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- Keywords c Jun;ketamine;nifedipine;global ischemia;NMDA receptor;L type voltage gated calcium channel （L VGCC）; 氯胺酮;硝苯吡啶;脑缺血;NMDA受体;L-型电压门控钙通道;
- Voltage gated Na + channel(VGSC)is the target of numerous natural neurotoxins. 电压门控钠通道(VGSC)是许多天然生物神经毒素特异作用的靶受体。
- Voltage- gated calcium channel 电压门控性钙通道
- Rasmusson RL, Morales MJ, Wang S, et al. Inactivation of voltage gated cardiac K+ channels[J]. Circ Res, 1998,82(7):739 50. 郭洪波;王帅;邹飞.;下丘脑神经元钙激活钾通道的温度效应[J]
- Voltage gated sodium channels (VGSC) are responsible for the rising phase of the action potential in the membrane of neurons and most electrically excitable cells. 电压门控钠通道(VGSC)在神经元及大多可兴奋性细胞动作电位的形成和传播过程中扮演着极为重要的角色。
- Human voltage-gated calcium channel，VGCC Elisa ... 人钙离子通道抗体（VGCC）试剂盒；
- The voltage gated sodium channel is the major target receptor for DDT and pyrethroids, and is the basis of their cross resistance (knockdown resistance). 电压门控的钠通道是拟除虫菊酯 (Pyrethroid)和滴滴涕 (dichloro diphenyl trichloroethane)的共同靶变点 ,是它们产生交互抗性 (击倒抗性 ,Knockdownresistance)的基础。
- Calcium Channel Regulation and Presynaptic Plasticity. Ca2+通道与突触前神经元的可塑性有关。
- So and they would affect brain with calcium channel blockers. 通过应用钙离子拮抗剂治疗脑血管疾病。
- Calcium channel blockers reduce afterload with little effect on preload. 钙通道阻滞剂降低后负荷，而对前负荷几乎没有作用。
- Cilnidipine is a new dihydropyridine (DHP) type of calcium channel antagonist. 西尼地平是新型的二氢吡啶类(DHP)钙通道拮抗剂，临床上用于治疗高血压和心绞痛；
- Amlodipine(ALDP) is a new kind of calcium channel blocker of dihydropyridine. 氨氯地平是新型二氢吡啶类钙通道阻滞剂。
- The calcium channel blocker had similar effect and was concerned by doctors. 而钙通道阻滞剂治疗消化性溃疡的疗效已引起广大医生的关注。
- Phenobarbital may also inhibit calcium channels, resulting in a decrease in excitatory transmitter release. 苯巴比妥还对钙通道起抑制作用，减少兴奋性递质的释放。
- Conclusions Ketamine inhihites the L-type calcium channels of ventricular myocytes in a good dose-response manner. 结论氯胺酮对心肌细胞膜L-型钙通道具有抑制作用，其抑制程度有浓度依赖性。
- Like opioid receptors, N-type calcium channels occur throughout the nervous system. 一如鸦片类受体，N型钙离子通道也分布在整个神经系统。
- Bre may decrease [Caa+]i through receptor-dependent calcium channels,while it can increase [Caa+]i through voltage-dependent calcium channels. Bre可能通过抑制受体依赖性钙通道而降低[Caa+]i,但却能增强电压依赖性钙通道而增高[Caa+]i。
- Preperfusing with Bay K 8644 (500 nmol/L), an agonist of calcium channels, also eliminated the effect of Agm on carotid baroreceptor activity. (4 )预先灌流Ca2 +通道激动剂BayK 86 44 (5 0 0nmol/L)亦可取消Agm对窦神经传入放电的影响。
- Collectively, VEGF can directly and specifically reduce the activities of HVA calcium channels in the hippocampal CA1 pyramidal neurons. 2． 首次提出VEGF具有快速抑制神经元细胞膜高电压激活的钙电流的作用。
- AIM To study the antifibrotic effect of calcium channel blockers)CCB)on chronic liver diseases. 目的:研究钙通道阻滞刑(CCB)抗肝纤维化的作用。
