Skin/muscle incision and retraction regulates the persistent postoperative pain in rats by the Epac1/PKC-βII pathway

Abstract Persistent postoperative pain causes influence the life quality of many patients. The Epac/PKC pathway has been indicated to regulate mechanical hyperalgesia. The present study used skin/muscle incision and retraction (SMIR) to induce postoperative pain in rats and evaluated the Epac/PKC pa...

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Main Authors: Jiashu Qian, Xuezheng Lin, Zhili Zhou
Format: Article
Language:English
Published: BMC 2022-07-01
Series:BMC Anesthesiology
Subjects:
Online Access:https://doi.org/10.1186/s12871-022-01771-w
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author Jiashu Qian
Xuezheng Lin
Zhili Zhou
author_facet Jiashu Qian
Xuezheng Lin
Zhili Zhou
author_sort Jiashu Qian
collection DOAJ
description Abstract Persistent postoperative pain causes influence the life quality of many patients. The Epac/PKC pathway has been indicated to regulate mechanical hyperalgesia. The present study used skin/muscle incision and retraction (SMIR) to induce postoperative pain in rats and evaluated the Epac/PKC pathway in postoperative pain. Mechanical allodynia was assessed by paw withdrawal threshold before and after incision. The levels of Epac, PKC, proinflammatory cytokines, and blood-nerve barrier-related proteins were assessed using Western blotting. We found that SMIR induced the activation of the Epac/PKC pathway, mechanical allodynia, and upregulation of Glut1, VEGF, and PGP9.5 proteins in dorsal root ganglia. Under the influence of agonists of Epac/PKC, normal rats showed mechanical allodynia and increased Glut1, VEGF, and PGP9.5 proteins. After inhibition of Epac1 in rats with SMIR, mechanical allodynia was alleviated, and proinflammatory cytokines and Glut1, VEGF, and PGP9.5 proteins were decreased. Moreover, dorsal root ganglia neurons showed abnormal proliferation under the activation of the Epac/PKC pathway. Using Captopril to protect vascular endothelial cells after SMIR had a positive effect on postoperative pain. In conclusion, SMIR regulates the persistent postoperative pain in rats by the Epac/PKC pathway.
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spelling doaj.art-565ef69d924c4218a390d2ef2bb84faf2022-12-22T00:44:18ZengBMCBMC Anesthesiology1471-22532022-07-012211910.1186/s12871-022-01771-wSkin/muscle incision and retraction regulates the persistent postoperative pain in rats by the Epac1/PKC-βII pathwayJiashu Qian0Xuezheng Lin1Zhili Zhou2Department of Anesthesiology, Taizhou Central Hospital (Affiliated Hospital of Taizhou University)Department of Anesthesiology, Taizhou Central Hospital (Affiliated Hospital of Taizhou University)Department of Anesthesiology, Taizhou Central Hospital (Affiliated Hospital of Taizhou University)Abstract Persistent postoperative pain causes influence the life quality of many patients. The Epac/PKC pathway has been indicated to regulate mechanical hyperalgesia. The present study used skin/muscle incision and retraction (SMIR) to induce postoperative pain in rats and evaluated the Epac/PKC pathway in postoperative pain. Mechanical allodynia was assessed by paw withdrawal threshold before and after incision. The levels of Epac, PKC, proinflammatory cytokines, and blood-nerve barrier-related proteins were assessed using Western blotting. We found that SMIR induced the activation of the Epac/PKC pathway, mechanical allodynia, and upregulation of Glut1, VEGF, and PGP9.5 proteins in dorsal root ganglia. Under the influence of agonists of Epac/PKC, normal rats showed mechanical allodynia and increased Glut1, VEGF, and PGP9.5 proteins. After inhibition of Epac1 in rats with SMIR, mechanical allodynia was alleviated, and proinflammatory cytokines and Glut1, VEGF, and PGP9.5 proteins were decreased. Moreover, dorsal root ganglia neurons showed abnormal proliferation under the activation of the Epac/PKC pathway. Using Captopril to protect vascular endothelial cells after SMIR had a positive effect on postoperative pain. In conclusion, SMIR regulates the persistent postoperative pain in rats by the Epac/PKC pathway.https://doi.org/10.1186/s12871-022-01771-wPersistent postoperative painSkin/muscle incision and retractionEpac1/PKC-βII
spellingShingle Jiashu Qian
Xuezheng Lin
Zhili Zhou
Skin/muscle incision and retraction regulates the persistent postoperative pain in rats by the Epac1/PKC-βII pathway
BMC Anesthesiology
Persistent postoperative pain
Skin/muscle incision and retraction
Epac1/PKC-βII
title Skin/muscle incision and retraction regulates the persistent postoperative pain in rats by the Epac1/PKC-βII pathway
title_full Skin/muscle incision and retraction regulates the persistent postoperative pain in rats by the Epac1/PKC-βII pathway
title_fullStr Skin/muscle incision and retraction regulates the persistent postoperative pain in rats by the Epac1/PKC-βII pathway
title_full_unstemmed Skin/muscle incision and retraction regulates the persistent postoperative pain in rats by the Epac1/PKC-βII pathway
title_short Skin/muscle incision and retraction regulates the persistent postoperative pain in rats by the Epac1/PKC-βII pathway
title_sort skin muscle incision and retraction regulates the persistent postoperative pain in rats by the epac1 pkc βii pathway
topic Persistent postoperative pain
Skin/muscle incision and retraction
Epac1/PKC-βII
url https://doi.org/10.1186/s12871-022-01771-w
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AT zhilizhou skinmuscleincisionandretractionregulatesthepersistentpostoperativepaininratsbytheepac1pkcbiipathway