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Introduction:The use of pharmaceutical anti-malaria drugs in many rural areas is not common. Various plant extracts have been used as anti-plasmodial agents.Myrsine africanaseed extracts are common anti-malaria agents amongst the Maasai community of Kenya.Aims:This study aimed at characterizing the chemical constituents of methanolic, aqua and n-hexane extracts of Myrsine africana seeds. Study Design:An independent measures design was used.Methodology:The extracts were obtained by maceration of the seeds before subjecting to physical-chemical analysis, functional groups, bio-metal concentrations and phytochemicals screening. Antibacterial studies were conducted using E. coliand S. aureus. The extracts were thereafter screened for presence of quinine and chloroquine by UV VIS spectroscopy. Results:The results indicated the extracts were weakly acidic with moderate solid content. The FT-IR peaks of the extracts indicated abundance of carboxylic acids and benzylic groups. The extracts had a moderate iron concentration with mild copper, cobalt and zinc concentrations. The extracts were also rich in tannins, phenols, saponins, alkaloids and steroids. The antibacterial proficiency of both stains used increased with concentration of extracts and were highest at 50.0mg/mL. Methanolic and water extracts of the seeds also showed appreciable quinines and chloroquinines concentrations. Conclusions:M. africanaseed methanolic and water extracts can be used as anti-plasmodial drugs to help curb malaria in rural tropical regions
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Effect of sodium chloride extract of Dacryodes edulis (African pear) and Chrysophyllum albidum (African star apple) seeds on enteric pathogens (Escherichia coli (ATCC25922); Salmonella typhi (clinical strain); Klebsiella pneumoniae (clinical strain); Pseudomonas spp. (ATCC4853); Enterococcus faecalis (ATCC29212) and Staphylococcus aureus (ATCC25923) were investigated using agar well diffusion and micro broth dilution methods. Results revealed that the extracts have antimicrobial activity against the test organisms. In agar well diffusion method, the extracts were most effective at concentration 100 mg/ml as inhibition zone diameter (IZD) values ranges from 16.5 mm to 23 mm for African pear seed extract and 16.5 mm to 21.9 mm for African star apple seed extract. In the broth dilution method, the extracts were bacteriostatic at lower concentration and bactericidal at higher concentration against all test organisms. Sodium chloride extract of African pear seed shows minimum inhibitory concentration (MIC) values ranges from 1.5625 mg/ml to 50 mg/ml and minimum bactericidal concentration (MBC) values ranges from 6.25 mg/ml to 50 mg/ml respectively while sodium chloride extract of African star apple seed shows MIC values ranges from 6.25 mg/ml to 50 mg/ml and MBC values ranges from 25 mg/ml to 100 mg/ml respectively. In liquid broth medium, sodium chloride extract of African pear seed exhibited the highest activity against Pseudomonas as the least MIC (1.5625 mg/ml) and MBC (6.25 mg/ml) were recorded against the test organism. It is concluded that the sodium chloride extract of African pear and African star apple seeds showed potential antimicrobial activity of MIC and MBC ≤ 100 mg/ml, thus they have antimicrobial activity against enteric pathogens. Hence, sodium chloride will be useful for extracting bioactive agents in African pear and African star apple seeds, thus this will help reduce the cost of extraction and incidence of intestinal diseases.
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Objective: To evaluate the potential efficacy of seed extracts of Annona squamosa and Annona muricata used as natural insecticides to control adult and larvae of the vectors Aedes albopictus and Culex quinquefasciatus under laboratory conditions. Methods: Aqueous and oil extracts of the two plants were prepared from dried seeds. Preliminary identifications of the chemical components of each seed extracts were performed using micro-reactional and GCP techniques. Larvae and adults of Aedes albopictus and Culex quinquefasciatus were collected from the breeding sites in coastal and highlands regions of Madagascar. WHO standardized tests of susceptibility for larvae and imaginal stage of mosquitoes were realized to determine mortality and LC50 of mosquitoes. Results: Chemical identifications showed that these extracts contain alkaloids and flavonoids compounds that probably confer their biological insecticidal proprieties. CPG analysis showed also the presence of various fatty acids. On adult mosquitoes, significant insecticidal effects were observed with both aqueous and oil extracts of the two plant seeds compared to mortality induced by deltamethrin, an insecticide used as reference. Extracts of Annona muricata induced high mortality rate to both species of mosquito compared to extracts of Annona squamosa at all concentrations tested. The LC50 of seed extracts ranged from 1% to 5% for adults and 0.5% to 1% for larvae. Conclusions: The seed extracts of these two plants may be used as mosquito controlling agents and offer a new approach to a less costly, practical and environmentally friendly control of vector borne diseases.
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Objective: To evaluate the potential efficacy of seed extracts of Annona squamosa and Annona muricata used as natural insecticides to control adult and larvae of the vectors Aedes albopictus and Culex quinquefasciatus under laboratory conditions. Methods:Aqueous and oil extracts of the two plants were prepared from dried seeds. Preliminary identifications of the chemical components of each seed extracts were performed using micro-reactional and GCP techniques. Larvae and adults of Aedes albopictus and Culex quinquefasciatus were collected from the breeding sites in coastal and highlands regions of Madagascar. WHO standardized tests of susceptibility for larvae and imaginal stage of mosquitoes were realized to determine mortality and LC50 of mosquitoes. Results: Chemical identifications showed that these extracts contain alkaloids and flavonoids compounds that probably confer their biological insecticidal proprieties. CPG analysis showed also the presence of various fatty acids. On adult mosquitoes, significant insecticidal effects were observed with both aqueous and oil extracts of the two plant seeds compared to mortality induced by deltamethrin, an insecticide used as reference. Extracts of Annona muricata induced high mortality rate to both species of mosquito compared to extracts of Annona squamosa at all concentrations tested. The LC50 of seed extracts ranged from 1% to 5% for adults and 0.5% to 1% for larvae. Conclusions: The seed extracts of these two plants may be used as mosquito controlling agents and offer a new approach to a less costly, practical and environmentally friendly control of vector borne diseases.
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Objective: To develop a quantitative analysis of multi-components with single marker (QAMS) and validate its accuracy and feasibility for simultaneously determining 3-n-butylphthalide (b), sedenenolide (sen), and sedanolide (san) in celery seed extracts (CSE). Methods: Three main effective components,3-n-butylphthalide, sedenenolide, and sedanolide, were selected as analytes for evaluating the quality of CSE. The relative correction factors (RCF, f) of 3-n-butylthalide to the other two thalides were calculated: fb/sen = 0. 226, fb/san = 0.702. The external standard method was used to determine the title compounds in 6 batches of CSE and the results were compared with those of QAMS. Results: The RSD of RCF calculated by different instruments was between 4.4%-6.7%. The RSD of RCF calculated by the same instrument with different chromatographic columns was between 2. 3%-3. 6%. The established RCF had a good reproducibility. The quantitative results of three thalides determined by external standard method and QAMS method were not significantly different. Conclusion: The present method can serve as a new mode to determine multi-components in CSE when standard substances are unavailable.
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This study assessed the antiproliferative and cytotoxic potential against tumor lines of ethanolic seed extracts of 21 plant species belonging to different families from Northeastern Brazil. In addition, some underlying mechanisms involved in this cytotoxicity were also investigated. Among the 21 extracts tested, the MTT assay after 72 h of incubation demonstrated that only the ethanolic extract obtained from Myracrodruon urundeuva seeds (EEMUS), which has steroids, alkaloids and phenols, showed in vitro cytotoxic activity against human cancer cells, being 2-fold more active on leukemia HL-60 line [IC50 value of 12.5 (9.5-16.7) μg/mL] than on glioblastoma SF-295 [IC50 of 25.1 (17.3-36.3) μg/mL] and Sarcoma 180 cells [IC50 of 38.1 (33.5-43.4) μg/mL]. After 72h exposure, flow cytometric and morphological analyses of HL-60-treated cells showed that EEMUS caused decrease in cell number, volume and viability as well as internucleosomal DNA fragmentation in a dose-dependent way, suggesting that the EEMUS triggers apoptotic pathways of cell death.
Este estudo avaliou o potencial antiproliferativo e citotóxico contra linhagens de células tumorais de extratos etanólicos de sementes de vinte e uma espécies vegetais pertencentes a diferentes famílias do Nordeste brasileiro. Além disso, alguns mecanismos subjacentes envolvidos nesta citotoxidade também foram investigados. Dentre os 21 extratos testados pelo ensaio do MTT após 72 h de incubação, apenas o extrato etanólico obtido a partir de sementes de Myracrodruon urundeuva (EEMUS), o qual apresentou traços de esteróides, alcalóides e fenóis em sua composição, demonstrou atividade citotóxica in vitro contra células tumorais humanas, sendo 2 vezes mais ativo sobre a linhagem leucêmica HL-60 [IC50 valor de 12,5 (9,5-16,7) μg/mL] do que sobre células de glioblastoma SF-295 [IC50 de 25,1 (17,3-36,3) μg/mL] e de sarcoma 180 [IC50 de 38,1 (33,5-43,4) μg/mL]. Após 72 h de exposição, as análises morfológicas e por citometria de fluxo de células HL-60 tratadas com EEMUS mostraram diminuição no número de células, seu volume e viabilidade, assim como fragmentação internucleosomal do DNA de forma dose-dependente, sugerindo que a ação antiproliferativa de EEMUS pode ser ativada por vias apoptóticas.
Subject(s)
Animals , Humans , Mice , Antineoplastic Agents, Phytogenic/pharmacology , Plant Extracts/pharmacology , Plants, Medicinal/chemistry , Brazil , Cell Line, Tumor/drug effects , Cell Proliferation/drug effects , Flow Cytometry , Plants, Medicinal/classification , Seeds/chemistryABSTRACT
The purpose of the present study was to investigate the effect of ethanol extracts from red pepper seeds on the antioxidative defense system and oxidative stress in rats fed a high fat . high cholesterol diet. Rats were divided into four experimental groups which were composed of high fat . high cholesterol diet group (HF), high fat . high cholesterol diet with 0.1% ethanol extracts from red pepper seeds supplemented group (HEA), high fat . high cholesterol diet with 0.2% ethanol extracts from red pepper seeds supplemented group (HEB) and high fat.high cholesterol diet with 0.5% ethanol extracts from red pepper seeds supplemented group (HEC). Supplementation of ethanol extracts from red pepper seeds groups (HEA, HEB and HEC) resulted in significantly increased activities of hepatic glutathione peroxidase and catalase. Hepatic superoxide radical contents in microsome and mitochondria were significantly reduced in the groups supplemented with red pepper seeds ethanol extracts. Hepatic hydrogen peroxide content in the mitochondria was reduced in ethanol extracts from red pepper seeds supplemented groups. TBARS values in the liver were reduced in red pepper seeds ethanol extracts supplemented groups. Especially, HEB and HEC groups were significantly decreased compared to the HF group. Hepatic carbonyl values were significantly reduced in mitochondria in these supplemented groups. These results suggest that red pepper seeds ethanol extracts may reduce oxidative damage, by activation of antioxidative defense system in rats fed high fat . high cholesterol diets.
Subject(s)
Animals , Rats , Capsicum , Catalase , Cholesterol , Diet , Ethanol , Glutathione Peroxidase , Hydrogen Peroxide , Liver , Microsomes , Mitochondria , Oxidative Stress , Seeds , Superoxides , Thiobarbituric Acid Reactive SubstancesABSTRACT
Very little research has been carried out on safflower seed for the prevention and treatment of the bone deficiency diseases, including osteoporosis, which are supported by scientific evidences. In the present study, 3microliter of 0.1% dried crude extract or 2microliter of 0.1% dried aqueous fraction were shown to significantly accelerate the rate of differentiation of osteoblast. Also, the crude extract and aqueous fraction increased the [Ca2+]i of the cultured osteoblast cells: 3microliter of 0.1% dried crude extract and 2microliter of 0.1% dried aqueous fraction significantly increased the [Ca2+]i of the cultured osteoblast cells (8x104) to the extent that it deserves a considerable attention. Furthermore, the crude extract and aqueous fraction increased the [Ca2+]i of the cultured osteoblast cells, and 300microM Cd2+, specific calcium channel blocker, completely blocked the increase. Therefore, the increased [Ca2+]i of the cultured osteoblast cells by safflower seed component continued to activate calcium channel.
Subject(s)
Calcium Channels , Calcium , Carthamus tinctorius , Deficiency Diseases , Osteoblasts , OsteoporosisABSTRACT
The ultimate goal of periodontal therapy is the regeneration of periodontal tissue and the repair of function. For more than a decade there have been many efforts to develop ma- terials and methods of treatment to promote periodontal tissue regeneration. Recently many efforts are concentrated on the regeneration potential of material used in traditional medicine. Safflower(Carthamus tinctorius L.) seed extract(SSE) have long clinically used in Korea to promote bone formation and prevent osteoporosis. The purpose of this study was to examine the effects of SSE on bone formation in human osteoblastic cell line. Human fetal osteoblastic cell line(hFOB 1.19) was cultured with DMEM and SSE(1microgram/ml, 10microgram/ml, 100microgram/ml, 1mg/ml) at 34degrees C with 5% CO2 in 100% humidity. The proliferation, differentiation of the cell was evaluated by several experiments. Cell proliferation was significantly increased at 10microgram/ml, 100microgram/ml, 1mg/ml of SSE after 3 and 7 days incubation(p<0.05). Cell spreading assay was significantly increased at 100microgram/ml of SSE after 3 days and 1microgram/ml, 10microgram/ml, 100microgram/ml, 1mg/ml of SSE after 7 days(p<0.05). Alkaline Phosphatase(ALP) level was significantly increased in 10microgram/ml, 100microgram/ml of SSE(p<0.05). Collagen synthesis was significantly increased at 10microgram/ml, 100microgram/ml, 1mg/ml of SSE(p<0.05). A quantified calcium accumulation was significantly increased at 10microgram/ml, 100microgram/ml of SSE(p<0.05). ALP and osteocalcin mRNA was expressed in 100microgram/ml of SSE by RT-PCR. These results indicate that SSE are capable of increasing osteoblasts mineralization and may play an important role in bone formation.