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

被引:18
作者
de Souza, Camila Oliveira [1 ]
Kurauti, Mirian Ayumi [1 ]
Silva, Flaviane de Fatima [1 ]
de Morais, Hely [1 ]
Borba-Murad, Glaucia Regina [1 ]
de Andrade, Fabio Goulart [2 ]
de Souza, Helenir Medri [1 ]
机构
[1] Univ Estadual Londrina, Dept Physiol Sci, BR-86051990 Londrina, PR, Brazil
[2] Univ Estadual Londrina, Dept Histol, BR-86051990 Londrina, PR, Brazil
关键词
Cancer; Non-steroidal anti-inflammatory drugs; Cachexia; Blood metabolic parameters; Insulin resistance; Hepatic glycolysis; ANOREXIA-CACHEXIA SYNDROME; FREE FATTY-ACIDS; INSULIN-RESISTANCE; CANCER CACHEXIA; ADIPOSE-TISSUE; BEARING RATS; FOOD-INTAKE; CYCLOOXYGENASE (COX)-2; PGE2; INHIBITION; HIT CELLS;
D O I
10.1007/s11010-014-2250-9
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
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.
引用
收藏
页码:237 / 246
页数:10
相关论文
共 50 条
  • [21] The urea cycle and related pathways in the liver of Walker-256 tumor-bearing rats
    Pereira, SRC
    Darronqui, E
    Constantin, J
    da Rocha, MH
    da Silva, A
    Yamamoto, NS
    Bracht, A
    BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE, 2004, 1688 (03): : 187 - 196
  • [22] Nonlinear Magnetochemical Effects in Nanotherapy of Walker-256 Carcinosarcoma
    Orel, Valerii E.
    Tselepi, Marina
    Mitrelias, Thanos
    Zabolotny, Mykhailo
    Krotevich, Mykhailo
    Shevchenko, Anatoliy
    Rykhalskyi, Alexander
    Romanov, Andriy
    Orel, Valerii B.
    Burlaka, Anatoliy
    Lukin, Sergey
    Stegnii, Vladyslav
    Barnes, Crispin H. W.
    ACS APPLIED BIO MATERIALS, 2019, 2 (09) : 3954 - 3963
  • [23] Decreased response to cAMP in the glucose and glycogen catabolism in perfused livers of Walker-256 tumor-bearing rats
    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
    Molecular and Cellular Biochemistry, 2012, 368 : 9 - 16
  • [24] Sesquiterpene lactones of Moquiniastrum polymorphum subsp floccosum have antineoplastic effects in Walker-256 tumor-bearing rats
    Martins, Gracianny Gomes
    dos Reis Liver, Francislaine Aparecida
    Stolf, Aline Maria
    Kopruszinski, Caroline Machado
    Cardoso, Cibele Campos
    Beltrame, Olair Carlos
    Queiroz-Telles, Jose Ederaldo
    Batista Strapasson, Regiane Lauriano
    Alves Stefanello, Maria Elida
    Oude-Elferink, Ronald
    Acco, Alexandra
    CHEMICO-BIOLOGICAL INTERACTIONS, 2015, 228 : 46 - 56
  • [25] Metabolic effects of Hedyotis diffusa on rats bearing Walker 256 tumor revealed by NMR-based metabolomics
    Wang, Zhiyong
    Gao, Kuo
    Xu, Can
    Gao, Jian
    Yan, Yujing
    Wang, Yingfeng
    Li, Zhongfeng
    Chen, Jianxin
    MAGNETIC RESONANCE IN CHEMISTRY, 2018, 56 (01) : 5 - 17
  • [26] Insulin secretion decline in Walker-256 tumor-bearing rats is early, follows the course of cachexia, and is not improved by lixisenatide
    Quintilhano, Debora Luiza
    Miksza, Daniele Romani
    de Souza Galia, Winny Beatriz
    Ramalho, Mahira Oliveira Ramalho Costa
    Lucena, Camila Ferraz
    Valle, Maira Mello Rezende
    Graciano, Maria Fernanda Rodrigues
    de Souza, Helenir Medri
    Bertolini, Gisele Lopes
    NAUNYN-SCHMIEDEBERGS ARCHIVES OF PHARMACOLOGY, 2021, 394 (04) : 697 - 705
  • [27] Creatine supplementation does not promote tumor growth or enhance tumor aggressiveness in Walker-256 tumor-bearing rats
    Cella, Paola Sanches
    Marinello, Poliana C.
    Padilha, Camila S.
    Testa, Mayra T.
    Guirro, Philippe B.
    Cecchini, Rubens
    Duarte, Jose A.
    Guarnier, Flavia A.
    Deminice, Rafael
    NUTRITION, 2020, 79-80
  • [28] Walker 256 tumor-bearing rats demonstrate altered interstitial cells of Cajal. Effects on ICC in the Walker 256 tumor model
    Fracaro, L.
    Frez, F. C. V.
    Silva, B. C.
    Vicentini, G. E.
    de Souza, S. R. G.
    Martins, H. A.
    Linden, D. R.
    Guarnier, F. A.
    Zanoni, J. N.
    NEUROGASTROENTEROLOGY AND MOTILITY, 2016, 28 (01) : 101 - 115
  • [29] Creatine supplementation in Walker-256 tumor-bearing rats prevents skeletal muscle atrophy by attenuating systemic inflammation and protein degradation signaling
    Cella, Paola S.
    Marinello, Poliana C.
    Borges, Fernando H.
    Ribeiro, Diogo F.
    Chimin, Patricia
    Testa, Mayra T. J.
    Guirro, Philippe B.
    Duarte, Jose A.
    Cecchini, Rubens
    Guarnier, Flavia A.
    Deminice, Rafael
    EUROPEAN JOURNAL OF NUTRITION, 2020, 59 (02) : 661 - 669
  • [30] Insulin secretion decline in Walker-256 tumor-bearing rats is early, follows the course of cachexia, and is not improved by lixisenatide
    Débora Luiza Quintilhano
    Daniele Romani Miksza
    Winny Beatriz de Souza Galia
    Mahira Oliveira Ramalho Costa Ramalho
    Camila Ferraz Lucena
    Maíra Mello Rezende Valle
    Maria Fernanda Rodrigues Graciano
    Helenir Medri de Souza
    Gisele Lopes Bertolini
    Naunyn-Schmiedeberg's Archives of Pharmacology, 2021, 394 : 697 - 705