Characterisation of the anticholinesterase activity of two new tacrine-huperzine A hybrids

Maria Del Mar Alcalá, Nuria María Vivas, Susana Hospital, Pelayo Camps, Diego Muñoz-Torrero, Albert Badia

Research output: Contribution to journalArticleResearchpeer-review

32 Citations (Scopus)

Abstract

The effects of two tacrine-huperzine A hybrids, (±)-huprine Y and (±)-huprine Z, have been evaluated. Bovine and human acetylcholinesterase (AChE) and human butyrylcholinesterase (BChE) inhibition were assayed by Ellman's method. The two huprines were more active than both tacrine and (-)-huperzine A as inhibitors of both human and bovine AChE, and they acted as mixed-type AChE inhibitors. Moreover, (±)-huprine Y exhibited a tight binding character seen in the experiments of reversibility of bovine AChE inhibitory activity. In addition, both compounds were more active toward AChE than toward BChE. Also, the selectivity for the human AChE was greater than for the bovine enzyme. In ex vivo studies performed in mice, both drugs showed a clear inhibitory activity of brain AChE, 20 min after i.p. injection, (±)-huprine Y being more potent than (±)-huprine Z [ID50 1.09 (0.39-2.98) vs. 5.77 (3.29-10.30) μmol/kg]. The time-course study of the inhibitory effect displayed a t1/2 of 1 h for the two compounds. These results show that these drugs are two potent, central AChE inhibitors of potential interest in the treatment of AD. © 2003 Elsevier Science Ltd. All rights reserved.
Original languageEnglish
Pages (from-to)749-755
JournalNeuropharmacology
Volume44
DOIs
Publication statusPublished - 1 Jan 2003

Keywords

  • (±)-Huprine Y
  • (±)-Huprine Z
  • AChE inhibitor
  • Alzheimer's disease
  • Huperzine A
  • Tacrine

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