author_facet Sun, Yang
Gui, Huan
Li, Qi
Luo, Zhu‐Min
Zheng, Min‐Jun
Duan, Jun‐Li
Liu, Xia
Sun, Yang
Gui, Huan
Li, Qi
Luo, Zhu‐Min
Zheng, Min‐Jun
Duan, Jun‐Li
Liu, Xia
author Sun, Yang
Gui, Huan
Li, Qi
Luo, Zhu‐Min
Zheng, Min‐Jun
Duan, Jun‐Li
Liu, Xia
spellingShingle Sun, Yang
Gui, Huan
Li, Qi
Luo, Zhu‐Min
Zheng, Min‐Jun
Duan, Jun‐Li
Liu, Xia
CNS Neuroscience & Therapeutics
MicroRNA‐124 Protects Neurons Against Apoptosis in Cerebral Ischemic Stroke
Pharmacology (medical)
Physiology (medical)
Psychiatry and Mental health
Pharmacology
author_sort sun, yang
spelling Sun, Yang Gui, Huan Li, Qi Luo, Zhu‐Min Zheng, Min‐Jun Duan, Jun‐Li Liu, Xia 1755-5930 1755-5949 Wiley Pharmacology (medical) Physiology (medical) Psychiatry and Mental health Pharmacology http://dx.doi.org/10.1111/cns.12142 <jats:title>Summary</jats:title><jats:sec><jats:title>Aims</jats:title><jats:p>To explore the role and underlying mechanism of miR‐124 in stroke.</jats:p></jats:sec><jats:sec><jats:title>Methods</jats:title><jats:p>miR‐124 expression was determined by real‐time PCR. The effect of miR‐124 on infarct area was assessed in middle cerebral artery occlusion (MCAO) mice. The influence of miR‐124 on oxygen and glucose deprivation (OGD) induced neuron apoptosis and death was examined by immunofluorescence. The effect of miR‐124 on apoptosis‐related proteins was determined by Western blot.</jats:p></jats:sec><jats:sec><jats:title>Results</jats:title><jats:p>The level of miR‐124 is significantly increased in ischemic penumbra as compared with that in nonischemic area of MACO mice. Brain tissue of stroke‐prone spontaneously hypertensive rats (SHR‐SP) also showed higher level of miR‐124 as compared with that of spontaneously hypertensive rats (SHR). Consistently, OGD treatment obviously increased miR‐124 level in primary neurons. <jats:italic>In vivo</jats:italic>, miR‐124 overexpression significantly decreased, while miR‐124 knockdown significantly increased, the infarct area of MCAO mice. <jats:italic>In vitro</jats:italic>, gain or loss of miR‐124 function resulted in reduced or increased neuron apoptosis and death induced by OGD, and increased or reduced antiapoptosis protein, Bcl‐2 and Bcl‐xl, respectively.</jats:p></jats:sec><jats:sec><jats:title>Conclusions</jats:title><jats:p>miR‐124 plays a neurons‐protective role <jats:italic>via</jats:italic> apoptosis‐inhibiting pathway in ischemic stroke.</jats:p></jats:sec> MicroRNA‐124 Protects Neurons Against Apoptosis in Cerebral Ischemic Stroke CNS Neuroscience & Therapeutics
doi_str_mv 10.1111/cns.12142
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series CNS Neuroscience & Therapeutics
source_id 49
title MicroRNA‐124 Protects Neurons Against Apoptosis in Cerebral Ischemic Stroke
title_unstemmed MicroRNA‐124 Protects Neurons Against Apoptosis in Cerebral Ischemic Stroke
title_full MicroRNA‐124 Protects Neurons Against Apoptosis in Cerebral Ischemic Stroke
title_fullStr MicroRNA‐124 Protects Neurons Against Apoptosis in Cerebral Ischemic Stroke
title_full_unstemmed MicroRNA‐124 Protects Neurons Against Apoptosis in Cerebral Ischemic Stroke
title_short MicroRNA‐124 Protects Neurons Against Apoptosis in Cerebral Ischemic Stroke
title_sort microrna‐124 protects neurons against apoptosis in cerebral ischemic stroke
topic Pharmacology (medical)
Physiology (medical)
Psychiatry and Mental health
Pharmacology
url http://dx.doi.org/10.1111/cns.12142
publishDate 2013
physical 813-819
description <jats:title>Summary</jats:title><jats:sec><jats:title>Aims</jats:title><jats:p>To explore the role and underlying mechanism of miR‐124 in stroke.</jats:p></jats:sec><jats:sec><jats:title>Methods</jats:title><jats:p>miR‐124 expression was determined by real‐time PCR. The effect of miR‐124 on infarct area was assessed in middle cerebral artery occlusion (MCAO) mice. The influence of miR‐124 on oxygen and glucose deprivation (OGD) induced neuron apoptosis and death was examined by immunofluorescence. The effect of miR‐124 on apoptosis‐related proteins was determined by Western blot.</jats:p></jats:sec><jats:sec><jats:title>Results</jats:title><jats:p>The level of miR‐124 is significantly increased in ischemic penumbra as compared with that in nonischemic area of MACO mice. Brain tissue of stroke‐prone spontaneously hypertensive rats (SHR‐SP) also showed higher level of miR‐124 as compared with that of spontaneously hypertensive rats (SHR). Consistently, OGD treatment obviously increased miR‐124 level in primary neurons. <jats:italic>In vivo</jats:italic>, miR‐124 overexpression significantly decreased, while miR‐124 knockdown significantly increased, the infarct area of MCAO mice. <jats:italic>In vitro</jats:italic>, gain or loss of miR‐124 function resulted in reduced or increased neuron apoptosis and death induced by OGD, and increased or reduced antiapoptosis protein, Bcl‐2 and Bcl‐xl, respectively.</jats:p></jats:sec><jats:sec><jats:title>Conclusions</jats:title><jats:p>miR‐124 plays a neurons‐protective role <jats:italic>via</jats:italic> apoptosis‐inhibiting pathway in ischemic stroke.</jats:p></jats:sec>
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author Sun, Yang, Gui, Huan, Li, Qi, Luo, Zhu‐Min, Zheng, Min‐Jun, Duan, Jun‐Li, Liu, Xia
author_facet Sun, Yang, Gui, Huan, Li, Qi, Luo, Zhu‐Min, Zheng, Min‐Jun, Duan, Jun‐Li, Liu, Xia, Sun, Yang, Gui, Huan, Li, Qi, Luo, Zhu‐Min, Zheng, Min‐Jun, Duan, Jun‐Li, Liu, Xia
author_sort sun, yang
container_issue 10
container_start_page 813
container_title CNS Neuroscience & Therapeutics
container_volume 19
description <jats:title>Summary</jats:title><jats:sec><jats:title>Aims</jats:title><jats:p>To explore the role and underlying mechanism of miR‐124 in stroke.</jats:p></jats:sec><jats:sec><jats:title>Methods</jats:title><jats:p>miR‐124 expression was determined by real‐time PCR. The effect of miR‐124 on infarct area was assessed in middle cerebral artery occlusion (MCAO) mice. The influence of miR‐124 on oxygen and glucose deprivation (OGD) induced neuron apoptosis and death was examined by immunofluorescence. The effect of miR‐124 on apoptosis‐related proteins was determined by Western blot.</jats:p></jats:sec><jats:sec><jats:title>Results</jats:title><jats:p>The level of miR‐124 is significantly increased in ischemic penumbra as compared with that in nonischemic area of MACO mice. Brain tissue of stroke‐prone spontaneously hypertensive rats (SHR‐SP) also showed higher level of miR‐124 as compared with that of spontaneously hypertensive rats (SHR). Consistently, OGD treatment obviously increased miR‐124 level in primary neurons. <jats:italic>In vivo</jats:italic>, miR‐124 overexpression significantly decreased, while miR‐124 knockdown significantly increased, the infarct area of MCAO mice. <jats:italic>In vitro</jats:italic>, gain or loss of miR‐124 function resulted in reduced or increased neuron apoptosis and death induced by OGD, and increased or reduced antiapoptosis protein, Bcl‐2 and Bcl‐xl, respectively.</jats:p></jats:sec><jats:sec><jats:title>Conclusions</jats:title><jats:p>miR‐124 plays a neurons‐protective role <jats:italic>via</jats:italic> apoptosis‐inhibiting pathway in ischemic stroke.</jats:p></jats:sec>
doi_str_mv 10.1111/cns.12142
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id ai-49-aHR0cDovL2R4LmRvaS5vcmcvMTAuMTExMS9jbnMuMTIxNDI
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imprint_str_mv Wiley, 2013
institution DE-Gla1, DE-Zi4, DE-15, DE-Pl11, DE-Rs1, DE-105, DE-14, DE-Ch1, DE-L229, DE-D275, DE-Bn3, DE-Brt1, DE-Zwi2, DE-D161
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spelling Sun, Yang Gui, Huan Li, Qi Luo, Zhu‐Min Zheng, Min‐Jun Duan, Jun‐Li Liu, Xia 1755-5930 1755-5949 Wiley Pharmacology (medical) Physiology (medical) Psychiatry and Mental health Pharmacology http://dx.doi.org/10.1111/cns.12142 <jats:title>Summary</jats:title><jats:sec><jats:title>Aims</jats:title><jats:p>To explore the role and underlying mechanism of miR‐124 in stroke.</jats:p></jats:sec><jats:sec><jats:title>Methods</jats:title><jats:p>miR‐124 expression was determined by real‐time PCR. The effect of miR‐124 on infarct area was assessed in middle cerebral artery occlusion (MCAO) mice. The influence of miR‐124 on oxygen and glucose deprivation (OGD) induced neuron apoptosis and death was examined by immunofluorescence. The effect of miR‐124 on apoptosis‐related proteins was determined by Western blot.</jats:p></jats:sec><jats:sec><jats:title>Results</jats:title><jats:p>The level of miR‐124 is significantly increased in ischemic penumbra as compared with that in nonischemic area of MACO mice. Brain tissue of stroke‐prone spontaneously hypertensive rats (SHR‐SP) also showed higher level of miR‐124 as compared with that of spontaneously hypertensive rats (SHR). Consistently, OGD treatment obviously increased miR‐124 level in primary neurons. <jats:italic>In vivo</jats:italic>, miR‐124 overexpression significantly decreased, while miR‐124 knockdown significantly increased, the infarct area of MCAO mice. <jats:italic>In vitro</jats:italic>, gain or loss of miR‐124 function resulted in reduced or increased neuron apoptosis and death induced by OGD, and increased or reduced antiapoptosis protein, Bcl‐2 and Bcl‐xl, respectively.</jats:p></jats:sec><jats:sec><jats:title>Conclusions</jats:title><jats:p>miR‐124 plays a neurons‐protective role <jats:italic>via</jats:italic> apoptosis‐inhibiting pathway in ischemic stroke.</jats:p></jats:sec> MicroRNA‐124 Protects Neurons Against Apoptosis in Cerebral Ischemic Stroke CNS Neuroscience & Therapeutics
spellingShingle Sun, Yang, Gui, Huan, Li, Qi, Luo, Zhu‐Min, Zheng, Min‐Jun, Duan, Jun‐Li, Liu, Xia, CNS Neuroscience & Therapeutics, MicroRNA‐124 Protects Neurons Against Apoptosis in Cerebral Ischemic Stroke, Pharmacology (medical), Physiology (medical), Psychiatry and Mental health, Pharmacology
title MicroRNA‐124 Protects Neurons Against Apoptosis in Cerebral Ischemic Stroke
title_full MicroRNA‐124 Protects Neurons Against Apoptosis in Cerebral Ischemic Stroke
title_fullStr MicroRNA‐124 Protects Neurons Against Apoptosis in Cerebral Ischemic Stroke
title_full_unstemmed MicroRNA‐124 Protects Neurons Against Apoptosis in Cerebral Ischemic Stroke
title_short MicroRNA‐124 Protects Neurons Against Apoptosis in Cerebral Ischemic Stroke
title_sort microrna‐124 protects neurons against apoptosis in cerebral ischemic stroke
title_unstemmed MicroRNA‐124 Protects Neurons Against Apoptosis in Cerebral Ischemic Stroke
topic Pharmacology (medical), Physiology (medical), Psychiatry and Mental health, Pharmacology
url http://dx.doi.org/10.1111/cns.12142