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敌草快可使大鼠血浆和组织中的半胱氨酸蛋白酶抑制剂大幅增加。

Diquat increases cysteine proteinase inhibitors greatly in rat plasma and tissues.

作者信息

Minakata K, Suzuki O, Oh-ishi S, Hayashi I, Saito S, Harada N

机构信息

Department of Legal Medicine, Hamamatsu University, School of Medicine, Japan.

出版信息

Arch Toxicol. 1995;69(5):318-21. doi: 10.1007/s002040050177.

Abstract

Biochemical and gross pathological effects of diquat were studied with special attention to cysteine proteinase inhibitor level which was often increased in acute and chronic disorder. Diquat was fed continuously to rats at the dose of 1000 ppm in the diet. After 10 days, anorexia and severe diarrhea were observed but epistaxis and hypokinesia were not apparent. The rats were killed after feeding the diet for 13.5 days and plasma components such as acute phase reactant proteins and some vitamins which act as antioxidants were examined. The results showed that alpha-cysteine proteinase inhibitor (alpha-CPI) increased to 9-fold and vitamin C radical increased to 1.6-fold, whereas alpha 1 proteinase inhibitor (alpha 1-PI) decreased to 0.9-fold and vitamins C and E were the same as the control. Among three components of alpha-CPI, the T kininogen level in intoxicated rat plasma was about 20-fold, whereas the high molecular weight kininogen level was about 2-fold of the control. Diquat also enhanced the cysteine proteinase inhibitor (CPI) level to 20-fold in kidney and to 7- to 10-fold in the other organs. The large increment of T kininogen in these organs was also confirmed immunologically. The kidney showed a granular degeneration and its weight increased to 1.2-fold of control. The other organs showed neither gross pathological alteration nor weight change, compared with the control. The diquat distribution was highest in spleen and next highest in kidney among several organs. These results were compared with those caused by paraquat.

摘要

研究了敌草快的生化和大体病理学效应,特别关注半胱氨酸蛋白酶抑制剂水平,该水平在急性和慢性疾病中常升高。以1000 ppm的剂量将敌草快持续喂给大鼠。10天后,观察到厌食和严重腹泻,但鼻出血和运动减退不明显。在喂食该饮食13.5天后处死大鼠,并检测血浆成分,如急性期反应蛋白和一些作为抗氧化剂的维生素。结果显示,α-半胱氨酸蛋白酶抑制剂(α-CPI)增加至9倍,维生素C自由基增加至1.6倍,而α1蛋白酶抑制剂(α1-PI)降至0.9倍,维生素C和E与对照组相同。在α-CPI的三个成分中,中毒大鼠血浆中的T激肽原水平约为对照组的20倍,而高分子量激肽原水平约为对照组的2倍。敌草快还使肾脏中的半胱氨酸蛋白酶抑制剂(CPI)水平增加至20倍,其他器官中的增加至7至10倍。这些器官中T激肽原的大幅增加也通过免疫学得到证实。肾脏出现颗粒变性,其重量增加至对照组的1.2倍。与对照组相比,其他器官既没有大体病理学改变,重量也没有变化。在几个器官中,敌草快的分布在脾脏中最高,其次在肾脏中最高。将这些结果与百草枯引起的结果进行了比较。

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