Abstract

Periodontitis is the leading cause of tooth loss in adults, and psychological factors play an important role in the development of periodontitis. To elucidate the adverse effects of psychological stress on the inflammatory process and redox status of periodontitis tissue, fifty male Sprague-Dawley rats were divided into the control, experimental periodontitis, psychological stress, experimental periodontitis plus psychological stress, and experimental periodontitis plus psychological stress plus fluoxetine groups. Chronic unpredictable mild stress (CUMS) was used to establish psychological stress, and silk ligature was used to induce experimental periodontitis. Four weeks later, stressed rats showed altered behaviour, serum hormone levels, and sucrose preference. More obvious alveolar bone loss and attachment loss and higher protein expressions of inflammatory cytokines were observed in the experimental periodontitis plus psychological stress group. The combination of CUMS and periodontitis had synergistic effects on increasing hypoxia-inducible factor-1α (HIF-1α) protein expression and reactive oxygen species (ROS) and malondialdehyde (MDA) contents and decreasing antioxidant enzyme activities compared with those in the stress or periodontitis groups. Moreover, psychological stress further increased p-IκBα and p-NF-κB p65 protein levels and decreased IκBα protein levels in periodontitis rats. Fluoxetine administration alleviated the adverse effects of psychological stress on the progression of periodontitis in rats. These results hint us that psychological stress could aggravate inflammation in periodontitis tissues, which may be partly due to local worsening of oxidative damage and further activation of the nuclear factor kappa-B (NF-κB) signalling pathway.

Highlights

  • As a chronic inflammatory disease, periodontitis is the main cause of tooth exfoliation due to severe inflammatory reactions and periodontal tissue destruction [1]

  • Fifty male Sprague-Dawley rats (8 weeks old, 210-230 g) were obtained from our university. They were randomly divided into five groups of 10 rats each, i.e., the C group, which comprised control rats; the EP group, which comprised rats with experimental periodontitis; the PS group, which comprised rats exposed to psychological stress; the EP+PS group, which comprised rats with experimental periodontitis exposed to psychological stress; and the EP+PS+DR group, which comprised rats with experimental periodontitis exposed to psychological stress and treated with fluoxetine

  • We found that periodontitis increased hypoxia-inducible factor-1α (HIF-1α) protein expression in gingival tissue (P < 0:05, Figure 7(b)), and a similar result was observed in the PS group rats (P < 0:05, Figure 7(b))

Read more

Summary

Introduction

As a chronic inflammatory disease, periodontitis is the main cause of tooth exfoliation due to severe inflammatory reactions and periodontal tissue destruction [1]. It is currently widely accepted that bacteria are the main aetiologic factor in periodontal disease [2], it cannot be ignored that the local, systemic, and behavioural host conditions that. Psychologic condition, especially psychological stress, plays an important role in daily life and can be caused by a variety of stressors that potentially threaten an individual’s homeostasis, well-being, overall health, or survival [5]. The association between psychological stress and periodontitis has been largely demonstrated recently [6, 7, 8] and has been identified as a potential risk factor for periodontal disease in some observational studies [9, 10]. Some studies even indicated that psychosocial stress has a greater influence than pathogenic bacteria on the severity of periodontal inflammation [13]. We previously observed the phenomenon of a delayed periodontitis healing process in psychologically stressed rats induced by chronic unpredictable mild stress (CUMS) [14]. Elucidating its important role in the progression of periodontitis will further enrich our knowledge of the pathological process of periodontal disease

Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call