Article · Volume 19, Issue 3 · pp. 581–591
Exploring the Potential of Spirulina (Arthrospira platensis) Aqueous Extract in Preventing Glycation of Hemoglobin and pBR322 Plasmid
Additiya Paramanya1, Mohammad Abul Farah2, Khalid Mashay Al-Anazi2, Hari Prasad Devkota3,4, Ahmad Ali1
- 1Department of Life Sciences, University of Mumbai, Mumbai, Maharashtra, India.
- 2Department of Zoology, College of Science, King Saud University, Riyadh, Saudi Arabia.
- 3Graduate School of Pharmaceutical Sciences, Kumamoto University, Kumamoto City, Kumamoto, Japan.
- 4Pharmacy Program, Gandaki University, Pokhara, Pokhara, Gandaki Province, Nepal.
Abstract
Background: Spirulina (Arthrospira platensis), a cyanobacterium, is being consumed worldwide owing to its high nutritional value and therapeutic potential.Objectives: This study aims to determine the phytochemical content, antioxidant capacity, and antiglycation property of A. platensis PCC 7345 aqueous extract against glucose, fructose, and ribose-mediated glycation of hemoglobin.Materials and Methods: The antioxidant property of the extract was determined by 2,2-diphenyl-1-picrylhydrazyl (DPPH), 2,2'-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) (ABTS), and a nitric oxide scavenging assay. Protein glycation and its subsequent prevention were interpreted by observing a reduction in browning, fructosamine, glycated hemoglobin (HbA1c) level, protein carbonyl content, advanced glycation end products (AGEs) formation, and protein aggregation using spectrophotometry and spectrofluorometry. The prevention of strand nicking/breaks in the pBR322 plasmid was analyzed using electrophoresis, and the change in integrated density was calculated using ImageJ software.Results: The extract showed very good antioxidant potential, which is evident and could be estimated from the inhibition concentration (IC50) values that were 45.97, 31.09, and 52.29 μg/mL in the DPPH, ABTS, and nitric oxide scavenging assays, respectively. A. platensis aqueous extract was found to be the most effective in preventing glucose-mediated glycation and protein aggregation, wherein 100 μg/mL of the extract could effectively cause ~50% inhibition in the formation of early and AGEs and prevented the formation of protein aggregates. The highest antiglycating potential of the extract was observed in glucose-mediated glycation, followed by fructose and ribose. The formation of four fluorescent AGEs, such as argpyrimidine, vesper lysine A, pentosidine, and crossline, was reduced. The extract could prevent 97% of DNA nicking in pBR322.Conclusion: The aqueous extract of A. platensis has a potent ability to prevent glycation and its secondary complications.
Keywords: Advanced glycation end products (AGEs); Arthrospira platensis; glycated hemoglobin; integrated density; protein aggregation
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