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Combined prostaglandin E1 and lithium exert potent neuroprotection in a rat model of cerebral ischemia
by
RuiSHENG Li-sha ZHANG Rong HAN Bo GAO Xiao-qian LIU Zheng-hong QIN
in
Alprostadil - therapeutic use
/ Animals
/ Antimanic Agents - therapeutic use
/ Bcl-2 protein
/ Biomedical and Life Sciences
/ Biomedicine
/ Brain injury
/ Brain Ischemia - drug therapy
/ Brain Ischemia - prevention & control
/ Cerebral blood flow
/ Disease Models, Animal
/ Drug Combinations
/ Heat shock proteins
/ Hsp60 protein
/ Hsp70 protein
/ Immunoblotting
/ Immunology
/ Internal Medicine
/ Intravenous administration
/ Ischemia
/ Lithium
/ Lithium Compounds - therapeutic use
/ Medical Microbiology
/ Neostriatum
/ Neurological diseases
/ Neuroprotection
/ Neuroprotective Agents - therapeutic use
/ Original
/ original-article
/ p53 protein
/ p53基因
/ Pharmacology/Toxicology
/ Prostaglandin E1
/ Random Allocation
/ Rats
/ Stroke
/ Vaccine
/ Vasodilator Agents - therapeutic use
/ 前列腺素E1
/ 大鼠模型
/ 混合配方
/ 热休克蛋白60
/ 神经保护作用
/ 脑缺血
2011
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Combined prostaglandin E1 and lithium exert potent neuroprotection in a rat model of cerebral ischemia
by
RuiSHENG Li-sha ZHANG Rong HAN Bo GAO Xiao-qian LIU Zheng-hong QIN
in
Alprostadil - therapeutic use
/ Animals
/ Antimanic Agents - therapeutic use
/ Bcl-2 protein
/ Biomedical and Life Sciences
/ Biomedicine
/ Brain injury
/ Brain Ischemia - drug therapy
/ Brain Ischemia - prevention & control
/ Cerebral blood flow
/ Disease Models, Animal
/ Drug Combinations
/ Heat shock proteins
/ Hsp60 protein
/ Hsp70 protein
/ Immunoblotting
/ Immunology
/ Internal Medicine
/ Intravenous administration
/ Ischemia
/ Lithium
/ Lithium Compounds - therapeutic use
/ Medical Microbiology
/ Neostriatum
/ Neurological diseases
/ Neuroprotection
/ Neuroprotective Agents - therapeutic use
/ Original
/ original-article
/ p53 protein
/ p53基因
/ Pharmacology/Toxicology
/ Prostaglandin E1
/ Random Allocation
/ Rats
/ Stroke
/ Vaccine
/ Vasodilator Agents - therapeutic use
/ 前列腺素E1
/ 大鼠模型
/ 混合配方
/ 热休克蛋白60
/ 神经保护作用
/ 脑缺血
2011
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Combined prostaglandin E1 and lithium exert potent neuroprotection in a rat model of cerebral ischemia
by
RuiSHENG Li-sha ZHANG Rong HAN Bo GAO Xiao-qian LIU Zheng-hong QIN
in
Alprostadil - therapeutic use
/ Animals
/ Antimanic Agents - therapeutic use
/ Bcl-2 protein
/ Biomedical and Life Sciences
/ Biomedicine
/ Brain injury
/ Brain Ischemia - drug therapy
/ Brain Ischemia - prevention & control
/ Cerebral blood flow
/ Disease Models, Animal
/ Drug Combinations
/ Heat shock proteins
/ Hsp60 protein
/ Hsp70 protein
/ Immunoblotting
/ Immunology
/ Internal Medicine
/ Intravenous administration
/ Ischemia
/ Lithium
/ Lithium Compounds - therapeutic use
/ Medical Microbiology
/ Neostriatum
/ Neurological diseases
/ Neuroprotection
/ Neuroprotective Agents - therapeutic use
/ Original
/ original-article
/ p53 protein
/ p53基因
/ Pharmacology/Toxicology
/ Prostaglandin E1
/ Random Allocation
/ Rats
/ Stroke
/ Vaccine
/ Vasodilator Agents - therapeutic use
/ 前列腺素E1
/ 大鼠模型
/ 混合配方
/ 热休克蛋白60
/ 神经保护作用
/ 脑缺血
2011
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Combined prostaglandin E1 and lithium exert potent neuroprotection in a rat model of cerebral ischemia
Journal Article
Combined prostaglandin E1 and lithium exert potent neuroprotection in a rat model of cerebral ischemia
2011
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Overview
Aim: To examine the effects of a mixed formulation composed of prostaglandin E1 and lithium (PGEI+Li mixture) on brain damage after cerebral ischemia. The effects of the mixture on protein expression of heat shock proteins (HSPs), p53, and Bcl-2 were also determined. Methods: Brain ischemia was induced with a permanent middle cerebral artery occlusion (pMCAO) in rats. Rats were treated with a single intravenous administration of PGE1, lithium or a PGEI+Li mixture immediately after the ischemic insult. The infarct volume and motor behavior deficits were analyzed 24 h after the ischemic insult. The protein levels of HSPTO, glucose-regulated protein 78 (GRP78), HSP60, Bcl-2, and p53 in the striatum of the ipsilateral hemisphere were examined using immunoblotting. Results: The mixture (PGE1 22.6 nmol/kg+Li 0.5 mmol/kg) reduced infarct volume and neurological deficits induced by focal cerebral ischemia. Moreover, the mixture had a greater neuroprotective effect against cerebral ischemia compared with PGE1 or lithium alone. The mixture was effective even if it was administered 3 h after ischemia. PGEI+Li also significantly upregulated cytoprotective HSPTO GRP78, HSP60, and Bcl-2 protein levels, while decreasing p53 expression. Conclusion: These results demonstrated a PGEI+Li mixture with a therapeutic window of up to 3 h for clinical treatment of cerebral ischemia. The PGEI+Li mixture potentially exerts a protective effect after stroke through the induction of HSPs and Bcl-2 proteins.
Publisher
Nature Publishing Group UK,Nature Publishing Group
Subject
/ Animals
/ Antimanic Agents - therapeutic use
/ Biomedical and Life Sciences
/ Brain Ischemia - drug therapy
/ Brain Ischemia - prevention & control
/ Ischemia
/ Lithium
/ Lithium Compounds - therapeutic use
/ Neuroprotective Agents - therapeutic use
/ Original
/ p53基因
/ Rats
/ Stroke
/ Vaccine
/ Vasodilator Agents - therapeutic use
/ 前列腺素E1
/ 大鼠模型
/ 混合配方
/ 热休克蛋白60
/ 神经保护作用
/ 脑缺血
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