Literature DB >> 2329123

The influence of mild body and brain hypothermia on ischemic brain damage.

H Minamisawa1, C H Nordström, M L Smith, B K Siesjö.   

Abstract

The influence of brain and body temperature on ischemic brain damage, notably on the density and distribution of selective neuronal vulnerability, was studied in SPF-Wistar rats subjected to 15 min of forebrain ischemia induced by bilateral occlusion of the common carotid arteries combined with arterial hypotension (50 mm Hg) in a room air environment. In one group of animals, the body temperature was maintained at 37 degrees C but no attempt was made to prevent heat losses from the ischemic brain; i.e., the head was not heated during ischemia. Under those conditions the temperature of the caudoputamen and at a subcutaneous site over the skull bone spontaneously fell to approximately 32 degrees C. In four other groups, both the rectal and the subcutaneous skull temperatures were maintained at 38, 37, 35, and 33 degrees C during the ischemia. Our results confirm those recently reported when brain temperature was varied during 20 min of ischemia, with body temperature kept constant. Thus, the histopathological outcome of the brain damage, as assessed after 7 days of recovery, was strongly temperature dependent. Whereas ischemia at 37-38 degrees C consistently caused neuronal necrosis in the hippocampus, neocortex, and caudoputamen, spontaneous cooling of the brain during ischemia at a rectal temperature of 37 degrees C significantly reduced the ischemic damage. Intentional lowering of temperature to 35 degrees C markedly reduced and to 33 degrees C virtually prevented neuronal necrosis in some but not all of the regions studied. While damage to the caudoputamen was extremely temperature sensitive, that affecting the CA1 sector of the hippocampus, and particularly the lateral reticular nucleus of the thalamus, was less so. Our results suggest that whatever biochemical events are responsible for selective neuronal vulnerability, they are temperature sensitive; however, since there are differences in sensitivity between different parts of the brain, more than one mechanism may be involved.

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Mesh:

Year:  1990        PMID: 2329123     DOI: 10.1038/jcbfm.1990.66

Source DB:  PubMed          Journal:  J Cereb Blood Flow Metab        ISSN: 0271-678X            Impact factor:   6.200


  30 in total

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Review 3.  Calcium, energy metabolism and the development of selective neuronal loss following short-term cerebral ischemia.

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4.  Multiscale entropy analysis of EEG for assessment of post-cardiac arrest neurological recovery under hypothermia in rats.

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5.  Heating of the brain to maintain normothermia during ischemia aggravates brain injury in the rat.

Authors:  T Miyazawa; P Bonnekoh; R Widmann; K A Hossmann
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6.  Endonuclease G expression in thalamic reticular nucleus after global cerebral ischemia.

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Journal:  Exp Brain Res       Date:  2008-06-21       Impact factor: 1.972

7.  Loss of parvalbumin immunoreactivity defines selectively vulnerable thalamic reticular nucleus neurons following cardiac arrest in the rat.

Authors:  K Kawai; T S Nowak; I Klatzo
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8.  Postischaemic changes in protein synthesis in the rat brain: effects of hypothermia.

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9.  Neuronal damage, glial response and cerebral metabolism after hypothermic forebrain ischemia in the rat.

Authors:  H Chen; M Chopp; Q Jiang; J H Garcia
Journal:  Acta Neuropathol       Date:  1992       Impact factor: 17.088

10.  The effect of focal cerebral cooling on perinatal hypoxic-ischemic brain damage.

Authors:  J Towfighi; C Housman; D F Heitjan; R C Vannucci; J Y Yager
Journal:  Acta Neuropathol       Date:  1994       Impact factor: 17.088

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