The Effect of Chemerin on Cardiac Parameters and Gene Expressions in Isolated Perfused Rat Heart

Background: Chemerin is a novel chemoattractant adipokine expressed in cardiovascular system, and its receptor has been detected in the epicardial adipose tissue. Aims: To determine the effects of chemerin on the cardiac parameters and gene expressions in the isolated perfused rat heart. Study Des...

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Main Authors: Özden Kutlay, Ziya Kaygısız, Bilgin Kaygısız
Format: Article
Language:English
Published: Galenos Publishing House 2019-01-01
Series:Balkan Medical Journal
Subjects:
Online Access:http://balkanmedicaljournal.org/text.php?lang=en&id=2042
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author Özden Kutlay
Ziya Kaygısız
Bilgin Kaygısız
author_facet Özden Kutlay
Ziya Kaygısız
Bilgin Kaygısız
author_sort Özden Kutlay
collection DOAJ
description Background: Chemerin is a novel chemoattractant adipokine expressed in cardiovascular system, and its receptor has been detected in the epicardial adipose tissue. Aims: To determine the effects of chemerin on the cardiac parameters and gene expressions in the isolated perfused rat heart. Study Design: Animal experiment. Methods: The hearts were retrogradely perfused with Langendorff technique to measure the cardiac parameters. The experimental groups were acutely treated with 10, 100, and 1000 nM doses of chemerin. Another group was given 10 μM L-nitric oxide synthase inhibitor for 5 min before 1000 nM chemerin administration. The real-time polymerase chain reaction was performed for detecting the expression of target genes. Results: All doses of chemerin significantly decreased the left ventricular developed pressure (max 35.33 ∆%, p<0.001), and +dP/dtmax (max 31.3 ∆%, p<0.001), which are the indexes of cardiac contractile force. In addition, 1000 nM chemerin reduced the coronary flow (max 31 ∆%, p<0.001). N(W)-nitro-L-arginine methyl ester antagonized the negative inotropic effect of chemerin on contractility. Chemerin induced a 2.16-fold increase in endothelial nitric oxide synthase mRNA and increased the cyclic guanosine monophosphate levels (p<0.001) but decreased the PI3Kγ gene expression (1.8-fold, p<0.001). Furthermore, all doses of chemerin decreased the CaV1.2 gene expression (1.69-fold, p<0.001). Conclusion: Acute chemerin treatment induces a negative inotropic action with the involvement of nitric oxide pathway, CaV1.2, and PI3Kγ on isolated rat heart.
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spelling doaj.art-2f0c324d82f348d49d7d8a3c7db2eff02023-02-15T16:18:12ZengGalenos Publishing HouseBalkan Medical Journal2146-31232146-31312019-01-01361434810.4274/balkanmedj.2017.1787The Effect of Chemerin on Cardiac Parameters and Gene Expressions in Isolated Perfused Rat HeartÖzden Kutlay0Ziya Kaygısız1Bilgin Kaygısız2Department of Physiology, Eskişehir Osmangazi University School of Medicine, Eskişehir, TurkeyDepartment of Physiology, Eskişehir Osmangazi University School of Medicine, Eskişehir, TurkeyDepartment of Pharmacology, Eskişehir Osmangazi University School of Medicine, Eskişehir, Turkey Background: Chemerin is a novel chemoattractant adipokine expressed in cardiovascular system, and its receptor has been detected in the epicardial adipose tissue. Aims: To determine the effects of chemerin on the cardiac parameters and gene expressions in the isolated perfused rat heart. Study Design: Animal experiment. Methods: The hearts were retrogradely perfused with Langendorff technique to measure the cardiac parameters. The experimental groups were acutely treated with 10, 100, and 1000 nM doses of chemerin. Another group was given 10 μM L-nitric oxide synthase inhibitor for 5 min before 1000 nM chemerin administration. The real-time polymerase chain reaction was performed for detecting the expression of target genes. Results: All doses of chemerin significantly decreased the left ventricular developed pressure (max 35.33 ∆%, p<0.001), and +dP/dtmax (max 31.3 ∆%, p<0.001), which are the indexes of cardiac contractile force. In addition, 1000 nM chemerin reduced the coronary flow (max 31 ∆%, p<0.001). N(W)-nitro-L-arginine methyl ester antagonized the negative inotropic effect of chemerin on contractility. Chemerin induced a 2.16-fold increase in endothelial nitric oxide synthase mRNA and increased the cyclic guanosine monophosphate levels (p<0.001) but decreased the PI3Kγ gene expression (1.8-fold, p<0.001). Furthermore, all doses of chemerin decreased the CaV1.2 gene expression (1.69-fold, p<0.001). Conclusion: Acute chemerin treatment induces a negative inotropic action with the involvement of nitric oxide pathway, CaV1.2, and PI3Kγ on isolated rat heart.http://balkanmedicaljournal.org/text.php?lang=en&id=2042Animal experimentchemerincyclic guanosine monophosphateendothelial nitric oxide synthaseheart contractility
spellingShingle Özden Kutlay
Ziya Kaygısız
Bilgin Kaygısız
The Effect of Chemerin on Cardiac Parameters and Gene Expressions in Isolated Perfused Rat Heart
Balkan Medical Journal
Animal experiment
chemerin
cyclic guanosine monophosphate
endothelial nitric oxide synthase
heart contractility
title The Effect of Chemerin on Cardiac Parameters and Gene Expressions in Isolated Perfused Rat Heart
title_full The Effect of Chemerin on Cardiac Parameters and Gene Expressions in Isolated Perfused Rat Heart
title_fullStr The Effect of Chemerin on Cardiac Parameters and Gene Expressions in Isolated Perfused Rat Heart
title_full_unstemmed The Effect of Chemerin on Cardiac Parameters and Gene Expressions in Isolated Perfused Rat Heart
title_short The Effect of Chemerin on Cardiac Parameters and Gene Expressions in Isolated Perfused Rat Heart
title_sort effect of chemerin on cardiac parameters and gene expressions in isolated perfused rat heart
topic Animal experiment
chemerin
cyclic guanosine monophosphate
endothelial nitric oxide synthase
heart contractility
url http://balkanmedicaljournal.org/text.php?lang=en&id=2042
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