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[胆汁淤积综合征的临床化学诊断]

[Clinico-chemical diagnosis of the cholestasis syndrome].

作者信息

Ohlen J, Drescher M, Selmair H

出版信息

Fortschr Med. 1982 Jan 14;100(1-2):10-15.

PMID:6120134
Abstract
  1. Cholestatic reactions of various etiology are biochemically established by determination of alkaline phosphatase, gamma-glutamyltranspeptidase (and leucinaminopeptidase) activities and of bile acid concentrations in serum. 2. The pathomechanisms of elevated serum activities of AP, gamma-GT and LAP in cholestatic diseases are - an induction of these canalicular membrane bound enzymes, probably due to an intracellular increase of bile acids, - a partial solubilization of canalicular membrane structure (detergent effect of bile acids), - a histochemically and morphologically demonstrable change of liver cell polarity. 3. A discrimination of intra- or extrahepatic cholestasis only by means of biochemical parameters is impossible. 4. Additional serological and immunological parameters often demonstrate the etiology of cholestatic diseases; a short review is given.
摘要
  1. 通过测定血清中的碱性磷酸酶、γ-谷氨酰转肽酶(和亮氨酰氨基肽酶)活性以及胆汁酸浓度,在生化层面确定各种病因引起的胆汁淤积反应。2. 胆汁淤积性疾病中血清碱性磷酸酶(AP)、γ-谷氨酰转肽酶(γ-GT)和亮氨酰氨基肽酶(LAP)活性升高的发病机制为:这些小管膜结合酶的诱导,可能是由于细胞内胆汁酸增加;小管膜结构的部分溶解(胆汁酸的去污剂作用);肝细胞极性在组织化学和形态学上可证实的变化。3. 仅通过生化参数来区分肝内或肝外胆汁淤积是不可能的。4. 额外的血清学和免疫学参数常常能表明胆汁淤积性疾病的病因;现给出简要综述。

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