2016
DOI: 10.1016/j.bjoms.2016.01.022
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Rabbit model for osteoarthrosis of the temporomandibular joint as a basis for assessment of outcomes after intervention

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Cited by 12 publications
(13 citation statements)
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“…An example of this advantage is the possibility to inject substances intra-articularly without the need to access the joint surgically, and this is one of the reasons why rabbit models have emerged as the animal models of choice for the experimental study of diseases and therapies in the human TMJ [42,43]. In addition, we decided to inject MIA directly into the rabbit joint cavity given the results of previous studies confirming the efficacy of OA induction in the TMJ and important late degenerative changes [36,41,44].…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…An example of this advantage is the possibility to inject substances intra-articularly without the need to access the joint surgically, and this is one of the reasons why rabbit models have emerged as the animal models of choice for the experimental study of diseases and therapies in the human TMJ [42,43]. In addition, we decided to inject MIA directly into the rabbit joint cavity given the results of previous studies confirming the efficacy of OA induction in the TMJ and important late degenerative changes [36,41,44].…”
Section: Discussionmentioning
confidence: 99%
“…CG animals were injected with 50 μL of saline (Fig 1). A 30G needle (8 mm x 0.3 mm) was used to inject the solutions, and the injection site was determined at 5 mm above and distal to the posterior border of the zygomatic process, according to a previously established model [36].…”
Section: Experimental Designmentioning
confidence: 99%
“…The transgenic model cannot completely simulate the pathological process of human OA. The KOA model [ 21 , 22 ] can be rapidly created by injecting papain and collagenase into the joint cavity, which causes cartilage damage, and has been commonly used in cartilage pathology and drug treatment research [ 23 ]. However, because of the effects of anatomic site, joint size, and animal species, the drug dose required for modeling was also somewhat different [ 24 , 25 ].…”
Section: Discussionmentioning
confidence: 99%
“…MIA (Cledes et al;Güler et al;Artuzi et al, 2016) and papain (Yang & Shi) have been used successfully to induce OA in rabbit TMJs in previous studies. The severity of the OA is directly related with the exposure time (Cledes et al) and the concentration of the drug applied (Guingamp et al, 1997;Güler et al).…”
Section: Discussionmentioning
confidence: 99%