Journal of Inflammation Research · 2021 · 24 citations · 33 references
DentistryOral BiologyPeriodonticsInflammationPeriodontal BiologyPeriodontal TherapyAnti-inflammatory PharmacologyHost Immune ResponseHost Modulation TherapyPeriodontal DiseasePeriodontal InflammationPeriodontal Tissue DestructionCollagen Fiber BreakdownMatrix MetalloproteinasesPeriodontal ImmunopathogenesisPeriodontal Ligament BreakdownPeriodontitis-induced Bone ResorptionPro-inflammatory Mediator ProductionPro-inflammatory Mediators In PeriodontitisSystemic Treatments
Purpose: Clinically, it is challenging to manage diabetic patients with periodontitis. Biochemically, both involve a wide range of inflammatory/collagenolytic conditions which exacerbate each other in a “bi-directional manner.” However, standard treatments for this type of periodontitis rely on reducing the bacterial burden and less on controlling hyper-inflammation/excessive-collagenolysis. Thus, there is a crucial need for new therapeutic strategies to modulate this excessive host response and to promote enhanced resolution of inflammation. The aim of the current study is to evaluate the impact of a novel chemically-modified curcumin 2.24 (CMC2.24) on host inflammatory response in diabetic rats. Methods: Type I diabetes was induced by streptozotocin injection; periodontal breakdown then results as a complication of uncontrolled hyperglycemia. Non-diabetic rats served as controls. CMC2.24, or the vehicle-alone, was administered by oral gavage daily for 3 weeks to the diabetics. Micro-CT was used to analyze morphometric changes and quantify bone loss. MMPs were analyzed by gelatin zymography. Cell function was examined by cell migration assay, and cytokines and resolvins were measured by ELISA. Results: In this severe inflammatory disease model, administration of the pleiotropic CMC2.24 was found to normalize the excessive accumulation and impaired chemotactic activity of macrophages in peritoneal exudates, significantly decrease MMP-9 and pro-inflammatory cytokines to near normal levels, and markedly increase resolvin D 1 (RvD 1 ) levels in the thioglycolate-elicited peritoneal exudates (tPE). Similar effects on MMPs and RvD 1 were observed in the non-elicited resident peritoneal washes (rPW). Regarding clinical relevance, CMC2.24 significantly inhibited the loss of alveolar bone height, volume and mineral density (ie, diabetes-induced periodontitis and osteoporosis). Conclusion: In conclusion, treating hyperglycemic diabetic rats with CMC2.24 (a tri-ketonic phenylaminocarbonyl curcumin) promotes the resolution of local and systemic inflammation, reduces bone loss, in addition to suppressing collagenolytic MMPs and pro-inflammatory cytokines, suggesting a novel therapeutic strategy for treating periodontitis complicated by other chronic diseases. Keywords: hyperglycemia, periodontitis, matrix metalloproteinases, inflammation, resolvins, host-modulatory therapy
33
Charles N. Serhan, Song Hong, Karsten Gronert et al. · The Journal of Experimental Medicine · 2002 · 1.6K citations · Full text
Minocycline reduces gingival collagenolytic activity during diabetes
Lorne M. Golub, H. M. Lee, Gerard M. Lehrer et al. · Journal of Periodontal Research · 1983 · 414 citations
Matrix Metalloproteinase-2 and -9 Levels in Obese Patients
Giuseppe Derosa, I. Ferrari, Angela D’Angelo et al. · Endothelium · 2008 · 164 citations