Kv7通道调节剂对糖尿病大鼠离体胃收缩性的影响

Gehan Badawi, S. Gad, Atef Abdel azeem Al seidi, Sabry Gad
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摘要

目的:研究KV7通道调节剂雷加滨(KV7开启剂)和xa -99 (KV7阻滞剂)对I型糖尿病大鼠胃底节和胃底节运动的影响。方法:将24只雄性Sprague Dawley大鼠分为2组(1)对照组和(2)糖尿病组(n=12),每组按所用部位(眼底或体)再分为2个亚组。各节段组分别给予瑞加滨和XE-991治疗基础运动和胆碱能刺激运动。使用Power Lab系统在体外记录运动。结果:糖尿病胃的基本收缩幅度和频率明显高于对照组。糖尿病胃对A.ch的反应。明显高于对照组。雷加滨可显著降低糖尿病组和对照组大鼠胃底肌和体肌的自发收缩力,但糖尿病组胃底肌和体肌自发收缩力的下降幅度明显大于对照组。雷吉比滨还能显著降低胆碱能刺激的基底条和体条的收缩力,且糖尿病患者体条收缩幅度的下降幅度明显大于对照组。糖尿病大鼠和对照组大鼠胃底自发收缩力和肌体自发收缩力均明显增加,但糖尿病组对XE-991的反应明显高于对照组。此外,在A.ch后,ex -991显著增加了糖尿病组和对照组的基底和肌体收缩幅度,糖尿病组的收缩幅度明显增加,但两组在A.ch后的张力均未增加。结论:KV7通道调节剂可影响I型糖尿病大鼠及对照组的胃活动。
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Effect of Kv7 channel modulators on the contractility of diabetic rat stomach in-vitro
Objectives:To study the effect of KV7 channel modulators, Retigabine(KV7 opener) and XE-99 (KV7 blocker), on motility of both fundal and corpal gastric segments in Type I diabetic rats . Method:24 Male Sprague Dawley rats were divided into 2 groups: (I) control& (II) diabetic group (n=12) each were subdivided into 2 subgroups according to the used segment whether fundus or corpus. Each segment group was treated with retigabine and XE-991 on basal and cholinergic stimulated motility. The motility was recorded in-vitro using the Power Lab system. Results: Diabetic stomach significantly showed higher fundal basal amplitude and frequency of contractions when compared with control. Diabetic gastric response to A.ch. was significantly higher as compaired to control. Retigabine, significantly decreased spontaneous contractility of gastric fundal and corpal muscle in diabetic and control rats but diabetic group exhibits significant more decrease in contractility than control. Also, retigabine significantly decreased contractility of cholinergic stimulated fundal and corpal strips with significant more decreased contraction amplitude in diabetic corpus than the control. XE-991, significantly increased spontaneous gastric fundal and corpal contractility in diabetic and control rats but diabetic group exhibits significant more increased contraction in response to XE-991 than the control. Also, XE-991 after A.ch significantly increased the amplitude of fundal and corpal contractility of both diabetic and control groups with significant higher contraction in diabetics , however there is no increase in the tone after A.ch in either groups. Conclusion: KV7 channel modulators could affect gastric activity in type I diabetic and control rats.
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