Effect of Nattokinase in D-galactose- and Aluminum Chloride-induced Alzheimer's Disease Model of Rat.

IF 1.8 4区 医学 Q3 MEDICINE, RESEARCH & EXPERIMENTAL
In vivo Pub Date : 2024-11-01 DOI:10.21873/invivo.13744
Takashi Tanikawa, James Yu, Kate Hsu, Shinder Chen, Ayako Ishii, Masashi Kitamura
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引用次数: 0

Abstract

Background/aim: Alzheimer's disease (AD) is the most common form of dementia worldwide. Nattokinase is a serine protease extracellularly produced by natto, a fermented product of Bacillus subtilis var. natto. In this study, we investigated the therapeutic effects of nattokinase in a rat model of AD induced by aluminum and D-galactose.

Materials and methods: Forty Wistar rats were randomly divided into four groups: normal, vehicle, and orally administered nattokinase (NK65 and NK130 groups). Except for the normal group, all groups were treated with AlCl3 and D-galactose for 10 weeks. The NK65 and NK130 groups additionally received 65 mg/kg/day and 130 mg/kg/day nattokinase, respectively. We analyzed β-amyloid levels in the cerebrospinal fluid (CSF), and the spatial reference test was evaluated using the Morris water maze test. After the Morris water maze test, rats of all groups were subjected to micro-computed tomography (μCT) to assess constructional changes in the brain. Aluminum concentration and β-amyloid levels were analyzed by histochemical staining in all brain tissues.

Results: Oral administration of nattokinase in the AD rat model increased free-form β-amyloid levels in the CSF and improved aluminum and amyloid plaque accumulation in the brain. Brain μCT images showed enhanced brain volume with fewer constructional changes after treatment with nattokinase. In the behavioral tests, both the escape latency time in the spatial reference test and the time taken to cross the platform area in the spatial probe test improved partially.

Conclusion: The results suggest that nattokinase has potential therapeutic applications in the treatment of AD.

纳豆激酶对 D-半乳糖和氯化铝诱导的阿尔茨海默病大鼠模型的影响
背景/目的:阿尔茨海默病(AD)是全球最常见的痴呆症。纳豆激酶是一种丝氨酸蛋白酶,由纳豆(一种枯草芽孢杆菌的发酵产物)在细胞外产生。本研究探讨了纳豆激酶对铝和D-半乳糖诱导的AD大鼠模型的治疗效果:将 40 只 Wistar 大鼠随机分为四组:正常组、给药组和口服纳豆激酶组(NK65 和 NK130 组)。除正常组外,其他各组均接受氯化铝和 D-半乳糖治疗 10 周。NK65组和NK130组还分别接受了65毫克/千克/天和130毫克/千克/天的纳豆激酶治疗。我们分析了脑脊液(CSF)中的β淀粉样蛋白水平,并使用莫里斯水迷宫测试评估了空间参照测试。在莫里斯水迷宫试验后,对所有组的大鼠进行显微计算机断层扫描(μCT),以评估大脑构造的变化。所有脑组织中的铝浓度和β-淀粉样蛋白水平均通过组织化学染色法进行分析:结果:在AD大鼠模型中口服纳豆激酶可增加脑脊液中游离态β淀粉样蛋白的水平,并改善铝和淀粉样斑块在大脑中的积聚。脑μCT图像显示,纳豆激酶治疗后脑容量增加,结构变化减少。在行为测试中,空间参照测试中的逃逸潜伏时间和空间探针测试中穿过平台区所需的时间都得到了部分改善:结果表明,纳豆激酶具有治疗AD的潜在应用价值。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
In vivo
In vivo 医学-医学:研究与实验
CiteScore
4.20
自引率
4.30%
发文量
330
审稿时长
3-8 weeks
期刊介绍: IN VIVO is an international peer-reviewed journal designed to bring together original high quality works and reviews on experimental and clinical biomedical research within the frames of physiology, pathology and disease management. The topics of IN VIVO include: 1. Experimental development and application of new diagnostic and therapeutic procedures; 2. Pharmacological and toxicological evaluation of new drugs, drug combinations and drug delivery systems; 3. Clinical trials; 4. Development and characterization of models of biomedical research; 5. Cancer diagnosis and treatment; 6. Immunotherapy and vaccines; 7. Radiotherapy, Imaging; 8. Tissue engineering, Regenerative medicine; 9. Carcinogenesis.
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