Objective: To provide a systematic review of the effects of the bite-raised condition in animal models, a widespread technique in modern orthodontics. Design: A systematic review of the literature was conducted. Original articles were searched through Pubmed, Cochrane Central database and Embase until December 2018. Results: 242 articles were identified through database searching. After removing the duplicates, 198 articles were screened by reviewing the abstracts. 27 full text articles were assessed for eligibility and, after 7 exclusions, 20 articles were included in the review process. Studies selected by the review process concerned animal models. Histological, molecular, biochemical and electromyographical studies were evaluated. The results, with a high level of agreement in different animals, showed that the bite-raised condition is a source of stress, inducing increased plasma corticosterone, urinary cortisol and HPA axis alterations; it predisposes the organism to react to subsequent stressful stimulation with a significantly greater incretion of glucocorticoids, thus inducing hypersensitivity to novel forms of stress; it affects the structure of the hippocampus, reducing the number of neurons, increasing the number of glial cells and worsening memory and spatial orientation; it alters the electromyographical activity of masticatory muscles. Conclusions: The results of research conducted on animal models do not necessarily apply directly to human beings. More clinical research, with special attention to adolescent patients, is necessary to clarify whether, in humans, the bite-raised condition is accompanied by adverse effects comparable to those observed in animals.

Adverse effects of the bite-raised condition in animal studies: A systematic review

Piancino M. G.
First
;
Tortarolo A.;Cannavale R.;Deregibus A.
Last
2019-01-01

Abstract

Objective: To provide a systematic review of the effects of the bite-raised condition in animal models, a widespread technique in modern orthodontics. Design: A systematic review of the literature was conducted. Original articles were searched through Pubmed, Cochrane Central database and Embase until December 2018. Results: 242 articles were identified through database searching. After removing the duplicates, 198 articles were screened by reviewing the abstracts. 27 full text articles were assessed for eligibility and, after 7 exclusions, 20 articles were included in the review process. Studies selected by the review process concerned animal models. Histological, molecular, biochemical and electromyographical studies were evaluated. The results, with a high level of agreement in different animals, showed that the bite-raised condition is a source of stress, inducing increased plasma corticosterone, urinary cortisol and HPA axis alterations; it predisposes the organism to react to subsequent stressful stimulation with a significantly greater incretion of glucocorticoids, thus inducing hypersensitivity to novel forms of stress; it affects the structure of the hippocampus, reducing the number of neurons, increasing the number of glial cells and worsening memory and spatial orientation; it alters the electromyographical activity of masticatory muscles. Conclusions: The results of research conducted on animal models do not necessarily apply directly to human beings. More clinical research, with special attention to adolescent patients, is necessary to clarify whether, in humans, the bite-raised condition is accompanied by adverse effects comparable to those observed in animals.
2019
107
104516
104524
http://www.journals.elsevier.com/archives-of-oral-biology/
Bite-raising; Hippocampus; Malocclusion; Occlusal disharmony; Occlusal instability; Stress; Animals; Glucocorticoids; Hippocampus; Humans; Neuroglia; Neurons; Dental Occlusion; Hypothalamo-Hypophyseal System; Models, Animal; Pituitary-Adrenal System
Piancino M.G.; Tortarolo A.; Polimeni A.; Cannavale R.; Tonni I.; Deregibus A.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2318/1729509
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