Regulation of NMDA-induced neuronal excitability by TRPC6 channels

来源 :The 4th International Ion Channel Conference(第四届国际离子通道会议) | 被引量 : 0次 | 上传用户:yzgsmallfish
下载到本地 , 更方便阅读
声明 : 本文档内容版权归属内容提供方 , 如果您对本文有版权争议 , 可与客服联系进行内容授权或下架
论文部分内容阅读
Overactivation of NMDA receptor is a key event in excitotoxicity that induces a sudden intracellular.Ca2+ elevation and finally leads to cell apoptosis and necrosis and inhibition of the Ca2+ overload by blocking NMDA receptor can be neuroprotective.TRPC6 channel, one of the Ca2+-permeable nonselective cation channels, plays multiple important roles in neurite outgrowth, synapse formation and neuronal survival during neuronal development.However, little is known about the mechanisms of TRPC6-mediated neuroprotection and the relationship between TRPC6 channels and NMDA receptors.
其他文献
Retinoids are structurally related derivatives of vitamin A and are required for normal vision as well as cell proliferation and differentiation.Clinically, retinoids are effective in treating many sk
Purinergic signaling contributes significantly to cutaneous, musculoskeletal and visceral nociception and on the roles played by P2X3, P2X2/3, P2X4, P2X7 ATP receptor channels in neuropathic and infla
M-type K+ channels, encoded by the KCNQ2-5 family of genes, play key roles in the regulation of neuronal excitability.We study the regulation of M-channel activity and transcriptional expression by A-
Transient receptor potential (TRP) channels are polymodal cation channels that provide one of the main pathways for cation influx in excitable and non-excitable cells.Among them, the six thermo-sensit
会议
TRP
Phosphoinositides are a family of phospholipids in the cytoplasmic leaflet of plasma membranes and cell organelles.They are minority lipids differing by the degree of phosphorylation of the inositol h
Neutrophils are the first line of host defense against invading microorganism or other inflammatory stimuli in the innate immune system, and contribute to inflammation-related tissue injuries, associa
Kv1.3 channels have become a novel target for the treatment of autoimmune diseases.Searching for specific Kv1.3 potassium channel inhibitors has become the current hot spot for the treatment of autoim
Inward rectifier potassium (Kir) channels regulate cell resting membrane potential andexcitability.Like many other types of ion channels, the activity of Kir channels transport K+ ions cross membranes
Necrosis is an important form of cell demise during organ development and diseases.Traditionally, necrosis has been considered as an accidental, uncontrolled form of cell death.Increasing evidence now
Potassium inward rectifying (Kir) channels are a class of transmembrane proteins which play important roles in various physiological processes, controlling the resting membrane potential, regulating e