Field Neurosciences Laboratory for Restorative Neurology, Central Michigan University, Mt. Pleasant, Michigan 48859, USA.
J Med Food. 2013 Apr;16(4):288-95. doi: 10.1089/jmf.2012.0131.
Alzheimer's disease (AD) is a progressive neurodegenerative disorder that affects more than five million Americans and is characterized by a progressive loss of memory, loss of cholinergic neurons in the basal forebrain, formation of amyloid plaques and neurofibrillary tangles, and an increase in oxidative stress. Recent studies indicate that dietary supplements of antioxidants and omega-3 and omega-6 fatty acids may reduce the cognitive deficits in AD patients. The current study tested a combinatorial treatment of antioxidants from tart cherry extract and essential fatty acids from Nordic fish and emu oils for reducing cognitive deficits in the mu-p75 saporin (SAP)-induced mouse model of AD. Mice were given daily gavage treatments of Cerise(®) Total-Body-Rhythm™ (TBR; containing tart cherry extract, Nordic fish oil, and refined emu oil) or vehicle (methylcellulose) for 2 weeks before intracerebroventricular injections of the cholinergic toxin, mu-p75 SAP, or phosphate-buffered saline. The TBR treatments continued for an additional 17 days, when the mice were tested on a battery of cognitive and motor tasks. Results indicate that TBR decreased the SAP-induced cognitive deficits assessed by the object-recognition, place-recognition, and Morris-water-maze tasks. Histological examination of the brain tissue indicated that TBR protected against SAP-induced inflammatory response and loss of cholinergic neurons in the area around the medial septum. These findings indicate that TBR has the potential to serve as an adjunctive treatment which may help reduce the severity of cognitive deficits in disorders involving cholinergic deficits, such as AD.
阿尔茨海默病(AD)是一种进行性神经退行性疾病,影响着超过 500 万的美国人,其特征是记忆逐渐丧失、基底前脑胆碱能神经元丧失、淀粉样斑块和神经原纤维缠结形成,以及氧化应激增加。最近的研究表明,抗氧化剂和欧米伽-3 和欧米伽-6 脂肪酸的膳食补充剂可能会减少 AD 患者的认知缺陷。本研究测试了抗氧化剂组合治疗,来自樱桃提取物和来自北欧鱼类和鸸鹋油的必需脂肪酸,用于减少 mu-p75 白喉毒素(SAP)诱导的 AD 小鼠模型中的认知缺陷。小鼠在脑室注射胆碱能毒素 mu-p75 SAP 或磷酸盐缓冲盐水前,每天接受 Cerise(®)Total-Body-Rhythm™(TBR;含有樱桃提取物、北欧鱼油和精炼鸸鹋油)或载体(甲基纤维素)的灌胃治疗 2 周。TBR 治疗持续另外 17 天,然后对小鼠进行一系列认知和运动任务测试。结果表明,TBR 可减少由对象识别、位置识别和 Morris 水迷宫任务评估的 SAP 诱导的认知缺陷。脑组织的组织学检查表明,TBR 可防止 SAP 诱导的炎症反应和中隔周围区域胆碱能神经元的丧失。这些发现表明,TBR 具有作为辅助治疗的潜力,可有助于减轻涉及胆碱能缺陷的疾病(如 AD)中认知缺陷的严重程度。