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Kv7 voltage-activated potassium channel inhibitors reduce fluid resuscitation requirements after hemorrhagic shock in rats

机译:Kv7电压激活的钾通道抑制剂可降低大鼠失血性休克后的液体复苏需求

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BackgroundRecent evidence suggests that drugs targeting Kv7 channels could be used to modulate vascular function and blood pressure. Here, we studied whether Kv7 channel inhibitors can be utilized to stabilize hemodynamics and reduce resuscitation fluid requirements after hemorrhagic shock.MethodsAnesthetized male Sprague-Dawley rats were instrumented with arterial and venous catheters for blood pressure monitoring, hemorrhage and fluid resuscitation. Series 1: Linopirdine (Kv7 channel blocker, 0.1–6 mg/kg) or retigabine (Kv7 channel activator, 0.1–12 mg/kg) were administered to normal animals. Series 2: Animals were hemorrhaged to a MAP of 25 mmHg for 30 min, followed by fluid resuscitation with normal saline (NS) to a MAP of 70 mmHg until t?=?75 min. Animals were treated with single bolus injections of vehicle, linopirdine (1–6 mg/kg), XE-991 (structural analogue of linopirdine with higher potency for channel blockade, 1 mg/kg) prior to fluid resuscitation. Series 3: Animals were resuscitated with NS alone or NS supplemented with linopirdine (1.25–200 μg/mL). Data were analyzed with 2-way ANOVA/Bonferroni post-hoc testing.ResultsSeries 1: Linopirdine transiently (10–15 min) and dose-dependently increased MAP by up to 15%. Retigabine dose-dependently reduced MAP by up to 60%, which could be reverted with linopirdine. Series 2: Fluid requirements to maintain MAP at 70 mmHg were 65?±?34 mL/kg with vehicle, and 57?±?13 mL/kg, 22?±?8 mL/kg and 22?±?11 mL/kg with intravenous bolus injection of 1, 3 and 6 mg/kg linopirdine, respectively. XE-991 (1 mg/kg), reduced resuscitation requirements comparable to 3 mg/kg linopirdine.Series 3: When resuscitation was performed with linopirdine-supplemented normal saline (NS), fluid requirements to stabilize MAP were 73?±?12 mL/kg with NS alone and 72?±?24, 61?±?20, 36?±?9 and 31?±?9 mL/kg with NS supplemented with 1.25, 6.25, 12.5 and 200 μg/mL linopirdine, respectively.ConclusionsOur data suggest that Kv7 channel blockers could be used to stabilize blood pressure and reduce fluid resuscitation requirements after hemorrhagic shock.
机译:背景技术最近的证据表明,靶向Kv7通道的药物可用于调节血管功能和血压。在这里,我们研究了是否可以使用Kv7通道抑制剂来稳定失血性休克后的血流动力学并降低其对复苏液的需求。系列1:将利诺比丁(Kv7通道阻断剂,0.1–6 mg / kg)或瑞替加滨(Kv7通道活化剂,0.1–12 mg / kg)施用于正常动物。系列2:使动物出血至25mmHg的MAP达30分钟,然后用生理盐水(NS)进行液体复苏至70mmHg的MAP,直到t≥75分钟。在进行液体复苏之前,通过单次大剂量注射溶媒,利诺吡丁(1-6 mg / kg),XE-991(利诺吡丁的结构类似物,对通道的阻断作用更高,1 mg / kg)对动物进行治疗。系列3:仅用NS或补充了利诺匹定(1.25-200μg/ mL)的NS可使动物复苏。结果数据1:利诺比尔定短暂(10-15分钟),剂量依赖性地使MAP升高15%。结果采用2通ANOVA / Bonferroni事后检验进行分析。瑞替加滨剂量依赖性地将MAP降低高达60%,这可以用利诺吡丁逆转。系列2:使用赋形剂将MAP维持在70 mmHg时所需的液体量为65?±?34 mL / kg,57?±?13 mL / kg,22?±?8 mL / kg和22?±?11 mL / kg分别静脉推注1、3和6 mg / kg利诺吡丁。 XE-991(1 mg / kg),降低的复苏要求相当于3 mg / kg利诺皮定。系列3:当使用补充了利诺皮定的生理盐水(NS)进行复苏时,稳定MAP所需的液体量为73?±?12 mL / kg(单独使用NS)和72?±?24、61?±?20、36?±?9和31?±?9 mL / kg,分别添加1.25、6.25、12.5和200μg/ mL利诺吡丁的NS。结论我们的数据表明,出血性休克后,Kv7通道阻滞剂可用于稳定血压和减少液体复苏的需求。

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