Modulation of Inflammatory Processes by Leaves Extract from Clusia nemorosa Both In Vitro and In Vivo Animal Models
The present study was carried out to investigate the anti-inflammatory effect of the hexane extract of the leaves from Clusia nemorosa G. Mey, called HECn, using carrageenan-induced mice pleurisy and cotton pellet-induced mice granuloma. Additionally, the ability of HECn to affect both neutrophil mi...
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Published in: | Inflammation Vol. 35; no. 2; pp. 764 - 771 |
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Main Authors: | , , , , , , , , , , |
Format: | Journal Article |
Language: | English |
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01-04-2012
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Abstract | The present study was carried out to investigate the anti-inflammatory effect of the hexane extract of the leaves from
Clusia nemorosa
G. Mey, called HECn, using carrageenan-induced mice pleurisy and cotton pellet-induced mice granuloma. Additionally, the ability of HECn to affect both neutrophil migration as viability was investigated by use of the Boyden chamber assay and flow cytometry, respectively. The HECn significantly inhibited exudation, total leukocytes and neutrophils influx, as well as TNFα levels in carrageenan-induced pleurisy. However, the extract not suppressed the granulomatous tissue formation in the cotton pellet-induced granuloma test. Experiments performed
in vitro
revealed that HECn on human neutrophils inhibited a dose-dependent manner the CXCL1-induced neutrophil chemotaxis. Furthermore, HECn also inhibited the chemoattraction of human neutrophils induced by formyl-methionyl-leucyl-phenylalanine (fMLP), leukotriene B4 (LTB4) and platelet activating factor (PAF) in a Boyden chamber. However, this same treatment not was able to induce apoptosis. The results obtained in this study showed that the extract from leaves of
C. nemorosa
possess a potent inhibitory activity in acute model of inflammation, being the effects mediated, in part, by inhibition of neutrophil responsiveness. These results indicate that
C. nemorosa
could be a good source for anti-inflammatory compounds. |
---|---|
AbstractList | The present study was carried out to investigate the anti-inflammatory effect of the hexane extract of the leaves from Clusia nemorosa G. Mey, called HECn, using carrageenan-induced mice pleurisy and cotton pellet-induced mice granuloma. Additionally, the ability of HECn to affect both neutrophil migration as viability was investigated by use of the Boyden chamber assay and flow cytometry, respectively. The HECn significantly inhibited exudation, total leukocytes and neutrophils influx, as well as TNF alpha levels in carrageenan-induced pleurisy. However, the extract not suppressed the granulomatous tissue formation in the cotton pellet-induced granuloma test. Experiments performed in vitro revealed that HECn on human neutrophils inhibited a dose-dependent manner the CXCL1-induced neutrophil chemotaxis. Furthermore, HECn also inhibited the chemoattraction of human neutrophils induced by formyl-methionyl-leucyl-phenylalanine (fMLP), leukotriene B4 (LTB4) and platelet activating factor (PAF) in a Boyden chamber. However, this same treatment not was able to induce apoptosis. The results obtained in this study showed that the extract from leaves of C. nemorosa possess a potent inhibitory activity in acute model of inflammation, being the effects mediated, in part, by inhibition of neutrophil responsiveness. These results indicate that C. nemorosa could be a good source for anti-inflammatory compounds. The present study was carried out to investigate the anti-inflammatory effect of the hexane extract of the leaves from Clusia nemorosa G. Mey, called HECn, using carrageenan-induced mice pleurisy and cotton pellet-induced mice granuloma. Additionally, the ability of HECn to affect both neutrophil migration as viability was investigated by use of the Boyden chamber assay and flow cytometry, respectively. The HECn significantly inhibited exudation, total leukocytes and neutrophils influx, as well as TNFα levels in carrageenan-induced pleurisy. However, the extract not suppressed the granulomatous tissue formation in the cotton pellet-induced granuloma test. Experiments performed in vitro revealed that HECn on human neutrophils inhibited a dose-dependent manner the CXCL1-induced neutrophil chemotaxis. Furthermore, HECn also inhibited the chemoattraction of human neutrophils induced by formyl-methionyl-leucyl-phenylalanine (fMLP), leukotriene B4 (LTB4) and platelet activating factor (PAF) in a Boyden chamber. However, this same treatment not was able to induce apoptosis. The results obtained in this study showed that the extract from leaves of C. nemorosa possess a potent inhibitory activity in acute model of inflammation, being the effects mediated, in part, by inhibition of neutrophil responsiveness. These results indicate that C. nemorosa could be a good source for anti-inflammatory compounds. The present study was carried out to investigate the anti-inflammatory effect of the hexane extract of the leaves from Clusia nemorosa G. Mey, called HECn, using carrageenan-induced mice pleurisy and cotton pellet-induced mice granuloma. Additionally, the ability of HECn to affect both neutrophil migration as viability was investigated by use of the Boyden chamber assay and flow cytometry, respectively. The HECn significantly inhibited exudation, total leukocytes and neutrophils influx, as well as TNFα levels in carrageenan-induced pleurisy. However, the extract not suppressed the granulomatous tissue formation in the cotton pellet-induced granuloma test. Experiments performed in vitro revealed that HECn on human neutrophils inhibited a dose-dependent manner the CXCL1-induced neutrophil chemotaxis. Furthermore, HECn also inhibited the chemoattraction of human neutrophils induced by formyl-methionyl-leucyl-phenylalanine (fMLP), leukotriene B4 (LTB4) and platelet activating factor (PAF) in a Boyden chamber. However, this same treatment not was able to induce apoptosis. The results obtained in this study showed that the extract from leaves of C. nemorosa possess a potent inhibitory activity in acute model of inflammation, being the effects mediated, in part, by inhibition of neutrophil responsiveness. These results indicate that C. nemorosa could be a good source for anti-inflammatory compounds. The present study was carried out to investigate the anti-inflammatory effect of the hexane extract of the leaves from Clusia nemorosa G. Mey, called HECn, using carrageenan-induced mice pleurisy and cotton pellet-induced mice granuloma. Additionally, the ability of HECn to affect both neutrophil migration as viability was investigated by use of the Boyden chamber assay and flow cytometry, respectively. The HECn significantly inhibited exudation, total leukocytes and neutrophils influx, as well as TNFα levels in carrageenan-induced pleurisy. However, the extract not suppressed the granulomatous tissue formation in the cotton pellet-induced granuloma test. Experiments performed in vitro revealed that HECn on human neutrophils inhibited a dose-dependent manner the CXCL1-induced neutrophil chemotaxis. Furthermore, HECn also inhibited the chemoattraction of human neutrophils induced by formyl-methionyl-leucyl-phenylalanine (fMLP), leukotriene B4 (LTB4) and platelet activating factor (PAF) in a Boyden chamber. However, this same treatment not was able to induce apoptosis. The results obtained in this study showed that the extract from leaves of C. nemorosa possess a potent inhibitory activity in acute model of inflammation, being the effects mediated, in part, by inhibition of neutrophil responsiveness. These results indicate that C. nemorosa could be a good source for anti-inflammatory compounds.[PUBLICATION ABSTRACT] |
Author | Ferraris, Fausto K. Barreto, Emiliano Oliveira, Fernando M. Ferro, Jamylle Nunes S. Candea, André Luiz P. Conserva, Lucia M. Conte, Fernando P. Silva, Juliane P. Henriques, Maria das Graças M. O. Agra, Isabela Karine R. Farias, José Alex C. |
Author_xml | – sequence: 1 givenname: José Alex C. surname: Farias fullname: Farias, José Alex C. organization: Laboratório de Biologia Celular, Instituto de Ciências Biológicas e da Saúde, Universidade Federal de Alagoas – sequence: 2 givenname: Jamylle Nunes S. surname: Ferro fullname: Ferro, Jamylle Nunes S. organization: Laboratório de Biologia Celular, Instituto de Ciências Biológicas e da Saúde, Universidade Federal de Alagoas – sequence: 3 givenname: Juliane P. surname: Silva fullname: Silva, Juliane P. organization: Laboratório de Biologia Celular, Instituto de Ciências Biológicas e da Saúde, Universidade Federal de Alagoas – sequence: 4 givenname: Isabela Karine R. surname: Agra fullname: Agra, Isabela Karine R. organization: Laboratório de Biologia Celular, Instituto de Ciências Biológicas e da Saúde, Universidade Federal de Alagoas – sequence: 5 givenname: Fernando M. surname: Oliveira fullname: Oliveira, Fernando M. organization: Laboratório de Pesquisa em Química dos Produtos Naturais, Instituto de Química e Biotecnologia, Universidade Federal de Alagoas – sequence: 6 givenname: André Luiz P. surname: Candea fullname: Candea, André Luiz P. organization: Laboratório de Farmacologia Aplicada, Farmanguinhos-Fiocruz – sequence: 7 givenname: Fernando P. surname: Conte fullname: Conte, Fernando P. organization: Laboratório de Farmacologia Aplicada, Farmanguinhos-Fiocruz – sequence: 8 givenname: Fausto K. surname: Ferraris fullname: Ferraris, Fausto K. organization: Laboratório de Farmacologia Aplicada, Farmanguinhos-Fiocruz – sequence: 9 givenname: Maria das Graças M. O. surname: Henriques fullname: Henriques, Maria das Graças M. O. organization: Laboratório de Farmacologia Aplicada, Farmanguinhos-Fiocruz – sequence: 10 givenname: Lucia M. surname: Conserva fullname: Conserva, Lucia M. organization: Laboratório de Pesquisa em Química dos Produtos Naturais, Instituto de Química e Biotecnologia, Universidade Federal de Alagoas – sequence: 11 givenname: Emiliano surname: Barreto fullname: Barreto, Emiliano email: emilianobarreto@optma.org organization: Laboratório de Biologia Celular, Instituto de Ciências Biológicas e da Saúde, Universidade Federal de Alagoas, Universidade Federal de Alagoas |
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Snippet | The present study was carried out to investigate the anti-inflammatory effect of the hexane extract of the leaves from
Clusia nemorosa
G. Mey, called HECn,... The present study was carried out to investigate the anti-inflammatory effect of the hexane extract of the leaves from Clusia nemorosa G. Mey, called HECn,... |
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SubjectTerms | Animals Anti-Inflammatory Agents - pharmacology Apoptosis - drug effects Biomedical and Life Sciences Biomedicine Carrageenan Cells, Cultured Chemotaxis, Leukocyte - drug effects Clusia Cotton Fiber Granuloma - chemically induced Granuloma - drug therapy Granuloma - immunology Humans Immunology Internal Medicine Mice Neutrophils - immunology Neutrophils - physiology Pathology Pharmacology/Toxicology Phytotherapy Plant Extracts - pharmacology Plant Leaves Pleurisy - chemically induced Pleurisy - drug therapy Pleurisy - immunology Rheumatology Tumor Necrosis Factor-alpha - biosynthesis |
Title | Modulation of Inflammatory Processes by Leaves Extract from Clusia nemorosa Both In Vitro and In Vivo Animal Models |
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