Co-Nanoencapsulation of Vitamin D 3 and Curcumin Regulates Inflammation and Purine Metabolism in a Model of Arthritis

  • PDF / 1,235,707 Bytes
  • 16 Pages / 595.276 x 790.866 pts Page_size
  • 48 Downloads / 200 Views

DOWNLOAD

REPORT


ORIGINAL ARTICLE

Co-Nanoencapsulation of Vitamin D3 and Curcumin Regulates Inflammation and Purine Metabolism in a Model of Arthritis Jean Lucas G. da Silva,1,2 Daniela F. Passos ,1,2 Viviane M. Bernardes,1,2 Fernanda L. Cabral,1,3 Paulo G. Schimites,1,3 Alessandra G. Manzoni,1,2 Edilene Gadelha de Oliveira,4 Cristiane de Bona da Silva,3 Ruy Carlos Ruver Beck,4 Matheus H. Jantsch,1 Roberto M. Maciel,5 and Daniela B. R. Leal1,2,6

We analyzed the effects of a nanoencapsulated association of curcumin and vitamin D3 on purine metabolism enzymes in neutrophils, lymphocytes, and platelets in a model of adjuvant-induced arthritis (AIA) in rats. Following AIA induction, the animals were treated for 15 days with free and nanoencapsulated curcumin (4 mg/kg), nanocapsules of vitamin D3 (VD3) (15.84 IU/day), a nanoencapsulated combination of curcumin and VD3, vehicle, or blank nanocapsules. The animals were euthanized, and blood was collected to evaluate the activities of E-NTPDase, adenosine deaminase (ADA), and myeloperoxidase (MPO), as well as reactive oxygen species (ROS) levels and biochemical parameters. Also, the liver and kidney were collected for histological analysis. The changes in the activities of purinergic enzymes indicated that inflammation was significantly reverted by vitamin D3 and curcumin co-nanoencapsulation treatments in the arthritic rats. The reduction of inflammation was confirmed by the reduction in the signs and symptoms of AIA, as well as in MPO activity by all formulations. The treatments with nanocapsules reverted histological alterations in the kidney. Serum parameters were not altered by the induction or treatments. Our results suggest that co-nanoencapsulation of vitamin D3 and curcumin is an efficient alternative adjuvant treatment for rheumatoid arthritis as it reverts the changes in the purine metabolism and reduces arthritis-associated inflammation. Abstract—

Electronic supplementary material The online version of this article (https://doi.org/10.1007/s10753-019-01021-1) contains supplementary material, which is available to authorized users. 1

Laboratório de Imunobiologia Experimental e Aplicada (LABIBIO), Departamento de Microbiologia e Parasitologia, Centro de Ciências da Saúde, Universidade Federal de Santa Maria, Av. Roraima, 1000, prédio 20, Santa Maria, RS 97105-900, Brazil 2 Programa de Pós-Graduação em Bioquímica Toxicológica, Centro de Ciências Naturais e Exatas, Universidade Federal de Santa Maria, Santa Maria, RS, Brazil 3 Programa de Pós-Graduação em Ciências Farmacêuticas, Universidade Federal de Santa Maria, Santa Maria, RS, Brazil

4

Programa de Pós-Graduação em Ciências Farmacêuticas, Universidade Federal do Rio Grande do Sul, Porto Alegre, RS, Brazil 5 Departamento de Patologia, Centro de Ciências Naturais e Exatas, Universidade Federal de Santa Maria, Santa Maria, RS, Brazil 6 To whom correspondence should be addressed at Laboratório de Imunobiologia Experimental e Aplicada (LABIBIO), Departamento de Microbiologia e Parasitologia, Centro de Ciências da Saúde, Univer