Hemodialysis stimulates muscle and whole body protein loss and alters substrate oxidation

被引:231
作者
Ikizler, TA
Pupim, LB
Brouillette, JR
Levenhagen, DK
Farmer, K
Hakim, RM
Flakoll, PJ
机构
[1] Vanderbilt Univ, Med Ctr, Div Nephrol, Dept Med, Nashville, TN 37232 USA
[2] Vanderbilt Univ, Med Ctr, Dept Surg, Nashville, TN 37232 USA
[3] Vanderbilt Univ, Med Ctr, Dept Biochem, Nashville, TN 37232 USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM | 2002年 / 282卷 / 01期
关键词
catabolism; malnutrition; inflammation; energy expenditure; metabolism;
D O I
10.1152/ajpendo.2002.282.1.E107
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The hemodialysis (HD) procedure has been implicated as a potential catabolic factor predisposing the chronic HD (CHD) patients to protein calorie malnutrition. To assess the potential effects of HD on protein and energy metabolism, we studied 11 CHD patients 2 h before, during, and 2 h after HD by use of primed constant infusion of L-[1-C-13] leucine and L-[ring-H-2(5)] phenylalanine. Our results showed that HD led to increased whole body (10%) and muscle protein (133%) proteolysis. Simultaneously, whole body protein synthesis did not change, and forearm synthesis increased (120%). The net result was increased net whole body protein loss (96%) and net forearm protein loss (164%). During the 2-h post-HD period, the muscle protein breakdown trended toward baseline, whereas whole body protein breakdown increased further. Substrate oxidation during the post-HD was significantly altered, with diminished carbohydrate and accelerated lipid and amino acid oxidation. These data demonstrate that hemodialysis is an overall catabolic event, decreasing the circulating amino acids, accelerating rates of whole body and muscle proteolysis, stimulating muscle release of amino acids, and elevating net whole body and muscle protein loss.
引用
收藏
页码:E107 / E116
页数:10
相关论文
共 38 条
  • [31] IMMUNAOASSAY OF INSULIN - 2 ANTIBODY SYSTEM - PLASMA INSULIN LEVELS OF NORMAL SUBDIABETIC AND DIABETIC RATS
    MORGAN, CR
    LAZAROW, A
    [J]. DIABETES, 1963, 12 (02) : 115 - &
  • [32] MEASUREMENT OF BRANCHED-CHAIN AMINO-ACIDS AND BRANCHED-CHAIN ALPHA-KETOACIDS IN PLASMA BY HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY
    NISSEN, SL
    VANHUYSEN, C
    HAYMOND, MW
    [J]. JOURNAL OF CHROMATOGRAPHY, 1982, 232 (01): : 170 - 175
  • [33] Nyboer J., 1972, J LIFE SCI, V2, P1
  • [34] Effect of the membrane biocompatibility on nutritional parameters in chronic hemodialysis patients
    Parker, TF
    Wingard, RL
    Husni, L
    Ikizler, TA
    Parker, RA
    Hakim, RM
    [J]. KIDNEY INTERNATIONAL, 1996, 49 (02) : 551 - 556
  • [35] Muscle wasting in insulinopenic rats results from activation of the ATP-dependent, ubiquitin-proteasome proteolytic pathway by a mechanism including gene transcription
    Price, SR
    Bailey, JL
    Wang, XN
    Jurkovitz, C
    England, BK
    Ding, XY
    Phillips, LS
    Mitch, WE
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1996, 98 (08) : 1703 - 1708
  • [36] SCHWENK WF, 1984, ANAL BIOCHEM, V141, P101
  • [37] AUTOMATED MEASUREMENT OF THE CONCENTRATION AND C-13 ENRICHMENT OF CARBON-DIOXIDE IN BREATH AND BLOOD-SAMPLES USING THE FINNIGAN MAT BREATH GAS-ANALYSIS SYSTEM
    SCRIMGEOUR, CM
    RENNIE, MJ
    [J]. BIOMEDICAL AND ENVIRONMENTAL MASS SPECTROMETRY, 1988, 15 (07): : 365 - 367
  • [38] Wolfe RR., 1992, Radioactive and Stable Isotope Tracers in Biomedicine: Principles and Practice of Kinetic Analysis, P283