Melatonin increases AKT and SOD gene and protein expressions in diabetic rats

Diabetes mellitus (DM) is a chronic metabolic disease marked by hyperglycemia due to insulin deficiency or insulin resistance leading to many chronic complications. It is thus important to manage diabetes effectively in order to prevent and or delay these complications. Melatonin is produced by the...

Full description

Bibliographic Details
Main Authors: Mohamed Lotfy, Aalaa Khattab, Mohammed Shata, Ahmad Alhasbani, Abdallah Khalaf, Saeed Alsaeedi, Mahdi Thaker, Hazza Said, Harun Tumi, Hassan Alzahmi, Omar Alblooshi, Mohamad Hamdan, Amjad Hussein, Biduth Kundu, Ernest A. Adeghate
Format: Article
Language:English
Published: Elsevier 2024-04-01
Series:Heliyon
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S240584402404670X
_version_ 1827572225936457728
author Mohamed Lotfy
Aalaa Khattab
Mohammed Shata
Ahmad Alhasbani
Abdallah Khalaf
Saeed Alsaeedi
Mahdi Thaker
Hazza Said
Harun Tumi
Hassan Alzahmi
Omar Alblooshi
Mohamad Hamdan
Amjad Hussein
Biduth Kundu
Ernest A. Adeghate
author_facet Mohamed Lotfy
Aalaa Khattab
Mohammed Shata
Ahmad Alhasbani
Abdallah Khalaf
Saeed Alsaeedi
Mahdi Thaker
Hazza Said
Harun Tumi
Hassan Alzahmi
Omar Alblooshi
Mohamad Hamdan
Amjad Hussein
Biduth Kundu
Ernest A. Adeghate
author_sort Mohamed Lotfy
collection DOAJ
description Diabetes mellitus (DM) is a chronic metabolic disease marked by hyperglycemia due to insulin deficiency or insulin resistance leading to many chronic complications. It is thus important to manage diabetes effectively in order to prevent and or delay these complications. Melatonin is produced by the pineal gland and regulates the wake-sleep circadian rhythm. Existing evidence suggests that melatonin may be effective in the management of DM. However, the evidence on the mechanism of the beneficial effect melatonin as a treatment for DM is limited. In this study, we investigated the effect of melatonin treatment on blood glucose, insulin (INS), AKT and superoxide dismutase (SOD) gene levels in diabetic rats. Non-diabetic and diabetic rats were treated orally for 4 weeks with either 25 mg or 50 mg/kg body weight of melatonin. At the end of the study, pancreatic and liver tissues morphology, glucose homeostasis, serum insulin and SOD levels, hepatic gene and protein expression of SOD as protecting antioxidant enzyme and AKT as central element involved in PI3K/AKT insulin signaling pathway were estimated. Melatonin treated diabetic rats showed reduced hyperglycemia, and increased serum insulin and SOD levels. In addition, melatonin induced an increased gene and protein expression of SOD and AKT. In conclusion, melatonin may play a role in treating diabetic rats via stimulation of insulin secretion, insulin signaling and reduction in oxidative stress.
first_indexed 2024-04-24T16:26:20Z
format Article
id doaj.art-ea9caedaf41644c5b82fdd916ed0f9c6
institution Directory Open Access Journal
issn 2405-8440
language English
last_indexed 2024-04-24T16:26:20Z
publishDate 2024-04-01
publisher Elsevier
record_format Article
series Heliyon
spelling doaj.art-ea9caedaf41644c5b82fdd916ed0f9c62024-03-31T04:37:37ZengElsevierHeliyon2405-84402024-04-01107e28639Melatonin increases AKT and SOD gene and protein expressions in diabetic ratsMohamed Lotfy0Aalaa Khattab1Mohammed Shata2Ahmad Alhasbani3Abdallah Khalaf4Saeed Alsaeedi5Mahdi Thaker6Hazza Said7Harun Tumi8Hassan Alzahmi9Omar Alblooshi10Mohamad Hamdan11Amjad Hussein12Biduth Kundu13Ernest A. Adeghate14Biology Department, College of Science, United Arab Emirates University, Al Ain, United Arab Emirates; Corresponding author. Biology Department, College of Science, United Arab Emirates University, Al Ain, United Arab Emirates.Faculty of Dentistry, The British University in Egypt, El Sherouk City, Cairo, EgyptBiology Department, College of Science, United Arab Emirates University, Al Ain, United Arab EmiratesBiology Department, College of Science, United Arab Emirates University, Al Ain, United Arab EmiratesBiology Department, College of Science, United Arab Emirates University, Al Ain, United Arab EmiratesBiology Department, College of Science, United Arab Emirates University, Al Ain, United Arab EmiratesBiology Department, College of Science, United Arab Emirates University, Al Ain, United Arab EmiratesBiology Department, College of Science, United Arab Emirates University, Al Ain, United Arab EmiratesBiology Department, College of Science, United Arab Emirates University, Al Ain, United Arab EmiratesBiology Department, College of Science, United Arab Emirates University, Al Ain, United Arab EmiratesBiology Department, College of Science, United Arab Emirates University, Al Ain, United Arab EmiratesBiology Department, College of Science, United Arab Emirates University, Al Ain, United Arab EmiratesBiology Department, College of Science, United Arab Emirates University, Al Ain, United Arab EmiratesBiology Department, College of Science, United Arab Emirates University, Al Ain, United Arab EmiratesDepartment of Anatomy, College of Medicine & Health Sciences, United Arab Emirates University, Al Ain, United Arab Emirates; Zayed Centre for Health Sciences, College of Science, United Arab Emirates University, Al Ain, United Arab Emirates; Corresponding author. Department of Anatomy, College of Medicine & Health Sciences, United Arab Emirates University, Al Ain, United Arab Emirates.Diabetes mellitus (DM) is a chronic metabolic disease marked by hyperglycemia due to insulin deficiency or insulin resistance leading to many chronic complications. It is thus important to manage diabetes effectively in order to prevent and or delay these complications. Melatonin is produced by the pineal gland and regulates the wake-sleep circadian rhythm. Existing evidence suggests that melatonin may be effective in the management of DM. However, the evidence on the mechanism of the beneficial effect melatonin as a treatment for DM is limited. In this study, we investigated the effect of melatonin treatment on blood glucose, insulin (INS), AKT and superoxide dismutase (SOD) gene levels in diabetic rats. Non-diabetic and diabetic rats were treated orally for 4 weeks with either 25 mg or 50 mg/kg body weight of melatonin. At the end of the study, pancreatic and liver tissues morphology, glucose homeostasis, serum insulin and SOD levels, hepatic gene and protein expression of SOD as protecting antioxidant enzyme and AKT as central element involved in PI3K/AKT insulin signaling pathway were estimated. Melatonin treated diabetic rats showed reduced hyperglycemia, and increased serum insulin and SOD levels. In addition, melatonin induced an increased gene and protein expression of SOD and AKT. In conclusion, melatonin may play a role in treating diabetic rats via stimulation of insulin secretion, insulin signaling and reduction in oxidative stress.http://www.sciencedirect.com/science/article/pii/S240584402404670XDiabetes mellitusMelatoninInsulin signalingSOD and PI3K/AKT
spellingShingle Mohamed Lotfy
Aalaa Khattab
Mohammed Shata
Ahmad Alhasbani
Abdallah Khalaf
Saeed Alsaeedi
Mahdi Thaker
Hazza Said
Harun Tumi
Hassan Alzahmi
Omar Alblooshi
Mohamad Hamdan
Amjad Hussein
Biduth Kundu
Ernest A. Adeghate
Melatonin increases AKT and SOD gene and protein expressions in diabetic rats
Heliyon
Diabetes mellitus
Melatonin
Insulin signaling
SOD and PI3K/AKT
title Melatonin increases AKT and SOD gene and protein expressions in diabetic rats
title_full Melatonin increases AKT and SOD gene and protein expressions in diabetic rats
title_fullStr Melatonin increases AKT and SOD gene and protein expressions in diabetic rats
title_full_unstemmed Melatonin increases AKT and SOD gene and protein expressions in diabetic rats
title_short Melatonin increases AKT and SOD gene and protein expressions in diabetic rats
title_sort melatonin increases akt and sod gene and protein expressions in diabetic rats
topic Diabetes mellitus
Melatonin
Insulin signaling
SOD and PI3K/AKT
url http://www.sciencedirect.com/science/article/pii/S240584402404670X
work_keys_str_mv AT mohamedlotfy melatoninincreasesaktandsodgeneandproteinexpressionsindiabeticrats
AT aalaakhattab melatoninincreasesaktandsodgeneandproteinexpressionsindiabeticrats
AT mohammedshata melatoninincreasesaktandsodgeneandproteinexpressionsindiabeticrats
AT ahmadalhasbani melatoninincreasesaktandsodgeneandproteinexpressionsindiabeticrats
AT abdallahkhalaf melatoninincreasesaktandsodgeneandproteinexpressionsindiabeticrats
AT saeedalsaeedi melatoninincreasesaktandsodgeneandproteinexpressionsindiabeticrats
AT mahdithaker melatoninincreasesaktandsodgeneandproteinexpressionsindiabeticrats
AT hazzasaid melatoninincreasesaktandsodgeneandproteinexpressionsindiabeticrats
AT haruntumi melatoninincreasesaktandsodgeneandproteinexpressionsindiabeticrats
AT hassanalzahmi melatoninincreasesaktandsodgeneandproteinexpressionsindiabeticrats
AT omaralblooshi melatoninincreasesaktandsodgeneandproteinexpressionsindiabeticrats
AT mohamadhamdan melatoninincreasesaktandsodgeneandproteinexpressionsindiabeticrats
AT amjadhussein melatoninincreasesaktandsodgeneandproteinexpressionsindiabeticrats
AT biduthkundu melatoninincreasesaktandsodgeneandproteinexpressionsindiabeticrats
AT ernestaadeghate melatoninincreasesaktandsodgeneandproteinexpressionsindiabeticrats