Halvorson D L, McCune S A
Lipids. 1984 Nov;19(11):851-6. doi: 10.1007/BF02534514.
The compound 5-(tetradecyloxy)-2-furoic acid (TOFA), a hypolipidemic agent, inhibits fatty acid synthesis, lactate and pyruvate accumulation and CO2 release in isolated rat adipocytes. TOFA stimulates the accumulation of citrate. ATP levels are not lowered by TOFA. In comparison with the natural fatty acid, oleate, TOFA exhibited a much greater inhibitory effect on lipogenesis. TOFyl-CoA formation within intact adipocytes was demonstrated. Although not inhibited by TOFA, acetyl-CoA carboxylase is inhibited by TOFyl-CoA. It is proposed that many of the metabolic effects of TOFA in isolated adipocytes can be explained by TOFyl-CoA inhibition of acetyl-CoA carboxylase. TOFA inhibits glycolysis as a secondary event with the primary event of inhibition of fatty acid synthesis causing an accumulation of citrate which is an inhibitor of phosphofructokinase.
化合物5-(十四烷氧基)-2-呋喃甲酸(TOFA)是一种降血脂剂,可抑制离体大鼠脂肪细胞中的脂肪酸合成、乳酸和丙酮酸积累以及二氧化碳释放。TOFA刺激柠檬酸盐的积累。TOFA不会降低ATP水平。与天然脂肪酸油酸相比,TOFA对脂肪生成的抑制作用要强得多。已证实在完整的脂肪细胞中会形成TOFyl-CoA。尽管TOFA不会抑制乙酰辅酶A羧化酶,但TOFyl-CoA会抑制该酶。有人提出,TOFA在离体脂肪细胞中的许多代谢作用可以用TOFyl-CoA对乙酰辅酶A羧化酶的抑制来解释。TOFA抑制糖酵解是次要事件,而抑制脂肪酸合成这一主要事件会导致柠檬酸盐积累,柠檬酸盐是磷酸果糖激酶的抑制剂。