The laboratory mouse in the wild is known as the common
mouse. Through introduction by man the common house mouse now
frequents most of the world. The wild mouse was originally
thought to be native to Asia, India, and western Europe.
There are both commensal and wild forms of the house mouse.
The commensal forms often move out from buildings into
surrounding fields in the spring and summer and return to the
shelter of the buildings in the fall. The common house mouse
is light brown to black above and whitish below, often with a
buffy wash and tail that is lighter below. Commensal forms of
Mus musculus tend to have longer tails and to be darker than
the wild forms. Commensal forms of the house mouse are active
at any hour; the wild forms seem to be active mainly at
night. The range of movement in a common house mouse is very
limited; it may be an area of only 15 square meters. They are
not afraid of water and swim well. Nests are often made of
soft shredded material wherever suitable cover and food are
present.
Commensal forms feed on any human food that is available
and also on paste, glue, soap, and other household articles.
They damage much more than they eat. They seem to survive on
very little, hence the term "poor as a church mouse". In the
wild they eat many kinds of vegetables such as seeds, fleshy
roots, and leaves and stems; insects and some meats may be
eaten when available. They will also store food at times.
They breed throughout the year at least in the warm parts of
the range, and may have five or more litters a year. Because
of this high fecundity, wild populations become very high at
times. Population increases occurred in 1926-1927 and in
1941-1942 in the central valley of California. A population
of more than 82,000, per acre was estimated in the first of
these ecological explosions. The mouse has worked the
sparsely vegetated soil until it appeared to be recently
cultivated. Millions of mice were warming around the area
until the population trend was reversed. "Sing", "waltzing",
and "shaker" genetic abnormalities are common in house mice.
"Singing" mice are so called because a fait but audible
uttering is emitted by house mice in their shelters and has
been reported from various parts of the world. The waltzing
or shaker mice are caused by a defect in the equilibrium
system; they "waltz" or "shake" instead of moving about like
normal mice. Common house mice cause food spoilage and damage
to household articles and also transport the hosts of typhus,
spotted fever, and possibly other human diseases. The albino
strains of M. musculus are used extensively for laboratory
work. The genetics of the house mouse have been more
thoroughly studied than that of any other mammal.
In handling laboratory mice, there are several things that
must be kept in mind. You must be firm but gentle and always
handle the animal in the same way. A mouse is best handled by
picking it up by the base of the tail, then gently grasping a
pinch of lose skin over the shoulder area between the thumb
and forefinger (Figure 1)
The mouse is restrained in such a way can be easily
manipulated. If the mice are excitable and moving around in
the cage so that grasping the base of the tail is difficult,
cup the hand over the top of the mouse and then grasp the
tail gently at the base with a thumb and forefinger. Care
must be taken not to attempt to grab the tail other than
close to the base because this may result in slippage of the
skin and subcutaneous tissue from the bone leading to
necrosis, infection, and sloughing of the tail area where the
skin has been pulled off.
The mouse, although the smallest of the common laboratory
animals, is in the greatest demand in terms of numbers as an
experimental animal. Up to 80% of all animals used in
laboratories are mice. The small size, rapid reproduction,
and relatively high position on the evolutionary scale
provide numerous characteristics useful in all areas of
research. The mouse is used in a wide variety of studies
including drug toxicity, microbiology, radiobiology, cancer
research, behavior research, nutrition, and genetic
studies.
There are more inbred strains of mice than any other
mammalian species. These inbred strains offer the
investigator a wide range of capabilities and are suitable
for almost any research protocol. These inbred strains have,
for the most part, been genetically defined to enable the
investigator to select a model to fit his particular need
with ease. A primary source of inbred laboratory mice in the
United States is the Jackson Memorial Laboratory in Bar
Harbor, Maine. The majority of inbred strains available are
maintained at this laboratory and are available for
investigator use. Other individual suppliers of laboratory
mice may have many of the strains available. Care must be
taken to investigate fully the supplier's reputation in the
research field before utilization of these mice. It is
recommended that once an individual supplier is selected and
a study is initiated, the researcher should resist changing
suppliers until the individual study is completed. Although
several suppliers may offer the same genetic strain, the
variability between one supplier and another can be great. It
cannot be over emphasized that extreme care and caution must
be taken when selecting a source and a strain of animals to
be used for specific research protocol. The laboratory mouse
is not specifically covered in the rules and regulations
under the various public laws administered by the U.S.
Department of Agriculture. Therefore no specific permits or
licenses are required to produce or handle these animals.
Mice should be kept in rooms with the temperature set at
about 70F and humidity at 50%. Lights should not be too
bright since most white mice are albinos and too much light
hurts their eyes. They are diurnal which means they need
about 12 hours of light and 12 hours of darkness each day.
Their bedding should not be wood shaving since some wood
emits toxic fumes to mice. They should have fresh mouse or
rat food and water available at all times. Their bedding
should be changed 2 or 3 times a week to prevent the buildup
of urea.
Data is from many sources and is meant only as a quick
reference. Figures are from Harkness, "The Biology and
Medicine of Rabbits and Rodents" Text is mostly from
Uniformed Services University of the Health Sciences.
|
ANESTHETIC, ANALGESIC
|
Dose
|
Comments /
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|
| ACETAMINOPHEN (TYLENOL) |
1-2 MG/ML DW (14) // 300 MG/KG IP |
NONSTEROIDAL ANTI-INFLAMMATORY, ANALGESIC |
| ACETHYLSALICYLICATE ACID (ASPIRIN) |
120-300 MG/KG PO OR 100-150 MG/KG PO q4h
(14) // 25 IP/20 SC/120 PO MG/KG Q4H(2) |
NONSTEROIDAL ANTI-INFLAMMATORY, ANALGESIC |
| ACETYLPROMAZINE (ACEPROMAZINE) - DOSAGE |
0.5-1.0 MG/KG IM (14) // 1-2 MG/KG
IM |
TRANQUILIZER-PHENOTHIAZINE |
| BUPIVACAINE (MARCAINE) |
AS NEEDED |
LOCAL ANESTHETIC |
| BUPRENORPHINE (BUPRENEX) |
0.05-0.1 MG/KG IP (1)12//2 MG/KG SC (1)
Q12H (2)/(4) 0.05-2.5 MG/KG SC, IP q6-12h (14) (USE
0.05) |
NARCOTIC AGONIST-ANTAGONIST V |
| BUTORPHANOL (STADOL OR TORBUTROL) |
1.5 MG/KG SC q2-4h (14) // 5.4 MG/KG SC (1) |
NARCOTIC AGONIST-ANTAGONIST V |
| DIAZAPAM (VALIUM) |
5 MG/KG IP // 3-5 MG/KG IM (14) |
TRANQUILIZER - BENZODIAZEPINE IV |
| DIAZAPAM - DURATION TO EFFECT |
1-2 HOURS |
TRANQUILIZER - BENZODIAZEPINE IV |
| DIAZAPAM - TIME TO EFFECT |
1-2 MIN |
TRANQUILIZER - BENZODIAZEPINE IV |
| FENTANYL/DROPERIDOL (INNOVAR-VET)-DOSAGE |
0.3-0.5 ML/KG IM (14) // 2-5 ML/KG (4) |
NEUROLEPTANALGESIC, NARCOTIC/BUTYROPHENONE
TRANQUILIZER II |
| FENTANYL/ DROPERDOL - DURATION EFFECT |
15-20 MIN |
NEUROLEPTANALGESIC, NARCOTIC/BUTYROPHENONE
TRANQUILIZER II |
| FENTANYL/DROPERIDOL - TIME TO EFFECT |
2 MIN |
NEUROLEPTANALGESIC, NARCOTIC/BUTYROPHENONE
TRANQUILIZER II |
| FENTANYL/DROPERIDOL/DIAZEPAM-DOSE |
5 MG/KG DIAZEPAM IP 1ST,/FOLLOWED BY 0.1 ML/30G IP OF
1:10 SALINE DILUTION INNOVAR (1) |
NEUROLEPTANALGESIC, NARCOTIC/BUTYROPHENONE
TRANQUILIZER, BUTYROPHENONE II |
| IBUPROFEN |
7-15 MG/KG PO q4h (14) |
ANTI-INFLAMMATORY, ANALGESIA |
| KETAMINE (KETASET, VETALAR) - DOSAGE |
44 MG/KG IM (14) // 100-200 MG/KG IM (1) |
DISSOCIATIVE |
| KETAMINE-ACEPROMAZINE |
100/2.5 MG/KG IM (1)/ (2) |
DISSOCIATIVE/TRANQUILIZER |
| KETAMINE-DIAZEPAM (VALIUM) |
200 IM/5 IP MG/KG (1)/ (2) |
DISSOCIATIVE/TRANQUILIZER |
| KETAMINE-XYLAZINE (ROMPUN) |
50/5 MG/KG IP (14) // 200 IM/10 IP MG/KG (1)/
(2) |
DISSOCIATIVE/ANALGESIC |
| MEPERIDINE (DEMEROL) |
20 MG/KG IM SC (14) (1) Q2-3H |
NARCOTIC II, ANALGESIC |
| METHOHEXITAL (BREVITAL/BREVANE) |
6 MG/KG IV (2) |
ULTRA SHORT BARBITURATE IV |
| MORPHINE |
2-5 MG./KG SC q2-5h (14) // 10 MG/KG IM SC (1)
Q2-4H (2) |
NARCOTIC II, ANALGESIC |
| NALBUPHINE (NUBAIN) |
4-8 MG/KG IM q3h (14) |
NARCOTIC AGONIST-ANTAGONISTS ANALGESIC |
| OXYMORPHONE (NUMORPHAN) DOSAGE |
0.2-0.5 MG/KG SC IM q6-12h (14) |
NARCOTIC II, ANALGESIC |
| PENTAZOCINE (TALWIN-V) |
10 MG/KG SC q2-4h (14)(2) IM IV Q3-4H (2) |
NON-NARCOTIC ANALGESIC IV |
| PENTOBARBITAL Na (NEMBUTAL) |
40 MG/KG IV IP SEDATION /50-90 MG/KG IP SURG.
ANEST.(14) (1)/ (4) |
BARBITURATE SHORT II, SEDATION, ANESTHETIC (NOT
RECOMMENDED -MARGINAL ANALGESIA (14)) |
| PHENYLBUTAZONE (BUTAZOLDIN) |
150 MG/KG IP (7) |
NONSTEROIDAL ANTI-INFLAMMATORY |
| PROCAINE (NOVOCAIN) |
NEVER |
ANESTHETIC LOCAL |
| PROPOFOL (RAPINOVET) |
12-26 MG/KG IV (14) |
ANESTHETIC |
| THIAMYLAL (SURITAL) |
20-50 MG/KG IV IP//25-50 IV (4) |
BARBITURATE ULTRA SHORT III |
| THIOPENTAL (PENTOTHAL) |
30-40 MG/KG IV (2) ONLY (1) //25-50 IV (4) |
BARBITURATE ULTRA SHORT III |
| TILETAMINE/ ZOLAZEPAM (TELAZOL) 50MG BASE/ML |
100-160 MG/KG IP IM (1) |
DISSOCIATE/TRANQUILIZER III |
| TRIBROMOETHANOL (AVERTIN) (0.25%) |
125 MG/KG IP (1)/0.25% (2) |
ANESTHETIC |
| XYLAZINE (ROMPUN)- DOSAGE |
4-8 MG/KG IM |
ALPHA-2-ADRENERGIC AGONIST SEDATIVE, ANALGESIC,
MUSCLE RELAXANT |
| YOHIMBINE. (YOBINE) |
0.5-1.0 MG/KG IV (14) |
XYLAZINE REVERSAL |
|
ANESTHETIC GAS
|
Dose
|
Comments /
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|
| HALOTHANE - MAC |
TO EFFECT |
INHALANT |
| ISOFLURANE - MAC |
TO EFFECT |
INHALANT |
| METHOXYFLURANE - MAC |
TO EFFECT |
INHALANT |
| NITROUS OXIDE-MAC |
TO EFFECT |
INHALANT |
|
ANTI-INFLAMMATORY
|
Dose
|
Comments /
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|
| DEXAMETHASONE (AZIUM) |
0.06 MG SC IM IV IP |
STEROID |
| PREDNISONE (METICORTIN) |
0.05-0.22 MG SC IM |
STEROID |
|
ANTIBIOTIC
|
Dose
|
Comments /
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|
| AMIKACIN |
2-5 MG/KG SC. IM q8-12h(14) |
ANTIBIOTIC |
| AMOXICILLIN |
100 MG/KG SC IM Q12H(2) |
ANTIBIOTIC |
| AMPICILLIN (POLYFLEX) |
20-100 MG/KG PO, SC, IM q12h (14) // 50-150 MG/KG SC
Q12H(2) // OR 30 MG/KG IM Q24H (4.5 MG/30 MG)(3) |
BETA LACTAM ANTIBIOTIC |
| BACITRACIN |
TOPICAL |
ANTIBIOTIC |
| CARBENICILLIN |
100 MG/KG PO q12h (14) |
|
| CEPHALORIDINE (LORIDINE) |
10-25 MG/KG SC, IM q24h (14) |
BETA LACTAM ANTIBIOTIC |
| CHLORAMPHENICOL PALMITATE (CHLOROMYCETIN) |
DW 0.5 MG/ML(3)(14) |
BACTERIAL STATIC BROAD SPEC. |
| CHLORAMPHENICOL SUCCINATE (CHLOROMYCETIN) |
50-200 MG/KG PO q8h OR 30-50 MG/KG SC, IM q24h (14)
// 50 MG/KG IM Q12H(2) // OR Q24H (1.5 MG/30 GM)(3) |
BACTERIAL STATIC BROAD SPEC. |
| DIHYDROSTREPTOMYCIN |
NEVER |
BACTERIAL |
| DOXYCYCLINE |
2.5MG/KG PO q12h (14) |
PNEUMONIA, NOT IN YOUNG OR PREGNANT |
| ENROFLOXACIN |
25-85 MG/KG q24h X 14 DAYS OR 0.05-0.20 MG/ML DW X 14
DAYS(14) |
PASTEURELLOSIS |
| ERYTHROMYCIN |
20 MG/KG PO (14) |
BACTERIAL |
| GENTAMICIN (GENTOCIN) |
5 MG/KG SC, IM q24h (14) // 5 MG/KG SC IM SID (0.15
MG/30GM) (3)14D |
AMINOGLYCOSIDES |
| GRISEOFULVIN (FULVICIN U/F) |
25-50 MG/KG PO q12h X 14-60 DAYS (14) // 75 MG/KG PO
SID 14D// OR 60 MG/KG PO IN FOOD(3) |
ANTIFUNGAL |
| KETOCONAZOLE |
10-40 MG/KG PO q24h X 14 DAYS |
SYSTEMIC MYCOSES, CANDIDIASIS |
| NEOMYCIN (BIOSOL) |
50 MG/KG SC q24h (14) // 2.6 MG/ML DW (14) |
DIARRHEA |
| OXYTETRACYCLINE (LIQUAMYCIN) |
0.4 MG/ML DW(3)(14) // 100 MG/KG SC Q12H(2)//
10-20 MG/KG PO q8h (14) |
BACTERIAL STATIC BROAD SPEC. |
| PENICILLIN PROCAINE (AZIMYCIN) |
NEVER |
BACTERIAL |
| STREPTOMYCIN (BIOTEC) |
NEVER |
BACTERIAL |
| SULFADIMETHAXINE |
10-15 MG/KG PO q12h (14) |
|
| SULFAMERAZINE |
1 MG/ML DW (14) // 1 MG/4G FEED (14) |
BACT. COCCIDIA, CIT,B |
| SULFAMETHAZINE |
1 MG/ML DW (14) |
|
| SULFAQUINOXALINE (SULQUIN) |
1MG/ML DW (14) // 0.025% 30days |
EIMERIA, KLOS. PAST. |
| TETRACYCLINES |
100 MG/KG SC SID (3 MG/30 GM)(3) // DW 3
MG/ML(3) |
BACTERIAL STATIC BROAD SPEC//FROG RED LEG |
| TRIMETHOPRIM (40MG/ML)/SULPHADOXINE (200MG/ML)
(TRIBRISSEN) |
30 MG/KG PO, SC, IM a12h (14) // 0.5 ML/KG SC
Q12H(2) |
TRIMETHOPRIM / SULPHONAMIDE |
| TYLOSIN |
0.5 MG/ML DW (14) // 10 MG/KG PO, SC, IM q24h (14) //
2-5 MG/ML DW10 MG/KG SC Q12H(2) // OR (0.3 MG/KG GM)
IM(3) |
MACROLIDES |
|
ANTICHOLINERGIC
|
Dose
|
Comments /
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|
| ATROPINE - DOSAGE |
0.04 MG/KG SC IM(2)/(3)(14) |
ANTICHOLINERGIC |
| ATROPINE - DURATION EFFECT |
25 MIN |
ANTICHOLINERGIC |
| ATROPINE - TIME TO EFFECT |
10MIN |
ANTICHOLINERGIC |
|
ANTIPARASITIC
|
Dose
|
Comments /
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|
| DICHLORVOS (TASK) |
250-500 MG/KG FOOD 1D |
ECTOPARASITIC-SYPH, HETER |
| DICHLORVOS (VOPONA STRIPS) |
STRIP 48H/WK//OR1 OVER CAGE 24 H/W(3) // Suspend 15
cm above cage x 24 hr, then 2 x /wk x 3 wk (14) |
ECTOPARASITIC |
| DIMETRIDAZOLE |
1 MG/ML DW (14) |
GASTROINTESTINAL PROTOZOA |
| DITHIAZANINE IODINE |
0.1 MG/KG FOOD 7D |
SYPH. HETER. STRONG.TR |
| FENBENDAZOLE |
0.3% FEED X 14 DAYS (14) // 20 (50 FOR GIARDIASIS)
MG/KG PO X 5 DAYS (14) |
CESTODES, PINWORMS, GIARDIASIS |
| FIPRONIL (FRONTLINE) |
7.5 MG/KG TOP q30-60d (14) |
FLEA ADULTCIDE |
| IVERMECTIN (IVOMEC) |
0.2 MG/KG PO, SC q7d X 3 WK (14) // 8 MG/L DW X 4
D/WK X 5 WK (14) // 200 MCG/KG PO SC(3) |
MITE, PINWORMS |
| MEBENDAZOLE (TELMIN) |
10 MG/KG PO 5D(3) |
NEMATODIASIS COSMOCE |
| METRONIDAZOLE (FLAGYL) |
15 MG/KG IP 1X |
GIARDIA |
| NICLOSAMIDE (YOMESAN) |
100 MG/KG PO(3) |
CESTODES-HYMENOLEPSIS |
| PIPERAZINE CITRATE |
2-5 MG/ML DW X 7 DAYS, OFF 7 DAY, REPEAT (14) // 100
MG/KG PO(3) // 16GM/GAL WATER + 200 ML KARO SYRUP SIDX3,
REPEAT IN 2 WKS (8) |
ANTI-NEMATODES-SYPHACIA & HET & PINWORMS |
| PRAZIQUANTEL |
6-10 MG/KG PO (14) // 30 MG/KG PO q14d X 3 TX
(14) |
CESTODES |
| PYRVINIUM PAMOATE |
1.6 MG/KG/D 30D |
SYPH. HETER.ENTEROBIU |
| SULFADIMETHOXINE |
10-15 MG/KG PO q12h (14) |
COCCIDIOSIS |
| SULFAMERAZINE |
1 MG/ML DW (14) |
EIMERIA/COCCIDIOSIS |
| THIABENDAZOLE (TBZ; OMIZOLE) |
1 MG/ML DW (14) // 100 MG/KG PO q24h X 5D(14)(3) |
COCCIDIOSIS/ASCARIDIASIS |
|
MISCELLANEOUS
|
Dose
|
Comments /
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|
| ATROPINE |
20-40 MG/ANIMAL PO (14) |
ANTICHOLINERGIC |
| DEXAMETHASONE |
0.5-2.0 MG/KG PO, SC, DECREASE DOSE q12h X 3-14 DAYS
(14) |
ANTI-INFLAMMATORY |
| DOXAPRAM |
5-10 MG/KG IP, IV (14) |
RESPIRATORY STIMULANT |
| FUROSEMIDE |
5-10 MG/KG SC, IM q12h (14) |
DIURETIC/PULMONARY CONGESTION/ASCITES |
| LACTATED RINGER'S SOLUTION |
50-100 ML/KG SC, IV, IO q12h (14) |
MAINTENANCE FLUID |
| LOPERAMIDE (IMODIUM A-D) |
0.1 MG/KG PO q8h X 3 DAYS THEN q24h X 2 DAYS (GIVEN
IN 1.0 ML WATER)(14) |
DIARRHEA |
| OXYTOCIN |
0.2-3 UNITS/KG SC IM IV (14)(9) |
DELAYED PARTURITION, UTERINE/MILK HORM. |
| PREDNISONE |
0.5-2.2 MG/KG SC IM (14) |
ANTI-INFLAMMATORY |
| VITAMIN B COMPLEX |
0.02-0.20 ML/KG SC IM (14) |
|
| VITAMIN D |
200-400 IU/KG SC IM (14) |
|
| VITAMIN E/SELENIUM |
0.1ML/100-250 G SC (14) |
|
| VITAMIN K1 |
1-10 MG/KG IM q214h X 4-6 DAYS (14) |
WARFARIN POISONING |
|
EUTHANASIA
|
Dose
|
Comments /
Back to Top
|
| Sodium pentobarbital |
150 mg/kg IP |
Controlled substance |
| Halothane |
To effect |
High Concentration, Rapid flow, High flow rates may
initially frighten the animal, If a chamber is used
Animal should not come into contact with liquid, Animals
should not be overcrowded, Animals should be
compatible |
| Isoflurane |
To effect |
High Concentration, Rapid flow, High flow rates may
initially frighten the animal, If a chamber is used
Animal should not come into contact with liquid, Animals
should not be overcrowded, Animals should be
compatible |
| CO2 |
To effect |
No breathing, no heart beat/pulse, no response to
toe/ear pinch for at least 2 minutes, Must use a gas
cylinder |
| CO |
To effect |
No breathing, no heart beat/pulse, no response to
toe/ear pinch for at least 2 minutes, Very hazardous,
Must use a gas cylinder |
| Potassium chloride |
1-2 mmol/kg IV or Intracardiac |
Requires general anesthesia |
| Cervical dislocation |
Conditionally acceptable |
Requires another method |
| Decapitation |
Conditionally acceptable |
Requires another method |
| Chloral hydrate |
Unacceptable |
|
|
NOTES
|
Abbreviations /
Back to Top
|
(1) = Anesthesia and Analgesia in
Laboratory Animals: American College of Laboratory Animal
Medicine: 1990
(2) = Laboratory Animal Anesthesia: Flecknell:
1989
(3) = Drug Dosages for Small Mammals: McKellar:
1989
(4) = Recognition and Alleviation of Pain and
Distress in Laboratory Animals: NRC: 1992
(5) = Current Veterinary Therapy 2 Food Animal
Practice
(6) = University of Calif., San Fran., Morrish
(7) = Basic Care of Experimental Animals
(8) = Therapeutic Guide and Anesthesia, O'Harndley
(9) = The Biology and Medicine of Rabbits and
Rodents
(10) = ???????? Continuing Education Vol. 5, No.
4, April 1992
(11) = USUHS Formulary
(12) = LAB ANIMAL OCT 91 PAGE 34
(13) = Anesthesia and Analgesia Doses, SCHAEFFER,
KNOXVILLE, TN
(14) = Exotic Animal Formulary, Carpenter,
Saunders:2001 |
EOD = Every Other Day
SID = Once a day
BID = Twice a day (generally every 12 hours)
TID = Three times a day (every 8 hours)
QID = Four times a day (every 6 hours)
Q?H = Every ? hours
IM = Intramuscular injection
IP = Intraperitoneal injection
SC or SQ = Subcutaneous injection
IV = Intravenous injection
PO = Per Os (By Mouth) (Orally)
DW = Drinking water
3DX4 = 3 days of treatment, repeated 4 times |