13-Plex UHPLC–MS/MS Analysis of Hexanal and Heptanal Using Multiplex Tags Chemical Isotope Labeling Technology

2020 ◽  
Vol 31 (9) ◽  
pp. 1965-1973
Author(s):  
Jingwen Hu ◽  
Shi-En Chen ◽  
Shuyun Zhu ◽  
Wenhui Jia ◽  
Jing Sun ◽  
...  
Keyword(s):  
Isotope Labeling ◽  
Ms Analysis ◽  
Chemical Isotope Labeling

12-Plex UHPLC-MS/MS analysis of sarcosine in human urine using integrated principle of multiplex tags chemical isotope labeling and selective imprint enriching

Talanta ◽  
2021 ◽  
Vol 224 ◽  
pp. 121788
Author(s):  
Shi-En Chen ◽  
Jingwen Hu ◽  
Ping Yan ◽  
Jing Sun ◽  
Wenhui Jia ◽  
...  
Keyword(s):  
Human Urine ◽  
Isotope Labeling ◽  
Ms Analysis ◽  
Chemical Isotope Labeling

scholarly journals Dexamethasone-Induced Perturbations in Tissue Metabolomics Revealed by Chemical Isotope Labeling LC-MS Analysis

Metabolites ◽  
2020 ◽  
Vol 10 (2) ◽  
pp. 42 ◽  
Author(s):  
Lina Dahabiyeh ◽  
Abeer Malkawi ◽  
Xiaohang Wang ◽  
Dilek Colak ◽  
Ahmed Mujamammi ◽  
...  
Keyword(s):  
Skeletal Muscle ◽  
Amino Acid ◽  
Side Effects ◽  
Isotope Labeling ◽  
Protein Biosynthesis ◽  
Chronic Administration ◽  
Therapeutic Interventions ◽  
Sprague Dawley ◽  
The Brain ◽  
Chemical Isotope Labeling

Dexamethasone (Dex) is a synthetic glucocorticoid (GC) drug commonly used clinically for the treatment of several inflammatory and immune-mediated diseases. Despite its broad range of indications, the long-term use of Dex is known to be associated with specific abnormalities in several tissues and organs. In this study, the metabolomic effects on five different organs induced by the chronic administration of Dex in the Sprague–Dawley rat model were investigated using the chemical isotope labeling liquid chromatography-mass spectrometry (CIL LC-MS) platform, which targets the amine/phenol submetabolomes. Compared to controls, a prolonged intake of Dex resulted in significant perturbations in the levels of 492, 442, 300, 186, and 105 metabolites in the brain, skeletal muscle, liver, kidney, and heart tissues, respectively. The positively identified metabolites were mapped to diverse molecular pathways in different organs. In the brain, perturbations in protein biosynthesis, amino acid metabolism, and monoamine neurotransmitter synthesis were identified, while in the heart, pyrimidine metabolism and branched amino acid biosynthesis were the most significantly impaired pathways. In the kidney, several amino acid pathways were dysregulated, which reflected impairments in several biological functions, including gluconeogenesis and ureagenesis. Beta-alanine metabolism and uridine homeostasis were profoundly affected in liver tissues, whereas alterations of glutathione, arginine, glutamine, and nitrogen metabolism pointed to the modulation of muscle metabolism and disturbances in energy production and muscle mass in skeletal muscle. The differential expression of multiple dipeptides was most significant in the liver (down-regulated), brain (up-regulation), and kidney tissues, but not in the heart or skeletal muscle tissues. The identification of clinically relevant pathways provides holistic insights into the tissue molecular responses induced by Dex and understanding of the underlying mechanisms associated with their side effects. Our data suggest a potential role for glutathione supplementation and dipeptide modulators as novel therapeutic interventions to mitigate the side effects induced by Dex therapy.

Accurate Determination of Protein Methionine Oxidation by Stable Isotope Labeling and LC-MS Analysis

2013 ◽  
Vol 85 (24) ◽  
pp. 11705-11709 ◽  
Author(s):  
Hongcheng Liu ◽  
Gomathinayagam Ponniah ◽  
Alyssa Neill ◽  
Rekha Patel ◽  
Bruce Andrien
Keyword(s):  
Stable Isotope ◽  
Isotope Labeling ◽  
Accurate Determination ◽  
Stable Isotope Labeling ◽  
Methionine Oxidation ◽  
Ms Analysis
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