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Updated: Sep 18, 2025
Development of a Direct Pulp-capping Model for the Evaluation of Pulpal Wound Healing and Reparative Dentin Formation in Mice
Published on: January 12, 2017
Dental pulp enhances dentin bonding durability: Evidence from a rat model
Bing-Jie Zhong1, Jing-Hui Lin1, Zheng-Xing Lin1
1Fujian Key Laboratory of Oral Diseases & Fujian Provincial Engineering Research Center of Oral Biomaterial & Stomatological Key Laboratory of Fujian College and University, School and Hospital of Stomatology, Fujian Medical University, Fuzhou, China; Research Center of Dental Esthetics and Biomechanics, Fujian Medical University, Fuzhou, China.
Objectives:
To develop a novel animal model for investigating dentin bonding and to examine how dental pulp vitality affects the long-term stability of dentin-resin bonds.
Methods:
1) A split-mouth design was employed in Sprague-Dawley rats. Mandibular first molars were assigned to the vital or nonvital group (n = 6). In vital teeth, 0.3 mm of the mesial surface was removed to expose the dentin, followed by the application of a self-etch adhesive and light-cured resin composite. For nonvital teeth, root canal treatment was performed before the same bonding procedure. Micro-CT analysis and hematoxylin-eosin staining were conducted for model validation. 2) A total of 116 rats were used for dentin bonding evaluation. The composite survival rates, microshear bond strength (μSBS), and interfacial structure were characterized at 0, 2, 4, and 6 weeks (with 29 rats sacrificed at each interval) via field emission scanning electron microscopy, atomic force microscopy, and confocal laser scanning microscopy. Additional biochemical analysis of bonded dentin (n = 3) was performed via data-independent acquisition mass spectrometry.
Results:
1) The animal model was validated successfully, with micro-CT and histology confirming that there were no pathological alterations in pulp or periapical tissues. 2) Vital teeth exhibited superior bonding durability, with significantly higher survival rates, stable μSBS values, and excellently characterized interface. Nonvital teeth exhibited decreased bond strength, microcracks, poor sealing, reduced mechanical properties, and increased matrix metalloproteinase (MMP) activity. Proteomic analysis suggested that pulp vitality regulates MMP expression, preserving interfacial stability.
Conclusions:
Dental pulp vitality enhances bonding durability by maintaining interface integrity and modulating endogenous enzymes, particularly MMPs.
Clinical Relevance:
The protective role of dental pulp vitality in stabilizing the dentin-resin interface and suppressing MMP activity may lead to the development of novel dentin bonding strategies.
