Impaired cholinergic dilator response of resistance arteries isolated from patients with Raynaud's disease

PJW Smith*, CJ Ferro, DS McQueen, DJ Webb

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

Abstract

Aims We examined the effect of cooling on the response to the endothelium-dependent and -independent dilators, acetylcholine (ACh) and sodium nitroprusside (SNP), respectively, in human microvessels in vitro, and compared the responses between Raynaud's disease (RD) patients and controls, in order to assess the pathogenic role of the endothelium in RD.

Methods Subcutaneous resistance arteries were dissected from gluteal fat biopsies taken from patients with RD (n = 18) and h-om age-and sex-matched control subjects (n = 17). Vessels were cannulated in a small vessel arteriograph, in which a pressure of 50 mmHg was maintained across the vessel wall. Cumulative concentration response curves for ACh (10(-10)-10(-4) M) and SNP (10(-10)-10(-3) M) were generated in vessels at either 37 degrees C or 24 degrees C, with endothelium intact for ACh and removed for SNP (n = 6 per group).

Results Neither dilator showed significant differences in sensitivity when comparing responses between vessels from RD patients and controls, at either temperature, but the maximal relaxation to ACh was depressed in vessels from RD patients compared with controls at 37 degrees C (E-max = 45 +/- 13 in RD vs 89 +/- 4 in controls; P = 0.004).

Conclusions These results support the hypothesis that impaired endothelium-dependent vasodilatation is involved in the pathophysiology of RD.

Original languageEnglish
Pages (from-to)507-513
Number of pages7
JournalBritish Journal of Clinical Pharmacology
Volume47
Issue number5
DOIs
Publication statusPublished - May 1999

Keywords

  • cooling
  • endothelium
  • human
  • nitric oxide
  • Raynaud's disease
  • resistance arteries
  • NORMOTENSIVE SUBJECTS
  • NITRIC-OXIDE
  • IN-VITRO
  • TEMPERATURE
  • INHIBITION
  • PREVALENCE
  • MIGRAINE
  • VESSELS
  • RELEASE

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