Evaluation of monosodium iodoacetate dosage to induce knee osteoarthritis: Relation with oxidative stress and pain

被引:32
作者
Yamada, Eloa Ferreira [1 ]
Salgueiro, Andreia Fernandes [1 ]
Goulart, Aline da Silva [1 ]
Mendes, Vanessa Pereira [2 ]
Anjos, Bruno Leite [2 ]
Folmer, Vanderlei [1 ]
da Silva, Morgana Duarte [1 ]
机构
[1] Univ Fed Pampa Unipampa, Postgrad Program Biochem, Uruguaiana, Brazil
[2] Univ Fed Pampa Unipampa, Vet Pathol Lab, Uruguaiana, Brazil
关键词
articular damage; knee osteoarthritis; monosodium iodoacetate; oxidative stress; pain; MODEL; BEHAVIOR; DISEASE; DAMAGE; JOINT; RATS; HYPERALGESIA; MECHANISMS; ARTHRITIS; CARTILAGE;
D O I
10.1111/1756-185X.13450
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aim To determine the dose of monosodium iodoacetate (MIA) required to induce oxidative stress, as well as pain and edema; to confirm the induction of knee osteoarthritis (OA) symptoms in rats by the presence of reactive oxygen species (ROS) and reduction of antioxidant agents; and to verify the presence of histopathological injury in these affected joints. Method Biological markers of oxidative stress, pain, knee edema, and cartilage degeneration provided by different doses of MIA (0.5; 1.0 or 1.5 mg) in rat knee joints were analyzed. The animal evaluations were conducted during 15 days for mechanical and cold hypersensitivity, spontaneous pain and edema. After that, blood serum, intra-articular lavage and structures of knee, spinal cord and brainstem were collected for biochemical analysis; moreover, the knees were removed for histological evaluation. Results This study demonstrates that the highest dose of MIA (1.5 mg) increased the oxidative stress markers and reduced the antioxidant reactions, both in the focus of the lesion and in distant sites. MIA also induced the inflammatory process, characterized by pain, edema, increase in neutrophil count and articular damage. Conclusion This model provides a basis for the exploration of underlying mechanisms in OA and the identification of mechanisms that may guide therapy and the discovery of OA signals and symptoms.
引用
收藏
页码:399 / 410
页数:12
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