首页> 外文期刊>Behavioural Brain Research: An International Journal >Disturbance of endogenous hydrogen sulfide generation and endoplasmic reticulum stress in hippocampus are involved in homocysteine-induced defect in learning and memory of rats
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Disturbance of endogenous hydrogen sulfide generation and endoplasmic reticulum stress in hippocampus are involved in homocysteine-induced defect in learning and memory of rats

机译:海马内源性硫化氢生成和内质网应激障碍与同型半胱氨酸诱导的大鼠学习记忆障碍有关

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摘要

Homocysteine (Hcy) is a risk factor for Alzheimer's disease (AD). Hydrogen sulfide (H2S) acts as an endogenous neuromodulator and neuroprotectant. It has been shown that endoplasmic reticulum (ER) stress is involved in the pathological mechanisms of the learning and memory dysfunctions and that H2S exerts its neuroprotective role via suppressing ER stress. In the present work, we explored the effects of intracerebroventricular injection of Hcy on the formation of learning and memory, the generation of endogenous H2S, and the expression of ER stress in the hippocampus of rats. We found that intracerebroventricular injection of Hcy in rats leads to learning and memory dysfunctions in the Morris water maze and novel of object recognition test and decreases in the expression of cystathionine-β-synthase, the major enzyme responsible for endogenous H2S generation, and the generation of endogenous H2S in the hippocampus of rats. We also showed that exposure of Hcy could up-regulate the expressions of glucose-regulated protein 78 (GRP78), CHOP, and cleaved caspase-12, which are the major mark proteins of ER stress, in the hippocampus of rats. Taken together, these results suggest that the disturbance of hippocampal endogenous H2S generation and the increase in ER stress in the hippocampus are related to Hcy-induced defect in learning and memory.
机译:同型半胱氨酸(Hcy)是阿尔茨海默氏病(AD)的危险因素。硫化氢(H2S)充当内源性神经调节剂和神经保护剂。已经显示,内质网(ER)应激与学习和记忆功能障碍的病理机制有关,H2S通过抑制ER应激发挥其神经保护作用。在本研究中,我们探讨了脑室内注射Hcy对大鼠海马学习记忆的形成,内源性H2S的产生以及ER应激表达的影响。我们发现,脑室内注射Hcy会导致莫里斯水迷宫中的学习和记忆功能障碍以及新的物体识别测试,并降低胱硫醚-β-合酶(负责内源性H2S生成的主要酶)及其生成的表达。大鼠海马内源性H2S的变化我们还表明,暴露于Hcy可以上调大鼠海马中葡萄糖调节蛋白78(GRP78),CHOP和裂解的caspase-12的表达,这是ER应激的主要标志蛋白。两者合计,这些结果表明,海马内源性H2S生成的紊乱和海马内质网应激的增加与Hcy诱导的学习和记忆缺陷有关。

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