Departamento de Química, Centro de Investigación y de Estudios Avanzados (Cinvestav), México DF, México.
Exp Neurol. 2012 Jan;233(1):182-92. doi: 10.1016/j.expneurol.2011.09.032. Epub 2011 Oct 1.
Manganese is essential for life, yet chronic exposure to this metal can cause a neurodegenerative disease named manganism that affects motor function. In the present study we have evaluated Mn neurotoxicity after its administration in the rat striatum. The participation of the calcium-dependent protease calpain and the apoptosis-related protease caspase-3, in Mn-induced cell death was monitored in the striatum and globus pallidus. Mn induced the activation of both proteases, although calpain activation seems to be an earlier event. Moreover, while the broad-spectrum caspase inhibitor QVD did not significantly prevent Mn-induced cell death, the specific calpain inhibitor MDL-28170 did. The role of NMDA glutamate receptors on calpain activity was also investigated; blockage of these receptors by MK-801 and memantine did not prevent calpain activation, nor Mn-induced cell death. Finally, studies in striatal homogenates suggest a direct activation of calpain by Mn ions. Altogether the present study suggests that additional mechanisms to excitotoxicity are involved in Mn-induced cell death, placing calpain as an important mediator of acute Mn neurotoxicity in vivo.
锰是生命所必需的,但长期接触这种金属会导致一种名为锰中毒的神经退行性疾病,影响运动功能。在本研究中,我们评估了锰在大鼠纹状体中的给药后的神经毒性。钙依赖性蛋白酶钙蛋白酶和凋亡相关蛋白酶半胱天冬酶-3在锰诱导的细胞死亡中的参与在纹状体和苍白球中进行了监测。锰诱导了这两种蛋白酶的激活,尽管钙蛋白酶的激活似乎是一个更早的事件。此外,虽然广谱半胱天冬酶抑制剂 QVD 不能显著阻止锰诱导的细胞死亡,但特异性钙蛋白酶抑制剂 MDL-28170 可以。还研究了 NMDA 谷氨酸受体对钙蛋白酶活性的作用;MK-801 和美金刚阻断这些受体不能阻止钙蛋白酶的激活,也不能阻止锰诱导的细胞死亡。最后,纹状体匀浆的研究表明锰离子直接激活钙蛋白酶。总之,本研究表明,兴奋性毒性以外的机制参与了锰诱导的细胞死亡,钙蛋白酶作为体内急性锰神经毒性的重要介质。