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腹膜炎大鼠中麻醉剂对回肠自发收缩的影响

Altered spontaneous contractions of the ileum by anesthetic agents in rats exposed to peritonitis.

作者信息

Aydin Cengiz, Bagcivan Ihsan, Gursoy Sinan, Altun Ahmet, Topcu Omer, Koyuncu Ayhan

机构信息

Department of General Surgery, Cumhuriyet University School of Medicine, Sivas, Turkey.

出版信息

World J Gastroenterol. 2009 Apr 7;15(13):1620-4. doi: 10.3748/wjg.15.1620.

Abstract

AIM

To investigate in vitro effects of propofol, midazolam and dexmedetomidine, which are commonly used anaesthesic or sedatives, on spontaneous contractions of the ileum both in normal rats and those exposed to hyperdynamic peritonitis.

METHODS

Spontaneous contractions of isolated ileum muscle segments from sham operated rats and those exposed to peritonitis, were studied in vitro. The amplitude and the frequency of spontaneous contractions of ileum muscle segments were studied after adding dexmedetomidine, propofol, and midazolam to the organ bath in a cumulative manner.

RESULTS

Both amplitude (85.2 +/- 6.6 vs 47.4 +/- 7.1) and frequency (32.8 +/- 4.6 vs 20.2 +/- 3.9) of spontaneous contractions in ileum smooth muscle segments were decreased significantly in the peritonitis group compared to the control group (P < 0.05). Dexmedetomidine significantly increased the amplitude of spontaneous contractions (85.2 +/- 6.6 vs 152.0 +/- 5.4, P < 0.05) whereas, propofol (85.2 +/- 6.6 vs 49.6 +/- 4.8, P < 0.05) and midazolam (85.2 +/- 6.6 vs 39.2 +/- 4.5, P < 0.05) decreased it in both control and peritonitis groups. The frequency of spontaneous contractions were significantly decreased by propofol in both control (32.8 +/- 4.6 vs 18.2 +/- 3.4, P < 0.05) and peritonitis groups 20.2 +/- 3.9 vs 11.6 +/- 3.2, P < 0.05). Dexmedetomidine and midazolam did not cause significant changes in the number of spontaneous contractions in both control and the peritonitis groups (P > 0.05).

CONCLUSION

Propofol, midazolam and dexmedetomidine have various in vitro effects on spontaneous contractions of the rat ileum. While dexmedetomidine augments the spontaneous contraction of the rat ileum, propofol attenuates it. However, the effects of these compounds were parallel in both control and peritonitis groups.

摘要

目的

研究常用麻醉剂或镇静剂丙泊酚、咪达唑仑和右美托咪定对正常大鼠以及患有高动力性腹膜炎大鼠回肠自发收缩的体外作用。

方法

对假手术大鼠和患有腹膜炎大鼠的离体回肠肌段的自发收缩进行体外研究。将右美托咪定、丙泊酚和咪达唑仑以累积方式添加到器官浴中后,研究回肠肌段自发收缩的幅度和频率。

结果

与对照组相比,腹膜炎组回肠平滑肌段自发收缩的幅度(85.2±6.6对47.4±7.1)和频率(32.8±4.6对20.2±3.9)均显著降低(P<0.05)。右美托咪定显著增加自发收缩的幅度(85.2±6.6对152.0±5.4,P<0.05),而丙泊酚(85.2±6.6对49.6±4.8,P<0.05)和咪达唑仑(85.2±6.6对39.2±4.5,P<0.05)在对照组和腹膜炎组中均使其降低。丙泊酚在对照组(32.8±4.6对18.2±3.4,P<0.05)和腹膜炎组(20.2±3.9对11.6±3.2,P<0.05)中均显著降低自发收缩的频率。右美托咪定和咪达唑仑在对照组和腹膜炎组中均未引起自发收缩次数的显著变化(P>0.05)。

结论

丙泊酚、咪达唑仑和右美托咪定对大鼠回肠的自发收缩具有不同的体外作用。右美托咪定增强大鼠回肠的自发收缩,而丙泊酚减弱其收缩。然而,这些化合物在对照组和腹膜炎组中的作用是相似的。

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