Glucocorticoids are potent anti-inflammatories, regardless of the inflammation's cause; their primary anti-inflammatory mechanism is lipocortin-1 (annexin-1) synthesis. Lipocortin-1 both suppresses phospholipase A2 , thereby blocking eicosanoid production, and inhibits various leukocyte inflammatory events ( epithelial adhesion , emigration , chemotaxis , phagocytosis , respiratory burst , etc.). In other words, glucocorticoids not only suppress immune response, but also inhibit the two main products of inflammation, prostaglandins and leukotrienes . They inhibit prostaglandin synthesis at the level of phospholipase A2 as well as at the level of cyclooxygenase /PGE isomerase (COX-1 and COX-2),  the latter effect being much like that of NSAIDs , potentiating the anti-inflammatory effect.
Stages of Liver Damage
A group of enzymes, that are located in the endoplasmic reticulum, known as cytochrome P-450, is the most important family of metabolizing enzymes found in the liver. Cytochrome P-450 is the terminal oxidase component of an electron transport chain. It’s not a single enzyme, but consists of a family of closely related 50 isoforms. Six of them metabolize 90% of drugs. There is a great diversity of individual P-450 gene products and this heterogeneity allows the liver to perform oxidation on a vast array of chemicals, which includes almost all drugs.
Information from the National Library of Medicine
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Ages Eligible for Study: 18 Years to 99 Years (Adult, Senior) Sexes Eligible for Study: All Accepts Healthy Volunteers: No Criteria