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- 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。
- Methods: Whole-cell patch clamp technique was used to determine sodium channel cur rent. 方法 :采用全细胞膜片钳技术 ,记录钠通道电流。
- Bepridil (Bep), an Ca 2+ channel blocker, ip 5 mg/kg 30 min prior to hypoxia served as positive control. 并以苄普地尔 5 m g/ kg ip给药作阳性对照。
- Sodium channel of dorsal root ganglion (DRG) plays an important role in the mechanisms of neuropathic pain. 摘要脊髓背根神经节的钠通道与神经性疼痛的形成有密切的关系。
- Conclusions:Coronary spasm can provoke lethal arrhythmia,but be tr eated effectively with Calcium Channel Blocker. 结论:冠状动脉痉挛可诱发严重的心律失常,钙拮抗剂治疗有效。
- Tetrodotoxin is one of the strong marine neural toxins which block sodium channels. 河豚毒素是钠离子通道阻断剂,是一种强海洋神经毒剂。
- These anaesthetics block sodium channels and thereby the excitability of all neurons, not just sensory neurons. 这些局麻剂可以阻断钠通道,因此不仅仅阻滞了感觉神经元,也同时阻滞了几乎所有其他神经元的兴奋性。
- The results suggest that RSM may be a kind of selective slow calcium channel blocker and able to prevent myocardium from injury of ISO. 提示:丹参可能为钙桔抗剂,并能对抗ISO引起的心肌钙超载性损伤。
- This review focuses on the relationship between the plasticity of voltage-gated sodium channel subunits and neuropathic pain states. 本文就目前研究较多的几种钠通道亚单位的可塑性与神经性疼痛的关系作一综述。
- The mechanism of treating traumatic cerebral edema with calcium channel blocker is to inhibit EAA releasing and to inhibit Ca 2+ influx directly. 钙通道阻断剂治疗外伤性脑水肿的机制是抑制脑外伤后EAA释放及直接减少Ca2+内流。
- It can activate sodium channel,inrease sodium current.it can inrease liber calcium concentration in the myocardial cell. 实验证明:As可激活钙通道,增加钙通道电流 As增加细胞内游离的钙离子浓度 As可激活钠通道,增加钠电流 关键词:龙牙葱木皂苷 培养心肌细胞 L-型钙电流 钠通道 膜片钳 正性肌力作用 Aralosides(As)are omni-glycosides extracted from roots;petiols and skins of Aralia (Miq) seem.
- AIM: To investigate the effects of nifedipine, a calcium channel blocker, on cellular proliferation of gingival fibroblasts in vitro . 目的:探讨钙拮抗剂硝苯地平对牙龈成纤维细胞的作用。
- These included mutations in the sodium channel gene SCN5A, preiously associated with LQTS and other unstable heart rhythm conditions and sudden death. 这其中包括钠通道基因SCN5A的突变,该基因以前发现与LQTS、其他不稳定心律失常以及猝死相关。
- Nifedipine (nifedipine) is the last century in the early 70 listed a calcium channel blocker treatment of cardiovascular disease category. 硝苯地平(心痛定)是上世纪70年代初上市的一种钙通道拮抗剂类心血管病治疗药物。
- They are lipophilic, so can enter virtually any neuron, where they indiscriminately block sodium channels in the membrane. 它们的亲油性使它们能进入几乎任何神经元,在那里,它们会不加甄别地阻断细胞膜中的钠通道。
- CONCLUSION GLB used as KATP channel blocker can reduce the extent of augmentation of TDR in the initial stage when coronary artery was ligated. 结论使用KATP通道阻断剂GLB可减小冠脉结扎后初期心室肌TDR增大程度。
- 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。
- Effects of neuromuscular blocker (NMB) of atracurium (ATC) and vecuronium (VCR ) in patients on calcium - channel blocker(CCB), nifedipine, therapy were studied with Accelograph. 观察了钙通道阻滞药(CCB)硝苯吡啶(Nif)与阿屈可林(ATC)或维库溴铵(VCR)联用对患者神经肌肉阻滞(NMB)效应的影响。
- To observe the effect of Garlicin on sodium channel in isolated ventricular cell of rats, to find out the mechanism of antiarrhythmia of Garlicin on the ionic channel level. 目的研究大蒜素对豚鼠心室肌细胞膜快钠通道的影响,探讨大蒜素在离子通道水平的抗心律失常作用机制。