Troxerutin flavonoid has neuroprotective properties and increases neurite outgrowth and migration of neural stem cells from the subventricular zone

被引:13
作者
Masood, Muhammad Irfan [1 ,2 ,3 ]
Schaefer, Karl Herbert [2 ]
Naseem, Mahrukh [4 ]
Weyland, Maximilian [2 ]
Meiser, Peter [5 ]
机构
[1] Saarland Univ, Sch Pharm, Div Bioorgan Chem, Saarbrucken, Germany
[2] Univ Appl Sci Kaiserslautern, ENS Grp, Zweibrucken, Germany
[3] Univ Vet & Anim Sci, Inst Pharmaceut Sci, Lahore, Pakistan
[4] Univ Balochistan, Dept Zool, Quetta, Pakistan
[5] URSAPHARM Arzneimittel GmbH, Med Sci Dept GM, Saarbrucken, Germany
来源
PLOS ONE | 2020年 / 15卷 / 08期
关键词
EPIDERMAL-GROWTH-FACTOR; STEM/PROGENITOR CELLS; IN-VITRO; NEURONAL DIFFERENTIATION; HIPPOCAMPAL-NEURONS; OXIDATIVE STRESS; NERVOUS-SYSTEM; RADIAL GLIA; GREEN TEA; PROLIFERATION;
D O I
10.1371/journal.pone.0237025
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Troxerutin (TRX) is a water-soluble flavonoid which occurs commonly in the edible plants. Recent studies state that TRX improves the functionality of the nervous system and neutralizes Amyloid-ss induced neuronal toxicity. In this study, anin vitroassay based upon Neural stem cell (NSCs) isolated from the subventricular zone of the postnatal balb/c mice was established to explore the impact of TRX on individual neurogenesis processes in general and neuroprotective effect against ss-amyloid 1-42 (Ass42) induced inhibition in differentiation in particular. NSCs were identified exploiting immunostaining of the NSCs markers. Neurosphere clonogenic assay and BrdU/Ki67 immunostaining were employed to unravel the impact of TRX on proliferation. Differentiation experiments were carried out for a time span lasting from 48 h to 7 days utilizing ss-tubulin III and GFAP as neuronal and astrocyte marker respectively. Protective effects of TRX on Ass42 induced depression of NSCs differentiation were determined after 48 h of application. A neurosphere migration assay was carried out for 24 h in the presence and absence of TRX. Interestingly, TRX enhanced neuronal differentiation of NSCs in a dose-dependent manner after 48 h and 7 days of incubation and significantly enhanced neurite growth. A higher concentration of TRX also neutralized the inhibitory effects of Ass42 on neurite outgrowth and length after 48 h of incubation. TRX significantly stimulated cell migration. Overall, TRX not only promoted NSCs differentiation and migration but also neutralized the inhibitory effects of Ass42 on NSCs. TRX, therefore, offers an interesting lead structure from the perspective of drug design especially to promote neurogenesis in neurological disorders i.e. Alzheimer's disease.
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页数:24
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