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Table 5 Antiplasmodial, antimalarial and toxicity studies of extracts and compounds isolated from plants reported in malaria phytotherapy of Bwambara Sub-County, Rukungiri District, Western Uganda

From: Ethnomedicinal plants used for malaria treatment in Rukungiri District, Western Uganda

Medicinal plant

Plant organ

Solvent1

Antiplasmodial/antimalarial (Plasmodium spp) efficacy2

Reported bioactive phytochemicals

Toxicity profile

References

Aloe vera

Leaves

Water

EC50 values for extract: 0.289 to 1056 μg/mL (MRC-2), 169.76 (3D7) for aloin

Aloin

Considered to be safe

[58, 59]

Albizia coriaria

Stem bark

MeOH

15.2 (D6); 16.8 (W2)

Triterpenoids, lupeol, lupenone

Cytotoxic to the human glioblastoma cell line U87 CD4 CXCR4 (​​CC50 = 6.4 and 14.9 μg/ml for ethanol and DMSO extracts)

[60,61,62,63]

Azadirachta indica

Leaves

Water, MeOH

17.9 (D6); 43.7 (W2)

Terpenoids, isoprenoids, gedunin, limonoids: khayanthone, meldenin, nimbinin

Cytotoxicity LD50 of 101.26 and 61.43 µg/ml for water and methanol extracts

[64,65,66,67,68]

Bidens pilosa

Leaves

DCM, water, MeOH

8.5, 5, 11, 70 (D10)

No reports

Hydro and ethanolic extracts are not toxic in mice (LD50 = 12.3 and 6.2 g/kg bw, respectively). Safe in humans

[69,70,71]

Carica papaya

Leaves

Ethyl acetate

2.96 (D10), 3.98 (DD2), 0.2 µM (carpaine)

Carpaine

Carpaine has high selectivity (106), nontoxic to normal red blood cells and rat skeletal myoblast (L6) cells

[72,73,74]

Clausena anisata

Twigs, Leaves

DCM/MeOH, water

18 (D10), > 100 (D10); 55, > 100 (D10)

No reports

Potentially toxic

[69, 75]

Cleome gynandra

Whole plant

Hexane, ethyl acetate, MeOH

Schizonticidal activity in vitro (NK65)

Apigenin, caffeic,

Ferulic, hexadecanoic acids, kaempferol, taraxasterol, pheophytin A, sitosterol, stigmasterol; 5,7,13,15-eicosatetraen-9, 12-diol and 9-hydroxy-5,7,13,15-eicosatetraen-12-one

No report

[76]

Clerodendrum capitatum

Leaves

Ethanol

65.3% chemosuppression at 400 mg/kg

Tannins, flavonoids, alkaloids, triterpenes

LD50 > 5000 mg/kg

[77]

Erythrina abyssinica

Stem bark

Ethyl acetate

83.6% inhibition of P. falciparum at 10 μg/ml

Chalcones (5-prenylbutein, homobutein), flavanones such as 5-deoxyabyssinin II, abyssinin III and abyssinone IV

Minimal toxicity reported in animal studies

[54, 78]

Kigelia africana

Bark, fruit

Chloroform/ethyl acetate, MeOH

59.9 (K39), 83.8 (V1/S); fruits had 165.9 (K39)

None reported

Aqueous fruit extract elicited hepatorenal toxic effects in rats

[79, 80]

Markhamia lutea

Leaves

Ethyl acetate

71% inhibition of P. falciparum at 10 μg/ml

Phenylpropanoid glycosides, cycloartane triterpenoids, musambins A-C, Candmusambiosides A-C

Aqueous leaf and ethanolic extracts with curative anti-inflammatory activity attenuated paclitaxel toxicity in rat’s intestine

[54, 81, 82]

Momordica foetida

Shoot

Water

6.16 (NF54); 0.35 (FCR3)

Saponins, alkaloids, cardiac glycosides

No toxicity against human hepatocellular (HepG2) and urinary bladder carcinoma (ECV-304, derivative of T-24) cells

[83,84,85]

Mondia whitei

Whole root

MeOH

2% parasitemia suppression (ANKA)

Chlorogenic acid

Low toxicity on mice exposed to extract for 90 days

[86, 87]

Moringa oleifera

Flower, leaves

Water, MeOH, acetone, hexane

Parasitemia suppression upto 99.48%

Flavonoids

Not toxic

[88]

Ocimum gratissimum

Leaves/twigs

DCM

8.6 (W2)

Flavonoids

LD50 of the butanolic and ethyl acetate fraction of MeOH leaf extract were 2154.1 and 3807.9 mg/kg

[64, 89, 90]

Ocimum kilimandscharicum

Leaves, twigs

DCM

0.843 (D6); 1.547 (W2)

No reports

No reports

[89]

Plectranthus barbatus

Leaves

DCM

No activity

No toxicity recorded

No reports

[89, 91]

Rootbark

Water (hot), chloroform/MeOH

100 mg/kg/day of extracts had 55.23% and 78.69% parasite chemosuppression

No report

No reports

Senna didymobotrya

Leaves twigs

MeOH, DCM/MeOH (1:1)

 > 100 (K39), 9.5 (D10)

Quinones

Root extracts were toxic (LD50 = 1927 mg/kg)

[55, 69, 92]

Solanecio mannii

Leaves

MeOH

21.6 (3D7), 26.2 (W2)

Phytosterols, n-alkanes and N-hexacosanol

No reports

[36, 93]

Tithonia diversifolia

Aerial parts, leaves

MeOH, ether

1.2 (3D7); 1.5 (W2), MeOH extract had 74% parasitemia suppression

Tagitinin C, sesquiterpene lactones

Aerial parts reportedly cytotoxic against cells from human foetal lung fibroblast cell line

[94,95,96,97]

Vernonia amygdalina

Leaves

MeOH/DCM, ethanol

2.7 (K1), 9.83. In vivo parasite suppression of between 57.2–72.7% in combination with chloroquine

Vernolepin, vernolin, vernolide, vernodalin and hydroxy vernodalin, steroid glucosides

Petroleum ether extract elicited strong cytotoxicity

[36, 54, 57, 85, 95, 98]

Warburgia ugandensis

Stem bark

MeOH, water, DCM

6.4 (D6); 6.9 (W2), 12.9 (D6); 15.6 (W2)

69% parasite suppression

Coloratane sesquiterpenes, e.g., muzigadiolide

Cytotoxic to the human glioblastoma cell line U87 CD4 CXCR4 (​​CC50 = 7.2 and 2.0 μg/ml for ethanol and DMSO extracts

[60, 61, 95, 99,100,101]

  1. 1Solvents used: DCM = dichloromethane, MeOH = methanol. 2Antiplasmodial activity are reported as IC50 (μg/mL). Plasmodium falciparum isolates: chloroquine sensitive strains are 3D7, MRC-2, D6, D10, FCR3, and NF54; chloroquine resistant strains include DD2, K1 and W2