No / Cajanus cajan L, a member of the family Fabaceae, was identified from the Nigerian antimalarial ethnobotany as possessing antimalarial properties. The bioassay-guided fractionation of the crude methanol extract of C. cajan leaves was done in vitro using the multiresistant strain of Plasmodium falciparum (K1) in the parasite lactate dehydrogenase assay. Isolation of compound was achieved by a combination of chromatographic techniques, while the structure of the compound was elucidated by spectroscopy. This led to the identification of a cajachalcone, 2′,6′-dihydroxy-4-methoxy chalcone, as the biologically active constituent from the ethyl acetate fraction. Cajachalcone had an IC50 value of 2.0 μg/mL (7.4 μM) and could be a lead for anti-malarial drug discovery.

Given the drawbacks associated with the use of antibiotics as feed additives and the imminent banning of its use in the European Union, the aim of this project was to develop an extract that could be used as an alternative feed additive in poultry production. The desired extract preferably had to be rich in antibacterial activity to control proliferation of undesired microorganisms, and antioxidant activity to boost the immune system of the poultry. A number of trial extraction procedures were employed on dried leaf material samples to identify the best extraction method. In preliminary extraction studies, direct extraction was performed on leaf samples from the Lowveld National Botanical Gardens (LNBG) and from University of Pretoria Botanical Garden (UP). The principle aim of preliminary studies was to identify the solvents that extracted high antibacterial and antioxidant activity while also extracting large quantities of material. The secondary objective was to test for differences in activities between samples collected from LNBG and UP. Five extractants of varying polarities; acetone, ethanol, ethylacetate, dichloromethane and hexane were used. Antibacterial activity of all extracts was quantified by a serial dilution microplate technique while bioautography was used in qualitative analysis of the antibacterial active compounds. ATCC strains of Staphylococcus aureus, Pseudomonas aeruginosa, Escherichia coli and Enterococcus faecalis were used as test organisms. Qualitative antioxidant activity was determined by using a DPPH assay on TLC plates. Results from preliminary extraction studies showed larger quantities of material were present in extracts from the LNBG sample than in the UP sample. Two major antioxidant compounds (Rf values of 0.85 and 0.35 in EMW solvent system) were seen on DPPH sprayed TLC plates, while bioautography showed the presence of a number antibacterial active compounds in the acetone, ethanol and ethylacetate extracts with Rr values ranging between 0.85 and 0.56 on TLC plates developed in the EMW solvent system. MIC values of the extracts tallied with the results from bioautography. The acetone, ethanol and ethyl acetate extracts had the highest antibacterial activity while the hexane extracts had the lowest activity with average MIC value of 0.55 mg/ml for both the LNBG and UP samples. MIC values as low as 0.04 mg/ml were measured in the acetone and ethylacetate extracts of the LNBG sample against S. aureus and E. faecalis. Based on results from preliminary extraction studies, hexane was identified as a possible pretreatment solvent for application in enrichment procedures, acetone and ethanol were chosen as the main extractants and only the LNBG sample was used for future work. Enrichment procedures were employed along two pathways; the first pathway involved the use of hexane "wash" as a pretreatment procedure prior to extraction with acetone or ethanol. The second pathway involved the use of various mixtures of acetone in water and ethanol in water as extractants. The rationale of using these various ratios was an attempt to identify solvent mixtures that would selectively extract the bioactive components or otherwise selectively remove inactive material. A serial dilution microplate method was used to determine Minimum Inhibitory Concentrations (MICs) and the Trolox Equivalent Antioxidant Capacity (TEAC) assay was used to quantify antioxidant activity of all extracts. The optimal extract was the one developed by pretreatment with a single direct extraction with hexane prior to extraction with acetone. It had a TEAC value of 2.3, an increase in TEAC value of 283% compared to that of the crude acetone extract. The average MIC of the crude acetone extract against ATCC stains of S. aureus, Ps. aeruginosa, E. coli and E. faecalis had dropped from 0.15 mg/ml to 0.08 mg/ml in the optimal extract (an improvement in antibacterial activity of 87.5%). Since the optimal extract is intended for commercial application in poultry production, its antibacterial activity was tested against Campylobacter jejuni, Clostridium perfringens, Salmonella enteritidis, E. coli and multi drug resistant E. coli isolated from chickens. Its in vitro toxicity was ascertained using the brine shrimp assay and the MTT cytotoxicity assay on monkey kidney cells. The optimal extract was effective against Campylobacter jejuni and Clostridium perfringens with MIC values ranging from 40 µ/ml to 80 µ/ml. It was also active against multi-resistant strains of E. coli and Salmonella enteritidis (MIC values of 125 µ/ml for both strains). LC50 results from the brine shrimp assay and the MTT cytotoxicity assay on monkey kidney cells gave values of 863 µ/ml and 226 µ/ml respectively indicating low toxicity. These results meant that though in some cases the MICs of the optimal extract were higher than befitting of typical antibiotics, due to its relatively low toxicity, large quantities of the extract may possibly be feed to achieve the desired activity without causing any toxicity in the poultry. The major antioxidant compound was isolated by silica gel column chromatography. The isolated compound was identified by nuclear magnetic resonance and mass spectroscopy as combretastatin BS (2', 3', 4-trihydroxyl, 3, S, 4'-trimethoxybibenzyl), previously isolated from the seeds of C. kraussii and also from C. woodii leaves. Famakin (2002) showed this compound to be the major antibacterial compound in C. woodii leaves. Combretastatin BS (CBS) demonstrated in vitro cytotoxicity in the MTT assay on monkey kidney cells with an LC50 value of 1 0 µ/ml. In vitro cytotoxicity of CBS could be due to its antimitotic activity. The TEAC value of 7.9 found in this study means that combretastatin BS has about 8 times the antioxidant capacity of vitamin E. This is the first report of the antioxidant activity of any of the combretastatins. Tolerance of broiler chickens to the optimal extract was assessed at clinically inferred doses of 2 mg/kg, Smg/kg and 10 mg/kg . After 21 days of infeed-dosing with the optimal extract, none of the chickens died or showed any behavioral signs of toxicity. There were no statistically significant differences in weight gain between broilers fed the optimal extract and the positive and negative control. There was also no positive correlation between weight gain and amount of the optimal extract incorporated in feed. Although the optimal extract did not result in significant growth promotion relative to the positive and negative control, 2 mg/kg dose regimens showed the best Feed Conversion Ratio (FCR), with a 6.2% improvement compared to the negative control. The positive control was the only other feed regimen to provide a positive FCR with an improvement of 1.73% compared to the negative control. Because purchase of feed could represent up to 80% of costs of broiler production, this is an important finding. If these results can be confirmed, the product may therefore have commercial value. Repetition of the experiment with lower doses of the optimal extract on poultry challenged with bacterial infections is required to confirm the commercial applicability of this product. Copyright / Dissertation (MSc (Paraclinical Science))--University of Pretoria, 2004. / Paraclinical Sciences / unrestricted

Magister Pharmaceuticae - MPharm / Syzygium cordatum is a medicinal plant indigenous to South Africa and Mozambique, commonly used to treat stomach aches, diabetes, respiratory problems and tuberculosis. In spite of the folklore use, adequate scientific data to credit its widespread traditional use is lacking. The objectives of this study were: to evaluate and validate scientifically the successful therapeutic claims by traditional medicine practitioners that Syzygium cordatum is effective in treating diarrhoea and diabetes; to determine the effects of the plant extract on gastrointestinal transit of a charcoal meal in mice; to determine the effects on castor oilinduced intestinal fluid accumulation; to determine the safety profile of the plant by carrying out acute toxicology study and to carry out preliminary screening of the active compounds present in the plant using standard phytochemical analytical procedures. The aqueous leaf extract of Syzygium cordatum (3.125 -50mg/kg, p.o) significantly reduced the faecal output caused by castor oil (0.7ml). All the doses used, reduced faecal output from 100% produced by castor oil to between 40 and 61%. S.cordatum (6.25 – 50mg/kg, p.o) significantly and in a dose dependent manner, delayed the onset of castor oil-induced diarrhoea. / South Africa

No description available.

Syzygium cordatum is a medicinal plant indigenous to South Africa and Mozambique, commonly used to treat stomach aches, diabetes, respiratory problems and tuberculosis. In spite of the folklore use, adequate scientific data to credit its widespread traditional use is lacking. The objectives of this study were: to evaluate and validate scientifically the successful therapeutic claims by traditional medicine practitioners that Syzygium cordatum is effective in treating diarrhoea and diabetes / to determine the effects of the plant extract on gastrointestinal transit of a charcoal meal in mice / to determine the effects on castor oilinduced intestinal fluid accumulation / to determine the safety profile of the plant by carrying out acute toxicology study and to carry out preliminary screening of the active compounds present in the plant using standard phytochemical analytical procedures. The aqueous leaf extract of Syzygium cordatum (3.125 -50mg/kg, p.o) significantly reduced the faecal output caused by castor oil (0.7ml). All the doses used, reduced faecal output from 100% produced by castor oil to between 40 and 61%. S.cordatum (6.25 &ndash / 50mg/kg, p.o) significantly and in a dose dependent manner, delayed the onset of castor oil-induced diarrhoea.

Syzygium cordatum is a medicinal plant indigenous to South Africa and Mozambique, commonly used to treat stomach aches, diabetes, respiratory problems and tuberculosis. In spite of the folklore use, adequate scientific data to credit its widespread traditional use is lacking. The objectives of this study were: to evaluate and validate scientifically the successful therapeutic claims by traditional medicine practitioners that Syzygium cordatum is effective in treating diarrhoea and diabetes / to determine the effects of the plant extract on gastrointestinal transit of a charcoal meal in mice / to determine the effects on castor oilinduced intestinal fluid accumulation / to determine the safety profile of the plant by carrying out acute toxicology study and to carry out preliminary screening of the active compounds present in the plant using standard phytochemical analytical procedures. The aqueous leaf extract of Syzygium cordatum (3.125 -50mg/kg, p.o) significantly reduced the faecal output caused by castor oil (0.7ml). All the doses used, reduced faecal output from 100% produced by castor oil to between 40 and 61%. S.cordatum (6.25 &ndash / 50mg/kg, p.o) significantly and in a dose dependent manner, delayed the onset of castor oil-induced diarrhoea.

Fruit rot caused by Aspergillus niger and Colletotrichum sp. could cause rapid and severe damage on orange fruits. Current control method of orange fruits is mainly applied by usage of harmful pesticides, leading to chemical residues on fruits, environmental pollution and human poisoning. One of alternative methods of reducing pesticides is to use botanical extracts. This study was conducted to evaluate the in vivo antifungal efficacy of aqueous extracts from the leaves of neem and basket plants against A. niger and Colletotrichum sp. Orange fruits artificially inoculated by fruit rot pathogens were immersed into leaf extracts of 6% (w/v) neem or basket plants for 30 s, and kept for 11 days to record lesion length at room temperature. Orange fruits immersed into sterile distilled water were used as the control treatment. The results showed that at 11 days after inoculation, extracts of neem and basket plants significantly reduced the Aspergillus rot lesions by 109.08 and 124.00 mm, respectively. In addition, anthracnose lesions on orange fruits were statistically inhibited by treatments of neem and basket plants, with the average lesion diameters approximately 160.00 and 154.75 mm, respectively, at day 11 of the conducting experiment. The results of this study showed that leaf extracts of neem and basket plant at the concentration of 6% could be used as a natural alternative to control the in vivo growth of rot pathogens of orange fruits. These extracts have a bright future in modern plant protection to replace conventional synthetic pesticides in agro-ecosystem. / Thối trái bởi Aspergillus niger và Colletotrichum sp. gây ra các thiệt hại nghiêm trọng trên cam. Biện pháp phòng trừ bệnh trên trái cam hiện nay chủ yếu dựa vào thuốc hóa học, dẫn đến tồn dư thuốc trên trái cây, ô nhiễm môi trường và gây độc cho con người. Một trong các phương pháp thay thế giúp giảm sử dụng thuốc hóa học là sử dụng dịch trích thực vật. Nghiên cứu này đã được thưc hiện để đánh giá hiệu quả in vivo của dịch trích ở nồng độ 6% của neem hoặc lược vàng đối với A. niger và Colletotrichum sp. Các trái cam đã lây nhiễm nhân tạo tác nhân gây thối trái thì được nhúng vào dịch trích ở nồng độ 6% của neem hoặc lược vàng trong 30 giây, và giữ đến 11 ngày để ghi nhận chiều dài vết bệnh ở nhiệt độ phòng. Cái trái cam được nhúng vào nước cất thì dùng như nghiệm thức đối chứng. Kết quả cho thấy ở 11 ngày sau khi chủng bệnh, dịch trích neem và lược vàng làm giảm đáng kể vết thối Aspergillus lần lượt là 109,08 và 124,00 mm. Bên cạnh đó, vết bệnh thán thư trên trái cam đã bị ức chế có ý nghĩa thống kê bởi các dịch trích neem và lược vàng, với đường kính trung bình các vết bệnh lần lượt là 160,00 và 154,75 mm, ở ngày 11 của thí nghiệm. Kết quả của nghiên cứu này đã chỉ ra rằng dịch trích neem và lược vàng ở nồng độ 6% có thể sử dụng như một biện pháp thay thế tự nhiên trong việc phòng trừ sự phát triển của tác nhân gây thối trái cam. Các loại dịch trích này có tương lai trong bảo vệ thực vật hiện đại, thay thế các loại thuốc hóa học tổng hợp truyền thống trong hệ sinh thái nông nghiệp.