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Effects of cardioplegic solutions on the vasoreactivity of the internal mammary artery

C I Chardigny1, V A Jebara, T J Verbeuren

  • 1Department of Cardiovascular Surgery, Broussais Hospital, Paris, France.

Insights

Blood cardioplegia appears less harmful to internal mammary artery grafts than other solutions, preserving vascular function. Storage in cardioplegic solutions impacts arterial graft vasoreactivity and endothelial function.

Area of Science:

  • Cardiovascular Surgery
  • Vascular Biology
  • Organ Preservation

Background:

  • Internal mammary artery (IMA) grafting is a common cardiac surgical procedure.
  • Cardioplegia is administered via the IMA during grafting.
  • The impact of cardioplegic solutions on IMA graft function is not fully understood.

Purpose of the Study:

  • To investigate the effects of different cardioplegic solutions on IMA graft vasoreactivity.
  • To assess potential endothelial damage caused by cardioplegic solutions.
  • To compare the functional outcomes of IMA segments stored in various solutions.

Main Methods:

  • Segments of IMA from 10 patients were used.
  • Forty IMA segments were incubated in four solutions: Krebs, University of Wisconsin (UW), Broussais Hospital (BH), and blood cardioplegia.
  • Vascular reactivity was assessed using norepinephrine and acetylcholine.

Main Results:

  • IMA segments in Krebs solution showed different norepinephrine sensitivity compared to UW and BH solutions.
  • Acetylcholine-induced relaxation varied significantly between Krebs solution and the other three solutions, and between blood cardioplegia and UW/BH solutions.
  • No significant differences in sodium nitroprusside-induced relaxation were observed across solutions.

Conclusions:

  • Storage in cardioplegic solutions does not preserve the initial vasoreactivity of the IMA.
  • Blood cardioplegia demonstrates a less detrimental effect on endothelial and myogenic vascular function compared to other solutions.
  • These findings suggest blood cardioplegia may be preferable for maintaining IMA graft viability.
Abstract

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