Document Detail


Cushing's mechanism maintains cerebral perfusion pressure in experimental subarachnoid haemorrhage.
MedLine Citation:
PMID:  22982148     Owner:  NLM     Status:  Publisher    
Abstract/OtherAbstract:
Mortality following subarachnoid haemorrhage (SAH) is high, especially within the first 48h. Poor outcome is predicted by high intracranial pressure which causes diminished cerebral perfusion pressure unless a compensatory increase in mean arterial blood pressure occurs. Therefore blood pressure elevation can be protective following subarachnoid haemorrhage despite the potential for rebleeding. This study investigated blood pressure responses to SAH and the impact on cerebral perfusion pressure and outcome, as demonstrated by two experimental models. Various blood pressure responses were demonstrated, both at the ictus and within the following 5h. Elevated MABP at the ictus and at 2h following experimental SAH was associated with maintenance of CPP in the presence of raised ICP. Poor outcome (arrest of the cerebral circulation) was predicted by failure of MABP to increase significantly above sham levels within 2h of SAH. Rat SAH provides relatively inexpensive models to investigate physiological mechanisms that maintain cerebral perfusion in the presence of intracranial hypertension.
Authors:
Christine M Barry; Corinna van den Heuvel; Stephen Helps; Robert Vink
Related Documents :
3308238 - Position may reduce or stop pneumothorax formation in dogs receiving mechanical ventila...
8547558 - Closed mitral valvotomy and elective ventilation in the postoperative period: effect of...
7249708 - A pulse method of measuring respiratory system compliance in ventilated patients.
3124238 - Regulation of ventilation and acid-base status in the elasmobranch scyliorhinus stellar...
22423118 - Update on the pathophysiology and management of idiopathic intracranial hypertension.
24728428 - Patterns of left ventricular remodeling among patients with essential and secondary hyp...
Publication Detail:
Type:  JOURNAL ARTICLE     Date:  2012-9-5
Journal Detail:
Title:  Neuroscience letters     Volume:  -     ISSN:  1872-7972     ISO Abbreviation:  Neurosci. Lett.     Publication Date:  2012 Sep 
Date Detail:
Created Date:  2012-9-17     Completed Date:  -     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  7600130     Medline TA:  Neurosci Lett     Country:  -    
Other Details:
Languages:  ENG     Pagination:  -     Citation Subset:  -    
Copyright Information:
Copyright © 2012. Published by Elsevier Ireland Ltd.
Affiliation:
Discipline of Anatomy and Histology, Centre for Neuroscience, Flinders University, Bedford Park, SA 5042, Australia. Electronic address: christine.barry@flinders.edu.au.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


Previous Document:  Effects of intrahippocampal l-NAME treatment on the behavioral long-term potentiation in dentate gyr...
Next Document:  cAMP stimulates the ubiquitin/proteasome pathway in rat spinal cord neurons.