Evidence map›Paper›PMID 21190949›Full record

ArticleAmerican journal of physiology. Renal physiology2011

A mathematical model of the myogenic response to systolic pressure in the afferent arteriole.

Jing Chen, Ioannis Sgouralis, Leon C Moore, Harold E Layton, Anita T Layton

Open access · greenAbstract read
In one paragraph

Article in American journal of physiology. Renal physiology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.1field-weighted citation impact, top 12% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

20 citing papers in PubMed, 51 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Renal medullary and urinary oxygen tension during cardiopulmonary bypass in the rat.Mathematical medicine and biology : a journal of the IMA · 2017
    Article
  5. Multiscale modeling methods in biomechanics.Wiley interdisciplinary reviews. Systems biology and medicine · 2017
    Review
  6. Article
  7. Conduction of feedback-mediated signal in a computational model of coupled nephrons.Mathematical medicine and biology : a journal of the IMA · 2016
    Article
  8. Article
  9. Renal autoregulation in health and disease.Physiological reviews · 2015
    Review
  10. Article
  11. Theoretical assessment of renal autoregulatory mechanisms.American journal of physiology. Renal physiology · 2014
    Article
  12. Article
  13. Calcium dynamics underlying the myogenic response of the renal afferent arteriole.American journal of physiology. Renal physiology · 2014
    Article
  14. Control and modulation of fluid flow in the rat kidney.Bulletin of mathematical biology · 2013
    Article
  15. Renal microvascular dysfunction, hypertension and CKD progression.Current opinion in nephrology and hypertension · 2013
    Review
  16. Article
  17. Article
  18. Delayed graft function in the kidney transplant.American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2011
    Review
  19. Mechanical control of cation channels in the myogenic response.American journal of physiology. Heart and circulatory physiology · 2011
    Article
  20. Mathematical modeling of kidney transport.Wiley interdisciplinary reviews. Systems biology and medicine
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 2 institutions in 1 country.

Jing ChenDepartment of Mathematics, Duke University, Durham, North Carolina; and State University of New York, Stony Brook, New York, USA.
Ioannis Sgouralis
Leon C Moore
Harold E Layton
Anita T Layton
Duke University · USState University of New York · US

Funding

MATHEMATICAL MODELS OF RENAL DYNAMICSR01DK042091 · NIDDK · DUKE UNIVERSITY · PI LAYTON, HAROLD E · 1995 to 2009
$1.9M
Modeling Solute Transport and Urine Concentrating Mechanism in the Rat KidneyR01DK089066 · NIDDK · DUKE UNIVERSITY · PI LAYTON, ANITA · 2010 to 2014
$1.2M
MATHEMATICAL MODELS OF RENAL DYNAMICSR29DK042091 · NIDDK · DUKE UNIVERSITY · PI LAYTON, HAROLD E · 1990 to 1994
–
NIDDK NIH HHS DK-42091NIDDK NIH HHS DK-89066
6 · The paper itself

Abstract

Elevations in systolic blood pressure are believed to be closely linked to the pathogenesis and progression of renal diseases. It has been hypothesized that the afferent arteriole (AA) protects the glomerulus from the damaging effects of hypertension by sensing increases in systolic blood pressure and responding with a compensatory vasoconstriction (Loutzenhiser R, Bidani A, Chilton L. Circ Res 90: 1316-1324, 2002). To investigate this hypothesis, we developed a mathematical model of the myogenic response of an AA wall, based on an arteriole model (Gonzalez-Fernandez JM, Ermentrout B. Math Biosci 119: 127-167, 1994). The model incorporates ionic transport, cell membrane potential, contraction of the AA smooth muscle cell, and the mechanics of a thick-walled cylinder. The model represents a myogenic response based on a pressure-induced shift in the voltage dependence of calcium channel openings: with increasing transmural pressure, model vessel diameter decreases; and with decreasing pressure, vessel diameter increases. Furthermore, the model myogenic mechanism includes a rate-sensitive component that yields constriction and dilation kinetics similar to behaviors observed in vitro. A parameter set is identified based on physical dimensions of an AA in a rat kidney. Model results suggest that the interaction of Ca(2+) and K(+) fluxes mediated by voltage-gated and voltage-calcium-gated channels, respectively, gives rise to periodicity in the transport of the two ions. This results in a time-periodic cytoplasmic calcium concentration, myosin light chain phosphorylation, and cross-bridge formation with the attending muscle stress. Furthermore, the model predicts myogenic responses that agree with experimental observations, most notably those which demonstrate that the renal AA constricts in response to increases in both steady and systolic blood pressures. The myogenic model captures these essential functions of the renal AA, and it may prove useful as a fundamental component in a multiscale model of the renal microvasculature suitable for investigations of the pathogenesis of hypertensive renal diseases.

Indexed as

Models, TheoreticalAnimalsArteriolesBlood PressureCalciumCalcium ChannelsKidneyMembrane PotentialsModels, AnimalMuscle, Smooth, VascularPotassiumRatsSystoleCalciumCalcium ChannelsPotassium

Identifiers

PMID21190949
PMCPMC3064127
OpenAlexW2082325856

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.