Cortisone

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'''Cortisone''' ({{pronEng|ˈkɔrtɨsoʊn}} or {{IPA|/ˈkɔrtɨzoʊn/}} (ˈkôrtəˌsōn or -zōn)) (17-hydroxy-11-dehydrocorticosterone) is a [[steroid]] [[hormone]]. Chemically, it is a [[corticosteroid]] closely related to [[corticosterone]].
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A naturally occurring glucocorticoid. It has been used in replacement therapy for adrenal insufficiency and as an anti-inflammatory agent. Cortisone itself is inactive. It is converted in the liver to the active metabolite HYDROCORTISONE. (From Martindale, The Extra Pharmacopoeia, 30th ed, p726).
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==History==
 +
Cortisone was first discovered by the American chemist [[Edward Calvin Kendall]] while a researcher at the [[Mayo Clinic]]. He was awarded the 1950 [[Nobel Prize for Physiology or Medicine]] along with [[Philip S. Hench]] and [[Tadeus Reichstein]] for the discovery of [[adrenal cortex]] hormones, their structures, and functions. Cortisone was first produced commercially by [[Merck & Co.]].
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==Production==
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Cortisone is one of several end products of a process called [[steroidogenesis]]. This process starts with the synthesis of [[cholesterol]] which then proceeds through a series of modifications in the [[adrenal gland]] (suprarenal) to become any one of many steroid hormones.  One end product of this pathway is cortisol. For cortisol to be released from the adrenal gland a cascade of signaling occurs. [[Corticotropin releasing hormone]] released from the [[hypothalamus]] stimulates corticotrophs in the [[anterior pituitary]] to release [[ACTH]] which relays the signal to the adrenal cortex. Here, the zona fasiculata and zona reticularis in response to ACTH secrete glucocorticoids, in particular [[cortisol]].  In the peripheral tissues cortisol is converted to cortisone by an [[enzyme]] called [[11-beta-steroid dehydrogenase]]. Cortisol has much greater [[glucocorticoid]] activity than cortisone and thus cortisone can be considered an inactive metabolite of cortisol. However 11-beta-steroid dehydrogenase can catalyze the reverse reaction as well and thus cortisone is also the inactive precursor molecule of the active hormone cortisol. Cortisone is activated through [[hydrogenation]] of the 11-keto-group and is thus sometimes referred to as [[hydrocortisone]].
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<uploadedFileContents>NPH133.SDF</uploadedFileContents>
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</jmol>
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==Description==
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A naturally occurring glucocorticoid. It has been used in replacement  therapy for adrenal insufficiency and as an anti-inflammatory agent.   Cortisone itself is inactive. It is converted in the liver to the   active metabolite HYDROCORTISONE. (From Martindale, The Extra  Pharmacopoeia, 30th ed, p726)
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==General Properties==
+
-
<b>*Molecular Weight</b>
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==Effects and uses==
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Cortisol, a [[glucocorticoid]], and [[adrenaline]] are the main hormones released by the body as a reaction to stress. They elevate blood pressure and prepare the body for a [[fight or flight response]].
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360.44
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Cortisone is sometimes used as a drug to treat a variety of ailments. It can be administered [[intravenous]]ly or [[cutaneous]]ly.
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<b>*Molecular Formula</b>
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One of cortisone's effects on the body, and a potentially harmful side effect when administered clinically, is the suppression of the immune system.  This could be the explanation for the apparent correlation between high [[Stress (medicine)|stress]] and sickness. The suppression of the immune system may be important in the treatment of inflammatory conditions such as severe [[IgE]]-mediated [[allergies]]. 
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Cortisone is less powerful than a similar steroid [[cortisol]]. Cortisol is responsible for 95% of the effects of the [[glucocorticosteroids]] while cortisone is about 4 or 5%. [[Corticosterone]] is even less important.{{Fact|date=January 2008}} Cortisol decreases the uptake of glucose by cells and increases glucose release by the liver. This may cause hyperglycemia in a well-fed state but can maintain blood glucose levels in (stressful) fasting states.
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C<sub>2</sub><sub>1</sub>H<sub>2</sub><sub>8</sub>O<sub>5</sub>
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==References==
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*''Merck Index'', 11th Edition, 2533
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*{{cite journal
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| author=  Woodward R. B., Sondheimer F., Taub D.
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| title= The Total Synthesis of Cortisone
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| journal=Journal of the American Chemical Society
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| year=1951
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| pages=4057–4057
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| volume=73
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| doi=10.1021/ja01152a551 }}
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*{{cite journal
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| author=  Ingle D. J.
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| title= The biologic properties of cortisone: a review
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| journal=Journal of Clinical Endocrinology
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| year=1950
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| pages=1312–1354
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| volume=10 }}
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<b>*IUPAC NAME</b>
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==See also==
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* [[Central serous retinopathy]]
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* [[Corticosterol]]
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(8S,9S,10R,13S,14S,17R)-17-hydroxy-17-(2-hydroxyacetyl)-10,13-dimethyl-1,2,6,7,8,9,12,14,15,16-decahydrocyclopenta[a]phenanthrene-3,11-dione
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==External links==
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*[http://www.chem.yorku.ca/hall_of_fame/essays97/cortisone/cortison.htm Cortisone: The Wonder Drug]
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{{Corticosteroids}}
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<b>*Canonical Smiles</b>
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[[Category:Corticosteroids]]
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CC12CCC(=O)C=C1CCC3C2C(=O)CC4(C3CCC4(C(=O)CO)O)C
 
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<b>*Isomeric Smiles</b>
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KEGG Pathway(C00762,D07749)
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*C21-Steroid hormone metabolism
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*Prostate cancer
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C[C@]12CCC(=O)C=C1CC[C@@H]3[C@@H]2C(=O)C[C@]4([C@H]3CC[C@@]4(C(=O)CO)O)C
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Activity Adrenal cortex hormone, glucocorticoid
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{| border="1;width:100%; height:200px;style=text-align:center"
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|+'''List of PDB file having CORTISONE as Ligands'''
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==PhysioChemical Properties==
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|-
-
 
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! style="background:brown; color:white" |MMDB ID
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<b>*Melting Point</b>
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! style="background:brown; color:white" |PDB ID
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! style="background:brown; color:white" |Reference
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222(EXP)
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|-
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|66962
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<b>*LogP</b>
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|3EB3
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|Gulbis JM, Zhou M, Mann S, MacKinnon RStructure of the cytoplasmic beta subunit-T1 assembly of voltage-dependent K+ channelsScience v289, p.123-127
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1.47(EXP)
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|-
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|}
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<b>*Water Solubility</b>
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{| border="1;width:100%; height:200px;style=text-align:center"
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|+'''Physiochemical Properties'''
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280(EXP) at 25C
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|-
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! style="background:brown; color:white" |Physical Property
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==External Links==
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! style="background:brown; color:white" |Value
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*[http://pubchem.ncbi.nlm.nih.gov/summary/summary.cgi?cid=222786]Pubchem
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! style="background:brown; color:white" |Units
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*[http://www.rcsb.org/pdb/cgi/explore.cgi?pdbId=3EB3]]3EB3,
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! style="background:brown; color:white" |Temp (deg C)
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*[http://www.genome.jp/dbget-bin/www_bget?compound+C00762]]KEGG Compound
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! style="background:brown; color:white" |Source
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*[http://www.genome.jp/dbget-bin/www_bget?drug+D07749]]KEGG Drug
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|-
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*[http://www.hmdb.ca/metabolites/HMDB02802]Human Metabolome DataBase
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|Melting Point
-
 
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|222
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|deg C
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[[Categories:Hormones]]
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| 
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|EXP
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|-
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|log P (octanol-water)
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|1.47
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|(none)  
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|  
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|EXP
 +
|-
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|Water Solubility
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|280
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|mg/L
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|25
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|EXP
 +
|-
 +
|Vapor Pressure
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|5.80E-13
 +
|mm Hg
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|25
 +
|EST
 +
|-
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|Henry's Law Constant
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|6.03E-10
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|atm-m3/mole
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|25
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|EST
 +
|-
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|Atmospheric OH Rate Constant
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|1.10E-10
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|cm3/molecule-sec
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|25
 +
|EST
 +
|-

Revision as of 07:10, 13 February 2009

Cortisone (Template:PronEng or Template:IPA (ˈkôrtəˌsōn or -zōn)) (17-hydroxy-11-dehydrocorticosterone) is a steroid hormone. Chemically, it is a corticosteroid closely related to corticosterone. A naturally occurring glucocorticoid. It has been used in replacement therapy for adrenal insufficiency and as an anti-inflammatory agent. Cortisone itself is inactive. It is converted in the liver to the active metabolite HYDROCORTISONE. (From Martindale, The Extra Pharmacopoeia, 30th ed, p726).

Contents

History

Cortisone was first discovered by the American chemist Edward Calvin Kendall while a researcher at the Mayo Clinic. He was awarded the 1950 Nobel Prize for Physiology or Medicine along with Philip S. Hench and Tadeus Reichstein for the discovery of adrenal cortex hormones, their structures, and functions. Cortisone was first produced commercially by Merck & Co..

Production

Cortisone is one of several end products of a process called steroidogenesis. This process starts with the synthesis of cholesterol which then proceeds through a series of modifications in the adrenal gland (suprarenal) to become any one of many steroid hormones. One end product of this pathway is cortisol. For cortisol to be released from the adrenal gland a cascade of signaling occurs. Corticotropin releasing hormone released from the hypothalamus stimulates corticotrophs in the anterior pituitary to release ACTH which relays the signal to the adrenal cortex. Here, the zona fasiculata and zona reticularis in response to ACTH secrete glucocorticoids, in particular cortisol. In the peripheral tissues cortisol is converted to cortisone by an enzyme called 11-beta-steroid dehydrogenase. Cortisol has much greater glucocorticoid activity than cortisone and thus cortisone can be considered an inactive metabolite of cortisol. However 11-beta-steroid dehydrogenase can catalyze the reverse reaction as well and thus cortisone is also the inactive precursor molecule of the active hormone cortisol. Cortisone is activated through hydrogenation of the 11-keto-group and is thus sometimes referred to as hydrocortisone.

Effects and uses

Cortisol, a glucocorticoid, and adrenaline are the main hormones released by the body as a reaction to stress. They elevate blood pressure and prepare the body for a fight or flight response.

Cortisone is sometimes used as a drug to treat a variety of ailments. It can be administered intravenously or cutaneously.

One of cortisone's effects on the body, and a potentially harmful side effect when administered clinically, is the suppression of the immune system. This could be the explanation for the apparent correlation between high stress and sickness. The suppression of the immune system may be important in the treatment of inflammatory conditions such as severe IgE-mediated allergies.

Cortisone is less powerful than a similar steroid cortisol. Cortisol is responsible for 95% of the effects of the glucocorticosteroids while cortisone is about 4 or 5%. Corticosterone is even less important.Template:Fact Cortisol decreases the uptake of glucose by cells and increases glucose release by the liver. This may cause hyperglycemia in a well-fed state but can maintain blood glucose levels in (stressful) fasting states.

References

  • Merck Index, 11th Edition, 2533
  • Woodward R. B., Sondheimer F., Taub D. (1951). "The Total Synthesis of Cortisone". Journal of the American Chemical Society 73: 4057–4057. doi:10.1021/ja01152a551. 
  • Ingle D. J. (1950). "The biologic properties of cortisone: a review". Journal of Clinical Endocrinology 10: 1312–1354. 

See also

External links

Template:Corticosteroids


KEGG Pathway(C00762,D07749)

  • C21-Steroid hormone metabolism
  • Prostate cancer

Activity Adrenal cortex hormone, glucocorticoid

List of PDB file having CORTISONE as Ligands
MMDB ID PDB ID Reference
66962 3EB3 Gulbis JM, Zhou M, Mann S, MacKinnon RStructure of the cytoplasmic beta subunit-T1 assembly of voltage-dependent K+ channelsScience v289, p.123-127
Physiochemical Properties
Physical Property Value Units Temp (deg C) Source
Melting Point 222 deg C EXP
log P (octanol-water) 1.47 (none) EXP
Water Solubility 280 mg/L 25 EXP
Vapor Pressure 5.80E-13 mm Hg 25 EST
Henry's Law Constant 6.03E-10 atm-m3/mole 25 EST
Atmospheric OH Rate Constant 1.10E-10 cm3/molecule-sec 25 EST
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