Late phase III acts as a retroperistaltic pump, retropelling duodenal contents to the stomach. In this physiologic duodenogastric reflux. bile is avoided by deviation to the gallbladder, probably by a phase lll-associated occlusion of the sphincter Oddi.
Normal and reticuloendothelial system (RES) stimulated rats were examined with dynamic liver RES scintigraphy using a computerized gamma camera. 99Tcm-labelled albumin colloid, albures (radius 250 nm) or nanocoll (radius 25 nm), or both were used as test substances to study the kinetics of vascular clearance after RES stimulation. Registrations were made of 30 s per frame for 5 min and 300 s per frame for 15 min or 25 min and a region of interest (ROI) was indicated over the liver. Whole body and liver RES clearance rate constants (k) were calculated from the liver uptake vs time curve. Liver parenchyma blood flow was estimated with 133Xe washout technique. The blood clearance rate constant of albures in non-activated rats was twice that for nanocoll (1.08 +/- 0.05 vs 0.49 +/- 0.02 10(-2)s-1). There was no mutual interaction between the two colloids, implying that they may be eliminated from the blood-stream by slightly different processes. In zymosan-stimulated animals, nanocoll given in a single injection showed a significantly increased k-value. Neither the albures clearance rate constant nor the nanocoll/albures k-value ratio revealed RES macrophage activation. By contrast the nanocoll/albures ratio, calculated for the liver, rose significantly. The final colloid uptake in the liver revealed RES macrophage activation. No changes in liver parenchyma blood flow per g tissue could be registered after administration of zymosan. The nanocoll and albures colloid particles did not impair the normal liver parenchyma blood flow.(ABSTRACT TRUNCATED AT 250 WORDS)
The liver consists essentially of two compartments, parenchymal cells (PC) and non parenchymal cells (NPC) i.e. Kupffer cells, endothelial cells, fat storing cells and pit cells. PC remain after transplantation but NPC are eventually exchanged with host cells. Dynamic liver scintigraphy with albumin colloid, extracted by NPC, and IODIDA, extracted by PC, were tested to evaluate function as determined by clearance rates in these two cellular compartments. Experimental liver transplantation was performed in 15 syngeneic rats. Following transplantation, we performed dynamic liver scintigraphy with 0.5 ml 5 MBq 9 9mTc-Nanocoll and 0.5 ml 20 MBq 99 mTc-IODIDA, 10 s per frame, 30 min for each examination. Percentage clearance rate, per minute was calculated from uptake curves over the liver. Uptake curves were nearly exponential and clearance rates could be estimated from a logarithmic plot of uptake versus time. The clearance rate was 25 ± 4 o/o per min (mean± SD) for NPC and 32 ± 15 o/o per min for PC in controls. After liver transplantation it was 31 ± 7 o/o per min for NPC and 30 ± 15 o/o per min for PC. Dynamic liver scintigraphy with 99 mTc-Nanocoii and 9 9mTc-IODIDA alloweds a separate assessment of the function of PC and NPC after experimental liver transplantation in rats.
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