Curcumin Prevents Renal Damage of l‐NAME Induced Hypertension in by Reducing MMP‐2 and MMP‐9

姜黄素 氧化应激 基质金属蛋白酶 内分泌学 肌酐 内科学 化学 炎症 肾功能 体内 药理学 超氧化物歧化酶 医学 生物 生物技术
作者
Bruna Pinheiro Pereira,Alessandra Oliveira Silva,Wanessa M.C. Awata,Gustavo Félix Pimenta,Jéssyca Milene Ribeiro,Carolina Aparecida de Faria Almeida,Carla Renata Kitanishi Antonietto,Luis Felipe Cunha dos Reis,Alessandra Esteves,Larissa Helena Torres,Fernanda Borges de Araújo Paula,Sílvia Graciela Ruginsk,Carlos R. Tirapelli,Élen Rizzi,Carla S. Ceron
出处
期刊:Cell Biochemistry and Function [Wiley]
卷期号:42 (7)
标识
DOI:10.1002/cbf.4119
摘要

ABSTRACT In the present study, we investigated whether curcumin administration would interfere with the main renal features of l ‐NAME‐induced hypertension model. For this purpose, we conducted both in vitro and in vivo experiments to evaluate renal indicators of inflammation, oxidative stress, and metalloproteinases (MMPs) expression/activity. Hypertension was induced by l ‐NAME (70 mg/kg/day), and Wistar rats from both control and hypertensive groups were treated with curcumin (50 or 100 mg/kg/day; gavage) or vehicle for 14 days. Blood and kidneys were collected to determine serum creatinine levels, histological alterations, oxidative stress, MMPs expression and activity, and ED1 expression. l ‐NAME increased blood pressure, but both doses of curcumin treatment reduced these values. l ‐NAME treatment increased creatinine levels, glomeruli area, Bowman's space, kidney MMP‐2 activity, as well as MMP‐9 and ED1 expression, and reduced the number of glomeruli. Curcumin treatment prevented the increase in creatinine levels, MMP‐2 activity, and reduced MMP‐2, MMP‐9, ED1, and superoxide levels, as well as increased superoxide dismutase activity and partially prevented glomeruli alterations. Moreover, curcumin directly inhibited MMP‐2 activity in vitro. Thus, our main findings demonstrate that curcumin reduced l ‐NAME‐induced hypertension and renal glomerular alterations, inhibited MMP‐2 and MMP‐9 expression/activity, and reduced oxidative stress and inflammatory processes, which may indirectly impact hypertension‐induced renal outcomes.

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