Document Detail


High blood glucose does not adversely affect outcome in moderately brain-injured rodents.
MedLine Citation:
PMID:  20504157     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
In a number of clinical studies researchers have reported that acute hyperglycemia is associated with increased mortality and worsened neurological outcome in patients with traumatic brain injury (TBI). In contrast, it has been demonstrated that intensive insulin therapy to lower blood glucose can lead to an increased frequency of hypoglycemic episodes and poor outcome. Consistent with this, experimental and clinical studies have shown that TBI causes a "metabolic crisis" in the injured brain, suggesting that a reduction in glucose availability may exacerbate brain damage. We therefore examined the consequences of hyperglycemia on cognitive and pathological measures. Using a rodent model of TBI, we find that when acute hyperglycemia is induced in animals prior to injury, there is little to no change in motor and cognitive performance, contusion volume, or cerebral edema. To examine the consequences of persistent hyperglycemia (as seen in diabetic patients), animals were treated with streptozotocin (STZ) to induce type 1 diabetes. We find that the presence of persistent STZ-induced hyperglycemia results in a reduction of brain edema. Insulin therapy to reduce blood glucose reverses this beneficial effect of hyperglycemia. Taken together, our results indicate that an acute increase in blood glucose levels may not be harmful, and that intervention with insulin therapy to lower blood glucose levels in TBI patients may increase secondary brain damage.
Authors:
Julia Hill; Jing Zhao; Pramod K Dash
Related Documents :
11252037 - 1-(13)c glucose magnetic resonance spectroscopy of pediatric and adult brain disorders.
226347 - Plasma free tryptophan, brain serotonin, and an endocrine profile of the genetically ob...
16283097 - Diabetes and cognitive impairment. clinical diagnosis and brain imaging in patients att...
9642647 - Carbohydrates as a cerebral metabolic fuel.
18178097 - Bone marrow angiogenesis and angiogenic factors in multiple myeloma treated with novel ...
3844417 - Obesity.
Publication Detail:
Type:  Journal Article; Research Support, N.I.H., Extramural    
Journal Detail:
Title:  Journal of neurotrauma     Volume:  27     ISSN:  1557-9042     ISO Abbreviation:  J. Neurotrauma     Publication Date:  2010 Aug 
Date Detail:
Created Date:  2010-08-17     Completed Date:  2010-12-02     Revised Date:  2011-08-03    
Medline Journal Info:
Nlm Unique ID:  8811626     Medline TA:  J Neurotrauma     Country:  United States    
Other Details:
Languages:  eng     Pagination:  1439-48     Citation Subset:  IM    
Affiliation:
Department of Neurobiology and Anatomy, The University of Texas Medical School, Houston, Texas 77225, USA.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:
Animals
Blood Glucose / physiology*
Brain Edema / etiology,  pathology
Brain Injuries / blood,  pathology*,  psychology*
Diabetes Mellitus, Experimental / complications
Glucose / pharmacology
Hyperglycemia / complications
Hypoglycemic Agents / pharmacology
Insulin / pharmacology
Male
Maze Learning / physiology
Mice
Mice, Inbred C57BL
Motor Skills / physiology
Psychomotor Performance / physiology
Rats
Rats, Sprague-Dawley
Reflex, Vestibulo-Ocular / physiology
Chemical
Reg. No./Substance:
0/Blood Glucose; 0/Hypoglycemic Agents; 11061-68-0/Insulin; 50-99-7/Glucose
Comments/Corrections

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


Previous Document:  Spontaneous epileptiform activity in rat neocortex after controlled cortical impact injury.
Next Document:  Hypothermia prior to decompression: buying time for treatment of acute spinal cord injury.