Altered thyroid status affects myocardial expression of connexin-43 and susceptibility of rat heart to malignant arrhythmias that can be partially normalized by red palm oil intake
Jazyk angličtina Země Německo Médium print-electronic
Typ dokumentu časopisecké články
PubMed
27600718
DOI
10.1007/s00418-016-1488-6
PII: 10.1007/s00418-016-1488-6
Knihovny.cz E-zdroje
- Klíčová slova
- Cardiac arrhythmias, Connexin-43, PKC, Red palm oil, Thyroid hormones,
- MeSH
- aplikace orální MeSH
- konexin 43 antagonisté a inhibitory genetika metabolismus MeSH
- krysa rodu Rattus MeSH
- messenger RNA antagonisté a inhibitory genetika metabolismus MeSH
- myokard metabolismus MeSH
- oleje rostlin aplikace a dávkování farmakologie MeSH
- palmový olej MeSH
- potkani Wistar MeSH
- srdce účinky léků MeSH
- srdeční arytmie farmakoterapie metabolismus MeSH
- štítná žláza účinky léků metabolismus MeSH
- zvířata MeSH
- Check Tag
- krysa rodu Rattus MeSH
- mužské pohlaví MeSH
- ženské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- Gja1 protein, rat MeSH Prohlížeč
- konexin 43 MeSH
- messenger RNA MeSH
- oleje rostlin MeSH
- palmový olej MeSH
We aimed to study the impact of altered thyroid status on myocardial expression of electrical coupling protein connexin-43 (Cx43), the susceptibility of rats to ventricular fibrillation (VF) and the effects of antioxidant-rich red palm oil (RPO). Adult male and female euthyroid, hyperthyroid (treated with T3/T4), hypothyroid (treated with methimazole) Wistar rats supplemented or not with RPO for 6 weeks were used. Function of isolated perfused heart and VF threshold were determined. Left ventricular tissue was used for assessment of mRNA and protein levels of Cx43, its phosphorylated forms and topology. Protein kinase C signaling (PKC) and gene transcripts of some proteins related to cardiac arrhythmias were assessed. Hyperthyroid state resulted in decrease of total and phosphorylated forms of Cx43 and suppression of PKC-ε expression in males and females, decrease of Cx43 mRNA in females, decrease of VF threshold and increase of functional parameters in male rat hearts. In contrast, hypothyroid status resulted in the increase of total and phosphorylated forms of Cx43, enhancement PKC-ε expression in males and females, increase of Cx43 mRNA in females, increase of VF threshold and decrease of functional parameters in male rat hearts. Function of the heart was partially normalized by RPO intake, which also enhanced myocardial Cx43 and PKC-ε expression as well as increased VF threshold in hyperthyroid male rats. We conclude that there is an inverse relationship between myocardial expression of Cx43, including its functional phosphorylated forms, and susceptibility of male rat hearts to VF in condition of altered thyroid status. RPO intake partly ameliorated adverse changes caused by excess of thyroid hormones.
Department of Physiology Faculty of Science Charles University Prague Czech Republic
Institute of Experimental Pharmacology and Toxicology SAS Bratislava Slovak Republic
Institute of Physiology v v i Academy of Sciences of the Czech Republic Prague Czech Republic
Zobrazit více v PubMed
Pflugers Arch. 2009 Oct;458(6):1061-8 PubMed
Physiol Res. 2005;54(6):705-8 PubMed
Endocrinology. 2009 Jan;150(1):546-54 PubMed
Circ Res. 1996 Sep;79(3):388-98 PubMed
J Hypertens. 2013 Sep;31(9):1876-85 PubMed
J Mol Cell Cardiol. 1995 Aug;27(8):1731-43 PubMed
J Clin Endocrinol Metab. 2000 Dec;85(12):4701-5 PubMed
Horm Metab Res. 2013 Jul;45(7):507-12 PubMed
Biochim Biophys Acta. 2005 Dec 20;1719(1-2):36-58 PubMed
Exp Physiol. 1998 Nov;83(6):763-70 PubMed
Can J Physiol Pharmacol. 2013 Aug;91(8):633-9 PubMed
Physiol Res. 2008;57 Suppl 2:S91-6 PubMed
Mol Cell Biochem. 1996 Apr 12-26;157(1-2):93-9 PubMed
Physiol Res. 2014;63 Suppl 1:S119-31 PubMed
Med Princ Pract. 2013;22(1):42-6 PubMed
Horm Metab Res. 2011 Jan;43(1):43-7 PubMed
Physiol Res. 2008;57 Suppl 2:S1-S13 PubMed
Physiol Res. 2013;62(4):445-53 PubMed
Int J Biochem Cell Biol. 2010 Nov;42(11):1767-70 PubMed
Circ Res. 2000 Apr 14;86(7):723-8 PubMed
Exp Physiol. 2004 Sep;89(5):629-36 PubMed
Mol Cell Biochem. 1993 Dec 22;129(2):145-59 PubMed
Heart Fail Rev. 2015 May;20(3):273-82 PubMed
J Mol Histol. 2004 Jun;35(5):463-70 PubMed
J Clin Invest. 2010 Jan;120(1):266-79 PubMed
J Physiol Pharmacol. 2008 Jun;59(2):271-85 PubMed
Histochem Cell Biol. 2014 Dec;142(6):677-84 PubMed
Physiol Res. 2014;63 Suppl 1:S133-40 PubMed
J Appl Physiol (1985). 2015 Dec 15;119(12 ):1487-93 PubMed
Thyroid. 2002 Jun;12(6):447-52 PubMed
Circ Res. 1981 Jul;49(1):1-15 PubMed
Life Sci. 2004 Jul 9;75(8):923-31 PubMed
Circulation. 2005 Nov 15;112(20):3122-30 PubMed
Cardiovasc Res. 1998 Nov;40(2):343-51 PubMed
Mol Cell Biochem. 2011 Jul;353(1-2):235-41 PubMed
J Physiol Pharmacol. 2015 Feb;66(1):83-9 PubMed
Physiol Res. 2001;50(6):619-26 PubMed
Physiol Res. 2008;57 Suppl 2:S39-48 PubMed
Adv Cardiol. 2006;42:243-54 PubMed
Cardiovasc Drugs Ther. 2006 Dec;20(6):463-9 PubMed
J Electrocardiol. 2015 May-Jun;48(3):434-40 PubMed
Vascul Pharmacol. 2010 Mar-Apr;52(3-4):102-12 PubMed
Anti-Fibrotic Potential of Angiotensin (1-7) in Hemodynamically Overloaded Rat Heart