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Cited by 7

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Methanolic Extract of Dill Leaves Inhibits AGEs Formation and Shows Potential Hepatoprotective Effects in CCl4 Induced Liver Toxicity in Rat

Oshaghi, Ebrahim Abbasi, Khodadadi, Iraj, Mirzaei, Fatemeh, Khazaei, Mozafar, Tavilani, Heidar, Goodarzi, Mohammad Taghi·2017·Journal of Pharmaceutics
DOI 10.1155/2017/6081374PMC PMC5274678
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Abstract

The research was aimed at evaluating the antiglycation, antioxidant, and hepatoprotective properties of methanolic extract of Anethum graveolens (dill). The antioxidant properties, photochemical characteristics, and antiglycation effects of dill extract were measured. Carbon tetrachloride-induced hepatotoxic rats were used to show the hepatoprotective activity of dill leaves. Different concentration of dill extract (0.032, 0.065, 0.125, 0.25, 0.5, and 1 mg/mL) showed potential antioxidant ability. The extract of dill leaves significantly reduced AGEs formation and also fructosamine and protein carbonyl levels in rats’ liver. Thiol groups’ oxidation, amyloid cross-β, and protein fragmentation (P<0.001) significantly reduced in treated rats. Liver damage markers significantly reduced in dill-treated animals (P<0.05). Dill with potential antioxidant, antiglycation, and hepatoprotective effects can be suggested for treatment of diabetes complications.

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Figure 1 Antioxidant and antiradical activity of dill extract. Values are the average of triplicate experiments and presented as mean ± SEM. (a) DPPH radical scavenging activity. (b) FRAP assays. (c) Superoxide radical scavenging activity. (d) Hydrogen peroxide radical scavenging activity. (e) Metal chelating activity. (f) Reducing power activity. (g) Nitric oxide scavenging activity.
Figure 1 Antioxidant and antiradical activity of dill extract. Values are the average of triplicate experiments and presented as mean ± SEM. (a) DPPH radical scavenging activity. (b) FRAP assays. (c) Superoxide radical scavenging activity. (d) Hydrogen peroxide radical scavenging activity. (e) Metal chelating activity. (f) Reducing power activity. (g) Nitric oxide scavenging activity.CC BY · PubMed Central
Figure 2 (a) The effect of dill extract on the level of protein aggregation. Data are represented as mean ± SEM (n = 3); ∗P < 0.001 compared with BSA/fructose at the same incubation time. AG: aminoguanidine. Data are represented as mean ± SEM (n = 3); ∗P < 0.001 compared with BSA/fructose at the same incubation time. (b) Protein fragmentation in BSA incubated with 200 mM fructose in the presence of Cu+2 ion, aminoguanidine, and dill extract for 7 days, detected by SDS-PAGE. Protein fragmentation inhibited by aminoguanidine (lane C) and dill extract (lane D) compared with BSA/fructose. A lane: 10 mg/mL BSA, B lane: 10 mg/mL BSA + 200 mM fructose, C lane: 10 mg/mL BSA + 200 mM fructose + aminoguanidine, and D lane: 10 mg/mL BSA + 200 mM fructose + dill extract.
Figure 2 (a) The effect of dill extract on the level of protein aggregation. Data are represented as mean ± SEM (n = 3); ∗P < 0.001 compared with BSA/fructose at the same incubation time. AG: aminoguanidine. Data are represented as mean ± SEM (n = 3); ∗P < 0.001 compared with BSA/fructose at the same incubation time. (b) Protein fragmentation in BSA incubated with 200 mM fructose in the presence of Cu+2 ion, aminoguanidine, and dill extract for 7 days, detected by SDS-PAGE. Protein fragmentation inhibited by aminoguanidine (lane C) and dill extract (lane D) compared with BSA/fructose. A lane: 10 mg/mL BSA, B lane: 10 mg/mL BSA + 200 mM fructose, C lane: 10 mg/mL BSA + 200 mM fructose + aminoguanidine, and D lane: 10 mg/mL BSA + 200 mM fructose + dill extract.CC BY · PubMed Central
Figure 3 Histopathological changes in the liver of different treated animals. Histology of liver in normal group showed regular structure, while CCl4-treated animals show the entire damage of hepatocytes. In dill-treated animals liver damage was restored.
Figure 3 Histopathological changes in the liver of different treated animals. Histology of liver in normal group showed regular structure, while CCl4-treated animals show the entire damage of hepatocytes. In dill-treated animals liver damage was restored.CC BY · PubMed Central

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Metadata

Authors
Oshaghi, E. A., Khodadadi, I., Mirzaei, F., Khazaei, M., Tavilani, H., & Goodarzi, M. T.
Affiliations
  • Department of Clinical Biochemistry, School of Medicine, Hamadan University of Medical Sciences, Hamadan, Iran
  • Student Research Committee, Kermanshah University of Medical Sciences, Kermanshah, Iran
  • Fertility and Infertility Research Center, Kermanshah University of Medical Sciences, Kermanshah, Iran
ORCID
Venue
Journal of Pharmaceutics
Publisher
Wiley
Published
2017-01-15
Volume
2017
Pages
1-9
ISSN
  • 2090-9918
  • 2090-7818
DOI
10.1155/2017/6081374
PMC
PMC5274678
Cited by
7
References
1
Language
en
Licence
creativecommons.org/licenses/by/4.0/ (unspecified)
Funders
Hamadan University of Medical Sciences

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