Gibson & Wiseman (1951) showed that when amino-acids were injected into the lumen of the intestine of the rat, the L-enantiomorph disappeared at a faster rate than the D-enantiomorph, and they postulated a stereochemically specific mechanism for the absorption of L-amino-acids. In support of this, Clarke, Gibson, Smyth & Wiseman (1951) showed that L-amino-acids also disappeared faster than D-amino-acids from the Thiry-Vella loop in the dog, and Wiseman (1953) showed with an in vitro technique that L-amino-acids could be transferred by the intestine against a concentration gradient, whereas D-amino-acids could not. While these experiments furnish strong evidence for the existence of a stereochemicaily specific mechanism for absorption of amino-acids from the intestine, they fail to supply any information about the concentration of the D-and L-amino-acids in the blood stream during absorption, and the present work was undertaken to investigate this aspect of the problem. Preliminary accounts of the results have been given by Matthews & Smyth (1952, 1953.
METHODSThe experiments were done on cats anaesthetized with pentobarbitone sodium. The carotid artery was cannulated by the procedure described by Crampton & Smyth (1953), which enables blood to be collected from or introduced into the carotid artery with simultaneous measurement of the blood pressure. A loop of the intestine was selected near to the caecum and spread out so that the arterial and venous supply could be inspected. A part of the intestine drained by a suitable vein was chosen, and this section of intestine was cannulated, washed out with warm saline (0-9 % NaCI) and tied off at each end. The vein draining the loop was now prepared for cannulation without any interference with the blood flow. There was thus an isolated section of intestine about 30 cm long with intact blood supply, and so arranged that on cannulation of the vein draining the loop, the blood from this section of the intestine could be collected. The loop of intestine was arranged on a heated plate and protected with a Perspex cover, so that it could be kept at a temperature of 370 C, moistened with saline and inspected during the experiment.The animal was then heparinized and the blood pressure measured in the carotid artery. Blood (30-50 ml.) was withdrawn from the carotid artery till the blood pressure had fallen to about 50 mm of mercury. The object of this was to reduce the rate of blood flow. Although this must