Comparative lytic efficacy of rt-PA and ultrasound in porcine versus human clots

PLoS One. 2017 May 17;12(5):e0177786. doi: 10.1371/journal.pone.0177786. eCollection 2017.

Abstract

Introduction: Porcine thrombi are employed routinely in preclinical models of ischemic stroke. In this study, we examined the differential lytic susceptibility of porcine and human whole blood clots with and without the use of microbubbles and ultrasound (US) as an adjuvant.

Materials and methods: An in vitro system equipped with time-lapse microscopy was used to evaluate recombinant tissue-plasminogen activator (rt-PA) lysis of porcine and human clots in the same species or cross species plasma. Human and porcine whole blood clots were treated with rt-PA and an echo contrast agent, Definity®, and exposed to intermittent 120 kHz US.

Results and conclusions: The rt-PA lytic efficacy observed for porcine clots in porcine plasma was 22 times lower than for human clots in human plasma reported previously. Further, porcine clots did not exhibit increased lysis with adjuvant Definity® and US exposure. However, the rt-PA lytic susceptibility of the porcine clots in human plasma was similar to that of human clots in human plasma. Human clots perfused with porcine plasma did not respond to rt-PA, but adjuvant use of Definity® and US enhanced lysis. These results reveal considerable differences in lytic susceptibility of porcine clots and human clots to rt-PA. The use of porcine clot models to test new human thrombolytic therapies may necessitate modulation of coagulation and thrombolytic factors to reflect human hemostasis accurately.

Publication types

  • Comparative Study

MeSH terms

  • Animals
  • Contrast Media
  • Humans
  • In Vitro Techniques
  • Microbubbles
  • Microscopy
  • Plasma / chemistry*
  • Recombinant Proteins / pharmacology*
  • Species Specificity
  • Swine
  • Thrombosis / drug therapy*
  • Time-Lapse Imaging
  • Tissue Plasminogen Activator / pharmacology*
  • Ultrasonography / methods

Substances

  • Contrast Media
  • Recombinant Proteins
  • Tissue Plasminogen Activator

Grants and funding

This work was supported by the National Institute of Neurological Diseases and Disorders (https://www.ninds.nih.gov/) (Grant number: R01 NS047603). SH is a member of the University of Cincinnati Medical Scientist Training Program, which is supported by the National Institute of General Medical Sciences (T32 GM 063483). HS was supported in part by the F. V. Hunt Postdoctoral research fellowship in Acoustics from the Acoustical Society of America. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.