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Neuroprotection Comparison of Rosmarinic Acid and Carnosic Acid in Primary Cultures of Cerebellar Granule Neurons

机译:迷迭香酸和肌酸在小脑颗粒神经元原代培养中的神经保护作用比较

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摘要

Neurodegenerative disorders such as amyotrophic lateral sclerosis (ALS), Alzheimer’s disease, and Parkinson’s disease, are characterized by the progressive loss of neurons in specific regions of the brain and/or spinal cord. Neuronal cell loss typically occurs by either apoptotic or necrotic mechanisms. Oxidative stress and nitrosative stress, along with excitotoxicity and caspase activation, have all been implicated as major underlying causes of neuronal cell death. Diverse nutraceuticals (bioactive compounds found in common foods) have been shown to have neuroprotective effects in a variety of in vitro and in vivo disease models. In the current study, we compared the neuroprotective effects of two polyphenolic compounds, rosmarinic acid and carnosic acid, which are both found at substantial concentrations in the herb rosemary. The capacity of these compounds to rescue primary cultures of rat cerebellar granule neurons (CGNs) from a variety of stressors was investigated. Both polyphenols significantly reduced CGN death induced by the nitric oxide donor, sodium nitroprusside (nitrosative stress). Rosmarinic acid uniquely protected CGNs from glutamate-induced excitotoxicity, while only carnosic acid rescued CGNs from caspase-dependent apoptosis induced by removal of depolarizing extracellular potassium (5K apoptotic condition). Finally, we found that carnosic acid protects CGNs from 5K-induced apoptosis by activating a phosphatidylinositol 3-kinase (PI3K) pro-survival pathway. The shared and unique neuroprotective effects of these two compounds against diverse modes of neuronal cell death suggest that future preclinical studies should explore the potential complementary effects of these rosemary polyphenols on neurodegenerative disease progression.
机译:诸如肌萎缩性侧索硬化症(ALS),阿尔茨海默氏病和帕金森氏病等神经退行性疾病的特征是大脑和/或脊髓特定区域神经元的逐渐丧失。神经细胞的丢失通常通过凋亡或坏死机制发生。氧化应激和亚硝化应激,以及兴奋性毒性和胱天蛋白酶的活化,都被认为是神经元细胞死亡的主要原因。在各种体外和体内疾病模型中,多种保健食品(在常见食品中发现的生物活性化合物)已显示出神经保护作用。在当前的研究中,我们比较了迷迭香中大量存在的两种多酚化合物(迷迭香酸和肌酸)的神经保护作用。研究了这些化合物从各种应激源中拯救大鼠小脑颗粒神经元(CGNs)原代培养物的能力。两种多酚均显着降低了由一氧化氮供体硝普钠(亚硝化应激)引起的CGN死亡。迷迭香酸独特地保护了CGNs免受谷氨酸诱导的兴奋性毒性,而只有肌苷酸才使CGNs摆脱了去极化细胞外钾的去除(5K细胞凋亡条件)而诱导的caspase依赖性细胞凋亡。最后,我们发现肌肽酸通过激活磷脂酰肌醇3激酶(PI3K)促存活途径来保护CGN免于5K诱导的细胞凋亡。这两种化合物对神经元细胞死亡的各种模式的共同和独特的神经保护作用表明,未来的临床前研究应探索这些迷迭香多酚对神经退行性疾病进展的潜在补充作用。

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