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Recent update on application of dihydromyricetin in metabolic related diseases
As a new type of natural flavonoids, dihydromyricetin (DMY) has attracted more and more attention. It has a series of pharmacological effects, such as anti-inflammatory, anti-tumor, anti-oxidation, antibacterial and so on, and it is almost no toxicity and with excellent safety. Therefore, even if th...
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Published in: | Biomedicine & pharmacotherapy 2022-04, Vol.148, p.112771-112771, Article 112771 |
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description | As a new type of natural flavonoids, dihydromyricetin (DMY) has attracted more and more attention. It has a series of pharmacological effects, such as anti-inflammatory, anti-tumor, anti-oxidation, antibacterial and so on, and it is almost no toxicity and with excellent safety. Therefore, even if the bioavailability is poor, it is often added to daily food, beverages and even medicines. In recent years, some researchers have found that DMY can treat some diseases by anti-oxidation, anti-inflammation, promoting cell death and regulate the activity of lipid and glucose metabolism. In addition, the mechanism of DMY on these diseases was also related to the signal pathway of AMPK, PI3K/Akt, PPAR and the participation of microRNAs. This review describes the mechanism of DMY in metabolic related diseases from three aspects: metabolic diseases, liver diseases, and cancers, hoping to provide some new ideas for clinical researches.
[Display omitted]
The mechanism of DMY with some associated metabolic diseases.
Abbreviations
DMY, dihydromyricetin; MAPK, mitogen-activated protein kinase; PI3K, phosphatidylinositol-3-kinase; mTOR, Mechanistic target of rapamycin; AMPK, adenosine monophosphate activated protein kinase; NF-κB, nuclear factor kappa-B; TGF-β, transforming growth factor-β; Bcl-2, B-cell lymphoma-2; ERK1/2, extracellular signal-regulated kinase 1/2.
•DMY has anti-inflammatory, anti-tumor, antioxidant, antibacterial and other pharmacological effects.•DMY can protect liver and alleviate metabolic syndrome.•DMY may be a potential natural drug for the treatment of cancers. |
doi_str_mv | 10.1016/j.biopha.2022.112771 |
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[Display omitted]
The mechanism of DMY with some associated metabolic diseases.
Abbreviations
DMY, dihydromyricetin; MAPK, mitogen-activated protein kinase; PI3K, phosphatidylinositol-3-kinase; mTOR, Mechanistic target of rapamycin; AMPK, adenosine monophosphate activated protein kinase; NF-κB, nuclear factor kappa-B; TGF-β, transforming growth factor-β; Bcl-2, B-cell lymphoma-2; ERK1/2, extracellular signal-regulated kinase 1/2.
•DMY has anti-inflammatory, anti-tumor, antioxidant, antibacterial and other pharmacological effects.•DMY can protect liver and alleviate metabolic syndrome.•DMY may be a potential natural drug for the treatment of cancers.</description><identifier>ISSN: 0753-3322</identifier><identifier>EISSN: 1950-6007</identifier><identifier>DOI: 10.1016/j.biopha.2022.112771</identifier><identifier>PMID: 35247719</identifier><language>eng</language><publisher>France: Elsevier Masson SAS</publisher><subject>AMP-Activated Protein Kinases - drug effects ; Anti-Inflammatory Agents - pharmacology ; Antioxidants - pharmacology ; Cancers ; Cell Death ; Dihydromyricetin ; Flavonols - pharmacology ; Glucose - metabolism ; Humans ; Lipid Metabolism - drug effects ; Liver diseases ; Liver Diseases - pathology ; Metabolic diseases ; Metabolic Diseases - pathology ; MicroRNAs - metabolism ; Neoplasms - pathology ; Oxidative Stress - drug effects ; Peroxisome Proliferator-Activated Receptors - drug effects ; Phosphatidylinositol 3-Kinases - drug effects ; Proto-Oncogene Proteins c-akt - drug effects ; Signal Transduction - drug effects</subject><ispartof>Biomedicine & pharmacotherapy, 2022-04, Vol.148, p.112771-112771, Article 112771</ispartof><rights>2022 The Authors</rights><rights>Copyright © 2022 The Authors. Published by Elsevier Masson SAS.. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c408t-1ed3b3b36dfab3bf6a5e5919123403bd5c973b715a937b48fd724ebcf60fc7c33</citedby><cites>FETCH-LOGICAL-c408t-1ed3b3b36dfab3bf6a5e5919123403bd5c973b715a937b48fd724ebcf60fc7c33</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35247719$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wang, Yirong</creatorcontrib><creatorcontrib>Wang, Junmin</creatorcontrib><creatorcontrib>Xiang, Hongjiao</creatorcontrib><creatorcontrib>Ding, Peilun</creatorcontrib><creatorcontrib>Wu, Tao</creatorcontrib><creatorcontrib>Ji, Guang</creatorcontrib><title>Recent update on application of dihydromyricetin in metabolic related diseases</title><title>Biomedicine & pharmacotherapy</title><addtitle>Biomed Pharmacother</addtitle><description>As a new type of natural flavonoids, dihydromyricetin (DMY) has attracted more and more attention. It has a series of pharmacological effects, such as anti-inflammatory, anti-tumor, anti-oxidation, antibacterial and so on, and it is almost no toxicity and with excellent safety. Therefore, even if the bioavailability is poor, it is often added to daily food, beverages and even medicines. In recent years, some researchers have found that DMY can treat some diseases by anti-oxidation, anti-inflammation, promoting cell death and regulate the activity of lipid and glucose metabolism. In addition, the mechanism of DMY on these diseases was also related to the signal pathway of AMPK, PI3K/Akt, PPAR and the participation of microRNAs. This review describes the mechanism of DMY in metabolic related diseases from three aspects: metabolic diseases, liver diseases, and cancers, hoping to provide some new ideas for clinical researches.
[Display omitted]
The mechanism of DMY with some associated metabolic diseases.
Abbreviations
DMY, dihydromyricetin; MAPK, mitogen-activated protein kinase; PI3K, phosphatidylinositol-3-kinase; mTOR, Mechanistic target of rapamycin; AMPK, adenosine monophosphate activated protein kinase; NF-κB, nuclear factor kappa-B; TGF-β, transforming growth factor-β; Bcl-2, B-cell lymphoma-2; ERK1/2, extracellular signal-regulated kinase 1/2.
•DMY has anti-inflammatory, anti-tumor, antioxidant, antibacterial and other pharmacological effects.•DMY can protect liver and alleviate metabolic syndrome.•DMY may be a potential natural drug for the treatment of cancers.</description><subject>AMP-Activated Protein Kinases - drug effects</subject><subject>Anti-Inflammatory Agents - pharmacology</subject><subject>Antioxidants - pharmacology</subject><subject>Cancers</subject><subject>Cell Death</subject><subject>Dihydromyricetin</subject><subject>Flavonols - pharmacology</subject><subject>Glucose - metabolism</subject><subject>Humans</subject><subject>Lipid Metabolism - drug effects</subject><subject>Liver diseases</subject><subject>Liver Diseases - pathology</subject><subject>Metabolic diseases</subject><subject>Metabolic Diseases - pathology</subject><subject>MicroRNAs - metabolism</subject><subject>Neoplasms - pathology</subject><subject>Oxidative Stress - drug effects</subject><subject>Peroxisome Proliferator-Activated Receptors - drug effects</subject><subject>Phosphatidylinositol 3-Kinases - drug effects</subject><subject>Proto-Oncogene Proteins c-akt - drug effects</subject><subject>Signal Transduction - drug effects</subject><issn>0753-3322</issn><issn>1950-6007</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNp9kE1LxDAQhoMo7rr6D0R69NI1H02yvQgifsGiIHoOaTJls7RNTVph_71ZunqUDMwcnjfDPAhdErwkmIib7bJyvt_oJcWULgmhUpIjNCclx7nAWB6jOZac5YxROkNnMW4xxlyw1SmaMU6LhJdz9PoOBrohG3urB8h8l-m-b5zRg0uzrzPrNjsbfLsLzsDguixVC4OufKKyAE2K2URF0BHiOTqpdRPh4tAX6PPx4eP-OV-_Pb3c361zU-DVkBOwrEpP2FqnXgvNgZekJJQVmFWWm1KyShKuSyarYlVbSQuoTC1wbaRhbIGup3_74L9GiINqXTTQNLoDP0ZFBROkoITjhBYTaoKPMUCt-uBaHXaKYLU3qbZqMqn2JtVkMsWuDhvGqgX7F_pVl4DbCYB057eDoKJx0BmwLoAZlPXu_w0_BeeHEQ</recordid><startdate>202204</startdate><enddate>202204</enddate><creator>Wang, Yirong</creator><creator>Wang, Junmin</creator><creator>Xiang, Hongjiao</creator><creator>Ding, Peilun</creator><creator>Wu, Tao</creator><creator>Ji, Guang</creator><general>Elsevier Masson SAS</general><scope>6I.</scope><scope>AAFTH</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>202204</creationdate><title>Recent update on application of dihydromyricetin in metabolic related diseases</title><author>Wang, Yirong ; Wang, Junmin ; Xiang, Hongjiao ; Ding, Peilun ; Wu, Tao ; Ji, Guang</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c408t-1ed3b3b36dfab3bf6a5e5919123403bd5c973b715a937b48fd724ebcf60fc7c33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>AMP-Activated Protein Kinases - drug effects</topic><topic>Anti-Inflammatory Agents - pharmacology</topic><topic>Antioxidants - pharmacology</topic><topic>Cancers</topic><topic>Cell Death</topic><topic>Dihydromyricetin</topic><topic>Flavonols - pharmacology</topic><topic>Glucose - metabolism</topic><topic>Humans</topic><topic>Lipid Metabolism - drug effects</topic><topic>Liver diseases</topic><topic>Liver Diseases - pathology</topic><topic>Metabolic diseases</topic><topic>Metabolic Diseases - pathology</topic><topic>MicroRNAs - metabolism</topic><topic>Neoplasms - pathology</topic><topic>Oxidative Stress - drug effects</topic><topic>Peroxisome Proliferator-Activated Receptors - drug effects</topic><topic>Phosphatidylinositol 3-Kinases - drug effects</topic><topic>Proto-Oncogene Proteins c-akt - drug effects</topic><topic>Signal Transduction - drug effects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wang, Yirong</creatorcontrib><creatorcontrib>Wang, Junmin</creatorcontrib><creatorcontrib>Xiang, Hongjiao</creatorcontrib><creatorcontrib>Ding, Peilun</creatorcontrib><creatorcontrib>Wu, Tao</creatorcontrib><creatorcontrib>Ji, Guang</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Biomedicine & pharmacotherapy</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wang, Yirong</au><au>Wang, Junmin</au><au>Xiang, Hongjiao</au><au>Ding, Peilun</au><au>Wu, Tao</au><au>Ji, Guang</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Recent update on application of dihydromyricetin in metabolic related diseases</atitle><jtitle>Biomedicine & pharmacotherapy</jtitle><addtitle>Biomed Pharmacother</addtitle><date>2022-04</date><risdate>2022</risdate><volume>148</volume><spage>112771</spage><epage>112771</epage><pages>112771-112771</pages><artnum>112771</artnum><issn>0753-3322</issn><eissn>1950-6007</eissn><abstract>As a new type of natural flavonoids, dihydromyricetin (DMY) has attracted more and more attention. It has a series of pharmacological effects, such as anti-inflammatory, anti-tumor, anti-oxidation, antibacterial and so on, and it is almost no toxicity and with excellent safety. Therefore, even if the bioavailability is poor, it is often added to daily food, beverages and even medicines. In recent years, some researchers have found that DMY can treat some diseases by anti-oxidation, anti-inflammation, promoting cell death and regulate the activity of lipid and glucose metabolism. In addition, the mechanism of DMY on these diseases was also related to the signal pathway of AMPK, PI3K/Akt, PPAR and the participation of microRNAs. This review describes the mechanism of DMY in metabolic related diseases from three aspects: metabolic diseases, liver diseases, and cancers, hoping to provide some new ideas for clinical researches.
[Display omitted]
The mechanism of DMY with some associated metabolic diseases.
Abbreviations
DMY, dihydromyricetin; MAPK, mitogen-activated protein kinase; PI3K, phosphatidylinositol-3-kinase; mTOR, Mechanistic target of rapamycin; AMPK, adenosine monophosphate activated protein kinase; NF-κB, nuclear factor kappa-B; TGF-β, transforming growth factor-β; Bcl-2, B-cell lymphoma-2; ERK1/2, extracellular signal-regulated kinase 1/2.
•DMY has anti-inflammatory, anti-tumor, antioxidant, antibacterial and other pharmacological effects.•DMY can protect liver and alleviate metabolic syndrome.•DMY may be a potential natural drug for the treatment of cancers.</abstract><cop>France</cop><pub>Elsevier Masson SAS</pub><pmid>35247719</pmid><doi>10.1016/j.biopha.2022.112771</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | AMP-Activated Protein Kinases - drug effects Anti-Inflammatory Agents - pharmacology Antioxidants - pharmacology Cancers Cell Death Dihydromyricetin Flavonols - pharmacology Glucose - metabolism Humans Lipid Metabolism - drug effects Liver diseases Liver Diseases - pathology Metabolic diseases Metabolic Diseases - pathology MicroRNAs - metabolism Neoplasms - pathology Oxidative Stress - drug effects Peroxisome Proliferator-Activated Receptors - drug effects Phosphatidylinositol 3-Kinases - drug effects Proto-Oncogene Proteins c-akt - drug effects Signal Transduction - drug effects |
title | Recent update on application of dihydromyricetin in metabolic related diseases |
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