Comparative phytochemical studies on the roots of Polygala azizsancarii and P. peshmenii and neuroprotective activities of the two xanthones
dc.contributor.author | Çalis, I | |
dc.contributor.author | Becer, E | |
dc.contributor.author | Ünlü, A | |
dc.contributor.author | Aydin, ZU | |
dc.contributor.author | Hanoglu, A | |
dc.contributor.author | Vatansever, HS | |
dc.contributor.author | Dönmez, AA | |
dc.date.accessioned | 2024-07-18T12:05:35Z | |
dc.date.available | 2024-07-18T12:05:35Z | |
dc.description.abstract | Six known sucrose mono-, di- and triesters and five xanthone derivatives were isolated from the roots of Polygala peshmenii Eren, Parolly, Raus & Kurschner which is a narrow species endemic to Turkiye. Among the xanthones, 1,7-dihydroxy-2,3-methylenedioxy-5,6-dimethoxy-xanthone is an undescribed compound isolated for the first time from a natural source. The studies on the roots of P. azizsancarii Do & BULL;nmez have resulted in the isolation of four known compounds including sucrose mono-, di- and triesters. The structures of the sucrose esters and xanthones isolated from P. azizsancarii and P. peshmenii were established by spectroscopic methods, including 1DNMR (1H NMR, 13C NMR, DEPT-135), 2D-NMR (COSY, NOESY, HSQC, HMBC). Neuroprotective activities of two xanthones, 1,3,6-trihydroxy-2,5,7-trimethoxyxanthone and 3-O-& beta;-D-glucopyranosyloxy-1,6-dihydroxy-2,5,7-trimethoxyxanthone isolated from the roots of P. azizsancarii were evaluated in vitro using in a cellular model of Alzheimer's disease. SKNAS human neuroblastoma cells were used in the study and treated with different consecrations of A & beta;25-35 oligomer for up to 48 h. Cell viability was evaluated using MTT assay. The distribution of & beta;-amyloid, & alpha;-synuclein, tau, JAK2, STAT3, caspase 3 and BMP-2 were investigated using indirect immunoperoxidase staining. Our results suggested that both xanthones control tau aggregation with no effect on & beta;-amyloid plaque formation. In addition, for neuronal pathophysiology in AD cell model, decreased distributions of JAK/ STAT3 and BMP2 signaling pathways were demonstrated, therefore they play a role in the protective effect on neurons in neurodegenerative disease. A significant decrease in caspase 3 immunoreactivity was detected after the administration of both compounds in AD cells. Therefore, both compounds control neuronal pathophysiology and rescue cell death in AD disease. | |
dc.identifier.issn | 0031-9422 | |
dc.identifier.other | 1873-3700 | |
dc.identifier.uri | http://akademikarsiv.cbu.edu.tr:4000/handle/123456789/9868 | |
dc.language.iso | English | |
dc.publisher | PERGAMON-ELSEVIER SCIENCE LTD | |
dc.subject | OLIGOSACCHARIDE MULTI-ESTERS | |
dc.subject | PERFORMANCE LIQUID-CHROMATOGRAPHY | |
dc.subject | VAR LATIFOLIA TORR | |
dc.subject | ALZHEIMERS-DISEASE | |
dc.subject | TRITERPENOID SAPONINS | |
dc.subject | TENUIFOLIA WILLDENOW | |
dc.subject | PHENOLIC GLYCOSIDES | |
dc.subject | BIOACTIVE SAPONINS | |
dc.subject | AERIAL PARTS | |
dc.subject | TAU-PROTEIN | |
dc.title | Comparative phytochemical studies on the roots of Polygala azizsancarii and P. peshmenii and neuroprotective activities of the two xanthones | |
dc.type | Article |