Berliocchi Laura, Maiarù Maria, Varano Giuseppe Pasquale, Russo Rossella, Corasaniti Maria Tiziana, Bagetta Giacinto, Tassorelli Cristina
Department of Health Sciences, University "Magna Græcia" of Catanzaro, 88100, Catanzaro, Italy.
Centre of Neuropharmacology of Normal and Pathological Synaptic Plasticity, University Consortium for Adaptive Disorders and Head Pain, 87036, Rende, Cosenza, Italy.
Mol Pain. 2015 Feb 2;11:3. doi: 10.1186/1744-8069-11-3.
Autophagy is a homeostatic degradative process essential for basal turnover of long-lived proteins and organelles as well as for removal of dysfunctional cellular components. Dysregulation of the autophagic machinery has been recently associated to several conditions including neurodegenerative diseases and cancer, but only very few studies have investigated its role in pain processing.
We previously described autophagy impairment at the spinal cord in the experimental model of neuropathic pain induced by spinal nerve ligation (SNL). In this study, we characterized the main autophagic markers in two other common experimental models of neuropathic pain, the chronic constriction injury (CCI) and the spared nerve injury (SNI). The different modulation of LC3-I, Beclin 1 and p62 suggested that autophagy is differentially affected in the spinal dorsal horn depending on the type of peripheral injury. Confocal analysis of p62 distribution in the spinal dorsal horn indicated its presence mainly in NeuN-positive cell bodies and occasionally in glial processes, thus suggesting a predominant expression in the neuronal compartment. Finally, we investigated the consequences of autophagy impairment on pain behaviour by using the autophagy blocker cloroquine. Intrathecal chloroquine injection in naïve mice induced spinal accumulation of LC3 and p62 paralleled by significant mechanical hypersensitivity thus confirming the block in autophagosome clearance and suggesting the participation of the autophagic process in spinal mechanisms of pain processing. Altogether, our data indicate that spinal autophagy is differentially altered in different experimental pain models of neuropathic pain and that this process may be relevant for pain control.
自噬是一种稳态降解过程,对于长寿蛋白和细胞器的基础更新以及清除功能失调的细胞成分至关重要。自噬机制的失调最近与包括神经退行性疾病和癌症在内的多种疾病相关,但只有极少数研究调查了其在疼痛处理中的作用。
我们之前在脊髓神经结扎(SNL)诱导的神经性疼痛实验模型中描述了脊髓中的自噬损伤。在本研究中,我们在另外两种常见的神经性疼痛实验模型,即慢性压迫损伤(CCI)和保留神经损伤(SNI)中,对主要的自噬标志物进行了表征。LC3-I、Beclin 1和p62的不同调节表明,根据外周损伤的类型,脊髓背角中的自噬受到不同影响。对脊髓背角中p62分布的共聚焦分析表明,它主要存在于NeuN阳性细胞体中,偶尔也存在于神经胶质细胞突起中,因此表明其在神经元区室中占主导性表达。最后,我们通过使用自噬阻断剂氯喹来研究自噬损伤对疼痛行为的影响。在未处理的小鼠中鞘内注射氯喹会诱导脊髓中LC3和p62的积累,同时伴有明显的机械性超敏反应,从而证实了自噬体清除的阻断,并表明自噬过程参与了脊髓疼痛处理机制。总之,我们的数据表明,在不同的神经性疼痛实验模型中,脊髓自噬会发生不同程度的改变,并且这一过程可能与疼痛控制有关。