Research in veterinary science
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The depolarising muscle relaxant suxamethonium (0.3 mg kg-1) and the non-depolarising muscle relaxant pipecuronium (0.05 mg kg-1) were administered to four dogs. In the first series of experiments pipecuronium was administered intravenously, followed at 50 per cent of return of neuromuscular activity by suxamethonium. At 50 per cent return of activity atropine and neostigmine were administered to reverse the neuromuscular block. ⋯ At 50 per cent recovery atropine and neostigmine were given. In the first series of experiments the time for the onset of suxamethonium block was significantly increased after prior administration of pipecuronium. However, in the second series of experiments the prior administration of suxamethonium had no significant effect on the duration of action of pipecuronium.
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Storage of plasma at -30 degrees C, with no prior treatment, resulted in significant (P less than 0.01) reductions in the biological and immunological activities of oxytocin after 10 days and further reductions after 20 days. Acidification with 0.1 N hydrochloric acid, or snap-freezing in solid carbon dioxide-acetone, before storage afforded some protection against these losses and a combination of both treatments preserved the biological and immunological activities for 20 days despite thawing and refreezing after 10 days.
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The non-depolarising muscle relaxants alcuronium (0.1 mg kg-1), gallamine (1 mg kg-1) and pancuronium (0.06 mg kg-1) were administered to six dogs. At 50 per cent return of neuromuscular activity, as measured by the train-of-four technique, the depolarising muscle relaxant suxamethonium (0.3 mg kg-1) was injected intravenously. At 50 per cent return of neuromuscular activity, atropine and neostigmine were administered to reverse the neuromuscular block. The duration of action of suxamethonium was reduced by each of the non-depolarising muscle relaxants.
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The depolarising muscle relaxant suxamethonium (0.3 mg kg-1) was administered to six dogs. At 50 per cent return of the neuromuscular activity, as measured by the train-of-four technique, a non-depolarising muscle relaxant was administered. ⋯ At the 50 per cent return of neuromuscular activity, atropine and neostigmine were administered to reverse the neuromuscular block. The duration of action of the three non-depolarising relaxants was reduced by the prior administration of suxamethonium.
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Ears of calves were made hyperaemic by using a rubefacient. Blood from the hyperaemic ear was sampled in capillary tubes and analysed for pO2, pCO2, pH and bicarbonate. ⋯ For pO2 and bicarbonate values a highly significant correlation was found between the two sets of results (P less than 0.001); for pH and pCO2 close correlations were found (P less than 0.01). The results indicate that blood samples from arterialised capillaries can be used as a substitute for blood obtained by arterial puncture.