MK-801和地塞米松给药后肾脏组织学检查。

Joanna Sekita-Krzak, Józef Visconti, Zbigniew Wójtowicz, Iwona Zebrowska-Lupina, Grazyna Ossowska, Bozena Klenk-Majewska
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摘要

本研究的目的是组织学评估MK-801 (NMDA受体拮抗剂)和地塞米松对肾脏的影响。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,连续给药8 d,地塞米松给药剂量为120 mg/kg/24 h。光镜下观察苏木精、伊红染色及PAS染色肾片。实验结果表明,MK-801引起肾小体尿腔和近曲小管管腔的轻微狭窄,毒性剂量地塞米松引起肾充血时尿腔的扩张。MK-801增强了地塞米松中毒剂量引起的肾脏形态学改变。
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Histological examination of the kidney 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 kidney. 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. Kidney slices stained with hematoxylin and eosin and with PAS method were examined with light microscope. The performed experiments revealed that MK-801 causes morphological changes in the shape of slight narrowing of the urinary spaces in renal corpuscles and narrowing of the lumen of the proximal convoluted tubules and dexamethasone administered in toxic doses causes dilatation of these spaces with kidney's hyperemia. MK-801 intensifies morphological changes of the kidney induced by toxic doses of dexamethasone.

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