TY - JOUR
T1 - Hesperidin Methylchalcone Suppresses Experimental Gout Arthritis in Mice by Inhibiting NF-κB Activation
AU - Ruiz-Miyazawa, Kenji W.
AU - Pinho-Ribeiro, Felipe A.
AU - Borghi, Sergio M.
AU - Staurengo-Ferrari, Larissa
AU - Fattori, Victor
AU - Amaral, Flavio A.
AU - Teixeira, Mauro M.
AU - Alves-Filho, Jose C.
AU - Cunha, Thiago M.
AU - Cunha, Fernando Q.
AU - Casagrande, Rubia
AU - Verri, Waldiceu A.
N1 - Funding Information:
This work was supported by grants from Coordenadoria de Aperfeico̧ amento de Pessoal de Niv́ el Superior (CAPES), Financiadora de Estudo e Projetos−Apoio à Infraestrutura (CT-INFRA 01/2011; process 01.13.0049.00), Central Multi-usuaŕ ia de Laboratorioś de Pesquisa da UEL (CMLP-UEL), Saõ Paulo Research Foundation (FAPESP), Center for Research on Inflammatory Diseases (CRID), Conselho Nacional de Desenvolvimento Cientifí co e Tecnologicó (CNPq), Pesquisa para o Sistema Único de Saudé(PPSUS) grant supported by Ministerío da Ciê Tecnologia e Inovaca̧ ̃o (MCTI), Secretaria da Ciencia, Tecnologia e Ensino Superior (SETI), Decit/SCTIE/MS through CNPq with the support of Fundaca̧ õ Araucaŕ ia and Secretaria da Saudé do Estado do Paraná (SESA-PR), and Parana State Government (Brazil).
Publisher Copyright:
© 2018 American Chemical Society.
PY - 2018/6/27
Y1 - 2018/6/27
N2 - Gout arthritis is a painful inflammatory disease induced by monosodium urate (MSU) crystals. We evaluate the therapeutic potential of the flavonoid hesperidin methylchalcone (HMC) in a mouse model of gout arthritis induced by intra-articular injection of MSU (100 μg/10 μL). Orally given HMC (3-30 mg/kg, 100 μL) reduced in a dose-dependent manner the MSU-induced hyperalgesia (44%, p < 0.05), edema (54%, p < 0.05), and leukocyte infiltration (70%, p < 0.05). HMC (30 mg/kg) inhibited MSU-induced infiltration of LysM-eGFP+ cells (81%, p < 0.05), synovitis (76%, p < 0.05), and oxidative stress (increased GSH, FRAP, and ABTS by 62, 78, and 73%, respectively; reduced O2- and NO by 89 and 48%, p < 0.05) and modulated cytokine production (reduced IL-1β, TNF-α, IL-6, and IL-10 by 35, 72, 37, and 46%, respectively, and increased TGF-β by 90%, p < 0.05). HMC also inhibited MSU-induced NF-κB activation (41%, p < 0.05), gp91phox (66%, p < 0.05) and NLRP3 inflammasome components mRNA expression in vivo (72, 77, 71, and 73% for NLRP3, ASC, pro-caspase-1, and pro-IL-1 β, respectively, p < 0.05), and induced Nrf2/HO-1 mRNA expression (3.9- and 5.1-fold increase, respectively, p < 0.05). HMC (30, 100, and 300 μM) did not inhibit IL-1β secretion by macrophages primed by LPS and challenged with MSU (450 μg/mL), demonstrating that the anti-inflammatory effect of HMC in gout arthritis depends on inhibiting NF-κB but not on direct inhibition of inflammasome. The pharmacological effects of HMC indicate its therapeutic potential for the treatment of gout.
AB - Gout arthritis is a painful inflammatory disease induced by monosodium urate (MSU) crystals. We evaluate the therapeutic potential of the flavonoid hesperidin methylchalcone (HMC) in a mouse model of gout arthritis induced by intra-articular injection of MSU (100 μg/10 μL). Orally given HMC (3-30 mg/kg, 100 μL) reduced in a dose-dependent manner the MSU-induced hyperalgesia (44%, p < 0.05), edema (54%, p < 0.05), and leukocyte infiltration (70%, p < 0.05). HMC (30 mg/kg) inhibited MSU-induced infiltration of LysM-eGFP+ cells (81%, p < 0.05), synovitis (76%, p < 0.05), and oxidative stress (increased GSH, FRAP, and ABTS by 62, 78, and 73%, respectively; reduced O2- and NO by 89 and 48%, p < 0.05) and modulated cytokine production (reduced IL-1β, TNF-α, IL-6, and IL-10 by 35, 72, 37, and 46%, respectively, and increased TGF-β by 90%, p < 0.05). HMC also inhibited MSU-induced NF-κB activation (41%, p < 0.05), gp91phox (66%, p < 0.05) and NLRP3 inflammasome components mRNA expression in vivo (72, 77, 71, and 73% for NLRP3, ASC, pro-caspase-1, and pro-IL-1 β, respectively, p < 0.05), and induced Nrf2/HO-1 mRNA expression (3.9- and 5.1-fold increase, respectively, p < 0.05). HMC (30, 100, and 300 μM) did not inhibit IL-1β secretion by macrophages primed by LPS and challenged with MSU (450 μg/mL), demonstrating that the anti-inflammatory effect of HMC in gout arthritis depends on inhibiting NF-κB but not on direct inhibition of inflammasome. The pharmacological effects of HMC indicate its therapeutic potential for the treatment of gout.
KW - cytokines
KW - gout arthritis
KW - NF-κB
KW - NLRP3 inflammasome
KW - oxidative stress
UR - http://www.scopus.com/inward/record.url?scp=85048043774&partnerID=8YFLogxK
U2 - 10.1021/acs.jafc.8b00959
DO - 10.1021/acs.jafc.8b00959
M3 - Article
C2 - 29852732
AN - SCOPUS:85048043774
SN - 0021-8561
VL - 66
SP - 6269
EP - 6280
JO - Journal of Agricultural and Food Chemistry
JF - Journal of Agricultural and Food Chemistry
IS - 25
ER -