Summary of project PR002191

This data is available at the NIH Common Fund's National Metabolomics Data Repository (NMDR) website, the Metabolomics Workbench, https://www.metabolomicsworkbench.org, where it has been assigned Project ID PR002191. The data can be accessed directly via it's Project DOI: 10.21228/M8DN9K This work is supported by NIH grant, U2C- DK119886.

See: https://www.metabolomicsworkbench.org/about/howtocite.php

Project ID: PR002191
Project DOI:doi: 10.21228/M8DN9K
Project Title:N-methyl-arginine is taken up into the liver, brain, and kidney of mice.
Project Type:Manuscript
Project Summary:N-methyl-arginine was identified as a transported substrate through multiple cationic amino acid transporters, which facilitate the uptake of lysine, arginine, and other structurally related amino acids. In cell culture, N-methyl-arginine inhibits the uptake and metabolism of lysine. In this project, we aimed to determine if N-methyl-arginine administered to mice at 80 mg/kg was sufficient to inhibit tissue lysine uptake and metabolism. Following a single injection, N-methyl-arginine significantly accumulated in mouse plasma and tissues but failed to significantly inhibit the level of lysine metabolites (e.g., saccharopine). These results are in-line with in vitro results suggesting that N-methyl-arginine is a relatively low affinity transport inhibitor.
Institute:University of British Columbia
Department:Biochemistry & Molecular Biology
Laboratory:Parker laboratory
Last Name:Parker
First Name:Seth
Address:950 W 28th Ave, Vancouver, British Columbia, V6H 0B3, Canada
Email:seth.parker@bcchr.ca
Phone:6048753121

Summary of all studies in project PR002191

Study IDStudy TitleSpeciesInstituteAnalysis
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(* : Contains raw data)
ST003557 Metabolomics analysis of kidney, brain, liver, and plasma from Aldh7a1-/- mice administered PBS or N-methyl-arginine (80 mg/kg) via a single intraperitoneal injection. Mus musculus University of British Columbia MS 2024-11-15 1 39 Uploaded data (8G)*
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