Affiliation:
1. SULEYMAN DEMIREL UNIVERSITY, SCHOOL OF MEDICINE
2. SÜLEYMAN DEMİREL ÜNİVERSİTESİ
Abstract
Objective
Acrylamide (ACR) is a harmful organic reactive compound
widely used in different industrial fields. Sele-
nium (SEL) is a trace element that takes part in some
chemical and enzymatic reactions in both animals
and human organisms and can cause some disorders
in many systems such as the cardiovascular
system in case of deficiency. The aim of this study is
to investigate whether SEL has a protective effect on
cardiac tissue in experimentally induced ACR toxicity
in rats.
Material and Method
A total of 28 rats were randomly and equally divided
into four groups: Control, SEL, ACR, SEL + ACR. At
the end of the study, cardiac markers such as creatine
kinase MB (CKMB), lactate dehydrogenase (LDH)
and ischemia-modified albumin (IMA) from blood
samples were measured. Oxidative stress markers
such as total oxidant status (TOS), total antioxidant
status (TAS) and oxidative stress index (OSI) in heart
tissue were analyzed. In addition, inducible nitric oxide
synthase iNOS activities were determined in heart
sections using immunohistochemical methods.
Results
The ACR + SEL group showed a significant decrease
in TOS, OSI, CKMB, LDH, IMA levels and significant
increase in TAS level compared to the ACR group.
In histopathological and immunohistochemical evaluation
of the heart sections; Disorganization in cardiac
muscle fibers, increased connective tissue between
muscle fibers and irregular eosinophilia in muscle
fibers were detected in ACR group. A decrease in
histopathological findings was observed in the SEL
treated groups compared to the ACR group. iNOS
immunoreactivities; moderate marking was observed
in the ACR group sections, while poor marking was
observed in the ACR + SEL group.
Conclusion
We determined that ACR caused damage to the heart
tissue of rats through various metabolic pathways and
that these damages were reversed in the groups given
the SEL.
Publisher
Medical Journal of Suleyman Demirel University