Ursolic Acid Inhibits Collagen Production and Promotes Collagen Degradation in Skin Dermal Fibroblasts: Potential Antifibrotic Effects
Tissue fibrosis, characterized by excessive collagen accumulation, leads to impaired organ function and is a hallmark of various chronic diseases. Fibroblasts play a central role in collagen production and deposition. This study examines the impact of ursolic acid, a pentacyclic triterpenoid compoun...
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Published in | Biomolecules (Basel, Switzerland) Vol. 15; no. 3; p. 365 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
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03.03.2025
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ISSN | 2218-273X 2218-273X |
DOI | 10.3390/biom15030365 |
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Abstract | Tissue fibrosis, characterized by excessive collagen accumulation, leads to impaired organ function and is a hallmark of various chronic diseases. Fibroblasts play a central role in collagen production and deposition. This study examines the impact of ursolic acid, a pentacyclic triterpenoid compound present in various fruits and vegetables, on collagen homeostasis in primary human dermal fibroblasts. Ursolic acid (UA) was observed to significantly reduce collagen production while markedly increasing the activity of matrix metalloproteinase-1 (MMP-1), an enzyme responsible for collagen degradation. Mechanistically, ursolic acid was found to inhibit TGF-β/Smad signaling, leading to decreased collagen production, and to activate mitogen-activated protein kinase (MAPK) pathways and activator protein 1 (AP-1), resulting in enhanced MMP-1 production. These in vitro findings were further validated in an in vivo mouse model of fibrosis, where ursolic acid significantly mitigated bleomycin-induced skin fibrosis. These results suggest that UA could be a promising candidate for treating skin fibrosis due to its dual effects on collagen homeostasis: inhibiting collagen production and promoting collagen degradation. |
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AbstractList | Tissue fibrosis, characterized by excessive collagen accumulation, leads to impaired organ function and is a hallmark of various chronic diseases. Fibroblasts play a central role in collagen production and deposition. This study examines the impact of ursolic acid, a pentacyclic triterpenoid compound present in various fruits and vegetables, on collagen homeostasis in primary human dermal fibroblasts. Ursolic acid (UA) was observed to significantly reduce collagen production while markedly increasing the activity of matrix metalloproteinase-1 (MMP-1), an enzyme responsible for collagen degradation. Mechanistically, ursolic acid was found to inhibit TGF-β/Smad signaling, leading to decreased collagen production, and to activate mitogen-activated protein kinase (MAPK) pathways and activator protein 1 (AP-1), resulting in enhanced MMP-1 production. These in vitro findings were further validated in an in vivo mouse model of fibrosis, where ursolic acid significantly mitigated bleomycin-induced skin fibrosis. These results suggest that UA could be a promising candidate for treating skin fibrosis due to its dual effects on collagen homeostasis: inhibiting collagen production and promoting collagen degradation. Tissue fibrosis, characterized by excessive collagen accumulation, leads to impaired organ function and is a hallmark of various chronic diseases. Fibroblasts play a central role in collagen production and deposition. This study examines the impact of ursolic acid, a pentacyclic triterpenoid compound present in various fruits and vegetables, on collagen homeostasis in primary human dermal fibroblasts. Ursolic acid (UA) was observed to significantly reduce collagen production while markedly increasing the activity of matrix metalloproteinase-1 (MMP-1), an enzyme responsible for collagen degradation. Mechanistically, ursolic acid was found to inhibit TGF-β/Smad signaling, leading to decreased collagen production, and to activate mitogen-activated protein kinase (MAPK) pathways and activator protein 1 (AP-1), resulting in enhanced MMP-1 production. These in vitro findings were further validated in an in vivo mouse model of fibrosis, where ursolic acid significantly mitigated bleomycin-induced skin fibrosis. These results suggest that UA could be a promising candidate for treating skin fibrosis due to its dual effects on collagen homeostasis: inhibiting collagen production and promoting collagen degradation.Tissue fibrosis, characterized by excessive collagen accumulation, leads to impaired organ function and is a hallmark of various chronic diseases. Fibroblasts play a central role in collagen production and deposition. This study examines the impact of ursolic acid, a pentacyclic triterpenoid compound present in various fruits and vegetables, on collagen homeostasis in primary human dermal fibroblasts. Ursolic acid (UA) was observed to significantly reduce collagen production while markedly increasing the activity of matrix metalloproteinase-1 (MMP-1), an enzyme responsible for collagen degradation. Mechanistically, ursolic acid was found to inhibit TGF-β/Smad signaling, leading to decreased collagen production, and to activate mitogen-activated protein kinase (MAPK) pathways and activator protein 1 (AP-1), resulting in enhanced MMP-1 production. These in vitro findings were further validated in an in vivo mouse model of fibrosis, where ursolic acid significantly mitigated bleomycin-induced skin fibrosis. These results suggest that UA could be a promising candidate for treating skin fibrosis due to its dual effects on collagen homeostasis: inhibiting collagen production and promoting collagen degradation. |
Audience | Academic |
Author | He, Tianyuan Liu, Yingchun Xiang, Yaping Quan, Hehui Guo, Chunfang Quan, Taihao |
AuthorAffiliation | 1 Department of Dermatology, University of Michigan Medical School, Ann Arbor, MI 48109, USA; tyhe@med.umich.edu (T.H.); 600850@csu.edu.cn (Y.X.); yingchun.liu@imau.edu.cn (Y.L.); cfguo@umich.edu (C.G.) 2 Lenox Hill Hospital, 100 E 77th St., New York, NY 10075, USA; hquan@northwell.edu |
AuthorAffiliation_xml | – name: 1 Department of Dermatology, University of Michigan Medical School, Ann Arbor, MI 48109, USA; tyhe@med.umich.edu (T.H.); 600850@csu.edu.cn (Y.X.); yingchun.liu@imau.edu.cn (Y.L.); cfguo@umich.edu (C.G.) – name: 2 Lenox Hill Hospital, 100 E 77th St., New York, NY 10075, USA; hquan@northwell.edu |
Author_xml | – sequence: 1 givenname: Tianyuan surname: He fullname: He, Tianyuan – sequence: 2 givenname: Yaping surname: Xiang fullname: Xiang, Yaping – sequence: 3 givenname: Hehui surname: Quan fullname: Quan, Hehui – sequence: 4 givenname: Yingchun surname: Liu fullname: Liu, Yingchun – sequence: 5 givenname: Chunfang surname: Guo fullname: Guo, Chunfang – sequence: 6 givenname: Taihao orcidid: 0000-0002-0954-5109 surname: Quan fullname: Quan, Taihao |
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Snippet | Tissue fibrosis, characterized by excessive collagen accumulation, leads to impaired organ function and is a hallmark of various chronic diseases. Fibroblasts... |
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SubjectTerms | Activator protein 1 Animals Antibodies Antifibrotic Agents - pharmacology Biopsy Bleomycin Cell culture Cells, Cultured Chronic diseases Chronic illnesses Collagen Collagen - metabolism Degradation Enzymes Ethylenediaminetetraacetic acid Fibroblasts Fibroblasts - drug effects Fibroblasts - metabolism Fibrosis Fibrosis - drug therapy Homeostasis Human subjects Humans Interstitial collagenase Kinases Liver cirrhosis MAKP MAP kinase Matrix metalloproteinase Matrix Metalloproteinase 1 - metabolism Medical research Metalloproteinase Mice MMP-1 Protein kinases Proteins Signal Transduction - drug effects Skin Skin - cytology Skin - drug effects Skin - metabolism Skin - pathology Smad protein TGF-β/Smad Transcription factors Transforming Growth Factor beta - metabolism Transforming growth factor-b Transforming growth factors Triterpenes - pharmacology Ursolic Acid |
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Title | Ursolic Acid Inhibits Collagen Production and Promotes Collagen Degradation in Skin Dermal Fibroblasts: Potential Antifibrotic Effects |
URI | https://www.ncbi.nlm.nih.gov/pubmed/40149901 https://www.proquest.com/docview/3181372887 https://www.proquest.com/docview/3182478283 https://pubmed.ncbi.nlm.nih.gov/PMC11939892 https://doaj.org/article/2d5676ae604049abacebecbc7342c2c6 |
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