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  2. GSTA2 - Wikipedia

    en.wikipedia.org/wiki/GSTA2

    The alpha class genes, located in a cluster mapped to chromosome 6, are the most abundantly expressed glutathione S-transferases in liver. In addition to metabolizing bilirubin and certain anti-cancer drugs in the liver, the alpha class of these enzymes exhibit glutathione peroxidase activity thereby protecting the cells from reactive oxygen ...

  3. Lipotropic - Wikipedia

    en.wikipedia.org/wiki/Lipotropic

    Choline functions as a methyl donor and it is required for proper liver function. Though choline can be synthesized from methionine or serine, mammals don't produce a sufficient amount on their own. Liver, eggs, wheat bran, meat, and broccoli are dietary sources of choline. Inositol exerts lipotropic effects as well.

  4. Glutathione - Wikipedia

    en.wikipedia.org/wiki/Glutathione

    The concentration of glutathione in the cytoplasm is significantly higher (ranging from 0.5-10 mM) compared to extracellular fluids (2-20 μM), reaching levels up to 1000 times greater. [7] [8] In healthy cells and tissue, more than 90% of the total glutathione pool is in the reduced form (GSH), with the remainder in the disulfide form (GSSG).

  5. What You Need to Know About Glutathione, a Powerful ... - AOL

    www.aol.com/know-glutathione-powerful...

    Here, find the health benefits of glutathione, an antioxidant that helps make proteins in the body. Plus, glutathione side effects and dosages. ... Plus, glutathione side effects and dosages. Skip ...

  6. Glutathione synthetase - Wikipedia

    en.wikipedia.org/wiki/Glutathione_synthetase

    Glutathione synthetase (GSS) (EC 6.3.2.3) is the second enzyme in the glutathione (GSH) biosynthesis pathway. It catalyses the condensation of gamma-glutamylcysteine and glycine, to form glutathione. [2] Glutathione synthetase is also a potent antioxidant. It is found in many species including bacteria, yeast, mammals, and plants. [3]

  7. Paracetamol poisoning - Wikipedia

    en.wikipedia.org/wiki/Paracetamol_poisoning

    NAPQI therefore remains in its toxic form in the liver and reacts with cellular membrane molecules, resulting in widespread hepatocyte damage and death, leading to acute liver necrosis. [35] [40] In animal studies, the liver's stores of glutathione must be depleted to less than 70% of normal levels before liver toxicity occurs. [36]