Left ventricular assist device effects on metabolic substrates in the failing heart.
Left ventricular assist device effects on metabolic substrates in the failing heart.
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DOI:
10.1371/journal.pone.0060292
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发表时间:
2013
期刊:
影响因子:
3.7
通讯作者:
Lowes BD
中科院分区:
文献类型:
--
作者:
Weitzel LB;Ambardekar AV;Brieke A;Cleveland JC;Serkova NJ;Wischmeyer PE;Lowes BD
Heart failure patients have inadequate nutritional intake and alterations in metabolism contributing to an overall energy depleted state. Left ventricular assist device (LVAD) support is a common and successful intervention in patients with end-stage heart failure. LVAD support leads to alterations in cardiac output, functional status, neurohormonal activity and transcriptional profiles but the effects of LVADs on myocardial metabolism are unknown. This study set out to measure cardiac metabolites in non-failing hearts, failing hearts, and hearts post-LVAD support. The study population consisted of 8 non-ischemic failing (at LVAD implant) and 8 post-LVAD hearts, plus 8 non-failing hearts obtained from the tissue bank at the University of Colorado. NMR spectroscopy was utilized to evaluate differences in myocardial energy substrates. Paired and non-paired t-tests were used to determine differences between the appropriate groups. Glucose and lactate values both decreased from non-failing to failing hearts and increased again significantly in the (paired) post-LVAD hearts. Glutamine, alanine, and aromatic amino acids decreased from non-failing to failing hearts and did not change significantly post-LVAD. Total creatine and succinate decreased from non-failing to failing hearts and did not change significantly post-LVAD. Measured metabolites related to glucose metabolism are diminished in failing hearts, but recovered their values post-LVAD. This differed from the amino acid levels, which decreased in heart failure but did not recover following LVAD. Creatine and the citric acid cycle intermediate succinate followed a similar pattern as the amino acid levels.
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影响因子:
37.8
作者:
Cheng S;Rhee EP;Larson MG;Lewis GD;McCabe EL;Shen D;Palma MJ;Roberts LD;Dejam A;Souza AL;Deik AA;Magnusson M;Fox CS;O'Donnell CJ;Vasan RS;Melander O;Clish CB;Gerszten RE;Wang TJ
通讯作者:
Wang TJ
影响因子:
158.5
作者:
Rose, EA;Gelijns, AC;Meier, P
通讯作者:
Meier, P
影响因子:
3.4
作者:
Wischmeyer, PE;Jayakar, D;Serkova, N
通讯作者:
Serkova, N
DOI:
10.1016/0735-1097(95)00555-2
发表时间:
1996-03-15
影响因子:
24
作者:
Nakatani, S;McCarthy, PM;Thomas, JD
通讯作者:
Thomas, JD
影响因子:
19.6
作者:
Serkova, N;Fuller, TF;Niemann, CU
通讯作者:
Niemann, CU