Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Pivot Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Target Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Query: UMLS:C1864663 (
HCC
)
2,985
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
High molecular weight hyaluronan (H-HA) has a pivotal role in the maintenance of normal functions of synovial fluid and structure of the articular joint, but it has been shown that its concentration is reduced in patients affected by degenerative cartilage diseases, such as osteoarthritis (OA). The aim of this study was to investigate the anti-inflammatory effects and properties of hybrid cooperative complexes based on high and low molecular weight hyaluronan (
HCC
) compared to H-HA on human primary cells derived by pathological joints. In addition, the rheological behavior of
HCC
was evaluated in order to define their potential as viscosupplement gel in degenerated joints. The experiments were performed using an
in vitro
model of OA based on human chondrocytes and synoviocytes isolated from degenerated joints of patients hospitalized for surgical replacement. In order to assess the anti-inflammatory effects of
HCC
, we evaluated NF-kB,
COMP
-2, IL-6, and IL-8 as specific markers at the transcriptional and/or protein level. Moreover, the proliferative properties of
HCC
were assessed using time lapse video microscopy. We showed that chondrocytes and synoviocytes clearly presented an altered cytokine profile compatible with a severe ongoing inflammation status. H-HA and, above all,
HCC
significantly reduced levels of the specific biomarkers evaluated and improved cartilage healing. The rheological profile indicated
HCC
suitability for intra-articular injection in joint diseases.
HCC
viscoelastic properties and the protective/anti-inflammatory effect on human chondrocytes and synoviocytes suggest the novel
HCC
-based gels as a valid support for OA management.
...
PMID:Novel Hybrid Gels Made of High and Low Molecular Weight Hyaluronic Acid Induce Proliferation and Reduce Inflammation in an Osteoarthritis
In Vitro
Model Based on Human Synoviocytes and Chondrocytes. 3277 39