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Hypothermia at 10°C Reduces Neurologic Injury After Hypothermic Circulatory Arrest in the Pig
Author(s) -
Ananiadou Olga G.,
Bibou Katerina,
Drossos George E.,
Bai Mary,
HajYahia Saleem,
Charchardi Antonia,
Johnson Elizabeth O.
Publication year - 2008
Publication title -
journal of cardiac surgery
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.428
H-Index - 58
eISSN - 1540-8191
pISSN - 0886-0440
DOI - 10.1111/j.1540-8191.2007.00485.x
Subject(s) - medicine , hypothermia , circulatory system , anesthesia , clinical death , intensive care medicine , resuscitation , cardiology , cardiopulmonary resuscitation
Background: We have previously reported that sensory, motor neocortex, and hippocampus are selectively vulnerable to injury in an acute porcine model of HCA at 18°C. This study was undertaken to assess whether further cooling to 10°C can reduce neurological injury during HCA. Methods: Twelve piglets underwent 75 minutes of HCA at 18°C (n = 6) and 10°C (n = 6). Four served as normal controls. After gradual rewarming and 80 minutes of reperfusion, treatment animals were sacrificed and brains were perfusion‐fixed and cryopreserved. Regional patterns of neuronal apoptosis after HCA were characterized by in situ DNA fragmentation using TUNEL histochemistry. Hematoxylin and eosin histology was used to characterize cell damage morphologically. TUNEL‐positive cells were scored on a scale of 0 to 5. Grade 0: no TUNEL‐positive cells; Grade 1: < 10%; Grade 2: 10% to 25%, Grade 3: 25% to 50%, Grade 4: 50% to 75%; and Grade 5: > 75%. Results: TUNEL‐positive cells indicating DNA fragmentation were scored in the motor and sensory neocortex, hippocampus, cerebellum, thalamus, and medulla of animals treated with 18°C and 10°C HCA and were significantly greater than in normal controls. Profound cooling to 10°C resulted in a significant reduction of neuronal injury in the neocortex and hippocampus. Conclusions: This data support that cerebral protection may be better at very cold temperatures compared to 18°C hypothermia. Regions selectively vulnerable to neuronal injury are offered more neural protection by profound hypothermia. These affects are observed in the acute state, suggesting activation of the apoptotic mechanisms at early stages can be inhibited by profound hypothermia.