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首页> 外文期刊>American Journal of Physiology >Rhythmic changes in colonic motility are regulated by period genes.
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Rhythmic changes in colonic motility are regulated by period genes.

机译:结肠运动性的节奏变化受到期间基因的调节。

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摘要

Human bowel movements usually occur during the day and seldom during the night, suggesting a role for a biological clock in the regulation of colonic motility. Research has unveiled molecular and physiological mechanisms for biological clock function in the brain; less is known about peripheral rhythmicity. This study aimed to determine whether clock genes such as period 1 (per1) and period2 (per2) modulate rhythmic changes in colonic motility. Organ bath studies, intracolonic pressure measurements, and stool studies were used to examine measures of colonic motility in wild-type and per1per2 double-knockout mice. To further examine the mechanism underlying rhythmic changes in circular muscle contractility, additional studies were completed in neuronal nitric oxide synthase (nNOS) knockout mice. Intracolonic pressure changes and stool output in vivo, and colonic circular muscle contractility ex vivo, are rhythmic with greatest activity at the start of night in nocturnal wild-type mice. In contrast, rhythmicity in these measures was absent in per1per2 double-knockout mice. Rhythmicity was also abolished in colonic circular muscle contractility of wild-type mice in the presence of N(omega)-nitro-L-arginine methyl ester and in nNOS knockout mice. These findings suggest that rhythms in colonic motility are regulated by both clock genes and a nNOS-mediated inhibitory process and suggest a connection between these two mechanisms.
机译:人的肠球通常发生在白天,很少在夜间很少发生,这表明在结肠运动的调节中对生物钟的作用。研究揭开了大脑生物钟功能的分子和生理机制;较少是关于外周节律的。本研究旨在确定时钟基因是否如1(PER1)和时期2(PER2)调节结肠运动性的节律变化。器官浴研究,沉体压力测量和粪便研究用于检查野生型和Per1per2双敲除小鼠的结肠运动措施。为了进一步检查圆形肌肉收缩性的节奏变化的基础变化的机制,在神经元一氧化氮合酶(NNOS)敲除小鼠中完成了额外的研究。体内的分子棒压力变化和粪便输出和结肠圆形肌肉收缩性exvivo,是夜间野生型小鼠的夜间夜间最大的活性。相反,在Per1per2双敲除小鼠中缺乏这些措施的节律性。在N(OMEGA) - 尼硝基-1-精氨酸甲酯和NNOS敲除小鼠的存在下,野生型小鼠的结肠圆形肌肉收缩性也被废除了节奏性。这些发现表明,结肠运动性的节奏由时钟基因和NNOS介导的抑制过程调节,并表明这两种机制之间的连接。

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