2000
DOI: 10.1016/s0006-2952(99)00400-1
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Reversal activity of the naturally occurring chemosensitizer malagashanine in Plasmodium malaria

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Cited by 31 publications
(12 citation statements)
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“…Data from studies with P. berghei have also shown that in chloroquine resistant strains, GSH can detoxify haemin within the food vacuole, thus precluding its polymerisation and preventing the activity of chloroquine and other quinoline containing drugs [10]. Our study shows that MG inhibits PfGST and it has been found to possess antimalarial activity by increasing the accumulation of CQ inside the parasite [15]. These two properties of MG may then act as a double edged sword in malaria therapy.…”
Section: Discussionsupporting
confidence: 52%
See 1 more Smart Citation
“…Data from studies with P. berghei have also shown that in chloroquine resistant strains, GSH can detoxify haemin within the food vacuole, thus precluding its polymerisation and preventing the activity of chloroquine and other quinoline containing drugs [10]. Our study shows that MG inhibits PfGST and it has been found to possess antimalarial activity by increasing the accumulation of CQ inside the parasite [15]. These two properties of MG may then act as a double edged sword in malaria therapy.…”
Section: Discussionsupporting
confidence: 52%
“…The crude alkaloids of Strychnos myrtoides Gilg and Busse, empirically used as an adjuvant to CQ in Malagasy herbal remedies, were found to be practically devoid of intrinsic in vitro and in vivo antimalarial activity. Malagashanine (MG, Figure 1) is the parent compound of a series of Nb,C[2I]-secocuran alkaloids isolated from two Malagasy Strychnos species [15]. It was found to display a good pharmacological profile by enhancing chloroquine (CQ) action in vitro against the CQ-resistant strain Fc29 of P. falciparum in a follow-up study of the empirical uses of Strychnos species as CQ adjuvants in the treatment of chronic malaria [16].…”
Section: R E S E a R C H A R T I C L Ementioning
confidence: 99%
“…This surprising cell death effect is likely due to a synthetic lethal effect of HSP90 inhibition on the EBNA1 Gly-Ala repeat domain interaction with infected cell proteasomes (36). Consideration has also been given to potentially unique protein interactions that arise from EBNA1 recruitment of Cdc6, ORC, and MCM to oriP DNA complexes for EBV episome replication (16,34,37,38). EBNA1 also interacts with USP7 and guanosine 5′ monophosphate synthetase to form a complex with DNA to promote EBNA1 oriP-binding (18,39).…”
Section: Discussionmentioning
confidence: 99%
“…The asexual erythrocytes' stages of Plasmodium falciparum FcM29-Cameroon, a highly chloroquine-resistant strain were grown continuously in stock cultures by a modification of the methods of Trager and Jensen (1976) using glucose-enriched RPMI 1640 medium, supplemented with 10% human serum at 37 °C as previously described (Rafatro et al, 2000).…”
Section: Parasites Strain and In Vitro Culture Conditionsmentioning
confidence: 99%