Ranganathan S, Jackson R L, Harmony J A
Atherosclerosis. 1982 Sep;44(3):261-73. doi: 10.1016/0021-9150(82)90002-8.
Pantethine [D-bis-(N-pantothenyl-beta-aminoethyl)-disulfide] is a compound used clinically to decrease plasma triglycerides and to increase HDL cholesterol. To understand the mechanism of action of this drug, its effect on the synthesis of cholesterol in cultured skin fibroblasts was assessed. The addition of pantethine (100-200 microM) to cultured cells caused an 80% inhibition in cholesterol synthesis as measured by the incorporation of radiolabeled acetate or mevalonolactone. Inhibition occurred within 4 h of adding the drug and was specific for pantethine; other sulfur-containing compounds such as dithiothreitol, glutathione, coenzyme A and cystine did not inhibit. The inhibition of cholesterol synthesis resulted in the accumulation of radiolabeled methyl sterols. The drug also inhibited total fatty acid synthesis. The amount of [14C]pantethine detected in the cells is very low and represented less than 0.5% of the radiolabeled pantethine added in the medium. At low pantethine concentrations, the drug had negligible effects on the biosynthesis of DNA, protein and phospholipid.
泛硫乙胺[D -双-(N -泛酰基-β -氨基乙基)-二硫化物]是一种临床上用于降低血浆甘油三酯和升高高密度脂蛋白胆固醇的化合物。为了解该药物的作用机制,评估了其对培养的皮肤成纤维细胞中胆固醇合成的影响。向培养细胞中添加泛硫乙胺(100 - 200微摩尔),通过放射性标记的乙酸盐或甲羟戊酸内酯的掺入量测定,导致胆固醇合成受到80%的抑制。在添加药物后4小时内出现抑制作用,且对泛硫乙胺具有特异性;其他含硫化合物如二硫苏糖醇、谷胱甘肽、辅酶A和胱氨酸均无抑制作用。胆固醇合成的抑制导致放射性标记的甲基甾醇积累。该药物还抑制总脂肪酸合成。在细胞中检测到的[14C]泛硫乙胺量非常低,占培养基中添加的放射性标记泛硫乙胺的不到0.5%。在低泛硫乙胺浓度下,该药物对DNA、蛋白质和磷脂的生物合成影响可忽略不计。