Literature DB >> 25359170

Effects of celecoxib and ibuprofen on metabolic disorders induced by Walker-256 tumor in rats.

Camila Oliveira de Souza1, Mirian Ayumi Kurauti, Flaviane de Fatima Silva, Hely de Morais, Glaucia Regina Borba-Murad, Fábio Goulart de Andrade, Helenir Medri de Souza.   

Abstract

The contribution of anti-inflammatory property of celecoxib in the improvement of metabolic disorders in cancer is unknown. The purpose of this study was to compare the effects of celecoxib and ibuprofen, non-steroidal anti-inflammatory drugs (NSAIDs), on several metabolic changes observed in Walker-256 tumor-bearing rats. The effects of these NSAIDs on the tumor growth were also assessed. Celecoxib or ibuprofen (both at 25 mg/Kg) was administered orally for 12 days, beginning on the day the rats were inoculated with Walker-256 tumor cells. Celecoxib treatment prevented the losses in body mass and mass of retroperitoneal adipose tissue, gastrocnemius, and extensor digitorum longus muscles in tumor-bearing rats. Celecoxib also prevented the rise in blood levels of triacylglycerol, urea, and lactate, the inhibition of peripheral response to insulin and hepatic glycolysis, and tended to attenuate the decrease in the food intake, but had no effect on the reduction of glycemia induced by the tumor. In addition, celecoxib treatment increased the number of Walker-256 cells with signs of apoptosis and the tumor necrosis area and prevented the tumor growth. In contrast, ibuprofen treatment had no effect on metabolic parameters affected by the Walker-256 tumor or tumor growth. It can be concluded that celecoxib, unlike ibuprofen, ameliorated several metabolic changes in rats with Walker-256 tumor due to its anti-tumor effect and not its anti-inflammatory property.

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Year:  2014        PMID: 25359170     DOI: 10.1007/s11010-014-2250-9

Source DB:  PubMed          Journal:  Mol Cell Biochem        ISSN: 0300-8177            Impact factor:   3.396


  48 in total

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4.  Decreased response to cAMP in the glucose and glycogen catabolism in perfused livers of Walker-256 tumor-bearing rats.

Authors:  Hely de Morais; Priscila Cassola; Carolina Campos Lima Moreira; Suéllen Kathiane Fernandes Vilas Bôas; Glaucia Regina Borba-Murad; Roberto Barbosa Bazotte; Helenir Medri de Souza
Journal:  Mol Cell Biochem       Date:  2012-05-26       Impact factor: 3.396

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7.  Changes in blood metabolic parameters during the development of Walker-256 tumour-induced cachexia in rats are not caused by decreased food intake.

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8.  Systemic biosynthesis of prostacyclin by cyclooxygenase (COX)-2: the human pharmacology of a selective inhibitor of COX-2.

Authors:  B F McAdam; F Catella-Lawson; I A Mardini; S Kapoor; J A Lawson; G A FitzGerald
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9.  The role of insulin resistance in the development of muscle wasting during cancer cachexia.

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Journal:  J Cachexia Sarcopenia Muscle       Date:  2011-12-01       Impact factor: 12.910

10.  Humoral mediation for cachexia in tumour-bearing rats.

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  3 in total

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2.  Effects of systemic administration of ibuprofen on stress response in a rat model of post-traumatic stress disorder.

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Review 3.  Cachexia as Evidence of the Mechanisms of Resistance and Tolerance during the Evolution of Cancer Disease.

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Journal:  Int J Mol Sci       Date:  2021-03-12       Impact factor: 5.923

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