Publication Cover
Chronobiology International
The Journal of Biological and Medical Rhythm Research
Volume 22, 2005 - Issue 3
74
Views
10
CrossRef citations to date
0
Altmetric
Original

Circadian Time‐Dependent Differences in Murine Tolerance to the Antihistaminic Agent Loratadine

, , , &
Pages 499-514 | Received 16 Jan 2005, Accepted 08 Feb 2005, Published online: 07 Jul 2009
 

Abstract

Loratadine is a second‐generation histamine H1‐receptor antagonist used in the treatment of allergic diseases. The aim of the study was to assess whether lethal toxicity and motor incoordination (neurotoxicity) of loratadine is circadian rhythm‐dependent. A total of 210 male Swiss mice, aged 10 wk, were synchronized for 3 wk to 12 h light (rest span)/12 h dark (activity span). The drug was administered per os. The choice of the sublethal (TD50=82 mg/kg body weight) and the lethal (LD50=4 g/kg body weight) dosage was based on preliminary studies. Each of these two doses was administered to comparable groups of animals at six different circadian time points (1, 5, 9, 13, 17, and 21 Hours After Light Onset [HALO]). The survival duration was dosing time‐dependent (χ2=16.96; p<0.001). Drug dosing at 17 HALO resulted in best (67%) survival rate; whereas, dosing at 9 HALO resulted in poorest (21%) survival rate. Cosinor analyses (with a trial period τ=24 h) validated a statistically significant circadian rhythm in survival rate (p<0.04) with an acrophase (peak time Ø of best tolerance to loratadine) being at 17.5 HALO±4.65 h. Troughs of motor incoordination were located at the administration times of 5 and 17 HALO (60% and 32% of animals affected, respectively), whereas peaks were located at 9 and 21 HALO (87% and 68% of animals affected, respectively). The 24 h mean of the motor incoordination was 61%, the mean proportion of animals affected by the treatment for the six different circadian times studies. The extent of this neurotoxic effect varied as a function of loratadine dosing time (p<0.001). A statistically significant ultradian component rhythm (p<0.01) with a trial period τ=12 h was also validated. The obtained results show that the dosing time of loratadine at the mid‐activity (dark) span seems to be optimal, since it corresponds to the longest (21 vs. 12 days) survival span and to least neurotoxicity.

Log in via your institution

Log in to Taylor & Francis Online

PDF download + Online access

  • 48 hours access to article PDF & online version
  • Article PDF can be downloaded
  • Article PDF can be printed
USD 61.00 Add to cart

Issue Purchase

  • 30 days online access to complete issue
  • Article PDFs can be downloaded
  • Article PDFs can be printed
USD 489.00 Add to cart

* Local tax will be added as applicable

Related Research

People also read lists articles that other readers of this article have read.

Recommended articles lists articles that we recommend and is powered by our AI driven recommendation engine.

Cited by lists all citing articles based on Crossref citations.
Articles with the Crossref icon will open in a new tab.