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Efficacy of ADIPOR1 and ADIPOR2 peptide-agonist AdipoRon in preventing contracture in a rabbit model of arthrofibrosis.
Salmons, Harold I; Carstens, Mason F; Limberg, Afton K; Bettencourt, Jacob W; Payne, Ashley N; Karczewski, Daniel C; Ryan, Zachary T; Morrey, Mark E; Sanchez-Sotelo, Joaquin; Berry, Daniel J; Dudakovic, Amel; Abdel, Matthew P.
  • Salmons HI; Department of Orthopedic Surgery, Mayo Clinic, Rochester, Minnesota, USA.
  • Carstens MF; Department of Orthopedic Surgery, Mayo Clinic, Rochester, Minnesota, USA.
  • Limberg AK; Department of Orthopedic Surgery, Mayo Clinic, Rochester, Minnesota, USA.
  • Bettencourt JW; Department of Orthopedic Surgery, Mayo Clinic, Rochester, Minnesota, USA.
  • Payne AN; Department of Orthopedic Surgery, Mayo Clinic, Rochester, Minnesota, USA.
  • Karczewski DC; Department of Orthopedic Surgery, Mayo Clinic, Rochester, Minnesota, USA.
  • Ryan ZT; Department of Orthopedic Surgery, Mayo Clinic, Rochester, Minnesota, USA.
  • Morrey ME; Department of Orthopedic Surgery, Mayo Clinic, Rochester, Minnesota, USA.
  • Sanchez-Sotelo J; Department of Orthopedic Surgery, Mayo Clinic, Rochester, Minnesota, USA.
  • Berry DJ; Department of Orthopedic Surgery, Mayo Clinic, Rochester, Minnesota, USA.
  • Dudakovic A; Department of Orthopedic Surgery, Mayo Clinic, Rochester, Minnesota, USA.
  • Abdel MP; Department of Orthopedic Surgery, Mayo Clinic, Rochester, Minnesota, USA.
J Orthop Res ; 42(9): 1916-1922, 2024 Sep.
Article en En | MEDLINE | ID: mdl-38605593
ABSTRACT
AdipoRon is an adiponectin receptor 1, 2 (ADIPOR1 and ADIPOR2) agonist with potential antifibrotic effects. Whether AdipoRon can mitigate joint stiffness in a rabbit model of arthrofibrosis is unknown. We examined the efficacy of intravenous (IV) AdipoRon at mitigating contracture in a rabbit model of knee arthrofibrosis. Fifty-six female New Zealand White rabbits were divided into three dosing groups vehicle (dimethyl sulfoxide, DMSO), 2.5 mg/kg AdipoRon, and 5 mg/kg AdipoRon. AdipoRon, in DMSO, was administered IV preoperatively and for 5 days postoperatively (30 rabbits, Aim 1). AdipoRon was again dosed similarly after Kirschner wire (K-wire) removal at 8 weeks (26 rabbits; Aim 2). The primary outcome of joint passive extension angle (PEA,°) was measured at 8, 10, 12, 16, and 24 weeks following index surgery. At 24 weeks, rabbits were euthanized and limbs were harvested to measure posterior capsular stiffness (N cm/°). In Aim 1, the 5 mg/kg treated rabbits had a significant increase in PEA when compared to controls at 16-week (p < 0.05). In Aim 2, the 5 mg/kg treated rabbits had a significant increase in PEA when compared to controls at 10-week (p < 0.05). In both aims, no significant differences were observed at later time points. Capsular stiffness was no different in any group. We are the first to report the efficacy of IV AdipoRon in a rabbit model of arthrofibrosis. We identified a significant dose-dependent decrease in joint PEA at early time points; however, no differences were observed between groups at later time points. Clinical

Significance:

The present investigation provided the first assessment of AdipoRon's efficacy in mitigating knee stiffness in the current gold standard rabbit model of arthrofibrosis. Results of this investigation provided further evidence as to the potential role of AdipoRon as a preventative for arthrofibrosis in large mammals.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Fibrosis / Receptores de Adiponectina Límite: Animals Idioma: En Año: 2024 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Fibrosis / Receptores de Adiponectina Límite: Animals Idioma: En Año: 2024 Tipo del documento: Article