Short‐term melatonin consumption protects the heart of obese rats independent of body weight change and visceral adiposity
Abstract
Chronic melatonin treatment has been shown to prevent the harmful effects of diet‐induced obesity and reduce myocardial susceptibility to ischaemia‐reperfusion injury (IRI). However, the exact mechanism whereby it exerts its beneficial actions on the heart in obesity/insulin resistance remains unknown. Herein, we investigated the effects of relatively short‐term melatonin treatment on the heart in a rat model of diet‐induced obesity. Control and diet‐induced obese Wistar rats (fed a high calorie diet for 20 wk) were each subdivided into three groups receiving drinking water with or without melatonin (4 mg/kg/day) for the last 6 or 3 wk of experimentation. A number of isolated hearts were perfused in the working mode, subjected to regional or global ischaemia‐reperfusion; others were nonperfused. Metabolic parameters, myocardial infarct sizes (IFS), baseline and postischaemic activation of PKB/Akt, ERK42/44, GSK‐3β and STAT‐3 were determined. Diet‐induced obesity caused increases in body weight gain, visceral adiposity, fasting blood glucose, serum insulin and triglyceride (TG) levels with a concomitant cardiac hypertrophy, large postischaemic myocardial IFS s and a reduced cardiac output. Melatonin treatment (3 and 6 wk) decreased serum insulin levels and the HOMA index (P < 0.05) with no effect on weight gain (after 3 wk), visceral adiposity, serum TG and glucose levels. It increased serum adiponectin levels, reduced myocardial IFSs in both groups and activated baseline myocardial STAT‐3 and PKB/Akt, ERK42/44 and GSK‐3β during reperfusion. Overall, short‐term melatonin administration to obese/insulin resistant rats reduced insulin resistance and protected the heart against ex vivo myocardial IRI independently of body weight change and visceral adiposity.
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Melatonin administration decreases the circulating leptin levels in most animal models, however, the results are inconsistent in human studies.
“Melatonin administration decreases the circulating leptin levels in most animal models, 29,30 however, the results are inconsistent in human studies. 19,31”
From Melatonin supplementation improves glycemic hemostasis, lipid profile, and adipokine concentrations of obese women: A double-blind randomized clinical trial (2024) · cites this paper as [30]
Different animal models and clinical studies approved the melatonin's effect on the treatment of circulating adiponectin.
“Different animal models and clinical studies approved the melatonin's effect on the treatment of circulating adiponectin. 19,29,30”
From Melatonin supplementation improves glycemic hemostasis, lipid profile, and adipokine concentrations of obese women: A double-blind randomized clinical trial (2024) · cites this paper as [30]
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MELATONIN AS POTENTIAL CARDIOPROTECTOR: EXPERIMENTAL - CLINICAL ANALISIS OF EFFECTITY
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- Authors
- Nduhirabandi, F., Huisamen, B., Strijdom, H., Blackhurst, D., & Lochner, A.
- Affiliations
- Stellenbosch University (ZA)
- University of Cape Town (ZA)
- Corresponding author
- Nduhirabandi, Frederic
- Venue
- Journal of Pineal Research
- Publisher
- Wiley
- Published
- 2014-09-20
- Volume
- 57
- Issue
- 3
- Pages
- 317-332
- ISSN
- 0742-3098 (ISSN-L)
- 1600-079X
- OpenAlex
- W2028739777
- Cited by
- 48
- References
- 71
- Citations by year
- 2026: 1 · 2024: 2 · 2023: 3 · 2022: 2 · 2021: 4 · 2020: 5 · 2019: 6 · 2018: 7 · 2017: 7 · 2016: 6 · 2015: 5
- FWCI
- 2.92
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Journal of Pineal Research (publishedVersion)
- PubMed (publishedVersion)
- Funders
- South African National Research Fundation and Harry Crossley Foundation
- Topics
- Life Sciences › Neuroscience › Endocrine and Autonomic Systems › Circadian rhythm and melatonin
- Health Sciences › Medicine › Pathology and Forensic Medicine › Cardiac Ischemia and Reperfusion
- Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Cardiac Fibrosis and Remodeling
- Keywords
- melatonin, diet-induced obesity, insulin resistance, myocardial ischemia-reperfusion injury, cardioprotection, visceral fat, adiponectin, STAT3 signaling, Akt signaling, GSK3β, myocardial infarct size, cardiac hypertrophy, HOMA index
- MeSH terms
- Animals, Body Weight, Heart, Melatonin, Obesity, Intra-Abdominal Fat, Rats
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