@phdthesis{Joseph2012, author = {Christy Joseph}, title = {Neuroprotection by prolonged hypothermia induced by hydrogen sulphide in focal cerebral ischemic rat model: Evidence from electrocortical activity and recruitment of polymorphonuclear cells}, journal = {Neuroprotektion durch anhaltende Hypothermie, induziert durch Hydrogensulfid im fokalen zerebralen isch{\"a}mischen Rattenmodel: Beleg durch elektrokortikale Aktivit{\"a}t und Rekrutierung polymorphonukle{\"a}rer Zellen.}, url = {https://nbn-resolving.org/urn:nbn:de:gbv:9-001328-5}, year = {2012}, abstract = {In aged humans, stroke is a major cause of disability for which no neuroprotective measures are available. In animal studies of focal ischemia, short-term hypothermia often reduces infarct size. Nevertheless, efficient neuroprotection requires long-term, regulated lowering of whole-body temperature. Previously, it is reported that post-stroke exposure to hydrogen sulfide (H2S) effectively lowers whole-body temperature and confers neuroprotection in aged animals. Here we report for the first time that the animals exposed to H2S the normal sleep–wake oscillations are replaced by a low-amplitude EEG dominated by a 4-Hz rhythmicactivity, reminiscent of EEG recordings in hibernating animals. In the present study using magnetic resonance imaging, reverse transcriptase polymerase chain reaction, western blotting and immunofluorescence, we characterized the central nervous system response to H2S -induced hypothermia and report, that annexin A1, a major constituent of peripheral leukocytes that is upregulated after stroke, was consistently downregulated in polymorphonuclear cells in the peri-lesional cortex of post-ischemic, aged rat brain after 48 hours of hypothermia induced by exposure to H2S. This might be due to the reduced kinetics of recruitment, adherence and infiltration of PMN cells by H2S -induced hypothermia. Our findings further suggest that, in contrast to monotherapies that have thus far uniformly failed in clinical practice, prolonged hypothermia has pleiotropic effects on brain physiology that may be necessary for effective protection of the brain after stroke.}, language = {en} }