The effect of human mesenchymal stem cell injection on pain behavior in chronic post-ischemia pain mice

被引:12
作者
Yoo, Sie Hyeon [1 ]
Lee, Sung Hyun [2 ]
Lee, Seunghwan [3 ]
Park, Jae Hong [3 ]
Lee, Seunghyeon [4 ]
Jin, Heecheol [4 ]
Park, Hue Jung [3 ]
机构
[1] Soonchunhyang Univ, Cheonan Hosp, Coll Med, Dept Anesthesiol & Pain Med, Cheonan, South Korea
[2] Sungkyunkwan Univ, Kangbuk Samsung Hosp, Sch Med, Dept Anesthesiol & Pain Med, Seoul, South Korea
[3] Catholic Univ Korea, Seoul St Marys Hosp, Coll Med, Dept Anesthesiol & Pain Med, 222 Banpo Daero, Seoul 06591, South Korea
[4] Soonchunhyang Univ, Bucheon Hosp, Coll Med, Dept Anesthesiol & Pain Med, Bucheon, South Korea
关键词
Ganglia; Spinal; Glial Fibrillary Acidic Protein; Hyperalgesia; Mesenchymal Stromal Cells; Mice; Neuralgia; Reperfusion Injury; Spinal Cord; Stem Cells; MARROW STROMAL CELLS; REFLEX SYMPATHETIC DYSTROPHY; NEUROPATHIC PAIN; TRANSPLANTATION; THERAPY; MODEL; REGENERATION;
D O I
10.3344/kjp.2020.33.1.23
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: Neuropathic pain (NP) is considered a clinically incurable condition despite various treatment options due to its diverse causes and complicated disease mechanisms. Since the early 2000s, multipotent human mesenchymal stem cells (hMSCs) have been used in the treatment of NP in animal models. However, the effects of hMSC injections have not been studied in chronic post-ischemia pain (CPIP) mice models. Here, we investigated whether intrathecal (IT) and intrapaw (IP) injections of hMSCs can reduce mechanical allodynia in CPIP model mice. Methods: Seventeen CPIP C57/BL6 mice were selected and randomized into four groups: IT sham (n = 4), IT stem (n = 5), IP sham (n = 4), and IP stem (n = 4). Mice in the IT sham and IT stem groups received an injection of 5 mu L saline and 2 x 10(4) hMSCs, respectively, while mice in the IP sham and IP stem groups received an injection of 5 mu L saline and 2 x 10(5) hMSCs, respectively. Mechanical allodynia was assessed using von Frey filaments from pre-injection to 30 days post-injection. Glial fibrillary acidic protein (GFAP) expression in the spinal cord and dorsal root ganglia were also evaluated. Results: IT and IP injections of hMSCs improved mechanical allodynia. GFAP expression was decreased on day 25 post-injection compared with the sham group. Injections of hMSCs improved allodynia and GFAP expression was decreased compared with the sham group. Conclusions: These results suggested that hMSCs may be also another treatment modality in NP model by ischemia-reperfusion.
引用
收藏
页码:23 / 29
页数:7
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