Meren H, Varin F, Ruwart M, Thurman R G
Hepatology. 1986 Sep-Oct;6(5):917-21. doi: 10.1002/hep.1840060518.
Previous work demonstrated that collagen deposition in the liver of rats fed a nutritionally deficient diet for 3 to 4 months was diminished markedly by 16,16-dimethyl prostaglandin E2 treatment. In this study, rats were fed a high-fat diet or a high-fat diet deficient in lipotropes for 2 to 4 weeks prior to liver perfusion. Rates of O2 uptake by the liver were not changed by dietary manipulation. Infusion of 16,16-dimethyl prostaglandin E2 (10 microM), however, decreased O2 uptake by the whole organ by 20 to 40% in both groups. O2 tension was measured at the liver surface with a miniature O2 electrode placed alternatively on periportal and pericentral regions of the liver lobule. Mean O2 tensions in both periportal and pericentral regions were reduced 2- to 3-fold during the infusion of 16,16-dimethyl prostaglandin E2 suggesting an action on the microcirculation. This hypothesis was supported by the observation that fluorescein isothiocyanate-dextran fluorescence detected from the liver surface as well as hepatic vascular volume determined by dye dilution techniques were decreased 30 to 50% by 16,16-dimethyl prostaglandin E2. In addition, 16,16-dimethyl prostaglandin E2 increased portal pressure by about 10 mm Hg in a reversible manner. Thus, it is concluded that pharmacological levels of 16,16-dimethyl prostaglandin E2 affects the microcirculation dramatically in the isolated perfused liver.
先前的研究表明,给大鼠喂食营养缺乏饮食3至4个月后,其肝脏中的胶原蛋白沉积会因16,16 - 二甲基前列腺素E2处理而显著减少。在本研究中,在肝脏灌注前2至4周,给大鼠喂食高脂饮食或缺乏促脂物质的高脂饮食。饮食操作并未改变肝脏的氧气摄取率。然而,在两组中,输注16,16 - 二甲基前列腺素E2(10微摩尔)均使整个器官的氧气摄取减少了20%至40%。用微型氧电极交替放置在肝小叶的门静脉周围和中央静脉周围区域,测量肝脏表面的氧张力。在输注16,16 - 二甲基前列腺素E2期间,门静脉周围和中央静脉周围区域的平均氧张力均降低了2至3倍,这表明其对微循环有作用。异硫氰酸荧光素 - 葡聚糖荧光从肝脏表面检测到的结果以及通过染料稀释技术测定的肝血管容积因16,16 - 二甲基前列腺素E2而降低了30%至50%,这一观察结果支持了该假设。此外,16,16 - 二甲基前列腺素E2以可逆的方式使门静脉压力升高约10毫米汞柱。因此,可以得出结论,药理学水平的16,16 - 二甲基前列腺素E2在离体灌注肝脏中对微循环有显著影响。