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Green tea and its active compound epigallocathechin-3-gallate (EGCG) inhibit neuronal apoptosis in a middle cerebral artery occlusion (MCAO) model

  • Abdulloh Machin EMAIL logo , Imam Susilo and Djoko A. Purwanto
Published/Copyright: June 25, 2021

Abstract

Objectives

To determine the effect of green tea with the active ingredient epigallocathechin-3-gallate (EGCG) on the inhibition of apoptosis in the middle cerebral artery occlusion (MCAO) model.

Methods

Four month old male Rattus norvegicus rats with a body weight of 200–275 g was used for the MCAO model and divided into five groups, and the treatment was carried out for 7 days. Before being sacrificed, the subject had 1 cc of blood drawn for high mobility group box 1 (HMGB-1) examination using enzyme-linked immunosorbent assay (ELISA), and after being sacrificed, the brain tissue specimen was taken to examine caspase-3 and B-cell lymphoma 3 (BCL-3) using immunohistochemistry methods.

Results

There was no significant difference in HMGB-1 results for the treatment group compared to the control group (P1: 384.20 ± 231.72 [p = 0.553]; P2: 379.11 ± 268.4 [p = 0.526]; P3: 284, 87 ± 276.19 [p = 0.140]; P4: 435.32 ± 279.95 [p = 0.912]). There is a significant increase in BCL-2 expression between the treatment group compared to the control group (P1: 2.58 ± 0.51 [p = 0.04]; P2: 3.36 ± 0.50 [p<0.001]; P3: 4.00 ± 0.42 [p<0.001]; P4: 3.60 ± 0.52 [p<0.001]). There was a significant difference in caspase-3 expression compared to the control group in the P3 group (P1: 4.33 ± 0.49 [p = 0.652]; P2: 4.09 ± 0.30 [p = 0.136]; P3: 3.58 ± 0.51 [p = 0.01]; P4: 3.89 ± 0.42 [p = 0.063]). There is no correlation between HMGB-1 and caspase-3 (r = −0.063; p = 0.613) or BCL-2 (r = −0.106; p = 0.396). There is significant negative correlation between caspase-3 and BCL-2 (r = −0.459; p = 0.000).

Conclusions

Green tea with the active ingredient EGCG can inhibit neuronal cell death through the apoptotic pathway and not through the activation of HMGB-1.


Corresponding author: Abdulloh Machin, Department Neurology, Faculty of Medicine, Universitas Airlangga, Surabaya, Indonesia, Phone: +62 813 3000 8306, E-mail:

Acknowledgments

Gratitude is due to the Head of the Department of Pathology, Faculty of Medicine, Universitas Airlangga, and Head of the Department of Pharmaceutical chemistry, Faculty of Pharmacy, Universitas Airlangga.

  1. Research funding: Research fund was obtained from Research and Community Service Management Information Systems Ministry of Research, Technology, and Higher Education of the Republic of Indonesia.

  2. Author contributions: All authors have accepted responsibility for the entire content of this manuscript and approved its submission.

  3. Competing interests: The authors state no conflict of interest.

  4. Ethical approval: Ethical approval was obtained from The Research Ethics Committee, Faculty of Veterinary Medicine, Universitas Airlangga, number: 2.KE.161.09.2018.

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Received: 2020-11-28
Accepted: 2021-02-20
Published Online: 2021-06-25

© 2021 Walter de Gruyter GmbH, Berlin/Boston

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