Low-intensity pulsed ultrasound reduces periodontal atrophy in occlusal hypofunctional teeth

Angle Orthod. 2017 Sep;87(5):709-716. doi: 10.2319/121216-893.1. Epub 2017 May 2.

Abstract

Objective: To clarify whether low-intensity pulsed ultrasound (LIPUS) exposure has recovery effects on the hypofunctional periodontal ligament (PDL) and interradicular alveolar bone (IRAB).

Materials and methods: Twelve-week-old male Sprague-Dawley rats were divided into three groups (n = 5 each): a normal occlusion (C) group, an occlusal hypofunction (H) group, and an occlusal hypofunction group subjected to LIPUS (HL) treatment. Hypofunctional occlusion of the maxillary first molar (M1) of the H and HL groups was induced by the bite-raising technique. Only the HL group was irradiated with LIPUS for 5 days. The IRAB and PDL of M1 were examined by microcomputed tomography (micro-CT) analysis. To quantify mRNA expression of cytokines involved in PDL proliferation and development, real-time reverse transcription quantitative PCR (qRT-PCR) was performed for twist family bHLH transcription factor 1 (Twist1), periostin, and connective tissue growth factor (CTGF) in the PDL samples.

Results: Micro-CT analysis showed that the PDL volume was decreased in the H group compared with that of the C and HL groups. Both bone volume per tissue volume (BV/TV) of IRAB was decreased in the H group compared with that in the C group. LIPUS exposure restored BV/TV in the IRAB of the HL group. qRT-PCR analysis showed that Twist1, periostin, and CTGF mRNA levels were decreased in the H group and increased in the HL group.

Conclusion: LIPUS exposure reduced the atrophic changes of alveolar bone by inducing the upregulation of periostin and CTGF expression to promote PDL healing after induction of occlusal hypofunction.

Keywords: Hypofunctional tooth; LIPUS; Orthodontics; Periodontal ligament; Periostin; Ultrasound.

MeSH terms

  • Alveolar Bone Loss / metabolism
  • Alveolar Bone Loss / pathology
  • Alveolar Bone Loss / radiotherapy
  • Alveolar Bone Loss / therapy
  • Animals
  • Cell Adhesion Molecules / genetics
  • Cell Adhesion Molecules / metabolism
  • Connective Tissue Growth Factor / genetics
  • Connective Tissue Growth Factor / metabolism
  • Cytokines / metabolism
  • Dental Occlusion*
  • Imaging, Three-Dimensional / methods
  • Male
  • Mandible / diagnostic imaging
  • Mandible / metabolism
  • Mandible / pathology
  • Mandible / radiation effects
  • Maxilla / diagnostic imaging
  • Maxilla / metabolism
  • Maxilla / pathology
  • Maxilla / radiation effects
  • Molar / diagnostic imaging
  • Molar / pathology
  • Nuclear Proteins / genetics
  • Nuclear Proteins / metabolism
  • Orthodontics
  • Periodontal Atrophy / metabolism
  • Periodontal Atrophy / pathology
  • Periodontal Atrophy / radiotherapy*
  • Periodontal Atrophy / therapy*
  • Periodontal Ligament / metabolism
  • Periodontal Ligament / pathology
  • Periodontal Ligament / radiation effects*
  • RNA, Messenger / analysis
  • RNA, Messenger / biosynthesis
  • Rats
  • Rats, Sprague-Dawley
  • Real-Time Polymerase Chain Reaction
  • Tooth / pathology
  • Tooth / radiation effects*
  • Twist-Related Protein 1 / genetics
  • Twist-Related Protein 1 / metabolism
  • Ultrasonic Therapy*
  • Ultrasonic Waves*
  • X-Ray Microtomography / methods

Substances

  • CCN2 protein, mouse
  • Cell Adhesion Molecules
  • Cytokines
  • Nuclear Proteins
  • Postn protein, mouse
  • RNA, Messenger
  • Twist-Related Protein 1
  • Twist1 protein, mouse
  • Connective Tissue Growth Factor