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Skeletal muscle mitochondria subjected to in vitro treatment with compounds inducing S-glutathionylation (diamide or disulfiram) produced less ROS as a by-product of aerobic oxidation of either carbohydrates or fatty acid derivatives

Our data provide another possible mechanism for this phenomenon, that enzymatic activity and/or protein-metabolite binding kinetics may account for time-dependent compound signal drift

mGluRs are divided into three groups based on their sequence homology, signal transduction pathways, and pharmacological profiles: Group I (mGluR1 and mGluR5), Group II (mGluR2 and mGluR3), and Group III (mGluR4, mGluR6, mGluR7, and mGluR8)

Nrf2 (Tables I and II) and CD44v9/xCT inhibition (Tables III and IV) can promote cancer initiation or inhibit cancer progression in a context-dependent manner

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Nahimana, A