期刊
PURINERGIC SIGNALLING
卷 5, 期 4, 页码 481-489出版社
SPRINGER
DOI: 10.1007/s11302-009-9150-6
关键词
P2X(4) receptor; P2Y(2) receptor; Amiloride-sensitive currents; ATP; Nucleotide; Kidney; Blood pressure
资金
- British Heart Foundation
- St Peter's Trust for Kidney, Bladder and Prostate Research
- Nuffield Foundation
Sodium balance determines the extracellular fluid volume and sets arterial blood pressure (BP). Chronically raised BP (hypertension) represents a major health risk in Western societies. The relationship between BP and renal sodium excretion (the pressure/natriuresis relationship) represents the key element in defining the BP homeostatic set point. The renin-angiotensin-aldosterone system (RAAS) makes major adjustments to the rates of renal sodium secretion, but this system works slowly over a period of hours to days. More rapid adjustments can be made by the sympathetic nervous system, although the kidney can function well without sympathetic nerves. Attention has now focussed on regulatory mechanisms within the kidney, including extracellular nucleotides and the P2 receptor system. Here, we discuss how extracellular ATP can control renal sodium excretion by altering the activity of epithelial sodium channels (ENaC) present in the apical membrane of principal cells. There remains considerable controversy over the molecular targets for released ATP, although the P2Y(2) receptor has received much attention. We review the available data and reflect on our own findings in which ATP-activated P2Y and P2X receptors make adjustments to ENaC activity and therefore sodium excretion.
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