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| 1 | A pharmacodynamic model of portal hypertension in isolated perfused rat liver显示文摘AIM:To develop a pharmacodynamic model of portal hypertension from chronic hepatitis.METHODS:Pathological changes and collagen depositions were analyzed using morphometry to confirm CCl 4-induced chronic hepatitis.At d 0,d 28,d 56 and d 84 of the process,the portal perfused velocities (μL/min) in isolated rat livers were exactly controlled with a quantified pump.The pressure (mmHg) was monitored with a Physiological System.The geometric concentrations of phenylephrine or acetylcholine were added to a fixed volume (300 mL) of the circulating perfusate.The equation,the median effective concentration and its 95% confidence intervals of phenylephrine or acetylcholine were regressed with Prism-4 software in nonlinear fit and various slopes.In the isolated perfused rat livers with chronic hepatitis,both median effective concentrations were defined as the pharmacodynamic model of portal hypertension.RESULTS:At d 0,d 28,d 56 and d 84,the equations of portal pressure potency from the concentrations of phenylephrine used to constrict the portal vein in isolated perfused rat livers were Y=0.1732 + 0.3970/[1 + 10 (-4.3061-0.4407 X) ],Y=-0.004934 + 0.12113/[1 + 10 (-3.1247-0.3262 X) ],Y=0.0104 + 0.2643/[1 + 10 (-8.8462-0.9579 X) ],and Y=0.01603 + 0.12107/[1 + 10 (-5.1134-0.563 X) ];the median effective concentrations were 1.69 × 10-10 mol/L,2.64 × 10-10 mol/L,5.82 × 10-10 mol/L,and 8.24 × 10-10 mol/L,respectively.The equations from the concentrations of acetylcholine used to relax the portal vein were Y =-0.4548 + 0.3274/[1 + 10 (6.1538 + 0.5554 X) ],Y=-0.05391 + 0.06424/[1 + 10 (3.8541 + 0.3469 X) ],Y=-0.2733 + 0.22978/[1 + 10 (3.0472 + 0.3008 X) ],and Y=-0.0559 + 0.053178/[1 + 10 (5.6336 + 0.5883 X) ];the median effective concentrations were 8.40 × 10-10 mol/L,7.73 × 10-12 mol/L,5.98 × 10-11 mol/L,and 2.66 × 10-10 mol/L,respectively.CONCLUSION:A pharmacodynamic model of portal hypertension in isolated perfused rat livers with chronic hepatitis was defined as the median effective concentrations of phenylephrine and acetylcholine. | Tao Zhang Xue-Yan Xu Hang Zhou Xin Zhao Meng Song Tao-Tao Zhang He Yin Ting Li Peng-Tao Li Da-Yong Cai | 2012 | World Journal of Gastroenterology2012,18,5: | 2 |
| 2 | 医学机能学教学实验中离体肝脏灌流大鼠模型的构建显示文摘目的构建医学机能学创新实验教学库的离体肝脏灌流大鼠模型。方法自门静脉进行灌流,按照不同灌流流出静脉,将大鼠分为下腔静脉与上腔静脉流出通路组。观察两组间手术时间、漏液情况。确定最佳流出通路后,分别灌流含或不含牛黄胆酸钠的K-H灌流液。检测不同时间点两种灌流液组的ALT、AST、LDH。结果上腔静脉流出通路比下腔静脉流出通路手术操作更简单。同一灌流液组不同灌流时间点ALT、AST、LDH的浓度变化无显著性差异。含牛黄胆酸钠的K-H灌流组AST的浓度低于不含牛黄胆酸钠的K-H灌流组。结论通过上述方法可构建离体肝脏灌流大鼠模型,上腔静脉流出组操作更简单,成功率更高。灌流液中增加(去除)牛磺胆酸钠并未影响灌流效果。 | 董晓敏 芦玲巧 郝刚 梁雪 | 2016 | 继续医学教育2016,30,11: | 0 |
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