Hayashi E, Yamada J, Kunitomo M, Terada M, Sato M
Jpn J Pharmacol. 1978 Feb;28(1):61-72. doi: 10.1254/jjp.28.61.
Effects of L-ascorbate 2-sulfate (AAS) on lipid metabolism and on pathological changes of aorta and visceral organs were investigated in cholesterol fed rabbits, with ascorbic acid (AA) and clofibrate (CPIB) as reference compounds. Administration of AAS (300 and 150 mg/kg) inhibited an increase in the levels of serum total cholesterol, free cholesterol, triglycerides and phospholipids caused by cholesterol feeding. A high dose of AAS prevented an increase of liver weight. An increase in the level of liver cholesterol was inhibited by a high dose of AAS. Both doses of AAS effectively prevented an accumulation of cholesterol in the aorta. The area rate of atheromatous plaque in aorta was less in specimens from both groups of AAS than in those from control I. Pathological changes in intima and media of aorta were milder in specimens from both groups of AAS. Developed of patholoigcal changes in arteries of various organs were prevented with both doses of AAS.
以抗坏血酸(AA)和氯贝丁酯(CPIB)作为参比化合物,研究了L -抗坏血酸2 -硫酸酯(AAS)对喂饲胆固醇的家兔脂质代谢以及主动脉和内脏器官病理变化的影响。给予AAS(300和150毫克/千克)可抑制因喂饲胆固醇引起的血清总胆固醇、游离胆固醇、甘油三酯和磷脂水平的升高。高剂量的AAS可防止肝脏重量增加。高剂量的AAS可抑制肝脏胆固醇水平的升高。两种剂量的AAS均能有效防止胆固醇在主动脉中蓄积。AAS两组标本中主动脉粥样斑块的面积率均低于对照组I。AAS两组标本中主动脉内膜和中膜的病理变化较轻。两种剂量的AAS均可防止各器官动脉病理变化的发展。