Evaluation on Efficacy and Safety of Tribromoethanol and Tribromoethanol plus alpha2-Adrenergic Agonists in Different Mouse Strains.
10.5625/lar.2010.26.3.241
- Author:
Yoon Ju CHO
1
;
Jae Won LEE
;
Jong In KIM
;
Young Ah LEE
;
Tae Yeon KIM
;
Jin Soo HAN
Author Information
1. Department of Laboratory Animal Medicine, College of Veterinary Medicine, Konkuk University, Seoul, Korea. labvet@konkuk.ac.kr
- Publication Type:Original Article
- Keywords:
Anesthetic dose;
strain difference;
tribromoethanol;
xylazine;
medetomidine
- MeSH:
Anesthesia;
Anesthetics;
Animals;
Ethanol;
Gastrointestinal Tract;
Injections, Intraperitoneal;
Light;
Medetomidine;
Mice;
Mice, Inbred ICR;
Peritonitis;
Reflex;
Retention (Psychology);
Sprains and Strains;
Xylazine
- From:Laboratory Animal Research
2010;26(3):241-247
- CountryRepublic of Korea
- Language:English
-
Abstract:
The present study was carried out to provide a guideline for injecting tribromoethanol (TBE) as the main anesthetic agent, while adjusting the doses of xylazine (X) and medetomidine (M) according to different strains of mice (male ICR, C57BL/6, and BALB/c). Seven intraperitoneal injection anesthesia protocols using TBE and mixtures of TBE and alpha2-adrenergic agonists (TBE/X and TBE/M) were compared in terms of their efficacy and safety (anesthetic duration, death rate, and the development of pathological lesions of abdominal organs). All animals that were injected with a low dose of TBE (200 mg/kg) displayed clear signs of light anesthesia with a strong pedal withdrawal reflex. Despite the good anesthetic effect, a high dose of TBE (400 mg/kg) was not a suitable anesthetic for major surgery in all mouse strains because of the risk of pathologic changes in the abdominal organs, such as retention of the digestive tract, peritonitis, and fibrinoid adhesion. TBE200/X10 and TBE200/M0.5 (TBE, 200 mg/kg; X, 10 mg/kg; M, 0.5 mg/kg) appeared to be safe and provided satisfactory anesthesia in ICR mice. Finally, there were clear differences in anesthetic efficacy among ICR, C57BL/6, and BALB/c strains. TBE/M and TBE/X did not anesthetize BALB/c mice, and it anesthetized C57BL/6 mice for a short time. When administered with TBE/X and TBE/M maintained the sedation of ICR mice. We were able to establish different regimes for each strain (TBE200/X20 for C57BL/6, TBE300/X10 and TBE200/M1 for BALB/c). Our results showed that TBE/X and TBE/M could be recommended as an anesthetic mixture, with the dose appropriately adjusted according to mouse strain.
