Skip to main content
Top
Published in: BMC Complementary Medicine and Therapies 1/2016

Open Access 01-12-2016 | Research article

Antimalarial properties of crude extracts of seeds of Brucea antidysenterica and leaves of Ocimum lamiifolium

Authors: Atetetgeb Kefe, Mirutse Giday, Hassen Mamo, Berhanu Erko

Published in: BMC Complementary Medicine and Therapies | Issue 1/2016

Login to get access

Abstract

Background

The search for new antimalarial drugs has become increasingly urgent due to plasmodial resistance to existing drugs. As part of this global effort, the present study aimed at evaluating the antimalarial activity of two traditionally used medicinal plants against the disease.

Methods

Acute toxicity and four-day suppressive effects of aqueous, methanol and chloroform extracts of the seed and leaf of Brucea antidysenterica and Ocimum lamiifolium, respectively, were investigated in Swiss albino mice using Plasmodium berghei using standard procedures.

Results

Methanol extract of the leaves of O. lamiifolium did not exhibit any sign of acute toxicity up to the dose of 2000 mg/kg body weight. However, all mice provided with seeds of B. antidesenterica at a dose of 2000 mg/kg body died within 24 h. The aqueous, methanol and chloroform crude extracts of B. antidesenterica significantly (p < 0.05) inhibited parasitaemia in a dose-dependent manner and prevented body weight loss at doses of 200, 400 and 600 mg/kg body weight. In addition, the extracts prolonged the mean survival time of P. berghei-infected mice compared to the non-treated control. However, it did not prevent reduction in packed cell volume except the chloroform extract in three doses and methanol extract at 200 mg/kg and 400 mg/kg. Extracts from O. lamiifolium also exhibited significant (p < 0.05) antiplasmodial activities. The extracts did not prevent body weight loss and PCV reduction, especially in chloroform. The highest suppression was recorded from aqueous crude extract of O. lamiifolium with 35.53 % in the dose of 600 mg/kg. On the other hand, a similar higher suppression was found in both methanol and chloroform of crude extracts of B. antidesenterica with 47.70 %, 46.44 % of chemosuppression, respectively, in its highest dose tested.

Conclusion

Crude aqueous, methanol and chloroform extracts of the two medicinal plants possess acceptable antimalarial effects. However, further investigation should be pursued on toxicity study and to isolate the bioactive components responsible for the observed antimalarial action of the plants.
Literature
1.
go back to reference WHO. World malaria report 2011. Geneva: World Health Organization; 2012. WHO. World malaria report 2011. Geneva: World Health Organization; 2012.
2.
go back to reference WHO. World malaria report 2012. Geneva: World Health Organization; 2013. WHO. World malaria report 2012. Geneva: World Health Organization; 2013.
3.
go back to reference Nkya TE, Akhouayri I, Poupardin R, Batengana B, Mosha F, Magesa S, Kisinza W, David JP. Insecticide resistance mechanisms associated with different environments in the malaria vector Anopheles gambiae: a case study in Tanzania. Malar J. 2014;13:28.CrossRefPubMedPubMedCentral Nkya TE, Akhouayri I, Poupardin R, Batengana B, Mosha F, Magesa S, Kisinza W, David JP. Insecticide resistance mechanisms associated with different environments in the malaria vector Anopheles gambiae: a case study in Tanzania. Malar J. 2014;13:28.CrossRefPubMedPubMedCentral
4.
go back to reference Fidock DA, Rosenthal PJ, Croft SL, Brun R, Nwaka S. Antimalarial drug discovery: efficacy models for compound screening. Nat Rev Drug Discov. 2004;3:509–20.CrossRefPubMed Fidock DA, Rosenthal PJ, Croft SL, Brun R, Nwaka S. Antimalarial drug discovery: efficacy models for compound screening. Nat Rev Drug Discov. 2004;3:509–20.CrossRefPubMed
5.
go back to reference Ashley EA, Dhorda M, Fairhurst RM, Amaratunga C, Lim P, Suon S, et al. Spread of artemisinin resistance in Plasmodium falciparum malaria. N Engl J Med. 2014;371:411–23.CrossRefPubMedPubMedCentral Ashley EA, Dhorda M, Fairhurst RM, Amaratunga C, Lim P, Suon S, et al. Spread of artemisinin resistance in Plasmodium falciparum malaria. N Engl J Med. 2014;371:411–23.CrossRefPubMedPubMedCentral
7.
go back to reference Krettli AU, Neto V, Brandao M, Ferrari W. The search for new antimalarial drugs from plants used to treat fever and malaria or plants randomly selected. Mem Inst Oswald Cruz. 2001;96:1033–42.CrossRef Krettli AU, Neto V, Brandao M, Ferrari W. The search for new antimalarial drugs from plants used to treat fever and malaria or plants randomly selected. Mem Inst Oswald Cruz. 2001;96:1033–42.CrossRef
8.
go back to reference Bero J, Frederich M, Quetin-Leclercq J. Antimalarial compounds isolated from plants used in traditional medicine. J Pharm Pharmacol. 2009;61:1401–33.CrossRefPubMed Bero J, Frederich M, Quetin-Leclercq J. Antimalarial compounds isolated from plants used in traditional medicine. J Pharm Pharmacol. 2009;61:1401–33.CrossRefPubMed
9.
go back to reference Zelalem P. The Need of standardized herbal remedies as alternate sources of antimalarial products in Ethiopia. J Pharmacol. 2011;3:1440–7. Zelalem P. The Need of standardized herbal remedies as alternate sources of antimalarial products in Ethiopia. J Pharmacol. 2011;3:1440–7.
10.
go back to reference Makonnen E, Debella A, Zerihun L, Abebe D, Teka F. Antipyretic properties of the aqueous and ethanol extracts of the leaves of Ocimum suave and Ocimum lamiifolium in mice. J Ethnopharmacol. 2003;88:85–91.CrossRefPubMed Makonnen E, Debella A, Zerihun L, Abebe D, Teka F. Antipyretic properties of the aqueous and ethanol extracts of the leaves of Ocimum suave and Ocimum lamiifolium in mice. J Ethnopharmacol. 2003;88:85–91.CrossRefPubMed
11.
go back to reference Dawit A, Asfaw D, Kelbessa U. Medicinal plants and other useful plants of Ethiopia. Addis Ababa: Addis Ababa University Press; 2003. Dawit A, Asfaw D, Kelbessa U. Medicinal plants and other useful plants of Ethiopia. Addis Ababa: Addis Ababa University Press; 2003.
12.
go back to reference Grace OM, Fowler DG. Brucea antidysenterica J.F. Mill. Medicinal plants/Plantes médicinales. Wageningen: PROTA; 2008. Grace OM, Fowler DG. Brucea antidysenterica J.F. Mill. Medicinal plants/Plantes médicinales. Wageningen: PROTA; 2008.
13.
go back to reference O'Neill MJ, Bray DH, Boardman P, Chan KL, Phillipson JD, Warhurst DC, Peters W. Plants as sources of antimalarial drugs, part 4: activity of Brucea javanica fruits against chloroquine-resistant Plasmodium falciparum in vitro and against Plasmodium berghei in vivo. J Nat Prod. 1987;50:41–8.CrossRefPubMed O'Neill MJ, Bray DH, Boardman P, Chan KL, Phillipson JD, Warhurst DC, Peters W. Plants as sources of antimalarial drugs, part 4: activity of Brucea javanica fruits against chloroquine-resistant Plasmodium falciparum in vitro and against Plasmodium berghei in vivo. J Nat Prod. 1987;50:41–8.CrossRefPubMed
14.
go back to reference Murithi CK, Fidahusein DS, Nguta JW, Lukhoba CW. Antimalarial activity and in vivo toxicity of selected medicinal plants naturalised in Kenya. Int J Educ Res. 2014;2:5. Murithi CK, Fidahusein DS, Nguta JW, Lukhoba CW. Antimalarial activity and in vivo toxicity of selected medicinal plants naturalised in Kenya. Int J Educ Res. 2014;2:5.
15.
go back to reference Tchoumbougnang F1, Zollo PH, Dagne E, Mekonnen Y. In vivo antimalarial activity of essential oils from Cymbopogon citratus and Ocimum gratissimum on mice infected with Plasmodium berghei. Planta Med. 2005;71:20–3.CrossRefPubMed Tchoumbougnang F1, Zollo PH, Dagne E, Mekonnen Y. In vivo antimalarial activity of essential oils from Cymbopogon citratus and Ocimum gratissimum on mice infected with Plasmodium berghei. Planta Med. 2005;71:20–3.CrossRefPubMed
16.
go back to reference Kayembe JS, Taba KM, Ntumba K, Tshiongo MTC, Kazadi TK. In vitro anti-malarial activity of 20 quinones isolated from four plants used by traditional healers in the Democratic Republic of Congo. J Med Plants Res. 2010;2010(4):991–4. Kayembe JS, Taba KM, Ntumba K, Tshiongo MTC, Kazadi TK. In vitro anti-malarial activity of 20 quinones isolated from four plants used by traditional healers in the Democratic Republic of Congo. J Med Plants Res. 2010;2010(4):991–4.
17.
go back to reference O’Neill MJ, Bray DH, Boardman P, Phillipson DJ, et al. Plants as sources of antimalarial drugs: in vitro antimalarial activities somequassinoids. Antimicrob Agents Chemother. 1986;30:101–4.CrossRefPubMedPubMedCentral O’Neill MJ, Bray DH, Boardman P, Phillipson DJ, et al. Plants as sources of antimalarial drugs: in vitro antimalarial activities somequassinoids. Antimicrob Agents Chemother. 1986;30:101–4.CrossRefPubMedPubMedCentral
18.
go back to reference Ogu GI, Aisuodionoe ME, Nwachukwu P. Antiplasmodial activity of Caesalpinia Pulcherrima (Swarts) stem. IJBPAS. 2012;1:168–78. Ogu GI, Aisuodionoe ME, Nwachukwu P. Antiplasmodial activity of Caesalpinia Pulcherrima (Swarts) stem. IJBPAS. 2012;1:168–78.
19.
go back to reference OECD. OECD guideline for testing of chemicals. Acute oral toxicity–Up-and-down procedure. 2001. OECD. OECD guideline for testing of chemicals. Acute oral toxicity–Up-and-down procedure. 2001.
20.
go back to reference Li QG, Si YZ, Lee P, Wong E, Xie LH, Kyle DE, Dow GS. Efficacy of comparison of intravenous artelinate and artesunate in Plasmodium berghei infected Sprangue-dawlery rats. Parasitology. 2003;126:283–91.CrossRefPubMed Li QG, Si YZ, Lee P, Wong E, Xie LH, Kyle DE, Dow GS. Efficacy of comparison of intravenous artelinate and artesunate in Plasmodium berghei infected Sprangue-dawlery rats. Parasitology. 2003;126:283–91.CrossRefPubMed
21.
go back to reference Devi CU, Atul PK, Pillal CR. Antiplasmodial effect of three medicinal plants: preliminary study. Curr Sci. 2001;80:917–9. Devi CU, Atul PK, Pillal CR. Antiplasmodial effect of three medicinal plants: preliminary study. Curr Sci. 2001;80:917–9.
22.
go back to reference Mengistie B, Makonnen E, Urga K. In vivo antimalarial activity of Dodonaea angustifolia seed extracts against plasmodium berghei in mice model. MEJS. 2012;4:47–63. Mengistie B, Makonnen E, Urga K. In vivo antimalarial activity of Dodonaea angustifolia seed extracts against plasmodium berghei in mice model. MEJS. 2012;4:47–63.
23.
go back to reference Franssen FJ, Smeijsters LW, Berger I, Aldana BM. In vitro and in vivo antiplasmodial activities of some plants traditionally used in Guatemala against malaria. Antimicrob Agent Chemother. 1997;41:1500–3. Franssen FJ, Smeijsters LW, Berger I, Aldana BM. In vitro and in vivo antiplasmodial activities of some plants traditionally used in Guatemala against malaria. Antimicrob Agent Chemother. 1997;41:1500–3.
24.
go back to reference Krettli AU, Adebayo JO, Krettli LG. Testing of natural products and synthetic molecules aiming at new antimalarials. Curr Drug Targ. 2009;10:261–70.CrossRef Krettli AU, Adebayo JO, Krettli LG. Testing of natural products and synthetic molecules aiming at new antimalarials. Curr Drug Targ. 2009;10:261–70.CrossRef
25.
go back to reference Alli LA, Adesokan AA, Salawu OA, Akanji MA, Tijani AY. Antiplasmodial activity of aqueous root extract of Acacia nilotica. Afr J Biochem Res. 2011;5:214–9. Alli LA, Adesokan AA, Salawu OA, Akanji MA, Tijani AY. Antiplasmodial activity of aqueous root extract of Acacia nilotica. Afr J Biochem Res. 2011;5:214–9.
26.
go back to reference Deressa T, Mekonnen Y, Animut A. In vivo antimalarial activities of Clerodendrum myricoides, Dodonea angustifolia and Aloe debrana against Plasmodium berghei. Ethiop J Health Dev. 2010;24:25–9. Deressa T, Mekonnen Y, Animut A. In vivo antimalarial activities of Clerodendrum myricoides, Dodonea angustifolia and Aloe debrana against Plasmodium berghei. Ethiop J Health Dev. 2010;24:25–9.
27.
go back to reference Dikasso D, Makonnen E, Debella A, Abebe D, Urga K, et al. In vivo anti-malarial activity of hydroalcoholic extracts from Asparagus africanus Lam. in mice infected with Plasmodium berghei. Ethiop J Health Dev. 2006;20:112–8. Dikasso D, Makonnen E, Debella A, Abebe D, Urga K, et al. In vivo anti-malarial activity of hydroalcoholic extracts from Asparagus africanus Lam. in mice infected with Plasmodium berghei. Ethiop J Health Dev. 2006;20:112–8.
28.
go back to reference Zhengming G, Suryanarayana V, Robert WS, Larry AW, Robert DS. Biologically active quassinoids and their chemistry: potential leads for drug design. Front Med Chem. 2009;4:1–22. Zhengming G, Suryanarayana V, Robert WS, Larry AW, Robert DS. Biologically active quassinoids and their chemistry: potential leads for drug design. Front Med Chem. 2009;4:1–22.
29.
go back to reference Muregi FW, Ishain A, Suzuki T, Kino H, Amano T, Mkoji GM, Miyase T, Terada M, et al. In vivo antimalarial activity of aqueous extracts from Kenyan medicinal plants and their chloroquinine potentiation effects against a blood-induced CQ resistant rodent malaria parasite in mice. Phytother Rev. 2007;21:337–43.CrossRef Muregi FW, Ishain A, Suzuki T, Kino H, Amano T, Mkoji GM, Miyase T, Terada M, et al. In vivo antimalarial activity of aqueous extracts from Kenyan medicinal plants and their chloroquinine potentiation effects against a blood-induced CQ resistant rodent malaria parasite in mice. Phytother Rev. 2007;21:337–43.CrossRef
30.
go back to reference Abdu KB, Khan ME, Rumah MM. Antimicrobial activity and phytochemical screening of extracts from the root bark of Carissa edulis, against human/animal. J Trop Med. 2008;2:1–6. Abdu KB, Khan ME, Rumah MM. Antimicrobial activity and phytochemical screening of extracts from the root bark of Carissa edulis, against human/animal. J Trop Med. 2008;2:1–6.
Metadata
Title
Antimalarial properties of crude extracts of seeds of Brucea antidysenterica and leaves of Ocimum lamiifolium
Authors
Atetetgeb Kefe
Mirutse Giday
Hassen Mamo
Berhanu Erko
Publication date
01-12-2016
Publisher
BioMed Central
Published in
BMC Complementary Medicine and Therapies / Issue 1/2016
Electronic ISSN: 2662-7671
DOI
https://doi.org/10.1186/s12906-016-1098-9

Other articles of this Issue 1/2016

BMC Complementary Medicine and Therapies 1/2016 Go to the issue