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However, the biocompatibility of a<jats:styled-content style=\"fixed-case\">HPG<\/jats:styled-content>\u2010based<jats:styled-content style=\"fixed-case\">PD<\/jats:styled-content>solution (<jats:styled-content style=\"fixed-case\">HPG<\/jats:styled-content>) in subjects with MetS has not been investigated. This study compared the local and systemic effects of a<jats:styled-content style=\"fixed-case\">HPG<\/jats:styled-content>solution with conventional physioneal (<jats:styled-content style=\"fixed-case\">PYS<\/jats:styled-content>) and icodextrin (<jats:styled-content style=\"fixed-case\">ICO<\/jats:styled-content>)<jats:styled-content style=\"fixed-case\">PD<\/jats:styled-content>solutions in rats with MetS. Obese type 2 diabetic<jats:styled-content style=\"fixed-case\">ZSF<\/jats:styled-content>1 rats received a daily intraperitoneal injection of<jats:styled-content style=\"fixed-case\">PD<\/jats:styled-content>solutions (10\u00a0<jats:styled-content style=\"fixed-case\">mL<\/jats:styled-content>) for 3\u00a0months. The peritoneal membrane (<jats:styled-content style=\"fixed-case\">PM<\/jats:styled-content>) function was determined by ultrafiltration (<jats:styled-content style=\"fixed-case\">UF<\/jats:styled-content>), and the systemic responses were determined by profiling blood metabolic substances, cytokines and oxidative status. Tissue damage was assessed by histology. At the end of the 3\u2010month treatment with<jats:styled-content style=\"fixed-case\">PD<\/jats:styled-content>solutions,<jats:styled-content style=\"fixed-case\">PM<\/jats:styled-content>damage and<jats:styled-content style=\"fixed-case\">UF<\/jats:styled-content>loss in both the<jats:styled-content style=\"fixed-case\">PYS<\/jats:styled-content>and<jats:styled-content style=\"fixed-case\">ICO<\/jats:styled-content>groups were greater than those in the<jats:styled-content style=\"fixed-case\">HPG<\/jats:styled-content>group. Blood analyses showed that compared to the baseline control, the rats in the<jats:styled-content style=\"fixed-case\">HPG<\/jats:styled-content>group exhibited a significant decrease only in serum albumin and<jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\u20106 and a minor glomerular injury, whereas in both the<jats:styled-content style=\"fixed-case\">PYS<\/jats:styled-content>and<jats:styled-content style=\"fixed-case\">ICO<\/jats:styled-content>groups, there were more significant decreases in serum albumin, antioxidant activity,<jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\u20106,<jats:styled-content style=\"fixed-case\">KC<\/jats:styled-content>\/<jats:styled-content style=\"fixed-case\">GRO<\/jats:styled-content>(<jats:styled-content style=\"fixed-case\">CXCL<\/jats:styled-content>1) and<jats:styled-content style=\"fixed-case\">TNF<\/jats:styled-content>\u2010\u03b1 (in<jats:styled-content style=\"fixed-case\">ICO<\/jats:styled-content>only) as well as a more substantial glomerular injury compared to the<jats:styled-content style=\"fixed-case\">HPG<\/jats:styled-content>group. Furthermore,<jats:styled-content style=\"fixed-case\">PYS<\/jats:styled-content>increased serum creatinine, serum glucose and urine production. In conclusion, compared to<jats:styled-content style=\"fixed-case\">PYS<\/jats:styled-content>or<jats:styled-content style=\"fixed-case\">ICO<\/jats:styled-content>solutions, the<jats:styled-content style=\"fixed-case\">HPG<\/jats:styled-content>solution had less adverse effects locally on the<jats:styled-content style=\"fixed-case\">PM<\/jats:styled-content>and systemically on distant organs (e.g. kidneys) and the plasma oxidative status in rats with MetS.<\/jats:p>","DOI":"10.1111\/bcpt.13038","type":"journal-article","created":{"date-parts":[[2018,5,12]],"date-time":"2018-05-12T23:00:31Z","timestamp":1526166031000},"page":"494-503","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":8,"title":["Peritoneal and Systemic Responses of Obese Type<scp>II<\/scp>Diabetic Rats to Chronic Exposure to a Hyperbranched Polyglycerol\u2010Based Dialysis Solution"],"prefix":"10.1111","volume":"123","author":[{"given":"Bo","family":"La 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