METHODSHens and cockerels (White Leghorns and Rhode Islands obtained commercially), weighing from 1.0 to 2.0 kg, were used. The birds were anaesthetized with pentobarbitone sodium (55 mg/kg) and received heparin 1,000 u./kg. Intravenous injections were given into the brachial vein and the blood samples were collected from a common carotid artery. Bufo marinus of either sex, weighing 150-300 g, obtained from the West Indies were used. Anaesthesia was produced by immersing the toads in a 0.2% solution of MS222 (Sandoz). Intravenous injections were given into the femoral vein and the blood samples were collected from the carotid arch after heparin (1,000 u./kg) had been administered. Adult albino rats of both sexes, weighing from 150 to 200 g were used for assays.
Assay of antidiuretic activityThe original technique of Jeffers, Livezey & Austin (1942) was employed with slight modifications. The rats were fasted overnight but were allowed to drink water. On the day of the assay warm tap water 50 ml./kg body weight was given by stomach tube and 45 min later the same volume of 12% ethanol by the same route. If the depth of anaesthesia produced by ethanol was not adequate for surgical operations, 3 mg of pentobarbitone sodium was administered intraperitoneally. As soon as surgical anaesthesia had been obtained a jugular vein was cannulated, as were the stomach and the urinary bladder, and the penile urethra was ligatured. Tracheotomy was also performed to ensure a free airway. The rat was then laid on its back