Chemical analysis of Punica granatum fruit peel and its in vitro and in vivo biological properties

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Abstract

Background: The medical application of pomegranate fruits and its peel is attracted human beings. The aim of the present study was to evaluate the in vitro α-Glucosidase inhibition, antimicrobial, antioxidant property and in vivo anti-hyperglycemic activity of Punica granatum (pomegranate) fruit peel extract using Caenorhabditis elegans. Methods: Various invitro antioxidant activity of fruit peel extracts was determined by standard protocol. Antibacterial and antifungal activities were determined using disc diffusion and microdilution method respectively. Anti-hyperglycemic activity of fruit peel was observed using fluorescence microscope for in vivo study. Results: The ethyl acetate extract of P. granatum fruit peel (PGPEa) showed α-Glucosidase inhibition upto 50 % at the concentration of IC50 285.21 ± 1.9 μg/ml compared to hexane and methanol extracts. The total phenolic content was highest (218.152 ± 1.73 mg of catechol equivalents/g) in ethyl acetate extract. PGPEa showed more scavenging activity on 2,2-diphenyl-picrylhydrazyl (DPPH) with IC50 value 302.43 ± 1.9 μg/ml and total antioxidant activity with IC50 294.35 ± 1.68 μg/ml. PGPEa also showed a significant effecton lipid peroxidation IC50 208.62 ± 1.68 μg/ml, as well as high reducing power. Among the solvents extracts tested, ethyl acetate extract of fruit peel showed broad spectrum of antimicrobial activity. Ethyl acetate extract supplemented C.elegans worms showed inhibition of lipid accumulation similar to acarbose indicating good hypoglycemic activity. The normal worms compared to test (ethyl acetate extract supplemented) showed the highest hypoglycaemic activity by increasing the lifespan of the worms. GC-MS analysis of PGPEa showed maximum amount of 5-hydroxymethylfurfural and 4-fluorobenzyl alcohol (48.59 %). Conclusion: In the present investigation we observed various biological properties of pomegranate fruit peel. The results clearly indicated that pomegranate peel extract could be used in preventing the incidence of long term complication of diabetics.

Figures

  • Table 1 α-Glucosidase inhibition of extracts of Punica granatum (Pomegranate) fruit peal
  • Fig. 1 DPPH scavenging effect of hexane, ethyl acetate, and methanol extracts of Punica granatum (Pomegranate) fruit peel extracts and Vitamin C at different concentrations (100–500 μg/ml). Each value represents the mean ± standard deviation of triplicate experiments
  • Fig. 2 Total antioxidant activity of hexane, ethyl acetate, and methanol ext C at different concentrations (100–500 μg/ml). Each value represents the m
  • Fig. 3 Reducing power of hexane, ethyl acetate, methanol extracts of Punica granatum (Pomegranate) fruit peel extractsand BHT at different concentrations (100–500 μg/ml). Each value represents the mean ± standard deviation of triplicate experiments
  • Fig. 4 Lipid peroxidation scavenging effect of hexane, ethyl acetate, metha BHT at different concentrations (100–500 μg/ml). Each value represents the
  • Table 2 Antibacterial activities of crude extracts of Punica granatum (Pomegranate) fruit peel
  • Table 3 Antifungal activities of crude extracts of Punica granatum (Pomegranate) fruit peel
  • Table 4 C. elegans Life span assay (Plate contain Glucose) of Punica granatum fruit peel

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Barathikannan, K., Venkatadri, B., Khusro, A., Al-Dhabi, N. A., Agastian, P., Arasu, M. V., … Kim, Y. O. (2016). Chemical analysis of Punica granatum fruit peel and its in vitro and in vivo biological properties. BMC Complementary and Alternative Medicine, 16(1). https://doi.org/10.1186/s12906-016-1237-3

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