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  2. Steroidogenic acute regulatory protein - Wikipedia

    en.wikipedia.org/wiki/Steroidogenic_acute...

    StAR has thus far been found in all tissues that can produce steroids, including the adrenal cortex, the gonads, the brain and the nonhuman placenta. [10] One known exception is the human placenta. Substances that suppress StAR activity, like those listed below, can cause endocrine disrupting effects, including altered steroid hormone levels ...

  3. Steroid hormone - Wikipedia

    en.wikipedia.org/wiki/Steroid_hormone

    A variety of synthetic steroids and sterols have also been contrived. Most are steroids, but some nonsteroidal molecules can interact with the steroid receptors because of a similarity of shape. Some synthetic steroids are weaker or stronger than the natural steroids whose receptors they activate. [8] Some examples of synthetic steroid hormones:

  4. 11β-Hydroxysteroid dehydrogenase - Wikipedia

    en.wikipedia.org/wiki/11β-Hydroxysteroid...

    This enzyme is most abundant in the liver but can be found in most tissues in the body. HSD11B- Type 1 amplifies glucocorticoid concentrations in the liver and adipose tissue, glucocorticoid excess induces obesity with other features such as hypertension and diabetes mellitus.

  5. Hepatotoxicity - Wikipedia

    en.wikipedia.org/wiki/Hepatotoxicity

    A group of enzymes located in the endoplasmic reticulum, known as cytochrome P-450, is the most important family of metabolizing enzymes in the liver. Cytochrome P-450 is not a single enzyme, but rather consists of a closely related family of 50 isoforms ; six of them metabolize 90% of drugs.

  6. Metandienone - Wikipedia

    en.wikipedia.org/wiki/Metandienone

    Estrogenic side effects such as gynecomastia and fluid retention can also occur. [1] Case reports of gynecomastia exist. [ 21 ] [ 22 ] As with other 17α-alkylated steroids, methandienone poses a risk of hepatotoxicity and use over extended periods of time can result in liver damage without appropriate precautions.

  7. Steroidogenic enzyme - Wikipedia

    en.wikipedia.org/wiki/Steroidogenic_enzyme

    Steroid numbering. Steroid reductases. 5α-Reductase (1, 2, 3) – androgen and neurosteroid synthesis, progestogen metabolism; 5β-Reductase – androgen and progestogen metabolism, neurosteroid synthesis; Conjugation (and deconjugation) Glucuronosyltransferase – steroid metabolism [6] Glucuronidase (β-glucuronidase) – steroid synthesis [7]

  8. Glucocorticoid - Wikipedia

    en.wikipedia.org/wiki/Glucocorticoid

    In the liver, they quickly metabolize by conjugation with a sulfate or glucuronic acid, and are secreted in the urine. [citation needed] Glucocorticoid potency, duration of effect, and the overlapping mineralocorticoid potency vary. Cortisol is the standard of comparison for glucocorticoid potency.

  9. Prednisolone - Wikipedia

    en.wikipedia.org/wiki/Prednisolone

    Gastrointestinal system effects: swelling of the stomach lining, reversible increase in liver enzymes, and risk of stomach ulcers; Muscular and skeletal abnormalities, such as muscle weakness/muscle loss, osteoporosis (see steroid-induced osteoporosis), long bone fractures, tendon rupture, and back fractures

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