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鼻内注射 AdipoRon 减轻了 6-OHDA 诱导的帕金森病大鼠模型的焦虑和抑郁样行为:超越运动症状。

Intranasal AdipoRon Mitigated Anxiety and Depression-Like Behaviors in 6-OHDA-Induced Parkinson 's Disease Rat Model: Going Beyond Motor Symptoms.

机构信息

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.

出版信息

Neurochem Res. 2024 Nov;49(11):3030-3042. doi: 10.1007/s11064-024-04223-8. Epub 2024 Aug 3.

Abstract

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.

摘要

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。

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