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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Veröffentlicht in:Journal of applied toxicology 2008-03, Vol.28 (2), p.156-163
Hauptverfasser: 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.
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container_issue 2
container_start_page 156
container_title Journal of applied toxicology
container_volume 28
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. 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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. 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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 &amp; Sons, Ltd.</abstract><cop>Chichester, UK</cop><pub>John Wiley &amp; 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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