Zhang Yaoyuan, Qu Zhenzhen, Mao Zhuofeng, Liu Hu, Wang Weiping, Jia Lijing
Key Laboratory of Neurology of Hebei Province, The Second Hospital of Hebei Medical University, Shijiazhuang, Hebei 050000, P.R. China.
Mol Med Rep. 2025 Mar;31(3). doi: 10.3892/mmr.2025.13429. Epub 2025 Jan 3.
Among patients with chronic epilepsy, 70‑80% have cognitive impairment. To investigate the relationship between adiponectin (ADPN) and the cognitive level in epilepsy and its mechanism, 20 epileptic patients and 20 healthy controls were included for the assessment of the cognitive level. An ELISA was used to evaluate the serum ADPN level. An epileptic rat model was established and treated with AdipoRon, an ADPN receptor (AdipoR) agonist, which binds to AdipoR1 and AdipoR2. The Morris water maze test was used to assess the cognitive function of rats, and the expression levels of the synapsis‑associated proteins postsynaptic density protein 95 (PSD95), synaptosomal associated protein 25 (SNAP25) and synaptophysin (SYP), as well as AMP‑activated protein kinase (AMPK), mTOR, phosphorylated (p‑)AMPK and p‑mTOR were determined by immunoblotting. Serum ADPN levels were positively correlated with the Montreal cognitive assessment score. AdipoRon improved the cognitive function of epileptic rats, maintained the structural integrity of hippocampal neurons and reduced neuronal damage. It also promoted the mRNA expression of AdipoR1 and AdipoR2 in the hippocampus. Furthermore, AdipoRon increased the expression of the synapsis‑associated proteins PSD95, SNAP25 and SYP by activating the AMPK/mTOR signaling pathway. ADPN improved cognitive impairment in epilepsy by targeting the AMPK/mTOR signaling pathway, providing novel insights for the treatment of epilepsy.
在慢性癫痫患者中,70%-80%存在认知障碍。为研究脂联素(ADPN)与癫痫认知水平之间的关系及其机制,纳入20例癫痫患者和20例健康对照者进行认知水平评估。采用酶联免疫吸附测定法(ELISA)评估血清ADPN水平。建立癫痫大鼠模型并用脂联素受体(AdipoR)激动剂AdipoRon进行治疗,AdipoRon可与AdipoR1和AdipoR2结合。采用Morris水迷宫试验评估大鼠的认知功能,通过免疫印迹法检测突触相关蛋白突触后致密蛋白95(PSD95)、突触体相关蛋白25(SNAP25)和突触素(SYP)以及AMP活化蛋白激酶(AMPK)、mTOR、磷酸化(p-)AMPK和p-mTOR的表达水平。血清ADPN水平与蒙特利尔认知评估评分呈正相关。AdipoRon改善了癫痫大鼠的认知功能,维持了海马神经元的结构完整性并减少了神经元损伤。它还促进了海马中AdipoR1和AdipoR2的mRNA表达。此外,AdipoRon通过激活AMPK/mTOR信号通路增加了突触相关蛋白PSD95、SNAP25和SYP的表达。ADPN通过靶向AMPK/mTOR信号通路改善癫痫中的认知障碍,为癫痫治疗提供了新的见解。