Effect of a cachectic factor on carbohydrate metabolism and attenuation by eicosapentaenoic acid

被引:23
作者
Hussey, HJ [1 ]
Tisdale, MJ [1 ]
机构
[1] Aston Univ, Inst Pharmaceut Sci, Birmingham B4 7ET, W Midlands, England
关键词
proteolysis-inducing factor (PIF); glucose utilization; eicosapentaenoic acid (EPA);
D O I
10.1038/sj.bjc.6690490
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The effect of a proteolysis-inducing factor (PIF), produced by cachexia-inducing tumours on glucose utilization by different tissues and the effect of pretreatment with the polyunsaturated fatty acid eicosapentaenoic acid (EPA), has been determined using the 2-deoxyglucose tracer technique. Mice receiving PIF showed a profound depression of body weight (2.3 g) over a 24-h period, which was completely abolished by pretreatment with a monoclonal antibody to PIF or by 3 days pretreatment with EPA at 500 mg kg(-1). Animals receiving PIF exhibited a marked hypoglycaemia, which was effectively reversed by both antibody and EPA pretreatment. There was an increase in glucose utilization by brain, heart and brown fat, but a decrease by kidney, white fat, diaphragm and gastrocnemius muscle after administration of PIF. Changes in organ glucose consumption were attenuated by either monoclonal antibody, EPA, or both. There was a decrease in 2-deoxyglucose uptake by C2C12 myoblasts in vitro, which was attenuated by EPA. This suggests a direct effect of PIF on glucose uptake by skeletal muscle. These results suggest that in addition to a direct catabolic effect on skeletal muscle PIF has a profound effect on glucose utilization during cachexia.
引用
收藏
页码:1231 / 1235
页数:5
相关论文
共 21 条
[11]   METABOLIC SUBSTRATE UTILIZATION BY TUMOR AND HOST TISSUES IN CANCER CACHEXIA [J].
MULLIGAN, HD ;
TISDALE, MJ .
BIOCHEMICAL JOURNAL, 1991, 277 :321-326
[12]  
NOLOP KB, 1987, CANCER, V60, P2682, DOI 10.1002/1097-0142(19871201)60:11<2682::AID-CNCR2820601118>3.0.CO
[13]  
2-H
[14]   Brown fat thermogenesis in rats fed high-fat diets enriched with n-3 polyunsaturated fatty acids [J].
Oudart, H ;
Groscolas, R ;
Calgari, C ;
Nibbelink, M ;
Leray, C ;
LeMaho, Y ;
Malan, A .
INTERNATIONAL JOURNAL OF OBESITY, 1997, 21 (11) :955-962
[15]  
SCHEIN PS, 1979, CANCER-AM CANCER SOC, V43, P2070, DOI 10.1002/1097-0142(197905)43:5+<2070::AID-CNCR2820430715>3.0.CO
[16]  
2-C
[17]   INHIBITION OF TUMOR-INDUCED LIPOLYSIS INVITRO AND CACHEXIA AND TUMOR-GROWTH INVIVO BY EICOSAPENTAENOIC ACID [J].
TISDALE, MJ ;
BECK, SA .
BIOCHEMICAL PHARMACOLOGY, 1991, 41 (01) :103-107
[18]   Biology of cachexia [J].
Tisdale, MJ .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1997, 89 (23) :1763-1773
[19]   Characterization of a cancer cachectic factor [J].
Todorov, P ;
Cariuk, P ;
McDevitt, T ;
Coles, B ;
Fearon, K ;
Tisdale, M .
NATURE, 1996, 379 (6567) :739-742
[20]  
Todorov PT, 1996, CANCER RES, V56, P1256