Evidence map›Paper›PMID 26173457›Full record

ArticleAmerican journal of physiology. Endocrinology and metabolism2015

Pendrin localizes to the adrenal medulla and modulates catecholamine release.

Yoskaly Lazo-Fernandez, Greti Aguilera, Truyen D Pham, Annie Y Park, William H Beierwaltes, Roy L Sutliff, Jill W Verlander, Karel Pacak, Adeboye O Osunkoya, Carla L Ellis and 7 more

Erratum issuedAbstract read
In one paragraph

Article in American journal of physiology. Endocrinology and metabolism, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.9field-weighted citation impact, top 8% 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, 24 citations in OpenAlex.

  1. Pendrin is upregulated by corticosterone and participates in its pressor response.American journal of physiology. Renal physiology · 2026
    Article
  2. Article
  3. Article
  4. Article
  5. Pendrin regulation is prioritized by anion in high-potassium diets.American journal of physiology. Renal physiology · 2023
    Article
  6. Pendrin-null mice develop severe hypokalemia following dietary NaAmerican journal of physiology. Renal physiology · 2022
    Article
  7. Review
  8. Review
  9. Article
  10. Article
  11. Article
  12. GABAPflugers Archiv : European journal of physiology · 2018
    Review
  13. Renal intercalated cells and blood pressure regulation.Kidney research and clinical practice · 2017
    Review
  14. Acute genetic ablation of pendrin lowers blood pressure in mice.Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association · 2017
    Article
  15. Article
  16. Pendrin-A New Target for Diuretic Therapy?Journal of the American Society of Nephrology : JASN · 2016
    Article
  17. Small-Molecule Inhibitors of Pendrin Potentiate the Diuretic Action of Furosemide.Journal of the American Society of Nephrology : JASN · 2016
    Article
  18. Inhibitors of pendrin anion exchange identified in a small molecule screen increase airway surface liquid volume in cystic fibrosis.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2016
    Article
  19. The role of pendrin in blood pressure regulation.American journal of physiology. Renal physiology · 2016
    Review
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

17 authors at 5 institutions in 1 country.

Yoskaly Lazo-FernandezDepartment of Medicine, Emory University School of Medicine, Atlanta, Georgia;
Greti AguileraSection on Endocrine Physiology, Developmental Endocrinology Branch, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland;
Truyen D PhamDepartment of Medicine, Emory University School of Medicine, Atlanta, Georgia;
Annie Y ParkDepartment of Medicine, Emory University School of Medicine, Atlanta, Georgia;
William H BeierwaltesHypertension and Vascular Research Division, Henry Ford Hospital and Wayne State School of Medicine, Detroit, Michigan;
Roy L SutliffDepartment of Medicine, Emory University School of Medicine, Atlanta, Georgia; Atlanta Veterans Affairs Hospital, Atlanta, Georgia;
Jill W VerlanderDepartment of Medicine, University of Florida, Gainesville, Florida;
Karel PacakProgram in Reproductive and Adult Endocrinology, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland;
Adeboye O OsunkoyaDepartment of Pathology, Emory University School of Medicine, Atlanta, Georgia;
Carla L EllisDepartment of Pathology, Emory University School of Medicine, Atlanta, Georgia;
Young Hee KimDepartment of Medicine, Emory University School of Medicine, Atlanta, Georgia;
Gregory L ShipleyDepartment of Integrative Biology and Pharmacology, University of Texas Medical School at Houston, Houston, Texas;
Brandi M WynneDepartment of Medicine, Emory University School of Medicine, Atlanta, Georgia;
Robert S HooverDepartment of Medicine, Emory University School of Medicine, Atlanta, Georgia; Atlanta Veterans Affairs Hospital, Atlanta, Georgia; Department of Physiology, Emory University School of Medicine, Atlanta, Georgia.
Shurjo K SenCardiovascular Disease Section, and National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland;
Paul M PlotskyDepartment of Psychiatry, Emory University School of Medicine, Atlanta, Georgia; and.
Susan M WallDepartment of Medicine, Emory University School of Medicine, Atlanta, Georgia; Department of Physiology, Emory University School of Medicine, Atlanta, Georgia smwall@emory.edu.
Emory University · USNational Institutes of Health · USHenry Ford Hospital · USUniversity of Florida · USVeterans Health Administration · US

Funding

Nephrology Institutional Training Grant FLSA SupplementT32DK007656 · NIDDK · EMORY UNIVERSITY · PI SANDS, JEFF M, WALL, SUSAN MARIE · 1990 to 2020
$3.5M
RENAL NET ACID SECRETION AND THE NA/K/2C1 CONTRANSPORTERR01DK046493 · NIDDK · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI WALL, SUSAN MARIE · 1999 to 2014
$2.0M
Mechanisms of Hormonal Regulation of the Sodium Chloride CotransporterR01DK085097 · NIDDK · EMORY UNIVERSITY · PI HOOVER, ROBERT S · 2010 to 2015
$1.5M
NH4+ TRANSPORT IN RENAL INNER MEDULLARY COLLECTING DUCTR29DK046493 · NIDDK · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI WALL, SUSAN MARIE · 1993 to 1997
–
Intramural NIH HHSNIDDK NIH HHS DK-085097NIDDK NIH HHS DK-46493NIDDK NIH HHS R01 DK085097NIDDK NIH HHS T32 DK-07656
6 · The paper itself

Abstract

Pendrin (Slc26a4) is a Cl(-)/HCO3 (-) exchanger expressed in renal intercalated cells and mediates renal Cl(-) absorption. With pendrin gene ablation, blood pressure and vascular volume fall, which increases plasma renin concentration. However, serum aldosterone does not significantly increase in pendrin-null mice, suggesting that pendrin regulates adrenal zona glomerulosa aldosterone production. Therefore, we examined pendrin expression in the adrenal gland using PCR, immunoblots, and immunohistochemistry. Pendrin protein was detected in adrenal lysates from wild-type but not pendrin-null mice. However, immunohistochemistry and qPCR of microdissected adrenal zones showed that pendrin was expressed in the adrenal medulla, rather than in cortex. Within the adrenal medulla, pendrin localizes to both epinephrine- and norepinephrine-producing chromaffin cells. Therefore, we examined plasma catecholamine concentration and blood pressure in wild-type and pendrin-null mice under basal conditions and then after 5 and 20 min of immobilization stress. Under basal conditions, blood pressure was lower in the mutant than in the wild-type mice, although epinephrine and norepinephrine concentrations were similar. Catecholamine concentration and blood pressure increased markedly in both groups with stress. With 20 min of immobilization stress, epinephrine and norepinephrine concentrations increased more in pendrin-null than in wild-type mice, although stress produced a similar increase in blood pressure in both groups. We conclude that pendrin is expressed in the adrenal medulla, where it blunts stress-induced catecholamine release.

Indexed as

Adrenal GlandsAdrenal MedullaAnimalsAnion Transport ProteinsBlood PressureChloride-Bicarbonate AntiportersEpinephrineGene Expression ProfilingImmunoblottingImmunohistochemistryKidneyMiceMice, KnockoutNorepinephrineRatsRestraint, PhysicalAnion Transport ProteinsChloride-Bicarbonate AntiportersEpinephrineNorepinephrineRNA, MessengerSlc26a4 protein, mouseSlc26A4 protein, ratSulfate Transporterschloridedopamineepinephrinenorepinephrinependrin

Identifiers

PMID26173457
PMCPMC4572452
OpenAlexW2167054013

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.