Drug Applied Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.
Department of Biomedical Education, College of Osteopathic Medicine, California Health Sciences University, Clovis, CA, USA.
Neurochem Res. 2024 Nov;49(11):3030-3042. doi: 10.1007/s11064-024-04223-8. Epub 2024 Aug 3.
Depression and anxiety are prevalent neuropsychiatric conditions among patients with Parkinson's disease (PD), which may manifest prior to motor symptoms. As levodopa, a prominent treatment for PD motor symptoms, provides few benefits for mood-related abnormalities, tackling non-motor symptoms is particularly important. AdipoRon (Ad), an adiponectin agonist, has demonstrated neuroprotective effects by suppressing neuroinflammatory responses and activating the AMPK/Sirt-1 signaling pathway. This study looked at the potential advantages and underlying mechanisms of intranasal Ad in a rat model of PD induced by 6-hydroxydopamine (6-OHDA). We found that Ad at doses of 1 and 10 µg for 21 days exhibited anxiolytic- and antidepressant effects in the open field (OF) test, elevated plus maze (EPM), sucrose splash test, and forced swimming test in a PD model caused by a unilateral 6-OHDA injection into the medial forebrain bundle (MFB). The Ad also lowered the levels of corticosterone in the blood, decreased inflammasome components (NLRP3, caspase 1, and IL-1β), and increased Sirt-1 protein levels in the prefrontal cortex (PFC) of PD rats. We conclude that Ad ameliorates anxious and depressive-like behaviors in the PD rat model through stimulating the AMPK/Sirt-1 signaling and blocking the NLRP3 inflammasome pathways in the PFC.
抑郁和焦虑是帕金森病(PD)患者常见的神经精神疾病,这些症状可能在运动症状出现之前就已经出现。由于左旋多巴是治疗 PD 运动症状的主要药物,但对与情绪相关的异常几乎没有益处,因此解决非运动症状尤为重要。AdipoRon(Ad)是一种脂联素激动剂,通过抑制神经炎症反应和激活 AMPK/Sirt-1 信号通路,显示出神经保护作用。本研究探讨了经鼻给予 Ad 在单侧内侧前脑束(MFB)注射 6-羟多巴胺(6-OHDA)诱导的 PD 大鼠模型中的潜在优势和潜在机制。我们发现,Ad 在 21 天内以 1 和 10μg 的剂量给药,在 PD 模型的旷场(OF)测试、高架十字迷宫(EPM)、蔗糖溅出测试和强迫游泳测试中表现出抗焦虑和抗抑郁作用。Ad 还降低了血液中皮质酮的水平,减少了炎症小体成分(NLRP3、caspase 1 和 IL-1β),并增加了 PD 大鼠前额叶皮层(PFC)中的 Sirt-1 蛋白水平。我们得出结论,Ad 通过刺激 AMPK/Sirt-1 信号通路并阻断 PFC 中的 NLRP3 炎症小体途径,改善了 PD 大鼠模型中的焦虑和抑郁样行为。