Evidence map›Paper›PMID 27534994›Full record

ArticleAmerican journal of physiology. Renal physiology2016

Activation of the metabolic sensor AMP-activated protein kinase inhibits aquaporin-2 function in kidney principal cells.

Mohammad M Al-Bataineh, Hui Li, Kazuhiro Ohmi, Fan Gong, Allison L Marciszyn, Sajid Naveed, Xiaoqing Zhu, Dietbert Neumann, Qi Wu, Lei Cheng and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in American journal of physiology. Renal physiology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.7field-weighted citation impact, top 15% 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

15 citing papers in PubMed, 26 citations in OpenAlex.

  1. Expression and distribution of MUC1 in the developing and adult kidney.American journal of physiology. Renal physiology · 2025
    Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. PKA-independent vasopressin signaling in renal collecting duct.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2020
    Article
  10. AMPK phosphorylation of the βAmerican journal of physiology. Renal physiology · 2019
    Article
  11. Article
  12. Article
  13. AMP-Activated Protein Kinase (AMPK)-Dependent Regulation of Renal Transport.International journal of molecular sciences · 2018
    Review
  14. Mammalian urine concentration: a review of renal medullary architecture and membrane transporters.Journal of comparative physiology. B, Biochemical, systemic, and environmental physiology · 2018
    Review
  15. Article
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

13 authors at 4 institutions in 3 countries.

Mohammad M Al-BatainehDepartment of Medicine, Renal-Electrolyte Division, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.
Hui LiDepartment of Medicine, University of Southern California/University Kidney Research Organization, Kidney Research Center, Division of Nephrology and Hypertension, Keck School of Medicine of University of Southern California, Los Angeles, California.
Kazuhiro OhmiDepartment of Medicine, University of Southern California/University Kidney Research Organization, Kidney Research Center, Division of Nephrology and Hypertension, Keck School of Medicine of University of Southern California, Los Angeles, California.
Fan GongDepartment of Medicine, Renal-Electrolyte Division, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.
Allison L MarciszynDepartment of Medicine, Renal-Electrolyte Division, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.
Sajid NaveedDepartment of Medicine, Renal-Electrolyte Division, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.
Xiaoqing ZhuDepartment of Molecular Genetics, School for Cardiovascular Diseases, Maastricht University, Maastricht, The Netherlands; and.
Dietbert NeumannDepartment of Molecular Genetics, School for Cardiovascular Diseases, Maastricht University, Maastricht, The Netherlands; and.
Qi WuDepartment of Biomedicine, InterPrET Center, Aarhus University, Aarhus, Denmark.
Lei ChengDepartment of Biomedicine, InterPrET Center, Aarhus University, Aarhus, Denmark.
Robert A FentonDepartment of Biomedicine, InterPrET Center, Aarhus University, Aarhus, Denmark.
Núria M Pastor-SolerDepartment of Medicine, University of Southern California/University Kidney Research Organization, Kidney Research Center, Division of Nephrology and Hypertension, Keck School of Medicine of University of Southern California, Los Angeles, California; nuria.pastor-soler@med.usc.edu.
Kenneth R HallowsDepartment of Medicine, University of Southern California/University Kidney Research Organization, Kidney Research Center, Division of Nephrology and Hypertension, Keck School of Medicine of University of Southern California, Los Angeles, California.
University of Pittsburgh · USUniversity of Southern California · USAarhus University · DKMaastricht University · NL

Funding

Single Nephron and MetabolomicsP30DK079307 · NIDDK · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI APODACA, GERARD L · 2008 to 2022
$13.4M
Mechanisms and Relevance of Sodium Transport Regulation by AMPKR01DK075048 · NIDDK · UNIVERSITY OF SOUTHERN CALIFORNIA · PI HALLOWS, KENNETH R · 2007 to 2015
$2.5M
Mechanisms of Kinase-dependent Regulation of the V-ATPase in KidneyR01DK084184 · NIDDK · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI PASTOR-SOLER, NURIA M. · 2009 to 2013
$1.5M
Role of Muc1 in the b-catenin Response to Acute Kidney InjuryK01DK109038 · NIDDK · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI AL-BATAINEH, MOHAMMAD · 2016 to 2021
$798k
Aquaporin-2 (AQP2) Regulation by AMP-activated kinase(AMPK) in the Kidney CollecF32DK097889 · NIDDK · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI AL-BATAINEH, MOHAMMAD · 2012 to 2015
$167k
NIDDK NIH HHS F32 DK097889NIDDK NIH HHS K01 DK109038NIDDK NIH HHS P30 DK079307NIDDK NIH HHS R01 DK075048NIDDK NIH HHS R01 DK084184
6 · The paper itself

Abstract

Aquaporin-2 (AQP2) is essential to maintain body water homeostasis. AQP2 traffics from intracellular vesicles to the apical membrane of kidney collecting duct principal cells in response to vasopressin [arginine vasopressin (AVP)], a hormone released with low intravascular volume, which causes decreased kidney perfusion. Decreased kidney perfusion activates AMP-activated kinase (AMPK), a metabolic sensor that inhibits the activity of several transport proteins. We hypothesized that AMPK activation also inhibits AQP2 function. These putative AMPK effects could protect interstitial ionic gradients required for urinary concentration during metabolic stress when low intravascular volume induces AVP release. Here we found that short-term AMPK activation by treatment with 5-aminoimidazole-4-carboxamide-1-β-d-ribofuranoside (AICAR; 75 min) in kidney tissue prevented baseline AQP2 apical accumulation in principal cells, but did not prevent AQP2 apical accumulation in response to the AVP analog desmopressin (dDAVP). Prolonged AMPK activation prevented AQP2 cell membrane accumulation in response to forskolin in mouse collecting duct mpkCCD

Indexed as

Aminoimidazole CarboxamideAMP-Activated Protein KinasesAnimalsAquaporin 2Cell LineKidneyKidney Tubules, CollectingMaleMicePhosphorylationRatsRats, Sprague-DawleyRibonucleotidesXenopusAICA ribonucleotideAminoimidazole CarboxamideAMP-Activated Protein KinasesAquaporin 2RibonucleotidesepithelialmetforminmpkCCDc14PKAwater transport

Identifiers

PMID27534994
PMCPMC5130465
OpenAlexW2514186136

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.