Calotropis proceraRoot Extract Has the Capability to Combat Free Radical Mediated Damage
Author(s) -
Shashank Kumar,
Ashutosh Gupta,
Abhay K. Pandey
Publication year - 2013
Publication title -
isrn pharmacology
Language(s) - English
Resource type - Journals
eISSN - 2090-5173
pISSN - 2090-5165
DOI - 10.1155/2013/691372
Subject(s) - chemistry , dpph , lipid peroxidation , antioxidant , flavonoid , calotropis procera , quercetin , hydroxyl radical , chelation , kidney , biochemistry , traditional medicine , nuclear chemistry , organic chemistry , biology , medicine , endocrinology
The present study reports the antioxidant and membrane protective activities of Calotropis procera aqueous root extract using several in vitro assays along with the determination of phenolic as well as flavonoid contents. Total phenol and flavonoid contents in extract were 15.67 ± 1.52 mg propyl gallate equivalent/g and 1.62 ± 0.05 mg quercetin equivalent/g, respectively. UV-visual spectroscopic scanning of the extract indicated the presence of glycoside-linked tannins or flavonoids. The extract exhibited appreciable reducing power signifying hydrogen donating potential. DPPH radical scavenging assay revealed substantial free radical scavenging activity (42–90%) in the extracts. Concentration dependent response was observed in the metal ion chelating activity (16–95%). Extracts also provided protection against iron induced lipid peroxidation in rat tissue (liver, brain, and kidney) homogenates. Comparatively better protective efficacy against peroxidative damage was observed in liver (71%) followed by kidney (65%) and brain (60%) tissues. Positive correlation ( r 2 = 0.756) was observed between DPPH free radical scavenging activity and reducing power of extract. Similarly strong positive correlation ( r 2 ≈ 0.756) was observed between metal ion chelating ability and percentage lipid peroxidation inhibition in different tissues. The study demonstrated considerable protective efficacy in C. procera root aqueous extracts against free radical and metal ion mediated oxidative damage.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom