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首页> 外文期刊>American Journal of Physiology >A new model of pacing in the mouse intestine.
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A new model of pacing in the mouse intestine.

机译:一种在小鼠肠中起搏的新模型。

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摘要

A simple model of pacing in mouse intestine to longitudinal (LM) as well as circular muscle (CM) has been developed. Undissected segments of LM or CM from mouse ileum or jejunum were prepared to record contractions, nerve functions were inhibited, and regular spontaneous contractions were recorded. These had the properties expected of interstitial cells of Cajal (ICC) paced contractions: ileum slower than jejunum, inhibited but not abolished by nicardipine, reduced in frequency by cyclopiazonic acid, abolished by Ca(2+)-free media, and high temperature dependence (Q10 approximately 2.6-3.2). Nicardipine significantly reduced the pacing frequency in LM and CM. Intestinal segments from W/W(V) mice had few irregular contractions in CM but had regular contractions in LM. Other differences were found between LM and CM that suggest that the control of pacing of LM differed from pacing of CM. Moreover, both LM and CM segments in wild-type and W/W(V) and after cyclopiazonic acid responded to electrical pacing (50 V/cm, 50 or 100 ms) at 1 pulse per second. Temperature <26 degrees C inhibited electrically paced contractions in CM. These findings suggest that the current models of ICC pacing need to be modified to apply to intact segments of mouse intestine.
机译:已经开发了在小鼠肠内向纵向(LM)以及环形肌肉(CM)起搏的简单模型。准备好来自小鼠回肠或空肠的未解剖的LM或CM片段以记录收缩,抑制神经功能,并记录规则的自发性收缩。这些具有预期的Cajal(ICC)间隔收缩间质细胞的特性:回肠比空肠慢,尼卡地平抑制但不消除,尼卡地平抑制回肠,环吡唑酸降低频率,无Ca(2+)培养基消除和高温依赖性(Q10约为2.6-3.2)。尼卡地平可显着降低LM和CM的起搏频率。 W / W(V)小鼠的肠段在CM中几乎没有不规则收缩,而在LM中则有规则收缩。在LM和CM之间发现了其他差异,这表明LM的起搏控制与CM的起搏不同。此外,野生型和W / W(V)以及环吡唑酸后的LM和CM段均以每秒1个脉冲的速度响应电起搏(50 V / cm,50或100 ms)。 <26摄氏度的温度抑制了CM中的电起搏收缩。这些发现表明,需要对当前的ICC起搏模型进行修改,以适用于小鼠肠道的完整节段。

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