Specific necroptosis inhibitor-1(Nec-1) attenuates glial scar formation in rat models with spinal cord injury

Objective To observe the effect of necroptosis inhibitor-1(Nec-1) on glial scar formation in rats with spinal cord injury and its mechanism. Methods The rats were randomly divided into sham group, model group (falling method) and RIPK1 inhibitor Nec-1 group (10 μmol/L Nec-1 10μL was injected into la...

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Published in:Jichu yixue yu linchuang
Main Author: CHEN Sheng, WANG Chun-ming, YAN Xue-fei, MAO Yuan-qing
Format: Article
Language:Chinese
Published: Institute of Basic Medical Sciences and Peking Union Medical College Hospital, Chinese Academy of Medical Sciences / Peking Union Medical College. 2022-01-01
Subjects:
Online Access:http://journal11.magtechjournal.com/Jwk_jcyxylc/fileup/1001-6325/PDF/1001-6325-2022-42-1-94.pdf
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author CHEN Sheng, WANG Chun-ming, YAN Xue-fei, MAO Yuan-qing
author_facet CHEN Sheng, WANG Chun-ming, YAN Xue-fei, MAO Yuan-qing
author_sort CHEN Sheng, WANG Chun-ming, YAN Xue-fei, MAO Yuan-qing
collection DOAJ
container_title Jichu yixue yu linchuang
description Objective To observe the effect of necroptosis inhibitor-1(Nec-1) on glial scar formation in rats with spinal cord injury and its mechanism. Methods The rats were randomly divided into sham group, model group (falling method) and RIPK1 inhibitor Nec-1 group (10 μmol/L Nec-1 10μL was injected into lateral ventricle). BBB method was used to measure the motor function of hind limbs, immunofluorescence was used to detect the formation of glial scar, and Western blot was used to detect the expression of cathepsin B, caspase-3, GFAP and vimentin. Results On the 14th day after operation, compared with the sham group, the BBB scores of the model group and Nec-1 group were significantly lower (P<0.05), compared with the model group, the BBB score of Nec-1 group was significantly higher (P<0.05). NF-200 fluorescence was not found in the sham operation group, but in the model group and Nec-1 group, the intensity of NF-200 fluorescence labeling in Nec-1 group decreased significantly(P<0.05). On the 7th and 14th day after operation, compared with the sham operation group, the protein level of cathepsin B, caspase-3, GFAP and vimentin in the model group and Nec-1 group was significantly higher(P<0.05),while the protein level of cathepsin B, caspase-3, GFAP and vimentin in Nec-1 group decreased significantly (P<0.05). Conclusions Nec-1 may regulate expression level of cathepsin B and caspase-3, reduce the expression of GFAP and vimentin proteins, reduce the formation of glial scar after spinal cord injury and promote the recovery of neural function.
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spelling doaj-art-e8f2a67c5bb4470bb8bcbc7ace1ec6e62025-08-20T00:50:17ZzhoInstitute of Basic Medical Sciences and Peking Union Medical College Hospital, Chinese Academy of Medical Sciences / Peking Union Medical College.Jichu yixue yu linchuang1001-63252022-01-01421949910.16352/j.issn.1001-6325.2022.01.014Specific necroptosis inhibitor-1(Nec-1) attenuates glial scar formation in rat models with spinal cord injuryCHEN Sheng, WANG Chun-ming, YAN Xue-fei, MAO Yuan-qing0Department of Orthopaedics,the Affiliated Jiangsu Shengze Hospital of Nanjing Medical University/Shengze Clinical Medical School, Kangda College of Nanjing Medical University, Suzhou 215228, ChinaObjective To observe the effect of necroptosis inhibitor-1(Nec-1) on glial scar formation in rats with spinal cord injury and its mechanism. Methods The rats were randomly divided into sham group, model group (falling method) and RIPK1 inhibitor Nec-1 group (10 μmol/L Nec-1 10μL was injected into lateral ventricle). BBB method was used to measure the motor function of hind limbs, immunofluorescence was used to detect the formation of glial scar, and Western blot was used to detect the expression of cathepsin B, caspase-3, GFAP and vimentin. Results On the 14th day after operation, compared with the sham group, the BBB scores of the model group and Nec-1 group were significantly lower (P<0.05), compared with the model group, the BBB score of Nec-1 group was significantly higher (P<0.05). NF-200 fluorescence was not found in the sham operation group, but in the model group and Nec-1 group, the intensity of NF-200 fluorescence labeling in Nec-1 group decreased significantly(P<0.05). On the 7th and 14th day after operation, compared with the sham operation group, the protein level of cathepsin B, caspase-3, GFAP and vimentin in the model group and Nec-1 group was significantly higher(P<0.05),while the protein level of cathepsin B, caspase-3, GFAP and vimentin in Nec-1 group decreased significantly (P<0.05). Conclusions Nec-1 may regulate expression level of cathepsin B and caspase-3, reduce the expression of GFAP and vimentin proteins, reduce the formation of glial scar after spinal cord injury and promote the recovery of neural function.http://journal11.magtechjournal.com/Jwk_jcyxylc/fileup/1001-6325/PDF/1001-6325-2022-42-1-94.pdfspinal cord injury|glial scar|necroptosis inhibitor-1(nec-1)|cathepsin b
spellingShingle CHEN Sheng, WANG Chun-ming, YAN Xue-fei, MAO Yuan-qing
Specific necroptosis inhibitor-1(Nec-1) attenuates glial scar formation in rat models with spinal cord injury
spinal cord injury|glial scar|necroptosis inhibitor-1(nec-1)|cathepsin b
title Specific necroptosis inhibitor-1(Nec-1) attenuates glial scar formation in rat models with spinal cord injury
title_full Specific necroptosis inhibitor-1(Nec-1) attenuates glial scar formation in rat models with spinal cord injury
title_fullStr Specific necroptosis inhibitor-1(Nec-1) attenuates glial scar formation in rat models with spinal cord injury
title_full_unstemmed Specific necroptosis inhibitor-1(Nec-1) attenuates glial scar formation in rat models with spinal cord injury
title_short Specific necroptosis inhibitor-1(Nec-1) attenuates glial scar formation in rat models with spinal cord injury
title_sort specific necroptosis inhibitor 1 nec 1 attenuates glial scar formation in rat models with spinal cord injury
topic spinal cord injury|glial scar|necroptosis inhibitor-1(nec-1)|cathepsin b
url http://journal11.magtechjournal.com/Jwk_jcyxylc/fileup/1001-6325/PDF/1001-6325-2022-42-1-94.pdf
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