Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/79151
Type: Artigo de periódico
Title: Comparative in vitro and in vivo antimalarial activity of the indole alkaloids ellipticine, olivacine, cryptolepine and a synthetic cryptolepine analog
Author: Silva, LFRE
Montoia, A
Amorim, RCN
Melo, MR
Henrique, MC
Nunomura, SM
Costa, MRF
Neto, VFA
Costa, DS
Dantas, G
Lavrado, J
Moreira, R
Paulo, A
Pinto, AC
Tadei, WP
Zacardi, RS
Eberlin, MN
Pohlit, AM
Abstract: Indole alkaloids ellipticine (1), cryptolepine triflate (2a), rationally designed 11-(4-piperidinamino)cryptolepine hydrogen dichloride (2b) and olivacine (3) (an isomer of 1) were evaluated in vitro against Plasmodium falciparum and in vivo in'Plasmodium berghei-infected mice. 1-3 inhibited P. falciparum (IC50 <= 1.4 mu M, order of activity: 2b >1 > 2a > 3). In vitro toxicity to murine macrophages was evaluated and revealed selectivity indices (SI) of 10-12 for 2a and SI> 2.8 x 102 for 1, 2b and 3.1 administered orally at 50 mg/kg/day was highly active against P. berghei (in vivo inhibition compared to untreated control (IVI) = 100%, mean survival time (MST)> 40 days, comparable activity to chloroquine control). 1 administered orally and subcutaneously was active at 10 mg/kg/day (IVI = 70-77%; MST= 27-29 days). 3 exhibited high oral activity at >= 50 mg/kg/day (IVI =90-97%, MST= 23-27 days). Cryptolepine (2a) administered orally and subcutaneously exhibited moderate activity at 50 mg/kg/day (IVI =43-63%, MST= 24-25 days). At 50 mg/kg/day, 2b administered subcutaneously was lethal to infected mice (MST= 3 days) and moderately active when administered orally (IVI =45-55%, MST = 25 days). 1 and 3 are promising compounds for development of antimalarials. (C) 2012 Elsevier GmbH. All rights reserved.
Subject: Plasmodium falciparum
Plasmodium berghei
Murine macrophages
Antiplasmodial activity
Indole alkaloids
Country: Alemanha
Editor: Elsevier Gmbh, Urban & Fischer Verlag
Rights: fechado
Identifier DOI: 10.1016/j.phymed.2012.09.008
Date Issue: 2012
Appears in Collections:Unicamp - Artigos e Outros Documentos

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