Department of Histology and Embryology, Faculty of Medicine, Gazi University, Ankara, Turkey
Department of Histology and Embryology, Faculty of Medicine, İstanbul Okan University, İstanbul, Turkey
Turk J Med Sci. 2021 Aug 30;51(4):2159-2166. doi: 10.3906/sag-2008-291.
BACKGROUND/AIM: Calcineurin, an inhibitor of calcium dependent phosphatase is highly presented in a brain of an Alzheimer’s disease. Aging brain gets more sensitive to hyperactivation of calcineurin, and this event causes tau neurofibrillary plaque accumulation, which is one of the outcomes of this disease. The regions of hippocampus are much effected from the results of this process. Our hypothesis is that a calcineurin inhibitor, tacrolimus, could prevent the accumulation and the decrease of the neuronal cells. Therefore, this immunosuppressive drug could be a candidate for an early treatment of Alzheimer disease.
Fifteen male Wistar albino rats were divided to three groups; control, Alzheimer, and Alzheimer+Tacrolimus. The Alzheimer group received an injection of streptozotocin intracerebroventricularly for the purpose of modelling the disease via generating free radicals leading a cognitive impairment. Alzheimer+Tacrolimus group first received an oral drug, a calcineurin inhibitor for 10 days afterwards prepared for the model as same as the Alzheimer group received. Finally, all groups performed the Morris water maze test for four days then sacrificed. For the aim of counting neurons in the hippocampus stereological methods, as well as for an evaluation of cellular response to stress in dentate gyrus, a c-Fos immunohistochemistry was performed.
According to the probe trial of Morris water maze test, the latency time was dramatically higher at both Alzheimer and Alzheimer+Tacrolimus group (p < 0.01). We confirmed these results with our stereology data. The results from stereology technique indicate that there was a neuronal decrease at the hippocampus regions in Alzheimer and Alzheimer+Tacrolimus group. Our outcomes from immunohistochemical data showed a significant increase in the number of c-Fos-positive cells in Alzheimer group when comparing with Alzheimer+Tacrolimus group (p < 0.001).
There was none preventive effect for neuronal loss in the hippocampus under the effect of tacrolimus drug according to stereological results. However, tacrolimus administration may have reduced cellular stress and cell damage.
背景/目的:钙调神经磷酸酶是一种钙依赖性磷酸酶抑制剂,在阿尔茨海默病患者的大脑中高度表达。衰老的大脑对钙调神经磷酸酶的过度激活更加敏感,而这一事件会导致 tau 神经原纤维缠结的积累,这是该疾病的结果之一。海马体的区域受到该过程的影响最大。我们的假设是,钙调神经磷酸酶抑制剂他克莫司可以防止神经元细胞的积累和减少。因此,这种免疫抑制剂可能是治疗阿尔茨海默病的早期候选药物。
将 15 只雄性 Wistar 白化大鼠分为三组;对照组、阿尔茨海默病组和阿尔茨海默病+他克莫司组。阿尔茨海默病组通过脑室注射链脲佐菌素来模拟疾病,通过产生自由基导致认知障碍。阿尔茨海默病+他克莫司组首先接受 10 天的口服药物治疗,一种钙调神经磷酸酶抑制剂,然后像阿尔茨海默病组一样准备进行模型制作。最后,所有组都进行了为期四天的 Morris 水迷宫测试,然后处死。为了对海马体中的神经元进行计数,采用立体学方法,以及评估齿状回细胞对应激的反应,进行了 c-Fos 免疫组织化学染色。
根据 Morris 水迷宫测试的探测试验,阿尔茨海默病组和阿尔茨海默病+他克莫司组的潜伏期时间明显延长(p < 0.01)。我们通过立体学数据证实了这些结果。立体学技术的结果表明,阿尔茨海默病组和阿尔茨海默病+他克莫司组的海马体区域神经元数量减少。我们的免疫组织化学数据结果表明,与阿尔茨海默病+他克莫司组相比,阿尔茨海默病组的 c-Fos 阳性细胞数量显著增加(p < 0.001)。
根据立体学结果,他克莫司药物对海马体神经元丢失没有预防作用。然而,他克莫司的给药可能减少了细胞应激和细胞损伤。