Porciúncula Lisiane O, Rocha João Batista, Tavares Rejane G, Ghisleni Gabriele, Reis Marcelo, Souza Diogo O
Departamento de Bioquímica, CCNE, Universidade Federal do Rio Grande do Sul, Porto Alegre/RS90035 003, Brasil.
Neuroreport. 2003 Mar 24;14(4):577-80. doi: 10.1097/00001756-200303240-00010.
Methylmercury (MeHg) is an environmental contaminant that continues to cause risk to human health. The toxic effects of MeHg on the CNS implicate the involvement of glutamatergic system. In this study, we evaluated the effects of MeHg on [3H]glutamate uptake by synaptic vesicles. MeHg inhibited [3H]glutamate uptake in a concentration dependent manner. Since glutamate uptake by synaptic vesicles is driven by an electrochemical gradient, formed across the vesicle membrane by a bafilomycin A(1)-sensitive H+-ATPase, we further investigated the effect of MeHg on activity of this enzyme. MeHg inhibited the H+-ATPase activity and also dissipated the proton gradient (DeltapH), indicating that MeHg decreased [3H]glutamate uptake involving the H+-ATPase activity. Until now, the toxic effects of MeHg on CNS were attributed mainly to an impairment of glial glutamate transporters. These findings contribute for the understanding of the neurotoxicity by MeHg, pointing to the involvement of vesicular glutamate.
甲基汞(MeHg)是一种环境污染物,持续对人类健康构成风险。MeHg对中枢神经系统的毒性作用表明谷氨酸能系统参与其中。在本研究中,我们评估了MeHg对突触小泡摄取[3H]谷氨酸的影响。MeHg以浓度依赖性方式抑制[3H]谷氨酸的摄取。由于突触小泡摄取谷氨酸是由一种对巴弗洛霉素A(1)敏感的H+-ATP酶在囊泡膜上形成的电化学梯度驱动的,我们进一步研究了MeHg对该酶活性的影响。MeHg抑制H+-ATP酶活性并消除质子梯度(ΔpH),表明MeHg通过影响H+-ATP酶活性降低了[3H]谷氨酸的摄取。到目前为止,MeHg对中枢神经系统的毒性作用主要归因于胶质谷氨酸转运体的损伤。这些发现有助于理解MeHg的神经毒性,表明囊泡谷氨酸参与其中。