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      <ref-type name="Journal Article">17</ref-type>
      <contributors>
        <authors>
          <author>Zhiyu Wang</author>
          <author>Lei Shi</author>
          <author>Weitong Chen</author>
          <author>Bo Feng</author>
        </authors>
      </contributors>
      <titles>
        <title>EFFECTS OF TGF-Β3/PDGF-BB-HEPARIN-HYALURONIC ACID HYDROGEL ON RABBIT KNEE OSTEOARTHRITIS</title>
        <secondary-title>Journal of Animal and Plant Sciences</secondary-title>
        <alt-title>JAPS</alt-title>
      </titles>
      <dates><year>2026</year><pub-dates><date>2026/01/20</date></pub-dates></dates>
      <volume>36</volume>
      <number>1</number>
      <pages>116-127</pages>
      <isbn>1018-7081</isbn>
      <electronic-resource-num>https://doi.org/10.36899/JAPS.2026.1.0010</electronic-resource-num>
      <abstract>&lt;p&gt;Current treatments for knee osteoarthritis (KOA) can alleviate symptoms but fail to repair damaged articular cartilage, while long-term use may lead to side effects. This study aimed to investigate the role of transforming growth factor (TGF)-&amp;beta;3-platelet-derived growth factor (PDGF)-B chain homodimer (BB)/heparin-hyaluronic acid (HA) hydrogel in rabbit KOA to achieve effective articular cartilage repair. Methacrylated hyaluronic acid (HAMA) and heparin (HepMA) were synthesized and utilized as matrices to prepare HepMA-HAMA hydrogel microspheres (MSs). Subsequently, the MSs were co-incubated with TGF-&amp;beta;3 and PDGF-BB to fabricate heparin-HA hydrogel MSs loaded with dual growth factors (HepMA-HAMA@DGFs). The drug loading, release , degradation and biocompatibility characteristics of the prepared hydrogel MSs were examined. New Zealand rabbits were utilized as experimental animals, and a KOA rabbit model was established. Physiological saline (Model group), HA (HA group), hydrogel MSs (HepMA-HAMA group and HepMA-HAMA@DGFs group) were injected into the joint cavity. Healthy rabbits served as the control. Behavioral analysis, knee joint histology, and expression differences of matrix metalloproteinase-13 (MMP-13), tissue inhibitor of metalloproteinases-1 (TIMP-1), and vascular endothelial growth factor (VEGF) in knee articular cartilage were calculated. The MSs exhibited sustained cumulative drug release and&amp;nbsp;&lt;em&gt;in vitro&lt;/em&gt;&amp;nbsp;degradation. Co-culturing HepMA-HAMA@DGFs MSs with mouse bone marrow mesenchymal stem cells (MSCs) showed minimal changes in cell growth. In rabbits, the model group exhibited increased Lequesne MG scores, upregulated expression of MMP-13 and VEGF in knee articular cartilage, and downregulated expression of TIMP-1 versus Control (&lt;em&gt;P&lt;/em&gt;&amp;lt;0.05). HepMA-HAMA and HepMA-HAMA@DGFs groups showed reduced Lequesne MG scores, downregulated expression of MMP-13 and VEGF in knee articular cartilage, and upregulated expression of TIMP-1 versus Model group (&lt;em&gt;P&lt;/em&gt;&amp;lt;0.05). Compared with the HepMA-HAMA group, HepMA-HAMA@DGFs group exhibited decreased Lequesne MG scores, downregulated expressions of MMP-13 and VEGF in knee articular cartilage of rabbits, and upregulated expression of TIMP-1 (&lt;em&gt;P&lt;/em&gt;&amp;lt;0.05). These findings indicate that HepMA-HAMA@DGFs hydrogel MSs have favorable drug release properties, degradation performance, and biocompatibility. Furthermore, HepMA-HAMA@DGFs hydrogel MSs can reduce the expression of MMP-13 and VEGF in KOA cartilage of rabbits, increase the expression of TIMP-1, and promote cartilage repair, thereby exerting therapeutic effects in the treatment of KOA in rabbits.&lt;/p&gt;</abstract>
      <keywords><keyword>TGF-β3-PDGF-BB/heparin-hyaluronic acid hydrogel, knee osteoarthritis, drug release rate, growth factor, cartilage repair</keyword></keywords>
      <publisher>Pakistan Agricultural Scientists Forum</publisher>
      <urls><related-urls><url>https://thejaps.org.pk/AbstractView.aspx?mid=2025-JAPS-376</url></related-urls></urls>
    </record>
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