Effect of a kynurenic acid analog on home-cage activity and body temperature in rats

Background N-(2-N,N-Dimethylaminoethyl)-4-oxo-1H-quinoline-2-carboxamide hydrochloride (SzR-72) is a kynurenic acid (KYNA) amide analog that displays neuroprotective action. Whereas its brain penetration ability and its solubility limit the therapeutic use of KYNA: the corresponding properties of th...

Teljes leírás

Elmentve itt :
Bibliográfiai részletek
Szerzők: Kassai Ferenc
Kedves Rita
Gyertyán István
Tuka Bernadett
Fülöp Ferenc
Toldi József
Lendvai Balázs
Vécsei László
Dokumentumtípus: Cikk
Megjelent: 2015
Sorozat:PHARMACOLOGICAL REPORTS 67 No. 6
doi:10.1016/j.pharep.2015.04.015

mtmt:30461871
Online Access:http://publicatio.bibl.u-szeged.hu/9904
Leíró adatok
Tartalmi kivonat:Background N-(2-N,N-Dimethylaminoethyl)-4-oxo-1H-quinoline-2-carboxamide hydrochloride (SzR-72) is a kynurenic acid (KYNA) amide analog that displays neuroprotective action. Whereas its brain penetration ability and its solubility limit the therapeutic use of KYNA: the corresponding properties of the analog exceed those of the parent compound. Although SzR-72 has been extensively studied, its exact mechanism of action has not yet been fully clarified. As KYNA induces hypothermia in laboratory rodents, it may be hypothesized that SzR-72 may have a similar effect. This would be of major importance, since the hypothermia generated by external cooling is neuroprotective, thus a putative hypothermic effect of SzR-72 could contribute to its neuroprotective action. Methods The effects of SzR-72 on the body temperature and home-cage activity of rats were studied by using a telemetry system. In order to follow the longitudinal changes in the effects of the compound, subchronic drug administration was applied. Results The initial administration of the compound induced substantial hypothermia and reduced the home-cage activity. During the 5 days of SzR-72 administration, partial tolerance developed to the hypothermic effect, while the inhibition of home-cage activity detected after the acute administration was completely tolerated. Conclusions On the basis of these results, it cannot be excluded that the hypothermic effect of SzR-72 contributes to its neuroprotective action. © 2015 Institute of Pharmacology, Polish Academy of Sciences. Published by Elsevier Sp. z o.o. © 2015 Institute of Pharmacology, Polish Academy of Sciences. Published by Elsevier Sp. z o.o. All rights reserved.
Terjedelem/Fizikai jellemzők:1188-1192
ISSN:1734-1140