RENAL TUBULAR PC02 AND ACID-BASE EQUILIBRIUM

肾小管 PC02 和酸碱平衡

基本信息

项目摘要

The proposed research is designed to gain insight into the process of CO2 transfer in the kidney cortex, and into the role of bicarbonate reabsorption in the early proximal tubule in the maintenance of acid-base equilibrium. Micropuncture and microelectrode measurements in rats will be coupled with mathematical modelling efforts to test specific hypotheses concerning: 1) the high PCO2 levels in the superficial renal cortex, 2) the influence of tubular bicarbonate and CO2 reabsorption on peritubular capillary PCO2, 3) the factors producing a transepithelial PCO2 gradient confined to the early proximal tubule, and 4) the factor influencing bicarbonate reabsorption along the proximal tubule. For each of these problems a mathematical model has been developed, based on physicochemical interactions between CO2, bicarbonate and hydrogen ions, and on the interaction of these species with-blood buffers. The models also consider the permeabilities and diffusivities of these species in their movement from one compartment to another. The assumptions used to develop the models will be tested by specific experimental maneuvers in Munich-Wistar rats designed to produce measurable changes in renal cortical PCO2. These experiments include acute plasma expansion, metabolic and respiratory acid-base disorders, carbonic anhydrase inhibition, inhibition or uncoupling of metabolic CO2 production, and diuretic administration. In these experiments, microelectrode PCO2 measurements as well as measurements of bicarbonate reabsorption will be carried out. Experimental PCO2 measurements will be compared with values calculated by the models for each setting to test specific hypotheses concerning CO2 and bicarbonate transfer from the tubular lumen to the peritubular capillaries. A separate group of experiments will focus on defining the factors influencing bircarbonate reabsorption in the first 1-2 mm of the proximal tubule. The effect of pH, filtered bicarbonate load, and transport inhibitors will be examined in micropuncture and microperfusion studies. Finally, we plan to measure Na+/H+ exchange activity in brush border membrane vesicles isolated from rat renal cortex. These studies should provide insight into the regulation of normal acid-base equilibrium, and ultimately into clinical disorders of acid-base equilibrium.
这项拟议的研究旨在深入了解二氧化碳的过程

项目成果

期刊论文数量(0)
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F JOHN GENNARI其他文献

F JOHN GENNARI的其他文献

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{{ truncateString('F JOHN GENNARI', 18)}}的其他基金

RENAL REGULATION OF PROTON TRANSPORT
质子运输的肾脏调节
  • 批准号:
    3023290
  • 财政年份:
    1991
  • 资助金额:
    $ 18.7万
  • 项目类别:
RENAL TUBULAR PC02 AND ACID-BASE EQUILIBRIUM
肾小管 PC02 和酸碱平衡
  • 批准号:
    3227998
  • 财政年份:
    1979
  • 资助金额:
    $ 18.7万
  • 项目类别:
RENAL TUBULAR PC02 AND ACID-BASE EQUILIBRIUM
肾小管 PC02 和酸碱平衡
  • 批准号:
    3228001
  • 财政年份:
    1979
  • 资助金额:
    $ 18.7万
  • 项目类别:
RENAL TUBULAR PC02 AND ACID-BASE EQUILIBRIUM
肾小管 PC02 和酸碱平衡
  • 批准号:
    3227994
  • 财政年份:
    1979
  • 资助金额:
    $ 18.7万
  • 项目类别:
RENAL TUBULAR PCO2 AND ACID-BASE EQUILIBRIUM
肾小管 PCO2 和酸碱平衡
  • 批准号:
    3151656
  • 财政年份:
    1979
  • 资助金额:
    $ 18.7万
  • 项目类别:
RENAL TUBULAR PC02 AND ACID-BASE EQUILIBRIUM
肾小管 PC02 和酸碱平衡
  • 批准号:
    3227999
  • 财政年份:
    1979
  • 资助金额:
    $ 18.7万
  • 项目类别:
EFFICACY OF LISINOPRIL IN HYPERTENSIVE PATIENTS
赖诺普利对高血压患者的疗效
  • 批准号:
    4701219
  • 财政年份:
  • 资助金额:
    $ 18.7万
  • 项目类别:
MK-421 (ENALAPRIL) AND HCTZ FOR MODERATE ESSENTIAL HYPERTENSION
MK-421(依那普利)和 HCTZ 治疗中度原发性高血压
  • 批准号:
    4701180
  • 财政年份:
  • 资助金额:
    $ 18.7万
  • 项目类别:
TERAZOSIN ABBOTT-45975 VERSES PLACEBO STUDY #M81-060
特拉唑嗪 ABBOTT-45975 对照安慰剂研究
  • 批准号:
    3973646
  • 财政年份:
  • 资助金额:
    $ 18.7万
  • 项目类别:
EFFICACY OF LISINOPRIL IN HYPERTENSIVE PATIENTS
赖诺普利对高血压患者的疗效
  • 批准号:
    3948384
  • 财政年份:
  • 资助金额:
    $ 18.7万
  • 项目类别:

相似海外基金

Studies of Aqueous Carbonates-Bicarbonates; Interactions of Ions in Natural Water Modeling (Chemistry)
含水碳酸盐-碳酸氢盐的研究;
  • 批准号:
    8406557
  • 财政年份:
    1984
  • 资助金额:
    $ 18.7万
  • 项目类别:
    Continuing Grant
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