Eunjin Sohn , Hye-Sun Lim , Bu-Yeo Kim , Yu Jin Kim , Joo-Hwan Kim , Soo-Jin Jeong
{"title":"Elaeagnus glabra f. oxyphylla 提取物对淀粉样β诱导的认知缺陷小鼠的神经保护作用:PKC-δ、MYL2 和 FER 通路的参与。","authors":"Eunjin Sohn , Hye-Sun Lim , Bu-Yeo Kim , Yu Jin Kim , Joo-Hwan Kim , Soo-Jin Jeong","doi":"10.1016/j.biopha.2024.117671","DOIUrl":null,"url":null,"abstract":"<div><div><em>Elaeagnus glabra</em> f. <em>oxyphylla</em> (EGFO), a member of the <em>Elaeagnaceae</em> family, is an evergreen plant distinct from other species in its genus<em>.</em> We previously reported that ethanol extract from EGFO has memory improvement effects in a short-term memory deficit mouse model and anti-inflammatory effects in a microglial cell line. However, little is known about the pharmacological effects of EGFO. In the present study, we further explored the effect of EGFO on cognitive impairment using amyloid-beta-induced Alzheimer's disease (AD)-like mice. EGFO extract significantly enhanced cognitive functions in the passive avoidance task and Morris water maze test. EGFO treatment led to a significant increase in neuronal nuclei expression in mouse hippocampal tissues and inhibited hydrogen peroxide-induced cell death in HT22 hippocampal cells, indicating the neuroprotective effects of EGFO. Antibody microarray analysis was performed to determine the molecular mechanisms underlying the effects of EGFO on cognitive improvement and neuroprotection. The data revealed that EGFO decreased the phosphorylation of protein kinase C delta and increased the phosphorylation of myosin regulatory light chain 2 and tyrosine kinase Fer. These findings were validated using immunoblotting both in <em>in vitro</em> and <em>in vivo</em> AD models. Overall, our findings suggest that EGFO could be a candidate therapeutic agent for AD or AD-like diseases due to its potential for cognitive improvement and neuroprotection.</div></div>","PeriodicalId":8966,"journal":{"name":"Biomedicine & Pharmacotherapy","volume":"181 ","pages":"Article 117671"},"PeriodicalIF":6.9000,"publicationDate":"2024-11-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Neuroprotective effects of Elaeagnus glabra f. oxyphylla extract in amyloid-beta-induced cognitive deficit mice: Involvement of the PKC-delta, MYL2, and FER pathways\",\"authors\":\"Eunjin Sohn , Hye-Sun Lim , Bu-Yeo Kim , Yu Jin Kim , Joo-Hwan Kim , Soo-Jin Jeong\",\"doi\":\"10.1016/j.biopha.2024.117671\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div><em>Elaeagnus glabra</em> f. <em>oxyphylla</em> (EGFO), a member of the <em>Elaeagnaceae</em> family, is an evergreen plant distinct from other species in its genus<em>.</em> We previously reported that ethanol extract from EGFO has memory improvement effects in a short-term memory deficit mouse model and anti-inflammatory effects in a microglial cell line. However, little is known about the pharmacological effects of EGFO. In the present study, we further explored the effect of EGFO on cognitive impairment using amyloid-beta-induced Alzheimer's disease (AD)-like mice. EGFO extract significantly enhanced cognitive functions in the passive avoidance task and Morris water maze test. EGFO treatment led to a significant increase in neuronal nuclei expression in mouse hippocampal tissues and inhibited hydrogen peroxide-induced cell death in HT22 hippocampal cells, indicating the neuroprotective effects of EGFO. Antibody microarray analysis was performed to determine the molecular mechanisms underlying the effects of EGFO on cognitive improvement and neuroprotection. The data revealed that EGFO decreased the phosphorylation of protein kinase C delta and increased the phosphorylation of myosin regulatory light chain 2 and tyrosine kinase Fer. These findings were validated using immunoblotting both in <em>in vitro</em> and <em>in vivo</em> AD models. Overall, our findings suggest that EGFO could be a candidate therapeutic agent for AD or AD-like diseases due to its potential for cognitive improvement and neuroprotection.</div></div>\",\"PeriodicalId\":8966,\"journal\":{\"name\":\"Biomedicine & Pharmacotherapy\",\"volume\":\"181 \",\"pages\":\"Article 117671\"},\"PeriodicalIF\":6.9000,\"publicationDate\":\"2024-11-12\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Biomedicine & Pharmacotherapy\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0753332224015579\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"MEDICINE, RESEARCH & EXPERIMENTAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biomedicine & Pharmacotherapy","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0753332224015579","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MEDICINE, RESEARCH & EXPERIMENTAL","Score":null,"Total":0}
引用次数: 0
摘要
榆叶梅(Elaeagnus glabra f. oxyphylla,EGFO)是榆叶梅科榆叶梅属的一种常绿植物,有别于同属的其他物种。我们以前曾报道过,EGFO 的乙醇提取物在短期记忆缺失小鼠模型中具有改善记忆的作用,在小胶质细胞系中具有抗炎作用。然而,人们对 EGFO 的药理作用知之甚少。在本研究中,我们利用淀粉样β诱导的阿尔茨海默病(AD)样小鼠进一步探讨了 EGFO 对认知障碍的影响。在被动回避任务和莫里斯水迷宫测试中,EGFO提取物能明显增强小鼠的认知功能。EGFO处理可使小鼠海马组织中神经元核表达明显增加,并可抑制过氧化氢诱导的HT22海马细胞死亡,这表明EGFO具有神经保护作用。为了确定EGFO对认知改善和神经保护作用的分子机制,研究人员进行了抗体微阵列分析。数据显示,EGFO减少了蛋白激酶C delta的磷酸化,增加了肌球蛋白调节轻链2和酪氨酸激酶Fer的磷酸化。这些发现通过免疫印迹法在体外和体内AD模型中得到了验证。总之,我们的研究结果表明,EGFO具有改善认知能力和保护神经的潜力,可以作为AD或类似AD疾病的候选治疗药物。
Neuroprotective effects of Elaeagnus glabra f. oxyphylla extract in amyloid-beta-induced cognitive deficit mice: Involvement of the PKC-delta, MYL2, and FER pathways
Elaeagnus glabra f. oxyphylla (EGFO), a member of the Elaeagnaceae family, is an evergreen plant distinct from other species in its genus. We previously reported that ethanol extract from EGFO has memory improvement effects in a short-term memory deficit mouse model and anti-inflammatory effects in a microglial cell line. However, little is known about the pharmacological effects of EGFO. In the present study, we further explored the effect of EGFO on cognitive impairment using amyloid-beta-induced Alzheimer's disease (AD)-like mice. EGFO extract significantly enhanced cognitive functions in the passive avoidance task and Morris water maze test. EGFO treatment led to a significant increase in neuronal nuclei expression in mouse hippocampal tissues and inhibited hydrogen peroxide-induced cell death in HT22 hippocampal cells, indicating the neuroprotective effects of EGFO. Antibody microarray analysis was performed to determine the molecular mechanisms underlying the effects of EGFO on cognitive improvement and neuroprotection. The data revealed that EGFO decreased the phosphorylation of protein kinase C delta and increased the phosphorylation of myosin regulatory light chain 2 and tyrosine kinase Fer. These findings were validated using immunoblotting both in in vitro and in vivo AD models. Overall, our findings suggest that EGFO could be a candidate therapeutic agent for AD or AD-like diseases due to its potential for cognitive improvement and neuroprotection.
期刊介绍:
Biomedicine & Pharmacotherapy stands as a multidisciplinary journal, presenting a spectrum of original research reports, reviews, and communications in the realms of clinical and basic medicine, as well as pharmacology. The journal spans various fields, including Cancer, Nutriceutics, Neurodegenerative, Cardiac, and Infectious Diseases.