Late administration of a specific COX-2 inhibitor does not treat and/or prevent progression of gastric tumors in rats submitted to duodenogastric reflux procedure
PURPOSE:To assess whether late introduction of a specific COX-2 inhibitor (Meloxicam) can treat and/or prevent the progression of tumors in the stomach of rats submitted to duodenogastric reflux. METHODS: Seventy five male Wistar rats, weighing 150 grams, were submitted to the induction of duodenoga...
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Format: | Article |
Language: | English |
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Sociedade Brasileira para o Desenvolvimento da Pesquisa em Cirurgia
2013-06-01
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Series: | Acta Cirúrgica Brasileira |
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Online Access: | http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0102-86502013000600009&tlng=en |
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author | Paulo Antônio Rodrigues Luiz Eduardo Naresse Maria Aparecida Marchesan Rodrigues Shoiti Kobayasi |
author_facet | Paulo Antônio Rodrigues Luiz Eduardo Naresse Maria Aparecida Marchesan Rodrigues Shoiti Kobayasi |
author_sort | Paulo Antônio Rodrigues |
collection | DOAJ |
description | PURPOSE:To assess whether late introduction of a specific COX-2 inhibitor (Meloxicam) can treat and/or prevent the progression of tumors in the stomach of rats submitted to duodenogastric reflux. METHODS: Seventy five male Wistar rats, weighing 150 grams, were submitted to the induction of duodenogastric reflux through the pylorus. At 36 weeks of follow-up were established three experimental groups: DGR36 sacrificed immediately, DGR54 and DGR54MLX both sacrificed at 54th week of follow-up . The animals of the latter group were fed with a rat chow premixed with Meloxicam (2.0 mg/ kg feed; 0.3 mg / kg bw / day) and the other two with standard rat chow. The lesions found in the pyloric mucosa and gastrojejunal anastomosis were analyzed macroscopically and histologically. For statistical analysis was adjusted a generalized linear model assuming a binomial distribution with LOGIT link function. RESULTS: No significant differences were found when comparing the incidences of benign tumor lesions (Adenomatous Hyperplasia), p=0.4915, or malignant (Mucinous Adenocarcinoma), p=0.2731, among groups. CONCLUSION: Late introduction of specific COX-2 inhibitor (Meloxicam) did not treat and was not able to prevent the progression of tumoral lesions induced by duodenogastric reflux in the rat stomachs. |
first_indexed | 2024-12-10T17:18:56Z |
format | Article |
id | doaj.art-ab93db19fab444719a5bc0ed170cd380 |
institution | Directory Open Access Journal |
issn | 0102-8650 |
language | English |
last_indexed | 2024-12-10T17:18:56Z |
publishDate | 2013-06-01 |
publisher | Sociedade Brasileira para o Desenvolvimento da Pesquisa em Cirurgia |
record_format | Article |
series | Acta Cirúrgica Brasileira |
spelling | doaj.art-ab93db19fab444719a5bc0ed170cd3802022-12-22T01:40:02ZengSociedade Brasileira para o Desenvolvimento da Pesquisa em CirurgiaActa Cirúrgica Brasileira0102-86502013-06-01286453457Late administration of a specific COX-2 inhibitor does not treat and/or prevent progression of gastric tumors in rats submitted to duodenogastric reflux procedurePaulo Antônio Rodrigues0Luiz Eduardo Naresse1Maria Aparecida Marchesan Rodrigues2Shoiti Kobayasi3UNESPUNESPUNESPUNESPPURPOSE:To assess whether late introduction of a specific COX-2 inhibitor (Meloxicam) can treat and/or prevent the progression of tumors in the stomach of rats submitted to duodenogastric reflux. METHODS: Seventy five male Wistar rats, weighing 150 grams, were submitted to the induction of duodenogastric reflux through the pylorus. At 36 weeks of follow-up were established three experimental groups: DGR36 sacrificed immediately, DGR54 and DGR54MLX both sacrificed at 54th week of follow-up . The animals of the latter group were fed with a rat chow premixed with Meloxicam (2.0 mg/ kg feed; 0.3 mg / kg bw / day) and the other two with standard rat chow. The lesions found in the pyloric mucosa and gastrojejunal anastomosis were analyzed macroscopically and histologically. For statistical analysis was adjusted a generalized linear model assuming a binomial distribution with LOGIT link function. RESULTS: No significant differences were found when comparing the incidences of benign tumor lesions (Adenomatous Hyperplasia), p=0.4915, or malignant (Mucinous Adenocarcinoma), p=0.2731, among groups. CONCLUSION: Late introduction of specific COX-2 inhibitor (Meloxicam) did not treat and was not able to prevent the progression of tumoral lesions induced by duodenogastric reflux in the rat stomachs.http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0102-86502013000600009&tlng=enAdenocarcinomaStomachChemopreventionCyclooxygenase InhibitorsRats |
spellingShingle | Paulo Antônio Rodrigues Luiz Eduardo Naresse Maria Aparecida Marchesan Rodrigues Shoiti Kobayasi Late administration of a specific COX-2 inhibitor does not treat and/or prevent progression of gastric tumors in rats submitted to duodenogastric reflux procedure Acta Cirúrgica Brasileira Adenocarcinoma Stomach Chemoprevention Cyclooxygenase Inhibitors Rats |
title | Late administration of a specific COX-2 inhibitor does not treat and/or prevent progression of gastric tumors in rats submitted to duodenogastric reflux procedure |
title_full | Late administration of a specific COX-2 inhibitor does not treat and/or prevent progression of gastric tumors in rats submitted to duodenogastric reflux procedure |
title_fullStr | Late administration of a specific COX-2 inhibitor does not treat and/or prevent progression of gastric tumors in rats submitted to duodenogastric reflux procedure |
title_full_unstemmed | Late administration of a specific COX-2 inhibitor does not treat and/or prevent progression of gastric tumors in rats submitted to duodenogastric reflux procedure |
title_short | Late administration of a specific COX-2 inhibitor does not treat and/or prevent progression of gastric tumors in rats submitted to duodenogastric reflux procedure |
title_sort | late administration of a specific cox 2 inhibitor does not treat and or prevent progression of gastric tumors in rats submitted to duodenogastric reflux procedure |
topic | Adenocarcinoma Stomach Chemoprevention Cyclooxygenase Inhibitors Rats |
url | http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0102-86502013000600009&tlng=en |
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