scholarly journals Regional Alterations of ATP and Heat-Shock Protein-72 mRNA following Hypoxia—Ischemia in Neonatal Rat Brain

1995 ◽  
Vol 15 (6) ◽  
pp. 1047-1056 ◽  
Author(s):  
Shuichi Kobayashi ◽  
Frank A. Welsh

Neonatal rats, 7 days of age, underwent unilateral carotid artery ligation followed by exposure to hypoxia (8% O2) for 80 min. At the end of the period of hypoxia, and after recovery for 2 or 24 h, regional levels of ATP and heat-shock protein-72 (hsp72) mRNA were measured in adjacent brain sections using ATP-luminescence histochemistry and in situ hybridization, respectively. At the end of hypoxia, ATP levels were decreased in a patchy pattern within the hemisphere ipsilateral to the carotid ligation. In the parietal cortex, the reduction of ATP often occurred in columns oriented perpendicular to the cortical surface. Expression of hsp72 mRNA was not detected prior to recovery, except in the ventricular lining of the ipsilateral hemisphere. However, by 2 h of recovery, hsp72 mRNA was expressed in a diffuse pattern in the ipsilateral hemisphere, even in regions in which the distribution of ATP remained patchy. Although the regional extent of expression varied in different animals, hsp72 mRNA was expressed consistently in the subcortical white matter, which, in some animals, was the only region showing expression. In contrast to the diffuse pattern of expression at 2 h of recovery, expression of hsp72 mRNA at 24 h was highly localized in the superficial layers of cerebral cortex and the pyramidal cell layer of hippocampus. The present results demonstrate that hypoxia–ischemia causes regionally distinct alterations in ATP and hsp72 mRNA that may be related to cell injury in this model.

1990 ◽  
Vol 53 (1) ◽  
pp. 145-150 ◽  
Author(s):  
Donna M. Ferriero ◽  
Hernani Q. Soberano ◽  
Roger P. Simon ◽  
Frank R. Sharp

1992 ◽  
Vol 12 (6) ◽  
pp. 987-995 ◽  
Author(s):  
Ken S. Blumenfeld ◽  
Frank A. Welsh ◽  
Valerie A. Harris ◽  
Michael A. Pesenson

Cerebral ischemia induces the expression of a number of proteins that may have an important influence on cellular injury. The purpose of this study was to compare the regional effects of hypoxia–ischemia on the expression of the proto-oncogene, c-fos, and the heat shock protein-70 (HSP-70) gene in developing brain. Unilateral hypoxia–ischemia was produced in the brain of immature rats (7, 15, and 23 days after birth) using a combination of carotid artery ligation and systemic hypoxia (8% O2). After recovery for 2 and 24 h, the regional expression of c-fos and HSP-70 mRNA was determined using in situ hybridization. Littermates were permitted to recover for 1 week for assessment of histologic injury. Hypoxia–ischemia increased the expression of both c-fos and HSP-70 mRNA, but the topography of expression varied with the age of the animal as well as the mRNA species. In the 7-day-old group, expression of c-fos at 2 h increased in multiple regions of the ipsilateral hemisphere in nearly one-half of the animals, while HSP-70 mRNA was not expressed until 24 h and, then, predominantly in the hippocampus. In 15- and 23-day-old rats, expression of c-fos was increased at 2 h in the entorhinal cortex and in the dendritic field of the upper blade of the hippocampal dentate gyrus, while HSP-70 mRNA was prominently expressed in neocortex and the cell layers of the hippocampus. Interestingly, the strong expression of HSP-70 mRNA in dentate granule cells did not occur in the innermost layer of cells. By 24 h of recovery, expression of c-fos had nearly normalized in all age groups, while HSP-70 mRNA was expressed in 15- and 23-day-old rats in many regions, including those undergoing histologic injury. These results suggest that expression of c-fos and HSP-70 mRNA may be useful regional markers of cell stress following hypoxia–ischemia.


1999 ◽  
Vol 180 (5) ◽  
pp. 1254-1262 ◽  
Author(s):  
Xiao Y. Xia ◽  
Tomoaki Ikeda ◽  
Arturo Ota ◽  
Yi X. Xia ◽  
Hiroshi Sameshima ◽  
...  

2009 ◽  
Vol 46 (7) ◽  
pp. 1326-1339 ◽  
Author(s):  
Fumito Tani ◽  
Michiko Ohno ◽  
Yuichi Furukawa ◽  
Masami Sakamoto ◽  
Seiji Masuda ◽  
...  

ACS Nano ◽  
2016 ◽  
Vol 10 (9) ◽  
pp. 8578-8590 ◽  
Author(s):  
Shouju Wang ◽  
Ying Tian ◽  
Wei Tian ◽  
Jing Sun ◽  
Shuang Zhao ◽  
...  

2007 ◽  
Vol 292 (2) ◽  
pp. H893-H903 ◽  
Author(s):  
Galina N. Antonova ◽  
Connie M. Snead ◽  
Alexander S. Antonov ◽  
Christiana Dimitropoulou ◽  
Richard C. Venema ◽  
...  

Large (pathological) amounts of nitric oxide (NO) induce cell injury, whereas low (physiological) NO concentrations often ameliorate cell injury. We tested the hypotheses that pretreatment of endothelial cells with low concentrations of NO (preconditioning) would prevent injury induced by high NO concentrations. Apoptosis, induced in bovine aortic endothelial cells (BAECs) by exposing them to either 4 mM sodium nitroprusside (SNP) or 0.5 mM N-(2-aminoethyl)- N-(2-hydroxy-2-nitrosohydrazino)-1,2-ethylenediamine (spermine NONOate) for 8 h, was abolished by 24-h pretreatment with either 100 μM SNP, 10 μM spermine NONOate, or 100 μM 8-bromo-cGMP (8-Br-cGMP). Repair of BAECs following wounding, measured as the recovery rate of transendothelial electrical resistance, was delayed by 8-h exposure to 4 mM SNP, and this delay was significantly attenuated by 24-h pretreatment with 100 μM SNP. NO preconditioning produced increased association and expression of soluble guanyl cyclase (sGC) and heat shock protein 90 (HSP90). The protective effect of NO preconditioning, but not the injurious effect of 4 mM SNP, was abolished by either a sGC activity inhibitor 1H-[1,2,4]oxadiazolo-[4,3- a]quinoxalin-1-one (ODQ) or a HSP90 binding inhibitor (radicicol) and was mimicked by 8-Br-cGMP. We conclude that preconditioning with a low dose of NO donor accelerates repair and maintains endothelial integrity via a mechanism that includes the HSP90/sGC pathway. HSP90/sGC may thus play a role in the protective effects of NO-generating drugs from injurious stimuli.


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