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洛哌丁胺和比沙可啶对大鼠肠道转运时间、粪便重量及短链脂肪酸排泄的影响

Effect of loperamide and bisacodyl on intestinal transit time, fecal weight and short chain fatty acid excretion in the rat.

作者信息

Bustos D, Ogawa K, Pons S, Soriano E, Bandi J C, Bustos Fernández L

机构信息

Instituto de Gastroenterología Dr. Jorge Pérez Companc, Buenos Aires, Rep. Argentina.

出版信息

Acta Gastroenterol Latinoam. 1991;21(1):3-9.

PMID:1811403
Abstract

We analyzed the effect of drugs that modify the colonic motility on rat intestinal transit time (ITT) (measured with radiopaque markers), fecal weight (FW) and fecal concentration of short chain fatty acids (FSCFA) (assayed by gas liquid chromatography), over a four-week period. Bisacodyl was used to accelerate and Loperamide to retard the intestinal transit in rats maintained on a conventional diet. The first and 3rd week were drug-free control periods. The mean values of these periods were: ITT = 28.9h +/- 1.9 FW: 9.2 +/- 1.2 g/24 h and FSCFA = 60.6 +/- 17.9 mmol/g. After loperamide administration, we observed an increase in the mean ITT as compared to the control period (40.4 +/- 8.0h) and decrease in FW (4.8 +/- 3.6 g/24h) and in FSCFA = 32.2 +/- 5.6 mmol/g). After bisacodyl administration, we found a shorter ITT in relation to controls (24.8 +/- 2.5h), and increases in FW (27.5 +/- 3.6g/24h) and in FSCFA (108.2 +/- 39.9 mmol/g). There was a negative correlation between ITT and FW (R = 0.67 p less than 0.01) and a positive correlation between total SCFA concentration and FW (R = 0.71 p less than 0.01). The concentration of acetic, propionic and butyric acids increased with progressive increments in fecal weight, whereas concentrations of isovaleric and caproic acids decreased. The results of this study show that the FW and the FSCFA may be influenced by modifications in the intestinal transit time.

摘要

我们在四周的时间里分析了改变结肠动力的药物对大鼠肠道转运时间(通过不透射线标志物测量)、粪便重量(FW)和短链脂肪酸粪便浓度(通过气相色谱法测定)的影响。使用比沙可啶加速、洛哌丁胺延缓维持常规饮食大鼠的肠道转运。第一周和第三周为无药物对照期。这些时期的平均值为:肠道转运时间 = 28.9小时±1.9,粪便重量:9.2±1.2克/24小时,短链脂肪酸粪便浓度 = 60.6±17.9毫摩尔/克。给予洛哌丁胺后,我们观察到与对照期相比平均肠道转运时间增加(40.4±8.0小时),粪便重量减少(4.8±3.6克/24小时),短链脂肪酸粪便浓度为32.2±5.6毫摩尔/克。给予比沙可啶后,我们发现与对照组相比肠道转运时间缩短(24.8±2.5小时),粪便重量增加(27.5±3.6克/24小时),短链脂肪酸粪便浓度增加(108.2±39.9毫摩尔/克)。肠道转运时间与粪便重量之间呈负相关(R = 0.67,p小于0.01),总短链脂肪酸浓度与粪便重量之间呈正相关(R = 0.71,p小于0.01)。随着粪便重量逐渐增加,乙酸、丙酸和丁酸的浓度升高,而异戊酸和己酸的浓度降低。本研究结果表明,粪便重量和短链脂肪酸粪便浓度可能受肠道转运时间改变的影响。

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