Anti-inflammatory and Anti-nociceptive Actions of Systemically or Locally Treated Adipose-Derived Mesenchymal Stem Cells in Experimental Inflammatory Model

被引:24
作者
Mert, Tufan [1 ]
Kurt, Akif H. [2 ]
Arslan, Mahmut [3 ]
Celik, Ahmet [4 ]
Tugtag, Berin [5 ]
Akkurt, Aysenur [6 ]
机构
[1] Kahramanmaras Sutcu Imam Univ, Dept Biophys, Sch Med, TR-46050 Kahramanmaras, Turkey
[2] Kahramanmaras Sutcu Imam Univ, Depertment Pharmacol, Sch Med, TR-46050 Kahramanmaras, Turkey
[3] Kahramanmaras Sutcu Imam Univ, Anaesthesiol & Reanimat, Sch Med, TR-46050 Kahramanmaras, Turkey
[4] Kahramanmaras Sutcu Imam Univ, Biochem, Sch Med, TR-46050 Kahramanmaras, Turkey
[5] Fatih Univ, Sch Med, Dept Anat, TR-34500 Istanbul, Turkey
[6] Kahramanmaras Sutcu Imam Univ, Sch Med, TR-46050 Kahramanmaras, Turkey
关键词
adipose-derived mesenchymal stem cells; inflammation; hyperalgesia; allodynia; cytokines; rats; NITRIC-OXIDE; RAT; MECHANISMS; CYTOKINES; PAIN; HYPERALGESIA; CHEMOKINES; MEDIATORS; PAW;
D O I
10.1007/s10753-014-0101-1
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Cell-based therapies using mesenchymal stem cells provide hopeful results. Therefore, in this present study, possible anti-inflammatory and anti-nociceptive actions of locally or systemically treated adipose-derived mesenchymal stem cells (ADMSCs) investigated in experimental inflammation model. ADMSCs were isolated from a male Wistar rat under anesthesia, and then they were cultured and expanded for transplantation in all the experimental animals. Effects of intraperitoneal or intraplantar ADMSC treatments on the hallmarks of the inflammatory nociception, such as hyperalgesia, allodynia, edema, and several biochemical parameters were investigated using a well-established carrageenan (CG)-induced hindpaw inflammation model in male rats. Both local and systemic ADMSC treatment increased the latencies, thresholds, and the development of edema in a time-dependent manner. In addition, administration of ADMSC suppressed the increased level of interleukin (IL)-1 beta, IL-6, and nitric oxide (NO), but further enhanced that of IL-10. Locally treated ADMSC at inflammatory sites effectively suppressed the CG-induced inflammatory responses when compared to the intraperitoneal route of administration. Findings suggest that therapeutic potential of ADMSC can change depending on its route of administration. Local ADMSC treatments may suppress the development of inflammatory-nociception and edema by decreasing the production of pro-inflammatory cytokines and NO level and increasing the anti-inflammatory cytokine production at inflammatory sites.
引用
收藏
页码:1302 / 1310
页数:9
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