Casals C, Garcia-Barreno P, Municio A M
Biochem J. 1983 May 15;212(2):339-44. doi: 10.1042/bj2120339.
Oleoylanilide was administered orally to groups of rats according to different patterns. Subcellular fractionation of liver, lung and adipose tissue was then carried out in order to study the main enzyme activities involved in the lipogenesis. The observed findings indicate that adipose tissue and lung are the main target organs for the anilide, adipose tissue being involved in a general decrease of the enzyme activities, whereas transacylation reaction exhibits the most marked depletion of all the enzyme activities in the lung. The enzyme activities in liver were not markedly affected by this oral administration, although some data support the existence of a latent liver toxicity. These data suggest that oleoylanilide has the capacity to alter lipid metabolism of lung and adipose tissue to a considerable extent, whereas no major effect was produced in the liver. This different organ response could be related to the lymphatic gland via absorption of the substance.
按照不同模式给几组大鼠口服油酰苯胺。然后对肝脏、肺和脂肪组织进行亚细胞分级分离,以研究参与脂肪生成的主要酶活性。观察结果表明,脂肪组织和肺是该苯胺的主要靶器官,脂肪组织参与酶活性的普遍降低,而转酰基反应在肺中所有酶活性的消耗最为显著。口服该物质后,肝脏中的酶活性未受到明显影响,尽管一些数据支持存在潜在的肝脏毒性。这些数据表明,油酰苯胺有能力在相当程度上改变肺和脂肪组织的脂质代谢,而对肝脏没有产生重大影响。这种不同的器官反应可能与该物质通过吸收进入淋巴结有关。