Recombinant human thyrotropin enhances endothelial-mediated vasodilation of conduit arteries

J Clin Endocrinol Metab. 2009 Mar;94(3):1012-6. doi: 10.1210/jc.2008-2298. Epub 2008 Dec 23.

Abstract

Context: Endothelial cells possess receptors to TSH. Their role is largely unknown.

Objectives: The objective of the study was to determine whether elevated serum TSH levels, as occur in hypothyroidism, affect endothelial function of large arteries and vascular risk biomarkers.

Subjects and methods: Thirty-four consecutively recruited patients, who had undergone thyroidectomy for thyroid carcinoma, were studied in connection with one of the monitoring procedures based on recombinant human (rh) TSH administration. Flow-mediated dilation (FMD) of the brachial artery and serum vascular risk markers were measured at baseline and for 5 d after the administration of rhTSH (0.9 mg im on d 1 and 2). Holter electrocardiogram and echocardiography were performed on d 2.

Results: rhTSH caused a rapid increase in flow-mediated dilation from the basal value of 10.2 to 15.6% at 6 h (P < 0.0000001), to 16.1% on d 2 (P < 0.0000001), and to 14.9% on d 6 (P = 0.0015). The results were identical when the analysis was made in a subgroup of 19 patients free of vascular risk conditions. Vascular cell adhesion molecule-1, TNFalpha, IL-6, and high sensitive C-reactive protein were unaffected by rhTSH, whereas homocysteine was decreased. Arterial blood pressure, mean 24-h heart rate, and left ventricular function were unaffected by rhTSH.

Conclusions: rhTSH causes marked and persistent activation of the endothelial mediated vasodilation, independent of systemic hemodynamic changes.

MeSH terms

  • Brachial Artery / drug effects
  • Brachial Artery / physiology
  • Electrocardiography / drug effects
  • Endothelium, Vascular / physiology*
  • Female
  • Hemodynamics / drug effects
  • Humans
  • Male
  • Middle Aged
  • Recombinant Proteins / pharmacology
  • Thyrotropin / blood
  • Thyrotropin / pharmacology*
  • Vasodilation / drug effects*

Substances

  • Recombinant Proteins
  • Thyrotropin