Park Sun Young, Kim Young Hun, Park Geuntae
Bio-IT Fusion Technology Research Institute, Busan, Republic of Korea.
Bio-IT Fusion Technology Research Institute, Busan, Republic of Korea; Department of Nanomaterials Engineering, Pusan National University, Busan, Republic of Korea.
Neurosci Lett. 2015 Nov 16;609:129-36. doi: 10.1016/j.neulet.2015.10.022. Epub 2015 Oct 22.
Emerging evidence suggests that neuroinflammatory responses are involved in the neuronal injury. Neuroinflammatory response is mediated by cellular components such as microglia and molecular components, including nitric oxide, prostaglandins and inflammatory cytokines, activation of complement proteins etc. Cucurbitacins is a class of highly oxidized tetracyclic triterpenoids isolated mainly from Cucurbitaceae but also from other plan families and has been reported to have pharmacological activities. The present study aimed to investigate the anti-neuroinflammatory effects of Cucurbitacins on TLR 2/4 agonists (amyloid-β, LTA, and LPS)-induced neuroinflammatory response in microglia and the underlying mechanism for Nrf2/ARE pathways. Results indicates that pretreatment with Cucurbitacins significantly reduced the pro-inflammatory cytokine (TNF-α, IL-1β and IL-6) and attenuated iNOS and COX-2 expression in TLR 2/4 agonists-stimulated microglia. In addition, Cucurbitacins inhibited JNK and p38 MAPKs activation and attenuated JAK-STAT and NF-κB activation in TLR 2/4 agonists-stimulated microglia. Next, we evaluate the potential involvement of Cucurbitacins in the activation of Nrf2/ARE signaling pathways and phase II detoxification enzymes activity. Results indicate that Cucurbitacins markedly promoted the activation of Nrf-2/ARE pathway-related downstream factors including NQO-1 and HO-1. Furthermore, anti-neuroinflammatory effects of Cucurbitacins are attenuated in the knockdown of Nrf2, HO-1 and NQO-1 respectively. Cucurbitacins also has neuroprotective effect against microglia over-activation related neuronal damage. This study demonstrates that Cucurbitacins is potent activator of the Nrf2/ARE pathway and is therapeutically relevant not only to neuroinflammatory responses of microglia but also neuroinflammation mediated neuronal injury.
新出现的证据表明,神经炎症反应与神经元损伤有关。神经炎症反应由小胶质细胞等细胞成分以及包括一氧化氮、前列腺素、炎性细胞因子、补体蛋白激活等分子成分介导。葫芦素是一类高度氧化的四环三萜类化合物,主要从葫芦科植物中分离得到,但也可从其他植物科中获得,并且据报道具有药理活性。本研究旨在探讨葫芦素对小胶质细胞中TLR 2/4激动剂(淀粉样蛋白-β、脂磷壁酸和脂多糖)诱导的神经炎症反应的抗神经炎症作用以及Nrf2/ARE通路的潜在机制。结果表明,用葫芦素预处理可显著降低促炎细胞因子(肿瘤坏死因子-α、白细胞介素-1β和白细胞介素-6),并减弱TLR 2/4激动剂刺激的小胶质细胞中诱导型一氧化氮合酶和环氧化酶-2的表达。此外,葫芦素抑制TLR 2/4激动剂刺激的小胶质细胞中JNK和p38丝裂原活化蛋白激酶的激活,并减弱JAK-STAT和NF-κB的激活。接下来,我们评估葫芦素在Nrf2/ARE信号通路激活和II期解毒酶活性中的潜在作用。结果表明,葫芦素显著促进了Nrf-2/ARE通路相关下游因子包括醌氧化还原酶-1和血红素加氧酶-1的激活。此外,分别敲低Nrf2、血红素加氧酶-1和醌氧化还原酶-1后,葫芦素的抗神经炎症作用减弱。葫芦素对小胶质细胞过度激活相关的神经元损伤也具有神经保护作用。本研究表明,葫芦素是Nrf2/ARE通路的有效激活剂,不仅与小胶质细胞的神经炎症反应有关,而且与神经炎症介导的神经元损伤治疗相关。