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Cancer Lett ; 201(2): 139-48, 2003 Nov 25.
Artículo en Inglés | MEDLINE | ID: mdl-14607327

RESUMEN

Cancer cachexia is characterized by anorexia and intense peripheral catabolism. We examine the potential benefits of combination of different anabolic agents such as insulin and clenbuterol associated to prostaglandin synthesis inhibitor (naproxen) on tumor growth, cachexia and renal function in Walker 256 tumor-bearing rats (WK). Groups were separated into WK, and WK with naproxen (WK N) or naproxen plus clenbuterol (WK NCb) or naproxen plus clenbuterol plus insulin (WK NCbI). Treatment begins at the 4th day after tumor inoculation, at the 14th day they were killed, glycemia, lacticidemia, glycogen content from liver, soleus and gastrocnemius muscles, tumor mass, body weight and kidney function were determined. Glycemia and glycogen content were reduced and lacticidemia increased in WK (p<0.05) as compared to control rats. The glycogen content recovered in all treated groups. Tumor weight was significantly reduced by the different treatments. At the 14th weight change (carcass-initial body weight) in the control increased by 38% and in the WK -2%. Naproxen treatment (WK N) induced an increased by 14%. The inclusion of clenbuterol (WK NCb) and insulin (WK NCbI) by 38 and 41%, respectively. Mean glomerular filtration rate (GFR) increased in the WK (p<0.05) as compared to control, but in the WK NCb the GFR was similar to control. Our results suggest that naproxen is able to reduce tumor growth and its association with insulin and clenbuterol induce mass weight gain and recovery energy fuel.


Asunto(s)
Caquexia/tratamiento farmacológico , Carcinoma 256 de Walker/tratamiento farmacológico , Clenbuterol/uso terapéutico , Insulina/uso terapéutico , Naproxeno/uso terapéutico , Agonistas Adrenérgicos beta/uso terapéutico , Animales , Glucemia/análisis , Peso Corporal/efectos de los fármacos , Carcinoma 256 de Walker/patología , Inhibidores de la Ciclooxigenasa/uso terapéutico , Quimioterapia Combinada , Ingestión de Alimentos/efectos de los fármacos , Ingestión de Energía , Glucógeno/metabolismo , Riñón/efectos de los fármacos , Riñón/patología , Hígado/efectos de los fármacos , Hígado/patología , Músculo Esquelético/efectos de los fármacos , Músculo Esquelético/patología , Ratas , Ratas Wistar
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