1. Academic Validation
  2. [Preclinical study of noopept toxicity]

[Preclinical study of noopept toxicity]

  • Eksp Klin Farmakol. 2002 Jan-Feb;65(1):62-4.
L P Kovalenko 1 N M Smol'nikova S V Alekseeva E P Nemova A V Sorokina M G Miramedova S P Kurapova E I Sidorina A V Kulakova N O Daugel'-Dauge
Affiliations

Affiliation

  • 1 Laboratory of Drug Toxicology, Institute of Pharmacology, Russian Academy of Medical Sciences, Baltiiskaya ul. 8, Moscow, 125315 Russia.
PMID: 12025790
Abstract

Within the framework of a preclinical investigation, the new nootrope drug noopept (N-phenyl-acetyl-L-propyl-glycine ethylate) was tested for chronic toxicity upon peroral administration in a dose of 10 or 100 mg/kg over 6 months in both male and female rabbits. The results of observations showed that noopept administered in this dose range induced no irreversible pathologic changes in the organs and systems studied and exhibited no allergenic, immunotoxic, and mutagen activity. The drug affected neither the generative function nor the antenatal or postnatal progeny development. Noopept produced a dose-dependent suppression of inflammation reaction to concanavalin A and stimulated the cellular and humoral immune response in mice.

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