Electrotonic vascular signal conduction and nephron synchronization

Research output: Contribution to journalJournal articleResearchpeer-review

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Electrotonic vascular signal conduction and nephron synchronization. / Marsh, Donald J; Toma, Ildiko; Sosnovtseva, Olga; Peti-Peterdi, Janos; Holstein-Rathlou, Niels-Henrik.

In: American Journal of Physiology - Renal Physiology, Vol. 296, No. 4, 2009, p. F751-61.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Marsh, DJ, Toma, I, Sosnovtseva, O, Peti-Peterdi, J & Holstein-Rathlou, N-H 2009, 'Electrotonic vascular signal conduction and nephron synchronization', American Journal of Physiology - Renal Physiology, vol. 296, no. 4, pp. F751-61. https://doi.org/10.1152/ajprenal.90669.2008

APA

Marsh, D. J., Toma, I., Sosnovtseva, O., Peti-Peterdi, J., & Holstein-Rathlou, N-H. (2009). Electrotonic vascular signal conduction and nephron synchronization. American Journal of Physiology - Renal Physiology, 296(4), F751-61. https://doi.org/10.1152/ajprenal.90669.2008

Vancouver

Marsh DJ, Toma I, Sosnovtseva O, Peti-Peterdi J, Holstein-Rathlou N-H. Electrotonic vascular signal conduction and nephron synchronization. American Journal of Physiology - Renal Physiology. 2009;296(4):F751-61. https://doi.org/10.1152/ajprenal.90669.2008

Author

Marsh, Donald J ; Toma, Ildiko ; Sosnovtseva, Olga ; Peti-Peterdi, Janos ; Holstein-Rathlou, Niels-Henrik. / Electrotonic vascular signal conduction and nephron synchronization. In: American Journal of Physiology - Renal Physiology. 2009 ; Vol. 296, No. 4. pp. F751-61.

Bibtex

@article{c9af0780359311df8ed1000ea68e967b,
title = "Electrotonic vascular signal conduction and nephron synchronization",
abstract = "Tubuloglomerular feedback (TGF) and the myogenic mechanism control afferent arteriolar diameter in each nephron and regulate blood flow. Both mechanisms generate self-sustained oscillations, the oscillations interact, TGF modulates the frequency and amplitude of the myogenic oscillation, and the oscillations synchronize; a 5:1 frequency ratio is the most frequent. TGF oscillations synchronize in nephron pairs supplied from a common cortical radial artery, as do myogenic oscillations. We propose that electrotonic vascular signal propagation from one juxtaglomerular apparatus interacts with similar signals from other nephrons to produce synchronization. We tested this idea in tubular-vascular preparations from mice. Vascular smooth muscle cells were loaded with a fluorescent voltage-sensitive dye; fluorescence intensity was measured with confocal microscopy. Perfusion of the thick ascending limb activated TGF and depolarized afferent arteriolar smooth muscle cells. The depolarization spread to the cortical radial artery and other afferent arterioles and declined with distance from the perfused juxtaglomerular apparatus, consistent with electrotonic vascular signal propagation. With a mathematical model of two coupled nephrons, we estimated the conductance of nephron coupling by fitting simulated vessel diameters to experimental data. With this value, we simulated nephron pairs to test for synchronization. In single-nephron simulations, the frequency of the TGF oscillation varied with nephron length. Coupling nephrons of different lengths forced TGF frequencies of both pair members to converge to a common value. The myogenic oscillations also synchronized, and the synchronization between the TGF and the myogenic oscillations showed an increased stability against parameter perturbations. Electronic vascular signal propagation is a plausible mechanism for nephron synchronization. Coupling increased the stability of the various oscillations.",
author = "Marsh, {Donald J} and Ildiko Toma and Olga Sosnovtseva and Janos Peti-Peterdi and Niels-Henrik Holstein-Rathlou",
note = "Keywords: Animals; Arterioles; Computer Simulation; Glomerular Filtration Rate; Homeostasis; Juxtaglomerular Apparatus; Membrane Potentials; Mice; Mice, Inbred C57BL; Microscopy, Fluorescence, Multiphoton; Models, Biological; Muscle, Smooth, Vascular; Oscillometry; Perfusion; Renal Circulation; Signal Transduction; Time Factors",
year = "2009",
doi = "10.1152/ajprenal.90669.2008",
language = "English",
volume = "296",
pages = "F751--61",
journal = "American Journal of Physiology - Renal Fluid and Electrolyte Physiology",
issn = "1931-857X",
publisher = "American Physiological Society",
number = "4",

}

RIS

TY - JOUR

T1 - Electrotonic vascular signal conduction and nephron synchronization

AU - Marsh, Donald J

AU - Toma, Ildiko

AU - Sosnovtseva, Olga

AU - Peti-Peterdi, Janos

AU - Holstein-Rathlou, Niels-Henrik

N1 - Keywords: Animals; Arterioles; Computer Simulation; Glomerular Filtration Rate; Homeostasis; Juxtaglomerular Apparatus; Membrane Potentials; Mice; Mice, Inbred C57BL; Microscopy, Fluorescence, Multiphoton; Models, Biological; Muscle, Smooth, Vascular; Oscillometry; Perfusion; Renal Circulation; Signal Transduction; Time Factors

PY - 2009

Y1 - 2009

N2 - Tubuloglomerular feedback (TGF) and the myogenic mechanism control afferent arteriolar diameter in each nephron and regulate blood flow. Both mechanisms generate self-sustained oscillations, the oscillations interact, TGF modulates the frequency and amplitude of the myogenic oscillation, and the oscillations synchronize; a 5:1 frequency ratio is the most frequent. TGF oscillations synchronize in nephron pairs supplied from a common cortical radial artery, as do myogenic oscillations. We propose that electrotonic vascular signal propagation from one juxtaglomerular apparatus interacts with similar signals from other nephrons to produce synchronization. We tested this idea in tubular-vascular preparations from mice. Vascular smooth muscle cells were loaded with a fluorescent voltage-sensitive dye; fluorescence intensity was measured with confocal microscopy. Perfusion of the thick ascending limb activated TGF and depolarized afferent arteriolar smooth muscle cells. The depolarization spread to the cortical radial artery and other afferent arterioles and declined with distance from the perfused juxtaglomerular apparatus, consistent with electrotonic vascular signal propagation. With a mathematical model of two coupled nephrons, we estimated the conductance of nephron coupling by fitting simulated vessel diameters to experimental data. With this value, we simulated nephron pairs to test for synchronization. In single-nephron simulations, the frequency of the TGF oscillation varied with nephron length. Coupling nephrons of different lengths forced TGF frequencies of both pair members to converge to a common value. The myogenic oscillations also synchronized, and the synchronization between the TGF and the myogenic oscillations showed an increased stability against parameter perturbations. Electronic vascular signal propagation is a plausible mechanism for nephron synchronization. Coupling increased the stability of the various oscillations.

AB - Tubuloglomerular feedback (TGF) and the myogenic mechanism control afferent arteriolar diameter in each nephron and regulate blood flow. Both mechanisms generate self-sustained oscillations, the oscillations interact, TGF modulates the frequency and amplitude of the myogenic oscillation, and the oscillations synchronize; a 5:1 frequency ratio is the most frequent. TGF oscillations synchronize in nephron pairs supplied from a common cortical radial artery, as do myogenic oscillations. We propose that electrotonic vascular signal propagation from one juxtaglomerular apparatus interacts with similar signals from other nephrons to produce synchronization. We tested this idea in tubular-vascular preparations from mice. Vascular smooth muscle cells were loaded with a fluorescent voltage-sensitive dye; fluorescence intensity was measured with confocal microscopy. Perfusion of the thick ascending limb activated TGF and depolarized afferent arteriolar smooth muscle cells. The depolarization spread to the cortical radial artery and other afferent arterioles and declined with distance from the perfused juxtaglomerular apparatus, consistent with electrotonic vascular signal propagation. With a mathematical model of two coupled nephrons, we estimated the conductance of nephron coupling by fitting simulated vessel diameters to experimental data. With this value, we simulated nephron pairs to test for synchronization. In single-nephron simulations, the frequency of the TGF oscillation varied with nephron length. Coupling nephrons of different lengths forced TGF frequencies of both pair members to converge to a common value. The myogenic oscillations also synchronized, and the synchronization between the TGF and the myogenic oscillations showed an increased stability against parameter perturbations. Electronic vascular signal propagation is a plausible mechanism for nephron synchronization. Coupling increased the stability of the various oscillations.

U2 - 10.1152/ajprenal.90669.2008

DO - 10.1152/ajprenal.90669.2008

M3 - Journal article

C2 - 19116241

VL - 296

SP - F751-61

JO - American Journal of Physiology - Renal Fluid and Electrolyte Physiology

JF - American Journal of Physiology - Renal Fluid and Electrolyte Physiology

SN - 1931-857X

IS - 4

ER -

ID: 18763678