Effects of second-generation histamine H1 receptor antagonists on the active avoidance response in rats.

Clin Exp Pharmacol Physiol

Department of Pharmacology, Faculty of Pharmaceutical Sciences, Okayama University, Okayama, Japan.

Published: November 2003

AI Article Synopsis

  • The study aimed to create a new method for testing how second-generation antihistamines affect memory in rats using an active avoidance response procedure.
  • In this new setup, rats had a delay before being shocked unless they moved to a safe, lit area, contrasting with a traditional method where no delay was present.
  • Results showed that drugs like cetirizine, olopatadine, and loratadine significantly impaired memory retrieval in rats, while ketotifen and epinastine had little to no effect.

Article Abstract

1. The aim of the present study was to establish a new schedule of active avoidance response in rats to estimate the central effects of second-generation histamine H1 receptor antagonists. 2. With the new schedule, a rat was placed into a dark room. A sliding door was opened after a delay of 5 s and, unless the animal moved into the lit room, an electric shock was delivered for 3 s. With the conventional schedule, the sliding door was opened immediately after the rat was placed into the dark room. 3. Ketotifen, at a dose of 50 mg/kg, showed no significant effect on the retrieval of active avoidance response with the conventional schedule. However, with the new schedule, the drug caused significant inhibition of retrieval of the response, even at a dose of 10 mg/kg. 4. Epinastine showed no significant effect on retrieval of the active avoidance response, even at a dose of 50 mg/kg with the new schedule. 5. Cetirizine, at a dose of 50 mg/kg, caused a significant effect, indicating that cetirizine, at this dose, markedly inhibits memory retrieval. 6. Both olopatadine and loratadine had potent effects; at doses of 20 and 50 mg/kg, respectively, these agents showed significant inhibitory effects on retrieval of the response. 7. In conclusion, we have developed a new schedule of active avoidance response that can be used to estimate the central effects of second-generation histamine H1 receptor antagonists.

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http://dx.doi.org/10.1046/j.1440-1681.2003.03791.xDOI Listing

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