General versus specific actions of mild-moderate hypothermia in attenuating cerebral ischemic damage

General versus specific actions of mild-moderate hypothermia in attenuating cerebral ischemic damage
Heng Zhao, Gary K Steinberg and Robert M Sapolsky
Journal of Cerebral Blood Flow & Metabolism, 2007

Mild or moderate hypothermia is generally thought to block all changes in signaling events that are detrimental to the ischemic brain but the effects are variable. It has been confirmed that mild hypothermia is clinically feasible for acute focal stroke treatment but no definite benefits have been reported yet.

Intravenous thrombolysis plus hypothermia for acute treatment of ischemic stroke (ICTuS-L): final results

Intravenous thrombolysis plus hypothermia for acute treatment of ischemic stroke (ICTuS-L): final results

Hemmen TM; Raman R; Guluma KZ; Meyer BC; Gomes JA; Cruz-Flores S; Wijman CA; Rapp KS; Grotta JC; Lyden
Stroke, 2010

The feasibility and safety of hypothermia and thrombolysis after acute ischemic stroke was studied in humans. Twenty-eight patients randomized to receive hypothermia and 30 to normothermia. At 3 months, 18% of patients treated with hypothermia had a modified Rankin Scale score of 0 or 1 versus 24% in the normothermia groups. This study demonstrates the feasibility and preliminary safety of combining endovascular hypothermia after stroke with thrombolysis.

Therapeutic hypothermia in stroke and traumatic brain injury

Therapeutic hypothermia in stroke and traumatic brain injury
Alireza Faridar, Eric M. Bershad, Tenbit Emiru, Paul A. Iaizzo, Jose I. Suarez and Afshin A. Divani
Frontiers in Neurology, 2011

Therapeutic hypothermia is considered to improve survival with favorable neurological outcome in the case of global cerebral ischemia after cardiac arrest and perinatal asphyxia. Among the various methods for hypothermia induction, intravascular cooling may have the most promise in the awake patient in terms of clinical outcomes. 

Dramatic Neuronal Rescue with Prolonged Selective Head Cooling after Ischemia in Fetal Lambs

Dramatic Neuronal Rescue with Prolonged Selective Head Cooling after Ischemia in Fetal Lambs
Alistair J. Gunn, Tania R. Gunn, Harmen H. de Haan, Christopher E. Williams, and Peter D. Gluckman
The American Society for Clinical Investigation, 1997

Unanesthetized near term fetal sheep were subject to 30 min of cerebral ischemia to determine whether prolonged head cooling improves outcome from severe ischemia.  Intrauterine cooling was induced by a coil around the fetal head leading to extradural temperatures of 5-10ºC and esophageal temperatures of 1.5-3ºC. Cerebral cooling reduced secondary cortical cytotoxic edema and caused a dramatic reduction in the extent of cortical infarction and neuronal loss in all regions assessed. Selective head cooling can improve neonatal outcome after perinatal asphyxia.

The effect of therapeutic hypothermia on the expression of inflammatory response genes following moderate traumatic brain injury in the rat

The effect of therapeutic hypothermia on the expression of inflammatory response genes following moderate traumatic brain injury in the rat
JS Truettner, T Suzuki, WD Dietrich
Molecular Brain research, 2005

Rats underwent moderate fluid-percussion brain injury with and without hypothermic treatment to detect genes that are differentially regulated after traumatic brain injury. Post-traumatic hypothermia had no significant effect on the acute expression of the majority of genes investigated but, the expression of TGF-beta2 at 24 h was significantly reduced by temperature manipulation.

Mild Hypothermia and Mg++ Protect Against Irreversible Damage During CNS Ischemia

Mild Hypothermia and Mg++ Protect Against Irreversible Damage During CNS Ischemia
FRANCIS X. VACANTI, ADELBERT AMES III
Stroke, 1984

Spinal cord ischemia was produced in rabbits by temporary occlusion of the abdominal aorta. Recovery, or failure to recover was assessed by examining the rabbits for permanent loss of sensory and motor function in the hind limbs. A temperature reduction of 3ºC during the period of circulatory impairment caused a doubling of the duration of ischemia that could be reversibly sustained. A combination of 5 mmoles/kg of MgCl2 and the 3ºC reduction tripled the duration of ischemia that could be sustained before irreversible damage occurred.

Prolonged hypothermia protects neonatal rat brain against hypoxic-ischemia by reducing both apoptosis and necrosis

Prolonged hypothermia protects neonatal rat brain against hypoxic-ischemia by reducing both apoptosis and necrosis
A.Ohmura, W Nakajima, A. Ishida, N. Yasuoka, M. Kawamura, S. Miura, G. Takada
Brain & Development, 2005

The effects of prolonged hypothermia on immature rat brain after hypoxic-ischemic injury and its protective mechanisms were examined by splitting the pups into a hypothermia group and a normothermia group. Prolonged hypothermia significantly reduced macroscopic brain injury, apoptotic cells, and necrotic cells. Results show that prolonged hypothermia protects neonatal brain after hypoxic-ischemic injury.

The effect of therapeutic hypothermia on the expression of inflammatory response genes following moderate traumatic brain injury in the rat

Effect of Moderate Hypothermia on Lipid Peroxidation in Canine Brain Tissue After Cardiac Arrest and Resuscitation
Lei Baiping, Tan Xiujuan, Cai Hongwei, Xu Qiming, Guo Quling
Stroke, 1994

Twenty-one dogs were divided into four groups: group A, nonischemic controls (shams); group B, 15-minute cardiac arrest without reperfusion; group C, 15-minute cardiac arrest and standard resuscitation; and group D, 15-minute cardiac arrest and hypothermic resuscitation. All dogs in groups C and D were successfully resuscitated. In cardiac arrest group D, after 2 hours of hypothermic reperfusion, there were lower values for tissue malondialdehyde and higher values for glutathione , superoxide dismutase , and glutathione peroxidase compared with normothermic resuscitation in group C. Moderate hypothermia initiated after resuscitation can significantly help the accumulation of lipid peroxidation products and the consumption of free radical scavengers in the brain tissue.

Cerebral Metabolism and Blood Flow after Circulatory Arrest During Deep Hypothermia

Rapid induction of brain hypothermia by endovascular intra-arterial perfusion
Motomasa Furuse, Mark C. Preul, Yoshihiko Kinoshita, Kentaro Nishihara, Naofumi Isono and Toshihiko Kuroiwa
Neurological Research, 2007

The effects of hypothermia and circulatory arrest on cerebral blood flow and cerebral oxygen in dogs 10 dogs was studied. Dogs underwent deep hypothermia and circulatory arrest for 45 minutes. Cerebral oxygen consumption after circulatory arrest and rewarming increased by 15%. The cerebral blood flow decreased by 18% and cerebral vascular resistance increased by 8%. Surface induced hypothermia with anesthesia was tolerated by the dogs with no evidence of impairment of cerebral metabolism.

Rapid induction of brain hypothermia by endovascular intra-arterial perfusion

Rapid induction of brain hypothermia by endovascular intra-arterial perfusion
Motomasa Furuse, Mark C. Preul, Yoshihiko Kinoshita, Kentaro Nishihara, Naofumi Isono and Toshihiko Kuroiwa
Neurological Research, 2007

Ringer’s solution cooled to approximately 6.5ºC l/kg/min for 30 minutes was infused into the right common carotid artery in six adult canines. Right brain temperature decreased from 37.7 +/- 1.1ºC to 33.6 +/- 2.0ºC 30 minutes after initiation of perfusion. The cooling rate of the right cerebral hemisphere was 4.2 +/- 1.1 degrees C/ 30 minutes. Brain hypothermia was rapidly and safely induced using an intra-arterial crystalloid infusion.