Laboratório de Síntese, Reatividade e Avaliação Farmacológica e Toxicológica de Organocalcogênios, Centro de Ciências Naturais e Exatas, Universidade Federal de Santa Maria, Santa Maria, Brazil.
J Alzheimers Dis. 2013;33(1):133-44. doi: 10.3233/JAD-2012-121150.
The purpose of this study was to investigate possible molecular targets involved in the neuroprotective effect of p,p'-methoxyl-diphenyl diselenide [(MeOPhSe)2], using a streptozotocin (STZ)-induced sporadic dementia of Alzheimer's type rat model. Male Wistar rats were injected with STZ (1.0 mg/8 μl; 4 μl/ventricle). After 21 days of STZ injection, regular diet-fed rats were supplemented with 10 ppm of (MeOPhSe)2 during 30 days. At the end of this period, rats performed object recognition and step-down passive avoidance tasks. Apoptosis was assessed by TUNEL staining and active caspase-3. Glial fibrillary acidic protein, ionized calcium binding adaptor molecule 1, and microtubule associated protein 2 were determined by immunofluorescence in rat hippocampus. The results demonstrate that the (MeOPhSe)2 dietary supplementation reversed STZ-induced memory impairment by enhancing memory in sham rats. (MeOPhSe)2 was also effective in reducing STZ-induced apoptosis and preserving dendrites and synapses. Moreover, (MeOPhSe)2 inhibited activation of microglia and astrogliosis induced by STZ in the rat hippocampus. We conclude that the (MeOPhSe)2 neuroprotective action is related to inhibition of apoptosis and suppression of inflammation.
本研究旨在探讨二苯并二硒醚[(MeOPhSe)2]的神经保护作用的可能分子靶点,使用链脲佐菌素(STZ)诱导的散发性阿尔茨海默病大鼠模型。雄性 Wistar 大鼠脑室注射 STZ(1.0 mg/8 μl;4 μl/脑室)。STZ 注射 21 天后,正常饮食喂养的大鼠在 30 天内补充 10 ppm 的(MeOPhSe)2。在此期间结束时,大鼠进行物体识别和下台阶被动回避任务。通过 TUNEL 染色和活性 caspase-3 评估细胞凋亡。通过免疫荧光在大鼠海马中测定神经胶质纤维酸性蛋白、离子钙结合接头分子 1 和微管相关蛋白 2。结果表明,(MeOPhSe)2 饮食补充通过增强假手术大鼠的记忆来逆转 STZ 诱导的记忆障碍。(MeOPhSe)2 还能有效减少 STZ 诱导的细胞凋亡并保护树突和突触。此外,(MeOPhSe)2 抑制了 STZ 在大鼠海马中诱导的小胶质细胞和星形胶质细胞的激活。我们得出结论,(MeOPhSe)2 的神经保护作用与抑制细胞凋亡和抑制炎症有关。