Lab Anim Res.  2021 Sep;37(3):193-202. 10.1186/s42826-021-00093-1.

Acute and 28-days subacute toxicity studies of Gαq-RGS2 signaling inhibitor

Affiliations
  • 1Department of Pharmacology, L. M. College of Pharmacy, Navarangpura, Gujarat 380009 Ahmedabad, India

Abstract

Background
The aim of study was to evaluate the single oral dose and 28 day repeated oral administration toxicity profile of the synthetic compound Gαq-RGS2 signaling inhibitor, (1-(5-chloro-2-hydroxyphenyl)-3-(4-(trifluoromethyl)phenyl)-1 H-1,2,4-triazol-5(4 H)-one) as per OECD guideline 425 (2008a) and 407 (2008b), respectively.
Results
In acute toxicity study, a single oral dose administration of Gαq-RGS2 signaling inhibitor did not show any mortality at doses of 5, 50, 300 and 2000 mg/kg within 24 h and 14 days. The treatment of GαqRGS2 signaling inhibitor at dose 10 and 100 mg/kg for 28 days did not show any mortality, significant changes in the increase of body weight, various organ damage markers, hematological parameters, relative organ/body weight ratio and microscopic anatomical texture of essential organs as compared to vehicle and normal control.
Conclusions
A single oral administration of Gαq-RGS2 signaling inhibitor up to dose of 2000 mg/kg in mice and repeated administration of Gαq-RGS2 signaling inhibitor at higher dose 100 mg/kg for 28 days in the rats is safe.

Keyword

Acute toxicity; Sub-acute toxicity; Gαq-RGS2 signaling inhibitor; 28-days repeated dose toxicity; Single oral dose toxicity
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