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Each rat was administered a placebo (the vehicle) or one of three active doses of a compound.
MTX/kg per rat was administered in 200 μl saline on days 8, 10 and 12, and rats were sacrificed on day 20 after pristane induction [ 26].
Therefore, each rat was administered s.c. 5 ml of warmed lactated ringer's solution (Ringer-Lactat nach Hartmann B. Braun, B. Braun, Melsungen, Germany) one hour after induction of anaesthesia.
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Adenoviral vectors (3 × 10 pfu per rat) were administered by direct injection into the left ventricular free wall with a 30-gauge needle.
The plasma of stress adapted rats was administered to naïve rats before subjecting to acute stress.
A group of 12-week-old male WKY rats was administered ACTH (0.2 mg/kg/day) subcutaneously for 4 weeks.
Rats were administered MDMA (20 mg/kg, s.c).
In Experiment 1, female rats were administered (P.O).
Eight-week-old rats were administered with STZ, which induced pancreatic injury and hyperglycemia.
Female adolescent Sprague Dawley rats were administered morphine at increasing doses (5 25 mg/kg, s.c).
The rats were administered, single dose of streptozotocin (STZ) for the induction of diabetes.
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