The Safety of Adiponectin Receptor Agonist AdipoRon in a Rabbit Model of Arthrofibrosis.


Journal

Tissue engineering. Part C, Methods
ISSN: 1937-3392
Titre abrégé: Tissue Eng Part C Methods
Pays: United States
ID NLM: 101466663

Informations de publication

Date de publication:
04 2023
Historique:
pmc-release: 01 04 2024
medline: 18 4 2023
pubmed: 17 3 2023
entrez: 16 3 2023
Statut: ppublish

Résumé

AdipoRon is an adiponectin receptor 1, 2 (ADIPOR1 and ADIPOR2) agonist with numerous reported physiological benefits in murine models of human disease, including a proposed reduction in fibrosis. However, AdipoRon has never been investigated in rabbits, which provide a robust model for orthopedic conditions. We examined the safety of intravenous (IV) AdipoRon in New Zealand White (NZW) female rabbits surgically stressed by a procedure that mimics human arthrofibrosis. Fifteen female NZW rabbits were prospectively studied using increasing AdipoRon doses based on established literature. AdipoRon was dissolved in dimethyl sulfoxide (DMSO), diluted in normal saline, and administered IV preoperatively and for 5 subsequent days postoperatively. The primary outcome was overall toxicity to rabbits, whereas secondary outcomes were change in rabbit weights and hemodynamics and defining acid-base characteristics of the drug formulation. Two rabbits expired during preoperative drug administration at 25 mg/kg. Remaining rabbits received preoperative doses of DMSO (vehicle), 2.5, 5, or 10 mg/kg of AdipoRon without complications. On postoperative day 1, one rabbit sustained a tonic-clonic seizure after their second dose of 10 mg/kg AdipoRon. The remaining 12 rabbits (4 in each group) received six serial doses of vehicle, 2.5, or 5 mg/kg of AdipoRon without adverse effects. All formulations of AdipoRon were within safe physiological pH ranges (4-5). We are the first to report the use of IV AdipoRon in a surgically stressed rabbit model of orthopedic disease. AdipoRon doses of 5 mg/kg or less appear to be well-tolerated in female NZW rabbits. Impact statement We provided the first

Identifiants

pubmed: 36924279
doi: 10.1089/ten.TEC.2023.0008
pmc: PMC10122264
doi:

Substances chimiques

AdipoRon 0
Receptors, Adiponectin 0
Adiponectin 0
Dimethyl Sulfoxide YOW8V9698H
Piperidines 0

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

154-159

Subventions

Organisme : NIAMS NIH HHS
ID : P30 AR076312
Pays : United States
Organisme : NIAMS NIH HHS
ID : R01 AR072597
Pays : United States
Organisme : NIAMS NIH HHS
ID : R01 AR073147
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL147155
Pays : United States

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Auteurs

Harold I Salmons (HI)

Department of Orthopedic Surgery and Mayo Clinic, Rochester, Minnesota, USA.

Christopher Gow (C)

Department of Comparative Medicine, Mayo Clinic, Rochester, Minnesota, USA.

Afton K Limberg (AK)

Department of Orthopedic Surgery and Mayo Clinic, Rochester, Minnesota, USA.

Jacob W Bettencourt (JW)

Department of Orthopedic Surgery and Mayo Clinic, Rochester, Minnesota, USA.

Mason F Carstens (MF)

Department of Orthopedic Surgery and Mayo Clinic, Rochester, Minnesota, USA.

Ashley N Payne (AN)

Department of Orthopedic Surgery and Mayo Clinic, Rochester, Minnesota, USA.

Mark E Morrey (ME)

Department of Orthopedic Surgery and Mayo Clinic, Rochester, Minnesota, USA.

Joaquin Sanchez-Sotelo (J)

Department of Orthopedic Surgery and Mayo Clinic, Rochester, Minnesota, USA.

Daniel J Berry (DJ)

Department of Orthopedic Surgery and Mayo Clinic, Rochester, Minnesota, USA.

Amel Dudakovic (A)

Department of Orthopedic Surgery and Mayo Clinic, Rochester, Minnesota, USA.

Matthew P Abdel (MP)

Department of Orthopedic Surgery and Mayo Clinic, Rochester, Minnesota, USA.

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Classifications MeSH