Transport asymmetry in peritoneal dialysis: application of a serial heteroporous peritoneal membrane model.
نویسندگان
چکیده
The transport of macromolecules during peritoneal dialysis is highly selective when they move from blood to dialysate but nearly completely unselective in the opposite direction. Aiming at describing this asymmetry, we modeled the peritoneal barrier as a series arrangement of two heteroporous membranes. First a three-pore membrane was considered, crossed by small [radius of the small pore (r(s)) approximately 45 A], large [radius of the large pore (r(L)) approximately 250 A], and transcellular pores accounting for 90, 8, and 2% to the hydraulic conductance, respectively, and with a corresponding pore area over diffusion distance (A(0)/Delta x) set to 50,000 cm. We calculated the second membrane parameters by fitting simultaneously the bidirectional clearance of molecules ranging from sucrose [molecular weight = 360, permeating solute radius (a(e)) approximately 5 A] to alpha(2)-macroglobulin (molecular weight = 820,000, a(e) approximately 90 A). The results describe a second two-pore membrane with very large pores (r(L) approximately 2,300 A) accounting for 95% of the hydraulic conductance, minor populations of small (r(s) approximately 67 A) and transcellular pores (3 and 2%, respectively), and an A(0)/Delta x approximately 65,000 cm. The estimated peritoneal lymph flow is approximately 0.3 ml/min. The two membranes can be identified as the capillary endothelium and an extracellular interstitium lumped with the peritoneal mesothelium.
منابع مشابه
Renal Replacement treatment for end Stage Renal Failure - the Role of capd
Before discussing clinical application and its complications, it is extremely important to have an understanding of the relevant peritoneal anatomy and physiology. In essence PD involves the transport of solutes and water across a ‘membrane’ that separates two fluid containing compartments: 1. Blood in peritoneal capillaries, which contains uremic toxins 2. Dialysis solution in the peritoneal c...
متن کاملFree water transport, small pore transport and the osmotic pressure gradient three-pore model of peritoneal transport.
In this issue of NDT, Flessner in a commentary [1] argues that the three-pore model (TPM) of peritoneal transport, although mathematically a powerful predictor of solute transport and ultrafiltration (UF) in peritoneal dialysis (PD), may be too simple as a tool for understanding the physiology of transperitoneal exchange. Flessner then disregards the fact that the TPM can be modified in a very ...
متن کاملمقایسه سلولهای مزانشیمی مغز استخوان و سلولهای مزوتلیومی مایع سروزی ازنظر میزان بیان مولکولهای کمپلکس سازگاری نسجی اصلی (MHC)
Abstract Background: Mesothelium is composed of a single layer of mesothelial cells attached to a thin basement membrane supported by subserosal connective tissue it plays an important role in homeostasis, wound healing, fluid transport and inflammation. The introduction of peritoneal dialysis (PD) as a modality of renal replacement therapy has provoked much interest in the biology of perito...
متن کاملThe impact of residual renal function on survival.
(See related article by A. Parikova et al. Free water transport, small pore transport and the osmotic pressure gradient. Free water transport, small pore transport and the osmotic pressure gradient three-pore model of peritoneal transport. Simonsen O et al. Fluid and electrolyte transport across the peritoneal membrane during CAPD according to the three-pore model. A et al. Aquaporin-1 plays an...
متن کاملTransport of peritoneal membrane assessed before and after the start of peritoneal dialysis.
BACKGROUND Patients on peritoneal dialysis (PD) with high small solute peritoneal membrane transport have an increased risk of morbidity and mortality. The membrane transport is currently assessed by peritoneal equilibration test (PET), usually performed after the first month of PD because of the early increase of membrane transport after the start of PD. The aim of this study was the assessmen...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
عنوان ژورنال:
- American journal of physiology. Renal physiology
دوره 280 4 شماره
صفحات -
تاریخ انتشار 2001