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Therapeutic Efficacy in Experimental Polyarthritis of Viral-Driven Enkephalin Overproduction in Sensory Neurons

机译:感官神经元中病毒驱动脑啡肽过量生产的实验性多关节炎的治疗功效

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摘要

Rheumatoid arthritis is characterized by erosive inflammation of the joints, new bone proliferation, and ankylosis, leading to severely reduced locomotion and intense chronic pain. In a model of this disease, adjuvant-induced polyarthritis in the rat, neurons involved in pain transmission and control undergo plastic changes, especially at the spinal level. These changes affect notably neurons that contain opioids, such as enkephalins deriving from preproenkephalin A (PA) precursor protein. Using recombinant herpes simplex virus containing rat PA cDNA, we enhanced enkephalin synthesis in sensory neurons of polyarthritic rats. This treatment markedly improved locomotion and reduced hyperalgesia. Furthermore, the progression of bone destruction slowed down, which is the most difficult target to reach in the treatment of patients suffering from arthritis. These data demonstrate the therapeutic efficacy of enkephalin overproduction in a model of systemic inflammatory and painful chronic disorder.
机译:类风湿关节炎的特征在于关节的糜烂性炎症,新的骨骼增生和强直性关节炎,从而导致运动能力大大降低和剧烈的慢性疼痛。在这种疾病的模型中,佐剂诱发的大鼠多关节炎,参与疼痛传递和控制的神经元发生塑性变化,尤其是在脊柱水平。这些变化尤其会影响包含阿片类药物的神经元,例如源自前脑啡肽原A(PA)前体蛋白的脑啡肽。使用包含大鼠PA cDNA的重组单纯疱疹病毒,我们增强了多关节炎大鼠感觉神经元中脑啡肽的合成。该治疗显着改善了运动并减少了痛觉过敏。此外,骨破坏的进程减慢了,这是治疗关节炎患者最困难的目标。这些数据证明了脑啡肽过量生产在系统性炎性和疼痛性慢性疾病模型中的治疗功效。

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