Pilocarpine (1) and other secretory stimulants (2-4) are known to increase the enzyme content of the blood and lymph. Numerous other investigations have indicated that these enzymes originate from the pancreas and enter the blood to a large extent by means of the lymphatic pathway (5-8). Recently, it has been shown that rat liver synthesized amylase in isolated perfusion experiments (9, 10). Relatively little information, however, is available on the contribution of hepatic lymph to the increased enzyme levels observed in the thoracic duct lymph after the administration of various secretory stimulants. In this series of experiments, enzyme levels were studied in normal dogs as well as in pancreatectomized dogs in order to evaluate the effect of pilocarpine on the production of serum enzymes by the liver as well as the pancreas. In addition, the enzyme levels of the hepatic and portal blood were studied in order to determine the relative importance of the venous versus the lymphatic pathways.Materials and Methods. Two series of experiments were performed. Mongrel dogs of either sex, weighing 15-20 kg, were used in these experiments. Six experiments were done in the first control series. The animals were subjected to laparotomy under pentobarbital anesthesia and controlled endo tracheal ven tilation. Lymphatic vessels were identified in the hilum of the liver after injecting Evan's blue dye subcapsularly in the liver. The efferent lymphatics from the hepatic lymph node were stripped of the surrounding tissue, and the largest one was incised. A polyethylene tube was inserted toward the liver, being held in place by ligatures.The remaining efferent lymphatics from the hepatic lymph node, as well as those * Supported by Grants AM-02723, HE-04182 from the National Institutes of Health. coming towards it from the direction of the pancreas and duodenum, were ligated ( 11). The right side of the thorax was then opened along the ninth intercostal space. A polyethylene tube was introduced into the inferior vena cava and passed down into the hepatic vein. This tube was available for sampling of hepatic venous blood.Cannulation for sampling of the portal vein was accomplished by passing a similar tube through the superior mesenteric vein into the portal vein. Peripheral blood was sampled from the femoral vein.Two control samples of heparinized lymph and blood were taken simultaneously at 20-min intervals from each of the catheters. Pilocarpine (20 mg diluted in 200 ml of normal saline) solution was administered intravenously by drip over a period of 40 min. Four samples of lymph and blood, each simultaneously at 20-min intervals, were taken after pilocarpine infusion (Table I A
and B).The lymph samples were collected continuously throughout each 20-min interval.In the second series of four experiments, hepatic lymphatic cannulation was done immediately after subjecting the animal to ,total pancreatectomy. Three samples of hepatic lymph and peripheral venous blood, each obtained at 15-min intervals, were taken simultaneousl...