Dihydroergocriptine in Parkinson's disease: clinical efficacy and comparison with other dopamine agonists

Acta Neurol Scand. 2003 May;107(5):349-55. doi: 10.1034/j.1600-0404.2003.02049.x.

Abstract

The present paper reviews clinical studies on the use of dihydroergocriptine (DHEC), an ergot derivative with dopamine agonist activity, for the treatment of Parkinson's disease. This compound is a hydrogenated ergot derivative structurally quite similar to bromocriptine, from which it differs because of the hydrogenation in C9 C10 and the lack of bromine in C2. DHEC has a potent D2-like receptor agonist and a partial D1-like receptor agonist activity; because of this biochemical profile, it has been suggested that DHEC may produce fewer side-effects and have clinical efficacy equal to that of a classical dopamine agonist. Several open-label and double-blind studies indicate that DHEC is an efficacious remedy for parkinsonian signs and symptoms. Further studies are necessary to compare DHEC to new dopamine agonists (pergolide, cabergoline, ropinirole, and pramipexole) which have been more recently marketed.

Publication types

  • Review

MeSH terms

  • Clinical Trials as Topic
  • Dihydroergocryptine / therapeutic use*
  • Dopamine Agonists / therapeutic use*
  • Humans
  • Parkinson Disease / drug therapy*
  • Treatment Outcome

Substances

  • Dopamine Agonists
  • Dihydroergocryptine