The objective of this study was to establish an effective post-operative an
algesic regimen tor Spraguc-Dawley (SD) and Dark Agouti (DA) rats. Buprenor
phine (0.01 or 0.05 mg/kg), a partial mu opioid agonist, was administered s
ubcutaneously immediately on completion of a standardized surgical procedur
e, involving anaesthesia, laparotomy and visceral manipulation. Two of tile
four treatment groups and the saline control group received a second injec
tion 9h later. Behavioural observations by three independent observers prov
ided no information in assessing pain in this model. All rats lost weight,
consumed less food and water after surgery. On the first day, both SD and D
A rats receiving buprenorphine lost less weight than untreated control grou
ps. Using weight loss as an efficacy criterion, low-dose buprenorphine, giv
en once or twice, provided effective analgesia in SD rats. A higher single
dose provided no additional benefit and a second dose was detrimental, redu
cing body weight and food intake. In DR rats, the high dose, given twice, a
ppeared to be more effective than the lower dose. All DA cage cohorts consu
med < 10% pre-operative food despite buprenorphine treatment, suggesting a
higher dosage may be necessary. However, all SD and 80% DA rats who receive
d no buprenorphine gained body weight on the second day, whereas most of th
e buprenorphine-treated rats continued to lose weight for another 2 days, d
espite increased food consumption by both strains. Buprenorphine may advers
ely affect intestinal function over a number of days due to its enterohepat
ic circulation; this effect may be more severe in DA rats. Adverse metaboli
c effects of buprenorphine and other opioids may preclude their use in the
future if it can be shown that non-steroidal anti-inflammatory drugs (NSAID
s) provide equally effective analgesia.