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  • Oral presentation
  • Open Access

Erythromycin induced neuroprotection during prolonged deep hypothermic circulatory arrest in an acute porcine model

  • 1Email author,
  • 1,
  • 1,
  • 1,
  • 2,
  • 2,
  • 1 and
  • 2
Journal of Cardiothoracic Surgery20138 (Suppl 1) :O24

  • Published:


  • Erythromycin
  • Motor Cortex
  • Neuronal Injury
  • Porcine Model
  • Cytoplasmic Vacuolation


The present study assesses whether preconditioning with erythromycin can improve neuronal viability in the neocortex following deep hypothermic circulatory arrest (DHCA) in the porcine model.


Piglets were treated with erythromycin (25mg/kg, iv) (n=8) or vehicle (n=6) and subjected to 75 minutes of DHCA at 18°C, 12 hours after pretreatment. Three served as normal controls. After gradual rewarming, treatment animals were sacrificed and brains were perfusion-fixed and cryopreserved. Motor cortex was dissected from the left hemisphere and paraffin embedded for histologic staining with hematoxylin and eosin (HE). To assess neuronal damage, HE-stained paraffin sections (10μm) were examined by light microscopic examination at x400 magnification. Layer V of the motor cortex was counted. Neuronal injury was recorded when there was evidence of eosinophilic cytoplasm, cytoplasmic vacuolation, cell body shrinkage or nuclear pyknosis. Neuronal injury was scored on a scale of 0-5.


The peri-operative physiological variables did show significant variations with erythromycin drug treatment. The motor cortex from piglets pretreated with vehicle undergoing DHCA showed diffuse edema. Neurons showed a diffuse loss of Nissl substance, shrinkage of the perikaryon, and nuclear pyknosis with a mean neuronal injury score of 3.74 + 1.47. Neuronal injury in the motor cortex was significantly lower in animals pretreated with erythromycin (2.53 + 1.22; p < 0.01). Normal controls showed minimal neuronal injury (0.42 + 0.51).


Pharmacologic preconditioning with erythromycin significantly improved neuronal viability in the motor neocortex of piglets undergoing HCA at 18°C. These findings suggest a potential clinical strategy of preemptive neuroprotection.

Authors’ Affiliations

Cardiothoracic Surgery Department, General Hospital "G. Papanikolaou", Thessaloniki, Greece
Department of Anatomy, University of Athens Medical School, Athens, Greece


© Koutsogiannidis et al; licensee BioMed Central Ltd. 2013

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.