Chobert M N, Bernard O, Bulle F, Lemonnier A, Guellaen G, Alagille D
Unité de Recherche de Pharmacologie et Physiologie Hépatique (INSERM U 99), Hôpital Henri Mondor, Créteil, France.
J Hepatol. 1989 Jan;8(1):22-5. doi: 10.1016/0168-8278(89)90157-8.
gamma-Glutamyl transferase (gamma-GT) was assayed in the serum and liver biopsies of children affected with either progressive idiopathic cholestasis (PIC, Byler's disease), or other types of cholestatic (biliary atresia, cholestasis of various origins) and non-cholestatic diseases. The mean liver gamma-GT activity was increased significantly only in PIC and biliary atresia. In contrast, the serum gamma-GT activity, raised in children with evident damage to the main bile ducts or to the interlobular bile ducts, was normal in children with PIC. Although the mechanism for such a discrepancy between high liver and normal serum gamma-GT activities in PIC is still speculative, this peculiarity could prove to be of use in leading to a better understanding of the disease.
在患有进行性特发性胆汁淤积症(PIC,比勒氏病)、其他类型胆汁淤积性疾病(胆道闭锁、各种原因引起的胆汁淤积)和非胆汁淤积性疾病的儿童的血清和肝活检组织中检测了γ-谷氨酰转移酶(γ-GT)。仅在PIC和胆道闭锁患儿中,肝脏γ-GT的平均活性显著升高。相比之下,主要胆管或小叶间胆管明显受损的患儿血清γ-GT活性升高,而PIC患儿的血清γ-GT活性正常。尽管PIC患儿肝脏γ-GT活性高而血清γ-GT活性正常这种差异的机制仍属推测,但这一特性可能有助于更好地理解该疾病。