Quercetin decreases the activity of matrix metalloproteinase-2 and ameliorates vascular remodeling in renovascular hypertension

Increased activity of matrix metalloproteinase (MMP)-2 is observed in aortas of different models of hypertension, and its activation is directly mediated by oxidative stress. As quercetin is an important flavonoid with significant antioxidant effects, the hypothesis here is that quercetin will reduc...

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Published inAtherosclerosis Vol. 270; pp. 146 - 153
Main Authors Pereira, Sherliane C., Parente, Juliana M., Belo, Vanessa A., Mendes, Atlante S., Gonzaga, Natália A., do Vale, Gabriel T., Ceron, Carla S., Tanus-Santos, José Eduardo, Tirapelli, Carlos R., Castro, Michele M.
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LanguageEnglish
Published Ireland Elsevier B.V 01.03.2018
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Abstract Increased activity of matrix metalloproteinase (MMP)-2 is observed in aortas of different models of hypertension, and its activation is directly mediated by oxidative stress. As quercetin is an important flavonoid with significant antioxidant effects, the hypothesis here is that quercetin will reduce increased MMP-2 activity by decreasing oxidative stress in aortas of hypertensive rats and then ameliorate hypertension-induced vascular remodeling. Male two-kidney one-clip (2K1C) hypertensive Wistar rats and controls were treated with quercetin (10 mg/kg/day) or its vehicle for three weeks by gavage. Rats were then analyzed at five weeks of hypertension. Systolic blood pressure (SBP) was determined by tail-cuff plethysmography. Aortas were used to determine MMP activity by in situ zymography and reactive oxygen species (ROS) levels by dihydroethidium. Western blot was performed to detect focal adhesion kinase (FAK) and phosphorylated-FAK levels. SBP was increased in 2K1C rats and only a borderline reduction in SBP was observed after treating 2K1C rats with quercetin. Cross-sectional area and the number of vascular smooth muscle cells were significantly increased in aortas of hypertensive rats, and quercetin reduced them. Quercetin reduced ROS levels in aortas of 2K1C rats and the increased activity of gelatinases in situ. However, quercetin did not affect the levels of tissue inhibitor of MMP (TIMP)-2 and did not interfere with FAK and p-FAK levels in aortas of hypertensive rats. Furthermore, different concentrations of quercetin did not directly reduce the activity of human recombinant MMP-2 in vitro. Quercetin reduces hypertension-induced vascular remodeling, oxidative stress and MMP-2 activity in aortas. •Quercetin decreased the number of vascular smooth muscle cells and increased aortic cross-sectional area in hypertension.•Quercetin reduces NAD(P)H oxidase activity and superoxide anion in hypertensive rats.•Quercetin reduced MMP-2 activity in aorta of hypertensive rats and its effect in hyperplasia of vascular smooth muscle cells.•Quercetin did not significantly reduce systolic blood pressure in hypertension although it ameliorated vascular remodeling.
AbstractList BACKGROUND AND AIMSIncreased activity of matrix metalloproteinase (MMP)-2 is observed in aortas of different models of hypertension, and its activation is directly mediated by oxidative stress. As quercetin is an important flavonoid with significant antioxidant effects, the hypothesis here is that quercetin will reduce increased MMP-2 activity by decreasing oxidative stress in aortas of hypertensive rats and then ameliorate hypertension-induced vascular remodeling.METHODSMale two-kidney one-clip (2K1C) hypertensive Wistar rats and controls were treated with quercetin (10 mg/kg/day) or its vehicle for three weeks by gavage. Rats were then analyzed at five weeks of hypertension. Systolic blood pressure (SBP) was determined by tail-cuff plethysmography. Aortas were used to determine MMP activity by in situ zymography and reactive oxygen species (ROS) levels by dihydroethidium. Western blot was performed to detect focal adhesion kinase (FAK) and phosphorylated-FAK levels.RESULTSSBP was increased in 2K1C rats and only a borderline reduction in SBP was observed after treating 2K1C rats with quercetin. Cross-sectional area and the number of vascular smooth muscle cells were significantly increased in aortas of hypertensive rats, and quercetin reduced them. Quercetin reduced ROS levels in aortas of 2K1C rats and the increased activity of gelatinases in situ. However, quercetin did not affect the levels of tissue inhibitor of MMP (TIMP)-2 and did not interfere with FAK and p-FAK levels in aortas of hypertensive rats. Furthermore, different concentrations of quercetin did not directly reduce the activity of human recombinant MMP-2 in vitro.CONCLUSIONSQuercetin reduces hypertension-induced vascular remodeling, oxidative stress and MMP-2 activity in aortas.
Increased activity of matrix metalloproteinase (MMP)-2 is observed in aortas of different models of hypertension, and its activation is directly mediated by oxidative stress. As quercetin is an important flavonoid with significant antioxidant effects, the hypothesis here is that quercetin will reduce increased MMP-2 activity by decreasing oxidative stress in aortas of hypertensive rats and then ameliorate hypertension-induced vascular remodeling. Male two-kidney one-clip (2K1C) hypertensive Wistar rats and controls were treated with quercetin (10 mg/kg/day) or its vehicle for three weeks by gavage. Rats were then analyzed at five weeks of hypertension. Systolic blood pressure (SBP) was determined by tail-cuff plethysmography. Aortas were used to determine MMP activity by in situ zymography and reactive oxygen species (ROS) levels by dihydroethidium. Western blot was performed to detect focal adhesion kinase (FAK) and phosphorylated-FAK levels. SBP was increased in 2K1C rats and only a borderline reduction in SBP was observed after treating 2K1C rats with quercetin. Cross-sectional area and the number of vascular smooth muscle cells were significantly increased in aortas of hypertensive rats, and quercetin reduced them. Quercetin reduced ROS levels in aortas of 2K1C rats and the increased activity of gelatinases in situ. However, quercetin did not affect the levels of tissue inhibitor of MMP (TIMP)-2 and did not interfere with FAK and p-FAK levels in aortas of hypertensive rats. Furthermore, different concentrations of quercetin did not directly reduce the activity of human recombinant MMP-2 in vitro. Quercetin reduces hypertension-induced vascular remodeling, oxidative stress and MMP-2 activity in aortas. •Quercetin decreased the number of vascular smooth muscle cells and increased aortic cross-sectional area in hypertension.•Quercetin reduces NAD(P)H oxidase activity and superoxide anion in hypertensive rats.•Quercetin reduced MMP-2 activity in aorta of hypertensive rats and its effect in hyperplasia of vascular smooth muscle cells.•Quercetin did not significantly reduce systolic blood pressure in hypertension although it ameliorated vascular remodeling.
Increased activity of matrix metalloproteinase (MMP)-2 is observed in aortas of different models of hypertension, and its activation is directly mediated by oxidative stress. As quercetin is an important flavonoid with significant antioxidant effects, the hypothesis here is that quercetin will reduce increased MMP-2 activity by decreasing oxidative stress in aortas of hypertensive rats and then ameliorate hypertension-induced vascular remodeling. Male two-kidney one-clip (2K1C) hypertensive Wistar rats and controls were treated with quercetin (10 mg/kg/day) or its vehicle for three weeks by gavage. Rats were then analyzed at five weeks of hypertension. Systolic blood pressure (SBP) was determined by tail-cuff plethysmography. Aortas were used to determine MMP activity by in situ zymography and reactive oxygen species (ROS) levels by dihydroethidium. Western blot was performed to detect focal adhesion kinase (FAK) and phosphorylated-FAK levels. SBP was increased in 2K1C rats and only a borderline reduction in SBP was observed after treating 2K1C rats with quercetin. Cross-sectional area and the number of vascular smooth muscle cells were significantly increased in aortas of hypertensive rats, and quercetin reduced them. Quercetin reduced ROS levels in aortas of 2K1C rats and the increased activity of gelatinases in situ. However, quercetin did not affect the levels of tissue inhibitor of MMP (TIMP)-2 and did not interfere with FAK and p-FAK levels in aortas of hypertensive rats. Furthermore, different concentrations of quercetin did not directly reduce the activity of human recombinant MMP-2 in vitro. Quercetin reduces hypertension-induced vascular remodeling, oxidative stress and MMP-2 activity in aortas.
Author Belo, Vanessa A.
do Vale, Gabriel T.
Gonzaga, Natália A.
Ceron, Carla S.
Parente, Juliana M.
Mendes, Atlante S.
Castro, Michele M.
Pereira, Sherliane C.
Tirapelli, Carlos R.
Tanus-Santos, José Eduardo
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  givenname: Carla S.
  surname: Ceron
  fullname: Ceron, Carla S.
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  givenname: José Eduardo
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  givenname: Carlos R.
  surname: Tirapelli
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Keywords Vascular remodeling
Hypertension
Oxidative stress
Matrix metalloproteinase
Antioxidant
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Snippet Increased activity of matrix metalloproteinase (MMP)-2 is observed in aortas of different models of hypertension, and its activation is directly mediated by...
BACKGROUND AND AIMSIncreased activity of matrix metalloproteinase (MMP)-2 is observed in aortas of different models of hypertension, and its activation is...
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SubjectTerms Animals
Antioxidant
Antioxidants - pharmacology
Aorta - drug effects
Aorta - enzymology
Aorta - pathology
Aorta - physiopathology
Disease Models, Animal
Focal Adhesion Kinase 1 - metabolism
Hypertension
Hypertension, Renovascular - drug therapy
Hypertension, Renovascular - enzymology
Hypertension, Renovascular - pathology
Hypertension, Renovascular - physiopathology
Male
Matrix metalloproteinase
Matrix Metalloproteinase 2 - metabolism
Oxidative stress
Oxidative Stress - drug effects
Phosphorylation
Quercetin - pharmacology
Rats, Wistar
Reactive Oxygen Species - metabolism
Signal Transduction - drug effects
Vascular remodeling
Vascular Remodeling - drug effects
Title Quercetin decreases the activity of matrix metalloproteinase-2 and ameliorates vascular remodeling in renovascular hypertension
URI https://dx.doi.org/10.1016/j.atherosclerosis.2018.01.031
https://www.ncbi.nlm.nih.gov/pubmed/29425960
https://search.proquest.com/docview/2001062955
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