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FRI0366 A pilot study on ischemia and reperfusion injury during a raynaud's attack: sequential assessment of redox stress parameters in a unique cooling and rewarming experiment
  1. AM Van Roon1,
  2. A Eman Abdulle1,
  3. AM van Roon1,
  4. JD Lefrandt1,
  5. AJ Smit1,
  6. H Bootsma2,
  7. BO Fernandez3,
  8. M Minnion3,
  9. M Feelisch3,
  10. H van Goor4,
  11. DJ Mulder1
  1. 1Internal Medicine - Vascular Medicine
  2. 2Rheumatology and Clinical Immunology, University of Groningen - University Medical Center Groningen, Groningen, Netherlands
  3. 3Clinical and Experimental Sciences, University of Southampton, Southampton, United Kingdom
  4. 4Pathology, University of Groningen - University Medical Center Groningen, Groningen, Netherlands

Abstract

Background Oxidative stress plays a role in systemic sclerosis (SSc), but the molecular mechanisms involved are incompletely understood. During an attack of Raynaud's phenomenon (RP) a period of ischemia (I), followed by reperfusion (R) occurs frequently, associated with the severity of vasculopathy. [1] Only in secondary RP digital ulcers develop. We hypothesized that I/R injury may play a role in the pathogenesis and could offer new therapeutic targets.

Objectives To explore the course of oxidative stress in patients with SSc compared with primary RP and healthy controls.

Methods A total of 30 patients were included: 10 with limited cutaneous SSc (age: 57 (53–61) yr, male/female 5/5), 10 with primary RP (age: 54 (41–58), 2/8), and 10 healthy controls (age: 25 (22–25), 3/7). A standardized cooling experiment was performed and digital perfusion was assessed in all 5 fingers using photo-electric plethysmography: at baseline (T=0) the dominant hand was submerged in water at 33°C, followed by cooling in steps of 3°C every 4 minutes, until 6°C or when pain became intolerable (T=1). Recording was continued 10 (T=2) and 30 (T=3) minutes of rewarming to ambient temperature (23°C). Blood was drawn from ipsilateral cubital vein at T0, 1, 2 and 3, markers for tissue injury (lactate, LDH, creatinine phosphokinase (CPK) [routine methods]), redox status (free thiols corrected for total protein) and nitric oxide (NO) activity (NO2, NO3, RXNO) were measured in plasma. [1–3] Numbers are in median (IQR).

Results Baseline free thiols were significantly decreased in RP vs. controls (5.18 (4.79–5.63) vs 5.87 (5.41–5.99) umol/g, p=0.013), with no differences in lactate, LDH, CPK, and NO activity. Raynaud's attack was induced in all RP patients but not in controls. Median duration of hypoperfusion was greater in SSc vs. PRP (30 (27–35) vs. 12 (9–14) min, p=0.010), with a considerably longer recovery time (8 (4–10) vs. 0 (0–1) min, p=0.006). No changes were observed in lactate, LDH, and CPK levels. A rise in free thiols occurred at recovery (T4) in all 3 groups (figure 1). The concentrations of NO-related products did not change during cooling or recovery. No association was detected between the extent of I/R and plasma parameters.

Conclusions In patients with RP free thiols were significantly reduced, indicating increased redox stress. During the cooling and rewarming experiment, a clear rise in free thiols was observed during rewarming, irrespective of the underlying disease or finger perfusion. Meanwhile, NO-related products remained stable. Although these findings need further study, they may suggest activation of ubiquitous antioxidant defense mechanisms during cooling and/or rewarming and should be explored for future use as a potential therapeutic target in RP.

References

  1. van Roon AM, et. al. Rheumatology (Oxford). 2016 Jun;55(6):1083–90.

  2. 2 Koning AM, et al. Pharmacol Res 2016 Sep;111:452–458.

  3. 3 Umbrello M, et al. J Physiol 2014 Mar 1;592(5):1061–1075.

References

Disclosure of Interest None declared

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