Dexmedetomidine to Help Nerve Regeneration in a Rat Sciatic Nerve Injury Model

Author:

Jeong Wook1,Kung Hsichiang2,Cheng Chia Chi2,Lim Changwoo2,Jung Min Jung3,Lee Jaeho4,Kim Doo Sik2,Shin Yusom2ORCID

Affiliation:

1. Department of Anesthesiology and Pain Medicine, Suryeoan Clinic, Busan, Republic of Korea

2. Department of Anesthesiology and Pain Medicine, Kosin University College of Medicine, Busan, Republic of Korea

3. Department of Pathology, Kosin University College of Medicine, Busan, Republic of Korea

4. Department of Anesthesiology and Pain Medicine, Ulsan University College of Medicine, Ulsan, Republic of Korea

Abstract

Background. Several studies have shown that dexmedetomidine (DXM), a selective α2-adrenoceptor agonist, also has neuroprotective effects. However, its effect on impaired peripheral nerve regeneration has not been studied. Materials and Methods. Forty-five Sprague-Dawley rats were randomly assigned to three groups: group 1 (control SHAM), group 2 (sciatic nerve injury + normal saline), and group 3 (sciatic nerve injury + DXM). The rats of group 3 were subdivided into the following three groups: DXM 0.5, 6, and 20 μg·kg−1 (groups 3A, 3B, and 3C, resp.). The sciatic nerve injury was assessed for nerve regeneration at 2 and 6 weeks. Results. There were no differences between groups 2 and 3 in their sciatic functional index (SFI) values or histological findings at 2 weeks postinjury. However, SFI differences were statistically significant at 6 weeks postinjury in group 3. The gross findings with H&E staining showed that the number of axons was higher in group 3 than in group 2. There was no histological difference according to the DXM concentration. Conclusion. The coincidental functional and histological assessment results of this study suggest that DXM for 6 weeks positively affects damaged peripheral nerves.

Publisher

Hindawi Limited

Subject

Anesthesiology and Pain Medicine,Neurology

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