Effects of Azadirachta indica seed kernel extracts on early erythrocytic schizogony of Plasmodium berghei and pro-inflammatory response in inbred mice

Medicinal plant research may contribute to develop new pharmacological control tools for vector borne diseases, such as malaria. The effects of methanol extracts (ME) obtained from seed kernel of ripe and unripe Azadirachta indica fruits were studied on erythrocytic proliferation of the rodent malar...

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Published inMalaria journal Vol. 18; no. 1; pp. 35 - 9
Main Authors Habluetzel, Annette, Pinto, Barbara, Tapanelli, Sofia, Nkouangang, Judith, Saviozzi, Michela, Chianese, Giuseppina, Lopatriello, Annalisa, Tenoh, Alain Rodrigue, Yerbanga, Rakiswendé Serge, Taglialatela-Scafati, Orazio, Esposito, Fulvio, Bruschi, Fabrizio
Format Journal Article
LanguageEnglish
Published England BioMed Central Ltd 08.02.2019
BioMed Central
BMC
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Summary:Medicinal plant research may contribute to develop new pharmacological control tools for vector borne diseases, such as malaria. The effects of methanol extracts (ME) obtained from seed kernel of ripe and unripe Azadirachta indica fruits were studied on erythrocytic proliferation of the rodent malaria parasite Plasmodium berghei strain ANKA and on mice pro-inflammatory response, as evaluated by measuring the matrix-metalloproteinase-9 (MMP-9) and tumour necrosis factor (TNF) plasma levels, in two mouse strains (C57BL/6 and BALB/c) which are considered as prototypical of Th1 and Th2 immune response, respectively. ME obtained from seed kernel of unripe Azadirachta indica fruits decreased by about 30% the proportion of erythrocytes infected with the malaria parasite in C57BL/6 mice in the 4 days suppressive test. In this treatment group, MMP-9 and TNF levels were notably higher than those measured in the same mouse strain treated with the anti-malarial drug artesunate, Azadirachta indica kernel extracts from ripe fruits or solvent. In BALB/c mice, treatment with kernel extracts did not influence parasitaemia. MMP-9 and TNF levels measured in this mouse strain were notably lower than those recorded in C57BL/6 mice and did not vary among treatment groups. The effects of the ME on the parasite-host interactions appeared to be mouse strain-dependent, but also related to the ripening stage of the neem fruits, as only the unripe fruit seed kernel extracts displayed appreciable bioactivity.
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ISSN:1475-2875
1475-2875
DOI:10.1186/s12936-019-2671-8