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Thyroxine Induces Acute Relaxation of Rat Skeletal Muscle Arteries Via Integrin αvβ3, ERK1/2 and Integrin-Linked Kinase

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Journal Front Physiol
Date 2021 Oct 1
PMID 34594239
Citations 1
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Abstract

Hyperthyroidism is associated with a decreased peripheral vascular resistance, which could be caused by the vasodilator genomic or non-genomic effects of thyroid hormones (TH). Non-genomic, or acute, effects develop within several minutes and involve a wide tissue-specific spectrum of molecular pathways poorly studied in vasculature. We aimed to investigate the mechanisms of acute effects of TH on rat skeletal muscle arteries. Sural arteries from male Wistar rats were used for isometric force recording (wire myography) and phosphorylated protein content measurement (Western blotting). Both triiodothyronine (T3) and thyroxine (T4) reduced contractile response of sural arteries to α-adrenoceptor agonist methoxamine. The effect of T4 was more prominent than T3 and not affected by iopanoic acid, an inhibitor of deiodinase 2. Endothelium denudation abolished the effect of T3, but not T4. Integrin αvβ3 inhibitor tetrac abolished the effect of T4 in endothelium-denuded arteries. T4 weakened methoxamine-induced elevation of phospho-MLC2 (Ser19) content in arterial samples. The effect of T4 in endothelium-denuded arteries was abolished by inhibiting ERK1/2 activation with U0126 as well as by ILK inhibitor Cpd22 but persisted in the presence of Src- or Rho-kinase inhibitors (PP2 and Y27632, respectively). Acute non-genomic relaxation of sural arteries induced by T3 is endothelium-dependent and that induced by T4 is endothelium-independent. The effect of T4 on α-adrenergic contraction is stronger compared to T3 and involves the suppression of extracellular matrix signaling via integrin αvβ3, ERK1/2 and ILK with subsequent decrease of MLC2 (Ser19) phosphorylation.

Citing Articles

Myography of isolated blood vessels: Considerations for experimental design and combination with supplementary techniques.

Schubert R, Gaynullina D, Shvetsova A, Tarasova O Front Physiol. 2023; 14:1176748.

PMID: 37168231 PMC: 10165122. DOI: 10.3389/fphys.2023.1176748.

References
1.
Hones G, Rakov H, Logan J, Liao X, Werbenko E, Pollard A . Noncanonical thyroid hormone signaling mediates cardiometabolic effects in vivo. Proc Natl Acad Sci U S A. 2017; 114(52):E11323-E11332. PMC: 5748168. DOI: 10.1073/pnas.1706801115. View

2.
Gaynullina D, Kudryashova T, Vorotnikov A, Schubert R, Tarasova O . MAPKs Are Highly Abundant but Do Not Contribute to α-Adrenergic Contraction of Rat Saphenous Arteries in the Early Postnatal Period. Int J Mol Sci. 2021; 22(11). PMC: 8199737. DOI: 10.3390/ijms22116037. View

3.
Cao X, Kambe F, Moeller L, Refetoff S, Seo H . Thyroid hormone induces rapid activation of Akt/protein kinase B-mammalian target of rapamycin-p70S6K cascade through phosphatidylinositol 3-kinase in human fibroblasts. Mol Endocrinol. 2004; 19(1):102-12. DOI: 10.1210/me.2004-0093. View

4.
Lin H, Mousa S, Davis P . Demonstration of the Receptor Site for Thyroid Hormone on Integrin αvβ3. Methods Mol Biol. 2018; 1801:61-65. DOI: 10.1007/978-1-4939-7902-8_7. View

5.
Vargas F, Manuel Moreno J, Rodriguez-Gomez I, Wangensteen R, Osuna A, Alvarez-Guerra M . Vascular and renal function in experimental thyroid disorders. Eur J Endocrinol. 2006; 154(2):197-212. DOI: 10.1530/eje.1.02093. View