Since Hahn demonstrated the clearing of alimentary lipemia by the intravenous injection of heparin, many excellent studies have been done on lipoprotein lipase (LPL). In these studies, however, LPL activities were compared in normal and pathological conditions at a certain time after heparin injection. If the level of LPL activity in the circulating blood changes continuously after heparin injection, under the influences of production and inactivation of LPL, it may be much more useful, under certain circumnstances, to measure the rate of change as well as the amount of such activity.One of the authors reported previously (1) the method of estimating the release or production rate and inactivation rate of LPL after heparin injection. This report will present the data on the metabolism of LPL activity in blood after the intravenous injection of heparin in normal subjects and patients with liver diseases, obesity, and coronary sclerosis, and in some animals.
EXPERIMENTAL METHODSPreparation of materials. Human subjects and experimental animals were fasted overnight before the experiment. Experimental animals (dogs and rabbits) were anesthetized with pentobarbital sodium (Nembutal) just before use.Heparin injection. The doses of heparin injected were 0.1 mg per kg of body weight throughout the experiment. The injection was done rapidly into the antecubital vein in men and dogs and into the ear vein in rabbits.Withdrawals of blood. At certain intervals after the injection, blood was withdrawn from the antecubital vein in human subj ects, from the femoral vein in dogs, and by heart puncture in rabbits. The blood specimen was immediately added to 1/9 vol of Y/10 M sodium oxalate solution kept in an ice-water bath.Assay of LPL activity. The test plasma weas obtained by centrifuging the blood for 5 minutes at 4,000 rpm in the cold. The substrate consisted of 0.1 vol of 2.5%o * Supported in part by a grant-in-aid for research from the Ministry of Education and a grant-in-aid for atherosclerosis study from the Ministry of \Velfare. Immediately after the mixing of 1 ml of test plasma with 1.5 ml of substrate, 1.0 ml of the mixture was pipetted into Dole's extraction mixture, and the remainder was incubated at 390 C for 30 minutes. The LPL activity was expressed by the difference of FFA concentrations (microequivalents per liter) in the mixture before and after the incubation. FFA was measured by Dole's method (2). The details of our method were discussed in the previous paper (1).
RESULTS AND DISCUSSIONLPL activity curve in normnal human beings, dogs, and rabbits. Eight healthy men aged 25 to 35 years, 4 dogs, and 3 rabbits were used. Figures 1 and 2 show the changes of LPL activity as a function of time in human subjects and dogs, respectively. Similar changes of LPL activity were observed also in rabbits. The rapid rise in LPL activity was observed immediately after heparin injection, and the peak was after about 9 minutes in human subjects, about 8 minutes in dogs, and about 3 minutes in rabbits. Thereafter, the activity...