Short-term immobilization of mice by methohexitone

被引:8
作者
Dörr, W
Weber-Frisch, M
机构
[1] Tech Univ Dresden, Med Fak Carl Gustav Carus, Klin & Poliklin Strahlentherapie, D-01307 Dresden, Germany
[2] GSF, Inst Strahlenbiol, Oberschleissheim, Germany
关键词
mouse; immobilization; chemical restraint; methohexitone; pentobarbitone;
D O I
10.1258/002367799780578543
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
The feasibility of short-term immobilization for <5 min of female mice by methohexitone sodium was studied. In C3H/Neu mice, methohexitone at a dose <40 mg/kg did not result in chemical restraint, doses >50 mg/kg caused considerable lethality. A dose of 44 mg/kg, applied intraperitoneally at a concentration of 6.46 mg/ml, is suitable for immobilization without complications. This concentration was chosen in order to achieve an injection volume of about 0.15 ml for a mouse with an average body weight of 22 g, corresponding to about 1 mg/mouse. Complete immobilization, defined as absence of the righting reflex, was observed within 3.3 +/- 0.8 min (mean +/- SD, n = 10) after the injection and lasted for 1.5 +/- 0.7 min. Recovery of the animals was complete after a total period of 10 to 15 min postinjection. No gross pathomorphological changes were induced when intraperitoneal injections of methohexitone were repeated 10 times within 10 days. In the present study, complete immobilization of the mice was safely achieved after 87 out of 90 injections. In conclusion, immobilization by intraperitoneal injection of methohexitone is a feasible and reliable method in the experimental studies of female mice.
引用
收藏
页码:35 / 40
页数:6
相关论文
共 28 条
[1]  
BREITNER A, 1989, THESIS LMU MUNCHEN
[2]   Observations on the use of medetomidine/ketamine and its reversal with atipamezole for chemical restraint in the mouse [J].
Cruz, JI ;
Loste, JM ;
Burzaco, OH .
LABORATORY ANIMALS, 1998, 32 (01) :18-22
[3]   METHOHEXITAL VERSUS PROPOFOL FOR OUTPATIENT ANESTHESIA .2. PROPOFOL IS SUPERIOR [J].
DEMBO, JB .
JOURNAL OF ORAL AND MAXILLOFACIAL SURGERY, 1995, 53 (07) :816-820
[4]   PROLIFERATION KINETICS OF MOUSE TONGUE EPITHELIUM UNDER NORMAL CONDITIONS AND FOLLOWING SINGLE DOSE IRRADIATION [J].
DORR, W ;
KUMMERMEHR, J .
VIRCHOWS ARCHIV B-CELL PATHOLOGY INCLUDING MOLECULAR PATHOLOGY, 1991, 60 (05) :287-294
[5]   Repopulation response of mouse oral mucosa during unconventional radiotherapy protocols [J].
Dorr, W ;
WeberFrisch, M .
RADIOTHERAPY AND ONCOLOGY, 1995, 37 (03) :230-236
[6]   EFFECT OF CHANGING WEEKLY DOSE ON ACCELERATED REPOPULATION DURING FRACTIONATED-IRRADIATION OF MOUSE TONGUE MUCOSA [J].
DORR, W ;
WEBERFRISCH, M .
INTERNATIONAL JOURNAL OF RADIATION BIOLOGY, 1995, 67 (05) :577-585
[7]   CAPACITY AND KINETICS OF SLD REPAIR IN MOUSE TONGUE EPITHELIUM [J].
DORR, W ;
BREITNER, A ;
KUMMERMEHR, J .
RADIOTHERAPY AND ONCOLOGY, 1993, 27 (01) :36-45
[8]   REPOPULATION IN MOUSE ORAL-MUCOSA - TREATMENT SPLITS [J].
DORR, W .
RADIOTHERAPY AND ONCOLOGY, 1994, 33 (02) :139-147
[9]   PROLIFERATION EQUIVALENT OF ACCELERATED REPOPULATION IN MOUSE ORAL-MUCOSA [J].
DORR, W ;
EMMENDORFER, H ;
HAIDE, E ;
KUMMERMEHR, J .
INTERNATIONAL JOURNAL OF RADIATION BIOLOGY, 1994, 66 (02) :157-167
[10]   ACCELERATED REPOPULATION OF MOUSE TONGUE EPITHELIUM DURING FRACTIONATED IRRADIATIONS OR FOLLOWING SINGLE DOSES [J].
DORR, W ;
KUMMERMEHR, J .
RADIOTHERAPY AND ONCOLOGY, 1990, 17 (03) :249-259