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In Vitro Effects of Astaxanthin Combined With Ginkgolide B on T Lymphocyte Activation in Peripheral Blood Mononuclear Cells From Asthmatic Subjects
This study was undertaken to identify novel approaches to pharmacological treatment of asthma. Here we hypothesize that the platelet-activating factor receptor antagonist ginkgolide B (GB) in combination with the antioxidant carotenoid astaxanthin (ASX) suppresses T cell activation comparably to two...
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Published in: | Journal of Pharmacological Sciences 2004, Vol.94(2), pp.129-136 |
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description | This study was undertaken to identify novel approaches to pharmacological treatment of asthma. Here we hypothesize that the platelet-activating factor receptor antagonist ginkgolide B (GB) in combination with the antioxidant carotenoid astaxanthin (ASX) suppresses T cell activation comparably to two commonly-used antihistamines: cetirizine dihydrochloride (CTZ) and azelastine (AZE). Peripheral blood mononuclear cells from asthmatics, cultured 24 h with either 50 μg/ml phytohemaglutinin (PHA) or PHA plus selected dosages of each drug are analyzed by flow cytometry for CD25+ or HLA-DR+ on CD3+ (T cells). Results are reported as stimulation indices (SI) of %CD3+CD25+ cells or %CD3+HLA-DR+ cells in cultures treated with PHA alone versus these subpopulations in cultures treated with both PHA and drugs. Combinations of ASX and GB exhibited optimal suppression at 10-7M GB + 10-8M ASX for CD3+CD25+ (SI = 0.79 ± 0.04, P = 0.001) and 10-7M GB + 10-7M ASX for CD3+HLA-DR+ (SI = 0.82 ± 0.05, P = 0.004). In conclusion, suppression of T cell activation below fully stimulated values by GB, ASX, and their combinations was comparable and for some combinations better than that mediated by CTZ and AZE. These results suggest that ASX and GB may have application as novel antiasthmatic formulations. |
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Here we hypothesize that the platelet-activating factor receptor antagonist ginkgolide B (GB) in combination with the antioxidant carotenoid astaxanthin (ASX) suppresses T cell activation comparably to two commonly-used antihistamines: cetirizine dihydrochloride (CTZ) and azelastine (AZE). Peripheral blood mononuclear cells from asthmatics, cultured 24 h with either 50 μg/ml phytohemaglutinin (PHA) or PHA plus selected dosages of each drug are analyzed by flow cytometry for CD25+ or HLA-DR+ on CD3+ (T cells). Results are reported as stimulation indices (SI) of %CD3+CD25+ cells or %CD3+HLA-DR+ cells in cultures treated with PHA alone versus these subpopulations in cultures treated with both PHA and drugs. Combinations of ASX and GB exhibited optimal suppression at 10-7M GB + 10-8M ASX for CD3+CD25+ (SI = 0.79 ± 0.04, P = 0.001) and 10-7M GB + 10-7M ASX for CD3+HLA-DR+ (SI = 0.82 ± 0.05, P = 0.004). In conclusion, suppression of T cell activation below fully stimulated values by GB, ASX, and their combinations was comparable and for some combinations better than that mediated by CTZ and AZE. These results suggest that ASX and GB may have application as novel antiasthmatic formulations.</description><identifier>ISSN: 1347-8613</identifier><identifier>EISSN: 1347-8648</identifier><identifier>DOI: 10.1254/jphs.94.129</identifier><identifier>PMID: 14978350</identifier><language>eng</language><publisher>Japan: Elsevier B.V</publisher><subject>Adjuvants, Immunologic - pharmacology ; Adult ; astaxanthin ; Asthma - immunology ; Asthma - metabolism ; azelastine ; beta Carotene - analogs & derivatives ; beta Carotene - pharmacology ; Cells, Cultured ; citirazine ; Diterpenes - pharmacology ; Drug Combinations ; Female ; ginkgolide ; Ginkgolides ; Humans ; Lactones - pharmacology ; Leukocytes, Mononuclear - drug effects ; Leukocytes, Mononuclear - metabolism ; Lymphocyte Activation - drug effects ; Male ; Plant Extracts ; Platelet Membrane Glycoproteins - antagonists & inhibitors ; Receptors, G-Protein-Coupled - antagonists & inhibitors ; T lymphocyte ; T-Lymphocytes - drug effects ; T-Lymphocytes - immunology ; T-Lymphocytes - metabolism ; Xanthophylls</subject><ispartof>Journal of Pharmacological Sciences, 2004, Vol.94(2), pp.129-136</ispartof><rights>2004 Elsevier B.V.</rights><rights>The Japanese Pharmacological Society 2004</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c612t-eb19ee9e23b38b383b3a688b6dbb09ee12b4a044e8ecda2ae94e49e1563f1c5d3</citedby><cites>FETCH-LOGICAL-c612t-eb19ee9e23b38b383b3a688b6dbb09ee12b4a044e8ecda2ae94e49e1563f1c5d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S1347861319325174$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>314,776,780,3535,4009,27902,27903,27904,45759</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/14978350$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mahmoud, Fadia F.</creatorcontrib><creatorcontrib>Haines, David D.</creatorcontrib><creatorcontrib>Abul, Habib T.</creatorcontrib><creatorcontrib>Abal, Adnan T.</creatorcontrib><creatorcontrib>Onadeko, Babatunde O.</creatorcontrib><creatorcontrib>Wise, John A.</creatorcontrib><title>In Vitro Effects of Astaxanthin Combined With Ginkgolide B on T Lymphocyte Activation in Peripheral Blood Mononuclear Cells From Asthmatic Subjects</title><title>Journal of Pharmacological Sciences</title><addtitle>J Pharmacol Sci</addtitle><description>This study was undertaken to identify novel approaches to pharmacological treatment of asthma. Here we hypothesize that the platelet-activating factor receptor antagonist ginkgolide B (GB) in combination with the antioxidant carotenoid astaxanthin (ASX) suppresses T cell activation comparably to two commonly-used antihistamines: cetirizine dihydrochloride (CTZ) and azelastine (AZE). Peripheral blood mononuclear cells from asthmatics, cultured 24 h with either 50 μg/ml phytohemaglutinin (PHA) or PHA plus selected dosages of each drug are analyzed by flow cytometry for CD25+ or HLA-DR+ on CD3+ (T cells). Results are reported as stimulation indices (SI) of %CD3+CD25+ cells or %CD3+HLA-DR+ cells in cultures treated with PHA alone versus these subpopulations in cultures treated with both PHA and drugs. Combinations of ASX and GB exhibited optimal suppression at 10-7M GB + 10-8M ASX for CD3+CD25+ (SI = 0.79 ± 0.04, P = 0.001) and 10-7M GB + 10-7M ASX for CD3+HLA-DR+ (SI = 0.82 ± 0.05, P = 0.004). In conclusion, suppression of T cell activation below fully stimulated values by GB, ASX, and their combinations was comparable and for some combinations better than that mediated by CTZ and AZE. These results suggest that ASX and GB may have application as novel antiasthmatic formulations.</description><subject>Adjuvants, Immunologic - pharmacology</subject><subject>Adult</subject><subject>astaxanthin</subject><subject>Asthma - immunology</subject><subject>Asthma - metabolism</subject><subject>azelastine</subject><subject>beta Carotene - analogs & derivatives</subject><subject>beta Carotene - pharmacology</subject><subject>Cells, Cultured</subject><subject>citirazine</subject><subject>Diterpenes - pharmacology</subject><subject>Drug Combinations</subject><subject>Female</subject><subject>ginkgolide</subject><subject>Ginkgolides</subject><subject>Humans</subject><subject>Lactones - pharmacology</subject><subject>Leukocytes, Mononuclear - drug effects</subject><subject>Leukocytes, Mononuclear - metabolism</subject><subject>Lymphocyte Activation - drug effects</subject><subject>Male</subject><subject>Plant Extracts</subject><subject>Platelet Membrane Glycoproteins - antagonists & inhibitors</subject><subject>Receptors, G-Protein-Coupled - antagonists & inhibitors</subject><subject>T lymphocyte</subject><subject>T-Lymphocytes - drug effects</subject><subject>T-Lymphocytes - immunology</subject><subject>T-Lymphocytes - metabolism</subject><subject>Xanthophylls</subject><issn>1347-8613</issn><issn>1347-8648</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNqFkcFu1DAQhiMEoqVw4o584oK22ImTODe2q7astAgkChwtx5lsHBI72N6KfQ5emFmyXS5ISJbtsf_5PJ4_SV4yesnSnL_tpy5cVhyD6lFyzjJeLkTBxePTnmVnybMQekpTQVnxNDljvCpFltPz5Nfakq8mekeu2xZ0DMS1ZBmi-qls7IwlKzfWxkJDvpnYkVtjv2_dYBogV8RZckc2-3HqnN5HIEsdzb2KBs8x8RN4M3Xg1UCuBuca8sFZZ3d6AOXJCoYhkBvvxsNj3YhZmnze1f2hhOfJk1YNAV4c14vky8313er9YvPxdr1abha6YGlcQM0qgArSrM4EDlxUIURdNHVN8YalNVeUcxCgG5UqqDjwClheZC3TeZNdJOuZ2zjVy8mbUfm9dMrIPwfOb6XyWNgAUgDned5CxZjmWjChFCAbyqwRtG0psl7PrMm7HzsIUY4maPylsuB2QWLjyzIv0_8KU5ZSSkWOwjezUHsXgof2VCGj8mC8PBgvK45BhepXR-yuHqH5qz06jYJ3s6BHc7dwEjz88AGWzhMyT1e6U16CRUQ-IwBNuTfgZdAGrIbGePQNu2b-WdtvQi3VkQ</recordid><startdate>2004</startdate><enddate>2004</enddate><creator>Mahmoud, Fadia F.</creator><creator>Haines, David D.</creator><creator>Abul, Habib T.</creator><creator>Abal, Adnan T.</creator><creator>Onadeko, Babatunde O.</creator><creator>Wise, John A.</creator><general>Elsevier B.V</general><general>The Japanese Pharmacological Society</general><general>Elsevier</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>7T5</scope><scope>H94</scope><scope>7X8</scope><scope>DOA</scope></search><sort><creationdate>2004</creationdate><title>In Vitro Effects of Astaxanthin Combined With Ginkgolide B on T Lymphocyte Activation in Peripheral Blood Mononuclear Cells From Asthmatic Subjects</title><author>Mahmoud, Fadia F. ; Haines, David D. ; Abul, Habib T. ; Abal, Adnan T. ; Onadeko, Babatunde O. ; Wise, John A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c612t-eb19ee9e23b38b383b3a688b6dbb09ee12b4a044e8ecda2ae94e49e1563f1c5d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Adjuvants, Immunologic - pharmacology</topic><topic>Adult</topic><topic>astaxanthin</topic><topic>Asthma - immunology</topic><topic>Asthma - metabolism</topic><topic>azelastine</topic><topic>beta Carotene - analogs & derivatives</topic><topic>beta Carotene - pharmacology</topic><topic>Cells, Cultured</topic><topic>citirazine</topic><topic>Diterpenes - pharmacology</topic><topic>Drug Combinations</topic><topic>Female</topic><topic>ginkgolide</topic><topic>Ginkgolides</topic><topic>Humans</topic><topic>Lactones - pharmacology</topic><topic>Leukocytes, Mononuclear - drug effects</topic><topic>Leukocytes, Mononuclear - metabolism</topic><topic>Lymphocyte Activation - drug effects</topic><topic>Male</topic><topic>Plant Extracts</topic><topic>Platelet Membrane Glycoproteins - antagonists & inhibitors</topic><topic>Receptors, G-Protein-Coupled - antagonists & inhibitors</topic><topic>T lymphocyte</topic><topic>T-Lymphocytes - drug effects</topic><topic>T-Lymphocytes - immunology</topic><topic>T-Lymphocytes - metabolism</topic><topic>Xanthophylls</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mahmoud, Fadia F.</creatorcontrib><creatorcontrib>Haines, David D.</creatorcontrib><creatorcontrib>Abul, Habib T.</creatorcontrib><creatorcontrib>Abal, Adnan T.</creatorcontrib><creatorcontrib>Onadeko, Babatunde O.</creatorcontrib><creatorcontrib>Wise, John A.</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>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Journal of Pharmacological Sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mahmoud, Fadia F.</au><au>Haines, David D.</au><au>Abul, Habib T.</au><au>Abal, Adnan T.</au><au>Onadeko, Babatunde O.</au><au>Wise, John A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>In Vitro Effects of Astaxanthin Combined With Ginkgolide B on T Lymphocyte Activation in Peripheral Blood Mononuclear Cells From Asthmatic Subjects</atitle><jtitle>Journal of Pharmacological Sciences</jtitle><addtitle>J Pharmacol Sci</addtitle><date>2004</date><risdate>2004</risdate><volume>94</volume><issue>2</issue><spage>129</spage><epage>136</epage><pages>129-136</pages><issn>1347-8613</issn><eissn>1347-8648</eissn><abstract>This study was undertaken to identify novel approaches to pharmacological treatment of asthma. Here we hypothesize that the platelet-activating factor receptor antagonist ginkgolide B (GB) in combination with the antioxidant carotenoid astaxanthin (ASX) suppresses T cell activation comparably to two commonly-used antihistamines: cetirizine dihydrochloride (CTZ) and azelastine (AZE). Peripheral blood mononuclear cells from asthmatics, cultured 24 h with either 50 μg/ml phytohemaglutinin (PHA) or PHA plus selected dosages of each drug are analyzed by flow cytometry for CD25+ or HLA-DR+ on CD3+ (T cells). Results are reported as stimulation indices (SI) of %CD3+CD25+ cells or %CD3+HLA-DR+ cells in cultures treated with PHA alone versus these subpopulations in cultures treated with both PHA and drugs. Combinations of ASX and GB exhibited optimal suppression at 10-7M GB + 10-8M ASX for CD3+CD25+ (SI = 0.79 ± 0.04, P = 0.001) and 10-7M GB + 10-7M ASX for CD3+HLA-DR+ (SI = 0.82 ± 0.05, P = 0.004). In conclusion, suppression of T cell activation below fully stimulated values by GB, ASX, and their combinations was comparable and for some combinations better than that mediated by CTZ and AZE. These results suggest that ASX and GB may have application as novel antiasthmatic formulations.</abstract><cop>Japan</cop><pub>Elsevier B.V</pub><pmid>14978350</pmid><doi>10.1254/jphs.94.129</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adjuvants, Immunologic - pharmacology Adult astaxanthin Asthma - immunology Asthma - metabolism azelastine beta Carotene - analogs & derivatives beta Carotene - pharmacology Cells, Cultured citirazine Diterpenes - pharmacology Drug Combinations Female ginkgolide Ginkgolides Humans Lactones - pharmacology Leukocytes, Mononuclear - drug effects Leukocytes, Mononuclear - metabolism Lymphocyte Activation - drug effects Male Plant Extracts Platelet Membrane Glycoproteins - antagonists & inhibitors Receptors, G-Protein-Coupled - antagonists & inhibitors T lymphocyte T-Lymphocytes - drug effects T-Lymphocytes - immunology T-Lymphocytes - metabolism Xanthophylls |
title | In Vitro Effects of Astaxanthin Combined With Ginkgolide B on T Lymphocyte Activation in Peripheral Blood Mononuclear Cells From Asthmatic Subjects |
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