Nameni Ghazaleh, Farhangi Mahdieh Abbasalizad, Hajiluian Ghazaleh, Shahabi Parviz, Abbasi Mehran Mesgari
Nutrition Research Center, Department of Community Nutrition, Tabriz University of Medical Sciences, Tabriz, Iran.
Drug Applied Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.
Int J Dev Neurosci. 2017 Jun;59:15-20. doi: 10.1016/j.ijdevneu.2017.02.008. Epub 2017 Mar 6.
Epidemiological studies proposed a linear connection between developing dementia including Alzheimer's disease (AD) and obesity. Adiposity, insulin resistance and dementia indicated probable mechanistic links in this process. Indeed, it has been known that optimum insulin action in the brain plays critical role in cognitive function; whereas, insulin resistance in obese individuals finally leads to insulin deficiency in central nervous system (CNS) and down regulation of the efficiency of insulin uptake from periphery into CSF. In the current study, we aimed to assess correlation between increased body weight and insulin resistance with CSF to serum ratio of insulin and to evaluate the correlation between CSF to serum ratio of insulin with cognitive function in high fat diet induced obese rats.
Twelve male Wister rats were randomly divided into two groups receiving Diet 1 (D1, 10% fat) and Diet 2 (D2, 59% fat) for 16 weeks. Weight was recorded weekly to assure body weight gain. Morris Water Maze (MWM) task was designed to assess spatial learning memory function. Finally, blood samples were collected for determining fasting serum glucose using enzymatic spectrophotometric method, insulin levels by ELISA kit and homeostasis model assessment of insulin resistance (HOMA-IR) were calculated. Fasting Cerebrospinal Fluid (CSF) insulin was also measured by ELISA kit.
D1 and D 2 groups both experienced weight gain but weight gain in D2 group were significantly higher. A significant correlation between CSF to serum ratio of insulin with weight (r=0.882, p=0.001) and HOMA-IR index (r=0.798, p=0.002) was reported. Moreover, the present study indicated significant correlations between CSF to serum ratio of insulin and escape latency time in first (r=0.631, p=0.028), second (r=0.716, p=0.009) and third (r=0.609, p=0.036) day of MWM test and probe time of MWM test (r=0.762, p=0.004).
Increased body weight induced by high fat diet and insulin resistance in rats led to down regulation of CSF to serum ratio of insulin in the current research. Brain insulin deficiency may be responsible for possible decline of cognitive function in obesity. More researches are needed to better clarify the underlying mechanisms and also to confirm the similar findings in human studies.
流行病学研究表明,包括阿尔茨海默病(AD)在内的痴呆症发展与肥胖之间存在线性关联。肥胖、胰岛素抵抗和痴呆症在这一过程中显示出可能的机制联系。事实上,已知大脑中最佳的胰岛素作用在认知功能中起着关键作用;然而,肥胖个体的胰岛素抵抗最终会导致中枢神经系统(CNS)胰岛素缺乏,并下调胰岛素从外周进入脑脊液的效率。在本研究中,我们旨在评估体重增加和胰岛素抵抗与脑脊液胰岛素与血清胰岛素比值之间的相关性,并评估高脂肪饮食诱导的肥胖大鼠脑脊液胰岛素与血清胰岛素比值与认知功能之间的相关性。
将12只雄性Wistar大鼠随机分为两组,分别给予饮食1(D1,10%脂肪)和饮食2(D2,59%脂肪),持续16周。每周记录体重以确保体重增加。设计莫里斯水迷宫(MWM)任务以评估空间学习记忆功能。最后,采集血样,采用酶分光光度法测定空腹血清葡萄糖,使用ELISA试剂盒测定胰岛素水平,并计算胰岛素抵抗的稳态模型评估(HOMA-IR)。空腹脑脊液(CSF)胰岛素也通过ELISA试剂盒测定。
D1组和D2组体重均增加,但D2组体重增加显著更高。报告显示脑脊液胰岛素与血清胰岛素比值与体重(r=0.882,p=0.001)和HOMA-IR指数(r=0.798,p=0.002)之间存在显著相关性。此外,本研究表明,在MWM测试的第一天(r=0.631,p=0.028)、第二天(r=0.716,p=0.009)和第三天(r=0.609,p=0.036)以及MWM测试的探测时间(r=0.762,p=0.004),脑脊液胰岛素与血清胰岛素比值与逃避潜伏期之间存在显著相关性。
在本研究中,高脂肪饮食诱导的大鼠体重增加和胰岛素抵抗导致脑脊液胰岛素与血清胰岛素比值下调。脑胰岛素缺乏可能是肥胖中认知功能可能下降的原因。需要更多研究来更好地阐明潜在机制,并在人体研究中证实类似发现。