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Bretschneider solution-induced alterations in the urine metabolome in cardiac surgery patients.
Lee, Cheng-Chia; Hsieh, Ya-Ju; Chen, Shao-Wei; Fu, Shu-Hsuan; Hsu, Chia-Wei; Wu, Chih-Ching; Han, Wei; Li, Yunong; Huan, Tao; Chang, Yu-Sun; Yu, Jau-Song; Li, Liang; Chang, Chih-Hsiang; Chen, Yi-Ting.
Afiliação
  • Lee CC; Kidney Research Center, Department of Nephrology, Chang Gung Memorial Hospital, Linkou branch, College of Medicine, Chang Gung University, Guishan, Taoyuan, Taiwan.
  • Hsieh YJ; Graduate Institute of Clinical Medical Sciences, College of medicine, Chang Gung University, Guishan, Taoyuan, Taiwan.
  • Chen SW; Molecular and Medicine Research Center, Chang Gung University, Guishan, Taoyuan, Taiwan.
  • Fu SH; Graduate Institute of Clinical Medical Sciences, College of medicine, Chang Gung University, Guishan, Taoyuan, Taiwan.
  • Hsu CW; Department of cardiothoracic and vascular surgery, Chang Gung Memorial Hospital, Linkou branch, College of Medicine, Chang Gung University, Guishan, Taoyuan, Taiwan.
  • Wu CC; Molecular and Medicine Research Center, Chang Gung University, Guishan, Taoyuan, Taiwan.
  • Han W; Molecular and Medicine Research Center, Chang Gung University, Guishan, Taoyuan, Taiwan.
  • Li Y; Molecular and Medicine Research Center, Chang Gung University, Guishan, Taoyuan, Taiwan.
  • Huan T; Department of Medical Biotechnology and Laboratory Science, Chang Gung University, Guishan, Taoyuan, 33302, Taiwan.
  • Chang YS; Department of Otolaryngology-Head & Neck Surgery, Chang Gung Memorial Hospital at Linkou, Guishan, Taoyuan, 33305, Taiwan.
  • Yu JS; Department of Chemistry, University of Alberta, Edmonton, AB, T6G2G2, Canada.
  • Li L; Department of Chemistry, University of Alberta, Edmonton, AB, T6G2G2, Canada.
  • Chang CH; Department of Chemistry, University of Alberta, Edmonton, AB, T6G2G2, Canada.
  • Chen YT; Molecular and Medicine Research Center, Chang Gung University, Guishan, Taoyuan, Taiwan.
Sci Rep ; 8(1): 17774, 2018 12 11.
Article em En | MEDLINE | ID: mdl-30538262
ABSTRACT
The development of Bretschneider's histidine-tryptophan-ketoglutarate (HTK) cardioplegia solution represented a major advancement in cardiac surgery, offering significant myocardial protection. However, metabolic changes induced by this additive in the whole body have not been systematically investigated. Using an untargeted mass spectrometry-based method to deeply explore the urine metabolome, we sought to provide a holistic and systematic view of metabolic perturbations occurred in patients receiving HTK. Prospective urine samples were collected from 100 patients who had undergone cardiac surgery, and metabolomic changes were profiled using a high-performance chemical isotope labeling liquid chromatography-mass spectrometry (LC-MS) method. A total of 14,642 peak pairs or metabolites were quantified using differential 13C-/12C-dansyl labeling LC-MS, which targets the amine/phenol submetabolome from urine specimens. We identified 223 metabolites that showed significant concentration change (fold change > 5) and assembled several potential metabolic pathway maps derived from these dysregulated metabolites. Our data indicated upregulated histidine metabolism with subsequently increased glutamine/glutamate metabolism, altered purine and pyrimidine metabolism, and enhanced vitamin B6 metabolism in patients receiving HTK. Our findings provide solid evidence that HTK solution causes significant perturbations in several metabolic pathways and establish a basis for further study of key mechanisms underlying its organ-protective or potential harmful effects.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Urina / Metaboloma Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Urina / Metaboloma Idioma: En Ano de publicação: 2018 Tipo de documento: Article