Guidelines for Rodent Analgesia
Because the anatomic structures and neurophysiologic mechanisms leading to the perception of pain are similar in humans and non-human
animals, it is reasonable to assume that if a stimulus:
is painful to humans,
is damaging or potentially damaging to tissues, or
induces escape and emotional responses in an animal,
it must be considered to be painful to that animal.
The choice of post-surgical analgesic drug must take into consideration (and be appropriate for) the estimated level and
duration of post-surgical/post-procedural pain/discomfort associated with the specific surgery/procedure.
Generally speaking, analgesics should be provided as early in the exercise as possible. Providing analgesic PRIOR to the initiation of the painful stimulus is most preferred; providing analgesia during the procedure (of an anesthetized animal) is considered the minimal standard when pre-procedural analgesia is not possible.
This concept of pre-emptive analgesic is important to the stability of the research animal and the outcome of the research data. An additional benefit of pre-emptive analgesia is that the amount of anesthetics required for proper anesthesia are often reduced, further benefiting the animal with a rapid return to normal, while saving critical research dollars.
For analgesic drugs that are administered via the oral route, the drug must:
be administered via oral gavage at the appropriate dosing frequency, or
if administered via the drinking water, the drug must be placed in the drinking water starting a minimum of 7 days
prior to the surgery/painful procedure in order for the animal to be “exposed”, and, presumably, adapted to the altered taste of the
water at the time of the surgery/procedure. This prepatory step is necessary to overcome ‘neophobia,’ a behavioral adaptation of rodents
(especially rats) whereby they may not consume adequate quantities of fluids when a new taste sensation is recognized. Placing a
flavored analgesic in the water post procedure may allow for association of the ‘pain’ with the new flavor and thereby rejection of the
flavored water resulting in inadequate analgesia.
Duke utilizes a tiered system of analgesic delivery, based upon generalized observations of degrees of pain or
discomfort. These include:
P1: Survival Surgery/Survival Procedures Estimated to Cause MARKED Post-Surgery/Post-Procedural Pain
P2: Survival Surgery/Survival Procedures Estimated to Cause MODERATE Post-Surgery/Post-Procedural Pain
P3: Survival Surgery/Survival Procedures Estimated to Cause MILD Post-Surgery/Post-Procedural Pain
Generally speaking, analgesics should be provided as early in the exercise as possible. Providing analgesic PRIOR to the initiation of the painful stimulus is most preferred; providing analgesia during the procedure (of an anesthetized animal) is considered the minimal standard when pre-procedural analgesia is not possible.
This concept of pre-emptive analgesic is important to the stability of the research animal and the outcome of the research data. An additional benefit of pre-emptive analgesia is that the amount of anesthetics required for proper anesthesia are often reduced, further benefiting the animal with a rapid return to normal, while saving critical research dollars.
For analgesic drugs that are administered via the oral route, the drug must:
P2: Survival Surgery/Survival Procedures Estimated to Cause MODERATE Post-Surgery/Post-Procedural Pain
P3: Survival Surgery/Survival Procedures Estimated to Cause MILD Post-Surgery/Post-Procedural Pain
P1: Survival Surgery/Survival Procedures Estimated to Cause MARKED Post-Surgery/Post-Procedural Pain.
(Examples: any surgery involving thoracotomy or celiotomy; transplantation of an organ; limb amputation; extensive orthopedic surgery;
cecal ligation and puncture):
| DRUG | MOUSE | RAT | HAMSTER | GERBIL | GUINEA PIG |
| Morhine | 10 mg/kg SQ or IM every 4 hours | 10 mg/kg SQ or IM every 4 hours | 10 mg/kg SQ or IM every 4 hours | 10 mg/kg SQ or IM every 4 hours | 10 mg/kg SQ or IM every 4 hours |
| Codeine | 20 mg/kg SQ every 4 hours | 50 mg/kg SQ every 4 hours | 40 mg/kg SQ every 4 hours | ||
| Oxymorphone | 0.15 mg/kg SQ or IM every 4 hours | 0.22-0.33 mg/kg SQ every 4 hours | 0.2-0.5 mg/kg SQ or IM every 6 hours | 0.2-0.5 mg/kg SQ or IM every 6 hours |
P2: Survival Surgery/Survival Procedures Estimated to Cause MODERATE Post-Surgery/Post-Procedural Pain
Examples: most laparoscopic (i.e. intra-abdominal) surgeries; limited orthopedic surgery; intra-cranial surgery):
Examples: most laparoscopic (i.e. intra-abdominal) surgeries; limited orthopedic surgery; intra-cranial surgery):
| DRUG | MOUSE | RAT | HAMSTER | GERBIL | GUINEA PIG |
| Ketoprofen | 5mg/kg SQ SID | 5mg/kg SQ SID | 5mg/kg SQ SID | 5mg/kg SQ SID | 5mg/kg SQ SID |
| Meperidine | 20 mg/kg SQ or IM every 3 hours | 20 mg/kg SQ or IM every 3 hours | 20 mg/kg SQ or IM every 3 hours | 20 mg/kg SQ or IM every 3 hours | |
| Nalbuphine | 4-8 mg/kg SQ or IM every 3 hours | 2-5 mg/kg SQ every 4 hours | 4-8 mg/kg SQ or IM every 3 hours | 4-8 mg/kg SQ or IM every 3 hours | 1-2 mg/kg IM every 4 hours |
| Pentazocine | 10 mg/kg SQ every 4 hours | 10 mg/kg SQ every 4 hours | |||
| Butorphanol | 2 mg/kg SQ every 4 hours | 5 mg/kg SQ every 4 hours | 5 mg/kg SQ every 4 hours | 5 mg/kg SQ every 4 hours | |
| Buprenorphine | 0.05-0.1 mg/kg SQ every 12 hours | 0.1-0.5 mg/kg SQ every 12 hours | 0.5 mg/kg SQ every 8 hours | 0.2 mg/kg every 8 hours | 0.05 mg/kg SQ every 12 hours |
| Carprofen | 5 mg/kg SQ every 12 hours | 5 mg/kg SQ every 12 hours | |||
| Aspirin | 300 mg/kg orally every 24 hours | 100 mg/kg orally every 24 hours | 86 mg/kg orally every 24 hours | ||
| Ibuprofen | 7.5 mg/kg orally every 24 hours | 30 mg/kg orally every 24 hours | |||
| Phenylbutazone | 30 mg/kg orally every 24 hours | 20 mg/kg orally every 24 hours | 40 mg/kg orally every 24 hours | ||
| Acetaminophen | 300 mg/kg orally every 24 hours | 300 mg/kg orally every 24 hours |
P3: Survival Surgery/Survival Procedures Estimated to Cause MILD Post-Surgery/Post-Procedural Pain:
(Examples: Placement of subcutaneous tumors or subcutaneous osmotic pumps; placement of chronic indwelling vascular
cannulaes; orchiectomy)
SQ=subcutaneous
IM=intramuscular
| DRUG | MOUSE | RAT | HAMSTER | GERBIL | GUINEA PIG |
| Ketoprofen | 5mg/kg SQ SID | 5mg/kg SQ SID | 5mg/kg SQ SID | 5mg/kg SQ SID | 5mg/kg SQ SID |
| Flunixin | 2.5 mg/kg IM every 12 hours | 2.5 mg/kg IM every 12 hours | |||
| Aspirin | 300 mg/kg orally every 24 hours | 100 mg/kg orally every 24 hours | 86 mg/kg orally every 24 hours | ||
| Ibuprofen | 7.5 mg/kg orally every 24 hours | 30 mg/kg orally every 24 hours | |||
| Phenylbutazone | 30 mg/kg orally every 24 hours | 20 mg/kg orally every 24 hours | 40 mg/kg orally every 24 hours | ||
| Acetaminophen | 300 mg/kg orally every 24 hours | 300 mg/kg orally every 24 hours |
SQ=subcutaneous
IM=intramuscular
For purposes of administering a drug via the drinking water:
*Animals that have been subjected to a painful procedure/surgery will not drink the “normal” amount of water for a minimum of 24 hours post-surgery/post-procedure. It is estimated that normal water consumption will be reduced by at least 50%.
Amount of orally-administered drug to mix/administer per ml of drinking water:
| MOUSE | RAT | HAMSTER | GERBIL | GUINEA PIG | |
| Normal* Daily Water Consumption | 15 ml/100 gm body weight/day | 8-11 ml/100 gm body weight/day | 30 ml/day | 4-7 ml/100gm body weight/day | 10 ml/100 gm body weight/day |
*Animals that have been subjected to a painful procedure/surgery will not drink the “normal” amount of water for a minimum of 24 hours post-surgery/post-procedure. It is estimated that normal water consumption will be reduced by at least 50%.
Amount of orally-administered drug to mix/administer per ml of drinking water:
| DRUG | Rat- Normal Water Consumption | Rat-50% Decrease in Water Consumption | Mouse-Normal Water Consumption | Mouse-50% Decrease in Water Consumption | Guinea Pig-Normal Water Consumption | Guinea Pig-50% Decrease in Water Consumption |
| Aspirin | 0.9 mg/ml | 1.8 mg/ml | 2 mg/ml | 4 mg/ml | 0.9 mg/ml | 1.8 mg/ml |
| Ibuprofen | 0.3 mg/ml | 0.6 mg/ml | .05 mg/ml | 0.1 mg/ml | ||
| Phenylbutazone | 0.2 mg/ml | 0.4 mg/ml | 0.2 mg/ml | 0.4 mg/ml | 0.4 mg/ml | 0.8 mg/ml |
| Acetaminophen | 2.7 mg/ml | 5.4 mg/ml | 2.0 mg/ml | 4.0 mg/ml |
Local Anesthetics:
Even with general anesthesia, the topical, subcutaneous (at surgical incision site), intra-articular, etc. administration of a local
anesthetic is recommended in order to provide additional post-surgical analgesia. Local anesthetics should not be used alone to provide
post-surgical/post-procedural analgesia.
* Duration is given for larger species. Duration in rodents (with their higher metabolic rate) should be considered less.
| Agent | Potency (Procaine=1) | Onset | Duration* | Topical Use | Infiltration Use | Nerve Block Use |
| Procaine (Novacaine) | 1 | Slow | 30-90 minutes | - | 1-2% | 1-2% |
| Chloroprocaine (Nesacaine) | 2.4:1 | Fast | Up to 2 hours | - | 1-2% | 1-2% |
| Lidocaine (Xylocaine) | 2:1 | Fast | 2 hours | 2-4% | 0.5-2% | 0.5-2% |
| Mipivacaine (Carbocaine) | 2.5:1 | Fast | 2-4 hours | - | 1-2% | 1-2% |
| Tetracaine (Ponticaine) | 12:1 | Slow | 3-8 hours | 0.2% | 0.1% | 0.1% |
| Hexycaine (Cyclaine) | 1-2:1 | Fast | 3-6 hours | 5% | 0.5-1% | 2% |
| Bupivicaine (Marcaine) | 8:1 | Intermediate | 24 -48 hours | - | 0.25% | 0.5% |
* Duration is given for larger species. Duration in rodents (with their higher metabolic rate) should be considered less.

