OBJECTIVE: The present study was designed to determine whether the predominant factor responsible for neuroprotection of hypothermia ranging from 31 to 34 degrees C is prolongation of onset of ischemic depolarization or suppression of neuronal injury during ischemic depolarization and to quantitatively determine the neuroprotective effects of hypothermia of 34 degrees C and 31 degrees C. DESIGN: Prospective animal study. SETTING: A university research laboratory. SUBJECTS: Eighty-nine gerbils. INTERVENTIONS: Bilateral common carotid arteries were occluded for 3-20 mins. The brain temperature was set at 37 degrees C, 34 degrees C, or 31 degrees C before and during ischemic depolarization. MEASUREMENTS AND MAIN RESULTS: DC potentials were measured in the CA1 region, where histologic evaluation was performed 7 days later. Onset times of ischemic depolarization were 1.3 +/- 0.2, 1.6 +/- 0.4, and 2.4 +/- 0.7 mins at 37 degrees C, 34 degrees C, and 31 degrees C, respectively. The logistic regression curve demonstrated a close relationship between duration of ischemic depolarization and neuronal damage and showed a rightward shift by lowering the brain temperature. In the 37 degrees C, 34 degrees C, and 31 degrees C groups, the durations of ischemic depolarization causing 50% neuronal damage were estimated to be 8.0, 14.2, and 26.0 mins, respectively, and the ischemia times causing 50% neuronal damage were estimated to be 4.9, 8.1, and 14.2 mins, respectively. CONCLUSIONS: The onset of ischemic depolarization was prolonged in the 34 degrees C and 31 degrees C groups by only 0.3 and 1.1 mins, respectively, compared with that in the 37 degrees C group. Most of the neuroprotection by hypothermia was attributed to the suppression of neuronal injury during ischemic depolarization, suggesting that hypothermia has neuroprotective effects if it is initiated during the ischemic depolarization period. The results also indicate that the neuroprotective effect at 31 degrees C is about three times greater than that at 34 degrees C and that neuronal cells can withstand 2.9 times longer duration of ischemia at 31 degrees C than at 37 degrees C.
OBJECTIVE: The present study was designed to determine whether the predominant factor responsible for neuroprotection of hypothermia ranging from 31 to 34 degrees C is prolongation of onset of ischemic depolarization or suppression of neuronal injury during ischemic depolarization and to quantitatively determine the neuroprotective effects of hypothermia of 34 degrees C and 31 degrees C. DESIGN: Prospective animal study. SETTING: A university research laboratory. SUBJECTS: Eighty-nine gerbils. INTERVENTIONS: Bilateral common carotid arteries were occluded for 3-20 mins. The brain temperature was set at 37 degrees C, 34 degrees C, or 31 degrees C before and during ischemic depolarization. MEASUREMENTS AND MAIN RESULTS: DC potentials were measured in the CA1 region, where histologic evaluation was performed 7 days later. Onset times of ischemic depolarization were 1.3 +/- 0.2, 1.6 +/- 0.4, and 2.4 +/- 0.7 mins at 37 degrees C, 34 degrees C, and 31 degrees C, respectively. The logistic regression curve demonstrated a close relationship between duration of ischemic depolarization and neuronal damage and showed a rightward shift by lowering the brain temperature. In the 37 degrees C, 34 degrees C, and 31 degrees C groups, the durations of ischemic depolarization causing 50% neuronal damage were estimated to be 8.0, 14.2, and 26.0 mins, respectively, and the ischemia times causing 50% neuronal damage were estimated to be 4.9, 8.1, and 14.2 mins, respectively. CONCLUSIONS: The onset of ischemic depolarization was prolonged in the 34 degrees C and 31 degrees C groups by only 0.3 and 1.1 mins, respectively, compared with that in the 37 degrees C group. Most of the neuroprotection by hypothermia was attributed to the suppression of neuronal injury during ischemic depolarization, suggesting that hypothermia has neuroprotective effects if it is initiated during the ischemic depolarization period. The results also indicate that the neuroprotective effect at 31 degrees C is about three times greater than that at 34 degrees C and that neuronal cells can withstand 2.9 times longer duration of ischemia at 31 degrees C than at 37 degrees C.
Authors: Kunjan R Dave; Sherri L Christian; Miguel A Perez-Pinzon; Kelly L Drew Journal: Comp Biochem Physiol B Biochem Mol Biol Date: 2012-02-03 Impact factor: 2.231
Authors: Marlene Davis Ekpo; George Frimpong Boafo; Suleiman Shafiu Gambo; Yuying Hu; Xiangjian Liu; Jingxian Xie; Songwen Tan Journal: Front Vet Sci Date: 2022-06-09
Authors: Kunjan R Dave; Richard Anthony Defazio; Ami P Raval; Oleksandr Dashkin; Isabel Saul; Kimberly E Iceman; Miguel A Perez-Pinzon; Kelly L Drew Journal: J Neurochem Date: 2009-05-30 Impact factor: 5.372