Stimulatory Effects of Areca Nut Extracts on Prostaglandin E2 Production by Human Polymorphonuclear Leukocytes

Background: Areca quid chewing increases the prevalence of periodontal diseases. Areca nut extract (ANE) inhibits the defensive functions of human polymorphonuclear leukocytes (PMNs). This in vitro study investigates the effects of ANE on the production of cyclooxygenase (COX)‐2 and the inflammatory...

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Veröffentlicht in:Journal of periodontology (1970) 2010-05, Vol.81 (5), p.758-766
Hauptverfasser: Lai, Yu‐Lin, Wu, Ching‐Yi, Lee, Ya‐Yun, Chang, Hui‐Wen, Liu, Tsung‐Yun, Hung, Shan‐Ling
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container_title Journal of periodontology (1970)
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creator Lai, Yu‐Lin
Wu, Ching‐Yi
Lee, Ya‐Yun
Chang, Hui‐Wen
Liu, Tsung‐Yun
Hung, Shan‐Ling
description Background: Areca quid chewing increases the prevalence of periodontal diseases. Areca nut extract (ANE) inhibits the defensive functions of human polymorphonuclear leukocytes (PMNs). This in vitro study investigates the effects of ANE on the production of cyclooxygenase (COX)‐2 and the inflammatory mediator prostaglandin E2 (PGE2) by PMNs. Methods: The possible effects of ANE on the production of COX‐2 were examined using Western blotting analysis. The viability and production of PGE2 of treated PMNs were determined using the propidium iodide staining method and the competition enzyme assay, respectively. The possible pathways involved were also examined using the COX‐2 inhibitor (NS398), the intracellular calcium chelator 1,2‐bis(2‐aminophenoxy)ethane‐N, N, N′, N′‐tetraacetic acid tetrakis (acetoxymethyl ester) (BAPTA‐AM), the p38 mitogen‐activated protein kinase (MAPK) inhibitor (SB203580), and the extracellular signal‐regulated protein kinase (ERK) inhibitor (U0126). The effects of ANE on the viability or PGE2 production were statistically assessed using a one‐way analysis of variance and Tukey multiple‐comparison intervals with α = 0.05. Results: ANE significantly induced the production of PGE2 in a time‐ and concentration‐dependent manner. This induction resulted from an increased expression of COX‐2. Moreover, the application of BAPTA‐AM, SB203580, and U0126 statistically significantly suppressed the induction of PGE2. Conclusions: ANE induced the production of PGE2. The activation of the intracellular calcium concentrations, p38 MAPK, and ERK may be involved in the inducing effects of ANE on PMNs. The findings suggest that areca nut chewing may induce an inflammatory response and affect the periodontal health of consumers.
doi_str_mv 10.1902/jop.2010.090660
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Areca nut extract (ANE) inhibits the defensive functions of human polymorphonuclear leukocytes (PMNs). This in vitro study investigates the effects of ANE on the production of cyclooxygenase (COX)‐2 and the inflammatory mediator prostaglandin E2 (PGE2) by PMNs. Methods: The possible effects of ANE on the production of COX‐2 were examined using Western blotting analysis. The viability and production of PGE2 of treated PMNs were determined using the propidium iodide staining method and the competition enzyme assay, respectively. The possible pathways involved were also examined using the COX‐2 inhibitor (NS398), the intracellular calcium chelator 1,2‐bis(2‐aminophenoxy)ethane‐N, N, N′, N′‐tetraacetic acid tetrakis (acetoxymethyl ester) (BAPTA‐AM), the p38 mitogen‐activated protein kinase (MAPK) inhibitor (SB203580), and the extracellular signal‐regulated protein kinase (ERK) inhibitor (U0126). The effects of ANE on the viability or PGE2 production were statistically assessed using a one‐way analysis of variance and Tukey multiple‐comparison intervals with α = 0.05. Results: ANE significantly induced the production of PGE2 in a time‐ and concentration‐dependent manner. This induction resulted from an increased expression of COX‐2. Moreover, the application of BAPTA‐AM, SB203580, and U0126 statistically significantly suppressed the induction of PGE2. Conclusions: ANE induced the production of PGE2. The activation of the intracellular calcium concentrations, p38 MAPK, and ERK may be involved in the inducing effects of ANE on PMNs. The findings suggest that areca nut chewing may induce an inflammatory response and affect the periodontal health of consumers.</description><identifier>ISSN: 0022-3492</identifier><identifier>EISSN: 1943-3670</identifier><identifier>DOI: 10.1902/jop.2010.090660</identifier><identifier>PMID: 20429655</identifier><language>eng</language><publisher>Chicago, IL: American Academy of Periodontology</publisher><subject>Adult ; Areca ; Biological and medical sciences ; Blotting, Western ; Butadienes - pharmacology ; calcium ; Calcium - metabolism ; Cell Survival - drug effects ; Cells, Cultured ; Chelating Agents - pharmacology ; Cyclooxygenase 2 - drug effects ; Cyclooxygenase 2 Inhibitors - pharmacology ; cyclooxygenase‐2 ; Dentistry ; Dinoprostone - analysis ; Dinoprostone - metabolism ; Dose-Response Relationship, Drug ; Egtazic Acid - analogs &amp; derivatives ; Egtazic Acid - pharmacology ; Enzyme Inhibitors - pharmacology ; Extracellular Signal-Regulated MAP Kinases - antagonists &amp; inhibitors ; Female ; Humans ; Imidazoles - pharmacology ; Inflammation Mediators - analysis ; Inflammation Mediators - metabolism ; Male ; Medical sciences ; mitogen‐activated protein kinase ; Neutrophils - drug effects ; Nitriles - pharmacology ; Nitrobenzenes - pharmacology ; Otorhinolaryngology. 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Areca nut extract (ANE) inhibits the defensive functions of human polymorphonuclear leukocytes (PMNs). This in vitro study investigates the effects of ANE on the production of cyclooxygenase (COX)‐2 and the inflammatory mediator prostaglandin E2 (PGE2) by PMNs. Methods: The possible effects of ANE on the production of COX‐2 were examined using Western blotting analysis. The viability and production of PGE2 of treated PMNs were determined using the propidium iodide staining method and the competition enzyme assay, respectively. The possible pathways involved were also examined using the COX‐2 inhibitor (NS398), the intracellular calcium chelator 1,2‐bis(2‐aminophenoxy)ethane‐N, N, N′, N′‐tetraacetic acid tetrakis (acetoxymethyl ester) (BAPTA‐AM), the p38 mitogen‐activated protein kinase (MAPK) inhibitor (SB203580), and the extracellular signal‐regulated protein kinase (ERK) inhibitor (U0126). The effects of ANE on the viability or PGE2 production were statistically assessed using a one‐way analysis of variance and Tukey multiple‐comparison intervals with α = 0.05. Results: ANE significantly induced the production of PGE2 in a time‐ and concentration‐dependent manner. This induction resulted from an increased expression of COX‐2. Moreover, the application of BAPTA‐AM, SB203580, and U0126 statistically significantly suppressed the induction of PGE2. Conclusions: ANE induced the production of PGE2. The activation of the intracellular calcium concentrations, p38 MAPK, and ERK may be involved in the inducing effects of ANE on PMNs. 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Stomatology</subject><subject>p38 Mitogen-Activated Protein Kinases - antagonists &amp; inhibitors</subject><subject>Plant Extracts - pharmacology</subject><subject>polymorphonuclear leukocytes</subject><subject>prostaglandin E2</subject><subject>Pyridines - pharmacology</subject><subject>Sulfonamides - pharmacology</subject><subject>Young Adult</subject><issn>0022-3492</issn><issn>1943-3670</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkctv1DAQxi0EokvhzA35gjiljB9x4mNVpbRoBRWPs-U4NqQkcfBDkP8eb3eB02jm-2leH0IvCVwQCfTtvV8vKJQMJAgBj9COSM4qJhp4jHYAlFaMS3qGnsV4X1LCGTxFZxQ4laKud2j5nMY5Tzr5sOHOOWtSxN7hy2CNxh9ywt3vFPRDdcF3wcekv016GcYFd_RQGLJJY9H6Dd_kWRfIT9vsw_rdL9lMVge8t_mHN1uy8Tl64vQU7YtTPEdfr7svVzfV_uO726vLfbWWa9qqYaxlrq9FL_TQwsAbLowBXg-94NxJRwzlzhICRnNr-kZCz62ujZWmGRxn5-jNse8a_M9sY1LzGI2dyubW56jKAMlo20AhX53I3M92UGsYZx029fdFBXh9AnQ0enJBL2aM_zlaejVEFK4-cr_GyW7_dALq4JQqTqmDU-rolHp_132Cpm7ZH00Kh4w</recordid><startdate>201005</startdate><enddate>201005</enddate><creator>Lai, Yu‐Lin</creator><creator>Wu, Ching‐Yi</creator><creator>Lee, Ya‐Yun</creator><creator>Chang, Hui‐Wen</creator><creator>Liu, Tsung‐Yun</creator><creator>Hung, Shan‐Ling</creator><general>American Academy of Periodontology</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>201005</creationdate><title>Stimulatory Effects of Areca Nut Extracts on Prostaglandin E2 Production by Human Polymorphonuclear Leukocytes</title><author>Lai, Yu‐Lin ; Wu, Ching‐Yi ; Lee, Ya‐Yun ; Chang, Hui‐Wen ; Liu, Tsung‐Yun ; Hung, Shan‐Ling</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p2018-73383fb56b6ad80d4746cc045db644f9f1c24fe110ca4ecb790b4ea5ce9c7df43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Adult</topic><topic>Areca</topic><topic>Biological and medical sciences</topic><topic>Blotting, Western</topic><topic>Butadienes - pharmacology</topic><topic>calcium</topic><topic>Calcium - metabolism</topic><topic>Cell Survival - drug effects</topic><topic>Cells, Cultured</topic><topic>Chelating Agents - pharmacology</topic><topic>Cyclooxygenase 2 - drug effects</topic><topic>Cyclooxygenase 2 Inhibitors - pharmacology</topic><topic>cyclooxygenase‐2</topic><topic>Dentistry</topic><topic>Dinoprostone - analysis</topic><topic>Dinoprostone - metabolism</topic><topic>Dose-Response Relationship, Drug</topic><topic>Egtazic Acid - analogs &amp; derivatives</topic><topic>Egtazic Acid - pharmacology</topic><topic>Enzyme Inhibitors - pharmacology</topic><topic>Extracellular Signal-Regulated MAP Kinases - antagonists &amp; inhibitors</topic><topic>Female</topic><topic>Humans</topic><topic>Imidazoles - pharmacology</topic><topic>Inflammation Mediators - analysis</topic><topic>Inflammation Mediators - metabolism</topic><topic>Male</topic><topic>Medical sciences</topic><topic>mitogen‐activated protein kinase</topic><topic>Neutrophils - drug effects</topic><topic>Nitriles - pharmacology</topic><topic>Nitrobenzenes - pharmacology</topic><topic>Otorhinolaryngology. Stomatology</topic><topic>p38 Mitogen-Activated Protein Kinases - antagonists &amp; inhibitors</topic><topic>Plant Extracts - pharmacology</topic><topic>polymorphonuclear leukocytes</topic><topic>prostaglandin E2</topic><topic>Pyridines - pharmacology</topic><topic>Sulfonamides - pharmacology</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lai, Yu‐Lin</creatorcontrib><creatorcontrib>Wu, Ching‐Yi</creatorcontrib><creatorcontrib>Lee, Ya‐Yun</creatorcontrib><creatorcontrib>Chang, Hui‐Wen</creatorcontrib><creatorcontrib>Liu, Tsung‐Yun</creatorcontrib><creatorcontrib>Hung, Shan‐Ling</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of periodontology (1970)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lai, Yu‐Lin</au><au>Wu, Ching‐Yi</au><au>Lee, Ya‐Yun</au><au>Chang, Hui‐Wen</au><au>Liu, Tsung‐Yun</au><au>Hung, Shan‐Ling</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Stimulatory Effects of Areca Nut Extracts on Prostaglandin E2 Production by Human Polymorphonuclear Leukocytes</atitle><jtitle>Journal of periodontology (1970)</jtitle><addtitle>J Periodontol</addtitle><date>2010-05</date><risdate>2010</risdate><volume>81</volume><issue>5</issue><spage>758</spage><epage>766</epage><pages>758-766</pages><issn>0022-3492</issn><eissn>1943-3670</eissn><abstract>Background: Areca quid chewing increases the prevalence of periodontal diseases. Areca nut extract (ANE) inhibits the defensive functions of human polymorphonuclear leukocytes (PMNs). This in vitro study investigates the effects of ANE on the production of cyclooxygenase (COX)‐2 and the inflammatory mediator prostaglandin E2 (PGE2) by PMNs. Methods: The possible effects of ANE on the production of COX‐2 were examined using Western blotting analysis. The viability and production of PGE2 of treated PMNs were determined using the propidium iodide staining method and the competition enzyme assay, respectively. The possible pathways involved were also examined using the COX‐2 inhibitor (NS398), the intracellular calcium chelator 1,2‐bis(2‐aminophenoxy)ethane‐N, N, N′, N′‐tetraacetic acid tetrakis (acetoxymethyl ester) (BAPTA‐AM), the p38 mitogen‐activated protein kinase (MAPK) inhibitor (SB203580), and the extracellular signal‐regulated protein kinase (ERK) inhibitor (U0126). The effects of ANE on the viability or PGE2 production were statistically assessed using a one‐way analysis of variance and Tukey multiple‐comparison intervals with α = 0.05. Results: ANE significantly induced the production of PGE2 in a time‐ and concentration‐dependent manner. This induction resulted from an increased expression of COX‐2. Moreover, the application of BAPTA‐AM, SB203580, and U0126 statistically significantly suppressed the induction of PGE2. Conclusions: ANE induced the production of PGE2. The activation of the intracellular calcium concentrations, p38 MAPK, and ERK may be involved in the inducing effects of ANE on PMNs. The findings suggest that areca nut chewing may induce an inflammatory response and affect the periodontal health of consumers.</abstract><cop>Chicago, IL</cop><pub>American Academy of Periodontology</pub><pmid>20429655</pmid><doi>10.1902/jop.2010.090660</doi><tpages>9</tpages></addata></record>
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subjects Adult
Areca
Biological and medical sciences
Blotting, Western
Butadienes - pharmacology
calcium
Calcium - metabolism
Cell Survival - drug effects
Cells, Cultured
Chelating Agents - pharmacology
Cyclooxygenase 2 - drug effects
Cyclooxygenase 2 Inhibitors - pharmacology
cyclooxygenase‐2
Dentistry
Dinoprostone - analysis
Dinoprostone - metabolism
Dose-Response Relationship, Drug
Egtazic Acid - analogs & derivatives
Egtazic Acid - pharmacology
Enzyme Inhibitors - pharmacology
Extracellular Signal-Regulated MAP Kinases - antagonists & inhibitors
Female
Humans
Imidazoles - pharmacology
Inflammation Mediators - analysis
Inflammation Mediators - metabolism
Male
Medical sciences
mitogen‐activated protein kinase
Neutrophils - drug effects
Nitriles - pharmacology
Nitrobenzenes - pharmacology
Otorhinolaryngology. Stomatology
p38 Mitogen-Activated Protein Kinases - antagonists & inhibitors
Plant Extracts - pharmacology
polymorphonuclear leukocytes
prostaglandin E2
Pyridines - pharmacology
Sulfonamides - pharmacology
Young Adult
title Stimulatory Effects of Areca Nut Extracts on Prostaglandin E2 Production by Human Polymorphonuclear Leukocytes
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