RT Journal Article
SR Electronic
T1 Age-dependent protein abundance of cytosolic alcohol and aldehyde dehydrogenases in human liver
JF Drug Metabolism and Disposition
JO Drug Metab Dispos
FD American Society for Pharmacology and Experimental Therapeutics
SP dmd.117.076463
DO 10.1124/dmd.117.076463
A1 Deepak Kumar Bhatt
A1 Andrea Gaedigk
A1 Robin E. Pearce
A1 J. Steven Leeder
A1 Bhagwat Prasad
YR 2017
UL http://dmd.aspetjournals.org/content/early/2017/06/12/dmd.117.076463.abstract
AB Hepatic cytosolic alcohol and aldehyde dehydrogenases (ADHs and ALDHs) catalyze the biotransformation of xenobiotics (e.g., cyclophosphamide and ethanol) and vitamin A. Because age-dependent hepatic abundance of these proteins is unknown, we quantified protein expression of ADHs and ALDH1A1 in a large cohort of pediatric and adult human livers by LC-MS/MS proteomics. Purified proteins were used as calibrators. Two to three surrogate peptides per protein were quantified in trypsin digests of liver cytosolic samples and calibrator proteins under optimal conditions of reproducibility. Neonatal levels of ADH1A, ADH1B, ADH1C and ALDH1A1 were 3, 8, 146 and 3-fold lower than the adult levels, respectively. For all proteins, the abundance steeply increased during the first year of life, which mostly reached adult levels during early childhood (age between 1 to 6 years). Only for ADH1A protein abundance in adults (age >18 yrs.) was ~40% lower relative to the early childhood group. Abundances of ADHs and ALDH1A1 were not associated with gender in samples with age > 1 year compared to males. Known single nucleotide polymorphisms (SNPs) had no effect on the protein levels of these proteins. Quantification of ADHs and ALDH1A1 protein levels could be useful in predicting disposition and response of substrates of these enzymes in younger children.