Prednisone: Difference between revisions

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{{Image|Prednisone structure.jpg|right|200px|Prednisone, a synthetic steroid.}}  
{{Image|Prednisone structure.jpg|right|200px|Prednisone, a synthetic steroid.}}  


'''Prednisone''', also called dehydrocortisone, prednisona, or prednisonum (IUPAC name (8S,9S,10R,13S,14S,17R)-17-hydroxy-17-(2-hydroxyacetyl)-10,13-dimethyl-6,7,8,9,12,14,15,16-octahydrocyclopenta[a]phenanthrene-3,11-dione) is a synthetic anti-inflammatory [[glucocorticoid]] [[steroid]] designed as a mimic of the naturally occurring steroid [[cortisone]].  It is used to treat many inflammatory conditions.  It is a prodrug that only becomes active after conversion to [[prednisolone]], a glucocorticoid agonist, in the liver.  Prednisolone binds to cytoplasmic receptors to control biosynthesis of [[prostaglandin]]s and [[leukotriene]]s.
'''Prednisone''', also called dehydrocortisone, prednisona, or prednisonum is a synthetic anti-inflammatory [[glucocorticoid]] [[steroid]] designed as a mimic of the naturally occurring steroid [[cortisone]].  It is used to treat many inflammatory conditions.  It is a prodrug that only becomes active after conversion to [[prednisolone]], a glucocorticoid agonist, in the liver.  Prednisolone binds to cytoplasmic receptors to control biosynthesis of prostaglandins and leukotrienes. IUPAC name = (8S,9S,10R,13S,14S,17R)-17-hydroxy-17-(2-hydroxyacetyl)-10,13-dimethyl-6,7,8,9,12,14,15,16-octahydrocyclopenta[a]phenanthrene-3,11-dione.


== indications ==
== Indications ==
Prednisone is use to treat allergies, [[carditis]], systemic [[dermatomyositis]], systemic [[lupus erythematosus]], [[dermatitis]], [[Stevens-Johnson syndrome]], [[psoriasis]], acute [[adrenocortical deficiency]], [[Addison's disease]], congenital [[adrenal hyperplasia]], [[hypercalcemia]] associated with neoplasms, [[thyroiditis]], [[ulceratice colitis]], [[Crohn's disease]], [[anemia]]s, [[erythroblastopenia]],[[thrombocytopenia]], [[bursitis]], epicondylitis, tenosynovitis, [[lymphocytic leukemia]], [[Hodgkin's lymphoma|Hodgkin's]] or [[non-Hodgkin's lymphomas]], [[Waldenstrom's macroglobulinemia]], primary brain tumors, [[nephrotic syndrome]], [[tuberculous meningitis]], [[multiple sclerosis]], [[myasthenia gravis]],  [[cerebral edema]], [[chorioretinitis]], [[diffuse posterior choroiditis]], [[allergic conjunctivitis]], [[Herpes zoster]] ophthalmicus, [[iridocyclitis]], [[iritis]], [[keratitis]], [[optoc neuritis]], [[sympathetic ophthalmia]], [[corneal marginal allergic ulcers]], symptomatic [[sarcoidosis]], [[Loeffler's syndrome]],  [[berylliosis]], and[[pulmonary tuberculosis]].  This is not a complete list of conditions for which prednisone is used.
This is a prescription drug only available by the order of a licensed physician, and its use must be carefully supervised by a physician. Prednisone is use to treat allergies, carditis, systemic [[dermatomyositis]], systemic lupus erythematosus, dermatitis, Stevens-Johnson syndrome, [[psoriasis]], acute [[adrenocortical deficiency]], [[Addison's disease]], congenital [[adrenal hyperplasia]], [[hypercalcemia]] associated with neoplasms, [[thyroiditis]], [[ulceratice colitis]], [[Crohn's disease]], [[anemia]]s, [[erythroblastopenia]],[[thrombocytopenia]], [[bursitis]], epicondylitis, tenosynovitis, lymphocytic leukemia, [[Hodgkin's lymphoma|Hodgkin's]] or [[non-Hodgkin's lymphomas]], [[Waldenstrom's macroglobulinemia]], primary brain tumors, [[nephrotic syndrome]], [[tuberculous meningitis]], [[multiple sclerosis]], [[myasthenia gravis]],  [[cerebral edema]], [[chorioretinitis]], [[diffuse posterior choroiditis]], [[allergic conjunctivitis]], [[Herpes zoster]] ophthalmicus, [[iridocyclitis]], [[iritis]], [[keratitis]], [[optoc neuritis]], [[sympathetic ophthalmia]], [[corneal marginal allergic ulcers]], symptomatic [[sarcoidosis]], [[Loeffler's syndrome]],  [[berylliosis]], and pulmonary tuberculosis.  This is not a complete list of conditions for which prednisone is used.


== comparison to cortisone and prednisolone ==
== Side effects==
Short-term use in humans is generally safe, even at high doses; for instance, a round of five days of treatment at 50 mg a day to reduce swelling after an acute injury. However, long-term use such as that for three months at a time can produce many side effects, some serious. After long-term use, it can be dangerous to suddenly stop taking the drug, so the dose must be tapered down gradually. Life-threatening adrenal insufficiency can occur if the drug is suddenly stopped after long-term use, e.g., for four months at 25 mg a day.
 
== Comparison to cortisone and prednisolone ==
[[Image:Cortisone_Prednisone_stickfig_DEVolk.jpg|left|thumb|350px|{{#ifexist:Template:Cortisone_Prednisone_stickfig_DEVolk.jpg/credit|{{Prednisone structure.jpg/credit}}<br/>|}}Prednisone is a synthetic mimic of cortisone.]]
[[Image:Cortisone_Prednisone_stickfig_DEVolk.jpg|left|thumb|350px|{{#ifexist:Template:Cortisone_Prednisone_stickfig_DEVolk.jpg/credit|{{Prednisone structure.jpg/credit}}<br/>|}}Prednisone is a synthetic mimic of cortisone.]]
Prednisone's structure is based on that of the naturally-occurring [[corticosteroid]] [[cortisone]].  The only difference between them is the presence of a carbon-carbon double bond in the A ring of prednisone that is not present in cortisone (note arrows in the figure).  The active form of the drug, prednisolone, as the name implies ("ol"), has a hydroxyl group on ring C in place of the carbonyl group present in prednisone.
Prednisone's structure is based on that of the naturally-occurring [[corticosteroid]] [[cortisone]].  The only difference between them is the presence of a carbon-carbon double bond in the A ring of prednisone that is not present in cortisone (note arrows in the figure).  The active form of the drug, prednisolone, as the name implies ("ol"), has a hydroxyl group on ring C in place of the carbonyl group present in prednisone.

Revision as of 09:07, 28 March 2023

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(CC) Image: David E. Volk
Prednisone, a synthetic steroid.

Prednisone, also called dehydrocortisone, prednisona, or prednisonum is a synthetic anti-inflammatory glucocorticoid steroid designed as a mimic of the naturally occurring steroid cortisone. It is used to treat many inflammatory conditions. It is a prodrug that only becomes active after conversion to prednisolone, a glucocorticoid agonist, in the liver. Prednisolone binds to cytoplasmic receptors to control biosynthesis of prostaglandins and leukotrienes. IUPAC name = (8S,9S,10R,13S,14S,17R)-17-hydroxy-17-(2-hydroxyacetyl)-10,13-dimethyl-6,7,8,9,12,14,15,16-octahydrocyclopenta[a]phenanthrene-3,11-dione.

Indications

This is a prescription drug only available by the order of a licensed physician, and its use must be carefully supervised by a physician. Prednisone is use to treat allergies, carditis, systemic dermatomyositis, systemic lupus erythematosus, dermatitis, Stevens-Johnson syndrome, psoriasis, acute adrenocortical deficiency, Addison's disease, congenital adrenal hyperplasia, hypercalcemia associated with neoplasms, thyroiditis, ulceratice colitis, Crohn's disease, anemias, erythroblastopenia,thrombocytopenia, bursitis, epicondylitis, tenosynovitis, lymphocytic leukemia, Hodgkin's or non-Hodgkin's lymphomas, Waldenstrom's macroglobulinemia, primary brain tumors, nephrotic syndrome, tuberculous meningitis, multiple sclerosis, myasthenia gravis, cerebral edema, chorioretinitis, diffuse posterior choroiditis, allergic conjunctivitis, Herpes zoster ophthalmicus, iridocyclitis, iritis, keratitis, optoc neuritis, sympathetic ophthalmia, corneal marginal allergic ulcers, symptomatic sarcoidosis, Loeffler's syndrome, berylliosis, and pulmonary tuberculosis. This is not a complete list of conditions for which prednisone is used.

Side effects

Short-term use in humans is generally safe, even at high doses; for instance, a round of five days of treatment at 50 mg a day to reduce swelling after an acute injury. However, long-term use such as that for three months at a time can produce many side effects, some serious. After long-term use, it can be dangerous to suddenly stop taking the drug, so the dose must be tapered down gradually. Life-threatening adrenal insufficiency can occur if the drug is suddenly stopped after long-term use, e.g., for four months at 25 mg a day.

Comparison to cortisone and prednisolone

(CC) Image: David E. Volk
Prednisone is a synthetic mimic of cortisone.

Prednisone's structure is based on that of the naturally-occurring corticosteroid cortisone. The only difference between them is the presence of a carbon-carbon double bond in the A ring of prednisone that is not present in cortisone (note arrows in the figure). The active form of the drug, prednisolone, as the name implies ("ol"), has a hydroxyl group on ring C in place of the carbonyl group present in prednisone.

Brand names

External Links

The most up-to-date information about Prednisone and other drugs can be found at the following sites.

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