Abstract | AIMS: MAIN METHODS: Male Wistar rats (190-210 g) were divided into 4 groups: Control, O2-treated control, untreated diabetes, and O2-treated diabetes. Diabetes was induced using high-fat diet followed by a low-dose of streptozotocin (30 mg/kg). Hyperoxia sessions were included 2-h exposure to 95% oxygen, repeated 6 days/week for 5 weeks. Serum fasting glucose, insulin, lactate, and lipid profile were measured before, during, and after hyperoxia. Glucose and pyruvate tolerance tests, and histological evaluations of interscapular and epididymal fats were done at the end of study. KEY FINDINGS: O2-treated diabetic rats compared to untreated ones, displayed lower weight gain, improved glucose-tolerance, insulin sensitivity, and more favorable lipid profile. In diabetic rats, hyperoxia increased surface area (6.36 ± 0.93 vs. 0.86 ± 0.16 mm2, P < 0.001), and volume density (1.53 ± 0.22 vs. 0.21 ± 0.04 mm3, P < 0.001) of interscapular adipose tissue; hyperoxia also increased protein levels of uncoupling protein 1 (UCP1), peroxisome proliferator activated receptor gamma ( PPAR-γ), and PPAR-γ coactivator 1 alpha (PGC1-α) in interscapular adipose tissue. The numerical density (541.7 ± 7.3 vs. 298.1 ± 11.7 mm3, P < 0.001) of epididymal fat were also higher. SIGNIFICANCE: This study showed that beneficial metabolic effects of hyperoxia in obese type 2 diabetic rats including improved insulin sensitivity and glucose tolerance are at least in part due to browning of adipose tissue.
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Authors | Reza Norouzirad, Mahboubeh Ghanbari, Zahra Bahadoran, Mohammad Amin Abdollahifar, Neda Rasouli, Asghar Ghasemi |
Journal | Life sciences
(Life Sci)
Vol. 220
Pg. 58-68
(Mar 01 2019)
ISSN: 1879-0631 [Electronic] Netherlands |
PMID | 30703383
(Publication Type: Journal Article)
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Copyright | Copyright © 2019 Elsevier Inc. All rights reserved. |
Chemical References |
- Insulin
- Streptozocin
- Glucose
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Topics |
- Adipocytes, Brown
- Adipocytes, White
- Adipose Tissue, Brown
(metabolism)
- Adipose Tissue, White
(metabolism)
- Animals
- Carbohydrate Metabolism
(physiology)
- Diabetes Mellitus, Experimental
(metabolism)
- Diabetes Mellitus, Type 2
(metabolism)
- Diet, High-Fat
- Disease Models, Animal
- Glucose
(metabolism)
- Glucose Tolerance Test
- Hyperoxia
(metabolism)
- Insulin
(metabolism)
- Insulin Resistance
- Male
- Obesity
(metabolism)
- Rats
- Rats, Wistar
- Streptozocin
(pharmacology)
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