Actinidia deliciosa Extract as a Promising Supplemental Agent for Hepatic and Renal Complication-Associated Type 2 Diabetes (In Vivo and In Silico-Based Studies)

Author:

El Azab Eman Fawzy1ORCID,Alakilli Saleha Y. M.2,Saleh Abdulrahman M.3ORCID,Alhassan Hassan H.4ORCID,Alanazi Hamad H.1,Ghanem Heba Bassiony45,Yousif Sara Osman16,Alrub Heba Abu1,Anber Nahla7,Elfaki Elyasa Mustafa1,Hamza Alneil1,Abdulmalek Shaymaa8ORCID

Affiliation:

1. Department of Clinical Laboratory Sciences, College of Applied Medical Sciences at Al-Qurayyat, Jouf University, Al-Qurayyat 77454, Saudi Arabia

2. Department of Biological Sciences, Faculty of Sciences, King Abdulaziz University, Jeddah 23761, Saudi Arabia

3. Pharmaceutical Medicinal Chemistry & Drug Design Department, Faculty of Pharmacy (Boys), Al-Azhar University, Cairo 11884, Egypt

4. Department of Clinical Laboratory Sciences, College of Applied Medical Sciences, Jouf University, Sakaka 72341, Saudi Arabia

5. Medical Biochemistry Department, Faculty of Medicine, Tanta University, Tanta 31527, Egypt

6. Department of Clinical Chemistry, Faculty of medical Laboratory Sciences, Sudan University of Science and Technology, Khartoum 13311, Sudan

7. Emergency Hospital, Mansoura University, Mansoura 35516, Egypt

8. Biochemistry Department, Faculty of Science, Alexandria University, Alexandria 21511, Egypt

Abstract

Type 2 diabetes (T2D) is a chronic metabolic condition associated with obesity, oxidative stress-mediated inflammation, apoptosis, and impaired insulin signaling. The utilization of phytochemical therapy generated from plants has emerged as a promising approach for the treatment of diabetes and its complications. Kiwifruit is recognized for its substantial content of antioxidative phenolics. Therefore, this work aimed to examine the effect of Actinidia deliciosa (kiwi fruit) on hepatorenal damage in a high-fat diet (HFD) and streptozotocin (STZ)-induced T2D in rats using in vivo and in silico analyses. An increase in hepatic and renal lipid peroxidation was observed in diabetic rats accompanied by a decrease in antioxidant status. Furthermore, it is important to highlight that there were observable inflammatory and apoptotic responses in the hepatic and renal organs of rats with diabetes, along with a dysregulation of the phosphorylation levels of mammalian target of rapamycin (mTOR), protein kinase B (Akt), and phosphoinositide 3-kinase (PI3K) signaling proteins. However, the administration of kiwi extract to diabetic rats alleviated hepatorenal dysfunction, inflammatory processes, oxidative injury, and apoptotic events with activation of the insulin signaling pathway. Furthermore, molecular docking and dynamic simulation studies revealed quercetin, chlorogenic acid, and melezitose as components of kiwi extract that docked well with potential as effective natural products for activating the silent information regulator 1(SIRT-1) pathway. Furthermore, phenolic acids in kiwi extract, especially syringic acid, P-coumaric acid, caffeic acid, and ferulic acid, have the ability to inhibit the phosphatase and tensin homolog (PTEN) active site. In conclusion, it can be argued that kiwi extract may present a potentially beneficial adjunctive therapy approach for the treatment of diabetic hepatorenal complications.

Funder

Deanship of Scientific Research Foundation of Jouf University

Publisher

MDPI AG

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Computer Science Applications,Spectroscopy,Molecular Biology,General Medicine,Catalysis

Reference52 articles.

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