Relevance of Porcine Stroke Models to Bridge the Gap from Pre-Clinical Findings to Clinical Implementation

Int J Mol Sci. 2020 Sep 8;21(18):6568. doi: 10.3390/ijms21186568.

Abstract

In the search of animal stroke models providing translational advantages for biomedical research, pigs are large mammals with interesting brain characteristics and wide social acceptance. Compared to rodents, pigs have human-like highly gyrencephalic brains. In addition, increasingly through phylogeny, animals have more sophisticated white matter connectivity; thus, ratios of white-to-gray matter in humans and pigs are higher than in rodents. Swine models provide the opportunity to study the effect of stroke with emphasis on white matter damage and neuroanatomical changes in connectivity, and their pathophysiological correlate. In addition, the subarachnoid space surrounding the swine brain resembles that of humans. This allows the accumulation of blood and clots in subarachnoid hemorrhage models mimicking the clinical condition. The clot accumulation has been reported to mediate pathological mechanisms known to contribute to infarct progression and final damage in stroke patients. Importantly, swine allows trustworthy tracking of brain damage evolution using the same non-invasive multimodal imaging sequences used in the clinical practice. Moreover, several models of comorbidities and pathologies usually found in stroke patients have recently been established in swine. We review here ischemic and hemorrhagic stroke models reported so far in pigs. The advantages and limitations of each model are also discussed.

Keywords: animal models; connectivity; gyrencephalic brain; pig; stroke; swine; translational research; white matter damage.

Publication types

  • Review

MeSH terms

  • Animals
  • Brain / physiopathology
  • Brain Ischemia / physiopathology
  • Cerebral Cortex / physiopathology
  • Disease Models, Animal*
  • Humans
  • Stroke / metabolism
  • Stroke / physiopathology*
  • Subarachnoid Hemorrhage / physiopathology
  • Swine / metabolism*
  • White Matter / physiopathology