In Vitro and In Vivo Biochemical Evaluations of the Methanolic Leaf Extract of Garcinia kola

  • Badmus J
  • Adedosu O
  • Adeleke E
  • et al.
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Abstract

Garcinia kola Heckel ( Guttiferae ) leaves have received limited scientific attention despite their traditionally acclaimed medicinal properties. The scavenging ability of the methanolic leaf extract (MLE) of G. kola was assayed for hydroxyl radical (OH • ), superoxide anion ( O 2 - ), 1,1-diphenyl-2-picrylhydrazyl (DPPH), azinobis-3-ethyl-benzothiazoline-6-sulfonic acid (ABTS •+ ), and lipid peroxidation (LP) activity in egg yolk, rat liver, and brain homogenates. Total phenolic and flavonoid contents of the extract were also evaluated. Group I animals were given oral doses of water, whereas Group II and Group III animals received 100 and 200 mg/kg body weight (bw) MLE, respectively, for 14 days. Plasma glucose, magnesium, γ -glutamyltransferase (GGT/ γ GT), alanine aminotransferase (ALT), aspartate aminotransferase (AST), creatinine, and urea were evaluated. Hepatic reduced glutathione (GSH), glutathione peroxidase (GPx), superoxide dismutase (SOD), LP, and liver histopathological appearance were also assessed. The extract scavenged OH • , O 2 - , DPPH, and ABTS •+ and inhibited LP in egg yolk, rat liver, and brain homogenates. Furthermore, oral administration of the extract showed no adverse effects on hepatic and renal function tests. Increased hepatic GSH and nonsignificant changes in LP, GPx and SOD activities, and liver histology were observed. These results suggest that G. kola leaves have antioxidant activities which may have application in traditional medicine.

Figures

  • Figure 1: The structure of the Garcinia biflavonoids (for GB1, R is H; GB2, R is OH) GB1 (3,4,4,5, 5,7,7-heptahydroxy-3,8-biflavanone) and GB2 (3,4,4,5, 5,5,7,7-hexahydroxy-3,8-biflavanone).
  • Figure 2: Hepatic GSH concentration and SOD and GPx activities in liver homogenates prepared from rats treated with distilled water as control (Group I), 100mg/kg (Group II) or 200mg/kg (Group III) MLE of G. kola. Data are presented as means ± SD (𝑛 = 6).
  • Table 1: Hydroxyl radical scavenging activity of the methanolic extract of Garcinia kola and quercetin.
  • Table 2: Superoxide anion scavenging activity of the methanolic extract of Garcinia kola and ascorbic acid.
  • Figure 3: Hepatic lipid peroxidation measured as malondialdehyde (MDA) generated in liver homogenates prepared from rats treated with distilled water as control (Group I), 100mg/kg (Group II) or 200mg/kg (Group III) MLE of G. kola. Data are presented as means ± SD (𝑛 = 6).
  • Figure 4: Histopathology of livers from rats in each treatment group. (a) Group I, distilled water control; (b) Group II, 100mg/kg; and (c) Group III, 200mg/kg MLE of G. kola. A portion of liver was fixed in 10% formalin and embedded in paraffin. Each liver section of 4-𝜇m thickness was stained with hematoxylin and eosin for light microscopic assessment at 100x.
  • Table 3: DPPH scavenging activity of the methanolic extract of Garcinia kola and ascorbic acid.
  • Table 4: ABTS∙+ scavenging activity of the methanolic extract of Garcinia kola and ascorbic acid.

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APA

Badmus, J. A., Adedosu, O. T., Adeleke, E. G., Akinboro, K. H., Odeyemi, B. I., Ayoola, B. I., & Hiss, D. C. (2014). In Vitro and In Vivo Biochemical Evaluations of the Methanolic Leaf Extract of Garcinia kola. International Scholarly Research Notices, 2014, 1–9. https://doi.org/10.1155/2014/391692

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