Yasuda Nodoka, Ishii Takayuki, Oyama Dai, Fukuta Tatsuya, Agato Yurika, Sato Akihiko, Shimizu Kosuke, Asai Tomohiro, Asakawa Tomohiro, Kan Toshiyuki, Yamada Shizuo, Ohizumi Yasushi, Oku Naoto
Department of Medical Biochemistry, School of Pharmaceutical Sciences, University of Shizuoka, 52-1 Yada, Suruga-ku, Shizuoka 422-8526, Japan.
Department of Synthetic Organic and Medicinal Chemistry, School of Pharmaceutical Sciences, University of Shizuoka, 52-1 Yada, Suruga-ku, Shizuoka 422-8526, Japan.
Brain Res. 2014 Apr 22;1559:46-54. doi: 10.1016/j.brainres.2014.02.007. Epub 2014 Feb 15.
Nobiletin, a citrus polymethoxylated flavone, is reported to possess various pharmacological activities such as anticancer, anti-inflammation, and antioxidant effects. Recently, nobiletin was shown to provide therapeutic benefit for the treatment of Alzheimer׳s disease by activating cAMP-response element-binding protein (CREB). In the present study, we investigated whether nobiletin could protect the brain against ischemia-reperfusion (I/R) injury and improve functional outcome in cerebral I/R model rats, since CREB activation is known to protect neuronal cells in cerebral ischemia. Nobiletin was injected twice at 0 and 1h after the start of reperfusion in transient middle cerebral artery occlusion (t-MCAO) rats. Cerebral I/R induced prominent brain damage in the ischemic hemisphere of t-MCAO rat brains; however, nobiletin treatment significantly reduced the infarct volume and suppressed the brain edema. Immunohistochemical and TUNEL staining indicated that nobiletin treatment significantly suppressed neutrophil invasion into the ischemic region and significantly decreased apoptotic brain cell death in ischemic hemisphere, suggesting that the anti-inflammatory effect and anti-apoptotic effect should be regarded as the neuroprotective mechanism of nobiletin. Moreover, nobiletin treatment ameliorated motor functional deficits in the ischemic rats compared with those deficits of the vehicle-treated group. These results indicate that nobiletin is a potential neuroprotectant for the treatment of cerebral I/R injury.
诺米林是一种柑橘类多甲氧基黄酮,据报道具有多种药理活性,如抗癌、抗炎和抗氧化作用。最近,诺米林被证明通过激活环磷酸腺苷反应元件结合蛋白(CREB)对阿尔茨海默病的治疗具有益处。在本研究中,我们研究了诺米林是否可以保护大脑免受缺血再灌注(I/R)损伤,并改善大脑I/R模型大鼠的功能结局,因为已知CREB激活可保护大脑缺血中的神经元细胞。在短暂性大脑中动脉闭塞(t-MCAO)大鼠再灌注开始后的0小时和1小时,诺米林注射两次。大脑I/R在t-MCAO大鼠大脑的缺血半球中引起了明显的脑损伤;然而,诺米林治疗显著减少了梗死体积并抑制了脑水肿。免疫组织化学和TUNEL染色表明,诺米林治疗显著抑制了中性粒细胞侵入缺血区域,并显著减少了缺血半球中凋亡性脑细胞死亡,这表明抗炎作用和抗凋亡作用应被视为诺米林的神经保护机制。此外,与载体处理组的缺陷相比,诺米林治疗改善了缺血大鼠的运动功能缺陷。这些结果表明,诺米林是治疗大脑I/R损伤的潜在神经保护剂。