Querobino Samyr Machado, Carrettiero Daniel Carneiro, Costa Maricilia Silva, Alberto-Silva Carlos
Natural and Humanities Sciences Center, Experimental Morphophysiology Laboratory Federal University of ABC (UFABC), Rua Arcturus, n° 03, Bloco Delta, São Bernardo do Campo, 09606-070, SP, Brazil.
Instituto de Pesquisa e Desenvolvimento - IP&D, Universidade do Vale do Paraíba-UNIVAP, Av. Shishima Hifumi 2911, São José dos Campos, Urbanova, 12244-000, SP, Brazil.
Toxicon. 2017 Apr;129:134-143. doi: 10.1016/j.toxicon.2017.02.015. Epub 2017 Feb 20.
In central nervous system cells, low molecular weight fractions (LMWF) from snake venoms can inhibit changes in mitochondrial membrane permeability, preventing the diffusion of cytochrome c to the cytoplasm, inhibiting the activation of pro-apoptotic factors. Here, we evaluated the neuroprotective activity of LMWF from Bothrops jararaca (Bj) snake venom in HO-induced cytotoxicity in cultured hippocampal cells. SDS-PAGE, FT-IR and MALDI-TOF analysis of LMWF (<14 kDa) confirmed the absence of high-molecular-weight proteins in the fraction. LMWF did not present cytotoxicity in all concentrations and time tested by MTT assay. Neuroprotection was evaluated in cells pretreated with LMWF for 4 h prior to the addition of 50 μM HO for 20 h. We demonstrated that LMWF reduced the argininosuccinate synthase (AsS) and superoxide dismutase (SOD1) expressions, suggesting that this fraction as an effective neuroprotective compound that could increase the hippocampal cells viability by attenuation of oxidative stress. In addition, LMWF protects against apoptosis induced by HO, reducing the expression of caspase-3 and caspase-8. Overall, this study opens new perspectives for the identification of new molecules for the development of drugs applied to the treatment of neurodegenerative diseases.
在中枢神经系统细胞中,蛇毒的低分子量组分(LMWF)可抑制线粒体膜通透性的改变,防止细胞色素c扩散至细胞质,抑制促凋亡因子的激活。在此,我们评估了巴西矛头蝮蛇毒的LMWF在HO诱导的培养海马细胞细胞毒性中的神经保护活性。对LMWF(<14 kDa)进行的SDS-PAGE、傅里叶变换红外光谱(FT-IR)和基质辅助激光解吸电离飞行时间质谱(MALDI-TOF)分析证实该组分中不存在高分子量蛋白质。通过MTT法检测,LMWF在所有测试浓度和时间下均未表现出细胞毒性。在加入50 μM HO处理20小时之前,先用LMWF预处理细胞4小时,评估其神经保护作用。我们证明LMWF降低了精氨酸琥珀酸合成酶(AsS)和超氧化物歧化酶(SOD1)的表达,表明该组分是一种有效的神经保护化合物,可通过减轻氧化应激来提高海马细胞的活力。此外,LMWF可保护细胞免受HO诱导的凋亡,降低caspase-3和caspase-8的表达。总体而言,本研究为鉴定用于开发治疗神经退行性疾病药物的新分子开辟了新的前景。