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

IF 2.8 3区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Bruna Pinheiro Pereira, Alessandra Oliveira Silva, Wanessa Mayumi Carvalho 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 Lobo Torres, Fernanda Borges de Araújo Paula, Sílvia Graciela Ruginsk, Carlos Renato Tirapelli, Ellen Rizzi, Carla Speroni Ceron
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引用次数: 0

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.

姜黄素通过减少 MMP-2 和 MMP-9 防止 l-NAME 诱导的高血压对肾脏的损伤
在本研究中,我们探讨了姜黄素是否会干扰l-NAME诱导的高血压模型的主要肾脏特征。为此,我们进行了体外和体内实验,以评估肾脏的炎症、氧化应激和金属蛋白酶(MMPs)表达/活性指标。用 l-NAME(70 毫克/千克/天)诱导高血压,用姜黄素(50 或 100 毫克/千克/天;灌胃)或药物治疗对照组和高血压组的 Wistar 大鼠 14 天。收集血液和肾脏以测定血清肌酐水平、组织学改变、氧化应激、MMPs表达和活性以及ED1表达。l-NAME会升高血压,但两种剂量的姜黄素治疗都会降低血压值;l-NAME会增加肌酐水平、肾小球面积、鲍曼氏间隙、肾脏MMP-2活性以及MMP-9和ED1表达,并减少肾小球数量。姜黄素能阻止肌酐水平和 MMP-2 活性的升高,降低 MMP-2、MMP-9、ED1 和超氧化物的水平,提高超氧化物歧化酶的活性,并部分阻止肾小球的改变。此外,姜黄素还能直接抑制体外 MMP-2 的活性。因此,我们的主要研究结果表明,姜黄素能降低l-NAME诱导的高血压和肾小球改变,抑制MMP-2和MMP-9的表达/活性,减少氧化应激和炎症过程,这可能会间接影响高血压诱导的肾脏结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Cell Biochemistry and Function
Cell Biochemistry and Function 生物-生化与分子生物学
CiteScore
6.20
自引率
0.00%
发文量
93
审稿时长
6-12 weeks
期刊介绍: Cell Biochemistry and Function publishes original research articles and reviews on the mechanisms whereby molecular and biochemical processes control cellular activity with a particular emphasis on the integration of molecular and cell biology, biochemistry and physiology in the regulation of tissue function in health and disease. The primary remit of the journal is on mammalian biology both in vivo and in vitro but studies of cells in situ are especially encouraged. Observational and pathological studies will be considered providing they include a rational discussion of the possible molecular and biochemical mechanisms behind them and the immediate impact of these observations to our understanding of mammalian biology.
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