Review Article

Alepidea amatymbica Eckl. & Zeyh.: A Review of Its Traditional Uses, Phytochemistry, Pharmacology, and Toxicology

Table 3

Pharmacological investigation of Alepidea amatymbica Eckl. & Zeyh.

Activity testedModel usedPlant part used/tested materialExtract typeDosageControlResultsReference

AntibacterialNutrient agar medium was mixed with extract and bacteria suspension.
Species strains: Bacillus subtilis ATCC 6051 and Staphylococcus aureus ATCC 12600 and Escherichia coli ATCC 11775 and Klebsiella pneumoniae ATCC 13883
RhizomeDCM, PE, water, and EtOH rhizome extracts1 mg mLWater and bacteria free broth (−ve), 0.1 mg/mL neomycin (+ve)The PE and DCM extracts of the rhizomes exhibited the best activity (MIC values of 0.39 mg/mL) against B. subtilis. The rest of the extracts showed low activity (MIC values >1 mg/mL)[6]

AntibacterialAgar dilution methods with the following organisms:
Bacillus cereus, Staphylococcus epidermidis, Staphylococcus aureus, Micrococcus kristinae, Streptococcus pyogenes, Escherichia coli, Salmonella poona, Serratia marcescens, Pseudomonas aeruginosa, and Klebsiella pneumoniae
Crude extracts of the leaf, stem, rhizome, and rootAcetone and methanol1–10 mg/mLPlates containing 1% acetone and methanol in agarThe acetone rhizome extract showed better activity than others especially on S. aureus and B. cereus
moderate activity that was recorded against the gram-positive bacteria tested with the exception of Micrococcus kristinae
[8]

AntimicrobialMicrodilution method on Mueller-Hinton broth. Species Bacillus subtilis, Staphylococcus aureus, Escherichia coli, and Klebsiella pneumoniae Rhizome and leaf (fresh, 90 days old, and one-year- old material) were assayedWater, ethanol, and hexane extracts12.5, 6.25, 3.13, 1.56, 0.78, 0.39, 0.20, and 0.1 mg/mLExtract-free solution and ethanol were used as a blank control and neomycin (+ve)The water extracts of plants tested for antibacterial activity showed no activity,
whereas the ethanol extracts generally showed an increase in activity. The antibacterial activity increase with storage or ageing of plant material
[33]

AntimicrobialAgar well diffusion method using H. pylori inocula prepared at McFarland’s turbidity standard 2 was plated onto BHI agar supplemented with 5% horse blood and Skirrow’s supplementRoots/rhizomesEthyl acetate, acetone, ethanol, methanol, and water100 mg/mLClarithromycin and 10% DMSO were used as positive and negative controls, respectivelyThe plants demonstrated anti-H. pylori activity with zone diameters of inhibition between 0 and 38 mm and 50% minimum inhibitory concentration (MIC50) values ranging from 0.06 to 5.0 mg/mL[9]

AntimicrobialAgar well diffusion method. Alepidea amatymbica were investigated against 30 clinical strains of H. pylori Roots/rhizomesEthyl acetate, acetone, ethanol, methanol, and water0.002–5.0 mg/mLReference control strain (NCTC 11638). Metronidazole and amoxicillin were included as positive control antibioticsMethanol was quantitatively the best solvent for all the plants while ethyl acetate had the lowest yields. A. amatymbica gave percentage susceptibilities of less than 50%[9]

AntifungalAgar dilution methods with the following organisms:
Aspergillus flavus, Aspergillus niger, and Penicillium notatum cultures were maintained on Potato Dextrose agar
Crude extracts of the leaf, stem, rhizome, and rootAcetone and methanolRadial pattern of streaking of organisms was usedPlates containing only PDA or PDA with the respective solventDiameter of the fungal growth was measured and expressed as percentage growth inhibition. All the extracts showed more than 50% mycotic inhibition with activity ranging from 51.39% to 81.11% at 5 mg/mL with the rhizome[8]

AntifungalThe antifungal activity of the extracts was evaluated against Candida albicans (ATCC 10231) and fungal culture was prepared in Yeast Malt (YM)RhizomeDCM, PE, water, and EtOH rhizome extracts0.1–5.0 mg/mLWater and bacteria free broth (−ve), 0.1 mg/mL neomycin (+ve)All the extracts showed activity against Candida albicans [6]

Anti-inflammatoryUsing the enzyme based cyclooxygenase assays COX-1 and COX-2RhizomeDCM, PE, water, and EtOH rhizome extracts1 mg mLWater and bacteria free broth (−ve), 0.1 mg/mL neomycin (+ve)The PE and DCM extracts had high COX-1 activity with percentage inhibitions above 70%. Ethanol extracts had inhibition less than 40%[6]

AntihypertensivePurified compounds on blood pressure and heart rate of anesthetized Wistar rats.Fresh rhizomesHexane extractive (AA/1), dichloromethane extractive, and methanol extractivei.p. injection of sodium thiopentone (40 mg/kg body weight)ChlorothiazideIn addition to the cardiovascular effects, distinct diuretic and natriuretic effects were found[24]

AntiplasmodiumPlasmodium falciparum strain D10 using the parasite lactate dehydrogenase (pLDH) assayWhole plantDichloromethane (DCM), DCM/methanol (MeOH) (1 : 1), MeOH, and purified water100–0.2 μg/mL)Chloroquine diphosphate served as the positive controlDetect plant-based antimalarial agents showing promising antiplasmodial activity with IC50 values of ≤10 g/mL[34]

DiureticThe Lipschitz test was used to determine the Diuretic and saluretic activity in ratsFresh rhizomeHexane/ethyl acetate extractThe test compound was applied orally at a dose of 50 mg/kgUrea (1 g/kg b.w.)
Hydrochlorothiazide (25 mg/kg b.w.)
The diuretic and natriuretic effects of the extractives were found to be similar to the effects of chlorothiazide[24]

CardiovascularPurified compounds on blood pressure and heart rate of anesthetized Wistar ratsPurified compound from fresh rhizomeHexane extract (AA/1), dichloromethane, and methanol portion of AA/1 were subjected to repeated flash chromatography with gradient elution (100–70% hexane/EtOAc) to give AA/3, a crystalline mixture of ent-kaur-en-19-oic acid, ent-kaura-9 (11), 16-dien-19-oic acid, and trachyloban-19-oic acid, AA/4, 16-methoxy-ent-kaur-11-en-19-oic acid, AA/5, 11-acetoxy-ent-kaur-16-en-19-oic acid, and AA/6, wedelia seco-kaurenolide20 mg/kg b.w. intraperitoneallyEthylene glycolModerate, but significant, decreasing systolic blood pressure (SBP) and heart rate (HT) effects after intraperitoneal application on conscious rats[24]

Anti-HIVExtracts and therein subfractions of A. amatymbica were assessed in a cell based assay targeting the replication of prototypic CXCR4-tropic (NL4-3) or CCR5-tropic
(NL-AD87) HIV-1 strains
Aerial parts and rootsAqueous500 μL of sample at a concentration of 25 mg/mLStandard retroviral inhibitorThe active ingredient identified in the aqueous extract does not support a direct application of this plant extract for treating HIV infection. The anti-HIV activity of the pure compound was found to be quite moderate[2, 12]

AntihelminthesNematode growth agar with Caenorhabditis elegans var. Bristol (N2) nematodesFresh and stored leaves and rootEthanol1 mg/mLLevamisole (+Ve) and nematode incubated with water (−Ve)Only fresh and stored water extracts showed a significant antihelminthes[33]

ToxicityThe bacterial cultures (100 μL) were added to 100 μL of plant extract in 500 μL phosphate buffer and 2 mL of agar containing biotin-histidine (0.5 mM)RhizomeDCM, PE, water, and EtOH rhizome extracts50, 500, and 5000 μg/mL4-Nitroquinoline-N-oxide (4NQO) was used as a positive control and water (−ve control)The Ames test revealed that none of the plant extracts significantly increased the number of His+ revertants with respect to the negative control[6]

CytoxicityHeLa, Vero, Jurkat E6.1, AA-2, or CEM-SS cellsFresh rhizomesAqueous1 mg/mLNot statedThe extract was not toxic at any concentration used in the test[35]

Acute toxicityEvaluation using brine shrimp Artemia salina intersection bioassayFresh rhizomesHexaneNot statedNot statedThe brine shrimp test showed that the crude hexane extracts have low toxicity with LC50 0.2[24]

ToxicityThe Hippocratic test on rats was usedFresh rhizomesIsolates from Alepidea amatymbica
Hexane extractive
0.1 mg/mLVerapamil (10 mg/kg)All extracts, crude and purified, showed low toxicity ranging from LC50 0.5 to 5 ng/mL apart from AA/4 and AA/5 that produced slight diarrhea on days 3, 4, and 5 and other extractives showed no toxicity at a dose of 20[24]