Zhang Zhen, Che Xinyue, Feng Tingyu, Zou Juntao, Chen Guangpei, Guo Wenping, Ma Chunmei, Yuan Haozhe, Chen Jingying, Xu Xiaowu
College of Basic Medical Sciences, Guangzhou University of Chinese Medicine, Guangzhou, China.
New York College of Traditional Chinese Medicine, New York, USA.
Brain Res Bull. 2025 Jun 15;226:111372. doi: 10.1016/j.brainresbull.2025.111372. Epub 2025 May 5.
Jujuboside A (JB-A) is the major component of Semen Ziziphi Spinosae (SZS), a traditional Chinese herbal medicine used to treat sleep with clinical efficacy. This is the first study to investigate the effects of JB-A on mitochondrial structure and function in the prefrontal cortex of the insomnia model mice.
Young adult C57BL/6 mice were induced to develop insomnia by P-chlorophenylalanine. After 14 d of JB-A treatment via gavage, anxiety level was assessed using the open field and elevated plus maze tests. Next, the mitochondrial metabolic activity and morphological changes in the prefrontal cortex of each group of mice, as well as their effects on mitochondrial membrane potential, oxidative phosphorylation levels, and cytochrome c (Cyt c) content in neurons were measured.
In our mouse model, JB-A ameliorated anxiety-like behaviors; up-regulated the membrane potential (Δψm) and had a therapeutic effect on the metabolic activity and damaged microscopic structure of mitochondria in the prefrontal cortex; effectively improved mitochondrial function by increasing the expression of Cyt c oxidase I and IV proteins, ATPase activity, and ATP content; and reduced the accumulation of Cyt c in the neuronal cytoplasm while inhibiting mitochondrial permeability transition pore (mPTP) opening.
JB-A can improve insomnia by restoring mitochondrial intracellular oxidative phosphorylation, regulating mPTP to maintain mitochondrial homeostasis, and alleviating structural damage, providing a scientific basis for finding new targets for insomnia treatment.
酸枣仁皂苷A(JB-A)是中药酸枣仁的主要成分,酸枣仁是一种用于治疗失眠且具有临床疗效的传统草药。本研究首次探讨JB-A对失眠模型小鼠前额叶皮质线粒体结构和功能的影响。
用对氯苯丙氨酸诱导年轻成年C57BL/6小鼠发生失眠。经口灌胃给予JB-A治疗14天后,通过旷场试验和高架十字迷宫试验评估焦虑水平。接下来,测定每组小鼠前额叶皮质的线粒体代谢活性和形态变化,以及它们对神经元线粒体膜电位、氧化磷酸化水平和细胞色素c(Cyt c)含量的影响。
在我们的小鼠模型中,JB-A改善了焦虑样行为;上调了膜电位(Δψm),并对前额叶皮质线粒体的代谢活性和受损微观结构具有治疗作用;通过增加细胞色素c氧化酶I和IV蛋白的表达、ATP酶活性和ATP含量有效改善了线粒体功能;减少了神经元细胞质中Cyt c的积累,同时抑制了线粒体通透性转换孔(mPTP)的开放。
JB-A可通过恢复线粒体细胞内氧化磷酸化、调节mPTP以维持线粒体稳态以及减轻结构损伤来改善失眠,为寻找失眠治疗的新靶点提供了科学依据。