Effect of Sodium Fluoride on the endogenous MMP Activity of Dentin Matrices.

Journal of nature and science Pub Date : 2015-06-01
Martha Goël Brackett, Kelli A Agee, William W Brackett, William O Key, Camila Sabatini, Melissa T Kato, Marilia A R Buzalaf, Leo Tjäderhane, David H Pashley
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Abstract

Objectives: This study evaluated the effect of incorporating increasing concentrations of sodium fluoride in incubation media, on the loss of dry mass and solubilization of collagen from demineralized dentin beams incubated for up to 7 days. The effect of fluoride on the inhibition of matrix-bound metalloproteinases (MMPs) was also measured.

Methods: Dentin beams were completely demineralized in 10% phosphoric acid. After baseline measurements of dry mass, the beams were divided into six groups (n=10) and incubated at 37°C either in buffered media containing sodium fluoride (NaF) at 75, 150, 300, 450, 600 ppm or in fluoride-free media (control) for seven days. Following incubation, dry mass was re-measured. The incubation media was hydrolyzed with HCl for the quantitation of hydroxyproline (HYP) as an index of solubilization of collagen by endogenous dentin proteases. Increasing concentrations of fluoride were also evaluated for their ability to inhibit rhMMP-9.

Results: Addition of NaF to the incubation media produced a progressive significant reduction (p<0.05) in the loss of mass of dentin matrices, with all concentrations demonstrating significantly less mass loss than the control group. Significantly less HYP release from the dentin beams was found in the higher fluoride concentration groups, while fluoride concentrations of 75 and 150 ppm significantly reduced rhMMP-9 activity by 6.5% and 79.2%, respectively.

Conclusions: The results of this study indicate that NaF inhibits matrix-bound MMPs and therefore may slow the degradation of dentin matrix by endogenous dentin MMPs.

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氟化钠对牙本质基质内源性MMP活性的影响。
目的:本研究评估了在培养培养基中加入浓度增加的氟化钠对培养长达7天的脱矿牙本质梁的干质量损失和胶原蛋白增溶的影响。测定了氟对基质结合金属蛋白酶(MMPs)的抑制作用。方法:牙本质梁在10%磷酸溶液中完全脱矿。在干质量基线测量后,将光束分为六组(n=10),并在37°C下,在含氟化钠(NaF)浓度为75、150、300、450、600 ppm的缓冲介质中或在无氟介质(对照)中孵育7天。孵育后,重新测量干质量。用盐酸水解培养培养基,定量测定羟脯氨酸(HYP),作为内源性牙本质蛋白酶对胶原增溶的指标。还评估了增加氟化物浓度对rhMMP-9的抑制能力。结论:本研究结果表明,NaF抑制基质结合的MMPs,因此可能减缓内源性牙本质MMPs对牙本质基质的降解。
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