The Effect of Super-Repressor IkB-Loaded Exosomes (Exo-srIκBs) in Chronic Post-Ischemia Pain (CPIP) Models

被引:7
作者
Chae, Ji Seon [1 ]
Park, Hyunju [2 ]
Ahn, So-Hee [3 ]
Han, Eun-Chong [3 ]
Lee, Yoonjin [2 ]
Kim, Youn Jin [1 ]
Ahn, Eun-Jin [4 ]
Oh, Hye-Won [1 ]
Lee, Hyun Jung [1 ]
Choi, Chulhee [3 ]
Choi, Youn-Hee [2 ]
Kim, Won-joong [1 ]
机构
[1] Ewha Womans Univ, Coll Med, Dept Anesthesiol & Pain Med, Seoul 07804, South Korea
[2] Ewha Womans Univ, Coll Med, Inflammat Canc Microenvironm Res Ctr, Dept Physiol, Seoul 07804, South Korea
[3] ILIAS Biol Inc, ILIAS Innovat Ctr, Daejeon 34014, South Korea
[4] Chung Ang Univ, Coll Med, Dept Anesthesiol & Pain Med, Seoul 06974, South Korea
基金
新加坡国家研究基金会;
关键词
exosomes; exosome loaded with super-repressor I kappa B; chronic post-ischemic pain model; complex regional pain syndrome (CRPS); allodynia; NF kappa B; inflammation; neuropathic pain; NEUROPATHIC PAIN; BIS(PHENYLIMIDAZOSELENAZOLYL) DISELENIDE; TRANSCRIPTION FACTOR; T-LYMPHOCYTES; ANIMAL-MODEL; SPINAL-CORD; RAT MODEL; MODULATION; CONTRIBUTES; ACTIVATION;
D O I
10.3390/pharmaceutics15020553
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Complex regional pain syndrome (CRPS) is a condition associated with neuropathic pain that causes significant impairment of daily activities and functioning. Nuclear factor kappa B (NF kappa B) is thought to play an important role in the mechanism of CRPS. Recently, exosomes loaded with super-repressor inhibitory kappa B (Exo-srI kappa B, I kappa B; inhibitor of NF kappa B) have been shown to have potential anti-inflammatory effects in various inflammatory disease models. We investigated the therapeutic effect of Exo-srI kappa B on a rodent model with chronic post-ischemia pain (CPIP), a representative animal model of Type I CRPS. After intraperitoneal injection of a vehicle, Exo-srI kappa B, and pregabalin, the paw withdrawal threshold (PWT) was evaluated up to 48 h. Administration of Exo-srI kappa B increased PWT compared to the vehicle and pregabalin, and the relative densities of p-I kappa B and I kappa B showed significant changes compared to the vehicle 24 h after Exo-srI kappa B injection. The levels of several cytokines and chemokines were reduced by the administration of Exo-srI kappa B in mice with CPIP. In conclusion, our results showed more specifically the role of NF kappa B in the pathogenesis of CRPS and provided a theoretical background for novel treatment options for CRPS.
引用
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页数:16
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