hidden pixel

Methysergide Information

Methysergide (UML-491) is a prescription drug used for prophylaxis of migraine headaches and is sold under the brand names Sansert and Deseril in 2 mg dosages.

Contents

Pharmacology

Methysergide interacts with serotonin (5-HT) receptors. Its therapeutic effect in migraine prophylaxis has been associated with its antagonism at the 5-HT2B receptor.[1] Furthermore, it is an antagonist at the 5-HT2C receptor and at the 5-HT1A receptor.[2][3] It is known to have partial agonist effects on some of the other 5-HT receptors as well.[4] Methysergide is metabolised into methylergometrine in humans, which is responsible for its psychedelic effects[5] .

Uses

Methysergide is used to treat headaches such as migraine and other recurrent throbbing headaches.[6] Methysergide is one of the most effective[7] medications for the prevention of migraine, but not for the treatment of an acute attack.

It is also used in carcinoid syndrome to treat severe diarrhea.[6]

Side effects

It has a known side effect, retroperitoneal fibrosis,[8] which is severe, although uncommon. Other severe but uncommon side effects include pleural fibrosis, and subendocardial fibrosis.

In addition, there is an increased risk of left-sided cardiac valve dysfunction.[7][9]

History

Methysergide was approved by the U.S. Food and Drug Administration (FDA) in 1962.

Novartis withdrew it from the U.S. market after taking over Sandoz, but currently lists it as a product.

Related compounds

Its molecular structure is closely related to that of LSD.

Like LSD, methysergide also produces psychedelic and hallucinogenic effects.[10]

About 4 mg is equal to 25mcg of LSD.[10]

Sandoz does not currently list this on their product guide.

See also

Triptan

References

  1. ^ Schmuck K, Ullmer C, Kalkman HO, Probst A, Lubbert H (May 1996). "Activation of meningeal 5-HT2B receptors: an early step in the generation of migraine headache?". Eur. J. Neurosci. 8 (5): 959–67. doi:10.1111/j.1460-9568.1996.tb01583.x. PMID 8743744.
  2. ^ Rang, H. P. (2003). Pharmacology. Edinburgh: Churchill Livingstone. ISBN 0-443-07145-4. Page 187
  3. ^ Saxena PR, Lawang A (October 1985). "A comparison of cardiovascular and smooth muscle effects of 5-hydroxytryptamine and 5-carboxamidotryptamine, a selective agonist of 5-HT1 receptors". Arch Int Pharmacodyn Ther 277 (2): 235–52. PMID 2933009.
  4. ^ Colpaert FC, Niemegeers CJ, Janssen PA (October 1979). "In vivo evidence of partial agonist activity exerted by purported 5-hydroxytryptamine antagonists". Eur. J. Pharmacol. 58 (4): 505–9. doi:10.1016/0014-2999(79)90326-1. PMID 510385.
  5. ^ Bredberg, U.; Eyjolfsdottir, G. S., Paalzow, L., Tfelt-Hansen, P., Tfelt-Hansen, V. (1 January 1986). "Pharmacokinetics of methysergide and its metabolite methylergometrine in man". European Journal of Clinical Pharmacology 30 (1): 75–77. doi:10.1007/BF00614199. PMID 3709634.
  6. ^ a b http://www.patient.co.uk/medicine/Methysergide.htm
  7. ^ a b Joseph T, Tam SK, Kamat BR, Mangion JR (2003). "Successful repair of aortic and mitral incompetence induced by methylsergide maleate: confirmation by intraoperative transesophageal echocardiography". Echocardiography 20 (3): 283–7. doi:10.1046/j.1540-8175.2003.03027.x. PMID 12848667.
  8. ^ emedicine.com (2002)
  9. ^ 1997 Mayo Clinic study linking heart disease to Fen Phen Valvular heart disease associated with fenfluramine-phentermine
  10. ^ a b Abramson HA, Rolo A (September 1965). "Lysergic acid diethylamide (LSD-25). 38. Comparison with action of methysergide and psilocybin on test subjects". J Asthma Res 3 (1): 81–96. doi:10.3109/02770906509106904. PMID 5318626.

External links

Antimigraine preparations (N02C)
Analgesic/abortive
Serotonin modulators
Ergot alkaloids DihydroergotamineErgotamineMethysergideLisuride
5-HT1 agonists Triptans (Almotriptan, Avitriptan, Eletriptan, Frovatriptan, Naratriptan, Rizatriptan, Sumatriptan, Zolmitriptan) Alniditan
Other Dotarizine
Other Paracetamol#Amidrine
Prevention of migraines
Beta blocker Propranolol#Timolol
CCB verapamil
corticosteroid flumedroxone
monosaccharide topiramate
adrenergic agonist Clonidine
tricyclic antidepressant amitriptylinenortriptylineimipramine
anticonvulsant valproatecarbamazepineoxcarbazepine
Ungrouped PizotifenIprazochromeDimetotiazineOxetoroneLomerizineTelcagepant

: CNS

(////////////)//

(/////)//, /,

, drug(////////)

Serotonergics
5-HT1 receptor ligands
5-HT1A
5-HT1B
5-HT1D
5-HT1E
5-HT1F
5-HT2 receptor ligands
5-HT2A
5-HT2B
5-HT2C
5-HT3
5-HT4
5-HT5A
5-HT6
5-HT7
Reuptake inhibitors
SERT
VMAT
Releasing agents
Enzyme inhibitors
Anabolism
TPH
AAAD
Catabolism
MAO
Others
Precursors
Cofactors
Others
Ergolines
Lysergic acid derivatives 2-Bromo-LSD (BOL-148)BromocriptineCabergolineDihydroergocornineDihydroergocristineDihydroergocryptine • Dihydroergometrine (Dihydroergonovine, Dihydroergobasine) • DihydroergotamineErgine (LSA; LA-111; Lysergamide) • ErgocornineErgocristineErgocryptineErgoloid (Dihydroergotoxine) • Ergometrine (Ergonovine, Ergobasine) • Ergometrinine • ErgotamineErgotoxineErgovalineLisurideLSDLSHLysergic Acid • Lysergic acid cyclobutylamide • Lysergic acid cyclopentylamide • Lysergic Acid Methyl EsterLysergolMesulergineMetergolineMethergine (Methylergometrine, Methylergonovine, Methylergobasine) • MethysergidePergolideSyntometrine
Psychedelic lysergamides AL-LADALD-52BU-LADCYP-LADDALDAM-57ErgonovineETH-LAD • IP-LAD • LAE-32LSDLPD-824LSM-775LSHLSD-PipLysergic Acid 2-ButylamideLysergic Acid 2,4-DimethylazetidideLysergic Acid 3-PentylamideMethylergonovineMethylisopropyllysergamideMLD-41PARGY-LADPRO-LAD
Other ergolines Ergoline
Natural sources Achnatherum robustum (Sleepy Grass) Argyreia nervosa (Hawaiian Baby Woodrose) • Claviceps spp. (Ergot) • Ipomoea spp. (Morning Glory, Tlitliltzin, Badoh Negro) • Rivea corymbosa (Coaxihuitl, Ololiúqui)

Categories:

 

The above information uses material from Wikipedia and is licensed under the GNU Free Documentation License.
Some facts may not have been fully verified for accuracy. [Disclaimers]
This page was last archived by our server on Sun Mar 4 14:52:46 2012.
Displaying this page or its contents does not use any Wikimedia Foundation's resources.
The owners of this site proudly support the Wikimedia Foundation.