In vitro and in vivo antitumor effect of 5-FU combined with piplartine and piperine
It has been reported that piplartine and piperine, alkaloid/amide compounds from Piper species, show antitumor activities. In the present paper, the effects of the combination of 5‐fluorouracil (5‐FU) with piplartine or piperine was determined using in vitro and in vivo experimental models. Hematolo...
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creator | Bezerra, Daniel P. Castro, Fernanda O. de Alves, Ana Paula N. N. Pessoa, Cláudia Moraes, Manoel Odorico de Silveira, Edilberto R. Lima, Mary Anne S. Elmiro, Francisca Juliana M. Alencar, Nylane M. N. de Mesquita, Rodney O. Lima, Michael W. Costa-Lotufo, Letícia V. |
description | It has been reported that piplartine and piperine, alkaloid/amide compounds from Piper species, show antitumor activities. In the present paper, the effects of the combination of 5‐fluorouracil (5‐FU) with piplartine or piperine was determined using in vitro and in vivo experimental models. Hematological and biochemical analyses, as well as histopathological and morphological analyses of the tumor and the organs, including liver, spleen and kidney, were performed in order to evaluate the toxicological aspects associated with different treatments. The incubation of tumor cell lines with 5‐FU in the presence of piplartine or piperine produced an increase in growth inhibition, as observed by lower IC50 values for 5‐FU. These effects were also observed in vivo, where the combination with piplartine but not piperine with 5‐FU led to a higher tumor growth inhibition. The results indicated that either piplartine‐ or 5‐FU‐treated animals showed a low inhibition rate when they were used individually at low doses of 28.67% and 47.71%, respectively, but when they were combined at the same dose, the inhibition rate increased significantly to 68.04%. The histopathological analysis showed that the livers and the kidneys of treated animals were only slightly and reversibly affected. Neither the enzymatic activity of transaminases nor the urea levels were significantly modified when compared with the control group. Hematological analysis showed leukopenia after 5‐FU treatment, which was reversed by the combined use of piplartine and piperine. These findings indicate that piplartine may enhance the therapeutic effectiveness of chemotherapeutic drugs, and moreover, this combination could improve immunocompetence hampered by 5‐FU. Copyright © 2007 John Wiley & Sons, Ltd. |
doi_str_mv | 10.1002/jat.1261 |
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N. ; Pessoa, Cláudia ; Moraes, Manoel Odorico de ; Silveira, Edilberto R. ; Lima, Mary Anne S. ; Elmiro, Francisca Juliana M. ; Alencar, Nylane M. N. de ; Mesquita, Rodney O. ; Lima, Michael W. ; Costa-Lotufo, Letícia V.</creator><creatorcontrib>Bezerra, Daniel P. ; Castro, Fernanda O. de ; Alves, Ana Paula N. N. ; Pessoa, Cláudia ; Moraes, Manoel Odorico de ; Silveira, Edilberto R. ; Lima, Mary Anne S. ; Elmiro, Francisca Juliana M. ; Alencar, Nylane M. N. de ; Mesquita, Rodney O. ; Lima, Michael W. ; Costa-Lotufo, Letícia V.</creatorcontrib><description>It has been reported that piplartine and piperine, alkaloid/amide compounds from Piper species, show antitumor activities. In the present paper, the effects of the combination of 5‐fluorouracil (5‐FU) with piplartine or piperine was determined using in vitro and in vivo experimental models. Hematological and biochemical analyses, as well as histopathological and morphological analyses of the tumor and the organs, including liver, spleen and kidney, were performed in order to evaluate the toxicological aspects associated with different treatments. The incubation of tumor cell lines with 5‐FU in the presence of piplartine or piperine produced an increase in growth inhibition, as observed by lower IC50 values for 5‐FU. These effects were also observed in vivo, where the combination with piplartine but not piperine with 5‐FU led to a higher tumor growth inhibition. The results indicated that either piplartine‐ or 5‐FU‐treated animals showed a low inhibition rate when they were used individually at low doses of 28.67% and 47.71%, respectively, but when they were combined at the same dose, the inhibition rate increased significantly to 68.04%. The histopathological analysis showed that the livers and the kidneys of treated animals were only slightly and reversibly affected. Neither the enzymatic activity of transaminases nor the urea levels were significantly modified when compared with the control group. Hematological analysis showed leukopenia after 5‐FU treatment, which was reversed by the combined use of piplartine and piperine. These findings indicate that piplartine may enhance the therapeutic effectiveness of chemotherapeutic drugs, and moreover, this combination could improve immunocompetence hampered by 5‐FU. Copyright © 2007 John Wiley & Sons, Ltd.</description><identifier>ISSN: 0260-437X</identifier><identifier>EISSN: 1099-1263</identifier><identifier>DOI: 10.1002/jat.1261</identifier><identifier>PMID: 17541943</identifier><identifier>CODEN: JJATDK</identifier><language>eng</language><publisher>Chichester, UK: John Wiley & Sons, Ltd</publisher><subject><![CDATA[5-fluorouracil ; Alanine Transaminase - blood ; Alkaloids - administration & dosage ; Animals ; Antimetabolites, Antineoplastic - administration & dosage ; Antineoplastic Agents, Phytogenic - administration & dosage ; Antineoplastic Combined Chemotherapy Protocols - pharmacology ; Antineoplastic Combined Chemotherapy Protocols - toxicity ; antitumor activity ; Aspartate Aminotransferases - blood ; Benzodioxoles - administration & dosage ; Biological and medical sciences ; Cell Proliferation - drug effects ; Dose-Response Relationship, Drug ; Female ; Fluorouracil - administration & dosage ; HL-60 Cells ; Humans ; Inhibitory Concentration 50 ; Kidney - drug effects ; Kidney - metabolism ; Leukopenia - chemically induced ; Leukopenia - prevention & control ; Liver - drug effects ; Liver - enzymology ; Medical sciences ; Mice ; Piperidines - administration & dosage ; Piperidones - administration & dosage ; piperine ; piplartine ; Polyunsaturated Alkamides - administration & dosage ; Sarcoma 180 - drug therapy ; Sarcoma 180 - metabolism ; Sarcoma 180 - pathology ; toxicity ; Toxicology ; Urea - blood]]></subject><ispartof>Journal of applied toxicology, 2008-03, Vol.28 (2), p.156-163</ispartof><rights>Copyright © 2007 John Wiley & Sons, Ltd.</rights><rights>2008 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4181-e8006bed805f4a688378810f584848312e54e7efa67e53f9181a84e0ba9291a63</citedby><cites>FETCH-LOGICAL-c4181-e8006bed805f4a688378810f584848312e54e7efa67e53f9181a84e0ba9291a63</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fjat.1261$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fjat.1261$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>315,782,786,1419,27933,27934,45583,45584</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=20171812$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17541943$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bezerra, Daniel P.</creatorcontrib><creatorcontrib>Castro, Fernanda O. de</creatorcontrib><creatorcontrib>Alves, Ana Paula N. N.</creatorcontrib><creatorcontrib>Pessoa, Cláudia</creatorcontrib><creatorcontrib>Moraes, Manoel Odorico de</creatorcontrib><creatorcontrib>Silveira, Edilberto R.</creatorcontrib><creatorcontrib>Lima, Mary Anne S.</creatorcontrib><creatorcontrib>Elmiro, Francisca Juliana M.</creatorcontrib><creatorcontrib>Alencar, Nylane M. N. de</creatorcontrib><creatorcontrib>Mesquita, Rodney O.</creatorcontrib><creatorcontrib>Lima, Michael W.</creatorcontrib><creatorcontrib>Costa-Lotufo, Letícia V.</creatorcontrib><title>In vitro and in vivo antitumor effect of 5-FU combined with piplartine and piperine</title><title>Journal of applied toxicology</title><addtitle>J. Appl. Toxicol</addtitle><description>It has been reported that piplartine and piperine, alkaloid/amide compounds from Piper species, show antitumor activities. In the present paper, the effects of the combination of 5‐fluorouracil (5‐FU) with piplartine or piperine was determined using in vitro and in vivo experimental models. Hematological and biochemical analyses, as well as histopathological and morphological analyses of the tumor and the organs, including liver, spleen and kidney, were performed in order to evaluate the toxicological aspects associated with different treatments. The incubation of tumor cell lines with 5‐FU in the presence of piplartine or piperine produced an increase in growth inhibition, as observed by lower IC50 values for 5‐FU. These effects were also observed in vivo, where the combination with piplartine but not piperine with 5‐FU led to a higher tumor growth inhibition. The results indicated that either piplartine‐ or 5‐FU‐treated animals showed a low inhibition rate when they were used individually at low doses of 28.67% and 47.71%, respectively, but when they were combined at the same dose, the inhibition rate increased significantly to 68.04%. The histopathological analysis showed that the livers and the kidneys of treated animals were only slightly and reversibly affected. Neither the enzymatic activity of transaminases nor the urea levels were significantly modified when compared with the control group. Hematological analysis showed leukopenia after 5‐FU treatment, which was reversed by the combined use of piplartine and piperine. These findings indicate that piplartine may enhance the therapeutic effectiveness of chemotherapeutic drugs, and moreover, this combination could improve immunocompetence hampered by 5‐FU. Copyright © 2007 John Wiley & Sons, Ltd.</description><subject>5-fluorouracil</subject><subject>Alanine Transaminase - blood</subject><subject>Alkaloids - administration & dosage</subject><subject>Animals</subject><subject>Antimetabolites, Antineoplastic - administration & dosage</subject><subject>Antineoplastic Agents, Phytogenic - administration & dosage</subject><subject>Antineoplastic Combined Chemotherapy Protocols - pharmacology</subject><subject>Antineoplastic Combined Chemotherapy Protocols - toxicity</subject><subject>antitumor activity</subject><subject>Aspartate Aminotransferases - blood</subject><subject>Benzodioxoles - administration & dosage</subject><subject>Biological and medical sciences</subject><subject>Cell Proliferation - drug effects</subject><subject>Dose-Response Relationship, Drug</subject><subject>Female</subject><subject>Fluorouracil - administration & dosage</subject><subject>HL-60 Cells</subject><subject>Humans</subject><subject>Inhibitory Concentration 50</subject><subject>Kidney - drug effects</subject><subject>Kidney - metabolism</subject><subject>Leukopenia - chemically induced</subject><subject>Leukopenia - prevention & control</subject><subject>Liver - drug effects</subject><subject>Liver - enzymology</subject><subject>Medical sciences</subject><subject>Mice</subject><subject>Piperidines - administration & dosage</subject><subject>Piperidones - administration & dosage</subject><subject>piperine</subject><subject>piplartine</subject><subject>Polyunsaturated Alkamides - administration & dosage</subject><subject>Sarcoma 180 - drug therapy</subject><subject>Sarcoma 180 - metabolism</subject><subject>Sarcoma 180 - pathology</subject><subject>toxicity</subject><subject>Toxicology</subject><subject>Urea - blood</subject><issn>0260-437X</issn><issn>1099-1263</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kMtOGzEUhq0KVMJF4gmQN626Gerr2LNEtBCiiEoQRNWN5UyOVdO5BNsB8vY4ZERXyItz_uPvXPQjdEzJKSWEfX-w6ZSykn5CI0qqqsg530EjwkpSCK5-76H9GB8IyX9Mf0Z7VElBK8FH6Paqw08-hR7bboH9Rjxt8uTTqu0DBuegTrh3WBYXd7ju27nvYIGfffqLl37Z2JBy4a07SwhZHKJdZ5sIR0M8QHcXP2fn42L66_Lq_Gxa1IJqWoAmpJzDQhPphC215kprSpzUIj9OGUgBCpwtFUjuqtxjtQAytxWrqC35Afq6nbsM_eMKYjKtjzU0je2gX0XDmRSVZCqD37ZgHfoYAzizDL61YW0oMRsDTTbQbAzM6MkwczVvYfEfHBzLwJcBsLG2jQu2q3185xihKh_KMldsuWffwPrDhWZyNhsWD7yPCV7eeRv-mVJxJc399aWZ_pj8mdyMZ-aevwIwwJQ4</recordid><startdate>200803</startdate><enddate>200803</enddate><creator>Bezerra, Daniel P.</creator><creator>Castro, Fernanda O. de</creator><creator>Alves, Ana Paula N. N.</creator><creator>Pessoa, Cláudia</creator><creator>Moraes, Manoel Odorico de</creator><creator>Silveira, Edilberto R.</creator><creator>Lima, Mary Anne S.</creator><creator>Elmiro, Francisca Juliana M.</creator><creator>Alencar, Nylane M. N. de</creator><creator>Mesquita, Rodney O.</creator><creator>Lima, Michael W.</creator><creator>Costa-Lotufo, Letícia V.</creator><general>John Wiley & Sons, Ltd</general><general>Wiley</general><scope>BSCLL</scope><scope>IQODW</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>8FD</scope><scope>FR3</scope><scope>KR7</scope></search><sort><creationdate>200803</creationdate><title>In vitro and in vivo antitumor effect of 5-FU combined with piplartine and piperine</title><author>Bezerra, Daniel P. ; Castro, Fernanda O. de ; Alves, Ana Paula N. N. ; Pessoa, Cláudia ; Moraes, Manoel Odorico de ; Silveira, Edilberto R. ; Lima, Mary Anne S. ; Elmiro, Francisca Juliana M. ; Alencar, Nylane M. N. de ; Mesquita, Rodney O. ; Lima, Michael W. ; Costa-Lotufo, Letícia V.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4181-e8006bed805f4a688378810f584848312e54e7efa67e53f9181a84e0ba9291a63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>5-fluorouracil</topic><topic>Alanine Transaminase - blood</topic><topic>Alkaloids - administration & dosage</topic><topic>Animals</topic><topic>Antimetabolites, Antineoplastic - administration & dosage</topic><topic>Antineoplastic Agents, Phytogenic - administration & dosage</topic><topic>Antineoplastic Combined Chemotherapy Protocols - pharmacology</topic><topic>Antineoplastic Combined Chemotherapy Protocols - toxicity</topic><topic>antitumor activity</topic><topic>Aspartate Aminotransferases - blood</topic><topic>Benzodioxoles - administration & dosage</topic><topic>Biological and medical sciences</topic><topic>Cell Proliferation - drug effects</topic><topic>Dose-Response Relationship, Drug</topic><topic>Female</topic><topic>Fluorouracil - administration & dosage</topic><topic>HL-60 Cells</topic><topic>Humans</topic><topic>Inhibitory Concentration 50</topic><topic>Kidney - drug effects</topic><topic>Kidney - metabolism</topic><topic>Leukopenia - chemically induced</topic><topic>Leukopenia - prevention & control</topic><topic>Liver - drug effects</topic><topic>Liver - enzymology</topic><topic>Medical sciences</topic><topic>Mice</topic><topic>Piperidines - administration & dosage</topic><topic>Piperidones - administration & dosage</topic><topic>piperine</topic><topic>piplartine</topic><topic>Polyunsaturated Alkamides - administration & dosage</topic><topic>Sarcoma 180 - drug therapy</topic><topic>Sarcoma 180 - metabolism</topic><topic>Sarcoma 180 - pathology</topic><topic>toxicity</topic><topic>Toxicology</topic><topic>Urea - blood</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bezerra, Daniel P.</creatorcontrib><creatorcontrib>Castro, Fernanda O. de</creatorcontrib><creatorcontrib>Alves, Ana Paula N. N.</creatorcontrib><creatorcontrib>Pessoa, Cláudia</creatorcontrib><creatorcontrib>Moraes, Manoel Odorico de</creatorcontrib><creatorcontrib>Silveira, Edilberto R.</creatorcontrib><creatorcontrib>Lima, Mary Anne S.</creatorcontrib><creatorcontrib>Elmiro, Francisca Juliana M.</creatorcontrib><creatorcontrib>Alencar, Nylane M. N. de</creatorcontrib><creatorcontrib>Mesquita, Rodney O.</creatorcontrib><creatorcontrib>Lima, Michael W.</creatorcontrib><creatorcontrib>Costa-Lotufo, Letícia V.</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Civil Engineering Abstracts</collection><jtitle>Journal of applied toxicology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bezerra, Daniel P.</au><au>Castro, Fernanda O. de</au><au>Alves, Ana Paula N. N.</au><au>Pessoa, Cláudia</au><au>Moraes, Manoel Odorico de</au><au>Silveira, Edilberto R.</au><au>Lima, Mary Anne S.</au><au>Elmiro, Francisca Juliana M.</au><au>Alencar, Nylane M. N. de</au><au>Mesquita, Rodney O.</au><au>Lima, Michael W.</au><au>Costa-Lotufo, Letícia V.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>In vitro and in vivo antitumor effect of 5-FU combined with piplartine and piperine</atitle><jtitle>Journal of applied toxicology</jtitle><addtitle>J. Appl. Toxicol</addtitle><date>2008-03</date><risdate>2008</risdate><volume>28</volume><issue>2</issue><spage>156</spage><epage>163</epage><pages>156-163</pages><issn>0260-437X</issn><eissn>1099-1263</eissn><coden>JJATDK</coden><abstract>It has been reported that piplartine and piperine, alkaloid/amide compounds from Piper species, show antitumor activities. In the present paper, the effects of the combination of 5‐fluorouracil (5‐FU) with piplartine or piperine was determined using in vitro and in vivo experimental models. Hematological and biochemical analyses, as well as histopathological and morphological analyses of the tumor and the organs, including liver, spleen and kidney, were performed in order to evaluate the toxicological aspects associated with different treatments. The incubation of tumor cell lines with 5‐FU in the presence of piplartine or piperine produced an increase in growth inhibition, as observed by lower IC50 values for 5‐FU. These effects were also observed in vivo, where the combination with piplartine but not piperine with 5‐FU led to a higher tumor growth inhibition. The results indicated that either piplartine‐ or 5‐FU‐treated animals showed a low inhibition rate when they were used individually at low doses of 28.67% and 47.71%, respectively, but when they were combined at the same dose, the inhibition rate increased significantly to 68.04%. The histopathological analysis showed that the livers and the kidneys of treated animals were only slightly and reversibly affected. Neither the enzymatic activity of transaminases nor the urea levels were significantly modified when compared with the control group. Hematological analysis showed leukopenia after 5‐FU treatment, which was reversed by the combined use of piplartine and piperine. These findings indicate that piplartine may enhance the therapeutic effectiveness of chemotherapeutic drugs, and moreover, this combination could improve immunocompetence hampered by 5‐FU. Copyright © 2007 John Wiley & Sons, Ltd.</abstract><cop>Chichester, UK</cop><pub>John Wiley & Sons, Ltd</pub><pmid>17541943</pmid><doi>10.1002/jat.1261</doi><tpages>8</tpages></addata></record> |
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subjects | 5-fluorouracil Alanine Transaminase - blood Alkaloids - administration & dosage Animals Antimetabolites, Antineoplastic - administration & dosage Antineoplastic Agents, Phytogenic - administration & dosage Antineoplastic Combined Chemotherapy Protocols - pharmacology Antineoplastic Combined Chemotherapy Protocols - toxicity antitumor activity Aspartate Aminotransferases - blood Benzodioxoles - administration & dosage Biological and medical sciences Cell Proliferation - drug effects Dose-Response Relationship, Drug Female Fluorouracil - administration & dosage HL-60 Cells Humans Inhibitory Concentration 50 Kidney - drug effects Kidney - metabolism Leukopenia - chemically induced Leukopenia - prevention & control Liver - drug effects Liver - enzymology Medical sciences Mice Piperidines - administration & dosage Piperidones - administration & dosage piperine piplartine Polyunsaturated Alkamides - administration & dosage Sarcoma 180 - drug therapy Sarcoma 180 - metabolism Sarcoma 180 - pathology toxicity Toxicology Urea - blood |
title | In vitro and in vivo antitumor effect of 5-FU combined with piplartine and piperine |
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