【摘 要】
:
As a main subtype of gtia in the central nervous system, astrocytes have diverse and comprehensive functions, from nutrient providing to synaptic transmission modulating.Astrocytes play protective rol
【机 构】
:
State Key Laboratory of Biomembrane and Membrane Biotechnology, College of Life Sciences, Peking Uni
【出 处】
:
中国神经科学学会第九届全国学术会议暨第五届会员代表大会
论文部分内容阅读
As a main subtype of gtia in the central nervous system, astrocytes have diverse and comprehensive functions, from nutrient providing to synaptic transmission modulating.Astrocytes play protective roles in ischemia injury by taking up glutamate, releasing neurotrophic factors, and so on.However, the function of gap junctions in this process is still controversial.Cultured cortical neurons were treated with 3-h oxygen-glucose deprivation (OGD) to induce cell damage.We found that astrocyte-conditioned medium (ACM) could reduce neuronal death from ~95% to ~30%, as indicated by MTT assay.With centrifugal filter devices, the molecular weight of protective factors released from astrocytes was speculated to be < 3 kDa.The protection of ACM was remarkably decreased when 50 tmol/L gap junction and hemichannel blocker carbenoxolone (CBX) was applied to the cultured astrocytes before ACM collection.Furthermore, ACM pretreatment raised neuronal level of reductive glutathione (GSH) and decreased reactive oxygen species (ROS) content, while ACM pretreated with CBX could block GSH increase in neurons.These results suggested that astrocytes enhanced neuronal tolerance against OGD injury by releasing protective factors dependent on hemichannels or gap junctions.
其他文献
目的 研究染料木素磺酸钠(genistein sulfonate sodium,GSS)对大鼠脑缺血再灌注损伤的保护作用.方法 采用大鼠大脑中动脉栓塞制作局灶性脑缺血再灌注损伤模型进行实验研究.在缺血后10分钟,假手术组与模型组经舌下静脉注射生理盐水,治疗组分别从舌下静脉注射等体积不同浓度的GSS (0.5 mg/kg,1 mg/kg或2 mg/kg).缺血1h,再灌注24 h后,行神经功能评分,
Electro-acupuncture (EA), especially high-frequency EA, has been frequently used as an alternative therapy for Parkinsons disease (PD) with reportedly effective for alleviating motor symptoms in patie
Objective Spinocerebellar ataxia type 3/Machado-Joseph disease (SCA3/MJD) is an autosomal dominant neurodegenerative disorder caused by an expansion of polyglutamine tract near the C-terminus of the M
Mutations in the parkin gene are currently thought to be the most common cause of familial Parkinsonism.Overexpression of parkin has been reported to prevent neuronal degeneration under various condit
Objective This study was performed with an in vitro blood-tumor barrier (BTB) model to investigate whether protein kinase C (PKC) and RhoA are involved in the low-dose endothelial monocyte-activating
Objective Epigenetic modifications such as DNA methylation are known to participate in the development of depression in both human and animal models.However, the role of DNA methyltransferases (DNMTs)
Completely transected rat lower thoracic spinal cord was bridged either immediately or lingeringly by microsurgically linking T7 intercostal nerves to L3 dorsal root stumps to establish a bridged bypa
Methylphenidate is widely used for the treatment of Attention-Deficit/Hyperactivity Disorder (ADHD), but the molecular mechanisms of its therapeutic action are not well understood.Here we examined the
Objective To identify the influence of ages of patients with hemispheric cerebral infarction on the mortality of large craniectomy decompression.Methods Thirteen cases underwent large craniectomy deco
Objective Generation and deposition of amyloid beta peptides (Aβ) and neurofibrillary tangle formation are key mechanisms involved in Alzheimers disease (AD) pathogenesis.There is evidence supporting