A MARKED increase in the concentration in the plasma of cholesterol and other lipoids can be induced in rabbits by feeding excessive amounts of cholesterol in the diet [Wacker and Hueck, 1913;Weinhouse and Hirsch, 1940]. The animals develop a visible lipaemia, which, unlike the lipaemia occurring normally during the absorption of a fat meal, does not disappear spontaneously in the intervals between feeding.The plasma turbidity in normal alimentary lipaemia is due to the entry of chyle, containing visible fat particles, into the blood stream from the thoracic duct [Gage and Fish, 1924]. These particles disappear from the blood following the injection of heparin [Hahn, 1943], and there is now evidence that a process analogous to this clearing reaction may be responsible for their rapid disappearance under physiological conditions [Robinson, Jeffries and French, 1954]. The persistence oflipeemia in rabbits fed cholesterol suggests that in these animals there is a deficiency in the normal mechanism for removal of particulate lipoid from the blood, and experiments were therefore undertaken to determine whether this could be attributed to the effects of cholesterol on the heparin clearing reaction.
METHODSThe method of measuring clearing activity at 370 C. by the addition of chyle to plasma, and the techniques of collecting chyle and of obtaining plasma in the rat, have been described previously [French, Robinson and Florey, 1953; Robinson, Jeifries and French, 1954].Rabbits were fed cholesterol in short-term experiments by introducing a measured volume of a 5 per cent solution of cholesterol in olive oil through a duodenal fistula, or, in long-term experiments, by mixing 15 ml. of a 5 per cent solution of cholesterol in olive oil with the daily ration of 80 g. " Oxo " rabbit pellets. Chyle was obtained from rabbits by cannulation of the thoracic duct in the neck, or, when small volumes only were required, by aspiration from the cysterna chyli. Blood in small quantities was withdrawn from the lateral ear vein. Larger volumes were obtained by exsanguination through a No. 3 polythene cannula inserted into the abdominal aorta under ether aneesthesia. Injections of heparin were made into the lateral ear vein.