{"title":"Quantitative analysis of erythrocyte velocity in rat liver after acute ethanol administration.","authors":"H Hamamatsu","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>Hepatic microcirculation is thought to be closely associated with the liver function. The present study was aimed to quantify changes in hepatic microcirculation after acute ethanol administration using a photometric device. Male Wistar rats were anesthetized with pentobarbital sodium (35 mg/kg) intraperitoneally. After laparotomy, a lobe of the liver was exposed and placed on the cover glass at the window of plastic stage, and observed using inverted intravital fluorescence microscopy assisted by a silicon intensified target camera. Erythrocytes were labeled with fluorescein isothiocyanate (FITC) according to the method of Zimmerhackl et al, and injected from the catheter placed at the aortic arch. FITC-labeled red blood cells (FITC-RBCs) recirculated continuously and resembled native cells in their flow properties. Ethanol (20%; 3 g/kg, 30%; 4.5 g/kg, 40%; 6 g/kg) was administered through the stomach tube. The microfluorograph of hepatic microcirculation was then recorded on a videotape. The velocity of FITC-RBCs in sinusoids was measured with a multipurpose computerized image analyzing system by replaying the video images. Portal pressure, mean arterial pressure, and central venous pressure were also monitored. The velocity of FITC-RBCs in the sinusoid increased by 54% at 10-20 min after 20% ethanol administration and remained at higher than the basal level throughout the period of the experiment. The velocity after 30% ethanol administration increased in some experiments and decreased in the others at the end of the experiment (60 min after acute ethanol administration). However, the velocity decreased by 26% at 60 min after 40% ethanol administration. Portal pressure increased by 16% at 45-60 min after 20% ethanol administration, and increased by 23% at 30 min after 40% ethanol administration, while mean arterial pressure and central venous pressure had no significant change. The method in this study is the first approach to visualize hepatic microcirculation by FITC-RBCs and measure erythrocyte velocity in the sinusoid using a multipurpose computerized image analysis system. The current results suggest that high concentration of ethanol may disturb hepatic microcirculation at the sinusoidal level.</p>","PeriodicalId":77015,"journal":{"name":"Arukoru kenkyu to yakubutsu izon = Japanese journal of alcohol studies & drug dependence","volume":"28 6","pages":"467-82"},"PeriodicalIF":0.0000,"publicationDate":"1993-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Arukoru kenkyu to yakubutsu izon = Japanese journal of alcohol studies & drug dependence","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Hepatic microcirculation is thought to be closely associated with the liver function. The present study was aimed to quantify changes in hepatic microcirculation after acute ethanol administration using a photometric device. Male Wistar rats were anesthetized with pentobarbital sodium (35 mg/kg) intraperitoneally. After laparotomy, a lobe of the liver was exposed and placed on the cover glass at the window of plastic stage, and observed using inverted intravital fluorescence microscopy assisted by a silicon intensified target camera. Erythrocytes were labeled with fluorescein isothiocyanate (FITC) according to the method of Zimmerhackl et al, and injected from the catheter placed at the aortic arch. FITC-labeled red blood cells (FITC-RBCs) recirculated continuously and resembled native cells in their flow properties. Ethanol (20%; 3 g/kg, 30%; 4.5 g/kg, 40%; 6 g/kg) was administered through the stomach tube. The microfluorograph of hepatic microcirculation was then recorded on a videotape. The velocity of FITC-RBCs in sinusoids was measured with a multipurpose computerized image analyzing system by replaying the video images. Portal pressure, mean arterial pressure, and central venous pressure were also monitored. The velocity of FITC-RBCs in the sinusoid increased by 54% at 10-20 min after 20% ethanol administration and remained at higher than the basal level throughout the period of the experiment. The velocity after 30% ethanol administration increased in some experiments and decreased in the others at the end of the experiment (60 min after acute ethanol administration). However, the velocity decreased by 26% at 60 min after 40% ethanol administration. Portal pressure increased by 16% at 45-60 min after 20% ethanol administration, and increased by 23% at 30 min after 40% ethanol administration, while mean arterial pressure and central venous pressure had no significant change. The method in this study is the first approach to visualize hepatic microcirculation by FITC-RBCs and measure erythrocyte velocity in the sinusoid using a multipurpose computerized image analysis system. The current results suggest that high concentration of ethanol may disturb hepatic microcirculation at the sinusoidal level.