. Correlating structure with solute and water transport in a chronic model of peritoneal inflammation. Am J Physiol Renal Physiol 290: F232-F240, 2006. First published August 23, 2005 doi:10.1152/ajprenal.00211.2005.-To study the process of chronic peritoneal inflammation from sterile solutions, we established an animal model to link structural changes with solute and water transport. Filtered solutions containing 4% N-acetylglucosamine (NAG) or 4% glucose (G) were injected intraperitoneally daily in 200-to 300-g rats and compared with controls (C). After 2 mo, each animal underwent transport studies using a chamber affixed to the parietal peritoneum to determine small-solute and protein mass transfer, osmotic filtration, and hydraulic flow. After euthanasia, parietal tissues were sampled for histological analysis, which demonstrated significant differences in peritoneal thickness (m; C, 42.6 Ϯ 7.5; G, 80.4 Ϯ 22.3; NAG, 450 Ϯ 104; P Ͻ 0.05). Staining for VEGF correlated with CD-31 vessel counts (no./mm 2 : C, 53.1 Ϯ 16.1; G, 166 Ϯ 32; NAG, 183 Ϯ 32; P Ͻ 0.05 ). Tissue analysis showed treatment effects on tissue hyaluronan (g/g: C, 962 Ϯ 73; G, 1,169 Ϯ 69; NAG, 1,428 Ϯ 69; P Ͻ 0.05) and collagen (g/g: C, 56.9 Ϯ 12.0; G, 107 Ϯ 12; NAG, 97.6 Ϯ 11.4; P Ͻ 0.05) but not sulfated glycosaminoglycan. Transport experiments revealed no significant differences in mannitol transfer or osmotic flow. Changes were seen in hydrostatic pressure-driven flux (l ⅐ min Ϫ1 ⅐ cm Ϫ2 : C, 0.676 Ϯ 0.133; G, 0.317 Ϯ 0.124; NAG, 0.284 Ϯ 0.117; P Ͻ 0.05) and albumin transfer (l ⅐ min Ϫ1 ⅐ cm Ϫ2 : C, 0.331 Ϯ 0.028; G, 0.286 Ϯ 0.026; NAG, 0.229 Ϯ 0.025; P Ͻ 0.04). We conclude that alteration of the interstitial matrix correlates with diminished hydraulic conductivity and macromolecular transport.