Betanin purification from red beetroots and evaluation of its anti-oxidant and anti-inflammatory activity on LPS-activated microglial cells.
Hosein AhmadiZahra NayeriZarrin MinuchehrFarzaneh SabouniMehdi MohammadiPublished in: PloS one (2020)
Microglial activation can release free radicals and various pro-inflammatory cytokines, which implicates the progress of a neurodegenerative disease. Therefore suppression of microglial activation can be an appropriate strategy for combating neurodegenerative diseases. Betanin is a red food dye that acts as free radical scavenger and can be a promising candidate for this purpose. In this study, purification of betanin from red beetroots was carried out by normal phase colum chromatography, yielding 500 mg of betanin from 100 g of red beetroot. The purified betanin was evaluated by TLC, UV-visible, HPLC, ESI-MASS, FT-IR spectroscopy. Investigation on the inhibitory effect of betanin on activated microglia was performed using primary microglial culture. The results showed that betanin significantly inhibited lipopolysaccharide induced microglial function including the production of nitric oxide free radicals, reactive oxygen species, tumor necrosis factor-alpha (TNF-α), interleukin-6 (IL-6) and interleukin-1 beta (IL-1β). Moreover, betanin modulated mitochondrial membrane potential, lysosomal membrane permeabilization and adenosine triphosphate. We further investigated the interaction of betanin with TNF-α, IL-6 and Nitric oxide synthase (iNOS or NOS2) using in silico molecular docking analysis. The docking results demonstrated that betanin have significant negative binding energy against active sites of TNF-α, IL-6 and iNOS.
Keyphrases
- lipopolysaccharide induced
- inflammatory response
- nitric oxide synthase
- nitric oxide
- molecular docking
- lps induced
- rheumatoid arthritis
- neuropathic pain
- ms ms
- molecular dynamics simulations
- induced apoptosis
- mass spectrometry
- anti inflammatory
- tandem mass spectrometry
- small molecule
- cell cycle arrest
- spinal cord
- spinal cord injury
- binding protein
- highly efficient
- protein kinase
- pi k akt