Kwon Hyunji, Lee Jihye, Lee Eunhong, Moon Somin, Cho Eunbi, Jeon Jieun, Park A Young, Hwang Joon-Ho, Cho Gun Hee, Kong Haram, Park Mi-Houn, Kim Sung-Kyu, Kim Dong Hyun, Jung Ji Wook
Department of Advanced Translational Medicine, School of Medicine, Konkuk University, 120 Neungdong-ro, Gwangjin-gu, Seoul 05029, Republic of Korea.
Industry Academic Cooperation Foundation, Daegu Haany University, 1 Hanuidae-ro, Gyeongsan-si 38610, Gyeongsangbuk-do, Republic of Korea.
Pharmaceutics. 2025 Aug 12;17(8):1045. doi: 10.3390/pharmaceutics17081045.
var. Kudo, a member of the Lamiaceae family, has been previously reported to reduce neuroinflammation and potentially decrease Aβ plaque accumulation in 5XFAD mice. In this study, we aimed to evaluate the anti-neuroinflammatory potential of a standardized 60% ethanol extract of Perilla leaves (PE), optimized for commercial application. : The inflammatory response was assessed in LPS-stimulated BV2 microglial cells, and the cognitive improvement was evaluated in an AD animal model induced by intracerebroventricular injection of Aβ. : Using LPS-stimulated BV2 microglial cells and an Aβ-injected ICR mouse model of Alzheimer's disease, we found that PE significantly suppressed the LPS-induced production of nitric oxide and pro-inflammatory mediators, including IL-6, TNF-α, NF-κB, iNOS, and COX-2, along with inhibition of JNK and p38 MAPK activation. Furthermore, PE upregulated CREB and BDNF expression. In vivo, PE administration alleviated Aβ-induced cognitive deficits, which were associated with reduced expression of JNK, NF-κB, iNOS, and COX and increased CREB/BDNF signaling in the hippocampus. Behavioral assessments-including passive avoidance, Morris water maze, novel object recognition, and Y-maze tests-confirmed the improvement in cognitive function. : Collectively, these findings demonstrate that PE exerts significant anti-neuroinflammatory and neuroprotective effects, supporting its potential as a functional ingredient for cognitive enhancement.
紫苏变种 Kudō 是唇形科植物的一员,此前有报道称其可减轻神经炎症,并有可能减少 5XFAD 小鼠脑中的 Aβ 斑块积累。在本研究中,我们旨在评估经标准化处理、适用于商业应用的 60% 紫苏叶乙醇提取物(PE)的抗神经炎症潜力。在脂多糖(LPS)刺激的 BV2 小胶质细胞中评估炎症反应,并在通过脑室内注射 Aβ 诱导的 AD 动物模型中评估认知改善情况。利用 LPS 刺激的 BV2 小胶质细胞和 Aβ 注射的 ICR 小鼠阿尔茨海默病模型,我们发现 PE 显著抑制 LPS 诱导的一氧化氮及促炎介质(包括 IL-6、TNF-α、NF-κB、诱导型一氧化氮合酶(iNOS)和环氧化酶-2(COX-2))的产生,同时抑制 JNK 和 p38 丝裂原活化蛋白激酶(MAPK)的激活。此外,PE 上调了 CREB 和脑源性神经营养因子(BDNF)的表达。在体内,PE 给药减轻了 Aβ 诱导的认知缺陷,这与海马体中 JNK、NF-κB、iNOS 和 COX 的表达降低以及 CREB/BDNF 信号通路增强有关。包括被动回避、莫里斯水迷宫、新物体识别和 Y 迷宫测试在内的行为评估证实了认知功能的改善。总体而言,这些发现表明 PE 具有显著的抗神经炎症和神经保护作用,支持其作为认知增强功能性成分的潜力。