THEORETICAL ANALYSIS OF SOLUTE & H2O TRANSPORT IN KIDNEY

溶质的理论分析

• 批准号: 3230156
• 负责人: JOHN L STEPHENSON
• 金额: $ 20.59万
• 依托单位: WEILL MEDICAL COLL OF CORNELL UNIV
• 依托单位国家: 美国
• 财政年份: 1984
• 资助国家: 美国
• 起止时间: 1984-01-01 至 1993-02-28
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/3230156
• 关键词: aldosterone; ammonia; apical membrane; basolateral membrane; biological fluid transport; body fluid osmolarity; carbonate dehydratase; diuretics; electrical potential; electrolyte balance; excretion; glucose; hormone regulation /control mechanism; hydrostatic pressure; ion transport; kidney circulation; mathematical model; membrane permeability; model design /development; nonblood rheology; radiotracer; renal cortex; renal medulla; renal tubular transport; scintillation cameras; solute; urea; vasopressins; water; water flow

The overall aim in this continuing project is to integrate experimental data on water and solute transport at the membrane level into a predictive model of whole kidney function that is useful in both experimental design and patient management. During this period the focus is on the handling of Na, K, urea, and water and their control by ADH and aldosterone. The specific aims are: 1. To model thick ascending limb of Henle's loop (TAHL). This model, based on models to toad bladder and proximal tubule (PT), will include both cellular and paracellular pathways and the following variables: Na+, K+, Cl-, urea, hydrostatic pressure, electric potential, and volume flow; it may also include the additional variables H+, HCO3+, HPO42-, H2PO4-, NH4+, and glucose and will utilize a linear non-equilibrium thermodynamic (NET) formalism to describe fluxes. A primary objective will be to understand transmural fluxes of Na+, K+, Cl- and NH4+ in terms of apical and basolateral membrane transport systems. Another will be to model the target action of ADH and diuretics on the apical co-transport system. 2. To incorporate the TAHL model together with the PT model into a central core model of the cortex and outer medulla. The extended model will be used to interpret cortical micropuncture data and certain clearance data, particularly from the isolated perfused kidney. 3. To model the cortical collecting tubule (CCT). By including the carbonic anhydrase (CA)-rich intercalated cell, this will be the first model of a cellularly heterogeneous epithelium. The model will be used to explore K+ handling, H+ secretion, HCO3-secretion, water absorption and their control and interaction in the experimentally isolated and perfused tubule, and will also be incorporated into the central core model of a cortical nephron. 4. To develop models of descending (DHL) and ascending (AHL) thin limbs of the loop of Henle that include cellular and paracellular pathways. These models will be used to explore the hypothesis that cycling of potassium from AHL to DHL generates the inner medullary concentration gradient. 5. To extend a two nephron model of the medulla to a) include the extended segmental models and b) to incorporate additional details of the architectural organization of the medulla; and to develop and to utilize new methods of parameter estimation.

这个持续项目的总体目标是整合实验性的 在膜水平上的水和溶质传输的数据转化为预测 在两种实验设计中均有用的全肾功能模型 病人管理。 在此期间，重点是处理 钠、钾、尿素和水，以及它们由ADH和醛固酮控制。 具体目标是： 1. 建立亨利袢粗升支模型。 这种模式， 基于蟾蜍膀胱和近端小管（PT）模型，将包括 细胞和细胞旁途径以及以下变量：Na+，K+， Cl-、尿素、静水压力、电势和体积流量;它 还可以包括另外的变量H+、HCO 3+、HPO 42-、H2 PO 4-、NH 4+， 和葡萄糖，并将利用线性非平衡热力学（NET） 形式主义来描述通量。 首要目标是了解 Na+、K+、Cl-和NH 4+的跨壁通量， 基底外侧膜转运系统。 另一个将是模拟 ADH和利尿剂对心尖共转运系统的靶向作用。 2. 将TAHL模型与PT模型合并到一个中央 皮质和外髓质的核心模型。 扩展模型将是 用于解释皮质微穿刺数据和某些清除数据， 特别是来自分离的灌注肾。 3. 建立皮质集合管（CCT）模型。 通过包括 碳酸酐酶（CA）丰富的插入细胞，这将是第一个 细胞异质上皮的模型。 该模型将用于 探索K+处理、H+分泌、HCO 3-分泌、水吸收和 它们在实验隔离和灌注的 小管，也将被纳入中央核心模型的一个 皮质肾单位 4. 开发下行（DHL）和上行（阿勒）模型 Henle袢的细肢，包括细胞和细胞旁 途径。 这些模型将被用来探索骑自行车的假设， 钾从阿勒到DHL产生了内髓浓度 梯度离心 5. 为了扩展髓质的两个肾单位模型，a）包括扩展的 分段模型和B）纳入额外的细节， 延髓的结构组织;并开发和利用 参数估计的新方法。