观察阴离子通道阻断剂对血管的舒张作用。
Vasorelaxing effects of anion channel blocker were observed.
目的研究l型钙通道阻断剂对曲马多镇痛作用的影响。
Aim To investigate the effects of L-type calcium channel blockers on tramadol-induced analgesia.
河豚毒素是钠离子通道阻断剂，是一种强海洋神经毒剂。
Tetrodotoxin is one of the strong Marine neural toxins which block sodium channels.
目的观察氯通道阻断剂对小鼠心室肌容积敏感性氯通道的影响。
Objective To examine the effect of chloride blockers on volume-sensitive chloride channels in mouse cardiac ventricular myocytes.
治疗高血压的钙离子通道阻断剂和治疗关节炎的药物都可能影响生育能力。
Calcium channel blockers used for high blood pressure and medications used to treat arthritis may affect fertility potential.
我相信，在不久的将来，将可以应用其它联合arb或者钙通道阻断剂的用药方案。
I believe other combinations will be available in the near future with ARB or with calcium channel blockers.
如果在围手术期给药钙通道阻断剂有减少移植后急性肾小管坏死(atn)的可能性。
Calcium channel blockers have the potential to reduce the incidence of post-transplant acute tubular necrosis (ATN) if given in the peri-operative period.
选择标准：比较对照和钙通道阻断剂围移植手术期给药的随机对照试验入选。半随机对照试验被排除。
SELECTION CRITERIA: Randomised controlled trials comparing calcium channel blockers given in the peri-transplant period with controls were included. Quasi-randomised trials were excluded.
氯通道阻断剂atp和NPPB可逆性地抑制此电流，ATP的抑制作用在外向电流显著强于内向电流。
Chloride channel blockers, NPPB and ATP, inhibited the currents reversibly. Moreover, the inhibition of ATP on the outward currents was stronger than that on the inward currents.
我们进一步用膜通道阻断剂验证，发现胞外钙的流入主要是通过N型钙通道和电压门控钠通道流入胞内的。
Furthermore, the external calcium was found to influx mainly through N-type calcium channels and voltage-gated sodium channels.
这表明钠离子通道阻断剂在与受体相互作用时具有共同的结构特征和作用方式，同时也为探讨受体结构提供了有价值的信息。
Studies of these results show that the sodium channel blockade has common structural features and way of action when interact with the receptor, thus leading to identical biological effect.
结果显示，应用TRPV 1激动剂能够使带电的钠通道阻断剂特异性地作用于疼痛感受器神经元而产生特异性局麻止痛效果。
Here we show that charged sodium-channel blockers can be targeted into nociceptors by the application of TRPV1 agonists to produce a pain-specific local anaesthesia.
结论：氯通道阻断剂NPPB或NFA能够在一定程度上减轻氧化应激引起的C6细胞损伤，可能与调节细胞膜功能和下调CLIC 4蛋白表达有关。
CONCLUSION: the chloride channel blockers NPPB or NFA lessen the oxidative injury of C6 cells through modulating the function of membrane and down-regulating the protein expression of CLIC4.
建立大鼠离体灌流心脏模型，观察钠通道特异性阻断剂河豚毒素对离体灌流心脏自发性节律即固有心率的影响。
The functional roles of the NaChs were tested by observing the effect of tetrodotoxin, a specific blocker of NaChs, on the intrinsic heart rate of isolated rat working heart.
建立大鼠离体灌流心脏模型，观察钠通道特异性阻断剂河豚毒素对离体灌流心脏自发性节律即固有心率的影响。
The functional roles of the NaChs were tested by observing the effect of tetrodotoxin, a specific blocker of NaChs, on the intrinsic heart rate of isolated rat working heart.
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