Dataset Information

Fetal to adult ontogeny of human cytochrome P450 activity, abundance, and expression

ABSTRACT: Activity-based and global proteomic analysis of fetal through late adulthood human samples, with a primary focus on cytochrome P450 enzyme expression and functional activity

INSTRUMENT(S): LTQ Orbitrap

ORGANISM(S): Homo Sapiens (human)

TISSUE(S): Liver

SUBMITTER: Matthew Monroe

LAB HEAD: Aaron T. Wright

PROVIDER: PXD002781 | Pride | 2018-10-24

REPOSITORIES: Pride

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Dataset's files

Source:

			Action	DRS
	FHLM_687_04_Run1_15Feb15_Lynx_15-01-23.mgf	Mgf
	FHLM_687_04_Run1_15Feb15_Lynx_15-01-23.pride.mgf.gz	Mgf
	FHLM_687_04_Run1_15Feb15_Lynx_15-01-23.raw	Raw
	FHLM_687_04_Run1_15Feb15_Lynx_15-01-23_msgfplus.mzid.gz	Mzid
	FHLM_687_04_Run1_15Feb15_Lynx_15-01-23_msgfplus.pride.mztab.gz	Mztab

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Publications

Hepatic Cytochrome P450 Activity, Abundance, and Expression Throughout Human Development.

Sadler Natalie C NC Nandhikonda Premchendar P Webb-Robertson Bobbie-Jo BJ Ansong Charles C Anderson Lindsey N LN Smith Jordan N JN Corley Richard A RA Wright Aaron T AT

Drug metabolism and disposition: the biological fate of chemicals 20160415 7

Cytochrome P450s are oxidative metabolic enzymes that play critical roles in the biotransformation of endogenous compounds and xenobiotics. The expression and activity of P450 enzymes varies considerably throughout human development; the deficit in our understanding of these dynamics limits our ability to predict environmental and pharmaceutical exposure effects. In an effort to develop a more comprehensive understanding of the ontogeny of P450 enzymes, we employed a multi-omic characterization ...[more]

PMID: 27084891

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Project description:The Göttingen Minipig is gaining ground as nonrodent species in safety testing of drugs for pediatric indications. Due to developmental changes in pharmacokinetics (PK) and pharmacodynamics (PD), physiologically-based pharmacokinetic (PBPK) models are built to better predict drug exposure in children and to aid species selection for nonclinical safety studies. These PBPK models require high quality physiological and PK/PD data such as protein abundance of drug metabolizing enzymes. These data are available for man and rat, but scarce for the Göttingen Minipig. The aim of this study was to assess hepatic cytochrome P450 (CYP) protein abundance in the developing Göttingen Minipig by using mass spectrometry. In addition, sex-related differences in CYP protein abundance and correlation of CYP enzyme activity with CYP protein abundance were assessed. The following age groups were included: gestational day (GD) 84 - 86 (n = 8), GD 108 (n = 6), postnatal day (PND) 1 (n = 8), PND 3 (n = 8), PND 7 (n = 8), PND 28 (n = 8) and adult (n = 8). Liver microsomes were extracted and protein abundance was compared to that in adult animals. Next, the CYP protein abundance was correlated to CYP enzyme activity in the same biological samples. In general, CYP protein abundance gradually increased during development. However, we observed a stable protein expression over time for CYP4A24 and CYP20A1 and for CYP51A1, a high protein expression during the fetal stages was followed by a decrease during the first month of life and an increase towards adulthood. Sex-related differences were observed for CYP4V2_2a and CYP20A1 at PND 1 with highest expression in females for both isoforms. In the adult samples, sex-related differences were detected for CYP1A1, CYP1A2, CYP2A19, CYP2E1_2, CYP3A22, CYP4V2_2a and CYP4V2_2b with higher values in female compared to male Göttingen Minipigs. The correlation analysis between CYP protein abundance and CYP enzyme activity showed that CYP3A22 protein abundance correlated clearly with the metabolism of midazolam at PND 7. These data are remarkably comparable to human data and provide a valuable step forward in the construction of a neonatal and juvenile Göttingen Minipig PBPK model.