The effect of active components from citrus fruits on dentin MMPs

Arch Oral Biol. 2017 Nov:83:111-117. doi: 10.1016/j.archoralbio.2017.07.006. Epub 2017 Jul 20.

Abstract

Objectives: This study was aimed to evaluate the anti-matrix metalloproteinases (MMPs) ability of active components from citrus fruits (hesperetin: Hst, hesperidin: Hsd and naringenin: Nge).

Methods: Inactivation effects of citrus flavonoids (Hst, Hsd, Nge) at different concentrations on soluble collagenase were measured using a fluorometric assay. Matrix-bound endogenous MMPs activity was evaluated via dry mass loss and hydroxyproline (HYP) release of demineralized human dentin. Demineralized dentin beams were pretreated with 500μg/mL citrus flavonoids for 10min. Chlorhexidine (CHX) was used as inhibitor control. Beams pretreated with distilled water served as blank control. Dentin slabs were used for in situ zymography and evaluated under confocal microscopy. Ultrastructure of demineralized collagen fibers was exhibited by Transmission Electron Microscopy (TEM).

Results: Citrus flavonoids exhibited inactivation function on soluble MMPs and the extent of inactivation increased in a dose-dependent manner. The inactivation percent of citrus flavonoids reached above 90% at the concentration of 500μg/mL. Compared with control group, citrus flavonoids pretreated demineralized dentin beams exhibited less dry mass loss, lower hydroxyproline release and more intact collagen architecture after 15days storage. Dentin samples pretreated with citrus flavonoids showed lower enzymes activities in in situ zymography.

Conclusions: Hst, Hsd or Nge have anti-MMPs ability and can preserve dentin collagen from degradation.

Clinical significance: Hst, Hsd and Nge may have the potential to be used in dentin bonding systems and improve the resin-dentin bonding durability.

Keywords: Citrus flavonoids; Hesperetin; Hesperidin; Matrix metalloproteinases inhibitor; Naringenin; Resin- dentin bonding.

MeSH terms

  • Chlorhexidine / pharmacology
  • Citrus / chemistry*
  • Dentin / metabolism*
  • Flavonoids / pharmacology*
  • Humans
  • Hydroxyproline / metabolism
  • In Vitro Techniques
  • Matrix Metalloproteinases / metabolism*
  • Microscopy, Electron, Transmission
  • Molar, Third
  • Surface Properties

Substances

  • Flavonoids
  • Matrix Metalloproteinases
  • Chlorhexidine
  • Hydroxyproline