实验给药MK-801和地塞米松后肝脏组织学检查。

Joanna Sekita-Krzak, Krystyna Czerny, Iwona Zebrowska-Lupina, Zofia Danilczuk, Maria Stepniewska
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摘要

本研究的目的是组织学评价MK-801 (NMDA受体拮抗剂)和地塞米松对肝脏的影响。该实验是在成年雄性白化瑞士小鼠身上进行的。MK-801给药剂量为0.3 mg/kg/24 h,连续8天;地塞米松给药剂量为120 mg/kg/24 h。光镜下观察苏木精和伊红染色肝片。实验结果表明,MK-801能引起肝脏的形态学改变,表现为肝细胞质透明度增加,肝窦变窄。MK-801加重毒性剂量地塞米松引起的肝损伤,导致肝细胞局灶性坏死。
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Histological examination of the liver after experimental administration of MK-801 and dexamethasone.

The aim of the research was histological assessment of the influence of MK-801 (NMDA receptor antagonist) and dexamethasone on the liver. The experiment was carried out on adult Albino-Swiss mouse males. MK-801 was administered in the dose of 0.3 mg/kg/24 h for 8 days, dexamethasone--in the toxic dose of 120 mg/kg/24 h. Liver slices stained with hematoxylin and eosin were examined with light microscope. The performed experiments revealed that MK-801 can cause morphological changes of the liver in the shape of increased transparence of hepatocyte cytoplasm and narrowing of the liver sinusoids. MK-801 intensifies liver damage induced by toxic doses of dexamethasone leading to focal necrosis of hepatocytes.

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