Effects of Glycyrrhizic Acid in Licorice on Prolongation of Murine Cardiac Allograft Survival
Recent evidence has pointed to the promising benefits of using specific immunosuppressive herbal compounds to prolong transplant allograft survival. In this study, we investigated the effects of glycyrrhizic acid (GA), a major component of licorice, in a model of murine heart transplantation. CBA (H...
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Veröffentlicht in: | Transplantation proceedings 2022-03, Vol.54 (2), p.476-481 |
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description | Recent evidence has pointed to the promising benefits of using specific immunosuppressive herbal compounds to prolong transplant allograft survival. In this study, we investigated the effects of glycyrrhizic acid (GA), a major component of licorice, in a model of murine heart transplantation. CBA (H2k) mice were transplanted with a fully-MHC mismatched C57BL/6 (H2b) heart allograft and subsequently received daily intraperitoneal administration of normal saline or 0.02, 0.2, or 2.0 mg/d of GA for 7 consecutive days. Untreated CBA recipients, with a median survival time (MST) of 7 days, and groups receiving 0.02mg/d (MST, 8 days) or 0.2mg/d (MST, 9 days) of GA acutely rejected C57BL/6 cardiac allografts. But mice treated with 2.0 mg/d of GA demonstrated significant prolongation of allografts (MST, 23 days). Histologic studies showed that cardiac allografts from GA-treated CBA recipients had preserved graft and vessel structure. Moreover, flow cytometric study showed that the percentage of CD4+CD25+Foxp3+ cell (regulatory T cell [Treg]) populations were increased in GA-treated CBA recipients. In a mixed leukocyte culture, splenocytes from GA-treated mice demonstrated suppressed allo-proliferation, in which interleukin (IL)-2 and interferon gamma production were downregulated and IL-10 secretion was upregulated. In conclusion, GA may be a novel promising therapeutic agent to prolong cardiac allograft survival through direct anti-inflammatory effects and induction of Treg populations. |
doi_str_mv | 10.1016/j.transproceed.2021.12.009 |
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In this study, we investigated the effects of glycyrrhizic acid (GA), a major component of licorice, in a model of murine heart transplantation. CBA (H2k) mice were transplanted with a fully-MHC mismatched C57BL/6 (H2b) heart allograft and subsequently received daily intraperitoneal administration of normal saline or 0.02, 0.2, or 2.0 mg/d of GA for 7 consecutive days. Untreated CBA recipients, with a median survival time (MST) of 7 days, and groups receiving 0.02mg/d (MST, 8 days) or 0.2mg/d (MST, 9 days) of GA acutely rejected C57BL/6 cardiac allografts. But mice treated with 2.0 mg/d of GA demonstrated significant prolongation of allografts (MST, 23 days). Histologic studies showed that cardiac allografts from GA-treated CBA recipients had preserved graft and vessel structure. Moreover, flow cytometric study showed that the percentage of CD4+CD25+Foxp3+ cell (regulatory T cell [Treg]) populations were increased in GA-treated CBA recipients. In a mixed leukocyte culture, splenocytes from GA-treated mice demonstrated suppressed allo-proliferation, in which interleukin (IL)-2 and interferon gamma production were downregulated and IL-10 secretion was upregulated. In conclusion, GA may be a novel promising therapeutic agent to prolong cardiac allograft survival through direct anti-inflammatory effects and induction of Treg populations.</description><identifier>ISSN: 0041-1345</identifier><identifier>EISSN: 1873-2623</identifier><identifier>DOI: 10.1016/j.transproceed.2021.12.009</identifier><identifier>PMID: 35101322</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Adoptive Transfer ; Allografts ; Animals ; Glycyrrhiza ; Glycyrrhizic Acid - pharmacology ; Graft Survival ; Heart Transplantation - adverse effects ; Humans ; Mice ; Mice, Inbred BALB C ; Mice, Inbred C57BL ; Mice, Inbred CBA ; T-Lymphocytes, Regulatory</subject><ispartof>Transplantation proceedings, 2022-03, Vol.54 (2), p.476-481</ispartof><rights>2022 Elsevier Inc.</rights><rights>Copyright © 2022 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c375t-38d265f9c855d0c2f80c5d067cfb76c8a52e79c3e20be5f8c07e48acd6a840f73</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.transproceed.2021.12.009$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>315,781,785,3551,27928,27929,45999</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35101322$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yamamoto, Yasuto</creatorcontrib><creatorcontrib>Uchiyama, Masateru</creatorcontrib><creatorcontrib>Iguchi, Kazuhito</creatorcontrib><creatorcontrib>Kawai, Kento</creatorcontrib><creatorcontrib>Imazuru, Tomohiro</creatorcontrib><creatorcontrib>Kawamura, Masafumi</creatorcontrib><creatorcontrib>Shimokawa, Tomoki</creatorcontrib><title>Effects of Glycyrrhizic Acid in Licorice on Prolongation of Murine Cardiac Allograft Survival</title><title>Transplantation proceedings</title><addtitle>Transplant Proc</addtitle><description>Recent evidence has pointed to the promising benefits of using specific immunosuppressive herbal compounds to prolong transplant allograft survival. In this study, we investigated the effects of glycyrrhizic acid (GA), a major component of licorice, in a model of murine heart transplantation. CBA (H2k) mice were transplanted with a fully-MHC mismatched C57BL/6 (H2b) heart allograft and subsequently received daily intraperitoneal administration of normal saline or 0.02, 0.2, or 2.0 mg/d of GA for 7 consecutive days. Untreated CBA recipients, with a median survival time (MST) of 7 days, and groups receiving 0.02mg/d (MST, 8 days) or 0.2mg/d (MST, 9 days) of GA acutely rejected C57BL/6 cardiac allografts. But mice treated with 2.0 mg/d of GA demonstrated significant prolongation of allografts (MST, 23 days). Histologic studies showed that cardiac allografts from GA-treated CBA recipients had preserved graft and vessel structure. Moreover, flow cytometric study showed that the percentage of CD4+CD25+Foxp3+ cell (regulatory T cell [Treg]) populations were increased in GA-treated CBA recipients. In a mixed leukocyte culture, splenocytes from GA-treated mice demonstrated suppressed allo-proliferation, in which interleukin (IL)-2 and interferon gamma production were downregulated and IL-10 secretion was upregulated. In conclusion, GA may be a novel promising therapeutic agent to prolong cardiac allograft survival through direct anti-inflammatory effects and induction of Treg populations.</description><subject>Adoptive Transfer</subject><subject>Allografts</subject><subject>Animals</subject><subject>Glycyrrhiza</subject><subject>Glycyrrhizic Acid - pharmacology</subject><subject>Graft Survival</subject><subject>Heart Transplantation - adverse effects</subject><subject>Humans</subject><subject>Mice</subject><subject>Mice, Inbred BALB C</subject><subject>Mice, Inbred C57BL</subject><subject>Mice, Inbred CBA</subject><subject>T-Lymphocytes, Regulatory</subject><issn>0041-1345</issn><issn>1873-2623</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkFtLxDAQhYMoul7-ggSffGnNpWm7vsm6XmBFQX2UkJ1ONEu30aRdWH-9kVXw0aeZYc6Zw3yEnHCWc8bLs0XeB9PF9-ABsckFEzznImdsvEVGvK5kJkoht8mIsYJnXBZqj-zHuGBpFoXcJXtSpUNSiBF5mVqL0EfqLb1u17AO4c19OqAX4BrqOjpz4IMDpL6jD8G3vns1vUtDMtwNwXVIJyY0ziRL2_rXYGxPH4ewcivTHpIda9qIRz_1gDxfTZ8mN9ns_vp2cjHLQFaqz2TdiFLZMdRKNQyErRmkpqzAzqsSaqMEVmOQKNgcla2BVVjUBprS1AWzlTwgp5u7icnHgLHXSxcB29Z06IeoE4-iVGUlWJKeb6QQfIwBrX4PbmnCWnOmv_Hqhf6LV3_j1VzohDeZj39yhvky7X6tvzyT4HIjwPTtymHQERx2gI0LCbNuvPtPzheq7pN5</recordid><startdate>202203</startdate><enddate>202203</enddate><creator>Yamamoto, Yasuto</creator><creator>Uchiyama, Masateru</creator><creator>Iguchi, Kazuhito</creator><creator>Kawai, Kento</creator><creator>Imazuru, Tomohiro</creator><creator>Kawamura, Masafumi</creator><creator>Shimokawa, Tomoki</creator><general>Elsevier Inc</general><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>202203</creationdate><title>Effects of Glycyrrhizic Acid in Licorice on Prolongation of Murine Cardiac Allograft Survival</title><author>Yamamoto, Yasuto ; Uchiyama, Masateru ; Iguchi, Kazuhito ; Kawai, Kento ; Imazuru, Tomohiro ; Kawamura, Masafumi ; Shimokawa, Tomoki</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c375t-38d265f9c855d0c2f80c5d067cfb76c8a52e79c3e20be5f8c07e48acd6a840f73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Adoptive Transfer</topic><topic>Allografts</topic><topic>Animals</topic><topic>Glycyrrhiza</topic><topic>Glycyrrhizic Acid - pharmacology</topic><topic>Graft Survival</topic><topic>Heart Transplantation - adverse effects</topic><topic>Humans</topic><topic>Mice</topic><topic>Mice, Inbred BALB C</topic><topic>Mice, Inbred C57BL</topic><topic>Mice, Inbred CBA</topic><topic>T-Lymphocytes, Regulatory</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yamamoto, Yasuto</creatorcontrib><creatorcontrib>Uchiyama, Masateru</creatorcontrib><creatorcontrib>Iguchi, Kazuhito</creatorcontrib><creatorcontrib>Kawai, Kento</creatorcontrib><creatorcontrib>Imazuru, Tomohiro</creatorcontrib><creatorcontrib>Kawamura, Masafumi</creatorcontrib><creatorcontrib>Shimokawa, Tomoki</creatorcontrib><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>Transplantation proceedings</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yamamoto, Yasuto</au><au>Uchiyama, Masateru</au><au>Iguchi, Kazuhito</au><au>Kawai, Kento</au><au>Imazuru, Tomohiro</au><au>Kawamura, Masafumi</au><au>Shimokawa, Tomoki</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effects of Glycyrrhizic Acid in Licorice on Prolongation of Murine Cardiac Allograft Survival</atitle><jtitle>Transplantation proceedings</jtitle><addtitle>Transplant Proc</addtitle><date>2022-03</date><risdate>2022</risdate><volume>54</volume><issue>2</issue><spage>476</spage><epage>481</epage><pages>476-481</pages><issn>0041-1345</issn><eissn>1873-2623</eissn><abstract>Recent evidence has pointed to the promising benefits of using specific immunosuppressive herbal compounds to prolong transplant allograft survival. In this study, we investigated the effects of glycyrrhizic acid (GA), a major component of licorice, in a model of murine heart transplantation. CBA (H2k) mice were transplanted with a fully-MHC mismatched C57BL/6 (H2b) heart allograft and subsequently received daily intraperitoneal administration of normal saline or 0.02, 0.2, or 2.0 mg/d of GA for 7 consecutive days. Untreated CBA recipients, with a median survival time (MST) of 7 days, and groups receiving 0.02mg/d (MST, 8 days) or 0.2mg/d (MST, 9 days) of GA acutely rejected C57BL/6 cardiac allografts. But mice treated with 2.0 mg/d of GA demonstrated significant prolongation of allografts (MST, 23 days). Histologic studies showed that cardiac allografts from GA-treated CBA recipients had preserved graft and vessel structure. Moreover, flow cytometric study showed that the percentage of CD4+CD25+Foxp3+ cell (regulatory T cell [Treg]) populations were increased in GA-treated CBA recipients. In a mixed leukocyte culture, splenocytes from GA-treated mice demonstrated suppressed allo-proliferation, in which interleukin (IL)-2 and interferon gamma production were downregulated and IL-10 secretion was upregulated. In conclusion, GA may be a novel promising therapeutic agent to prolong cardiac allograft survival through direct anti-inflammatory effects and induction of Treg populations.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>35101322</pmid><doi>10.1016/j.transproceed.2021.12.009</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adoptive Transfer Allografts Animals Glycyrrhiza Glycyrrhizic Acid - pharmacology Graft Survival Heart Transplantation - adverse effects Humans Mice Mice, Inbred BALB C Mice, Inbred C57BL Mice, Inbred CBA T-Lymphocytes, Regulatory |
title | Effects of Glycyrrhizic Acid in Licorice on Prolongation of Murine Cardiac Allograft Survival |
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