Raju Jayadev, Bird Ranjana P
Department of Foods and Nutrition, University of Manitoba, Winnipeg, Canada.
Mol Cell Biochem. 2002 Feb;231(1-2):139-46. doi: 10.1023/a:1014468932482.
Platelets are implicated in the pathogenesis of various chronic diseases including cancer. The main objective of the present study was to determine if dietary fish oil and piroxicam, known modulators of colon tumorigenesis, effect transforming growth factor (TGF)-betas and cyclooxygenase (COX) isozymes in the platelets of colon tumor-bearing male F344 rats. TGF-betas and COXs are important in the development of chronic illnesses including colon cancer. Animals harboring preneoplastic colonic lesions were randomly allocated to a low fat diet (5% by weight--low corn oil, LFC) and three high fat diets (23% by weight--high corn oil, HFC; high corn oil containing 150-ppm piroxicam, HFC+P; and high fish oil, HFF) for 16 weeks. TGF-beta1, TGF-beta2, COX-1 and COX-2 protein levels were assessed in the platelets by Western blot analysis. Active TGF-beta1 (12.5 kDa) level was significantly lower in the platelets of the HFC+P group (p < 0.001), whereas precursor TGF-beta1 (39 kDa) level was significantly lower in the platelets of the HFF group (p < 0.001). The anti-rabbit TGF-beta2 polyclonal antibody did not detect the 13-kDa active TGF-beta2 protein in the platelets. However a 29-kDa protein, potentially a precursor of TGF-beta2, was detected in the platelets of all the groups and was significantly lower in the HFC+P and HFF groups than in LFC and HFC (p < 0.001). COX-1 level was significantly lower in the HFF group than the other three groups (p < 0.001). COX-2 protein was detected in the platelets of all diet groups. Piroxicam in the presence of high corn oil (HFC+P) significantly lowered the level of COX-2 (p < 0.001), without having any effect on COX-1 level. These findings conclusively show that LFC and HFC differ from HFF and HFC+P, and piroxicam differs from fish oil, in regulating the levels of TGF-betas and COX in the platelets. This supports the conjecture that the levels of bioactive constituents of the platelets are profoundly modulated by dietary lipids, which in turn could influence the pathogenesis of chronic illnesses.
血小板与包括癌症在内的多种慢性疾病的发病机制有关。本研究的主要目的是确定已知的结肠肿瘤发生调节剂膳食鱼油和吡罗昔康是否会影响荷瘤雄性F344大鼠血小板中的转化生长因子(TGF)-βs和环氧化酶(COX)同工酶。TGF-βs和COXs在包括结肠癌在内的慢性疾病发展中起重要作用。将患有癌前结肠病变的动物随机分为低脂饮食(5%重量——低玉米油,LFC)和三种高脂饮食(23%重量——高玉米油,HFC;含150 ppm吡罗昔康的高玉米油,HFC+P;以及高鱼油,HFF),持续16周。通过蛋白质印迹分析评估血小板中TGF-β1、TGF-β2、COX-1和COX-2蛋白水平。HFC+P组血小板中活性TGF-β1(12.5 kDa)水平显著降低(p<0.001),而HFF组血小板中前体TGF-β1(39 kDa)水平显著降低(p<0.001)。抗兔TGF-β2多克隆抗体未在血小板中检测到13 kDa的活性TGF-β2蛋白。然而,在所有组的血小板中均检测到一种29 kDa的蛋白,可能是TGF-β2的前体,且HFC+P组和HFF组中的该蛋白水平显著低于LFC组和HFC组(p<0.001)。HFF组的COX-1水平显著低于其他三组(p<0.001)。在所有饮食组的血小板中均检测到COX-2蛋白。高玉米油(HFC+P)存在时的吡罗昔康显著降低了COX-2水平(p<0.001),而对COX-1水平无任何影响。这些发现确凿地表明,在调节血小板中TGF-βs和COX水平方面,LFC和HFC与HFF和HFC+P不同,吡罗昔康与鱼油不同。这支持了这样的推测,即膳食脂质可深刻调节血小板生物活性成分的水平,进而可能影响慢性疾病的发病机制。