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corticosteroid

 
Medical Encyclopedia: Corticosteroids

Definition

Corticosteriods are a group of natural and synthetic analogues of the hormones secreted by the hypothalamic-anterior pituitary-adrenocortical (HPA) axis, more commonly referred to as the pituitary gland. These include glucocorticoids, which are anti-inflammatory agents with a large number of other functions; mineralocorticoids, which control salt and water balance primarily through action on the kidneys; and corticotropins, which control secretion of hormones by the pituitary gland.

— Samuel Uretsky, PharmD



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Dictionary: cor·ti·co·ste·roid   (kôr'tĭ-kō-stîr'oid',-stĕr'-) pronunciation
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n.
Any of the steroid hormones produced by the adrenal cortex or their synthetic equivalents, such as cortisol and aldosterone.


Oncology Encyclopedia: Corticosteroids
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Key Terms: Autoimmune disease.

Definition

Corticosteroids are a group of related drugs used in cancer treatment to reduce the growth of tumors, stimulate the appetite, and treat skin rashes, nausea and vomiting, allergic reactions, inflammation, accumulation of fluid in the brain, and autoimmune disease.

Purpose

Corticosteroids have broad use in cancer treatment. Some are used to treat adult leukemias, adult lymphomas, acute childhood leukemia, multiple myeloma, and advanced prostate cancer. Others are used in creams to treat skin rashes from radiation therapy. Corticosteroids are also used to reduce swelling, especially in the brain and spinal column, reduce nausea and vomiting, and improve appetite.

Description

Corticosteroids occur naturally in the body. They are produced by the cortex of the adrenal glands, a small, pea-sized pair of glands that are located in the lower back, just above the kidney. Some corticosteroids regulate fluid balance in the body. Others influence fat and sugar (glucose) usage. Corticosteroids are chemically related to the sex hormones estrogen and testosterone.

Many different corticosteroids are produced artificially to use as drugs. They are administered as creams, tablets, liquids, or intravenously (or injection directly into a vein). Many people are already familiar with hydrocortisone, a corticosteroid found in low doses in over-the-counter creams.

The most common corticosteroids used in cancer treatment are:

  • dexamethasone (Decadron)
  • hydrocortisone
  • methylprednisolone (Medrol)
  • prednisone
  • cortisone
  • betamethasone
  • prednisolone There are many trade names for drugs containing these corticosteroids.

Recommended Dosage

Corticosteroids come in tablets, liquids, intravenous solutions, and creams. Because of their wide variety of uses and forms, there is no standard recommended dose. Dosage is individualized, and depends on the type of cancer, the patient's body weight and general health, the goal of the treatment, the other drugs being given, and the way a patient's cancer responds to the drug. Corticosteroids should be stored away from heat.

Precautions

People taking corticosteroids may want to go on a low-salt, high-potassium diet in order to reduce water retention. They may also want to watch their calorie intake unless corticosteroids are being given to improve appetite. Patients taking large doses of corticosteroids are more susceptible to infection and should try to avoid contact with crowds or any individuals that may have an infection. Patients should seek immediate medical advice if they are exposed to chicken pox or measles.

Side Effects

Corticosteroids have several side effects. Not every side effect is seen in every patient. The most serious, although rare, side effect is an allergic reaction to corticosteroids when given intravenously (IV). Other side effects can include:

  • salt and water retention
  • excessive potassium loss
  • high blood pressure
  • other fluid and electrolyte imbalances
  • loss of muscle tissue
  • loss of bone strength (osteoporosis)
  • easily fractured bones
  • heartburn and ulcers
  • thin, fragile skin
  • slow wound healing
  • skin rashes
  • masking of infection
  • convulsions
  • headache
  • dizziness
  • reproductive irregularities
  • strong mood changes
  • changes in the functioning of the adrenal gland
  • increased pressure in the eye
  • glaucoma, cataracts, and blindness (rare)
  • nausea
  • fatigue
  • increased appetite
  • weight gain
  • increased urination

Interactions

Many drugs interact with nonprescription (over-thecounter) drugs and herbal remedies. Patients should always tell their health care providers about these remedies, as well as any prescription drugs they are taking. Patients should also notify their physician if they are on a special diet.

Corticosteroids can also interact with anticoagulants (blood thinners such as Coumadin), cyclosporine, phenobarbitol, and antidepressants.

—Tish Davidson, A.M.

Food and Fitness: corticosteroids
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Hormones released from the outer part of the adrenal gland (adrenal cortex). Drugs similar to corticosteroids are produced synthetically. There are two main groups of corticosteroids: glucocorticoids are essential for carbohydrate, fat, and protein metabolism; and mineralocorticoids which are involved in salt and water balance. The glucocorticoids are also powerful anti-inflammatories and painkillers, normally involved in reactions to stress. Synthetic glucocorticoids are used to treat sports injuries. They are administered in and around damaged muscles, tendons, or joints. They are not given directly into damaged structures because of the risk of weakening them and hindering the healing process. Except under certain conditions, use of artificial corticosteroids is banned by the International Olympic Committee and many other sports federations.

Veterinary Dictionary: corticosteroid
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Any of the hormones produced by the adrenal cortex; also, their synthetic equivalents. Called also adrenocortical hormone and adrenocorticosteroid. All the hormones are steroids having similar chemical structures, but quite different physiological effects. Generally they are divided into glucocorticoids (cortisol, or hydrocortisone, and corticosterone), mineralocorticoids (aldosterone and desoxycorticosterone, and also corticosterone) and androgens.

  • c.-binding globulin — α-globulin that binds unconjugated corticosteroid and transports it in the plasma; called also transcortin.
Wikipedia: Corticosteroid
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Corticosteroids are a class of steroid hormones that are produced in the adrenal cortex. Corticosteroids are involved in a wide range of physiologic systems such as stress response, immune response and regulation of inflammation, carbohydrate metabolism, protein catabolism, blood electrolyte levels, and behavior.

Some common natural hormones are corticosterone (C21H30O4), cortisone (C21H28O5, 17-hydroxy-11-dehydrocorticosterone) and aldosterone.

Contents

Biosynthesis

Corticosteroid biosynthetic pathway in rat

The corticosteroids are synthesized from cholesterol within the adrenal cortex. Most steroidogenic reactions are catalysed by enzymes of the cytochrome P450 family. They are located within the mitochondria and require adrenodoxin as a cofactor (except 21-hydroxylase and 17α-hydroxylase).

Aldosterone and corticosterone share the first part of their biosynthetic pathway. The last part is either mediated by the aldosterone synthase (for aldosterone) or by the 11β-hydroxylase (for corticosterone). These enzymes are nearly identical (they share 11β-hydroxylation and 18-hydroxylation functions). But aldosterone synthase is also able to perform an 18-oxidation. Moreover, aldosterone synthase is found within the zona glomerulosa at the outer edge of the adrenal cortex; 11β-hydroxylase is found in the zona fasciculata and reticularis.

Classes of corticosteroids

Corticosteroids are generally grouped into four classes, based on chemical structure. Allergic reactions to one member of a class typically indicate an intolerance of all members of the class. This is known as the "Coopman classification",[1] after S. Coopman, who defined this classification in 1989.[2]

The highlighted steroids are often used in the screening of allergies to topical steroids.[3]

Group A

(short to medium acting glucocorticoids) Hydrocortisone, Hydrocortisone acetate, Cortisone acetate, Tixocortol pivalate, Prednisolone, Methylprednisolone, and Prednisone.

Group B

Triamcinolone acetonide, Triamcinolone alcohol, Mometasone, Amcinonide, Budesonide, Desonide, Fluocinonide, Fluocinolone acetonide, and Halcinonide.

Group C

Betamethasone, Betamethasone sodium phosphate, Dexamethasone, Dexamethasone sodium phosphate, and Fluocortolone.

Group D

Hydrocortisone-17-butyrate, Hydrocortisone-17-valerate, Aclometasone dipropionate, Betamethasone valerate, Betamethasone dipropionate, Prednicarbate, Clobetasone-17-butyrate, Clobetasol-17-propionate, Fluocortolone caproate, Fluocortolone pivalate, and Fluprednidene acetate.

Types of Corticosteroids

1. Topical steroid for use topically on the skin, eye, and mucous membranes.

2. Inhaled steroids for use to treat the nasal mucosa, sinuses, bronchii, and lungs.[4]

3. Oral forms - such as prednisone and prednisolone.[5]

4. Systemic forms - available in injectibles for use intravenously and parenteral routes.[6]

Uses

Synthetic drugs with corticosteroid-like effect are used in a variety of conditions, ranging from brain tumors to skin diseases. Dexamethasone and its derivatives are almost pure glucocorticoids, while prednisone and its derivatives have some mineralocorticoid action in addition to the glucocorticoid effect. Fludrocortisone (Florinef) is a synthetic mineralocorticoid. Hydrocortisone (cortisol) is available for replacement therapy, e.g. in adrenal insufficiency and congenital adrenal hyperplasia.

Synthetic glucocorticoids are used in the treatment of joint pain or inflammation (arthritis), temporal arteritis, dermatitis, allergic reactions, asthma, hepatitis, systemic lupus erythematosus, inflammatory bowel disease (ulcerative colitis and Crohn's disease), sarcoidosis and for glucocorticoid replacement in Addison's disease or other forms of adrenal insufficiency. Topical formulations are also available for the skin, eyes, lungs, nose, and bowels. Corticosteroids are also used supportively to prevent nausea, often in combination with 5-HT3 antagonists (e.g. ondansetron).

Typical undesired effects of glucocorticoids present quite uniformly as drug-induced Cushing's syndrome. Typical mineralocorticoid side effects are hypertension (abnormally high blood pressure), hypokalemia (low potassium levels in the blood), hypernatremia (high sodium levels in the blood) without causing peripheral edema, metabolic alkalosis and connective tissue weakness.[7] There may also be impaired wound healing or ulcer formation because of the immunosuppressive effects.

Clinical and experimental evidence indicates that corticosteroids can cause permanent eye damage by inducing central serous retinopathy (CSR, also known as central serous chorioretinopathy, CSC). A variety of steroid medications, from anti-allergy nasal sprays (Nasonex, Flonase) to topical skin creams, to eye drops (Tobradex), to Prednisone have been implicated in the development of CSR.

History

Tadeusz Reichstein together with Edward Calvin Kendall and Philip Showalter Hench were awarded the Nobel Prize for Physiology and Medicine in 1950 for their work on hormones of the adrenal cortex which culminated in the isolation of cortisone.

Corticosteroids have been used as drug treatment for some time. Lewis Sarett of Merck & Co. was the first to synthesize cortisone, using a complicated 36-step process that started with deoxycholic acid, which was extracted from ox bile. The low efficiency of converting deoxycholic acid into cortisone led to a cost of US $200 per gram. Russell Marker, at Syntex, discovered a much cheaper and more convenient starting material, diosgenin from wild Mexican yams. His conversion of diosgenin into progesterone by a four-step process now known as Marker degradation was an important step in mass production of all steroidal hormones, including cortisone and chemicals used in hormonal contraception. In 1952, D.H. Peterson and H.C. Murray of Upjohn Co. developed a process that used Rhizopus mold to oxidize progesterone into a compound that was readily converted to cortisone. The ability to cheaply synthesize large quantities of cortisone from the diosgenin in yams resulted in a rapid drop in price to US $6 per gram, falling to $0.46 per gram by 1980. Percy Julian's research also aided progress in the field. The exact nature of cortisone's anti-inflammatory nature remained a mystery for years after however, until the leukocyte adhesion cascade and the role of phospholipase A2 in the production of prostaglandins and leukotrienes was fully understood in the early 1980s.

Side effects

Long-term corticosteroids use has several severe side effects as for example: hyperglycemia, insulin resistance, diabetes mellitus, osteoporosis, anxiety, depression, gastritis, colitis, hypertension, ictus, erectile dysfunction, hypogonadism, hypothyroidism, amenorrhoea, retinopathy and as well as making people short tempered.

Safety

Corticosteroids were voted Allergen of the Year in 2005 by the American Contact Dermatitis Society.

See also

References

  1. ^ Rietschel, Robert L. (2007). Fisher's Contact Dermatitis, 6/e. Hamilton, Ont: BC Decker Inc. pp. 256. ISBN 1-55009-378-9. 
  2. ^ Coopman S, Degreef H, Dooms-Goossens A (July 1989). "Identification of cross-reaction patterns in allergic contact dermatitis from topical corticosteroids". Br. J. Dermatol. 121 (1): 27–34. doi:10.1111/j.1365-2133.1989.tb01396.x. PMID 2757954. 
  3. ^ Wolverton, SE. Comprehensive Dermatologic Drug Therapy. WB Saunders, 2001. p. 562
  4. ^ http://www.webmd.com/asthma/guide/asthma_control_with_anti-inflammatory-drugs
  5. ^ http://dermnetnz.org/treatments/systemic-steroids.html
  6. ^ http://dermnetnz.org/treatments/systemic-steroids.html
  7. ^ Werner R (2005). A massage therapist's guide to Pathology. 3rd edition. Lippincott Williams & Wilkins, Pennsylvania, USA.

 
 

 

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