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

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 t...

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Main Authors: Wook Jeong, Hsichiang Kung, Chia Chi Cheng, Changwoo Lim, Min Jung Jung, Jaeho Lee, Doo Sik Kim, Yusom Shin
Format: Article
Language:English
Published: Wiley 2017-01-01
Series:Pain Research and Management
Online Access:http://dx.doi.org/10.1155/2017/9045608
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author Wook Jeong
Hsichiang Kung
Chia Chi Cheng
Changwoo Lim
Min Jung Jung
Jaeho Lee
Doo Sik Kim
Yusom Shin
author_facet Wook Jeong
Hsichiang Kung
Chia Chi Cheng
Changwoo Lim
Min Jung Jung
Jaeho Lee
Doo Sik Kim
Yusom Shin
author_sort Wook Jeong
collection DOAJ
description 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.
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spelling doaj-art-ef9248389f8c42d6851a3972576484192025-02-03T01:22:08ZengWileyPain Research and Management1203-67651918-15232017-01-01201710.1155/2017/90456089045608Dexmedetomidine to Help Nerve Regeneration in a Rat Sciatic Nerve Injury ModelWook Jeong0Hsichiang Kung1Chia Chi Cheng2Changwoo Lim3Min Jung Jung4Jaeho Lee5Doo Sik Kim6Yusom Shin7Department of Anesthesiology and Pain Medicine, Suryeoan Clinic, Busan, Republic of KoreaDepartment of Anesthesiology and Pain Medicine, Kosin University College of Medicine, Busan, Republic of KoreaDepartment of Anesthesiology and Pain Medicine, Kosin University College of Medicine, Busan, Republic of KoreaDepartment of Anesthesiology and Pain Medicine, Kosin University College of Medicine, Busan, Republic of KoreaDepartment of Pathology, Kosin University College of Medicine, Busan, Republic of KoreaDepartment of Anesthesiology and Pain Medicine, Ulsan University College of Medicine, Ulsan, Republic of KoreaDepartment of Anesthesiology and Pain Medicine, Kosin University College of Medicine, Busan, Republic of KoreaDepartment of Anesthesiology and Pain Medicine, Kosin University College of Medicine, Busan, Republic of KoreaBackground. 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.http://dx.doi.org/10.1155/2017/9045608
spellingShingle Wook Jeong
Hsichiang Kung
Chia Chi Cheng
Changwoo Lim
Min Jung Jung
Jaeho Lee
Doo Sik Kim
Yusom Shin
Dexmedetomidine to Help Nerve Regeneration in a Rat Sciatic Nerve Injury Model
Pain Research and Management
title Dexmedetomidine to Help Nerve Regeneration in a Rat Sciatic Nerve Injury Model
title_full Dexmedetomidine to Help Nerve Regeneration in a Rat Sciatic Nerve Injury Model
title_fullStr Dexmedetomidine to Help Nerve Regeneration in a Rat Sciatic Nerve Injury Model
title_full_unstemmed Dexmedetomidine to Help Nerve Regeneration in a Rat Sciatic Nerve Injury Model
title_short Dexmedetomidine to Help Nerve Regeneration in a Rat Sciatic Nerve Injury Model
title_sort dexmedetomidine to help nerve regeneration in a rat sciatic nerve injury model
url http://dx.doi.org/10.1155/2017/9045608
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