Analysis of spatiotemporal pattern and quantification of gastrointestinal slow waves caused by anticholinergic drugs.

IF 1.6 4区 生物学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
Organogenesis Pub Date : 2017-04-03 Epub Date: 2017-02-23 DOI:10.1080/15476278.2017.1295904
Kelvin K L Wong, Lauren C Y Tang, Jerry Zhou, Vincent Ho
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引用次数: 6

Abstract

Anticholinergic drugs are well-known to cause adverse effects, such as constipation, but their effects on baseline contractile activity in the gut driven by slow waves is not well established. In a video-based gastrointestinal motility monitoring (GIMM) system, a mouse's small intestine was placed in Krebs solution and recorded using a high definition camera. Untreated controls were recorded for each specimen, then treated with a therapeutic concentration of the drug, and finally, treated with a supratherapeutic dose of the drug. Next, the video clips showing gastrointestinal motility were processed, giving us the segmentation motions of the intestine, which were then converted via Fast Fourier Transform (FFT) into their respective frequency spectrums. These contraction quantifications were analyzed from the video recordings under standardised conditions to evaluate the effect of drugs. Six experimental trials were included with benztropine and promethazine treatments. Only the supratherapeutic dose of benztropine was shown to significantly decrease the amplitude of contractions; at therapeutic doses of both drugs, neither frequency nor amplitude was significantly affected. We have demonstrated that intestinal slow waves can be analyzed based on the colonic frequency or amplitude at a supratherapeutic dose of the anticholinergic medications. More research is required on the effects of anticholinergic drugs on these slow waves to ascertain the true role of ICC in neurologic control of gastrointestinal motility.

Abstract Image

Abstract Image

抗胆碱能药物引起胃肠慢波的时空格局分析及定量分析。
众所周知,抗胆碱能药物会引起便秘等不良反应,但它们对肠道慢波驱动的基线收缩活动的影响尚未得到很好的证实。在基于视频的胃肠运动监测(GIMM)系统中,将小鼠的小肠置于克雷布斯溶液中,并使用高清摄像机进行记录。记录每个标本的未处理对照,然后用治疗浓度的药物治疗,最后用超治疗剂量的药物治疗。接下来,对显示胃肠运动的视频片段进行处理,得到肠道的分割运动,然后通过快速傅里叶变换(FFT)将其转换为各自的频谱。在标准化条件下,从录像中分析这些收缩量,以评价药物的效果。6项试验纳入苯托品和异丙嗪治疗。只有超治疗剂量的苯托品能显著降低收缩幅度;在两种药物的治疗剂量下,频率和振幅都没有明显影响。我们已经证明,在超治疗剂量的抗胆碱能药物下,肠道慢波可以根据结肠频率或振幅进行分析。抗胆碱能药物对这些慢波的影响需要更多的研究来确定ICC在胃肠运动的神经控制中的真正作用。
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来源期刊
Organogenesis
Organogenesis BIOCHEMISTRY & MOLECULAR BIOLOGY-DEVELOPMENTAL BIOLOGY
CiteScore
4.10
自引率
4.30%
发文量
6
审稿时长
>12 weeks
期刊介绍: Organogenesis is a peer-reviewed journal, available in print and online, that publishes significant advances on all aspects of organ development. The journal covers organogenesis in all multi-cellular organisms and also includes research into tissue engineering, artificial organs and organ substitutes. The overriding criteria for publication in Organogenesis are originality, scientific merit and general interest. The audience of the journal consists primarily of researchers and advanced students of anatomy, developmental biology and tissue engineering. The emphasis of the journal is on experimental papers (full-length and brief communications), but it will also publish reviews, hypotheses and commentaries. The Editors encourage the submission of addenda, which are essentially auto-commentaries on significant research recently published elsewhere with additional insights, new interpretations or speculations on a relevant topic. If you have interesting data or an original hypothesis about organ development or artificial organs, please send a pre-submission inquiry to the Editor-in-Chief. You will normally receive a reply within days. All manuscripts will be subjected to peer review, and accepted manuscripts will be posted to the electronic site of the journal immediately and will appear in print at the earliest opportunity thereafter.
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