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p53-mediated neuronal cell death in ischemic brain injury 被引量:7
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作者 洪荔枝 赵晓媛 张慧灵 《Neuroscience Bulletin》 SCIE CAS CSCD 2010年第3期232-240,共9页
p53 is a key modulator of cellular stress responses.It is activated in the ischemic areas of brain,and contributes to neuronal apoptosis.In various stroke models,p53 deficiency or applications of p53 inhibitors can si... p53 is a key modulator of cellular stress responses.It is activated in the ischemic areas of brain,and contributes to neuronal apoptosis.In various stroke models,p53 deficiency or applications of p53 inhibitors can significantly attenuate brain damage.p53-mediated neuronal apoptosis occurs through various molecular mechanisms.The transcriptional pathway is an important mechanism through which p53 induces neuronal apoptosis by up-regulating the expression of its target gene p21WAF,Peg3/Pw1 or p53-up-regulated modulator of apoptosis (PUMA) .In addition,p53 disrupts NF-κB binding to p300 and blocks NF-κB-mediated survival signaling.On the other hand,the transcription-independent pathway mechanism is also of great importance.In this pathway,p53 is translocated to mitochondrial and mediates the release of cytochrome c.In both pathways,p53 seems to play a key role in post-ischemic brain damage and has become a therapeutic target against stroke pathology. 展开更多
关键词 P53 cerebral ischemia APOPTOSIS
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PPARγ参与吡格列酮的镇痛作用 被引量:1
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作者 赵晓媛 史红 +2 位作者 魏超 洪荔枝 张慧灵 《中国新药杂志》 CAS CSCD 北大核心 2010年第3期229-232,235,共5页
目的:在动物疼痛模型上,观察过氧化物酶体增殖剂激活受体γ(peroxisome proliferator-activa-ted receptor gamma,PPARγ)激动剂吡格列酮(pioglitazone,Piog)的镇痛作用及其与PPARγ的关系。方法:采用腹腔注射(0.78,1.25和2 mg.kg-1,ip... 目的:在动物疼痛模型上,观察过氧化物酶体增殖剂激活受体γ(peroxisome proliferator-activa-ted receptor gamma,PPARγ)激动剂吡格列酮(pioglitazone,Piog)的镇痛作用及其与PPARγ的关系。方法:采用腹腔注射(0.78,1.25和2 mg.kg-1,ip)和脑室注射(0.02和0.04 mg.kg-1,icv)给予Piog,应用小鼠扭体反应测定痛阈;预先注射PPARγ的特异性抑制剂GW9662(0.5和1 mg.kg-1,ip或5和10μg.kg-1,icv)研究Piog的镇痛作用与PPARγ的关系。结果:Piog(0.78,1.25和2 mg.kg-1,ip)在小鼠扭体实验中呈现出剂量依赖性镇痛作用。脑室注射Piog(0.02和0.04 mg.kg-1,icv,外周剂量的1/50)亦出现镇痛作用。PPARγ的特异性抑制剂GW9662(1 mg.kg-1,ip或5,10μg.kg-1,icv)均能取消Piog的镇痛作用。结论:Pi-og具有镇痛作用,中枢神经系统可能参与Piog的镇痛作用。PPARγ尤其是中枢的PPARγ可能与Piog的镇痛作用有关。 展开更多
关键词 吡格列酮 镇痛 中枢神经系统 过氧化物酶体增殖剂激活受体γ GW9662
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