Multiscale biomechanical responses of adapted bone–periodontal ligament–tooth fibrous joints

• Published in: Bone (New York, N.Y.) Vol. 81; pp. 196 - 207
• Main Authors: Jang, Andrew T, Merkle, Arno P, Fahey, Kevin P, Gansky, Stuart A, Ho, Sunita P
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 01-12-2015
• Subjects: Animals; Biomechanical Phenomena - physiology; Biomechanics; Bone–PDL–tooth fibrous joint; Dental Cementum - physiology; Joints - physiology; Male; Mastication - physiology; Multiscale; Orthopedics; Periodontal ligament; Periodontal Ligament - physiology; Rat; Rats; Rats, Sprague-Dawley; Stiffness; Tooth - physiology; Biomechanics; Bone–PDL–tooth fibrous joint; Periodontal ligament; Stiffness; Rat; Multiscale
• ISSN: 8756-3282; 1873-2763
• DOI: 10.1016/j.bone.2015.07.004

Abstract Reduced functional loads cause adaptations in organs. In this study, temporal adaptations of bone-ligament-tooth fibrous joints to reduced functional loads were mapped using a holistic approach. Systematic studies were performed to evaluate organ-level and tissue-level adaptations in specimens harvested periodically from rats (N = 60) given powder food for 6 months over 8,12,16,20, and 24 weeks. Bone–periodontal ligament (PDL)–tooth fibrous joint adaptation was evaluated by comparing changes in joint stiffness with changes in functional space between the tooth and alveolar bony socket. Adaptations in tissues included mapping changes in the PDL and bone architecture as observed from collagen birefringence, bone hardness and volume fraction in rats fed soft foods (soft diet, SD) compared to those fed hard pellets as a routine diet (hard diet, HD). In situ biomechanical testing on harvested fibrous joints revealed increased stiffness in SD groups (SD:239–605 N/mm) (p < 0.05) at 8 and 12 weeks. Increased joint stiffness in early development phase was due to decreased functional space (at 8 weeks change in functional space was − 33 μm, at 12 weeks change in functional space was − 30 μm) and shifts in tissue quality as highlighted by birefringence, architecture and hardness. These physical changes were not observed in joints that were well into function, that is, in rodents older than 12 weeks of age. Significant adaptations in older groups were highlighted by shifts in bone growth (bone volume fraction 24 weeks: Δ–0.06) and bone hardness (8 weeks: Δ–0.04 GPa, 16 weeks: Δ–0.07 GPa, 24 weeks: Δ–0.06 GPa). The response rate (N/s) of joints to mechanical loads decreased in SD groups. Results from the study showed that joint adaptation depended on age. The initial form-related adaptation (observed change in functional space) can challenge strain-adaptive nature of tissues to meet functional demands with increasing age into adulthood. The coupled effect between functional space in the bone–PDL–tooth complex and strain-adaptive nature of tissues is necessary to accommodate functional demands, and is temporally sensitive despite joint malfunction. From an applied science perspective, we propose that adaptations are registered as functional history in tissues and joints.