Sabolovic N, Gérard A, Maréchal J, Gérard H
Biomed Pharmacother. 1984;38(3):159-67.
ALP activity has been studied during hepatitis (infection) in two genetically controlled mouse strains having different degrees of susceptibility ot MHV3 virus: A/JAX (resistant) and DBA/2 (susceptible). During the 8 days following viral infection we have compared ALP activity in serum and liver homogenates with ALP cytological localization in liver tissue (light and electron microscopy). Firstly, liver ALP activity has been demonstrated in the Disse's spaces, on the membrane of the hepatocytes microvilli whilst serum ALP was still very low. The serum ALP activity begins to increase markedly since the third day in sensitive mice (DBA/2), i.e., when the electron microscopy hepatocytes look very damaged; hepatocytes have lost most of their microvilli; necrotic vesicles, degenerative cytoplasmic organelles, lipid vesicles occurred in numerous hepatocytes. ALP activity has disappeared at the biliary pole of the cells whilst it increased at the vascular pole. Moreover, electron microscopic studies demonstrated that ALP positive cells are exclusively of lymphoid type whereas Kupffer cells remain ALP negative.
在两种对MHV3病毒具有不同易感性的基因控制小鼠品系(A/JAX,抗性;DBA/2,易感)的肝炎(感染)过程中,对碱性磷酸酶(ALP)活性进行了研究。在病毒感染后的8天里,我们将血清和肝匀浆中的ALP活性与肝组织中的ALP细胞定位(光学显微镜和电子显微镜)进行了比较。首先,在狄氏间隙、肝细胞膜微绒毛上证实了肝脏ALP活性,而血清ALP仍然很低。在敏感小鼠(DBA/2)中,血清ALP活性从第三天开始显著增加,即当电子显微镜下肝细胞看起来受损严重时;肝细胞失去了大部分微绒毛;许多肝细胞中出现坏死小泡、变性的细胞质细胞器、脂质小泡。细胞胆管极的ALP活性消失,而血管极的ALP活性增加。此外,电子显微镜研究表明,ALP阳性细胞仅为淋巴细胞类型,而库普弗细胞仍为ALP阴性。