Yue Sun , Dezheng Zhou , Yue Wang , Zehao Wang , Dalong Zhang , Zhiyong Qian , Jing Yan , Zhenshu Li , Guowei Huang , Wen Li
{"title":"中链甘油三酯结合 DHA 可抑制 SAMP8 小鼠大脑神经细胞的凋亡,从而改善认知功能。","authors":"Yue Sun , Dezheng Zhou , Yue Wang , Zehao Wang , Dalong Zhang , Zhiyong Qian , Jing Yan , Zhenshu Li , Guowei Huang , Wen Li","doi":"10.1016/j.exger.2024.112520","DOIUrl":null,"url":null,"abstract":"<div><p>Medium-chain triglycerides (MCTs) and docosahexaenoic acid (DHA, C<sub>n-3, 22:6</sub>) are essential in improving cognitive function and protecting neurocytes. This study explored the effects of the combined intervention of MCTs and DHA on inhibiting neurocyte apoptosis of the brain and improving cognitive function in senescence-accelerated mouse-prone 8 (SAMP8). Four-month-old male SAMP8 mice were randomly divided into four treatment groups (12 mice/group): DHA, MCT, DHA + MCT, and control groups, which intervened for seven months. Twelve age-matched male senescence-accelerated mouse resistant 1 (SAMR1) was used as the natural aging group. TUNEL assay and HE staining were used to assess neurocyte apoptosis and damage in the brain of mice. Moreover, the cognitive function was analyzed using the Morris water maze (MWM) and open field (OF) tests. The results showed that the cognitive function of 11-month-old SAMP8 mice decreased with age, and further pathological examination revealed the damaged neurocyte structure, karyopyknosis, cell atrophy, and even apoptosis. MCTs combined with DHA supplementation could increase octanoic acid (C8:0), decanoic acid (C10:0), and DHA levels in the serum, inhibit neurocyte apoptosis, improve neurocyte damage, moreover delay age-related cognitive decline after seven-month treatment. Furthermore, combining MCTs and DHA was significantly more beneficial than MCTs or DHA alone. In conclusion, MCTs combined with DHA could delay cognitive decline by inhibiting neurocyte apoptosis of the brain in SAMP8 mice.</p></div>","PeriodicalId":94003,"journal":{"name":"Experimental gerontology","volume":null,"pages":null},"PeriodicalIF":3.9000,"publicationDate":"2024-07-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S0531556524001621/pdfft?md5=18571e31f1b1ce5323941d1dede7cde5&pid=1-s2.0-S0531556524001621-main.pdf","citationCount":"0","resultStr":"{\"title\":\"Medium-chain triglycerides combined with DHA improve cognitive function by inhibiting neurocyte apoptosis of the brain in SAMP8 mice\",\"authors\":\"Yue Sun , Dezheng Zhou , Yue Wang , Zehao Wang , Dalong Zhang , Zhiyong Qian , Jing Yan , Zhenshu Li , Guowei Huang , Wen Li\",\"doi\":\"10.1016/j.exger.2024.112520\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Medium-chain triglycerides (MCTs) and docosahexaenoic acid (DHA, C<sub>n-3, 22:6</sub>) are essential in improving cognitive function and protecting neurocytes. This study explored the effects of the combined intervention of MCTs and DHA on inhibiting neurocyte apoptosis of the brain and improving cognitive function in senescence-accelerated mouse-prone 8 (SAMP8). Four-month-old male SAMP8 mice were randomly divided into four treatment groups (12 mice/group): DHA, MCT, DHA + MCT, and control groups, which intervened for seven months. Twelve age-matched male senescence-accelerated mouse resistant 1 (SAMR1) was used as the natural aging group. TUNEL assay and HE staining were used to assess neurocyte apoptosis and damage in the brain of mice. Moreover, the cognitive function was analyzed using the Morris water maze (MWM) and open field (OF) tests. The results showed that the cognitive function of 11-month-old SAMP8 mice decreased with age, and further pathological examination revealed the damaged neurocyte structure, karyopyknosis, cell atrophy, and even apoptosis. MCTs combined with DHA supplementation could increase octanoic acid (C8:0), decanoic acid (C10:0), and DHA levels in the serum, inhibit neurocyte apoptosis, improve neurocyte damage, moreover delay age-related cognitive decline after seven-month treatment. Furthermore, combining MCTs and DHA was significantly more beneficial than MCTs or DHA alone. 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引用次数: 0
摘要
中链甘油三酯(MCTs)和二十二碳六烯酸(DHA,Cn-3,22:6)对改善认知功能和保护神经细胞至关重要。本研究探讨了 MCTs 和 DHA 联合干预对抑制大脑神经细胞凋亡和改善衰老加速小鼠易感基因 8(SAMP8)认知功能的影响。将四个月大的雄性 SAMP8 小鼠随机分为四个治疗组(每组 12 只):DHA组、MCT组、DHA + MCT组和对照组,干预7个月。12只年龄匹配的雄性抗衰老加速小鼠1(SAMR1)作为自然衰老组。采用 TUNEL 法和 HE 染色法评估小鼠大脑中神经细胞的凋亡和损伤。此外,还使用莫里斯水迷宫(MWM)和开阔地(OF)测试分析了小鼠的认知功能。结果显示,11 个月大的 SAMP8 小鼠的认知功能随着年龄的增长而下降,进一步的病理检查显示神经细胞结构受损、核分裂、细胞萎缩甚至凋亡。补充 MCTs 和 DHA 可以增加血清中辛酸(C8:0)、癸酸(C10:0)和 DHA 的含量,抑制神经细胞凋亡,改善神经细胞损伤,而且在治疗 7 个月后,还能延缓与年龄相关的认知能力下降。此外,结合使用 MCTs 和 DHA 比单独使用 MCTs 或 DHA 更有益。总之,MCTs 与 DHA 的结合可以通过抑制 SAMP8 小鼠大脑神经细胞的凋亡来延缓认知能力的衰退。
Medium-chain triglycerides combined with DHA improve cognitive function by inhibiting neurocyte apoptosis of the brain in SAMP8 mice
Medium-chain triglycerides (MCTs) and docosahexaenoic acid (DHA, Cn-3, 22:6) are essential in improving cognitive function and protecting neurocytes. This study explored the effects of the combined intervention of MCTs and DHA on inhibiting neurocyte apoptosis of the brain and improving cognitive function in senescence-accelerated mouse-prone 8 (SAMP8). Four-month-old male SAMP8 mice were randomly divided into four treatment groups (12 mice/group): DHA, MCT, DHA + MCT, and control groups, which intervened for seven months. Twelve age-matched male senescence-accelerated mouse resistant 1 (SAMR1) was used as the natural aging group. TUNEL assay and HE staining were used to assess neurocyte apoptosis and damage in the brain of mice. Moreover, the cognitive function was analyzed using the Morris water maze (MWM) and open field (OF) tests. The results showed that the cognitive function of 11-month-old SAMP8 mice decreased with age, and further pathological examination revealed the damaged neurocyte structure, karyopyknosis, cell atrophy, and even apoptosis. MCTs combined with DHA supplementation could increase octanoic acid (C8:0), decanoic acid (C10:0), and DHA levels in the serum, inhibit neurocyte apoptosis, improve neurocyte damage, moreover delay age-related cognitive decline after seven-month treatment. Furthermore, combining MCTs and DHA was significantly more beneficial than MCTs or DHA alone. In conclusion, MCTs combined with DHA could delay cognitive decline by inhibiting neurocyte apoptosis of the brain in SAMP8 mice.