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MEASUREMENTS OF RETICULOENDOTHEILLA SYSTEM PHAGOCYTIC ACTIVITY IN THE RAT AFTER TREATMENT WITH SILICA, LIPOSOMES, AND CYCLOSPORINE
Author(s) -
Robert M. Merion
Publication year - 1985
Publication title -
transplantation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.45
H-Index - 204
eISSN - 1534-6080
pISSN - 0041-1337
DOI - 10.1097/00007890-198507000-00017
Subject(s) - mononuclear phagocyte system , phagocytosis , liposome , spleen , in vivo , phospholipid , distribution (mathematics) , endocrinology , medicine , albumin , pharmacology , chemistry , immunology , biology , biochemistry , mathematical analysis , microbiology and biotechnology , mathematics , membrane
Reticuloendothelial system phagocytosis was evaluated in vivo by the clearance and tissue distribution of 99mTc-albumin millimicrospheres in rats. Administration of i.p. silica 2 days prior to clearance measurement increased the half-life of millimicrospheres 24% compared with control animals (P less than 0.01). Impairment of phagocytic activity was maintained at 5 days to 22% over control values (P less than 0.01). Tissue distribution studies showed that liver uptake was reduced and splenic and pulmonary uptake was increased compared with control. Cyclosporine i.v. increased half-life by 14% 1 hr after administration )P = NS) and half-life returned to control values by 8 hr. Hepatosplenic shift was less marked than after silica treatment. Phospholipid liposomes i.v. produced prompt impairment of millimicrosphere clearance after 1 hr; half-life was prolonged 46% over control values (P less than 0.001 vs. control) and marked radiolabel shift to the spleen and lung was seen. Measurements done 18 hr after a dose of liposomes revealed an increase of 55% over control half-life (P less than 0.001). Liposomes appear to be potent, nontoxic--and, in some cases, reversible agents--for blockade of reticuloendothelial phagocytosis and examination of non-phagocytic reticuloendothelial functions. These results help to explain some of the results obtained in pancreatic islet grafting and suggest that phospholipid liposomes may be useful in this form of transplantation.

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