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1.
Indian J Biochem Biophys ; 2014 Apr; 51(2): 127-134
Article Dans Anglais | IMSEAR | ID: sea-154250

Résumé

The peptides produced enzymatically from various plants have shown various biological activities including cytotoxicity. Different types of cytotoxic peptides have been reported from the seeds and leaves of Violaceae, Rubiaceae and Annonaceae families. In this study, we report purification and characterization of peptide(s) showing cytotoxic activity against A549 and HeLa cancer cell lines from the seeds of Polyalthia longifolia (Annonaceae). Seed proteins of P. longifolia were extracted and hydrolyzed using trypsin. The enzyme hydrolysate was applied on to a Sephadex G10 column and eluted using Tris-HCl buffer (pH 7.5). Two fractions F1 and F2 were obtained, of which F2 showed significant cytotoxic activity against lung (A549) cancer cells at 10 µg/mL and cervical (HeLa) cancer cell lines at 30 µg/mL, as revealed by the MTT assay. DNA fragmentation was observed in the tested cancer cell lines treated with F2 peptide at a concentration of 10 µg/mL and 30 µg/mL, respectively. Further, increased number of apoptotic cells was observed in sub-G0 phase of cell cycle of A549 and HeLa cell lines, when treated with 10 µg/mL and 30 µg/mL of F2, as revealed by the flow cytometric analyses. FTIR spectrum of F2 peptide detected the presence of stretching vibrations of carboxylic acid OH residue with peak at 3420 cm-1 and carbonyl (C=O) groups at 1636 cm-1, respectively. RP-HPLC analysis of F2 peptide showed a single peak at a retention time of 12.8 min detected at 280 nm, depicting the purity of F2 to be more than 90%. LC-ESI-MS/MS analysis showed the average theoretical mass of F2 to be 679.8 using m/z ratios. In conclusion, the findings suggest that F2 peptide is an effective inducer of apoptosis of cancer cells, thus offers an important strategy in the development of cancer therapeutics.


Sujets)
Apoptose/effets des médicaments et des substances chimiques , Cycle cellulaire/effets des médicaments et des substances chimiques , Prolifération cellulaire/effets des médicaments et des substances chimiques , Chromatographie en phase liquide à haute performance , Cellules HeLa , Humains , Tumeurs du poumon/traitement médicamenteux , Tumeurs du poumon/anatomopathologie , Fragments peptidiques/isolement et purification , Fragments peptidiques/pharmacologie , Polyalthia/composition chimique , Graines/composition chimique , Spectrométrie de masse ESI , Spectroscopie infrarouge à transformée de Fourier , Spectrométrie de masse en tandem , Cellules cancéreuses en culture
2.
Asian Pacific Journal of Tropical Medicine ; (12): 673-679, 2011.
Article Dans Anglais | WPRIM | ID: wpr-820073

Résumé

OBJECTIVE@#To explore antiulcer and antimicrobial properties of methanolic extract of Polyalthia longifolia var. pendula.@*METHODS@#Gastroprotective potential of Polyalthia longifolia was studied on ethanol and ethanol/HCl induced ulcers at 2 different doses (270 and 540 mg/kg/body weight). Antimicrobial efficacy of Polyalthia longifolia (25 mg/mL) was also studied against six gram positive, seven gram negative bacteria and five fungi by agar well diffusion method. Minimum inhibitory concentration was determined by agar well diffusion method in two fold serial dilution, in the range of 97-25,000 μg/mL.@*RESULTS@#The reduction of ulcer index in Polyalthia longifolia treated animals was found to be statistically significant with respect to control animals. The Polyalthia longifolia exhibited ulcer protection activity in dose dependent manner and was also better than the standard. In antimicrobial activity, gram positive bacteria were more susceptible to Polyalthia longifolia than gram negative bacteria and fungal strains.@*CONCLUSIONS@#Results obtained confirm the antiulcer and antimicrobial potential of the Polyalthia longifolia.


Sujets)
Animaux , Femelle , Humains , Mâle , Rats , Antibactériens , Anti-infectieux , Bactéries , Modèles animaux de maladie humaine , Éthanol , Champignons , Acide chlorhydrique , Extraits de plantes , Feuilles de plante , Chimie , Polyalthia , Chimie , Agents protecteurs , Rat Wistar , Ulcère , Traitement médicamenteux , Microbiologie
3.
China Journal of Chinese Materia Medica ; (24): 1024-1027, 2011.
Article Dans Chinois | WPRIM | ID: wpr-252950

Résumé

<p><b>OBJECTIVE</b>To investigate the chemical constituents of the branches and leaves of Polyalthia nemoralis.</p><p><b>METHOD</b>The compounds were isolated and purified by silica gel, macroporous adsorption resin and Sephadex LH-20 column chromatographic methods. Their chemical structures were elucidated on the basis of physicochemical properties and spectral data.</p><p><b>RESULT</b>Fourteen compounds were isolated and identified as syringic acid (1), 3-methoxy-4-hydroxycinnamic acid (2), vanillic acid (3), 4-hydroxybenzoic acid (4), mauritianin (5), (+)-xylopinidine (6), (+)-oblongine(7), (+)-tembetarine (8), eythritol (9), D-mannitol (10), ethyl-beta-D-glucopyranoside (11), (+)-magnoflorine (12), stepharanine (13), (2S, 4R)-4-hydroxy-2-piperidine-carboxylic acid (14), respectively.</p><p><b>CONCLUSION</b>All the compounds were isolated from the genus Polyalthia for the first time; compounds 6 and 13 showed inhibitation activities against multi tumor cell lines.</p>


Sujets)
Humains , Alcaloïdes , Chimie , Pharmacologie , Antinéoplasiques d'origine végétale , Chimie , Pharmacologie , Aporphines , Chimie , Pharmacologie , Lignée cellulaire tumorale , Survie cellulaire , Chromatographie sur agarose , Méthodes , Acides coumariques , Chimie , Pharmacologie , Acide gallique , Chimie , Pharmacologie , Kaempférols , Chimie , Pharmacologie , Parabènes , Chimie , Pharmacologie , Extraits de plantes , Chimie , Pharmacologie , Feuilles de plante , Chimie , Tiges de plante , Chimie , Polyalthia , Chimie , Acide vanillique , Chimie , Pharmacologie
4.
China Journal of Chinese Materia Medica ; (24): 53-57, 2010.
Article Dans Chinois | WPRIM | ID: wpr-346947

Résumé

<p><b>OBJECTIVE</b>To investigate the active constituents of the branches and leaves of Polyalthia nemoralis.</p><p><b>METHOD</b>The compounds were isolated and purified by silica gel, macroporous adsorption resin and Sephadex LH-20 column chromatographic methods. Their chemical structures were elucidated on the basis of physicochemical properties and spectral data.</p><p><b>RESULT</b>Eight compounds were isolated and identified as: zincpolyanemin (1), nickel bis-(pyridine-N-oxide-2-thiolate) (2), cupric bis (pyridine-N-oxide-2-thiolate (3), 2-methanesulfonyl-pyridine (4), 2-pyridinethiolate N-oxide (5), 2,2'-dithiodipyridine (6), 2-thiohydroxypyridin-N-oxide-2-S-beta-D-gluco pyranoside (7) and pyridine-N-oxide (8), respectively.</p><p><b>CONCLUSION</b>Compounds 2, 4-6, 8 were new natural products. The bioassays in vitro against five human tumor cell lines with MTT method showed stronger cytotoxic activities (IC50 0.05-0.09 mg x L(-1)) for compounds 1-3 and 6, and weaker cytotoxic activities (IC50 5.49-7.71 mg x L(-1)) for compound 5.</p>


Sujets)
Humains , Lignée cellulaire tumorale , Survie cellulaire , Médicaments issus de plantes chinoises , Chimie , Pharmacologie , Spectroscopie par résonance magnétique , Feuilles de plante , Chimie , Tiges de plante , Chimie , Polyalthia , Chimie , Pyridines , Chimie
5.
China Journal of Chinese Materia Medica ; (24): 2343-2345, 2009.
Article Dans Chinois | WPRIM | ID: wpr-307588

Résumé

<p><b>OBJECTIVE</b>To investigate the aporphine alkaloids in the branches and leaves of Polyalthia nemoralis.</p><p><b>METHOD</b>The compounds were isolated and purified by silica gel and Sephadex LH-20 column chromatographies. Their chemical structures were elucidated on the basis of physicochemical properties and spectral data.</p><p><b>RESULT</b>Five aporphine alkaloids were isolated and identified as: bidebiline A (1), annobraine (2), lanuginosine (3), liriodenine (4), oxostephanosine (5), respectively.</p><p><b>CONCLUSION</b>For the first time, Compounds 2 and 5 were obtained from Polyalthia while 1, 3 and 4 isolated from this plant. The bioassays in vitro against five human tumor cell lines with MTT method showed moderate cytotoxic activities (IC50 1 mg x L(-1)) of compounds 3-5.</p>


Sujets)
Humains , Antinéoplasiques d'origine végétale , Chimie , Pharmacologie , Aporphines , Chimie , Pharmacologie , Lignée cellulaire tumorale , Feuilles de plante , Chimie , Tiges de plante , Chimie , Polyalthia , Chimie
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