even at a 100 microM concentration. 4. The present findings indicate that the trypanocide effects exerted by isradipine and lacidipine are not related with a disruption of the calcium homeostasis of the parasite.
Subject(s)
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Collection: 01-internacional Database: MEDLINE Main subject: Trypanocidal Agents / Trypanosoma cruzi / Dihydropyridines / Calcium Channel Blockers / Isradipine Limits: Animals Language: En Journal: Gen Pharmacol Year: 1998 Document type: Article Affiliation country: Chile Country of publication: United kingdom
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Collection: 01-internacional Database: MEDLINE Main subject: Trypanocidal Agents / Trypanosoma cruzi / Dihydropyridines / Calcium Channel Blockers / Isradipine Limits: Animals Language: En Journal: Gen Pharmacol Year: 1998 Document type: Article Affiliation country: Chile Country of publication: United kingdom