Examining the Effects of Hyperbaric Oxygen Therapy on the Cardiovascular System and Oxidative Stress in Insulin-Treated and Non-Treated Diabetic Rats

Author:

Ristic Petar1,Savic Maja2ORCID,Bolevich Sergey3,Bolevich Stefani34,Orlova Alexandra3,Mikhaleva Anastasiya3,Kartashova Anna3,Yavlieva Koka3,Nikolic Turnic Tamara25ORCID,Pindovic Bozidar2ORCID,Djordjevic Katarina2,Srejovic Ivan67ORCID,Zivkovic Vladimir67,Jakovljevic Vladimir36ORCID

Affiliation:

1. Clinic of Endocrinology, Military Medical Academy, 11000 Belgrade, Serbia

2. Department of Pharmacy, Faculty of Medical Sciences, University of Kragujevac, 34000 Kragujevac, Serbia

3. Department of Human Pathology, I.M. Sechenov First Moscow State Medical University, 119991 Moscow, Russia

4. Department of Pathophysiology, I.M. Sechenov First Moscow State Medical University, 119991 Moscow, Russia

5. N.A. Semashko Public Health and Healthcare Department, F.F. Erismann Institute of Public Health, I.M. Sechenov First Moscow State Medical University, 119991 Moscow, Russia

6. Department of Physiology, Faculty of Medical Sciences, University of Kragujevac, 34000 Kragujevac, Serbia

7. Departmennt of Pharmacology, Institute of Biodesign and Complex System Modeling, I.M. Sechenov First Moscow State Medical University, 119991 Moscow, Russia

Abstract

Background: This study explored the effects of hyperbaric oxygen therapy (HBOT) on the cardiovascular system and oxidative stress in streptozotocin-induced diabetic rats. Wistar albino rats were divided into four groups: DM group (diabetic rats), DM+HBOT group (diabetic rats exposed to HBOT for 1 h daily, five days a week, at 2.8 atmosphere absolute (ATA) with 100% oxygen for two weeks), DM+INS group (diabetic rats treated with neutral protamine hagedorn (NPH) insulin at a dosage of 3–5 U/day), and DM+HBOT+INS group (diabetic rats treated with both NPH insulin and HBOT for two weeks). Methods: Evaluations included glycemic control, oxidative stress parameters, and cardiac function measurements. Results: NPH insulin treatment reduced blood glucose levels, although normoglycemia was not achieved. The DM+HBOT+INS group demonstrated the lowest pro-oxidative marker levels. NPH insulin treatment improved cardiac function, and combination therapy effectively restored cardiac function in diabetic animals. Conclusions: NPH insulin treatment reduced hyperglycemia and improved cardiac function in diabetic rats. The combined approach of NPH insulin and HBOT resulted in decreased pro-oxidative markers. These findings provide valuable insights for managing cardiovascular complications and oxidative stress in diabetes.

Publisher

MDPI AG

Subject

General Veterinary,Animal Science and Zoology

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