Study of estimation and variation of alpha-amyrin content among individuals of Suaeda maritima (L.) Dumort. growing along the south-east coast of India
Автор: Pati Maniklal, Nandi Asis Kumar
Журнал: Журнал стресс-физиологии и биохимии @jspb
Статья в выпуске: 3 т.20, 2024 года.
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Suaeda maritima (L.) Dumort. of the family Chenopodiaceae, is an annual succulent herb growing on salty marshy habitat as one of the dominant mangrove associate species and also as pure vegetation of that. It is regularly harnessed by the local people for use as food as well as for alleviating different maladies. Alpha-amyrin, a triterpenoid, is a remarkable biomolecule available in S. maritima . It is reported to have cardioprotective, anti-inflammatory and anti-oxidant properties. A survey of the amount of alpha-amyrin content available in the individuals of S. maritima, collected from eight different regions of the sea coast of the bay of Bengal like, Digha, Sankarpur, Tajpur, Dadanpatrabarh, Shoula, Bankiput and Petuaghat, was conducted with normal phase high performance thin layer chromatography (HPTLC) in this study. It also portrayed variation in the amount of alpha-amyrin among the plant individuals of the species growing in the said zones. The existence of variation in the amount of alpha-amyrin seems to be prospective for selecting the best producer out of them.
Alpha-amyrin, hptlc, suaeda maritima
Короткий адрес: https://sciup.org/143182805
IDR: 143182805
Список литературы Study of estimation and variation of alpha-amyrin content among individuals of Suaeda maritima (L.) Dumort. growing along the south-east coast of India
- Aragao G.F., Carneiro L.M. and Rota-Junior A.P. (2015). Alterations in brain amino acid metabolism and inhibitory effects on PK are possibly correlated with anticonvulsant effects of the isomeric mixture alpha and beta-amyrin from Protium heptaphyllum. Pharm. Biol, 53(3), 407- 413.
- Barros F.W.A., Bandeira P.N. and Lima D.J.B. (2011). Amyrin esters induce cell death by apoptosis in HL-60 leukemia cells. Bioorg. Med. Chem. Lett., 19, 1268-1276.
- Behera L.M. and Hembram P. (2021). Advances on plant salinity stress responses in the post-genomic era: A review. J. Crop Sci. Biotech., 24, 117-126.
- Beulah G., Divya D., Kumar N.S.S., Sravya M.V.N., Govinda R.K., Chintagunta A.D., Divya G., Hari-Chandana S., Blessy B. D. and Simhachalam G. (2021). Purification and characterization of bioactive compounds extracted from Suaeda maritima leaf and its impact on pathogenicity of Pseudomonas aeruginosa in Catla catla fingerlings. AMB Expr., 11, 135.
- Choi S.C., Lim S.H. and Kim S.H. (2012). Growth and solute pattern of Suaeda maritima and Suaeda asparagoides in an abandoned salt field. J. Ecol. Field Biol., 35(4), 351-358.
- Das D.C., Pati M. and Mahato G. (2015). Study of the tidal vegetation of Purba Medinipur district of West Bengal, India. Int. J. Bioassays., 4 (5), 3915-3921.
- Ekalu A., Ayo R.G. and Habila J.D. (2019). Bioactivities of Phaeophytin a, a-Amyrin, and lupeol from Brachystelma togoense Schltr. J. Turkish chem. soc., 6(3), 411-418.
- Ferreira M.J., Diana C.G.A., Pinto A.C. and Silva H. (2022). Halophytes as Medicinal Plants against Human Infectious Diseases. Appl. Sci., 12(15), 7493.
- Fortunato S., Lasorella C., Dipierro N., Vita F. and de Pinto M.C. (2023). Redox Signaling in Plant Heat Stress Response. Antioxidants, 12(3), 605.
- Ghosh A., Misra S. and Dutta A.K. (1985). Pentacyclic triterpenoids and sterols from seven species of mangrove. Phytochem., 24(8), 1725-1727.
- Gill S.S. and Tuteja N. (2010). Reactive oxygen species and antioxidant machinery in abiotic stress tolerance in crop plants. Plant Physiol. Biochem., 48, 909-930.
- Guan B., Yu J., Lu Z., Zhang Y. and Wang X. (2011). Effects of water-salt stresses on seedling growth and activities of antioxidative enzyme of Suaeda salsa in coastal wetlands of the Yellow River Delta. Environ. Sci., 32, 2422-2429.
- Han N. and Bakovic M. (2015). Biologically Active Tri-terpenoids and Their Cardio protective and Anti-Inflammatory Effects. J. Bioanal. Biomed., 12, 005.
- Holanda P.S.A., Pinto L.M.S. and Guedes M.A. (2008). Antinoceptive effect of triterpenoid a, p-amyrin in rats onorofacial pain induced by formalin and capsaicin. Phytomedicine, 15, 630-634.
- Hossain M.S. and Dietz K.J. (2016). Tuning of Redox Regulatory Mechanisms, Reactive Oxygen Species and Redox Homeostasis under Salinity Stress. Front. Plant Sci., 7, 548.
- Lakshmi K.P. and Rao N.G.M. (2023). Antimicrobial Screening of the Solvent Extracts of Halophytic Plant Suaeda maritima (L.) Dumort. Against Selected Pathogens. Sch. Acad. J. Biosci., 11, 315-322.
- Martelanc M., Vovk I. and Simonovska B. (2009). Separation and identification of some common isomeric plant triterpenoids by thin-layer chromatography and high-performance liquid chromatography. J. Chromatogr., 1216(38), 66626670.
- Melo C.M., Morais T.C. and Tome A.R. (2011). Anti-inflammatory effect of a, b-amyrin, a triterpene from Protium heptaphyllum on cerulein-induced acute pancreatitis in mice. J. Inflamm. Res., 60(7), 673681.
- Mondal S., Burgert S., Asch J., Rahaman E. H. M. S. and Asch F. (2023). Salinity effects on the activities of ROS scavenging enzymes in leaves of two sweet potato clones. J. Agron. Crop Sci., 209, 841853.
- Oliveira F.A., Costa C.L. and Chaves M.H. (2005). Attenuation of capsaicin-induced acute and visceral nociceptive pain by alpha-and beta-amyrin, a triterpene mixture isolated from Protium heptaphyllum resin in mice. Life Sci., 77, 29422952.
- Oliveira F.A., Vieira-Junior G.M. and Chaves M.H. (2004). Gastro protective effect of the mixture of alpha- and beta-amyrin from Protium heptaphyllum: role of capsaicin-sensitive primary afferent neurons. Planta Med., 70, 780-782.
- Oliveira R.C., Bandeira P.N., Lemos T.L.G., Dos Santos H.S., Scherf J.R., Rocha J.E., Pereira R.L.S., Freitas T.S., Freitas P.R., Pereira-Junior F.N., Marinho M.M., Marinho E.M., Marinho E.S., Nogueira C.E.S., Coutinho H.D.M. and Teixeira A.M.R. (2022). In silico and in vitro evaluation of efflux pumps inhibition of a, p-amyrin. J. Biomol. Struct. Dyn., 40(23), 12785-12799.
- Pant P. and Rastogr R.P. (1979). The terpenoids. Phytochem., 18(7), 1095-1108.
- Pati M. and Nandi A.K. (2022). Morphological and phytochemical studies of Suaeda maritima (L.) Dumort. growing along the coastal belt of Purba Medinipur District, West Bengal, India in search of the prospective variation. Curr. Bot., 13, 34-39.
- Pinto S.A.H., Pinto L.M.S. and Cunha G.M.A. (2007). Anti-inflammatory effect of a, b-Amyrin, a pentacyclic triterpene from Protium heptaphyllum in rat model of acute periodontitis. Inflammopharmacology, 15, 1-5.
- Prabhakar P., Reeta K.H. and Maulik S.K. (2017). a-Amyrin attenuates high fructose diet-induced metabolic syndrome in rats. Appl. Physiol. Nutr. Metab., 42, 23-32.
- Pucciariello C., Banti V. and Perata P. (2012). ROS signaling as common element in low oxygen and heat stresses. Plant Physiol. Biochem., 59, 3-10.
- Roy M. and Dutta T.K. (2021). Evaluation of Phytochemicals and Bioactive Properties in Mangrove Associate Suaeda monoica Forssk. ex J.F.Gmel. of Indian Sundarbans. Front Pharmacol., 12, 584019,
- Sachdev S., Ansari S.A., Ansari M.I., Fujita M. and Hasanuzzaman M. (2021). Abiotic Stress and Reactive Oxygen Species: Generation, Signaling, and Defense Mechanisms. Antioxidants, 10(2), 277.
- Sahu B.B. and Shaw B.P. (2009). Isolation, identification and expression analysis of salt induced genes in Suaeda maritima, a natural halophyte, using PCR-based suppression subtractive hybridization. BMC Plant Biol., 9, 69.
- Santos F.A., Frota J.T. and Arruda B.R. (2012). Antihyperglycemic and hypolipidemic effects of a, ß-amyrin, a triterpenoid mixture from Protium heptaphyllum in mice. Lipids Health Dis., 11, 98.
- Singh S., Mann R. and Sharma S.K. (2013). Antihyperlipidemic activity of Suaeda maritima (L.) Dumortier Stem in Triton induced hyperlipidemic rat. Int J Ayurveda Pharma Res., 4(2), 203-206.
- Stahl E. (1969). Thin Layer Chromatography Handbook", (2nd ed.). Springer-Verlage, Berlin, Heidelberg, New York, pp.873.
- Trease and Evans (2002). Pharmacognosy, (15th ed.). University of Nottingham, Nottingham, UK, pp.22.
- Viet T.D., Xuan T.D. and Anh H. (2021). a-Amyrin and ß-Amyrin isolated from Celastrus hindsii leaves and their antioxidant, anti-xanthine oxidase, and antityrosinase potentials. Molecules, 26(23), 7248.
- Wang B., Luttge U. and Ratajczak R. (2004). Specific regulation of SOD isoforms by NaCl and osmotic stress in leaves of the C3 halophyte Suaeda salsa L. J. Plant Physiol., 161(3), 285-293.
- Yang Y. and Guo Y. (2018). Elucidating the molecular mechanisms mediating plant salt-stress responses. New Phytol., 217(2), 523-539.
- Yu B., Zheng W. and Xing L. (2022). Root twisting drives halotropism via stress-induced microtubule reorientation. Dev. Cell., 57, 2412-2425.
- Yu W., Wu W., Zhang N., Wang L., Wang Y., Wang B., Lan Q. and Wang Y. (2022). Research Advances on Molecular Mechanism of Salt Tolerance in Suaeda. Biology, 11(9),1273.
- Zang W., Miao R., Zhang Y., Yuan Y., Pang Q. and Zhou Z. (2021). Metabolic and molecular basis for the salt and alkali responses of Suaeda corniculate. Environ. Exp. Bot., 192, 104643.