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

被引:5
作者
Azizifar, Negin [1 ]
Mohaddes, Gisou [2 ]
Keyhanmanesh, Rana [1 ]
Athari, Seyed Zanyar [1 ]
Alimohammadi, Soraya [1 ]
Farajdokht, Fereshteh [3 ]
机构
[1] Tabriz Univ Med Sci, Drug Appl Res Ctr, Tabriz, Iran
[2] Calif Hlth Sci Univ, Coll Osteopath Med, Dept Biomed Educ, Clovis, CA USA
[3] Tabriz Univ Med Sci, Neurosci Res Ctr, Tabriz, Iran
关键词
Anxiety and depression; Parkinson's disease; 6-OHDA; AdipoRon; Sirt1; Inflammasome; MICROGLIAL ACTIVATION; NLRP3; INFLAMMASOME; OXIDATIVE STRESS; SIRT1; NEUROINFLAMMATION; ADIPONECTIN; NEUROGENESIS; PATHOGENESIS; INVOLVEMENT; DYSFUNCTION;
D O I
10.1007/s11064-024-04223-8
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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 mu g 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-1 beta), 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.
引用
收藏
页码:3030 / 3042
页数:13
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