OXIDATION OF PARENTERAL LIPID EMULSION BY AMBIENT AND PHOTOTHERAPY LIGHTS - POTENTIAL TOXICITY OF ROUTINE PARENTERAL-FEEDING

被引:118
作者
NEUZIL, J
DARLOW, BA
INDER, TE
SLUIS, KB
WINTERBOURN, CC
STOCKER, R
机构
[1] HEART RES INST, BIOCHEM GRP, SYDNEY, NSW 2050, AUSTRALIA
[2] CHRISTCHURCH HOSP, CHRISTCHURCH SCH MED, DEPT PAEDIAT, CHRISTCHURCH, NEW ZEALAND
[3] CHRISTCHURCH HOSP, CHRISTCHURCH SCH MED, DEPT PATHOL, CHRISTCHURCH, NEW ZEALAND
基金
英国医学研究理事会;
关键词
D O I
10.1016/S0022-3476(95)70412-4
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Vitamin E can be a prooxidant in isolated lipoprotein suspensions, Because lipid emulsions used in parenteral nutrition are lipoprotein-like suspensions rich in polyunsaturated fatty acids and vitamin E, we hypothesized that vitamin E may act as a prooxidant in lipid emulsions, as it is in lipoprotein suspensions, We therefore exposed an intravenously administered lipid emulsion (Intralipid) to a single spotlight commonly used in the treatment of neonatal jaundice, and measured the formation of triglyceride hydroperoxides by using high-performance liquid chromatography with postcolumn chemiluminescence detection, Concentrations of these hydroperoxides in different batches of fresh Intralipid were usually approximately 10 mu mol/L but increased up to 60 times after exposure to phototherapy light for a period of 24 hours, even though significant amounts of vitamin E were present at the end of the exposure, Triglyceride hydroperoxides were formed during phototherapy light exposure whether the Intralipid was in plastic tubing used routinely for infusion or in glass containers, Ambient light also caused significant peroxidation of the formula lipids, although to a much lesser extent than observed with phototherapy light, For infants in the neonatal intensive care unit who were receiving intralipid but not phototherapy, solutions being infused at the end of 24 hours contained a mean of 40 mu mol/L hydroperoxides, For infants receiving phototherapy, the mean was 97 mu mol/L. Phototherapy light-induced formation of triglyceride hydroperoxides was prevented by covering the Intralipid with aluminum foil or supplementation with sodium ascorbate before light exposure, We conclude that Intralipid is highly susceptible to oxidation and that elevated levels of oxidized lipids can be formed during its clinical use, especially when Intralipid infusion is combined with phototherapy, Because lipid hydroperoxides are cytotoxic and can cause adverse effects, inadvertent infusion of rancid Intralipid may add to the numerous problems encountered by premature neonates.
引用
收藏
页码:785 / 790
页数:6
相关论文
共 25 条
[11]   THE INCREASE IN VASOMOTOR TONE INDUCED BY A PARENTERAL LIPID EMULSION IS LINKED TO AN INHIBITION OF PROSTACYCLIN PRODUCTION [J].
LAVOIE, JC ;
CHESSEX, P .
FREE RADICAL BIOLOGY AND MEDICINE, 1994, 16 (06) :795-799
[12]   FORMATION OF NON-CYCLOOXYGENASE-DERIVED PROSTANOIDS (F-2-ISOPROSTANES) IN PLASMA AND LOW-DENSITY-LIPOPROTEIN EXPOSED TO OXIDATIVE STRESS IN-VITRO [J].
LYNCH, SM ;
MORROW, JD ;
ROBERTS, LJ ;
FREI, B .
JOURNAL OF CLINICAL INVESTIGATION, 1994, 93 (03) :998-1004
[13]  
MARKEY CM, 1987, J BIOL CHEM, V262, P6266
[14]   PHOTOTHERAPY FOR NEONATAL HYPERBILIRUBINEMIA - THE IMPORTANCE OF DOSE [J].
MODI, N ;
KEAY, AJ .
ARCHIVES OF DISEASE IN CHILDHOOD, 1983, 58 (06) :406-409
[15]   RADICAL-MEDIATED OXIDATION OF ISOLATED HUMAN VERY-LOW-DENSITY LIPOPROTEIN [J].
MOHR, D ;
STOCKER, R .
ARTERIOSCLEROSIS AND THROMBOSIS, 1994, 14 (07) :1186-1192
[16]  
NEUZIL J, 1994, J BIOL CHEM, V269, P16712
[17]   DETERMINATION OF ALPHA-TOCOPHEROL AND ALPHA-TOCOPHERYLQUINONE IN SMALL BIOLOGICAL SAMPLES BY HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY WITH ELECTROCHEMICAL DETECTION [J].
PASCOE, GA ;
DUDA, CT ;
REED, DJ .
JOURNAL OF CHROMATOGRAPHY-BIOMEDICAL APPLICATIONS, 1987, 414 (02) :440-448
[18]   GENERATION OF FREE-RADICALS IN LIPID EMULSION USED IN PARENTERAL-NUTRITION [J].
PITKANEN, O ;
HALLMAN, M ;
ANDERSSON, S .
PEDIATRIC RESEARCH, 1991, 29 (01) :56-59
[19]   PHYSICOCHEMICAL CHARACTERIZATION OF INTRALIPID EMULSIONS [J].
ROTENBERG, M ;
RUBIN, M ;
BOR, A ;
MEYUHAS, D ;
TALMON, Y ;
LICHTENBERG, D .
BIOCHIMICA ET BIOPHYSICA ACTA, 1991, 1086 (03) :265-272
[20]  
SATTLER W, 1994, METHOD ENZYMOL, V233, P469