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

IF 2.7 4区 医学 Q3 CELL & TISSUE ENGINEERING Tissue engineering. Part C, Methods Pub Date : 2023-04-01 DOI:10.1089/ten.TEC.2023.0008
Harold I Salmons, Christopher Gow, Afton K Limberg, Jacob W Bettencourt, Mason F Carstens, Ashley N Payne, Mark E Morrey, Joaquin Sanchez-Sotelo, Daniel J Berry, Amel Dudakovic, Matthew P Abdel
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Abstract

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 in vivo toxicity assessment and dose optimization of a new antifibrotic experimental medication, AdipoRon, in a surgically stressed rabbit model of knee arthrofibrosis.

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脂肪素受体激动剂 AdipoRon 在兔关节纤维化模型中的安全性
AdipoRon 是一种脂肪连接素受体 1 和 2(ADIPOR1 和 ADIPOR2)激动剂,据报道在人类疾病的小鼠模型中具有许多生理益处,包括减少纤维化。然而,AdipoRon 从未在兔子身上进行过研究,而兔子是骨科疾病的可靠模型。我们研究了在新西兰白(NZW)雌性兔子体内静脉注射 AdipoRon 的安全性。根据已有的文献资料,对 15 只雌性新西兰白兔进行了前瞻性研究,使用的 AdipoRon 剂量不断增加。AdipoRon溶于二甲基亚砜(DMSO),用生理盐水稀释,术前静脉注射,术后连续注射5天。主要结果是兔子的总体毒性,次要结果是兔子体重和血液动力学的变化以及药物制剂的酸碱特性。两只兔子在术前注射 25 毫克/千克的药物时死亡。其余兔子术前接受了二甲基亚砜(载体)、2.5、5 或 10 毫克/千克 AdipoRon 的剂量,未出现并发症。术后第 1 天,一只兔子在第二次服用 10 毫克/千克 AdipoRon 后出现强直阵挛发作。其余 12 只兔子(每组 4 只)接受了 6 次连续剂量的载体、2.5 或 5 毫克/千克 AdipoRon,均未出现不良反应。所有配方的 AdipoRon 都在安全的生理 pH 值范围内(4-5)。我们首次报告了静脉注射 AdipoRon 在骨科疾病手术应激兔模型中的应用。雌性 NZW 兔子对 5 毫克/千克或更低剂量的 AdipoRon 似乎耐受良好。影响声明 我们首次在膝关节纤维化的手术应激兔模型中对新型抗纤维化实验药物 AdipoRon 进行了体内毒性评估和剂量优化。
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来源期刊
Tissue engineering. Part C, Methods
Tissue engineering. Part C, Methods Medicine-Medicine (miscellaneous)
CiteScore
5.10
自引率
3.30%
发文量
136
期刊介绍: Tissue Engineering is the preeminent, biomedical journal advancing the field with cutting-edge research and applications that repair or regenerate portions or whole tissues. This multidisciplinary journal brings together the principles of engineering and life sciences in the creation of artificial tissues and regenerative medicine. Tissue Engineering is divided into three parts, providing a central forum for groundbreaking scientific research and developments of clinical applications from leading experts in the field that will enable the functional replacement of tissues. Tissue Engineering Methods (Part C) presents innovative tools and assays in scaffold development, stem cells and biologically active molecules to advance the field and to support clinical translation. Part C publishes monthly.
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