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Tytuł pozycji:

High-intensity exercise in hypoxia improves endothelial function via increased nitric oxide bioavailability in C57BL/6 mice.

Tytuł:
High-intensity exercise in hypoxia improves endothelial function via increased nitric oxide bioavailability in C57BL/6 mice.
Autorzy:
Lavier J; Division of Angiology, Heart and Vessel Department, Lausanne University Hospital (CHUV), Lausanne, Switzerland.; Institute of Sport Sciences, University of Lausanne, Lausanne, Switzerland.
Beaumann M; Neonatal Research Laboratory, Clinic of Neonatology, Department Woman-Mother-Child, Lausanne University Hospital (CHUV), Lausanne, Switzerland.
Menétrey S; Neonatal Research Laboratory, Clinic of Neonatology, Department Woman-Mother-Child, Lausanne University Hospital (CHUV), Lausanne, Switzerland.
Bouzourène K; Division of Angiology, Heart and Vessel Department, Lausanne University Hospital (CHUV), Lausanne, Switzerland.
Rosenblatt-Velin N; Division of Angiology, Heart and Vessel Department, Lausanne University Hospital (CHUV), Lausanne, Switzerland.
Pialoux V; Inter-University Laboratory of Human Movement Biology EA7424, University of Lyon, Villeurbanne, France.
Mazzolai L; Division of Angiology, Heart and Vessel Department, Lausanne University Hospital (CHUV), Lausanne, Switzerland.
Peyter AC; Neonatal Research Laboratory, Clinic of Neonatology, Department Woman-Mother-Child, Lausanne University Hospital (CHUV), Lausanne, Switzerland.
Pellegrin M; Division of Angiology, Heart and Vessel Department, Lausanne University Hospital (CHUV), Lausanne, Switzerland.
Millet GP; Institute of Sport Sciences, University of Lausanne, Lausanne, Switzerland.
Źródło:
Acta physiologica (Oxford, England) [Acta Physiol (Oxf)] 2021 Oct; Vol. 233 (2), pp. e13700. Date of Electronic Publication: 2021 Jun 19.
Typ publikacji:
Journal Article
Język:
English
Imprint Name(s):
Publication: Oxford : Wiley-Blackwell
Original Publication: Oxford : Blackwell Pub., c2006-4
MeSH Terms:
Nitric Oxide*/metabolism
Nitric Oxide Synthase Type III*/metabolism
Animals ; Biological Availability ; Endothelium, Vascular/metabolism ; Hypoxia/metabolism ; Mice ; Mice, Inbred C57BL
References:
Sleep. 2017 Aug 1;40(8):. (PMID: 28633495)
PLoS One. 2013;8(3):e59678. (PMID: 23527249)
PLoS One. 2014 Jan 20;9(1):e85450. (PMID: 24465565)
Front Physiol. 2016 Dec 21;7:631. (PMID: 28066264)
Cell Mol Immunol. 2015 Jan;12(1):5-23. (PMID: 25263488)
J Appl Physiol (1985). 2005 Sep;99(3):1029-35. (PMID: 15831799)
J Vis Exp. 2019 Mar 15;(145):. (PMID: 30933059)
Anal Biochem. 1988 Oct;174(1):331-6. (PMID: 3064653)
Sports Med. 2015 Feb;45(2):279-96. (PMID: 25281334)
J Clin Invest. 2002 Mar;109(6):765-75. (PMID: 11901185)
Basic Res Cardiol. 2013 Nov;108(6):389. (PMID: 24105420)
Acta Physiol (Oxf). 2021 Oct;233(2):e13700. (PMID: 34089562)
J Appl Physiol (1985). 2011 Mar;110(3):687-94. (PMID: 21193565)
Nitric Oxide. 2015 Feb 15;45:7-14. (PMID: 25619203)
J Transl Med. 2016 Jul 19;14(1):213. (PMID: 27435231)
Atherosclerosis. 2007 Jan;190(1):35-42. (PMID: 16529753)
Anal Biochem. 1993 Oct;214(1):11-6. (PMID: 7504409)
Korean J Physiol Pharmacol. 2020 Jan;24(1):53-68. (PMID: 31908575)
Methods Enzymol. 1984;105:457-64. (PMID: 6547201)
J Am Coll Cardiol. 2001 Feb;37(2):392-7. (PMID: 11216952)
J Physiol. 2012 Dec 15;590(24):6321-6. (PMID: 22988134)
J Appl Physiol (1985). 2011 Dec;111(6):1527-38. (PMID: 21885800)
Eur Heart J. 2021 Jan 1;42(1):17-96. (PMID: 32860412)
Med Sci Sports Exerc. 2015 Dec;47(12):2628-35. (PMID: 26057942)
Am J Cardiovasc Dis. 2017 Apr 15;7(2):64-71. (PMID: 28533932)
Eur Heart J. 2003 Sep;24(18):1681-9. (PMID: 14499232)
Hypertens Res. 2016 Feb;39(2):70-8. (PMID: 26537830)
J Sport Health Sci. 2018 Jan;7(1):109-119. (PMID: 30356452)
Circ Res. 2000 Nov 10;87(10):840-4. (PMID: 11073878)
J Appl Physiol (1985). 2003 Jul;95(1):20-5. (PMID: 12794092)
Med Sci Sports Exerc. 2021 Mar 1;53(3):559-573. (PMID: 32890201)
Curr Vasc Pharmacol. 2012 Jan;10(1):4-18. (PMID: 22112350)
Braz J Med Biol Res. 2015 Nov;48(11):996-1003. (PMID: 26397974)
Mol Cell Biochem. 2013 Mar;375(1-2):199-206. (PMID: 23242603)
Int J Health Sci (Qassim). 2020 Jan-Feb;14(1):3-8. (PMID: 31983915)
Front Physiol. 2019 Aug 16;10:1009. (PMID: 31474873)
Nat Rev Cardiol. 2016 Apr;13(4):193-209. (PMID: 26843289)
Cardiovasc Res. 2005 Jul 1;67(1):161-72. (PMID: 15949480)
J Am Coll Cardiol. 2004 Sep 15;44(6):1320-7. (PMID: 15364339)
Circ Res. 2016 Jul 8;119(2):375-96. (PMID: 27390338)
Kidney Int. 1996 May;49(5):1304-13. (PMID: 8731095)
Physiol Rev. 2015 Apr;95(2):549-601. (PMID: 25834232)
J Cereb Blood Flow Metab. 2007 Apr;27(4):776-84. (PMID: 16926845)
Med Sci Sports Exerc. 2018 Jan;50(1):124-130. (PMID: 28817509)
Sports Med. 2016 Nov;46(11):1725-1736. (PMID: 27286988)
Med Sci Sports Exerc. 2005 Jun;37(6):979-85. (PMID: 15947723)
Medicine (Baltimore). 2020 Sep 25;99(39):e22411. (PMID: 32991471)
Biochem J. 2002 Oct 15;367(Pt 2):467-73. (PMID: 12099887)
Glob Cardiol Sci Pract. 2014 Oct 16;2014(3):291-308. (PMID: 25780786)
Life Sci. 2019 Apr 1;222:36-45. (PMID: 30825543)
Sports Med. 2009;39(10):797-812. (PMID: 19757859)
Cardiovasc Res. 2009 Mar 1;81(4):723-32. (PMID: 19047339)
Am J Physiol Heart Circ Physiol. 2000 Oct;279(4):H1999-2005. (PMID: 11009490)
Clin Exp Pharmacol Physiol. 2015 Feb;42(2):179-85. (PMID: 25399833)
Contributed Indexing:
Keywords: endothelial function; exercise training; high-intensity; hypoxia; nitric oxide bioavailability
Substance Nomenclature:
31C4KY9ESH (Nitric Oxide)
EC 1.14.13.39 (Nitric Oxide Synthase Type III)
Entry Date(s):
Date Created: 20210605 Date Completed: 20211028 Latest Revision: 20211028
Update Code:
20240105
PubMed Central ID:
PMC8518730
DOI:
10.1111/apha.13700
PMID:
34089562
Czasopismo naukowe
Aim: The optimal exercise intensity to improve endothelial function remains unclear, as well as whether the addition of hypoxia could potentiate this function. Therefore, the aim of this study was to compare the effects of different exercise intensities in normoxia and hypoxia on vascular reactivity and nitric oxide (NO) bioavailability in mice.
Methods: C57BL/6 mice underwent treadmill running three times per week, for 4 weeks at either low, maximal or supramaximal intensity in normoxia or hypoxia (inspire oxygen fraction = 0.13). Vascular reactivity and expression of genes and proteins involved in NO production/bioavailability were assessed in aorta using isolated vessel tension experiments, RT-qPCR and western blot, respectively. Circulating NO metabolites and pro-/antioxidant markers were measured.
Results: Hypoxic exercise improved both acetylcholine-induced vasorelaxation and phenylephrine-induced vasoconstriction compared to normoxic exercise, independently of intensity. In hypoxia, a higher acetylcholine-induced vasorelaxation was observed with high intensities (supramaximal and maximal) compared to low intensity. Exercise protocols modulated endothelial nitric oxide synthase (eNOS) and α1-adrenergic receptor (α 1 -AR) mRNA level, but not superoxide dismutase 3 (SOD3) and p47phox. No significant differences were observed for protein expression of α 1 -AR, total eNOS, phosphorylated eNOS, SOD isoforms and p47phox. However, plasma SOD and catalase activities were significantly increased in hypoxic supramaximal compared to hypoxic low intensity, while concentration of nitrotyrosine significantly decreased. The latter was also observed in hypoxic maximal and supramaximal compared to the same intensities in normoxia.
Conclusion: Hypoxic high-intensity exercise increases NO bioavailability and improves vascular function, opening promising clinical perspectives for cardiovascular disease prevention.
(© 2021 The Authors. Acta Physiologica published by John Wiley & Sons Ltd on behalf of Scandinavian Physiological Society.)

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