The Effect of Omega-3-enriched Fish oil on the Inflammation of Mice Colon Induced by AOM and DSS: Study on COX-2

Method: 30 Swiss Webster mice divided into 6 groups: (1) Negative control group (KN); (2) test group of fish oil with a dose of 1.5 mg / day (Dose-I); (3) test group of fish oil with a dose of 3 mg / day (Dose-II); (4) solvent-control group of corn oil (KP); (5) Positive control group of aspirin (AS...

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Veröffentlicht in:Research journal of pharmacy and technology 2019-11, Vol.12 (11), p.5265-5268
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description Method: 30 Swiss Webster mice divided into 6 groups: (1) Negative control group (KN); (2) test group of fish oil with a dose of 1.5 mg / day (Dose-I); (3) test group of fish oil with a dose of 3 mg / day (Dose-II); (4) solvent-control group of corn oil (KP); (5) Positive control group of aspirin (ASP); (6) Normal group (KNO). Some studies have shown that omega-3 which is one of the polyunsaturated fatty acids (PUFA) can reduce inflammation in humans.6 Omega-3 derived from fish oil are natural ingredients that can be obtained from fish rich in fat, such as salmon, tuna and mackerel.7 Omega-3 have inhibitory action against COX-2 which ultimately inhibits the accumulation of ß-catenin which is considered to play an important role in the development and progression of CRC.8 Omega-3 can act as an alternative substrate of AA in COX-2, causing reduction of formation PGE2. Group I negative control, mice were given induction of AOM and DSS (KN); Group 2 mice were given AOM and DSS, and given fish oil with a dose of 1.5mg (Dose-I); Group 3 mice were given AOM and DSS, and were given fish oil dose of 3mg (Dose-II); Group 4 mice were given AOM and DSS, and were given corn oil as solvent control (KP); Group 5 mice were given AOM and DSS, and were given acetosal (ASP) as a positive control group; Group 6 is a normal group and is not given special treatment. [...]referring to figure 1 above, there is a tendency for suppression of COX-2 expression in the positive control group (ASP, KP) and the fish oil treatment group (Dose-I, Dose-II).This result may be due to the treatment time being too short (6 weeks), compared to study conducted by Kusmardi13 which stated in the second month, there is a decrease in the number of inflammation foci occurred between the control and low dose groups with medium and high dose groups (p
doi_str_mv 10.5958/0974-360X.2019.00911.9
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Some studies have shown that omega-3 which is one of the polyunsaturated fatty acids (PUFA) can reduce inflammation in humans.6 Omega-3 derived from fish oil are natural ingredients that can be obtained from fish rich in fat, such as salmon, tuna and mackerel.7 Omega-3 have inhibitory action against COX-2 which ultimately inhibits the accumulation of ß-catenin which is considered to play an important role in the development and progression of CRC.8 Omega-3 can act as an alternative substrate of AA in COX-2, causing reduction of formation PGE2. Group I negative control, mice were given induction of AOM and DSS (KN); Group 2 mice were given AOM and DSS, and given fish oil with a dose of 1.5mg (Dose-I); Group 3 mice were given AOM and DSS, and were given fish oil dose of 3mg (Dose-II); Group 4 mice were given AOM and DSS, and were given corn oil as solvent control (KP); Group 5 mice were given AOM and DSS, and were given acetosal (ASP) as a positive control group; Group 6 is a normal group and is not given special treatment. [...]referring to figure 1 above, there is a tendency for suppression of COX-2 expression in the positive control group (ASP, KP) and the fish oil treatment group (Dose-I, Dose-II).This result may be due to the treatment time being too short (6 weeks), compared to study conducted by Kusmardi13 which stated in the second month, there is a decrease in the number of inflammation foci occurred between the control and low dose groups with medium and high dose groups (p&lt;0,05).</description><identifier>ISSN: 0974-3618</identifier><identifier>EISSN: 0974-360X</identifier><identifier>EISSN: 0974-306X</identifier><identifier>DOI: 10.5958/0974-360X.2019.00911.9</identifier><language>eng</language><publisher>Raipur: A&amp;V Publications</publisher><subject>Colorectal cancer ; Drinking water ; Fish oils ; Humidity ; Inflammation ; Studies</subject><ispartof>Research journal of pharmacy and technology, 2019-11, Vol.12 (11), p.5265-5268</ispartof><rights>Copyright A&amp;V Publications Nov 2019</rights><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids></links><search><creatorcontrib>Kusmardi, Kusmardi</creatorcontrib><creatorcontrib>Adare, Pater Dean</creatorcontrib><creatorcontrib>Kodariah, Ria</creatorcontrib><title>The Effect of Omega-3-enriched Fish oil on the Inflammation of Mice Colon Induced by AOM and DSS: Study on COX-2</title><title>Research journal of pharmacy and technology</title><description>Method: 30 Swiss Webster mice divided into 6 groups: (1) Negative control group (KN); (2) test group of fish oil with a dose of 1.5 mg / day (Dose-I); (3) test group of fish oil with a dose of 3 mg / day (Dose-II); (4) solvent-control group of corn oil (KP); (5) Positive control group of aspirin (ASP); (6) Normal group (KNO). Some studies have shown that omega-3 which is one of the polyunsaturated fatty acids (PUFA) can reduce inflammation in humans.6 Omega-3 derived from fish oil are natural ingredients that can be obtained from fish rich in fat, such as salmon, tuna and mackerel.7 Omega-3 have inhibitory action against COX-2 which ultimately inhibits the accumulation of ß-catenin which is considered to play an important role in the development and progression of CRC.8 Omega-3 can act as an alternative substrate of AA in COX-2, causing reduction of formation PGE2. Group I negative control, mice were given induction of AOM and DSS (KN); Group 2 mice were given AOM and DSS, and given fish oil with a dose of 1.5mg (Dose-I); Group 3 mice were given AOM and DSS, and were given fish oil dose of 3mg (Dose-II); Group 4 mice were given AOM and DSS, and were given corn oil as solvent control (KP); Group 5 mice were given AOM and DSS, and were given acetosal (ASP) as a positive control group; Group 6 is a normal group and is not given special treatment. [...]referring to figure 1 above, there is a tendency for suppression of COX-2 expression in the positive control group (ASP, KP) and the fish oil treatment group (Dose-I, Dose-II).This result may be due to the treatment time being too short (6 weeks), compared to study conducted by Kusmardi13 which stated in the second month, there is a decrease in the number of inflammation foci occurred between the control and low dose groups with medium and high dose groups (p&lt;0,05).</description><subject>Colorectal cancer</subject><subject>Drinking water</subject><subject>Fish oils</subject><subject>Humidity</subject><subject>Inflammation</subject><subject>Studies</subject><issn>0974-3618</issn><issn>0974-360X</issn><issn>0974-306X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNo9kMlqwzAQhkVpoSHNKxRBz3YlS9bSW3CTNpDgQ1LITciy1Dh4Sb0c_PaVm5K5zPb_M_AB8IxRGMtYvCLJaUAYOoYRwjJESGIcyjswuy3ubzUWj2DRdWfkg4k4omIGLoeThSvnrOlh42Ba2W8dkMDWbWFONofrojvBpihhU8PeSze1K3VV6b7wA2_YFcbCpCl9t6nzwXhLNsJluoO6zuH7fv8G9_2Qj5M_SY9B9AQenC47u_jPc_C1Xh2Sz2CbfmyS5TYwmMZ9YDWLiCSxFDk3mRVaY-SotdJRyjNDGJHMaMOwJlmOBHcYc46oYHHkDCExmYOX691L2_wMtuvVuRna2r9UEeE8YoJy5lXsqjJt03WtderSFpVuR4WRmgCriZ2aOKoJsPoDrCT5BeXAayA</recordid><startdate>20191101</startdate><enddate>20191101</enddate><creator>Kusmardi, Kusmardi</creator><creator>Adare, Pater Dean</creator><creator>Kodariah, Ria</creator><general>A&amp;V Publications</general><scope>AAYXX</scope><scope>CITATION</scope><scope>04Q</scope><scope>04S</scope><scope>04W</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope></search><sort><creationdate>20191101</creationdate><title>The Effect of Omega-3-enriched Fish oil on the Inflammation of Mice Colon Induced by AOM and DSS: Study on COX-2</title><author>Kusmardi, Kusmardi ; 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(2) test group of fish oil with a dose of 1.5 mg / day (Dose-I); (3) test group of fish oil with a dose of 3 mg / day (Dose-II); (4) solvent-control group of corn oil (KP); (5) Positive control group of aspirin (ASP); (6) Normal group (KNO). Some studies have shown that omega-3 which is one of the polyunsaturated fatty acids (PUFA) can reduce inflammation in humans.6 Omega-3 derived from fish oil are natural ingredients that can be obtained from fish rich in fat, such as salmon, tuna and mackerel.7 Omega-3 have inhibitory action against COX-2 which ultimately inhibits the accumulation of ß-catenin which is considered to play an important role in the development and progression of CRC.8 Omega-3 can act as an alternative substrate of AA in COX-2, causing reduction of formation PGE2. Group I negative control, mice were given induction of AOM and DSS (KN); Group 2 mice were given AOM and DSS, and given fish oil with a dose of 1.5mg (Dose-I); Group 3 mice were given AOM and DSS, and were given fish oil dose of 3mg (Dose-II); Group 4 mice were given AOM and DSS, and were given corn oil as solvent control (KP); Group 5 mice were given AOM and DSS, and were given acetosal (ASP) as a positive control group; Group 6 is a normal group and is not given special treatment. [...]referring to figure 1 above, there is a tendency for suppression of COX-2 expression in the positive control group (ASP, KP) and the fish oil treatment group (Dose-I, Dose-II).This result may be due to the treatment time being too short (6 weeks), compared to study conducted by Kusmardi13 which stated in the second month, there is a decrease in the number of inflammation foci occurred between the control and low dose groups with medium and high dose groups (p&lt;0,05).</abstract><cop>Raipur</cop><pub>A&amp;V Publications</pub><doi>10.5958/0974-360X.2019.00911.9</doi><tpages>4</tpages></addata></record>
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subjects Colorectal cancer
Drinking water
Fish oils
Humidity
Inflammation
Studies
title The Effect of Omega-3-enriched Fish oil on the Inflammation of Mice Colon Induced by AOM and DSS: Study on COX-2
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