Glucose effects on lung surfactant kinetics in conscious pigs

被引:9
作者
Martini, WZ
Irtun, O
Chinkes, DL
Barrow, RE
Wolfe, RR
机构
[1] Shriners Burns Hosp, Galveston, TX 77550 USA
[2] Univ Texas, Med Branch, Dept Surg, Galveston, TX 77555 USA
[3] Univ Texas, Med Branch, Dept Anesthesiol, Galveston, TX 77555 USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM | 2000年 / 279卷 / 04期
关键词
phosphatidylcholine; isotope; synthesis; secretion;
D O I
10.1152/ajpendo.2000.279.4.E920
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The primary goal of this study was to investigate the effects of glucose infusion on surfactant phosphatidylcholine (PC) metabolic kinetics in the lungs. A new stable isotope tracer model was used in which [1,2-C-13(2)]acetate and uniformly labeled [U-C-13(16)]palmitate were infused in 12 normal overnight-fasted pigs to quantify lung surfactant kinetics with or without glucose infusion (24 mg.kg(-1).min(-1)). With glucose infusion, the rate of surfactant PC incorporation from de novo synthesized palmitate increased from the control value of 2.1 +/- 0.2 to 15.5 +/- 1.9 nmol PC-bound palmitate.h(=1).g wet lung(-1) (P < 0.05), whereas the incorporation rate from plasma preformed palmitate decreased from the control value of 20.9 +/- 1.9 to 11.6 +/- 1.1 nmol palmitate.h(-1).g wet lung(-1) (P < 0.05). The palmitate composition in lamellar body surfactant PC increased from the control value of 61.7 +/- 2.1% to 75.9 +/- 0.6% (P < 0.05). The surfactant PC secretion rate decreased from the control value of 239.0 +/- 26.1 to 81.9 +/- 5.3 nmol PC-bound palmitate.h(-1).g wet lung(-1) (P < 0.05). We conclude that, whereas surfactant secretion was inhibited by glucose infusion, neither total surfactant PC synthesis nor the surfactant PC pool size was significantly affected due to an increased reliance on de novo synthesized fatty acids.
引用
收藏
页码:E920 / E926
页数:7
相关论文
共 23 条
[1]   Contributions of de novo synthesis of fatty acids to total VLDL-triglyceride secretion during prolonged hyperglycemia hyperinsulinemia in normal man [J].
Aarsland, A ;
Chinkes, D ;
Wolfe, RR .
JOURNAL OF CLINICAL INVESTIGATION, 1996, 98 (09) :2008-2017
[2]   Hepatic and whole-body fat synthesis in humans during carbohydrate overfeeding [J].
Aarsland, A ;
Chinkes, D ;
Wolfe, RR .
AMERICAN JOURNAL OF CLINICAL NUTRITION, 1997, 65 (06) :1774-1782
[3]   SYNTHESIS OF FATTY-ACIDS AND CHOLESTEROL BY LIVER, ADIPOSE-TISSUE AND INTESTINAL-MUCOSA FROM OBESE AND CONTROL PATIENTS [J].
ANGEL, A ;
BRAY, GA .
EUROPEAN JOURNAL OF CLINICAL INVESTIGATION, 1979, 9 (05) :355-362
[4]   CHEMICAL-STRUCTURE OF PHOSPHOLIPIDS IN THE LUNGS AND AIRWAYS OF SHEEP [J].
BARROW, RE .
RESPIRATION PHYSIOLOGY, 1990, 79 (01) :1-8
[5]  
BARTLETT GR, 1959, J BIOL CHEM, V234, P466
[7]  
EPSTEIN MF, 1976, PEDIATRICS, V57, P722
[8]  
GOODRIDGE AG, 1991, BIOCH LIPIDS LIPOPRO, P111
[9]   THE INFLUENCE OF HORMONES ON THE BIOCHEMICAL DEVELOPMENT OF FETAL-RAT LUNG IN ORGAN-CULTURE .2. INSULIN [J].
GROSS, I ;
SMITH, GJW ;
WILSON, CM ;
MANISCALCO, WM ;
INGLESON, LD ;
BREHIER, A ;
ROONEY, SA .
PEDIATRIC RESEARCH, 1980, 14 (06) :834-838
[10]   DISTRIBUTION AND CHEMICAL COMPOSITION OF ULTRACENTRIFUGALLY SEPARATED LIPOPROTEINS IN HUMAN SERUM [J].
HAVEL, RJ ;
EDER, HA ;
BRAGDON, JH .
JOURNAL OF CLINICAL INVESTIGATION, 1955, 34 (09) :1345-1353