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Are anti-inflammatory properties of lipoic acid associated with the formation of hydrogen sulfide?
Lipoic acid (LA) was shown to possess anti-inflammatory properties. In this study, we present evidence supporting the hypothesis that the anti-inflammatory properties of LA are associated with the formation of hydrogen sulfide (H2S). The study was conducted on male albino Swiss mice. The animals wer...
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Published in: | Pharmacological reports 2013, Vol.65 (4), p.1018-1024 |
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creator | Dudek, Magdalena Bilska-Wilkosz, Anna Knutelska, Joanna Mogilski, Szczepan Bednarski, Marek Zygmunt, Małgorzata Iciek, Małgorzata Sapa, Jacek Bugajski, Dominik Filipek, Barbara Włodek, Lidia |
description | Lipoic acid (LA) was shown to possess anti-inflammatory properties. In this study, we present evidence supporting the hypothesis that the anti-inflammatory properties of LA are associated with the formation of hydrogen sulfide (H2S).
The study was conducted on male albino Swiss mice. The animals were treated with carrageenan by subcutaneous (sc) injection into the right hind paw to induce acute inflammation. Animals were treated intraperitoneally (ip) with LA (30, 50 and 100mg/kg) or indomethacin (20mg/kg) 30min before carrageenan administration. The control group was given ip the vehicle (1% Tween 80) 30min before carrageenan administration. Additional experiment involved ip combined treatment of mice with glibenclamide (10mg/kg) or glibenclamide (10mg/kg) and LA(100mg/kg) 30min before carrageenan administration. LA, indomethacin and glibenclamide were suspended in 1% Tween 80. At 1, 2 and 3h after treatment with carrageenan the degree of the paw edema was evaluated by the measurement of the paw volume using aqueous plethysmometer.
Injection of carrageenan into the mouse hind paw increased paw volume. The increase in paw edema was completely suppressed by pretreatment with LA. The reduction of paw edema by LAwas abolished by pretreatment with the KATP channel antagonist, glibenclamide.
Our findings demonstrate for the first time in vivo that the anti-inflammatory activity of LA might be connected with the formation of H2S. |
doi_str_mv | 10.1016/S1734-1140(13)71084-3 |
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The study was conducted on male albino Swiss mice. The animals were treated with carrageenan by subcutaneous (sc) injection into the right hind paw to induce acute inflammation. Animals were treated intraperitoneally (ip) with LA (30, 50 and 100mg/kg) or indomethacin (20mg/kg) 30min before carrageenan administration. The control group was given ip the vehicle (1% Tween 80) 30min before carrageenan administration. Additional experiment involved ip combined treatment of mice with glibenclamide (10mg/kg) or glibenclamide (10mg/kg) and LA(100mg/kg) 30min before carrageenan administration. LA, indomethacin and glibenclamide were suspended in 1% Tween 80. At 1, 2 and 3h after treatment with carrageenan the degree of the paw edema was evaluated by the measurement of the paw volume using aqueous plethysmometer.
Injection of carrageenan into the mouse hind paw increased paw volume. The increase in paw edema was completely suppressed by pretreatment with LA. The reduction of paw edema by LAwas abolished by pretreatment with the KATP channel antagonist, glibenclamide.
Our findings demonstrate for the first time in vivo that the anti-inflammatory activity of LA might be connected with the formation of H2S.</description><identifier>ISSN: 1734-1140</identifier><identifier>EISSN: 2299-5684</identifier><identifier>DOI: 10.1016/S1734-1140(13)71084-3</identifier><identifier>PMID: 24145097</identifier><language>eng</language><publisher>Cham: Elsevier B.V</publisher><subject>Animals ; Anti-Inflammatory Agents - pharmacology ; Anti-Inflammatory Agents - therapeutic use ; anti-inflammatory properties ; Carrageenan ; carrageenan-induced paw edema ; dihydrolipoic acid ; Dose-Response Relationship, Drug ; Drug Safety and Pharmacovigilance ; Edema - chemically induced ; Edema - drug therapy ; glibenclamide ; Glyburide - pharmacology ; Hindlimb - drug effects ; hydrogen sulfide ; Hydrogen Sulfide - metabolism ; Indomethacin - pharmacology ; Indomethacin - therapeutic use ; lipoic acid ; Male ; Mice ; Pharmacotherapy ; Pharmacy ; Potassium Channel Blockers - pharmacology ; Short Communication ; Thioctic Acid - antagonists & inhibitors ; Thioctic Acid - pharmacology ; Thioctic Acid - therapeutic use</subject><ispartof>Pharmacological reports, 2013, Vol.65 (4), p.1018-1024</ispartof><rights>2013 Institute of Pharmacology Polish Academy of Sciences</rights><rights>Maj Institute of Pharmacology, Polish Academy of Sciences 2013</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c412t-52cecfad66977d591497a1754fc4ce89c91b78c558b03b9a76a845f3776b7c7a3</citedby><cites>FETCH-LOGICAL-c412t-52cecfad66977d591497a1754fc4ce89c91b78c558b03b9a76a845f3776b7c7a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S1734114013710843$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3536,27901,27902,45756</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24145097$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Dudek, Magdalena</creatorcontrib><creatorcontrib>Bilska-Wilkosz, Anna</creatorcontrib><creatorcontrib>Knutelska, Joanna</creatorcontrib><creatorcontrib>Mogilski, Szczepan</creatorcontrib><creatorcontrib>Bednarski, Marek</creatorcontrib><creatorcontrib>Zygmunt, Małgorzata</creatorcontrib><creatorcontrib>Iciek, Małgorzata</creatorcontrib><creatorcontrib>Sapa, Jacek</creatorcontrib><creatorcontrib>Bugajski, Dominik</creatorcontrib><creatorcontrib>Filipek, Barbara</creatorcontrib><creatorcontrib>Włodek, Lidia</creatorcontrib><title>Are anti-inflammatory properties of lipoic acid associated with the formation of hydrogen sulfide?</title><title>Pharmacological reports</title><addtitle>Pharmacol. Rep</addtitle><addtitle>Pharmacol Rep</addtitle><description>Lipoic acid (LA) was shown to possess anti-inflammatory properties. In this study, we present evidence supporting the hypothesis that the anti-inflammatory properties of LA are associated with the formation of hydrogen sulfide (H2S).
The study was conducted on male albino Swiss mice. The animals were treated with carrageenan by subcutaneous (sc) injection into the right hind paw to induce acute inflammation. Animals were treated intraperitoneally (ip) with LA (30, 50 and 100mg/kg) or indomethacin (20mg/kg) 30min before carrageenan administration. The control group was given ip the vehicle (1% Tween 80) 30min before carrageenan administration. Additional experiment involved ip combined treatment of mice with glibenclamide (10mg/kg) or glibenclamide (10mg/kg) and LA(100mg/kg) 30min before carrageenan administration. LA, indomethacin and glibenclamide were suspended in 1% Tween 80. At 1, 2 and 3h after treatment with carrageenan the degree of the paw edema was evaluated by the measurement of the paw volume using aqueous plethysmometer.
Injection of carrageenan into the mouse hind paw increased paw volume. The increase in paw edema was completely suppressed by pretreatment with LA. The reduction of paw edema by LAwas abolished by pretreatment with the KATP channel antagonist, glibenclamide.
Our findings demonstrate for the first time in vivo that the anti-inflammatory activity of LA might be connected with the formation of H2S.</description><subject>Animals</subject><subject>Anti-Inflammatory Agents - pharmacology</subject><subject>Anti-Inflammatory Agents - therapeutic use</subject><subject>anti-inflammatory properties</subject><subject>Carrageenan</subject><subject>carrageenan-induced paw edema</subject><subject>dihydrolipoic acid</subject><subject>Dose-Response Relationship, Drug</subject><subject>Drug Safety and Pharmacovigilance</subject><subject>Edema - chemically induced</subject><subject>Edema - drug therapy</subject><subject>glibenclamide</subject><subject>Glyburide - pharmacology</subject><subject>Hindlimb - drug effects</subject><subject>hydrogen sulfide</subject><subject>Hydrogen Sulfide - metabolism</subject><subject>Indomethacin - pharmacology</subject><subject>Indomethacin - therapeutic use</subject><subject>lipoic acid</subject><subject>Male</subject><subject>Mice</subject><subject>Pharmacotherapy</subject><subject>Pharmacy</subject><subject>Potassium Channel Blockers - pharmacology</subject><subject>Short Communication</subject><subject>Thioctic Acid - antagonists & inhibitors</subject><subject>Thioctic Acid - pharmacology</subject><subject>Thioctic Acid - therapeutic use</subject><issn>1734-1140</issn><issn>2299-5684</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><recordid>eNqFkMFOHSEUhkmjqVfbR9CwtIupMMAwrIwxbTUx6UK7JgwcvJiZ4QpMm_v2cr3Wrauz4Pv_c_gQOqXkOyW0u7inkvGGUk7OKfsmKel5wz6hVdsq1Yiu5wdo9Y4coeOcnwjhtGXiMzpqOeWCKLlCw1UCbOYSmjD70UyTKTFt8SbFDaQSIOPo8Rg2MVhsbHDY5BxtMAUc_hfKGpc1YB9TzYU47-D11qX4CDPOy-iDg8sv6NCbMcPXt3mC_vz88XB909z9_nV7fXXX2HpWaURrwXrjuk5J6YSiXElDpeDecgu9sooOsrdC9ANhgzKyMz0XnknZDdJKw07Q-b63Hv-8QC56CtnCOJoZ4pI15ZwzxUhHKyr2qE0x5wReb1KYTNpqSvROr37Vq3fuNGX6Va9mNXf2tmIZJnDvqf8-K9DtgVyf5kdI-ikuaa7f_rD5ch-EauhvqMFsA8wWXEhgi3YxfNDwAuGtmzs</recordid><startdate>2013</startdate><enddate>2013</enddate><creator>Dudek, Magdalena</creator><creator>Bilska-Wilkosz, Anna</creator><creator>Knutelska, Joanna</creator><creator>Mogilski, Szczepan</creator><creator>Bednarski, Marek</creator><creator>Zygmunt, Małgorzata</creator><creator>Iciek, Małgorzata</creator><creator>Sapa, Jacek</creator><creator>Bugajski, Dominik</creator><creator>Filipek, Barbara</creator><creator>Włodek, Lidia</creator><general>Elsevier B.V</general><general>Springer International Publishing</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>2013</creationdate><title>Are anti-inflammatory properties of lipoic acid associated with the formation of hydrogen sulfide?</title><author>Dudek, Magdalena ; Bilska-Wilkosz, Anna ; Knutelska, Joanna ; Mogilski, Szczepan ; Bednarski, Marek ; Zygmunt, Małgorzata ; Iciek, Małgorzata ; Sapa, Jacek ; Bugajski, Dominik ; Filipek, Barbara ; Włodek, Lidia</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c412t-52cecfad66977d591497a1754fc4ce89c91b78c558b03b9a76a845f3776b7c7a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Animals</topic><topic>Anti-Inflammatory Agents - pharmacology</topic><topic>Anti-Inflammatory Agents - therapeutic use</topic><topic>anti-inflammatory properties</topic><topic>Carrageenan</topic><topic>carrageenan-induced paw edema</topic><topic>dihydrolipoic acid</topic><topic>Dose-Response Relationship, Drug</topic><topic>Drug Safety and Pharmacovigilance</topic><topic>Edema - chemically induced</topic><topic>Edema - drug therapy</topic><topic>glibenclamide</topic><topic>Glyburide - pharmacology</topic><topic>Hindlimb - drug effects</topic><topic>hydrogen sulfide</topic><topic>Hydrogen Sulfide - metabolism</topic><topic>Indomethacin - pharmacology</topic><topic>Indomethacin - therapeutic use</topic><topic>lipoic acid</topic><topic>Male</topic><topic>Mice</topic><topic>Pharmacotherapy</topic><topic>Pharmacy</topic><topic>Potassium Channel Blockers - pharmacology</topic><topic>Short Communication</topic><topic>Thioctic Acid - antagonists & inhibitors</topic><topic>Thioctic Acid - pharmacology</topic><topic>Thioctic Acid - therapeutic use</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Dudek, Magdalena</creatorcontrib><creatorcontrib>Bilska-Wilkosz, Anna</creatorcontrib><creatorcontrib>Knutelska, Joanna</creatorcontrib><creatorcontrib>Mogilski, Szczepan</creatorcontrib><creatorcontrib>Bednarski, Marek</creatorcontrib><creatorcontrib>Zygmunt, Małgorzata</creatorcontrib><creatorcontrib>Iciek, Małgorzata</creatorcontrib><creatorcontrib>Sapa, Jacek</creatorcontrib><creatorcontrib>Bugajski, Dominik</creatorcontrib><creatorcontrib>Filipek, Barbara</creatorcontrib><creatorcontrib>Włodek, Lidia</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>Pharmacological reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Dudek, Magdalena</au><au>Bilska-Wilkosz, Anna</au><au>Knutelska, Joanna</au><au>Mogilski, Szczepan</au><au>Bednarski, Marek</au><au>Zygmunt, Małgorzata</au><au>Iciek, Małgorzata</au><au>Sapa, Jacek</au><au>Bugajski, Dominik</au><au>Filipek, Barbara</au><au>Włodek, Lidia</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Are anti-inflammatory properties of lipoic acid associated with the formation of hydrogen sulfide?</atitle><jtitle>Pharmacological reports</jtitle><stitle>Pharmacol. Rep</stitle><addtitle>Pharmacol Rep</addtitle><date>2013</date><risdate>2013</risdate><volume>65</volume><issue>4</issue><spage>1018</spage><epage>1024</epage><pages>1018-1024</pages><issn>1734-1140</issn><eissn>2299-5684</eissn><abstract>Lipoic acid (LA) was shown to possess anti-inflammatory properties. In this study, we present evidence supporting the hypothesis that the anti-inflammatory properties of LA are associated with the formation of hydrogen sulfide (H2S).
The study was conducted on male albino Swiss mice. The animals were treated with carrageenan by subcutaneous (sc) injection into the right hind paw to induce acute inflammation. Animals were treated intraperitoneally (ip) with LA (30, 50 and 100mg/kg) or indomethacin (20mg/kg) 30min before carrageenan administration. The control group was given ip the vehicle (1% Tween 80) 30min before carrageenan administration. Additional experiment involved ip combined treatment of mice with glibenclamide (10mg/kg) or glibenclamide (10mg/kg) and LA(100mg/kg) 30min before carrageenan administration. LA, indomethacin and glibenclamide were suspended in 1% Tween 80. At 1, 2 and 3h after treatment with carrageenan the degree of the paw edema was evaluated by the measurement of the paw volume using aqueous plethysmometer.
Injection of carrageenan into the mouse hind paw increased paw volume. The increase in paw edema was completely suppressed by pretreatment with LA. The reduction of paw edema by LAwas abolished by pretreatment with the KATP channel antagonist, glibenclamide.
Our findings demonstrate for the first time in vivo that the anti-inflammatory activity of LA might be connected with the formation of H2S.</abstract><cop>Cham</cop><pub>Elsevier B.V</pub><pmid>24145097</pmid><doi>10.1016/S1734-1140(13)71084-3</doi><tpages>7</tpages></addata></record> |
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subjects | Animals Anti-Inflammatory Agents - pharmacology Anti-Inflammatory Agents - therapeutic use anti-inflammatory properties Carrageenan carrageenan-induced paw edema dihydrolipoic acid Dose-Response Relationship, Drug Drug Safety and Pharmacovigilance Edema - chemically induced Edema - drug therapy glibenclamide Glyburide - pharmacology Hindlimb - drug effects hydrogen sulfide Hydrogen Sulfide - metabolism Indomethacin - pharmacology Indomethacin - therapeutic use lipoic acid Male Mice Pharmacotherapy Pharmacy Potassium Channel Blockers - pharmacology Short Communication Thioctic Acid - antagonists & inhibitors Thioctic Acid - pharmacology Thioctic Acid - therapeutic use |
title | Are anti-inflammatory properties of lipoic acid associated with the formation of hydrogen sulfide? |
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