Cavallini Gabriella, Sgarbossa Antonella, Parentini Ilaria, Bizzarri Ranieri, Donati Alessio, Lenci Francesco, Bergamini Ettore
Interdepartmental Research Centre on Biology and Pathology of Aging, University of Pisa, Via Roma 55, 56126, Pisa, Italy.
Biophysics Institute of the National Research Council (IBF-CNR), Pisa, Italy.
Lipids. 2016 Apr;51(4):477-86. doi: 10.1007/s11745-016-4137-x. Epub 2016 Mar 11.
Dolichol, an end product of the mevalonate pathway, has been proposed as a biomarker of aging, but its biological role, not to mention its catabolism, has not been fully understood. UV-B radiation was used to induce oxidative stress in isolated rat hepatocytes by the collagenase method. Effects on dolichol, phospholipid-bound polyunsaturated fatty acids (PL-PUFA) and known lipid soluble antioxidants [coenzyme Q (CoQ) and α-tocopherol] were studied. The increase in oxidative stress was detected by a probe sensitive to reactive oxygen species (ROS). Peroxidation of lipids was assessed by measuring the release of thiobarbituric acid reactive substances (TBARS). Dolichol, CoQ, and α-tocopherol were assessed by high-pressure liquid chromatography (HPLC), PL-PUFA by gas-liquid chromatography (GC). UV-B radiation caused an immediate increase in ROS as well as lipid peroxidation and a simultaneous decrease in the levels of dolichol and lipid soluble antioxidants. Decrease in dolichol paralleled changes in CoQ levels and was smaller to that in α-tocopherol. The addition of mevinolin, a competitive inhibitor of the enzyme 3-hydroxy-3-methylglutaryl CoA reductase (HMG-CoAR), magnified the loss of dolichol and was associated with an increase in TBARS production. Changes in PL-PUFA were minor. These findings highlight that oxidative stress has very early and similar effects on dolichol and lipid soluble antioxidants. Lower levels of dolichol are associated with enhanced peroxidation of lipids, which suggest that dolichol may have a protective role in the antioxidant machinery of cell membranes and perhaps be a key to understanding some adverse effects of statin therapy.
多萜醇是甲羟戊酸途径的终产物,已被提议作为衰老的生物标志物,但其生物学作用,更不用说其分解代谢,尚未完全了解。采用胶原酶法用紫外线B辐射诱导分离的大鼠肝细胞产生氧化应激。研究了对多萜醇、磷脂结合多不饱和脂肪酸(PL-PUFA)和已知脂溶性抗氧化剂[辅酶Q(CoQ)和α-生育酚]的影响。通过对活性氧(ROS)敏感的探针检测氧化应激的增加。通过测量硫代巴比妥酸反应性物质(TBARS)的释放来评估脂质过氧化。多萜醇、CoQ和α-生育酚通过高压液相色谱(HPLC)进行评估,PL-PUFA通过气液色谱(GC)进行评估。紫外线B辐射导致ROS立即增加以及脂质过氧化,同时多萜醇和脂溶性抗氧化剂水平降低。多萜醇的降低与CoQ水平的变化平行,且小于α-生育酚的降低。添加美伐他汀,一种3-羟基-3-甲基戊二酰辅酶A还原酶(HMG-CoAR)的竞争性抑制剂,放大了多萜醇的损失,并与TBARS产生的增加有关。PL-PUFA的变化较小。这些发现突出表明,氧化应激对多萜醇和脂溶性抗氧化剂具有非常早期且相似的影响。较低水平的多萜醇与脂质过氧化增强有关,这表明多萜醇可能在细胞膜的抗氧化机制中具有保护作用,也许是理解他汀类药物治疗某些不良反应的关键。