(-)-Epigallocatechin gallate (EGCG) pharmacokinetics and molecular interactions towards amelioration of hyperglycemia, hyperlipidemia associated hepatorenal oxidative injury in alloxan induced diabetic mice.


Journal

Chemico-biological interactions
ISSN: 1872-7786
Titre abrégé: Chem Biol Interact
Pays: Ireland
ID NLM: 0227276

Informations de publication

Date de publication:
01 Dec 2022
Historique:
received: 30 08 2022
revised: 29 09 2022
accepted: 19 10 2022
pubmed: 30 10 2022
medline: 29 11 2022
entrez: 29 10 2022
Statut: ppublish

Résumé

Diabetes mellitus has become a serious problem associated with health complications, such as metabolism disorders and liver-kidney dysfunction. The inadequacies associated with conventional medicines have led to a determined search for alternative natural therapeutic agents. The present study was conducted to evaluate the hypoglycemic, antilipidemic, and antioxidant effects of EGCG in surviving diabetic mice. Alloxan diabetic mice were treated with EGCG. Their bloods were collected and submitted to various biochemical measurements, including blood glucose, cholesterol, triglycerides, urea, creatinine, and transaminases. Their livers and kidneys were isolated to assess oxidative damage and to perform histological analysis. Both EGCG and insulin treatment of diabetic mice resulted in a significant reduction in fasting blood glucose levels. EGCG supplementation also ameliorated hepatic as well as renal toxicity indices. Moreover, diabetic mice injected with EGCG exhibited significant changes in antioxidant enzyme activities in the liver and kidney. Histological analyses also showed that it exerted an ameliorative action on these organs and efficiently protected the liver-kidney functions of diabetic mice. EGCG was found to bind α-amylase, PTP1B, and α-glucosidase with good affinities ranging from -6.1 to -8.4 kcal/mol. The findings revealed that EGCG administration induced attractive curative effects on diabetic mice, particularly in terms of liver-kidney function. EGCG can, therefore, be considered as a potential strong candidate for future applications to treat and alleviate diabetic burden. Its pharmacokinetics, high affinities, and molecular interactions with the targeted receptors satisfactory explain the in vivo findings.

Identifiants

pubmed: 36309138
pii: S0009-2797(22)00435-5
doi: 10.1016/j.cbi.2022.110230
pii:
doi:

Substances chimiques

Alloxan 6SW5YHA5NG
epigallocatechin gallate BQM438CTEL
Blood Glucose 0
Catechin 8R1V1STN48
Antioxidants 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

110230

Informations de copyright

Copyright © 2022 Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: Riadh Badraoui reports financial support was provided by University of Hail.

Auteurs

Ahlem Soussi (A)

Laboratory of Animal Ecophysiology, Faculty of Sciences, Sfax, University of Sfax, Tunisia.

Manel Gargouri (M)

Laboratory of Animal Ecophysiology, Faculty of Sciences, Sfax, University of Sfax, Tunisia.

Christian Magné (C)

EA 7462 Géoarchitecture_Territoires, Urbanisation, Biodiversité, Environnement, Faculté des Sciences, Université de Western Brittany, CS 93837, 29238, Brest Cedex 3, France.

Hmed Ben-Nasr (H)

Laboratory of Pharmacology, Medicine Faculty of Sfax, Majida Boulila Road, 3029, Sfax, Tunisia.

Mohd Adnan Kausar (MA)

Laboratory of Biochemistry, College of Medicine, University of Ha'il, 81451, Ha'il, Saudi Arabia; Molecular Diagnostic and Personalized Therapeutics Unit, University of Ha'il, Ha'il, 81451, Saudi Arabia.

Arif J Siddiqui (AJ)

Laboratory of General Biology, Biology Department, College of Science, University of Ha'il, 81451, Ha'il, Saudi Arabia.

Mohd Saeed (M)

Laboratory of General Biology, Biology Department, College of Science, University of Ha'il, 81451, Ha'il, Saudi Arabia.

Mejdi Snoussi (M)

Laboratory of General Biology, Biology Department, College of Science, University of Ha'il, 81451, Ha'il, Saudi Arabia.

Mohd Adnan (M)

Laboratory of General Biology, Biology Department, College of Science, University of Ha'il, 81451, Ha'il, Saudi Arabia.

Abdelfattah El-Feki (A)

Laboratory of Animal Ecophysiology, Faculty of Sciences, Sfax, University of Sfax, Tunisia.

Daniel Chappard (D)

Groupes d'Etudes Remodelage Osseux et Biomateriaux, Universite d'Angers, Angers, 94100, France.

Riadh Badraoui (R)

Molecular Diagnostic and Personalized Therapeutics Unit, University of Ha'il, Ha'il, 81451, Saudi Arabia; Laboratory of General Biology, Biology Department, College of Science, University of Ha'il, 81451, Ha'il, Saudi Arabia; Section of Histology-Cytology, Medicine Faculty of Tunis, University of Tunis El Manar, 1007 La Rabta-Tunis, Tunisia. Electronic address: riadh.badraoui@fmt.utm.tn.

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Classifications MeSH