Kumar Sonu, Kumar Hansraj, Mudgal Shiv K, Kumar Subodh, Singh Harminder
Pharmacology and Therapeutics, Phulo Jhano Medical College and Hospital, Dumka, IND.
Pharmacology and Therapeutics, All India Institute of Medical Sciences, Deoghar, IND.
Cureus. 2025 Jul 2;17(7):e87148. doi: 10.7759/cureus.87148. eCollection 2025 Jul.
Cognitive impairment, including drug-induced amnesia, poses significant challenges in neurological research and therapy. Current treatments like donepezil provide limited benefits by targeting only cholinergic dysfunction. This study aimed to compare the cognitive-enhancing effects of the combination of liraglutide and R-alpha lipoic acid (R-ALA) with donepezil in a rat model of diazepam-induced amnesia.
Twenty adult Albino rats were randomized into four groups (n = 5 each): negative control, positive control (diazepam + saline), test (diazepam + liraglutide + R-ALA), and standard comparator (diazepam + donepezil). Diazepam (0.1 mg/kg, i.p.) induced amnesia, followed by treatments administered one hour before Morris Water Maze (MWM) trials. Escape latency times were recorded weekly at zero, one, two, three, and four hours post-treatment over five weeks. Data were analyzed by one-way ANOVA with Tukey's HSD post hoc test (p < 0.05).
The liraglutide-R-ALA group showed a significant and progressive reduction in escape latency compared to the positive control across all weeks and time points, with mean differences at the four-hour mark, ranging from 39.3 to 48.5 seconds (p < 0.001). Compared to donepezil, this combination showed statistically significant superiority at the third and fourth hours in weeks 1-5 (p-values ranging from 0.001 to 0.0001), with mean latency reductions of up to 20.65 seconds at four hours in week 5. Donepezil produced moderate improvements with higher variability and less consistent significance.
The liraglutide-R-ALA combination provides superior cognitive enhancement over donepezil in diazepam-induced amnesia by targeting multiple pathogenic mechanisms, highlighting the potential of multimodal therapies for cognitive impairment.
认知障碍,包括药物性失忆,给神经学研究和治疗带来了重大挑战。目前的治疗方法,如多奈哌齐,仅针对胆碱能功能障碍,益处有限。本研究旨在比较利拉鲁肽和R-α硫辛酸(R-ALA)联合用药与多奈哌齐在大鼠地西泮诱导失忆模型中的认知增强作用。
将20只成年白化大鼠随机分为四组(每组n = 5):阴性对照组、阳性对照组(地西泮+生理盐水)、试验组(地西泮+利拉鲁肽+R-ALA)和标准对照比较组(地西泮+多奈哌齐)。地西泮(0.1 mg/kg,腹腔注射)诱导失忆,随后在莫里斯水迷宫(MWM)试验前1小时进行治疗。在五周的时间里,每周在治疗后0、1、2、3和4小时记录逃避潜伏期。数据采用单因素方差分析和Tukey's HSD事后检验进行分析(p < 0.05)。
与阳性对照组相比,利拉鲁肽-R-ALA组在所有周和时间点的逃避潜伏期均显著且逐渐降低,在4小时标记处的平均差异为39.3至48.5秒(p < 0.001)。与多奈哌齐相比,该联合用药在第1 - 5周的第3和第4小时显示出统计学上的显著优势(p值范围为0.001至0.0001),在第5周的4小时平均潜伏期减少高达20.65秒。多奈哌齐产生了适度改善,但变异性较高且显著性不太一致。
在大鼠地西泮诱导失忆模型中,利拉鲁肽-R-ALA联合用药通过针对多种致病机制,在认知增强方面优于多奈哌齐,突出了多模式疗法对认知障碍的潜力。