Different Effects of Arborinine Alkaloid Obtained from Brazilian Erthela baihensis on Spleen and Thymus Cells Stimulated in Vitro with Different Mitogens
The present study has examined the effects of arborinine, an alkaloid obtained from Erthela bahiensis, a Brazilian plant popularly used as diuretic, antidiabetic, antithermic and expectorant, on the viability and function of immune system cells in vitro using a murine model. Rat spleen and thymus ce...
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creator | Roseghini, R. Moreira, P. Vale, V. Pinheiro, A.M. Costa, J.F.O. Bittencourt, T. Nascimento, I. Schaer, R. Velozo, E. El-Bachá, R. Meyer, R. Freire, S. |
description | The present study has examined the effects of arborinine, an alkaloid obtained from Erthela bahiensis, a Brazilian plant popularly used as diuretic, antidiabetic, antithermic and expectorant, on the viability and function of immune system cells in vitro using a murine model. Rat spleen and thymus cells were cultured with 10nM, 1µM e 10µM of the drug in the presence or absence of pokeweed (PWM), lipopolysaccharide (LPS), or concanavallin (ConA) mitogens. Cellular proliferation was analyzed by H3-thymidin uptake after 48 and 72 hr. Our results showed an inhibitory effect of arborinine on splenocytes proliferation under ConA or PWM stimulation and increased apoptosis on splenocytes and thymocytes stimulated with PWM in 24 hr. A decrease was observed on Interferon gamma (IFN- ) production by ConA- or LPS-stimulated splenocytes in 48 hr and 72 hr and ConA- or PWM-stimulated thymocytes in 72 hr. In contrast, an increase on lymphoproliferation was observed on LPS-stimulated splenocytes and ConA- or PWM-stimulated thymocytes in 48 hr. On this period, apoptosis decreased on LPS- or PWM-stimulated splenocytes and IFN- production increased in PWM stimulated thymocytes. Arborinine also induced a decrease on Interleukin-10 production by splenocytes and thymocytes stimulated with ConA or PWM. There was no significant variation on the necrosis rate of the cells treated with arborinine or any change on their viability or function values in the absence of mitogenic stimulus. |
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Rat spleen and thymus cells were cultured with 10nM, 1µM e 10µM of the drug in the presence or absence of pokeweed (PWM), lipopolysaccharide (LPS), or concanavallin (ConA) mitogens. Cellular proliferation was analyzed by H3-thymidin uptake after 48 and 72 hr. Our results showed an inhibitory effect of arborinine on splenocytes proliferation under ConA or PWM stimulation and increased apoptosis on splenocytes and thymocytes stimulated with PWM in 24 hr. A decrease was observed on Interferon gamma (IFN- ) production by ConA- or LPS-stimulated splenocytes in 48 hr and 72 hr and ConA- or PWM-stimulated thymocytes in 72 hr. In contrast, an increase on lymphoproliferation was observed on LPS-stimulated splenocytes and ConA- or PWM-stimulated thymocytes in 48 hr. On this period, apoptosis decreased on LPS- or PWM-stimulated splenocytes and IFN- production increased in PWM stimulated thymocytes. Arborinine also induced a decrease on Interleukin-10 production by splenocytes and thymocytes stimulated with ConA or PWM. There was no significant variation on the necrosis rate of the cells treated with arborinine or any change on their viability or function values in the absence of mitogenic stimulus.</description><identifier>ISSN: 0892-3973</identifier><identifier>EISSN: 1532-2513</identifier><identifier>DOI: 10.1080/08923970600809579</identifier><identifier>PMID: 16873102</identifier><language>eng</language><publisher>England: Informa UK Ltd</publisher><subject>Acridones ; Alkaloids ; Alkaloids - chemistry ; Alkaloids - pharmacology ; Animals ; Apoptosis ; Arborinine ; Cell Proliferation - drug effects ; Cell Survival - drug effects ; Cells, Cultured ; Drug Evaluation, Preclinical ; Interferon-gamma - immunology ; Interleukin-10 - immunology ; Male ; Mitogens ; Mitogens - pharmacology ; Plants - chemistry ; Quinazolines - chemistry ; Quinazolines - pharmacology ; Quinazolinones ; Rats ; Rats, Wistar ; Spleen - cytology ; Spleen - immunology ; Thymus Gland - cytology ; Thymus Gland - immunology</subject><ispartof>Immunopharmacology and immunotoxicology, 2006, Vol.28 (2), p.361-376</ispartof><rights>2006 Informa UK Ltd All rights reserved: reproduction in whole or part not permitted 2006</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c435t-315ffa5eb3bf294e0b12449b737f98bf807b91918b803b890347d0f91a0328663</citedby><cites>FETCH-LOGICAL-c435t-315ffa5eb3bf294e0b12449b737f98bf807b91918b803b890347d0f91a0328663</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.tandfonline.com/doi/pdf/10.1080/08923970600809579$$EPDF$$P50$$Ginformahealthcare$$H</linktopdf><linktohtml>$$Uhttps://www.tandfonline.com/doi/full/10.1080/08923970600809579$$EHTML$$P50$$Ginformahealthcare$$H</linktohtml><link.rule.ids>314,780,784,4024,27923,27924,27925,59647,59753,60436,60542,61221,61256,61402,61437</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16873102$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Roseghini, R.</creatorcontrib><creatorcontrib>Moreira, P.</creatorcontrib><creatorcontrib>Vale, V.</creatorcontrib><creatorcontrib>Pinheiro, A.M.</creatorcontrib><creatorcontrib>Costa, J.F.O.</creatorcontrib><creatorcontrib>Bittencourt, T.</creatorcontrib><creatorcontrib>Nascimento, I.</creatorcontrib><creatorcontrib>Schaer, R.</creatorcontrib><creatorcontrib>Velozo, E.</creatorcontrib><creatorcontrib>El-Bachá, R.</creatorcontrib><creatorcontrib>Meyer, R.</creatorcontrib><creatorcontrib>Freire, S.</creatorcontrib><title>Different Effects of Arborinine Alkaloid Obtained from Brazilian Erthela baihensis on Spleen and Thymus Cells Stimulated in Vitro with Different Mitogens</title><title>Immunopharmacology and immunotoxicology</title><addtitle>Immunopharmacol Immunotoxicol</addtitle><description>The present study has examined the effects of arborinine, an alkaloid obtained from Erthela bahiensis, a Brazilian plant popularly used as diuretic, antidiabetic, antithermic and expectorant, on the viability and function of immune system cells in vitro using a murine model. Rat spleen and thymus cells were cultured with 10nM, 1µM e 10µM of the drug in the presence or absence of pokeweed (PWM), lipopolysaccharide (LPS), or concanavallin (ConA) mitogens. Cellular proliferation was analyzed by H3-thymidin uptake after 48 and 72 hr. Our results showed an inhibitory effect of arborinine on splenocytes proliferation under ConA or PWM stimulation and increased apoptosis on splenocytes and thymocytes stimulated with PWM in 24 hr. A decrease was observed on Interferon gamma (IFN- ) production by ConA- or LPS-stimulated splenocytes in 48 hr and 72 hr and ConA- or PWM-stimulated thymocytes in 72 hr. In contrast, an increase on lymphoproliferation was observed on LPS-stimulated splenocytes and ConA- or PWM-stimulated thymocytes in 48 hr. On this period, apoptosis decreased on LPS- or PWM-stimulated splenocytes and IFN- production increased in PWM stimulated thymocytes. Arborinine also induced a decrease on Interleukin-10 production by splenocytes and thymocytes stimulated with ConA or PWM. There was no significant variation on the necrosis rate of the cells treated with arborinine or any change on their viability or function values in the absence of mitogenic stimulus.</description><subject>Acridones</subject><subject>Alkaloids</subject><subject>Alkaloids - chemistry</subject><subject>Alkaloids - pharmacology</subject><subject>Animals</subject><subject>Apoptosis</subject><subject>Arborinine</subject><subject>Cell Proliferation - drug effects</subject><subject>Cell Survival - drug effects</subject><subject>Cells, Cultured</subject><subject>Drug Evaluation, Preclinical</subject><subject>Interferon-gamma - immunology</subject><subject>Interleukin-10 - immunology</subject><subject>Male</subject><subject>Mitogens</subject><subject>Mitogens - pharmacology</subject><subject>Plants - chemistry</subject><subject>Quinazolines - chemistry</subject><subject>Quinazolines - pharmacology</subject><subject>Quinazolinones</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Spleen - cytology</subject><subject>Spleen - immunology</subject><subject>Thymus Gland - cytology</subject><subject>Thymus Gland - immunology</subject><issn>0892-3973</issn><issn>1532-2513</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkctuFDEQRS0EIpPAB7BBXrHr4Ec_bMFmGIaHFJRFAttWudumHdz2YLsVDX_C3-JoRooQUljZLp86uqpC6AUl55QI8poIybjsSEvKSzadfIRWtOGsYg3lj9Hq7r8qAD9BpyndEEIL3DxFJ7QVHaeErdDv99YYHbXPeFsuQ044GLyOKkTrrdd47X6AC3bElypDKYzYxDDjdxF-WWfB423Mk3aAFdhJ-2SLwOOrndPaY_Ajvp7285LwRjuX8FW28-IgF431-JvNMeBbmyd8H-OLzeF7ET1DTwy4pJ8fzzP09cP2evOpurj8-HmzvqiGmje54rQxBhqtuDJM1pooyupaqo53RgplBOmUpJIKJQhXQhJedyMxkgLhTLQtP0OvDt5dDD8XnXI_2zSUtOB1WFLfiraMseX_BVlRU8brAtIDOMSQUtSm30U7Q9z3lPR3i-v_WVzpeXmUL2rW433HcVMFeHsArDchznAbohv7DHsXoongB5t6_pD_zV_tkwaXpwGi7m_CEn2Z8APp_gAEUbm_</recordid><startdate>2006</startdate><enddate>2006</enddate><creator>Roseghini, R.</creator><creator>Moreira, P.</creator><creator>Vale, V.</creator><creator>Pinheiro, A.M.</creator><creator>Costa, J.F.O.</creator><creator>Bittencourt, T.</creator><creator>Nascimento, I.</creator><creator>Schaer, R.</creator><creator>Velozo, E.</creator><creator>El-Bachá, R.</creator><creator>Meyer, R.</creator><creator>Freire, S.</creator><general>Informa UK Ltd</general><general>Taylor & Francis</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>7T5</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>2006</creationdate><title>Different Effects of Arborinine Alkaloid Obtained from Brazilian Erthela baihensis on Spleen and Thymus Cells Stimulated in Vitro with Different Mitogens</title><author>Roseghini, R. ; Moreira, P. ; Vale, V. ; Pinheiro, A.M. ; Costa, J.F.O. ; Bittencourt, T. ; Nascimento, I. ; Schaer, R. ; Velozo, E. ; El-Bachá, R. ; Meyer, R. ; Freire, S.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c435t-315ffa5eb3bf294e0b12449b737f98bf807b91918b803b890347d0f91a0328663</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Acridones</topic><topic>Alkaloids</topic><topic>Alkaloids - chemistry</topic><topic>Alkaloids - pharmacology</topic><topic>Animals</topic><topic>Apoptosis</topic><topic>Arborinine</topic><topic>Cell Proliferation - drug effects</topic><topic>Cell Survival - drug effects</topic><topic>Cells, Cultured</topic><topic>Drug Evaluation, Preclinical</topic><topic>Interferon-gamma - immunology</topic><topic>Interleukin-10 - immunology</topic><topic>Male</topic><topic>Mitogens</topic><topic>Mitogens - pharmacology</topic><topic>Plants - chemistry</topic><topic>Quinazolines - chemistry</topic><topic>Quinazolines - pharmacology</topic><topic>Quinazolinones</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Spleen - cytology</topic><topic>Spleen - immunology</topic><topic>Thymus Gland - cytology</topic><topic>Thymus Gland - immunology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Roseghini, R.</creatorcontrib><creatorcontrib>Moreira, P.</creatorcontrib><creatorcontrib>Vale, V.</creatorcontrib><creatorcontrib>Pinheiro, A.M.</creatorcontrib><creatorcontrib>Costa, J.F.O.</creatorcontrib><creatorcontrib>Bittencourt, T.</creatorcontrib><creatorcontrib>Nascimento, I.</creatorcontrib><creatorcontrib>Schaer, R.</creatorcontrib><creatorcontrib>Velozo, E.</creatorcontrib><creatorcontrib>El-Bachá, R.</creatorcontrib><creatorcontrib>Meyer, R.</creatorcontrib><creatorcontrib>Freire, S.</creatorcontrib><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><jtitle>Immunopharmacology and immunotoxicology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Roseghini, R.</au><au>Moreira, P.</au><au>Vale, V.</au><au>Pinheiro, A.M.</au><au>Costa, J.F.O.</au><au>Bittencourt, T.</au><au>Nascimento, I.</au><au>Schaer, R.</au><au>Velozo, E.</au><au>El-Bachá, R.</au><au>Meyer, R.</au><au>Freire, S.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Different Effects of Arborinine Alkaloid Obtained from Brazilian Erthela baihensis on Spleen and Thymus Cells Stimulated in Vitro with Different Mitogens</atitle><jtitle>Immunopharmacology and immunotoxicology</jtitle><addtitle>Immunopharmacol Immunotoxicol</addtitle><date>2006</date><risdate>2006</risdate><volume>28</volume><issue>2</issue><spage>361</spage><epage>376</epage><pages>361-376</pages><issn>0892-3973</issn><eissn>1532-2513</eissn><abstract>The present study has examined the effects of arborinine, an alkaloid obtained from Erthela bahiensis, a Brazilian plant popularly used as diuretic, antidiabetic, antithermic and expectorant, on the viability and function of immune system cells in vitro using a murine model. Rat spleen and thymus cells were cultured with 10nM, 1µM e 10µM of the drug in the presence or absence of pokeweed (PWM), lipopolysaccharide (LPS), or concanavallin (ConA) mitogens. Cellular proliferation was analyzed by H3-thymidin uptake after 48 and 72 hr. Our results showed an inhibitory effect of arborinine on splenocytes proliferation under ConA or PWM stimulation and increased apoptosis on splenocytes and thymocytes stimulated with PWM in 24 hr. A decrease was observed on Interferon gamma (IFN- ) production by ConA- or LPS-stimulated splenocytes in 48 hr and 72 hr and ConA- or PWM-stimulated thymocytes in 72 hr. In contrast, an increase on lymphoproliferation was observed on LPS-stimulated splenocytes and ConA- or PWM-stimulated thymocytes in 48 hr. On this period, apoptosis decreased on LPS- or PWM-stimulated splenocytes and IFN- production increased in PWM stimulated thymocytes. Arborinine also induced a decrease on Interleukin-10 production by splenocytes and thymocytes stimulated with ConA or PWM. There was no significant variation on the necrosis rate of the cells treated with arborinine or any change on their viability or function values in the absence of mitogenic stimulus.</abstract><cop>England</cop><pub>Informa UK Ltd</pub><pmid>16873102</pmid><doi>10.1080/08923970600809579</doi><tpages>16</tpages></addata></record> |
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subjects | Acridones Alkaloids Alkaloids - chemistry Alkaloids - pharmacology Animals Apoptosis Arborinine Cell Proliferation - drug effects Cell Survival - drug effects Cells, Cultured Drug Evaluation, Preclinical Interferon-gamma - immunology Interleukin-10 - immunology Male Mitogens Mitogens - pharmacology Plants - chemistry Quinazolines - chemistry Quinazolines - pharmacology Quinazolinones Rats Rats, Wistar Spleen - cytology Spleen - immunology Thymus Gland - cytology Thymus Gland - immunology |
title | Different Effects of Arborinine Alkaloid Obtained from Brazilian Erthela baihensis on Spleen and Thymus Cells Stimulated in Vitro with Different Mitogens |
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