UPLC-ESI-Q-TOF-MSE-based metabolomics analysis of Acer mono sap and evaluation of osteogenic activity in mouse osteoblast cells

被引:0
作者
Natesan, Karthi [1 ]
Srivalli, Thimmarayan [2 ,3 ]
Mohan, Harshavardhan [4 ]
Jayaprakash, Arul [2 ,3 ]
Ramalingam, Vaikundamoorthy [5 ,6 ]
机构
[1] REVA Univ, Sch Allied Hlth Sci, Bengaluru, India
[2] Scared Heart Coll Autonomous, PG & Res Dept Biochem, Tirupattur 635601, Tamil Nadu, India
[3] Thiruvalluvar Univ, Vellore 632115, Tamil Nadu, India
[4] Jeonbuk Natl Univ, Res Inst Phys & Chem, Dept Chem, Jeonju 54896, South Korea
[5] CSIR Indian Inst Chem Technol, Ctr Nat Prod & Tradit Knowledge, Hyderabad, India
[6] Acad Sci & Innovat Res AcSIR, Ghaziabad 201002, India
关键词
DIFFERENTIATION; IDENTIFICATION; PROLIFERATION; ACID;
D O I
10.1039/d2fo01948e
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Investigation of phytochemicals and bioactive molecules is tremendously vital for the applications of new plant resources in chemistry, food, and medicine. In this study, the chemical profiling of sap of Acer mono (SAM), a Korean syrup known for its anti-osteoporosis effect, was performed using UPLC-ESI-Q-TOF-MSE analysis. A total of 23 compounds were identified based on the mass and fragmentation characteristics and most of the compounds have significant biomedical applications. The in vitro antioxidant assessment of SAM indicated excellent activity by scavenging DPPH and ABTS-free radicals and were found to be 23.35 mg mL(-1) and 29.33 mg mL(-1), respectively, as IC50 concentrations. As well, the in vitro proliferation effect of the SAM was assessed against mouse MC3T3-E1 cells, and the results showed that the SAM enhanced the proliferation of the cells, and 12.5 mg mL(-1) and 25 mg mL(-1) of SAM were selected for osteogenic differentiation. The morphological analysis clearly evidenced the SAM enhanced the osteogenic activity in MC3T3-E1 cells by the increased deposition of extracellular calcium and nodule formation. Moreover, the qRT-PCR analysis confirmed the increased expression of osteoblast marker gene expression including ALP, osteocalcin, osteopontin, collagen1 alpha 1, Runx2, and osterix in SAM-treated MC3T3-E1 cells. Together, these results suggest that SAM possesses osteogenic effects and can be used for bone regeneration and bone loss-associated diseases such as osteoporosis.
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收藏
页码:13002 / 13013
页数:12
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