Antimicrobial activity of selected Malaysian plants

Methanolic extracts of seventeen Malaysian plants were screened against fungi, including yeast and candida, as well as gram negative and gram positive bacteria. Antimicrobial activities were present in extracts prepared from Borreria latifolia, B. selidens, Hedyotis diffusa, H. nudicaulis, Morinda elliptica, M. umbellata (Rubiaceae), Sida rhombifolia (malvaceae) and Vitex ovata (Verbenaceae). Extracts from S. rhombifolia and B. latifolia showed exreptionally high activity against Candida albicans, Ca. intermedia, Aspergillus ochraceous, Cunninghamella clegans and Pseudomonas aeruginosa. However, only moderate activity was observed against Bacillus cereus, Ba. megaterium and Ca. Iipolyuca. Extracts from Calophyllum inophyllum (Guttiferae), Entada sp. (Leguminosae), Eclipta alba (Compositae), Dendrotrophe umbellata (Santalaceae), Cardiospermum halicacabum (Sapindaceae), Glochidion lutcscens and Euphorbia prunifolia (Euphorbiaceae) gave negative results

Mechanism of apoptosis induced by curcumin in colorectal cancer

Colorectal cancer (CRC) is among the top three cancer with higher incident and mortality rate worldwide. It is estimated that about over than 1.1 million of death and 2.2 million new cases by the year 2030. The current treatment modalities with the usage of chemo drugs such as FOLFOX and FOLFIRI, surgery and radiotherapy, which are usually accompanied with major side effects, are rarely cured along with poor survival rate and at higher recurrence outcome. This trigger the needs of exploring new natural compounds with anti-cancer properties which possess fewer side effects. Curcumin, a common spice used in ancient medicine was found to induce apoptosis by targeting various molecules and signaling pathways involved in CRC. Disruption of the homeostatic balance between cell proliferation and apoptosis could be one of the promoting factors in colorectal cancer progression. In this review, we describe the current knowledge of apoptosis regulation by curcumin in CRC with regard to molecular targets and associated signaling pathways

Metabolite characterization of different palm date varieties and the correlation with their NO inhibitory activity, texture and sweetness

The aim of this study was to examine the variation in metabolite constituents of five commercial varieties of date fruits; Ajwa, Safawi and Ambar which originated from Madinah, the Iranian Bam and Tunisian Deglet Noor. The differences of metabolome were inves-tigated using proton nuclear magnetic resonance (1HNMR) spectroscopy combined with multivariate data analysis (MVDA). Principal Component Analysis (PCA) revealed clear separation between the date varieties. The Tunisian Deglet Noor demonstrated distinct cluster from the rest of the palm date samples based on the metabolite composition as shown by the pattern observed in Hierarchical Clustering Analysis (HCA) and PCA. Deglet Noor exhibited a significant higher level of sucrose (d5.40) and fructose (d4.16) in comparison with the other four varieties which can be associated with the distinctive sweet taste of this variety.Dates originated from Madinah and Tunisia exhibited a contrast manner in the amount of xylose and moisture content. These two aspects may contribute towards the soft texture of Tunisian dates. All Madinah dates were found to contain phenolic compounds which were well established as great antioxidant and anti-inflammatory agent. Ajwa dates exerted greater effect in inhibiting the generation of nitric oxide (NO) from the stimulated RAW264.7 cells at 95.37% inhibition. Succinic acid was suggested to have the most significant correlation with the trend of NO inhibitory shown by the selected date palm varieties

Antiviral and cytotoxic activities of some plants used in Malaysian indigenous medicine

Ethanolic extracts of 61 medicinal plants used in Malaysia were screened for antiviral and cytotoxic activities. Antiviral activity was tested against the herpes simplex type-1 (HSV-1) and vesicular stomatitis (VSV) viruses, and cytotoxicity was assayed using the HeLa cell line. Antiviral activity against both viruses was present in the extracts from Calotropis gigantea, Costus speciosus, Eugenia michelii, Hedyotis auricularia, Mentha arvensis, Orthosiphon aristatus, Polygonum minus and Ricinus communis (MIG: 0.002-0.1 mg/ml). The extracts from Alternanthera sessilis, Blumea chinensis, Eleusine indica, Euphorbia hirta, Freycinetia malaccensis, Leea indica and Solanum americanum were active in selectively inhibiting HSV-1 (0.001-0.1 mg/ml). Selective activity against VSV was shown by the extracts from Acalypha indica, Bertholletia excelsa, Cerbera manghas, Codiaeum variegatum, Plectranthus amboinicus, Centella asiatica, Mirabilis jalapa, Morinda elliptica, Oenanthe javanica, Piper sarmentosum and Premna odorata (MIG: 0.005-0.1 mg/ml). Gytotoxic activity was present in the extracts from Acalypha indica, Andrographis paniculata, Cerbera manghas, Codiaeum variegatum, Cosmos caudatus, Elephantopus scaber, Etlingera elatior, Eugenia michelii, Freycinetia malaccensis, Hibiscus rosa-sinensis,Cen~ella asiati~a, Lecythis ollaria, Mentha arvensis, Mirabilis jalapa, Morinda elliptica, Ocimum tenUlflorum, PIper sarmentosum and Polygonum minus (CD50: 0.001-0.1 mgjml).Co-existing antiviral and cytotoxic activities were shown by Eugenia michelii, Mentha arvensis and Polygonum minus

Antiviral, cyototoxic and antimicrobial activities of anthraquinones isolated from the roots of Morinda elliptica

2-Formyl-1-hydroxyanthraquinone, along with ten other known anthraquinones (1-hydroxy-2-methylanthraquinone, nordamnacanthal, damnacanthal, lucidin-?-methyl ether, rubiadin, rubiadin-1-methyl ether, soranjidiol, morindone, morindone-5-methyl ether and alizarin-1-methyl ether), isolated from the roots of Morinda elliptica , were assayed for anti-HIV, cytotoxic and antimicrobial activites. Only damnacanthal showed moderate activity against HIV. It was cytotoxic towards the MCF-7 (breast carcinoma) and CEM-SS (T-lymphoblastic leukaemia) cell line. Nordamnacanthal was very cytotoxic against the CEM-SS cell lines. Other anthraquinones that showed strong cytotoxicity towards the cell lines tested were lucidin-?-methyl ether (CEM-SS and MCF-7) and rubiadin (CEM-SS). Three anthraquinones viz., nordamnacanthal, damnacanthal and morindone, were found to have strong antimicrobial activity

Securinega alkaloids: Reinvestigation on the fresh leaves of Breynia coronate (Euphorbiaceae)

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Mechanistic understanding of curcumin’s therapeutic effects in lung cancer

Lung cancer is among the most common cancers with a high mortality rate worldwide. Despite the significant advances in diagnostic and therapeutic approaches, lung cancer prognoses and survival rates remain poor due to late diagnosis, drug resistance, and adverse effects. Therefore, new intervention therapies, such as the use of natural compounds with decreased toxicities, have been considered in lung cancer therapy. Curcumin, a natural occurring polyphenol derived from turmeric (Curcuma longa) has been studied extensively in recent years for its therapeutic effects. It has been shown that curcumin demonstrates anti-cancer effects in lung cancer through various mechanisms, including inhibition of cell proliferation, invasion, and metastasis, induction of apoptosis, epigenetic alterations, and regulation of microRNA expression. Several in vitro and in vivo studies have shown that these mechanisms are modulated by multiple molecular targets such as STAT3, EGFR, FOXO3a, TGF-β, eIF2α, COX-2, Bcl-2, PI3KAkt/mTOR, ROS, Fas/FasL, Cdc42, E-cadherin, MMPs, and adiponectin. In addition, limitations, strategies to overcome curcumin bioavailability, and potential side effects as well as clinical trials were also reviewed

Application of BATMAN and BAYESIL for quantitative ¹H-NMR based metabolomics of urine: discriminant analysis of lean, obese, and obese-diabetic rats

Introduction: BATMAN and BAYESIL are software tools, which can provide a solution for automated metabolite quantifications based on the proton nuclear magnetic resonance (1H-NMR) spectral data of bio-fluids. However, their specific application for the quantitative 1H-NMR based metabolomics of urine has not been investigated. Objectives: The aim of this study is to evaluate the performance of BATMAN and BAYESIL in the quantitative metabolite analysis of urine based on its 1H-NMR spectra. Methods: BATMAN and BAYESIL were used for automated metabolite quantification based on the 1H-NMR spectra of the urine from the lean, obese and obese-diabetic rat groups. PLS-DA model was used to discriminate the three different groups based on the results from the quantifications. Results:BATMAN was found to be superior to BAYESIL in identifying and quantifying the metabolites in the urine samples, owing to its flexibility that allows users to define and adjust the relevant signals of the pure standard metabolites in the database in order to fit the signals in the samples, a necessary step since variations and peak shift are natural in most 1H-NMR spectra. The results of BATMAN also agreed well with that of the manual deconvolution method, which indicated the higher accuracy in metabolite quantification, despite the need of pre-processing and longer processing time than BAYESIL. However, in the case where the problems in baseline correction and peak shift of 1H-NMR spectra are absent, the use of BAYESIL is more advantageous. Application of quantitative 1H-NMR based metabolomics of the urine showed that PLS-DA model derived from BATMAN could satisfactorily discriminate the lean, obese, and obese-diabetic rat groups. Conclusion: Both BATMAN and BAYESIL are useful for the quantitative automation of urine metabolites based on its 1H-NMR spectra. The results from BATMAN method is superior to BAYESIL but require expertise in spectroscopy and longer computer time. Both methods help in simplifying the interpretation of metabolite status in the VIP analysis

Vasorelaxant activity of indole alkaloids from Tabernaemontana dichotoma.

The aim of this study was to search for bioactive natural products from medicinal plants targeting vasorelaxant activity and we found the methanol extract from bark of Tabernaemontana dichotoma showed vasorelaxant activity on rat aorta. We isolated eight indole alkaloids including 10-methoxyalstonerine (1), a new macroline type indole alkaloid, from bark of T. dichotoma. These were respectively identified as 10-methoxyaffinisine (2), lochnerine (3), cathafoline (4), (−)-alstonerine (5), 19,20-dehydro-10-methoxytalcarpine (6), alstonisine (7), and alstonal (8) based on spectroscopic analysis. Among them, sarpagine type (2 and 3), akuammiline type (4), and macroline oxindole type (7 and 8) showed potent vasorelaxant activity. Mechanism of action on vasorelaxant activity of 10-methoxyaffinisine (2), cathafoline (4), and alstonisine (7) was clarified. Effects of 10-methoxyaffinisine (2), cathafoline (4), and alstonisine (7) were partially mediated the NO release from endothelial cells. Furthermore, 10-methoxyaffinisine (2) and alstonisine (7) attribute to the inhibitory effect of VDC and ROC, and cathafoline (4) have inhibitory effect on Ca2+ influx via ROC. In addition, 10-methoxyaffinisine (2) as a major compound from bark of T. dichotoma showed hypotensive effect on normotensive rats in vivo