Whole body hypothermia broadens the therapeutic window of intranasally administered IGF-1 in a neonatal rat model of cerebral hypoxia-ischemia

To investigate whether whole body hypothermia after neonatal cerebral hypoxia-ischemia (HI) could broaden the therapeutic window of intranasal treatment of IGF-1 (iN-IGF-1), postnatal day 7 rat pups were subjected to right common carotid artery ligation, followed by 8% oxygen inhalation for 2 h. After HI, one group of pups were returned to their dams and kept at room temperature (24.5 +/- 0.2 degrees C). A second group of pups were subjected to whole body hypothermia in a cool environment (21.5 +/- 0.3 degrees C) for 2 or 4 h before being returned to their dams. Two doses of 50 mu g recombinant human IGF-1 were administered intranasally at a 1 h interval starting at 0, 2 or 4 h after hypothermia. Hypothermia decreased the rectal temperature of pups by 4.5 degrees C as compared to those kept at room temperature. While hypothermia or iN-IGF-1 administered 2 h after HI alone did not provide neuroprotection, the combined treatment of hypothermia with iN-IGF-1 significantly protected the neonatal rat brain from HI injury. Hypothermia treatment extended the therapeutic window of IGF-1 to 6 h after HI. The extended IGF-1 therapeutic window by hypothermia was associated with decreases in infiltration of polymorphonuclear leukocytes and activation of microglia/macrophages and with attenuation of NF-kappa B activation in the ipsilateral hemisphere following HI. (C) 2011 Elsevier B.V. All rights reserved.