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抗肿瘤坏死因子-α治疗会干扰肿瘤恶病质模型中脂质代谢的变化。

Anti-tumour necrosis factor-alpha treatment interferes with changes in lipid metabolism in a tumour cachexia model.

作者信息

Carbó N, Costelli P, Tessitore L, Bagby G J, López-Soriano F J, Baccino F M, Argilés J M

机构信息

Departament de Bioquímica i Fisiologia, Universitat de Barcelona, Spain.

出版信息

Clin Sci (Lond). 1994 Sep;87(3):349-55. doi: 10.1042/cs0870349.

Abstract
  1. Rats bearing the Yoshida ascites hepatoma AH-130 showed an important decrease in white adipose tissue lipoprotein lipase activity as compared with non-tumour bearing rats. This was associated with a lower adipose tissue mass, as estimated from the weight of the lumbar fat-pads. Conversely, lipoprotein lipase activity was markedly increased in brown adipose tissue and heart. 2. These changes were associated with a distinct hyperlipaemia, essentially manifested as an increase in circulating triacylglycerol levels, whereas no changes were observed in glycaemia. 3. Tumour-bearing rats were treated with a polyclonal anti-murine tumour necrosis factor-alpha antibody or with a non-immune IgG preparation. Control animals were either untreated or received a non-immune IgG preparation. Anti-tumour necrosis factor-alpha treatment resulted in a significant increase in lipoprotein lipase activity in white adipose tissue in animals bearing a tumour growing exponentially (day 4 after inoculation) as compared with the animals receiving a non-immune goat IgG preparation. In addition, animals bearing an stationary tumour (day 7 after inoculation) and submitted to anti-tumour necrosis factor-alpha treatment had a higher adipose tissue lipoprotein lipase activity as compared with the IgG- or the non-treated groups. Correspondingly, circulating triacylglycerol levels were markedly decreased, with a lower hyperlipaemia than in control tumour-bearing rats. 4. These observations suggest that tumour necrosis factor-alpha is involved in activating the lipid metabolic changes that develop in rats after transplantation of a fast-growing tumour.
摘要
  1. 与未患肿瘤的大鼠相比,携带吉田腹水肝癌AH - 130的大鼠白色脂肪组织脂蛋白脂肪酶活性显著降低。根据腰椎脂肪垫的重量估算,这与较低的脂肪组织量相关。相反,棕色脂肪组织和心脏中的脂蛋白脂肪酶活性明显增加。2. 这些变化与明显的高脂血症相关,主要表现为循环三酰甘油水平升高,而血糖水平未见变化。3. 给患肿瘤的大鼠注射多克隆抗小鼠肿瘤坏死因子-α抗体或非免疫IgG制剂。对照动物未接受治疗或接受非免疫IgG制剂。与接受非免疫山羊IgG制剂的动物相比,抗肿瘤坏死因子-α治疗使接种后第4天肿瘤呈指数生长的患肿瘤动物白色脂肪组织中的脂蛋白脂肪酶活性显著增加。此外,接种后第7天肿瘤生长稳定且接受抗肿瘤坏死因子-α治疗的动物,其脂肪组织脂蛋白脂肪酶活性高于IgG治疗组或未治疗组。相应地,循环三酰甘油水平显著降低,高脂血症程度低于对照患肿瘤大鼠。4. 这些观察结果表明,肿瘤坏死因子-α参与激活快速生长肿瘤移植后大鼠体内发生的脂质代谢变化。

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