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Research Article

Protective effect of epigallocatechin gallate against N-nitrosodiethylamine (NDEA) induced toxicity in rats

& | (Reviewing Editor)
Article: 1141451 | Received 09 Oct 2015, Accepted 04 Jan 2016, Published online: 23 Feb 2016

Figures & data

Figure 1. Rat liver sections stained with haematoxylin-eosin (200× magnification) (a) control; (b) rats exposed to NDEA (0.1 mg/ml) for 21 days, and (c) rats exposed to 0.1 mg/ml of NDEA along with 15 mg/ml of epigallocatechin gallate.

Notes: SN: swollen nucleus, SD: sinusoidal dilation.
Figure 1. Rat liver sections stained with haematoxylin-eosin (200× magnification) (a) control; (b) rats exposed to NDEA (0.1 mg/ml) for 21 days, and (c) rats exposed to 0.1 mg/ml of NDEA along with 15 mg/ml of epigallocatechin gallate.

Figure 2. Aspartate aminotransferase (AST) activity measured after 21 days of treatment of N-nitrosodiethylamine separately and along with different doses of epigallocatechin gallate in rats.

Notes: NDEA: N-nitrosodiethylamine; EGCG1: Epigallocatechin gallate (5 mg/ml); EGCG2: Epigallocatechin gallate (10 mg/ml); EGCG3: Epigallocatechin gallate (15 mg/ml); Negative control: Dimethyl sulphoxide (3 μl/ml); SE: standard error; asignificant with respect to untreated (p < 0.01); bsignificant with respect to NDEA treatment (p < 0.05).
Figure 2. Aspartate aminotransferase (AST) activity measured after 21 days of treatment of N-nitrosodiethylamine separately and along with different doses of epigallocatechin gallate in rats.

Figure 3. Alanine transaminase (ALT) activity measured after 21 days of treatment of N-nitrosodiethylamine separately and along with different doses of epigallocatechin gallate in rats.

Notes: NDEA: N-nitrosodiethylamine; EGCG1: Epigallocatechin gallate (5 mg/ml); EGCG2: Epigallocatechin gallate (10 mg/ml); EGCG3: Epigallocatechin gallate (15 mg/ml); Negative control: Dimethyl sulphoxide (3 μl/ml); SE: standard error; asignificant with respect to untreated (p < 0.01); bsignificant with respect to NDEA treatment (p < 0.05).
Figure 3. Alanine transaminase (ALT) activity measured after 21 days of treatment of N-nitrosodiethylamine separately and along with different doses of epigallocatechin gallate in rats.

Figure 4. Alkaline phosphatase (ALP) activity measured after 21 days of treatment of N-nitrosodiethylamine separately and along with different doses of epigallocatechin gallate in rats.

Notes: NDEA: N-nitrosodiethylamine; EGCG1: Epigallocatechin gallate (5 mg/ml); EGCG2: Epigallocatechin gallate (10 mg/ml); EGCG3: Epigallocatechin gallate (15 mg/ml); Negative control: Dimethyl sulphoxide (3 μl/ml); SE: standard error; asignificant with respect to untreated (p < 0.01); bsignificant with respect to NDEA treatment (p < 0.05).
Figure 4. Alkaline phosphatase (ALP) activity measured after 21 days of treatment of N-nitrosodiethylamine separately and along with different doses of epigallocatechin gallate in rats.

Figure 5. Lactate dehydrogenase (LDH) activity measured after 21 days of treatment of N-nitrosodiethylamine separately and along with different doses of epigallocatechin gallate in rats.

Notes: NDEA: N-nitrosodiethylamine; EGCG1: Epigallocatechin gallate (5 mg/ml); EGCG2: Epigallocatechin gallate (10 mg/ml); EGCG3: Epigallocatechin gallate (15 mg/ml); Negative control: Dimethyl sulphoxide (3 μl/ml); SE:standard error; asignificant with respect to untreated (p < 0.01); bsignificant with respect to NDEA treatment (p < 0.05).
Figure 5. Lactate dehydrogenase (LDH) activity measured after 21 days of treatment of N-nitrosodiethylamine separately and along with different doses of epigallocatechin gallate in rats.

Figure 6. Lipid peroxidation measured in rat liver after 21 days of treatment with NDEA alone and together with different amounts of epigallocatechin gallate.

Notes: NDEA: N-nitrosodiethylamine; EGCG1: Epigallocatechin gallate (5 mg/ml); EGCG2: Epigallocatechin gallate (10 mg/ml); EGCG3: Epigallocatechin gallate (15 mg/ml); Negative control: Dimethyl sulphoxide (3 μl/ml); SE: standard error; asignificant with respect to untreated (p < 0.01); bsignificant with respect to NDEA treatment (p < 0.05).
Figure 6. Lipid peroxidation measured in rat liver after 21 days of treatment with NDEA alone and together with different amounts of epigallocatechin gallate.

Figure 7. Protein carbonyl content measured in rat liver after 21 days of treatment with NDEA alone and together with different amounts of epigallocatechin gallate.

Notes: NDEA: N-nitrosodiethylamine; EGCG1: Epigallocatechin gallate (5 mg/ml); EGCG2: Epigallocatechin gallate (10 mg/ml); EGCG3: Epigallocatechin gallate (15 mg/ml); Negative control: Dimethyl sulphoxide (3 μl/ml); SE: standard error; asignificant with respect to untreated (p < 0.01); bsignificant with respect to NDEA treatment (p < 0.05).
Figure 7. Protein carbonyl content measured in rat liver after 21 days of treatment with NDEA alone and together with different amounts of epigallocatechin gallate.

Figure 8. (a) Hepatocytes with control, (b) treated with NDEA (0.1 m/ml), and (c) Micronucleus formation in hepatocytes after 21 days of treatment of rats with NDEA alone and together with different amounts of epigallocatechin gallate.

Notes: NDEA: N-nitrosodiethylamine; EG1: Epigallocatechin gallate (5 mg/ml); EG2: Epigallocatechin gallate (10 mg/ml); EG3: Epigallocatechin gallate (15 mg/ml); Negative control: Dimethyl sulphoxide (3 μl/ml); SE: standard error; asignificant with respect to untreated (p < 0.01); bsignificant with respect to NDEA treatment (p < 0.05).
Figure 8. (a) Hepatocytes with control, (b) treated with NDEA (0.1 m/ml), and (c) Micronucleus formation in hepatocytes after 21 days of treatment of rats with NDEA alone and together with different amounts of epigallocatechin gallate.

Figure 9. (a) Control, (b) treated with NDEA (0.1 mg/ml), and (c) Rats exposed to 0.1 mg/ml of NDEA along with 15 mg/ml of epigallocatechin gallate (d) Comet tail length in rat hepatocytes after 21 days of treatment of rats with NDEA alone and together with different amounts of epigallocatechin gallate.

Notes: NDEA: N-nitrosodiethylamine; EG1: Epigallocatechin gallate (5 mg/ml); EG2: Epigallocatechin gallate (10 mg/ml); EG3: Epigallocatechin gallate (15 mg/ml); Negative control: Dimethyl sulphoxide (3 μl/ml); SE: standard error; asignificant with respect to untreated (p < 0.01); bsignificant with respect to NDEA treatment (p < 0.05).
Figure 9. (a) Control, (b) treated with NDEA (0.1 mg/ml), and (c) Rats exposed to 0.1 mg/ml of NDEA along with 15 mg/ml of epigallocatechin gallate (d) Comet tail length in rat hepatocytes after 21 days of treatment of rats with NDEA alone and together with different amounts of epigallocatechin gallate.

Figure 10. (a) Control, (b) treated with NDEA (0.1 mg/ml), and (c) Rats exposed to 0.1 mg/ml of NDEA along with 15 mg/ml of epigallocatechin gallate (d) Comet tail length in rat blood lymphocytes after 21 days of treatment of rats with NDEA alone, or together with different amounts of epigallocatechin gallate.

Notes: NDEA: N-nitrosodiethylamine; EG1: Epigallocatechin gallate (5 mg/ml); EG2: Epigallocatechin gallate (10 mg/ml); EG3: Epigallocatechin gallate (15 mg/ml); Negative control: Dimethyl sulphoxide (3 μl/ml); SE: standard error; asignificant with respect to untreated (p < 0.01); bsignificant with respect to NDEA treatment (p < 0.05).
Figure 10. (a) Control, (b) treated with NDEA (0.1 mg/ml), and (c) Rats exposed to 0.1 mg/ml of NDEA along with 15 mg/ml of epigallocatechin gallate (d) Comet tail length in rat blood lymphocytes after 21 days of treatment of rats with NDEA alone, or together with different amounts of epigallocatechin gallate.