Effect of Atorvastatin, Curcumin, and Quercetin on miR-21 and miR-122 and their correlation with TGFβ1 expression in experimental liver fibrosis

Liver fibrosis is an inflammatory and fibrogenic process that occurs following chronic liver damage. TGFβ1 is the key inducer of fibrosis. MiR-21 and miR-122 are two miRNAs that their expression changes during fibrosis. In the present study, we investigate the effects of curcumin, quercetin, and ato...

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Published inLife sciences (1973) Vol. 259; p. 118293
Main Authors Nozari, Elham, Moradi, Ali, Samadi, Morteza
Format Journal Article
LanguageEnglish
Published New York Elsevier Inc 15.10.2020
Elsevier BV
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Abstract Liver fibrosis is an inflammatory and fibrogenic process that occurs following chronic liver damage. TGFβ1 is the key inducer of fibrosis. MiR-21 and miR-122 are two miRNAs that their expression changes during fibrosis. In the present study, we investigate the effects of curcumin, quercetin, and atorvastatin on the expression levels of miR-21 and miR-122 and evaluated their correlation with TGFβ1 expression in bile duct ligation (BDL)-induced fibrotic rats. Thirty two adult male Wistar rats were divided into 8 groups (n = 8 for each): Sham, Sham + curcumin (100 mg/kg/day), Sham + quercetin (30 mg/kg/day), Sham + atorvastatin (15 mg/kg/day), BDL, BDL + curcumin, BDL + quercetin, BDL + atorvastatin and treated for four weeks via oral gavage. The expression of miR-21, miR-122, and TGFβ1 was evaluated via RT-qPCR. The expression levels of TGFβ1 and miR-21 were significantly increased in the BDL group compared to the Sham group (P < 0.05), but the expression of miR-122 was significantly decreased in the BDL group compared to the Sham group (P < 0.05). Curcumin, quercetin, and atorvastatin treatment lead to down-regulation of miR-21 and TGFβ1 and up-regulation of miR-122 in the BDL groups. There was no significant difference between these drugs in altering gene expression and all had the same effects. Moreover, a direct significant correlation was observed between mir-21 and TGFβ1 and an inverse significant correlation between mir-122 and TGFβ1 expression. In summary, targeting these molecular pathways may partially prevent the progression of liver fibrosis.
AbstractList AIMSLiver fibrosis is an inflammatory and fibrogenic process that occurs following chronic liver damage. TGFβ1 is the key inducer of fibrosis. MiR-21 and miR-122 are two miRNAs that their expression changes during fibrosis. In the present study, we investigate the effects of curcumin, quercetin, and atorvastatin on the expression levels of miR-21 and miR-122 and evaluated their correlation with TGFβ1 expression in bile duct ligation (BDL)-induced fibrotic rats. MATERIALS AND METHODSThirty two adult male Wistar rats were divided into 8 groups (n = 8 for each): Sham, Sham + curcumin (100 mg/kg/day), Sham + quercetin (30 mg/kg/day), Sham + atorvastatin (15 mg/kg/day), BDL, BDL + curcumin, BDL + quercetin, BDL + atorvastatin and treated for four weeks via oral gavage. The expression of miR-21, miR-122, and TGFβ1 was evaluated via RT-qPCR. KEY FINDINGSThe expression levels of TGFβ1 and miR-21 were significantly increased in the BDL group compared to the Sham group (P < 0.05), but the expression of miR-122 was significantly decreased in the BDL group compared to the Sham group (P < 0.05). Curcumin, quercetin, and atorvastatin treatment lead to down-regulation of miR-21 and TGFβ1 and up-regulation of miR-122 in the BDL groups. There was no significant difference between these drugs in altering gene expression and all had the same effects. Moreover, a direct significant correlation was observed between mir-21 and TGFβ1 and an inverse significant correlation between mir-122 and TGFβ1 expression. SIGNIFICANCEIn summary, targeting these molecular pathways may partially prevent the progression of liver fibrosis.
Liver fibrosis is an inflammatory and fibrogenic process that occurs following chronic liver damage. TGFβ1 is the key inducer of fibrosis. MiR-21 and miR-122 are two miRNAs that their expression changes during fibrosis. In the present study, we investigate the effects of curcumin, quercetin, and atorvastatin on the expression levels of miR-21 and miR-122 and evaluated their correlation with TGFβ1 expression in bile duct ligation (BDL)-induced fibrotic rats. Thirty two adult male Wistar rats were divided into 8 groups (n = 8 for each): Sham, Sham + curcumin (100 mg/kg/day), Sham + quercetin (30 mg/kg/day), Sham + atorvastatin (15 mg/kg/day), BDL, BDL + curcumin, BDL + quercetin, BDL + atorvastatin and treated for four weeks via oral gavage. The expression of miR-21, miR-122, and TGFβ1 was evaluated via RT-qPCR. The expression levels of TGFβ1 and miR-21 were significantly increased in the BDL group compared to the Sham group (P < 0.05), but the expression of miR-122 was significantly decreased in the BDL group compared to the Sham group (P < 0.05). Curcumin, quercetin, and atorvastatin treatment lead to down-regulation of miR-21 and TGFβ1 and up-regulation of miR-122 in the BDL groups. There was no significant difference between these drugs in altering gene expression and all had the same effects. Moreover, a direct significant correlation was observed between mir-21 and TGFβ1 and an inverse significant correlation between mir-122 and TGFβ1 expression. In summary, targeting these molecular pathways may partially prevent the progression of liver fibrosis.
Aims Liver fibrosis is an inflammatory and fibrogenic process that occurs following chronic liver damage. TGFβ1 is the key inducer of fibrosis. MiR-21 and miR-122 are two miRNAs that their expression changes during fibrosis. In the present study, we investigate the effects of curcumin, quercetin, and atorvastatin on the expression levels of miR-21 and miR-122 and evaluated their correlation with TGFβ1 expression in bile duct ligation (BDL)-induced fibrotic rats. Materials and methods Thirty two adult male Wistar rats were divided into 8 groups (n = 8 for each): Sham, Sham + curcumin (100 mg/kg/day), Sham + quercetin (30 mg/kg/day), Sham + atorvastatin (15 mg/kg/day), BDL, BDL + curcumin, BDL + quercetin, BDL + atorvastatin and treated for four weeks via oral gavage. The expression of miR-21, miR-122, and TGFβ1 was evaluated via RT-qPCR. Key findings The expression levels of TGFβ1 and miR-21 were significantly increased in the BDL group compared to the Sham group (P < 0.05), but the expression of miR-122 was significantly decreased in the BDL group compared to the Sham group (P < 0.05). Curcumin, quercetin, and atorvastatin treatment lead to down-regulation of miR-21 and TGFβ1 and up-regulation of miR-122 in the BDL groups. There was no significant difference between these drugs in altering gene expression and all had the same effects. Moreover, a direct significant correlation was observed between mir-21 and TGFβ1 and an inverse significant correlation between mir-122 and TGFβ1 expression. Significance In summary, targeting these molecular pathways may partially prevent the progression of liver fibrosis.
ArticleNumber 118293
Author Moradi, Ali
Nozari, Elham
Samadi, Morteza
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Quercetin
Atorvastatin
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Liver fibrosis
MiR-122
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  ident: 10.1016/j.lfs.2020.118293_bb0035
  article-title: Curcumin-phospholipid complex: preparation, therapeutic evaluation and pharmacokinetic study in rats
  publication-title: Int. J. Pharm.
  doi: 10.1016/j.ijpharm.2006.09.025
  contributor:
    fullname: Maiti
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Snippet Liver fibrosis is an inflammatory and fibrogenic process that occurs following chronic liver damage. TGFβ1 is the key inducer of fibrosis. MiR-21 and miR-122...
Aims Liver fibrosis is an inflammatory and fibrogenic process that occurs following chronic liver damage. TGFβ1 is the key inducer of fibrosis. MiR-21 and...
AIMSLiver fibrosis is an inflammatory and fibrogenic process that occurs following chronic liver damage. TGFβ1 is the key inducer of fibrosis. MiR-21 and...
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StartPage 118293
SubjectTerms Atorvastatin
Bile
Bile ducts
Correlation
Curcumin
Fibrosis
Gene expression
Inflammation
Liver
Liver fibrosis
MiR-122
MiR-21
Quercetin
Rat
Rodents
TGFβ1
Transforming growth factor-b1
Title Effect of Atorvastatin, Curcumin, and Quercetin on miR-21 and miR-122 and their correlation with TGFβ1 expression in experimental liver fibrosis
URI https://dx.doi.org/10.1016/j.lfs.2020.118293
https://www.proquest.com/docview/2505418456
https://search.proquest.com/docview/2436403197
Volume 259
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