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Lack of effect of the cytokine suppressive agent FR167653 on tumour growth and cachexia in rats bearing the Yoshida AH-130 ascites hepatoma.

作者信息

Busquets S, Alvarez B, van Royen M, Carbó N, López-Soriano F J, Argilés J M

机构信息

Departament de Bioquímica i Biologia Molecular,Universitat de Barcelona, Spain.

出版信息

Cancer Lett. 2000 Aug 31;157(1):99-103. doi: 10.1016/s0304-3835(00)00476-6.

DOI:10.1016/s0304-3835(00)00476-6
PMID:10893448
Abstract

Daily s.c. administration of 6 mg/kg of FR167653 (an inhibitor of the synthesis of interleukin-1 and tumour necrosis factor-alpha) to rats bearing the ascites hepatoma Yoshida AH-130 (a highly cachectic tumour) did not prevent either the anorexia or the massive weight loss - affecting both adipose tissue and skeletal muscle - present in the cachectic animals. The compound did not affect the circulating levels of triacylglycerols or other metabolites such as glucose or lactate. Nor did the administration of FR167653 influence tumour growth. It is concluded that the drug is unable to reverse the cachectic state in this particular experimental tumour model.

摘要

相似文献

1
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Cancer Lett. 2000 Aug 31;157(1):99-103. doi: 10.1016/s0304-3835(00)00476-6.
2
Effects of the phosphodiesterase-IV inhibitor EMD 95832/3 on tumour growth and cachexia in rats bearing the Yoshida AH-130 ascites hepatoma.
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Interleukin-1 receptor antagonist (IL-1ra) is unable to reverse cachexia in rats bearing an ascites hepatoma (Yoshida AH-130).白细胞介素-1受体拮抗剂(IL-1ra)无法逆转荷腹水肝癌(吉田AH-130)大鼠的恶病质。
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Humoral mediation for cachexia in tumour-bearing rats.荷瘤大鼠恶病质的体液介导作用
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Interleukin-15 is able to suppress the increased DNA fragmentation associated with muscle wasting in tumour-bearing rats.白细胞介素-15能够抑制荷瘤大鼠中与肌肉萎缩相关的DNA片段化增加。
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