PMID- 20005922 OWN - NLM STAT- MEDLINE DCOM- 20100504 LR - 20191210 IS - 1873-7544 (Electronic) IS - 0306-4522 (Linking) VI - 166 IP - 1 DP - 2010 Mar 10 TI - Caloric restriction provided after global ischemia does not reduce hippocampal cornu ammonis injury or improve functional recovery. PG - 263-70 LID - 10.1016/j.neuroscience.2009.11.076 [doi] AB - Since caloric restriction (CR) can modify multiple pathways central to the ischemic cascade and enhance neuroplasticity mechanisms, we hypothesized that CR should exert protective effects following brain ischemia. Previous studies have suggested benefit when CR was administered prior to ischemia. We investigated whether prolonged CR beginning after global ischemia would result in lasting protection as assessed by performance in the open field, as a measure of functional outcome, and hippocampal CA1 neuronal counts. Adult, male Mongolian gerbils were subjected to 5 min bilateral carotid artery occlusion (ISCH) or sham surgery (SHAM) with tympanic temperature maintained at 36.5+/-0.2 degrees C during the intra-ischemic period. After screening out gerbils with incomplete ischemia, each of the two surgical groups were randomly assigned to control diet (CON) or 30% CR for the duration of the study (60 d). Gerbils were tested in the open field on d3, 7, 10, 30 and 60. ISCH-CON animals showed a significantly higher level of activity in the open field (impaired habituation) compared to SHAM-CON gerbils on all test days (P<0.001). Open field activity was significantly lower in the ISCH-CR group than in ISCH-CON gerbils only on d7 (P=0.024). Open field activity of the SHAM-CR gerbils showed a trend to increase relative to that of SHAM-CON gerbils during the last 30 d of the study (P=0.055 on d60), raising the question of suitability of the open field test for long-term studies of CR and ischemia. Brain sections obtained at d60 were stained with hematoxylin and eosin. Hippocampal CA1 neuron counts were significantly reduced by ischemia (P<0.001), and there was no sparing effect of CR. Our findings suggest that prolonged 30% CR administered beginning after global ischemia cannot diminish brain injury or enhance long-term recovery. CI - Copyright 2010 IBRO. Published by Elsevier Ltd. All rights reserved. FAU - McEwen, B R AU - McEwen BR AD - College of Pharmacy and Nutrition and Cameco Multiple Sclerosis Neuroscience Research Center, University of Saskatchewan, 110 Science Place, Saskatoon, SK, Canada. FAU - Paterson, P G AU - Paterson PG LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20091228 PL - United States TA - Neuroscience JT - Neuroscience JID - 7605074 SB - IM MH - Animals MH - Brain Ischemia/*metabolism/physiopathology/*therapy MH - CA1 Region, Hippocampal/*metabolism/pathology/physiopathology MH - Caloric Restriction/*methods MH - Cell Count MH - Cognition Disorders/metabolism/pathology/physiopathology MH - Disease Models, Animal MH - Eating/physiology MH - Energy Metabolism/physiology MH - Food Deprivation/*physiology MH - Food, Formulated MH - Gerbillinae MH - Learning Disabilities/metabolism/pathology/physiopathology MH - Male MH - Nerve Degeneration/physiopathology/prevention & control/*therapy MH - Neurons/metabolism/pathology MH - Recovery of Function/physiology EDAT- 2009/12/17 06:00 MHDA- 2010/05/05 06:00 CRDT- 2009/12/17 06:00 PHST- 2009/07/21 00:00 [received] PHST- 2009/11/15 00:00 [revised] PHST- 2009/11/28 00:00 [accepted] PHST- 2009/12/17 06:00 [entrez] PHST- 2009/12/17 06:00 [pubmed] PHST- 2010/05/05 06:00 [medline] AID - S0306-4522(09)01988-5 [pii] AID - 10.1016/j.neuroscience.2009.11.076 [doi] PST - ppublish SO - Neuroscience. 2010 Mar 10;166(1):263-70. doi: 10.1016/j.neuroscience.2009.11.076. Epub 2009 Dec 28.