Study of the Early Effects of Chitosan Nanoparticles with Glutathione in Rats with Osteoarthrosis

Author:

Ramírez-Noguera Patricia1ORCID,Zetina Marín Iliane1,Gómez Chavarin Blanca Margarita2,Valderrama Moisés Eduardo3,López-Barrera Laura Denise1ORCID,Díaz-Torres Roberto1ORCID

Affiliation:

1. Multidisciplinary Research Unit, Facultad de Estudios Superiores Cuautitlán, Universidad Nacional Autónoma de México, Carretera Cuautitlán-Teoloyucan Km. 2.5, San Sebastián Xhala, Cuautitlán Izcalli CP 54714, Mexico

2. School of Medicine, Universidad Nacional Autónoma de México, Circuito Interior, Ciudad Universitaria, Av. Universidad 3000, Mexico City CP 04510, Mexico

3. Equine Hospital, Facultad de Estudios Superiores Cuautitlán, Universidad Nacional Autónoma de México, Carretera Cuautitlán-Teoloyucan Km. 2.5, San Sebastián Xhala, Cuautitlán Izcalli CP 54714, Mexico

Abstract

Due to cartilage’s limited capacity for regeneration, numerous studies have been conducted to find new drugs that modify osteoarthrosis’s progression. Some evidence showed the capability of chitosan nanoparticles with glutathione (Np-GSH) to regulate the oxide-redox status in vitro in human chondrocytes. This work aimed to evaluate the capacity of Np-GSH in vivo, using Wistar rats with induced surgical osteoarthritis. Radiographic, biochemical (GSH and TBARS quantification), histopathological, and immunohistochemical (Col-2 and MMP-13) analyses were performed to evaluate the progress of the osteoarthritic lesions after the administration of a single dose of Np-GSH. According to the results obtained, the GSH contained in the NPs could be vectored to chondrocytes and used by the cell to modulate the oxidative state reduction, decreasing the production of ROS and free radicals induced by agents oxidizing xenobiotics, increasing GSH levels, as well as the activity of GPx, and decreasing lipid peroxidation. These results are significant since the synthesis of GSH develops exclusively in the cell cytoplasm, and its quantity under an oxidation–reduction imbalance may be defective. Therefore, the results allow us to consider these nanostructures as a helpful study tool to reduce the damage associated with oxidative stress in various diseases such as osteoarthritis.

Funder

Universidad Nacional Autónoma de México

Facultad de Estudios Superiores Cuautitlán, UNAM Cátedra de Investigación

Publisher

MDPI AG

Subject

Pharmaceutical Science

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