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Parathyroid hormone promotes cartilage healing after free reduction of mandibular condylar fractures by upregulating Sox9
After high fractures of the mandibular condyle, the insufficient blood supply to the condyle often leads to poor bone and cartilage repair ability and poor clinical outcome. Parathyroid hormone (PTH) can promote the bone formation and mineralization of mandibular fracture, but its effects on cartila...
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Published in: | Experimental biology and medicine (Maywood, N.J.) N.J.), 2021-11, Vol.246 (21), p.2249-2258 |
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description | After high fractures of the mandibular condyle, the insufficient blood supply to the condyle often leads to poor bone and cartilage repair ability and poor clinical outcome. Parathyroid hormone (PTH) can promote the bone formation and mineralization of mandibular fracture, but its effects on cartilage healing after the free reduction and internal fixation of high fractures of the mandibular condyle are unknown. In this study, a rabbit model of free reduction and internal fixation of high fractures of the mandibular condyle was established, and the effects and mechanisms of PTH on condylar cartilage healing were explored. Forty-eight specific-pathogen-free (SPF) grade rabbits were randomly divided into two groups. In the experimental group, PTH was injected subcutaneously at 20 µg/kg (PTH (1–34)) every other day, and in the control group, PTH was replaced with 1 ml saline. The healing cartilages were assessed at postoperative days 7, 14, 21, and 28. Observation of gross specimens, hematoxylin eosin staining and Safranin O/fast green staining found that every-other-day subcutaneous injection of PTH at 20 µg/kg promoted healing of condylar cartilage and subchondral osteogenesis in the fracture site. Immunohistochemistry and polymerase chain reaction showed that PTH significantly upregulated the chondrogenic genes Sox9 and Col2a1 in the cartilage fracture site within 7–21 postoperative days in the experimental group than those in the control group, while it downregulated the cartilage inflammation gene matrix metalloproteinase-13 and chondrocyte terminal differentiation gene ColX. In summary, exogenous PTH can stimulate the formation of cartilage matrix by triggering Sox9 expression at the early stage of cartilage healing, and it provides a potential therapeutic protocol for high fractures of the mandibular condyle. |
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Parathyroid hormone (PTH) can promote the bone formation and mineralization of mandibular fracture, but its effects on cartilage healing after the free reduction and internal fixation of high fractures of the mandibular condyle are unknown. In this study, a rabbit model of free reduction and internal fixation of high fractures of the mandibular condyle was established, and the effects and mechanisms of PTH on condylar cartilage healing were explored. Forty-eight specific-pathogen-free (SPF) grade rabbits were randomly divided into two groups. In the experimental group, PTH was injected subcutaneously at 20 µg/kg (PTH (1–34)) every other day, and in the control group, PTH was replaced with 1 ml saline. The healing cartilages were assessed at postoperative days 7, 14, 21, and 28. Observation of gross specimens, hematoxylin eosin staining and Safranin O/fast green staining found that every-other-day subcutaneous injection of PTH at 20 µg/kg promoted healing of condylar cartilage and subchondral osteogenesis in the fracture site. Immunohistochemistry and polymerase chain reaction showed that PTH significantly upregulated the chondrogenic genes Sox9 and Col2a1 in the cartilage fracture site within 7–21 postoperative days in the experimental group than those in the control group, while it downregulated the cartilage inflammation gene matrix metalloproteinase-13 and chondrocyte terminal differentiation gene ColX. In summary, exogenous PTH can stimulate the formation of cartilage matrix by triggering Sox9 expression at the early stage of cartilage healing, and it provides a potential therapeutic protocol for high fractures of the mandibular condyle.</description><identifier>ISSN: 1535-3702</identifier><identifier>EISSN: 1535-3699</identifier><identifier>DOI: 10.1177/15353702211027114</identifier><identifier>PMID: 34233524</identifier><language>eng</language><publisher>London, England: SAGE Publications</publisher><subject>Animals ; Cartilage - drug effects ; Cartilage - physiology ; Collagen Type II - drug effects ; Collagen Type II - physiology ; Female ; Fracture Fixation, Internal - methods ; Male ; Mandibular Condyle - drug effects ; Mandibular Condyle - injuries ; Mandibular Condyle - physiopathology ; Mandibular Fractures - drug therapy ; Mandibular Fractures - surgery ; Matrix Metalloproteinase 13 - metabolism ; Original Research ; Osteogenesis - drug effects ; Parathyroid Hormone - pharmacology ; Rabbits ; SOX9 Transcription Factor - agonists ; SOX9 Transcription Factor - physiology ; Up-Regulation - drug effects ; Wound Healing - drug effects</subject><ispartof>Experimental biology and medicine (Maywood, N.J.), 2021-11, Vol.246 (21), p.2249-2258</ispartof><rights>2021 by the Society for Experimental Biology and Medicine</rights><rights>2021 by the Society for Experimental Biology and Medicine 2021 The Society for Experimental Biology and Medicine</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c438t-1d85a114dc17cd28010b8636502ef1bc001c613104b991cef0c75d20fb566b5b3</citedby><cites>FETCH-LOGICAL-c438t-1d85a114dc17cd28010b8636502ef1bc001c613104b991cef0c75d20fb566b5b3</cites><orcidid>0000-0001-6309-0486</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8581833/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8581833/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,27923,27924,53790,53792</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34233524$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Jia, Yuanyuan</creatorcontrib><creatorcontrib>Xie, Liuqin</creatorcontrib><creatorcontrib>Tang, Zhenglong</creatorcontrib><creatorcontrib>Wang, Dongxiang</creatorcontrib><creatorcontrib>Hu, Yun</creatorcontrib><creatorcontrib>Zhang, Guoxing</creatorcontrib><creatorcontrib>Chen, Youli</creatorcontrib><creatorcontrib>Gao, Qiong</creatorcontrib><title>Parathyroid hormone promotes cartilage healing after free reduction of mandibular condylar fractures by upregulating Sox9</title><title>Experimental biology and medicine (Maywood, N.J.)</title><addtitle>Exp Biol Med (Maywood)</addtitle><description>After high fractures of the mandibular condyle, the insufficient blood supply to the condyle often leads to poor bone and cartilage repair ability and poor clinical outcome. Parathyroid hormone (PTH) can promote the bone formation and mineralization of mandibular fracture, but its effects on cartilage healing after the free reduction and internal fixation of high fractures of the mandibular condyle are unknown. In this study, a rabbit model of free reduction and internal fixation of high fractures of the mandibular condyle was established, and the effects and mechanisms of PTH on condylar cartilage healing were explored. Forty-eight specific-pathogen-free (SPF) grade rabbits were randomly divided into two groups. In the experimental group, PTH was injected subcutaneously at 20 µg/kg (PTH (1–34)) every other day, and in the control group, PTH was replaced with 1 ml saline. The healing cartilages were assessed at postoperative days 7, 14, 21, and 28. Observation of gross specimens, hematoxylin eosin staining and Safranin O/fast green staining found that every-other-day subcutaneous injection of PTH at 20 µg/kg promoted healing of condylar cartilage and subchondral osteogenesis in the fracture site. Immunohistochemistry and polymerase chain reaction showed that PTH significantly upregulated the chondrogenic genes Sox9 and Col2a1 in the cartilage fracture site within 7–21 postoperative days in the experimental group than those in the control group, while it downregulated the cartilage inflammation gene matrix metalloproteinase-13 and chondrocyte terminal differentiation gene ColX. In summary, exogenous PTH can stimulate the formation of cartilage matrix by triggering Sox9 expression at the early stage of cartilage healing, and it provides a potential therapeutic protocol for high fractures of the mandibular condyle.</description><subject>Animals</subject><subject>Cartilage - drug effects</subject><subject>Cartilage - physiology</subject><subject>Collagen Type II - drug effects</subject><subject>Collagen Type II - physiology</subject><subject>Female</subject><subject>Fracture Fixation, Internal - methods</subject><subject>Male</subject><subject>Mandibular Condyle - drug effects</subject><subject>Mandibular Condyle - injuries</subject><subject>Mandibular Condyle - physiopathology</subject><subject>Mandibular Fractures - drug therapy</subject><subject>Mandibular Fractures - surgery</subject><subject>Matrix Metalloproteinase 13 - metabolism</subject><subject>Original Research</subject><subject>Osteogenesis - drug effects</subject><subject>Parathyroid Hormone - pharmacology</subject><subject>Rabbits</subject><subject>SOX9 Transcription Factor - agonists</subject><subject>SOX9 Transcription Factor - physiology</subject><subject>Up-Regulation - drug effects</subject><subject>Wound Healing - drug effects</subject><issn>1535-3702</issn><issn>1535-3699</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNp9kV1rFTEQhoNYbK3-AG8kl96cmkk2-3EjSPELChZar0O-9pyU3eQ4yRb335vDaYsieDXDzDvPZPIS8gbYBUDXvQcppOgY5wCMdwDNM3J2qG1EOwzPH_MqOCUvc75jDGTH2xfkVDRcCMmbM7Jea9Rlt2IKju4Szil6usc0p-IztRpLmPTW053XU4hbqsfikY7oPUXvFltCijSNdNbRBbNMGqlN0a2HZERty4KVY1a67NFva78cKDfp1_CKnIx6yv71QzwnPz5_ur38urn6_uXb5cerjW1EXzbgeqnrac5CZx3vGTDTt6KVjPsRjK1H2RYEsMYMA1g_MttJx9loZNsaacQ5-XDk7hcze2d9LKgntccwa1xV0kH93Ylhp7bpXvWyh16ICnj3AMD0c_G5qDlk66dJR5-WrLhshrbvpGRVCkepxZQz-vFpDTB1sEz9Y1mdefvn-54mHj2qgoujIFcj1F1aMNb_-g_xN3fLoY8</recordid><startdate>20211101</startdate><enddate>20211101</enddate><creator>Jia, Yuanyuan</creator><creator>Xie, Liuqin</creator><creator>Tang, Zhenglong</creator><creator>Wang, Dongxiang</creator><creator>Hu, Yun</creator><creator>Zhang, Guoxing</creator><creator>Chen, Youli</creator><creator>Gao, Qiong</creator><general>SAGE Publications</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-6309-0486</orcidid></search><sort><creationdate>20211101</creationdate><title>Parathyroid hormone promotes cartilage healing after free reduction of mandibular condylar fractures by upregulating Sox9</title><author>Jia, Yuanyuan ; Xie, Liuqin ; Tang, Zhenglong ; Wang, Dongxiang ; Hu, Yun ; Zhang, Guoxing ; Chen, Youli ; Gao, Qiong</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c438t-1d85a114dc17cd28010b8636502ef1bc001c613104b991cef0c75d20fb566b5b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Animals</topic><topic>Cartilage - drug effects</topic><topic>Cartilage - physiology</topic><topic>Collagen Type II - drug effects</topic><topic>Collagen Type II - physiology</topic><topic>Female</topic><topic>Fracture Fixation, Internal - methods</topic><topic>Male</topic><topic>Mandibular Condyle - drug effects</topic><topic>Mandibular Condyle - injuries</topic><topic>Mandibular Condyle - physiopathology</topic><topic>Mandibular Fractures - drug therapy</topic><topic>Mandibular Fractures - surgery</topic><topic>Matrix Metalloproteinase 13 - metabolism</topic><topic>Original Research</topic><topic>Osteogenesis - drug effects</topic><topic>Parathyroid Hormone - pharmacology</topic><topic>Rabbits</topic><topic>SOX9 Transcription Factor - agonists</topic><topic>SOX9 Transcription Factor - physiology</topic><topic>Up-Regulation - drug effects</topic><topic>Wound Healing - drug effects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jia, Yuanyuan</creatorcontrib><creatorcontrib>Xie, Liuqin</creatorcontrib><creatorcontrib>Tang, Zhenglong</creatorcontrib><creatorcontrib>Wang, Dongxiang</creatorcontrib><creatorcontrib>Hu, Yun</creatorcontrib><creatorcontrib>Zhang, Guoxing</creatorcontrib><creatorcontrib>Chen, Youli</creatorcontrib><creatorcontrib>Gao, Qiong</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Experimental biology and medicine (Maywood, N.J.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jia, Yuanyuan</au><au>Xie, Liuqin</au><au>Tang, Zhenglong</au><au>Wang, Dongxiang</au><au>Hu, Yun</au><au>Zhang, Guoxing</au><au>Chen, Youli</au><au>Gao, Qiong</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Parathyroid hormone promotes cartilage healing after free reduction of mandibular condylar fractures by upregulating Sox9</atitle><jtitle>Experimental biology and medicine (Maywood, N.J.)</jtitle><addtitle>Exp Biol Med (Maywood)</addtitle><date>2021-11-01</date><risdate>2021</risdate><volume>246</volume><issue>21</issue><spage>2249</spage><epage>2258</epage><pages>2249-2258</pages><issn>1535-3702</issn><eissn>1535-3699</eissn><abstract>After high fractures of the mandibular condyle, the insufficient blood supply to the condyle often leads to poor bone and cartilage repair ability and poor clinical outcome. Parathyroid hormone (PTH) can promote the bone formation and mineralization of mandibular fracture, but its effects on cartilage healing after the free reduction and internal fixation of high fractures of the mandibular condyle are unknown. In this study, a rabbit model of free reduction and internal fixation of high fractures of the mandibular condyle was established, and the effects and mechanisms of PTH on condylar cartilage healing were explored. Forty-eight specific-pathogen-free (SPF) grade rabbits were randomly divided into two groups. In the experimental group, PTH was injected subcutaneously at 20 µg/kg (PTH (1–34)) every other day, and in the control group, PTH was replaced with 1 ml saline. The healing cartilages were assessed at postoperative days 7, 14, 21, and 28. Observation of gross specimens, hematoxylin eosin staining and Safranin O/fast green staining found that every-other-day subcutaneous injection of PTH at 20 µg/kg promoted healing of condylar cartilage and subchondral osteogenesis in the fracture site. Immunohistochemistry and polymerase chain reaction showed that PTH significantly upregulated the chondrogenic genes Sox9 and Col2a1 in the cartilage fracture site within 7–21 postoperative days in the experimental group than those in the control group, while it downregulated the cartilage inflammation gene matrix metalloproteinase-13 and chondrocyte terminal differentiation gene ColX. In summary, exogenous PTH can stimulate the formation of cartilage matrix by triggering Sox9 expression at the early stage of cartilage healing, and it provides a potential therapeutic protocol for high fractures of the mandibular condyle.</abstract><cop>London, England</cop><pub>SAGE Publications</pub><pmid>34233524</pmid><doi>10.1177/15353702211027114</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0001-6309-0486</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Animals Cartilage - drug effects Cartilage - physiology Collagen Type II - drug effects Collagen Type II - physiology Female Fracture Fixation, Internal - methods Male Mandibular Condyle - drug effects Mandibular Condyle - injuries Mandibular Condyle - physiopathology Mandibular Fractures - drug therapy Mandibular Fractures - surgery Matrix Metalloproteinase 13 - metabolism Original Research Osteogenesis - drug effects Parathyroid Hormone - pharmacology Rabbits SOX9 Transcription Factor - agonists SOX9 Transcription Factor - physiology Up-Regulation - drug effects Wound Healing - drug effects |
title | Parathyroid hormone promotes cartilage healing after free reduction of mandibular condylar fractures by upregulating Sox9 |
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