Literature DB >> 2584273

Sequential metabolic changes in rat brain following middle cerebral artery occlusion: a 2-deoxyglucose study.

K Shiraishi1, F R Sharp, R P Simon.   

Abstract

The distribution and time course of altered cerebral metabolism following permanent focal ischemia was studied in rat using the 2-deoxyglucose (2DG) technique. Increased 2DG uptake preceded decreased 2DG uptake and infarction in the caudate putamen and cortex. Decreased 2DG uptake without infarction was observed for 72 h in thalamus and for 24 h in hippocampus (areas remote from the ischemic zones). This study supports the concept of cell excitation as a pathophysiologic process in permanent focal ischemia. The time course of increased metabolism may demarcate the time window of opportunity for the previously demonstrated attenuation of stroke size with inhibition of cell excitation by pharmacologic blockade of excitatory amino acid neurotransmission.

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Year:  1989        PMID: 2584273     DOI: 10.1038/jcbfm.1989.110

Source DB:  PubMed          Journal:  J Cereb Blood Flow Metab        ISSN: 0271-678X            Impact factor:   6.200


  5 in total

1.  Proteomic analysis of hypoxia/ischemia-induced alteration of cortical development and dopamine neurotransmission in neonatal rat.

Authors:  Xiaoming Hu; Harriett C Rea; John E Wiktorowicz; J Regino Perez-Polo
Journal:  J Proteome Res       Date:  2006-09       Impact factor: 4.466

2.  Energy metabolism and NAD-NADH redox state in brain slices in response to glutamate exposure and ischemia.

Authors:  S S Kannurpatti; N B Joshi
Journal:  Metab Brain Dis       Date:  1999-03       Impact factor: 3.584

3.  Early detection of secondary damage in ipsilateral thalamus after acute infarction at unilateral corona radiata by diffusion tensor imaging and magnetic resonance spectroscopy.

Authors:  Chuo Li; Xueying Ling; Sirun Liu; Anding Xu; Yusheng Zhang; Shihui Xing; Zhong Pei; Jinsheng Zeng
Journal:  BMC Neurol       Date:  2011-05-05       Impact factor: 2.474

Review 4.  Mitochondrial dysfunction induced by nuclear poly(ADP-ribose) polymerase-1: a treatable cause of cell death in stroke.

Authors:  Paul Baxter; Yanting Chen; Yun Xu; Raymond A Swanson
Journal:  Transl Stroke Res       Date:  2013-09-07       Impact factor: 6.829

Review 5.  Opposing effects of glucose on stroke and reperfusion injury: acidosis, oxidative stress, and energy metabolism.

Authors:  Nathaniel M Robbins; Raymond A Swanson
Journal:  Stroke       Date:  2014-04-17       Impact factor: 7.914

  5 in total

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