Evaluation of combined fibroblast growth factor-2 and moderate hypothermia therapy in traumatically brain injured rats
- PMID: 11134598
- DOI: 10.1016/s0006-8993(00)03002-x
Evaluation of combined fibroblast growth factor-2 and moderate hypothermia therapy in traumatically brain injured rats
Abstract
Both the exogenous administration of fibroblast growth factor-2 (FGF-2) or the induction of moderate hypothermia have been shown to attenuate histopathology and improve functional outcome after traumatic brain injury (TBI). Since combined therapeutic strategies may be more beneficial than single therapies, we examined the potential synergistic effect of FGF-2 combined with moderate hypothermia treatment induced 10 min after TBI on functional and histological outcome following controlled cortical impact (CCI) injury. Fifty male Sprague-Dawley rats were randomized to one sham and four CCI treatment groups: Sham+vehicle (VEH); FGF-2 (45 microg/kg/h for 3 h i.v.)+Normothermia (37+/-0.5 degrees C); FGF-2+Hypothermia (32+/-0.5 degrees C for 3 h); VEH+Norm; VEH+Hypo. Vestibulomotor performance on the beam balance and beam-walk (BW) tasks on post-operative days 1-5 and spatial memory acquisition in the Morris water maze (MWM) on days 14-18 were assessed. After 4 weeks survival, histological evaluations (CA(1) and CA(3) cell counts and lesion volume) were performed. MWM performance improved in all treatment groups, but combined treatment was not more efficacious than either alone. The FGF-2+Hypo group performed significantly better than the other injured treatment groups in the BW task. Lastly, no significant group differences in beam balance or histological outcome were observed. These data suggest a suboptimal and incomplete synergy of combined FGF-2 and hypothermia treatment. These data may indicate that either our dose of FGF-2 or combination therapy was not optimized in our model.
Similar articles
-
Acute systemic administration of interleukin-10 suppresses the beneficial effects of moderate hypothermia following traumatic brain injury in rats.Brain Res. 2002 May 24;937(1-2):22-31. doi: 10.1016/s0006-8993(02)02458-7. Brain Res. 2002. PMID: 12020858
-
Attenuation of working memory and spatial acquisition deficits after a delayed and chronic bromocriptine treatment regimen in rats subjected to traumatic brain injury by controlled cortical impact.J Neurotrauma. 2002 Apr;19(4):415-25. doi: 10.1089/08977150252932370. J Neurotrauma. 2002. PMID: 11990348
-
Galantamine and Environmental Enrichment Enhance Cognitive Recovery after Experimental Traumatic Brain Injury But Do Not Confer Additional Benefits When Combined.J Neurotrauma. 2017 Apr 15;34(8):1610-1622. doi: 10.1089/neu.2016.4790. Epub 2016 Dec 20. J Neurotrauma. 2017. PMID: 27806662 Free PMC article.
-
No long-term benefit from hypothermia after severe traumatic brain injury with secondary insult in rats.Crit Care Med. 2000 Sep;28(9):3218-23. doi: 10.1097/00003246-200009000-00017. Crit Care Med. 2000. PMID: 11008985
-
Protective effects of moderate hypothermia on behavioral deficits but not necrotic cavitation following cortical impact injury in the rat.J Neurotrauma. 1998 Feb;15(2):95-103. doi: 10.1089/neu.1998.15.95. J Neurotrauma. 1998. PMID: 9512085
Cited by
-
The effect of thioredoxin-1 in a rat model of traumatic brain injury depending on diurnal variation.Brain Behav. 2023 Jun;13(6):e3031. doi: 10.1002/brb3.3031. Epub 2023 May 8. Brain Behav. 2023. PMID: 37157915 Free PMC article.
-
FGF2 Attenuates Neural Cell Death via Suppressing Autophagy after Rat Mild Traumatic Brain Injury.Stem Cells Int. 2017;2017:2923182. doi: 10.1155/2017/2923182. Epub 2017 Oct 17. Stem Cells Int. 2017. PMID: 29181034 Free PMC article.
-
Endogenous repair signaling after brain injury and complementary bioengineering approaches to enhance neural regeneration.Biomark Insights. 2015 May 12;10(Suppl 1):43-60. doi: 10.4137/BMI.S20062. eCollection 2015. Biomark Insights. 2015. PMID: 25983552 Free PMC article. Review.
-
Regional calcineurin subunit B isoform expression in rat hippocampus following a traumatic brain injury.Brain Res. 2010 Oct 28;1358:211-20. doi: 10.1016/j.brainres.2010.08.029. Epub 2010 Aug 13. Brain Res. 2010. PMID: 20713027 Free PMC article.
-
Acute treatment with the 5-HT(1A) receptor agonist 8-OH-DPAT and chronic environmental enrichment confer neurobehavioral benefit after experimental brain trauma.Behav Brain Res. 2007 Feb 27;177(2):186-94. doi: 10.1016/j.bbr.2006.11.036. Epub 2006 Dec 12. Behav Brain Res. 2007. PMID: 17166603 Free PMC article.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources
Miscellaneous