Compartmental and muscular response to closed soft tissue injury in rats investigated by oxygen-to-see and intravital fluorescence microscopy

J Trauma Acute Care Surg. 2012 Jul;73(1):73-9. doi: 10.1097/TA.0b013e31824afddd.

Abstract

Background: Closed soft tissue injury (CSTI) induces local inflammation and progressive microvascular dysfunction. The aim of the study was to evaluate and compare the microvascular changes systematically in a precompartmental tissue injury by oxygen-to-see (O2C), a combined laser Doppler flowmetry and spectrophotometry system, and intravital fluorescence microscopy (IVM).

Methods: Fourteen Wistar rats were subjected to a trauma and a control group (both n = 7). CSTI was performed on the left lower limb by means of a standardized impact device. Controls received a sham CSTI. Capillary blood flow (QRBC), oxygen saturation (sO2), and postcapillary filling pressure (rHb) were measured noninvasively by O2C assessed in 2-mm and 8-mm depth underneath the skin. Measurements were done before and after trauma and hourly up to 24 hours. IVM of the soleus muscle was performed after 24 hours.

Results: Before CSTI, O2C parameters did not reveal a difference between both groups. Up to 2 hours after trauma, QRBC was significantly increased in 8-mm tissue depth. No significant changes of sO2 and rHb were noted compared with controls. In 2-mm depth, significantly reduced QRBC and rHb levels were observed compared with 8 mm but with no significant changes after CSTI. IVM showed a significant increase of postcapillary blood flow with decreased functional capillary density, increased macromolecular leakage, and increased nicotinamide adenine dinucleotide hydride.

Conclusions: After CSTI in rats, there was an immediate increase of compartmental capillary blood flow with a slight increase of muscle oxygen saturation and unchanged postcapillary venous filling pressures as sign of a redistribution of blood between soft and muscle tissue. The severity of pathologic changes in the compartment was not reflected by O2C but by IVM.

MeSH terms

  • Animals
  • Capillaries / injuries
  • Capillaries / pathology
  • Capillaries / physiopathology
  • Laser-Doppler Flowmetry
  • Male
  • Microcirculation
  • Microscopy, Fluorescence
  • Microvessels / injuries
  • Microvessels / pathology*
  • Muscle, Skeletal / blood supply
  • Muscle, Skeletal / injuries*
  • Muscle, Skeletal / pathology
  • Muscle, Skeletal / physiopathology
  • Oxygen / metabolism
  • Rats
  • Rats, Wistar
  • Soft Tissue Injuries / pathology*
  • Soft Tissue Injuries / physiopathology

Substances

  • Oxygen