Role of Nrf2 dysfunction in the pathogenesis of diabetic nephropathy: Therapeutic prospect of epigallocatechin-3-gallate.


Journal

Free radical biology & medicine
ISSN: 1873-4596
Titre abrégé: Free Radic Biol Med
Pays: United States
ID NLM: 8709159

Informations de publication

Date de publication:
20 11 2020
Historique:
received: 11 05 2020
revised: 21 07 2020
accepted: 26 07 2020
pubmed: 10 8 2020
medline: 28 5 2021
entrez: 10 8 2020
Statut: ppublish

Résumé

Diabetic nephropathy (DN), a progressive kidney disease afflicts more than 20 and up to 40% of the diabetic population and it is characterized by persistent microalbuminuria declined glomerular filtration rate. The interesting feature associated with DN is that, even though the progression of the disease correlates with oxidative stress, Nrf2, the master regulator of antioxidant defense system involved in counteracting oxidative stress is also upregulated in the diabetic kidneys of both human as well as experimental animals in early stages of DN. Despite the increased expression, the ability of this protein to get translocated into the nucleus is diminished signifying the functional impairment of Nrf2, implying redox imbalance. Hence, it is understood that agents that boost the translocation of Nrf2 might be beneficial rather than those that quantitatively overexpress Nrf2 in treating DN. The deleterious effects of synthetic Nrf2 activators have instigated the researchers to search for phytochemicals that have ambient Nrf2 boosting ability with no side effects, one such phytochemical is Epigallocatechin-3-gallate (EGCG) and it has shown beneficial effects by preventing the progression of DN via influencing Nrf2/ARE pathway, however, the modus operandi is unclear, despite speculations. This study was designed to find out whether supplementation of Nrf2 booster like EGCG at the crucial time of Nrf2 dysfunction can mitigate the progression of DN. Based on the findings of the present study, it might be concluded that the beneficial effect of EGCG in mitigating DN is mediated mainly through its ability to activate the Nrf2/ARE signaling pathway at multiple stages i.e., by downregulating Keap1 and boosting the nuclear Nrf2 level by disrupting Nrf2-Keap1 interaction. These results emphasize that supplementation of EGCG might be more beneficial at an early stage of DN, where dysfunctional Nrf2 accumulation occurs, which should be further validated.

Identifiants

pubmed: 32768570
pii: S0891-5849(20)31184-9
doi: 10.1016/j.freeradbiomed.2020.07.037
pii:
doi:

Substances chimiques

Kelch-Like ECH-Associated Protein 1 0
NF-E2-Related Factor 2 0
NFE2L2 protein, human 0
Catechin 8R1V1STN48
epigallocatechin gallate BQM438CTEL

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

227-238

Informations de copyright

Copyright © 2020 Elsevier Inc. All rights reserved.

Auteurs

Thangarajeswari Mohan (T)

Department of Medical Biochemistry, University of Madras, Taramani, Chennai, 600113, India.

Kishore Kumar S Narasimhan (KKS)

Department of Medical Biochemistry, University of Madras, Taramani, Chennai, 600113, India; Department of Pathology, University of Alabama at Birmingham, Birmingham, AL 35294, USA.

Divya Bhavani Ravi (DB)

Department of Medical Biochemistry, University of Madras, Taramani, Chennai, 600113, India.

Prema Velusamy (P)

Department of Medical Biochemistry, University of Madras, Taramani, Chennai, 600113, India.

Navvi Chandrasekar (N)

Department of Biochemistry, University of Madras, Guindy, Chennai, 600025, India.

Lakshmi Narasimhan Chakrapani (LN)

Department of Medical Biochemistry, University of Madras, Taramani, Chennai, 600113, India.

Ashokkumar Srinivasan (A)

Department of Medical Biochemistry, University of Madras, Taramani, Chennai, 600113, India.

Porkodi Karthikeyan (P)

Department of Medical Biochemistry, University of Madras, Taramani, Chennai, 600113, India.

Pugazhendhi Kannan (P)

Department of Medical Biochemistry, University of Madras, Taramani, Chennai, 600113, India.

Bhavani Tamilarasan (B)

Department of Medical Biochemistry, University of Madras, Taramani, Chennai, 600113, India.

Thanka Johnson (T)

Department of Pathology, Sri Ramachandra University, Chennai, 600116, India.

Parkavi Kalaiselvan (P)

Chettinad Hospital and Research Institute, Chennai, 603103, India.

Kalaiselvi Periandavan (K)

Department of Medical Biochemistry, University of Madras, Taramani, Chennai, 600113, India. Electronic address: pkalaiselvi2011@gmail.com.

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Classifications MeSH