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镉对大鼠脑内钙调蛋白及钙调蛋白调节酶的体内效应。

In vivo effects of cadmium on calmodulin and calmodulin regulated enzymes in rat brain.

作者信息

Vig P J, Nath R

机构信息

Department of Neurology, University of Mississippi Medical Center, Jackson 39216.

出版信息

Biochem Int. 1991 Mar;23(5):927-34.

PMID:1652964
Abstract

Effect of chronic cadmium (Cd) exposure and the influence of diethyldithiocarbamate (DDC) on Cd absorption was studied on the brain of young male Wistar rats. A significant amount of Cd accumulated in cerebral cortices of rats after 4 weeks of Cd (6 mg/kg body wt) exposure (through gastric intubation). The biological activity of calmodulin (CaM) decreased significantly (p less than 0.001) in the cerebral cortices of these animals in comparison to the control group. 3'-5' Phosphodiesterase and synaptic membrane Ca(2+)-Mg(2+) ATPase were also significantly affected (p less than 0.01 and p less than 0.001 respectively). However, Cd treatment did not alter synaptic membrane adenylate cyclase activity and DDC (9.2 mg/kg body wt, intraperitoneal) treatment along with Cd (6 mg/kg body wt) enhanced Cd accumulation in cerebral cortices of treated animals resulting in an increased inhibition of CaM and CaM dependent enzymes. These data suggest that Cd may be acting via binding to CaM and uncoupling it from its normal cellular control of calcium.

摘要

研究了慢性镉(Cd)暴露的影响以及二乙基二硫代氨基甲酸盐(DDC)对年轻雄性Wistar大鼠大脑中镉吸收的影响。在通过胃插管给予镉(6毫克/千克体重)4周后,大鼠大脑皮层中积累了大量镉。与对照组相比,这些动物大脑皮层中钙调蛋白(CaM)的生物活性显著降低(p<0.001)。3'-5'磷酸二酯酶和突触膜Ca(2+)-Mg(2+)ATP酶也受到显著影响(分别为p<0.01和p<0.001)。然而,镉处理并未改变突触膜腺苷酸环化酶的活性,并且DDC(9.2毫克/千克体重,腹腔注射)与镉(6毫克/千克体重)联合处理增强了受试动物大脑皮层中镉的积累,导致对CaM和CaM依赖性酶的抑制增加。这些数据表明,镉可能通过与CaM结合并使其与正常的细胞钙控制解偶联而发挥作用。

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