Pharmacokinetics of heptastigmine in rats

Pharmacol Res. 1992 Feb-Mar;25(2):139-46. doi: 10.1016/1043-6618(92)91382-q.

Abstract

Heptastigmine is a new long acting cholinesterase inhibitor that affects behaviour in a number of cognitive tests in animals. We have studied its pharmacokinetics in rats: plasma kinetics were evaluated after single intravenous dose (2 mg/kg), intramuscular (4 mg/kg) and oral (4 and 8 mg/kg) administration. Tissue distribution (heart, liver, kidney and brain) was studied after single intramuscular (4 mg/kg) and oral (8 mg/kg) administration. Plasma and tissue kinetics were also investigated after repeated oral doses (8 mg/kg b.i.d. for 7 days). Heptastigmine levels in plasma and tissues were determined using an HPLC method with an electrochemical detector. After a single dose, heptastigmine remained for a long time in plasma (the terminal half-life was about 12 h), distributed widely in tissues (the volume of distribution was about 61) and brain concentrations were very high (4-22 times those found in plasma). After repeated oral doses, the drug levels increased in plasma and, to a lesser extent, in liver and kidney.

Publication types

  • Comparative Study

MeSH terms

  • Administration, Oral
  • Animals
  • Cholinesterase Inhibitors / pharmacokinetics*
  • Injections, Intramuscular
  • Injections, Intravenous
  • Male
  • Physostigmine / administration & dosage
  • Physostigmine / analogs & derivatives*
  • Physostigmine / blood
  • Physostigmine / pharmacokinetics
  • Rats
  • Rats, Inbred Strains
  • Tissue Distribution

Substances

  • Cholinesterase Inhibitors
  • physostigmine heptyl
  • Physostigmine