Intervertebral disk regeneration in a rat model by allopurinol–loaded chitosan/alginate hydrogel

Intervertebral disk degeneration remains one of the most challenging health problems. In the current study, allopurinol was loaded into the chitosan nanoparticles and then incorporated into chitosan/alginate hydrogels and then further studied for its disk regeneration potential in a rat model. In vi...

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Main Authors: Linhui Ye, Zengxin Gao, Saeed Rohani
Format: Article
Language:English
Published: Association of Basic Medical Sciences of Federation of Bosnia and Herzegovina 2023-07-01
Series:Biomolecules & Biomedicine
Subjects:
Online Access:https://www.bjbms.org/ojs/index.php/bjbms/article/view/8550
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author Linhui Ye
Zengxin Gao
Saeed Rohani
author_facet Linhui Ye
Zengxin Gao
Saeed Rohani
author_sort Linhui Ye
collection DOAJ
description Intervertebral disk degeneration remains one of the most challenging health problems. In the current study, allopurinol was loaded into the chitosan nanoparticles and then incorporated into chitosan/alginate hydrogels and then further studied for its disk regeneration potential in a rat model. In vitro studies were performed to characterize the hydrogel system, including scanning electron microscopy, cell viability assay, cytoprotection assay, cell migration assay, swelling assay, and drug release assay. In vivo study was performed in a rat model of the intervertebral disk injury. Animal studies showed that allopurinol-loaded hydrogels had significantly higher disk regeneration potential compared with other experimental groups. The gene expression studies showed that the animals treated with allopurinol–loaded hydrogel had significantly higher tissue expression levels of type I and type II collagen genes than other groups. Furthermore, the tissue expression levels of nuclear factor κB (NF-κB) and glutathione peroxidase (GPx) genes were significantly lower in this group. The relative expression levels of type I collagen, type II collagen, NF-κB, and GPx genes in the allopurinol-loaded hydrogel group were 2.77 ± 0.2%, 2.86 ± 0.25%, 0.58 ± 0.03%, and 0.45 ± 0.02%, respectively. We showed for the first time that allopurinol-loaded hydrogel promoted intervertebral disk repair, which could be due to its potential to modulate oxidative stress, reduce inflammation, and improve matrix synthesis.
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spelling doaj.art-9adf7f0d77cd405591ba45cc004c5dd72024-03-15T13:22:35ZengAssociation of Basic Medical Sciences of Federation of Bosnia and HerzegovinaBiomolecules & Biomedicine2831-08962831-090X2023-07-0123410.17305/bb.2022.8550Intervertebral disk regeneration in a rat model by allopurinol–loaded chitosan/alginate hydrogelLinhui Ye0Zengxin Gao1Saeed Rohani2Department of Orthopedics, Nanjing Lishui People’s Hospital, Zhongda Hospital, Lishui Branch, Southeast University, Nanjing, ChinaDepartment of Orthopedics, Nanjing Lishui People’s Hospital, Zhongda Hospital, Lishui Branch, Southeast University, Nanjing, China; Department of Orthopedic Surgery, Zhongda Hospital, School of Medicine, Southeast University, Nanjing, ChinaDepartment of Tissue Engineering, Tehran University of Medical Sciences, Tehran, IranIntervertebral disk degeneration remains one of the most challenging health problems. In the current study, allopurinol was loaded into the chitosan nanoparticles and then incorporated into chitosan/alginate hydrogels and then further studied for its disk regeneration potential in a rat model. In vitro studies were performed to characterize the hydrogel system, including scanning electron microscopy, cell viability assay, cytoprotection assay, cell migration assay, swelling assay, and drug release assay. In vivo study was performed in a rat model of the intervertebral disk injury. Animal studies showed that allopurinol-loaded hydrogels had significantly higher disk regeneration potential compared with other experimental groups. The gene expression studies showed that the animals treated with allopurinol–loaded hydrogel had significantly higher tissue expression levels of type I and type II collagen genes than other groups. Furthermore, the tissue expression levels of nuclear factor κB (NF-κB) and glutathione peroxidase (GPx) genes were significantly lower in this group. The relative expression levels of type I collagen, type II collagen, NF-κB, and GPx genes in the allopurinol-loaded hydrogel group were 2.77 ± 0.2%, 2.86 ± 0.25%, 0.58 ± 0.03%, and 0.45 ± 0.02%, respectively. We showed for the first time that allopurinol-loaded hydrogel promoted intervertebral disk repair, which could be due to its potential to modulate oxidative stress, reduce inflammation, and improve matrix synthesis. https://www.bjbms.org/ojs/index.php/bjbms/article/view/8550Allopurinolintervertebral disk regenerationcomposite hydrogel
spellingShingle Linhui Ye
Zengxin Gao
Saeed Rohani
Intervertebral disk regeneration in a rat model by allopurinol–loaded chitosan/alginate hydrogel
Biomolecules & Biomedicine
Allopurinol
intervertebral disk regeneration
composite hydrogel
title Intervertebral disk regeneration in a rat model by allopurinol–loaded chitosan/alginate hydrogel
title_full Intervertebral disk regeneration in a rat model by allopurinol–loaded chitosan/alginate hydrogel
title_fullStr Intervertebral disk regeneration in a rat model by allopurinol–loaded chitosan/alginate hydrogel
title_full_unstemmed Intervertebral disk regeneration in a rat model by allopurinol–loaded chitosan/alginate hydrogel
title_short Intervertebral disk regeneration in a rat model by allopurinol–loaded chitosan/alginate hydrogel
title_sort intervertebral disk regeneration in a rat model by allopurinol loaded chitosan alginate hydrogel
topic Allopurinol
intervertebral disk regeneration
composite hydrogel
url https://www.bjbms.org/ojs/index.php/bjbms/article/view/8550
work_keys_str_mv AT linhuiye intervertebraldiskregenerationinaratmodelbyallopurinolloadedchitosanalginatehydrogel
AT zengxingao intervertebraldiskregenerationinaratmodelbyallopurinolloadedchitosanalginatehydrogel
AT saeedrohani intervertebraldiskregenerationinaratmodelbyallopurinolloadedchitosanalginatehydrogel