دورية أكاديمية

Evaluation of the Canonical Wnt Signaling Pathway in the Hearts of Hypertensive Rats of Various Etiologies.

التفاصيل البيبلوغرافية
العنوان: Evaluation of the Canonical Wnt Signaling Pathway in the Hearts of Hypertensive Rats of Various Etiologies.
المؤلفون: Młynarczyk MA; Department of Histology and Cytophysiology, Medical University of Bialystok, 15-222 Bialystok, Poland., Domian N; Department of Histology and Cytophysiology, Medical University of Bialystok, 15-222 Bialystok, Poland., Kasacka I; Department of Histology and Cytophysiology, Medical University of Bialystok, 15-222 Bialystok, Poland.
المصدر: International journal of molecular sciences [Int J Mol Sci] 2024 Jun 11; Vol. 25 (12). Date of Electronic Publication: 2024 Jun 11.
نوع المنشور: Journal Article
اللغة: English
بيانات الدورية: Publisher: MDPI Country of Publication: Switzerland NLM ID: 101092791 Publication Model: Electronic Cited Medium: Internet ISSN: 1422-0067 (Electronic) Linking ISSN: 14220067 NLM ISO Abbreviation: Int J Mol Sci Subsets: MEDLINE
أسماء مطبوعة: Original Publication: Basel, Switzerland : MDPI, [2000-
مواضيع طبية MeSH: Wnt Signaling Pathway* , Hypertension*/metabolism , Hypertension*/etiology , Hypertension*/chemically induced , Hypertension*/pathology , Glycogen Synthase Kinase 3 beta*/metabolism , Myocardium*/metabolism , Myocardium*/pathology , beta Catenin*/metabolism , beta Catenin*/genetics, Animals ; Rats ; Male ; Wnt1 Protein/metabolism ; Wnt1 Protein/genetics ; Rats, Inbred SHR ; Frizzled Receptors/metabolism ; Frizzled Receptors/genetics ; Desoxycorticosterone Acetate
مستخلص: Wnt/β-catenin signaling dysregulation is associated with the pathogenesis of many human diseases, including hypertension and heart disease. The aim of this study was to immunohistochemically evaluate and compare the expression of the Fzd8, WNT1, GSK-3β, and β-catenin genes in the hearts of rats with spontaneous hypertension (SHRs) and deoxycorticosterone acetate (DOCA)-salt-induced hypertension. The myocardial expression of Fzd8, WNT1, GSK-3β, and β-catenin was detected by immunohistochemistry, and the gene expression was assessed with a real-time PCR method. In SHRs, the immunoreactivity of Fzd8, WNT1, GSK-3β, and β-catenin was attenuated in comparison to that in normotensive animals. In DOCA-salt-induced hypertension, the immunoreactivity of Fzd8, WNT1, GSK-3β, and β-catenin was enhanced. In SHRs, decreases in the expression of the genes encoding Fzd8, WNT1, GSK-3β, and β-catenin were observed compared to the control group. Increased expression of the genes encoding Fzd8, WNT1, GSK-3β, and β-catenin was demonstrated in the hearts of rats with DOCA-salt-induced hypertension. Wnt signaling may play an essential role in the pathogenesis of arterial hypertension and the accompanying heart damage. The obtained results may constitute the basis for further research aimed at better understanding the role of the Wnt/β-catenin pathway in the functioning of the heart.
References: Dev Cell. 2009 Jul;17(1):9-26. (PMID: 19619488)
Circulation. 1993 Sep;88(3):1222-7. (PMID: 8353884)
Pharmacol Rev. 2018 Jan;70(1):68-141. (PMID: 29247129)
Adv Med Sci. 2022 Mar;67(1):87-94. (PMID: 35101653)
Int J Mol Sci. 2020 May 30;21(11):. (PMID: 32486158)
Cardiovasc Res. 2011 Oct 1;92(1):95-105. (PMID: 21693625)
JACC Heart Fail. 2017 Aug;5(8):543-551. (PMID: 28711447)
Acta Pharmacol Sin. 2019 Jan;40(1):9-12. (PMID: 30002488)
J Am Soc Nephrol. 2015 Jan;26(1):107-20. (PMID: 25012166)
Diabetes. 2015 Oct;64(10):3342-4. (PMID: 26405272)
Front Mol Biosci. 2021 Nov 03;8:771208. (PMID: 34805278)
Nat Rev Dis Primers. 2018 Mar 22;4:18014. (PMID: 29565029)
Nat Commun. 2017 Sep 28;8(1):712. (PMID: 28959037)
EMBO J. 2012 Jan 18;31(2):429-42. (PMID: 22085926)
Proc Natl Acad Sci U S A. 2008 Dec 16;105(50):19762-7. (PMID: 19073933)
Biochem Biophys Res Commun. 2016 May 6;473(3):698-703. (PMID: 26626076)
Sci Rep. 2018 Jun 12;8(1):8996. (PMID: 29895976)
Dev Dyn. 2016 Mar;245(3):294-306. (PMID: 26638115)
Cells. 2021 Sep 14;10(9):. (PMID: 34572061)
Cell Regen. 2015 Jul 08;4(1):3. (PMID: 26157574)
Basic Res Cardiol. 2010 Sep;105(5):597-608. (PMID: 20376467)
Trends Endocrinol Metab. 2012 Dec;23(12):628-36. (PMID: 22902904)
Cardiovasc Pathol. 2017 Nov - Dec;31:9-16. (PMID: 28802159)
PLoS One. 2020 Mar 2;15(3):e0229462. (PMID: 32119722)
J Mol Cell Cardiol. 1999 Feb;31(2):333-43. (PMID: 10093046)
Circ Res. 2010 Jul 23;107(2):186-99. (PMID: 20651295)
Physiology (Bethesda). 2017 Mar;32(2):112-125. (PMID: 28202622)
Exp Biol Med (Maywood). 2018 Nov;243(15-16):1199-1206. (PMID: 30472885)
Biochim Biophys Acta Mol Basis Dis. 2019 Jun 1;1865(6):1313-1322. (PMID: 30710617)
J Mol Histol. 2013 Oct;44(5):565-73. (PMID: 23591738)
Adv Med Sci. 2014 Sep;59(2):190-5. (PMID: 25323756)
Postepy Hig Med Dosw (Online). 2013 Nov 26;67:1098-108. (PMID: 24379251)
J Hum Hypertens. 2021 May;35(5):383-386. (PMID: 33046827)
Cell. 2017 Jun 1;169(6):985-999. (PMID: 28575679)
Hum Mol Genet. 2015 Feb 1;24(3):802-13. (PMID: 25274778)
Am Fam Physician. 2017 Oct 1;96(7):453-461. (PMID: 29094913)
فهرسة مساهمة: Keywords: Wnt/β-catenin; arterial hypertension; essential hypertension; myocardium; secondary hypertension
المشرفين على المادة: EC 2.7.11.1 (Glycogen Synthase Kinase 3 beta)
0 (beta Catenin)
0 (Wnt1 Protein)
0 (Frizzled Receptors)
6E0A168OB8 (Desoxycorticosterone Acetate)
0 (Wnt1 protein, rat)
تواريخ الأحداث: Date Created: 20240627 Date Completed: 20240627 Latest Revision: 20240629
رمز التحديث: 20240629
مُعرف محوري في PubMed: PMC11204257
DOI: 10.3390/ijms25126428
PMID: 38928134
قاعدة البيانات: MEDLINE
الوصف
تدمد:1422-0067
DOI:10.3390/ijms25126428