Carrageenin-Induced Periodontitis as an Experimental Model in Rats Analyzed by Micro-Computerized Tomography

Periodontitis is a common disease worldwide and is a cause of tooth loss. For these reasons, many investigators have examined periodontitis not only by in vivo studies but also in vitro studies. For in vivo studies, it is very important which animal is used and how to make experimental periodontitis easily and efficiently in animals. Although the process of periodontitis in monkeys and dogs is similar to that in humans, rats and mice are much more useful animals for experiments because of ease of handling and low cost. For the induction of periodontitis, bacterial inoculation and wire ligature methods were examined previously; however, these methods had temporal and technical problems. Therefore, a simple, easy and reliable experimental model for periodontitis using rats and/or mice is required. In this study, the authors attempted to establish a novel experimental model for periodontitis in the rat lower jaw using carrageenin-immersed silk ligature wire, and examined the change of alveolar bone morphology by micro-computerized tomography. As a result, carrageeninimmersed silk ligature wire induced inflammation of the periodontium with severe alveolar bone loss in all experimental rats. In addition, the degree of absorption of the alveolar bone depended on the dosage times of carrageenin treatment. These findings suggested that this experimental model of periodontitis using carrageenin in rats may be a useful experimental model for periodontal research.

[1]  P. Bartold,et al.  Pre-existing periodontitis exacerbates experimental arthritis in a mouse model. , 2011, Journal of clinical periodontology.

[2]  D. Puleo,et al.  Animal Models for Periodontal Disease , 2011, Journal of biomedicine & biotechnology.

[3]  A. Kuijpers-Jagtman,et al.  Inflammatory responses in two commonly used rat models for experimental tooth movement: comparison with ligature-induced periodontitis. , 2011, Archives of oral biology.

[4]  L. Wen,et al.  Micro-computerized tomography analysis of alveolar bone loss in ligature- and nicotine-induced experimental periodontitis in rats. , 2010, Journal of periodontal research.

[5]  Elizabeth A. Novak,et al.  Autoinducer-2 and QseC Control Biofilm Formation and In Vivo Virulence of Aggregatibacter actinomycetemcomitans , 2010, Infection and Immunity.

[6]  M. Onozuka,et al.  Cervical sympathectomy causes alveolar bone loss in an experimental rat model. , 2009, Journal of periodontal research.

[7]  T. Tomofuji,et al.  Preventive effects of a cocoa-enriched diet on gingival oxidative stress in experimental periodontitis. , 2009, Journal of periodontology.

[8]  D. Fairlie,et al.  The use of live-animal micro-computed tomography to determine the effect of a novel phospholipase A2 inhibitor on alveolar bone loss in an in vivo mouse model of periodontitis. , 2009, Journal of periodontal research.

[9]  E. Weiss,et al.  Mouse model of experimental periodontitis induced by Porphyromonas gingivalis/Fusobacterium nucleatum infection: bone loss and host response. , 2009, Journal of clinical periodontology.

[10]  S. Shi,et al.  The miniature pig: a useful large animal model for dental and orofacial research. , 2007, Oral diseases.

[11]  S. Sathishkumar,et al.  Rat Model of Polymicrobial Infection, Immunity, and Alveolar Bone Resorption in Periodontal Disease , 2007, Infection and Immunity.

[12]  K. Tsukinoki,et al.  Restraint stress enhances alveolar bone loss in an experimental rat model. , 2006, Journal of periodontal research.

[13]  K. Niikura,et al.  A novel inhibitor of vacuolar ATPase, FR202126, prevents alveolar bone destruction in experimental periodontitis in rats. , 2005, The Journal of toxicological sciences.

[14]  U. Skalerič,et al.  Measurement of total antioxidant capacity in gingival crevicular fluid and serum in dogs with periodontal disease. , 2004, American journal of veterinary research.

[15]  P. Opstad,et al.  Effects of hypothalamic-pituitary-adrenal axis reactivity on periodontal tissue destruction in rats. , 2000, European journal of oral sciences.

[16]  S. Schou,et al.  Non-human primates used in studies of periodontal disease pathogenesis: a review of the literature. , 1993, Journal of periodontology.

[17]  T. Moyana,et al.  Carrageenan-induced intestinal injury in the rat--a model for inflammatory bowel disease. , 1990, Annals of clinical and laboratory science.

[18]  S. Holt,et al.  Implantation of Bacteroides gingivalis in nonhuman primates initiates progression of periodontitis. , 1988, Science.

[19]  Y. Fukuda,et al.  Induction by degraded carrageenan of colorectal tumors in rats. , 1978, Cancer letters.

[20]  S. Murota,et al.  Effect of salicyclic acid on gluccorticoid receptor in cultured fibroblasts derived from rat carrageenin granuloma. , 1976, Biochimica et biophysica acta.

[21]  H. Löe,et al.  Experimental periodontitis in the beagle dog. , 1973, Journal of periodontal research.

[22]  R. Marcus,et al.  Colonic ulceration in young rats fed degraded carrageenan. , 1971, Lancet.

[23]  D. B. Cater,et al.  Plasminogen activator of the blood vessels in tumours and in carrageenin-induced granulomas. , 1971, British journal of experimental pathology.

[24]  C. Niemegeers,et al.  Effect of various drugs on carrageenin‐induced oedema in the rat hind paw , 1964, The Journal of pharmacy and pharmacology.

[25]  C A WINTER,et al.  Carrageenin-Induced Edema in Hind Paw of the Rat as an Assay for Antiinflammatory Drugs , 1962, Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine.

[26]  Heineken Ts Carrageenan in the management of peptic ulcer. A preliminary report. , 1961 .

[27]  T. Heineken Carrageenan in the management of peptic ulcer. A preliminary report. , 1961, The American journal of gastroenterology.