Evidence mapPaperPMID 38586324Full record

ArticleHeliyon2024

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

Mohamed Lotfy, Aalaa Khattab, Mohammed Shata, Ahmad Alhasbani, Abdallah Khalaf, Saeed Alsaeedi, Mahdi Thaker, Hazza Said, Harun Tumi, Hassan Alzahmi and 5 more

Abstract read
In one paragraph

Article in Heliyon, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

7 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

15 authors.

Mohamed LotfyBiology Department, College of Science, United Arab Emirates University, Al Ain, United Arab Emirates.
Aalaa KhattabFaculty of Dentistry, The British University in Egypt, El Sherouk City, Cairo, Egypt.
Mohammed ShataBiology Department, College of Science, United Arab Emirates University, Al Ain, United Arab Emirates.
Ahmad AlhasbaniBiology Department, College of Science, United Arab Emirates University, Al Ain, United Arab Emirates.
Abdallah KhalafBiology Department, College of Science, United Arab Emirates University, Al Ain, United Arab Emirates.
Saeed AlsaeediBiology Department, College of Science, United Arab Emirates University, Al Ain, United Arab Emirates.
Mahdi ThakerBiology Department, College of Science, United Arab Emirates University, Al Ain, United Arab Emirates.
Hazza SaidBiology Department, College of Science, United Arab Emirates University, Al Ain, United Arab Emirates.
Harun TumiBiology Department, College of Science, United Arab Emirates University, Al Ain, United Arab Emirates.
Hassan AlzahmiBiology Department, College of Science, United Arab Emirates University, Al Ain, United Arab Emirates.
Omar AlblooshiBiology Department, College of Science, United Arab Emirates University, Al Ain, United Arab Emirates.
Mohamad HamdanBiology Department, College of Science, United Arab Emirates University, Al Ain, United Arab Emirates.
Amjad HusseinBiology Department, College of Science, United Arab Emirates University, Al Ain, United Arab Emirates.
Biduth KunduBiology Department, College of Science, United Arab Emirates University, Al Ain, United Arab Emirates.
Ernest A AdeghateDepartment of Anatomy, College of Medicine & Health Sciences, United Arab Emirates University, Al Ain, United Arab Emirates.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

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.

Indexed as

Diabetes mellitusInsulin signalingMelatoninSOD and PI3K/AKT

Identifiers

PMID38586324
PMCPMC10998142

What Socratic holds

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LicenceCC BY-NC
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.