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30 November 1999, Volume 11 Issue 6
氯丙嗪、尼莫地平单用和合用对小鼠镉中毒肝、肾毒效应的影响
Tang lingfang , Chen Yanmeg , Zhang Zhenling , Songling , Yang Yongnian , Feng Zhiying
1999, 11(6):  334-337.  doi:10.3969/j.issn.1004-616x.1999.06.016
Abstract ( 3410 )   PDF (82KB) ( 3037 )  
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Abstract  The influences of calmodulin antagonist CPZ , and calcium channel blocker NIMO and the combination on cadmiumpoisoning of mice were studied. Animal models for cadmiumpoisoning were established by peritoneal injection of 1/ 5 LD50CdCl2 , The experimental groups were protected by administering of CPZ、NIMO and combination of CPZ and NIMO respectively one hour before the injection of CdCl2 . Five consecutive days later , samples were collected for analysis. The data showed that the Cd content in blood and the urinaryγ2GT and NAG activities were reduced significantly by CPZ. Both CPZ and NIMO showed considerable protective effect against the decrease of Ca2 + - Mg2 + - ATPase activity , and a remarkable synergistic action between them was observed. Both CPZ and NIMO could considerably increase MT contents in livers and kidneys of Cd poisonig mice. The results indicated that the inhibitors could protect mice against the toxic effects of Cd on liver and kidney , while CPZ was more efficient than NIMO. The combination of CPZ and NIMO could exert a synergistic action in some aspects. The protective action of these two drugs might be relevent to the function of MT.
钙调素拮抗剂对镉接触小鼠脑突触小体蛋白质合成的影响
Tang lingfang , Chen Yanmeng , Zhang Zhenling , SongLing , Yang Yongnian , Feng Zhiying
1999, 11(6):  337-339.  doi:10.3969/j.issn.1004-616x.1999.06.017
Abstract ( 2707 )   PDF (84KB) ( 2945 )  
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Abstract  The isolated mice brain synaptosome was measured in vitro. The experiment explored protein biosynthesis by 3H - Leu in2 corporation technique , meanwhile , the influence of Calmodulin(CaM) inhibitor Chlorpromazine (CPZ) on this toxicity was investigated as well. The result indicated that Cd prevented 3H - Leu from incorporating into synaptosome , in which the concentration of Cd and the amount incorporated showed negative correlation and this toxic effect may be antagonized by CaM inibitor CPZ to some extend. It is concluded that CaM may be involved in the mechanism of Cd toxicity in brain synaptosome.