Innis S M, Boyd M C
Am J Clin Nutr. 1983 Jul;38(1):95-100. doi: 10.1093/ajcn/38.1.95.
The origin of excess plasma free cholesterol known to accumulate in plasma of patients or animals given total parenteral nutrition (TPN) with lipid emulsion was investigated. Rats were infused for 8 days with a specially formulated TPN solution plus either lipid emulsion (lipid-TPN) or an equicaloric volume of 25% dextrose (dextrose-TPN). Laboratory diet-fed controls were sham operated. Lipid-TPN suppressed hepatic HMG CoA reductase (HMG CoAR) activity but elevated cholesterol 7 alpha-hydroxylase (7 alpha-OH) activity. HMG CoAR activity, however, was increased in adipose tissue and skeletal muscle by lipid-TPN when compared to dextrose-TPN. Plasma lecithin/cholesterol acyl transfer activity was similar among all groups. It is suggested that in lipid-TPN excess plasma free cholesterol does not arise from decreased hepatic clearance or plasma esterification but may originate from extrahepatic tissue, possibly through leaching of membrane cholesterol by mesophase phospholipid present in the lipid emulsion. The changes in hepatic HMG CoAR and 7 alpha-OH activity imply that during lipid-TPN plasma free cholesterol is cleared by the liver and catabolized to bile acid.
对接受含脂质乳剂的全胃肠外营养(TPN)的患者或动物血浆中积累的过量血浆游离胆固醇的来源进行了研究。给大鼠输注特制的TPN溶液加脂质乳剂(脂质-TPN)或等热量的25%葡萄糖(葡萄糖-TPN),持续8天。以实验室饲料喂养的大鼠作为假手术对照。脂质-TPN抑制肝脏羟甲基戊二酸单酰辅酶A还原酶(HMG CoAR)活性,但提高胆固醇7α-羟化酶(7α-OH)活性。然而,与葡萄糖-TPN相比,脂质-TPN使脂肪组织和骨骼肌中的HMG CoAR活性增加。所有组间血浆卵磷脂/胆固醇酰基转移活性相似。提示在脂质-TPN中,过量的血浆游离胆固醇并非源于肝脏清除率降低或血浆酯化作用减弱,而是可能源于肝外组织,可能是通过脂质乳剂中存在的中间相磷脂对膜胆固醇的浸出作用。肝脏HMG CoAR和7α-OH活性的变化表明,在脂质-TPN期间,血浆游离胆固醇由肝脏清除并分解代谢为胆汁酸。