Bell F P
Atherosclerosis. 1981 Jan-Feb;38(1-2):81-8. doi: 10.1016/0021-9150(81)90106-4.
The local anesthetics lidocaine, tetracaine, benzocaine and dibucaine were found to inhibit sterol esterification by acylCoA:cholesterol acyltransferase (ACAT, EC 2.3.1.26) in the microsomal fraction isolated from rabbit aortas. In arterial microsomes, the incorporation of [14C]oleoylCoA into [14C]steryl esters was inhibited in a dose-dependent way by the anesthetics over the concentration range 0.25-5.0 mM. The potency of inhibition was dibucaine greater than benzocaine greater than tetracaine greater than lidocaine greater than procaine with inhibition of about 85% occurring with 0.25 mM dibucaine. Sterol esterification to [14C]oleic acid was also inhibited by the anesthetics in intact aortic tissue from the rabbit, dog, and rat. A detailed study of the effects of 5 mM lidocaine on lipid biosynthesis in the rabbit aorta in vitro revealed that lidocaine not only inhibited sterol esterification to [14C]oleate but stimulated [14C]oleate incorporation into glycerides.
研究发现,局部麻醉药利多卡因、丁卡因、苯佐卡因和地布卡因可抑制从兔主动脉分离出的微粒体部分中酰基辅酶A:胆固醇酰基转移酶(ACAT,EC 2.3.1.26)介导的甾醇酯化。在动脉微粒体中,麻醉药在0.25 - 5.0 mM的浓度范围内以剂量依赖的方式抑制[14C]油酰辅酶A掺入[14C]甾醇酯。抑制效力为地布卡因大于苯佐卡因大于丁卡因大于利多卡因大于普鲁卡因,0.25 mM地布卡因的抑制率约为85%。在兔、犬和大鼠的完整主动脉组织中,麻醉药也抑制甾醇酯化生成[14C]油酸。对5 mM利多卡因体外作用于兔主动脉脂质生物合成的详细研究表明,利多卡因不仅抑制甾醇酯化生成[14C]油酸酯,还刺激[14C]油酸酯掺入甘油酯。