Abstract
In order to study the in vivo clearance of model immune complexes, radiolabelled aggregated rat gamma globulin (ARG), aggregated human serum albumin (AHSA) and 59Fe-tagged erythrocytes were intravenously injected into control, and insulin-deficient and insulin-treated rats with streptozotocin-induced diabetes. Plasma clearance and organ uptake were measured. The rate of plasma clearance of ARG was studied at trace (18 micrograms) and near-saturating (10 mg) doses. AHSA was cleared slowly from the circulation, and there were no observed differences between the study groups. At trace doses of ARG, plasma clearance was similar in the three animal groups; however, at the higher dose, clearance was significantly slowed in both insulin-deficient and insulin-treated diabetic rats as compared to control animals (P less than 0.01). Organ uptake of AHSA was similar in all study groups. Hepatic uptake at 10 min after injection of ARG was comparable in control and insulin-deficient rats; however, the rate of removal from the liver was significantly slowed in these diabetic rats. Insulin-treated diabetic rats had less hepatic-associated ARG, as compared to the other animals, throughout the study. Splenic uptake of ARG was comparable in both control and insulin-treated animals, but was significantly less in insulin-deficient diabetic animals. These alterations in plasma clearance and tissue localization of ARG in diabetic animals suggest that abnormal phagocytosis may contribute to the elevated levels of circulating immune complexes that have been demonstrated in diabetic subjects.
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Selected References
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- Abrass C. K. Evaluation of the presence of circulating immune complexes and their relationship to glomerular IgG deposits in streptozotocin-induced diabetic rats. Clin Exp Immunol. 1984 Jul;57(1):17–24. [PMC free article] [PubMed] [Google Scholar]
- Abrass C. K., Heber D., Lieberman J. Circulating immune complexes in patients with diabetes mellitus. Clin Exp Immunol. 1983 Apr;52(1):164–172. [PMC free article] [PubMed] [Google Scholar]
- Abrass C. K., Hori M. Alterations in Fc receptor function of macrophages from streptozotocin-induced diabetic rats. J Immunol. 1984 Sep;133(3):1307–1312. [PubMed] [Google Scholar]
- Bar R. S., Kahn C. R., Koren H. S. Insulin inhibition of antibody-dependent cytoxicity and insulin receptors in macrophages. Nature. 1977 Feb 17;265(5595):632–635. doi: 10.1038/265632a0. [DOI] [PubMed] [Google Scholar]
- Brown E. J., Hosea S. W., Frank M. M. The role of the spleen in experimental pneumococcal bacteremia. J Clin Invest. 1981 Apr;67(4):975–982. doi: 10.1172/JCI110148. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hill H. R., Augustine N. H., Rallison M. L., Santos J. I. Defective monocyte chemotactic responses in diabetes mellitus. J Clin Immunol. 1983 Jan;3(1):70–77. doi: 10.1007/BF00919141. [DOI] [PubMed] [Google Scholar]
- Irvine W. J., Al-Khateeb S. F., Di Mario U., Feek C. M., Gray R. S., Edmond B., Duncan L. J. Soluble immune complexes in the sera of newly diagnosed insulin-dependent diabetics and in treated diabetics. Clin Exp Immunol. 1977 Oct;30(1):16–21. [PMC free article] [PubMed] [Google Scholar]
- Irvine W. J., Di Mario U., Guy K., Iavicoli M., Pozzilli P., Lumbroso B., Andreani D. Immune complexes and diabetic microangiopathy. J Clin Lab Immunol. 1978 Nov;1(3):187–191. [PubMed] [Google Scholar]
- Kadish A. H., Hall D. A. A new method for the continuous monitoring of blood glucose by measurement of dissolved oxygen. Clin Chem. 1965 Sep;11(9):869–875. [PubMed] [Google Scholar]
- Kitahara M., Eyre H. J., Lynch R. E., Rallison M. L., Hill H. R. Metabolic activity of diabetic monocytes. Diabetes. 1980 Apr;29(4):251–256. doi: 10.2337/diab.29.4.251. [DOI] [PubMed] [Google Scholar]
- Knutson D. W., Chia D., Barnett E. V., Levy L. Blood clearance and tissue localization of soluble aggregates of IgG in NZB/W and NZB mice. Immunology. 1985 Mar;54(3):439–448. [PMC free article] [PubMed] [Google Scholar]
- Knutson D. W., Kijlstra A., Lentz H., van Es L. A. Isolation of stable aggregates of IgG by zonal ultracentrifugation in sucrose gradients containing albumin. Immunol Commun. 1979;8(3):337–345. doi: 10.3109/08820137909050047. [DOI] [PubMed] [Google Scholar]
- Lawrence S., Charlesworth J. A., Pussell B. A., Campbell L. V., Kotowicz M. A. Factors influencing reticulophagocytic function in insulin-treated diabetes. Diabetes. 1984 Sep;33(9):813–818. doi: 10.2337/diab.33.9.813. [DOI] [PubMed] [Google Scholar]
- Mantovani B., Rabinovitch M., Nussenzweig V. Phagocytosis of immune complexes by macrophages. Different roles of the macrophage receptor sites for complement (C3) and for immunoglobulin (IgG). J Exp Med. 1972 Apr 1;135(4):780–792. doi: 10.1084/jem.135.4.780. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Mauer S. M., Michael A. F., Fish A. J., Brown D. M. Spontaneous immunoglobulin and complement deposition in glomeruli of diabetic rats. Lab Invest. 1972 Nov;27(5):488–494. [PubMed] [Google Scholar]
- McDonald T. L., Quenette L., Phares C. K. Isolation and quantitation of immune complexes in diabetic syrian hamsters: a chronological study. J Clin Lab Immunol. 1983 Jul;11(3):129–133. [PubMed] [Google Scholar]
- Minick C. R., Murphy G. E. Experimental induction of atheroarteriosclerosis by the synergy of allergic injury to arteries and lipid-rich diet. II. Effect of repeatedly injected foreign protein in rabbits fed a lipid-rich, cholesterol-poor diet. Am J Pathol. 1973 Nov;73(2):265–300. [PMC free article] [PubMed] [Google Scholar]
- Ptak W., Rewicka M., Bielecka J. Macrophage function in alloxan-diabetic mice: expression and activity of Fc receptors. J Clin Lab Immunol. 1981 Mar;5(2):121–124. [PubMed] [Google Scholar]
- Rhodes J. Modulation of macrophage Fc receptor expression in vitro by insulin and cyclic nucleotides. Nature. 1975 Oct 16;257(5527):597–599. doi: 10.1038/257597a0. [DOI] [PubMed] [Google Scholar]
- Subbaiah P. V., Bagdade J. D. Host defense mellitus: defective membrane synthesis during phagocytosis. Horm Metab Res. 1982 Sep;14(9):445–448. doi: 10.1055/s-2007-1019044. [DOI] [PubMed] [Google Scholar]
