Remote Myocardial Injury: The Protective Role of Fluoxetine

Autor: Hafize Uzun, Hayriye Erman, Nermin Yelmen, Ibrahim Guner, Mukaddes Pala, Gulderen Sahin, Mukaddes Esrefoglu, Onur M. Yaman, Remise Gelisgen, Olgu Enis Tok, Uğur Aksu
Přispěvatelé: EŞREFOĞLU, MUKADDES, Biruni Üniversitesi
Jazyk: angličtina
Rok vydání: 2017
Předmět:
0301 basic medicine
Lipid Peroxides
Infrarenal abdominal aorta
Cardiotonic Agents
Oxidant/Anti-Oxidant Balance
Physiology
Iron
Inflammation
medicine.disease_cause
Thiobarbituric Acid Reactive Substances
Antioxidants
Rats
Sprague-Dawley

03 medical and health sciences
Acute Cardiac Injury
Physiology (medical)
Fluoxetine
medicine
Animals
Creatine Kinase
Peroxidase
Ischemia-Reperfusion
Pharmacology
business.industry
Myocardium
Hemodynamics
Infrarenal Abdominal Aorta
General Medicine
Aortic surgery
Oxidants
Oxidative Stress
030104 developmental biology
Anesthesia
Reperfusion Injury
The Protective Role of Fluoxetine-
CANADIAN JOURNAL OF PHYSIOLOGY AND PHARMACOLOGY
cilt.3
ss.1-22
2017 [Yaman O.
Erman H.
Güner İ.
TOK O. E.
EŞREFOĞLU M.
Pala M.
Gelisgen R.
Uzun H.
Uğur A.
Yelmen N.
et al.
-Remote Myocardial Injury]

Cytokines
medicine.symptom
business
Oxidation-Reduction
Oxidative stress
Biomarkers
medicine.drug
Popis: Aortic cross-clamping-induced ischemia–reperfusion (IR) is an important factor in the development of postoperative acute cardiac injury following abdominal aortic surgery. We investigated the possible anti-oxidant/anti-inflammatory effects of fluoxetine (FLX), which is used widely as a preoperative anxiolytic on cardiac injury induced by IR of the infrarenal abdominal aorta. FLX was administered to IR-performed (60 min of ischemia and 120 min of reperfusion) rats for 3 days, once daily at 20 mg/kg i.p. dosage. Results were compared to control and non-FLX-treated IR-performed rats. Serum creatine kinase (CK) and CK-MB levels, lipid hydroperoxide, thiobarbituric acid reactive substances, and pro-oxidant/anti-oxidant balance levels in the IR group were significantly higher whereas superoxide dismutase activity, glutathione, and ferric reducing/anti-oxidant power levels were lower than for the control. IR also increased myeloperoxidase activity, tumor necrosis factor-α, interleukin-1β, and interleukin-6 and decreased interleukin-10 levels. FLX decreased CK, CK-MB, lipid hydroperoxide, thiobarbituric acid reactive substances, and pro-oxidant/anti-oxidant balance levels while increasing superoxide dismutase activity, glutathione, and ferric reducing/anti-oxidant power levels. FLX also decreased myeloperoxidase activity, tumor necrosis factor-α, interleukin-1β, and interleukin-6 levels and increased interleukin-10 levels compared to IR. FLX attenuated the morphological changes associated with cardiac injury. Our study clearly demonstrates that FLX confers protection against aortic IR-induced cardiac injury, tissue leucocyte infiltration, and cellular integrity via its anti-oxidant/anti-inflammatory effects.
Databáze: OpenAIRE