Evaluation of cell protection by Psephellus pyrrhoblepharus (Boiss.) Wagenitz extracts in MPP⁺-induced dopaminergic cell damage

References

• Aktümsek, A., 2013. Antioxidant potentials on anticholinesterase activities of methanolic and aqueous extracts of three endemic Centaurea L. species. Food and Chemical Toxicology, 55, 290–296.
   PubMed Web of Science ®Google Scholar
• Aktümsek, A., et al., 2013. Assesment of the antioxidant potential and fatty acid composition of four Centaurea L. taxa from Turkey. Food Chemistry, 141(1), 91–97.
   PubMed Web of Science ®Google Scholar
• Ashraf, A., et al., 2015. Antioxidant, antimicrobial, antitumor, and cytotoxic activities of an important medicinal plant (Euphorbia royleana) from Pakistan. Journal of Food and Drug Analysis, 13, 109–115.
   Google Scholar
• Barrero, A.F., et al., 1997. Cytotoxic activity of flavonoids from Carthamus arborescens, Ononis natrix ssp. ramosissima and Centaurea malacitana. Fitoterapia, 68(3), 281–283.
   Google Scholar
• Baykan-Erel, S., et al., 2010. Secondary metabolites from Centaurea ensiformis P.H. Davis. Biochemical Systematics and Ecology, 38(5), 1056–1058.
   Web of Science ®Google Scholar
• Benzie, I.F. and Strain, J.J., 1996. The ferric reducing ability of plasma (FRAP) as a measure of "antioxidant power": the FRAP assay. Analytical Biochemistry, 239(1), 70–76.
   PubMed Web of Science ®Google Scholar
• Chia-Chi, C., et al., 2002. Estimation of total flavonoid content in propolis by two complementary colorimetric methods. Journal of Food and Drug Analysis, 10(3), 178–182.
   Web of Science ®Google Scholar
• Csupor, D., et al., 2013. Anti-inflammatory activities of eleven Centaurea species occurring in the Carpathian Basin. Phytotherapy Research, 27(4), 540–544.
   PubMed Web of Science ®Google Scholar
• Dalar, A. and Konczak, I., 2012. Botanicals from Eastern Anatolia Region of Turkey: antioxidant capacity and phenolic constituents of endemic herbal medicines. Journal of Herbal Medicine, 2(4), 126–135.
   Web of Science ®Google Scholar
• Djeddi, S., et al., 2008. Analgesic activity of secondary metabolites from two Centaurea species. Planta Medica, 74(09), 37.
   Google Scholar
• Ekim, T., 2007. Türkiye’nin nadir endemikleri. Türkiye İş Bankası Kültür Yayınları: İstanbul.
   Google Scholar
• Fjaeraa, C. and Nånberg, E., 2009. Effect of ellagic acid on proliferation, cell adhesion and apoptosis in SH-SY5Y human neuroblastoma cells. Biomedicine & Pharmacotherapy, 63(4), 254–261.
   PubMed Web of Science ®Google Scholar
• Fukumoto, L.R. and Mazza, G., 2000. Assessing antioxidant and proantioxidant activites of phenolic compounds. Journal of Agricultural and Food Chemistry, 48(8), 3597–3604.
   PubMed Web of Science ®Google Scholar
• Gonzălez, A.G., et al., 1980. The cytotoxic activity of the chlorohyssopifolins, chlorinated sesquiterpene lactones from Centaurea. Planta Medica, 40(2), 179–184.
   PubMed Web of Science ®Google Scholar
• Greuter, W., 2003. The Euro + Med treatment of Cardueae (Compositae)—generic concepts and required new names. Willdenowia, 33(1), 49–61.
   Google Scholar
• Gülcemal, D., et al., 2010. Phenolic glycosides with antiproteasomal activity from Centaurea urvillei DC. subsp. urvillei. Carbohydrate Research, 345(17), 2529–2533.
   PubMed Web of Science ®Google Scholar
• Güner, A., et al., 2012. Türkiye Bitkileri Listesi (Damarlı Bitkiler) [Turkey Plant List (Vascular Plants)]. Nezahat Gökyiğit Botanical Garden and Flora Research Association Publication: İstanbul.
   Google Scholar
• Gürbüz, I. and Yesilada, E., 2007. Evaluation of the anti-ulcerogenic effect of sesquiterpene lactones from Centaurea solstitialis L. ssp. solstitialis by using various in vivo and biochemical techniques. Journal of Ethnopharmacology, 112(2), 284–291.
   PubMed Web of Science ®Google Scholar
• Hayta, S. and Bagci, E., 2015. Composition of the essential oil of endemic Psephellus pyrrhoblephara Boiss. (Asteraceae) from Turkey. Journal of Essential Oil Bearing Plants, 18(3), 627–632.
   Web of Science ®Google Scholar
• Jouha, J., et al., 2017. Synthesis of new heterocyclic compounds based on pyrazolopyridine scaffold and evaluation of their neuroprotective potential in MPP+-induced neurodegeneration. European Journal of Medicinal Chemistry, 31(129), 41–52.
   Google Scholar
• Kich, D.M., et al., 2016. Neuromodulatory effects of Calyptranthes grandifolia extracts against 6-hydroxydopamine-induced neurotoxicity in SH-SY5Y cells. Biomedicine & Pharmacotherapy, 84, 382–386.
   PubMed Web of Science ®Google Scholar
• Korkmaz, N., et al., 2019. Determination of phenolic contents by HPLC, and antioxidant, antimicrobial, antityrosinase, and anticholinesterase activities of Psephellus huber-morathii. Journal of Pharmaceutical Research International, 26(1), 1–10.
   Web of Science ®Google Scholar
• Nawrot, J., Budzianowski, J., and Nowak, G., 2019. Phytochemical profiles of the leaves of Stizolophus balsamita and Psephellus sibiricus and their chemotaxonomic implications. Phytochemistry, 159, 172–178.
   PubMed Web of Science ®Google Scholar
• Nowak, G., 1992. A chemotaxonomic study of sesquiterpene lactones from subtribe Centaureinae of the Compositae. Phytochemistry, 31(7), 2363–2368.
   Web of Science ®Google Scholar
• Nowak, G., 1993. Isolation and chromatography of 15-deoxyrepin and 25 other sesquiterpene lactones from Centaurea bella Trautv. Acta Societatis Botanicorum Poloniae, 62(1–2), 33–36.
   Web of Science ®Google Scholar
• Nowak, G., et al., 2014. Sesquiterpene lactones. XXXIII. Guaianolides in the genus Psephellus (Cass.) Schmalh., genus Centaurea L. Acta Societatis Botanicorum Poloniae, 55(4), 629–637.
   Google Scholar
• Nowak, G., Holub, M., and Buděšĺnský, M., 1989. Sesquiterpene lactones in several subgenera of the genus Centaurea L. Acta Societatis Botanicorum Poloniae, 58(1), 95–102.
   Web of Science ®Google Scholar
• Nowak, G., et al., 1986. Sesquiterpene lactones. XXIX. Cynaropicrin in species of the subtribe Centaureinae Dumort. Acta Societatis Botanicorum Poloniae, 55(1), 17–22.
   Web of Science ®Google Scholar
• Orallo, F., et al., 1998. Preliminary study of the potential vasodilator effects on rat aorta of centaurein and centaureidin, two flavonoids from Centaurea corcubionensis. Planta Medica, 64(02), 116–119.
   PubMedGoogle Scholar
• Pandey, K.B. and Rizvi, S.I., 2009. Plant polyphenols as dietary antioxidants in human health and disease. Oxidative Medicine and Cellular Longevity, 2(5), 270–278.
   PubMed Web of Science ®Google Scholar
• Pehlivan, S., 1995. Pollen morphology of some Turkish Endemic Centaurea. Grana, 34(1), 29–38.
   Web of Science ®Google Scholar
• Pirvu, L., et al., 2012. Vegetal extracts with gastroprotective activity. Part. I. extracts obtained from Centaurea cyanus L. raw material. Romanian Biotechnological Letters, 17(2), 7169–7176.
   Web of Science ®Google Scholar
• Pollock, J.L., et al., 2011. (±)-Catechin, a root exudate of the invasive Centaurea stoebe Lam. (Spotted knapweed) exhibits bacteriostatic activity against multiple soil bacterial populations. Journal of Chemical Ecology, 37(9), 1044–1053.
   PubMed Web of Science ®Google Scholar
• Przedborski, S. and Vila, M., 2003. The 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine mouse model: a tool to explore the pathogenesis of Parkinson's disease. Annals of the New York Academy of Sciences, 991, 189–198.
   PubMed Web of Science ®Google Scholar
• Radi, E., et al., 2014. Apoptosis and oxidative stress in neurodegenerative diseases. Journal of Alzheimer's Disease, 42(3), 125–152.
   Google Scholar
• Ragazzi, E. and Veronese, G., 1973. Quantitative analysis of phenolic compounds after thin-layer chromatographic separation. Journal of Chromatography A, 77(2), 369–375.
   PubMed Web of Science ®Google Scholar
• Rascol, O., et al., 2003. Limitations of current Parkinson's disease therapy. Annals of Neurology, 53(S3), S3–S12.
   PubMedGoogle Scholar
• Rashid, M.A., et al., 2018. Chemical composition and antioxidant, antimicrobial and haemolytic activities of Crambe cordifolia roots. Framacia, 66(1), 165–171.
   Web of Science ®Google Scholar
• Re, R., et al., 1999. Antioxidant activity applying an improved ABTS radical cation decolorization assay. Free Radical Biology and Medicine, 26(9–10), 1231–1237.
   PubMed Web of Science ®Google Scholar
• Ross, J.A. and Kasum, C.M., 2002. Dietary flavonoids: bioavailability, metabolic effects and safety. Annual Review of Nutrition, 22(1), 19–34.
   PubMed Web of Science ®Google Scholar
• Sagiroglu, M., et al., 2012. An ethnobotanical survey from Hayrat (Trabzon) and Kalkandere (Rize/Turkey). Biodiversity and Conservation, 5(1), 31–43.
   Google Scholar
• Sapkota, K., et al., 2010. A detoxified extract of Rhus verniciflua Stokes upregulated the expression of BDNF and GDNF in the rat brain and the human dopaminergic cell line SH-SY5Y. Bioscience, Biotechnology, and Biochemistry, 74(10), 1997–2004.
   PubMed Web of Science ®Google Scholar
• Singer, T.P. and Ramsay, R.R., 1990. Mechanism of the neurotoxicity of MPTP. An update. FEBS Letters, 274(1–2), 1–8.
   PubMed Web of Science ®Google Scholar
• Spinola, V., Pinto, J., and Castilho, P.C., 2015. Identification and quantification of phenolic compounds of selected fruits from Madeira Island by HPLC-DAD-ESI-MS and screening for their antioxidant activity. Food Chemistry, 173, 14–30.
   PubMed Web of Science ®Google Scholar
• Vajs, V., et al., 1999. Guaianolides from Centaurea nicolai: antifungal activity. Phytochemistry, 52(3), 383–386.
   PubMed Web of Science ®Google Scholar
• Wagenitz, G., Ertugrul, K., and Dural, H., 1998. A new species of Centaurea sect. Psephelloideae (Compositae) from SW Turkey. Willdenowia, 28(1–2), 157–161.
   Google Scholar
• Wagenitz, G. and Hellwig, H., 2000. The genus Psephellus Cass. (Compositae, Cardueae) revisited with a broadened concept. Willdenowia, 30(1), 29–44.
   Google Scholar
• Wagenitz, G. and Kandemir, A., 2008. Two new species of the genus Psephellus (Compositae, Cardueae) from Eastern Turkey. Willdenowia, 38(2), 521–526.
   Google Scholar
• Wu, F., et al., 2009. Alphasynuclein knockdown attenuates MPP+ induced mitochondrial dysfunction of SH-SY5Y cells. Brain Research, 1292, 173–179.
   PubMed Web of Science ®Google Scholar
• Xicoy, H., Wieringa, B., and Martens, G.J.M., 2017. The SH-SY5Y cell line in Parkinson’s disease research: a systematic review. Molecular Neurodegeneration, 12(1), 10.
   PubMed Web of Science ®Google Scholar
• Xie, H.R., Hu, L.S., and Li, G.Y., 2010. SH-SY5Y human neuroblastoma cell line: in vitro cell model of dopaminergic neurons in Parkinson’s disease. Chinese Medical Journal, 123(8), 1086–1092.
   PubMed Web of Science ®Google Scholar