Comparison of the anesthetic effects of 2,2,2-tribromoethanol on ICR mice derived from three different sources.
10.5625/lar.2018.34.4.270
- Author:
Mi Ree LEE
1
;
Hye Rin SUH
;
Myeong Whan KIM
;
Joon Young CHO
;
Hyun Keun SONG
;
Young Suk JUNG
;
Dae Youn HWANG
;
Kil Soo KIM
Author Information
1. College of Veterinary Medicine, Kyungpook National University, Daegu, Korea. kskim728@knu.ac.kr
- Publication Type:Original Article
- Keywords:
Anesthesia effect;
Korl:ICR mice;
pulse oximeter;
sex difference;
tribromoethanol
- MeSH:
Anesthesia;
Anesthetics*;
Animals;
Arterial Pressure;
Biomarkers;
Body Temperature;
Female;
Heart Rate;
Humans;
Hydrogen-Ion Concentration;
Kidney;
Liver;
Lung;
Male;
Mice;
Mice, Inbred ICR*;
Oxygen;
Sex Characteristics
- From:Laboratory Animal Research
2018;34(4):270-278
- CountryRepublic of Korea
- Language:English
-
Abstract:
This study was conducted to compare the anesthetic effects of 2,2,2-tribromoethanol (TBE, Avertin®) in ICR mice obtained from three different sources. TBE (2.5%) was intraperitoneally injected at three doses: high-dose group (500 mg/kg), intermediate-dose group (250 mg/kg), and low-dose group (125 mg/kg). Anesthesia time, recovery time, end-tidal peak CO2 (ETCO₂), mean arterial blood pressure, heart rate, oxygen saturation (SpO₂), body temperature, pH, PCO₂, and PO₂ of the arterial blood were measured. Stable anesthesia was induced by all doses of TBE and the anesthesia time was maintained exhibited dose dependency. No significant differences in anesthetic duration were found among the three different strains. However, the anesthesia time was longer in female than in male mice, and the duration of anesthesia was significantly longer in female than in male mice in the high-dose group. The recovery time was significantly longer for female than male mice in the intermediate- and high-dose groups. In the ICR strains tested, there were no significant differences in the mean arterial blood pressure, SPO₂, arterial blood PCO₂, and PO₂, which decreased after TBE anesthesia, or in heart rate and ETCO₂, which increased after TBE anesthesia. In addition, body temperature, blood biochemical markers, and histopathological changes of the liver, kidney, and lung were not significantly changed by TBE anesthesia. These results suggested that ICR mice from different sources exhibited similar overall responses to a single exposure to TBE anesthesia. In conclusion, TBE is a useful drug that can induce similar anesthetic effects in three different strains of ICR mice.
