Evidence map›Paper›PMID 27009163›Full record

ArticleJournal of neurophysiology2016

Inflammatory stimuli acutely modulate peripheral taste function.

Devaki Kumarhia, Lianying He, Lynnette Phillips McCluskey

Abstract read
In one paragraph

Article in Journal of neurophysiology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
–field-weighted citation impact
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

25 citing papers in PubMed.

  1. Blood biomarkers for the prediction of idiopathic taste dysfunction: a case-control study.European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery · 2026
    Article
  2. Article
  3. Article
  4. Article
  5. Organoid models for chemosensing cell studies.American journal of physiology. Cell physiology · 2025
    Review
  6. Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Review
  14. Review
  15. Do Gut Microbes Taste?Nutrients · 2021
    Review
  16. Review
  17. Salt sensitivity and hypertension.Journal of human hypertension · 2021
    Review
  18. Article
  19. Review
  20. Osmotic Adaptation by NaBiomedicines · 2020
    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

3 authors.

Devaki KumarhiaDepartment of Neuroscience and Regenerative Medicine, Medical College of Georgia at Augusta University, Augusta, Georgia; and Graduate Program in Molecular Medicine, Medical College of Georgia at Augusta University, Augusta, Georgia.
Lianying HeDepartment of Neuroscience and Regenerative Medicine, Medical College of Georgia at Augusta University, Augusta, Georgia; and.
Lynnette Phillips McCluskeyDepartment of Neuroscience and Regenerative Medicine, Medical College of Georgia at Augusta University, Augusta, Georgia; and lmccluskey@augusta.edu.

Funding

Degenerative Changes in the Taste SystemR01DC005811 · NIDCD · MEDICAL COLLEGE OF GEORGIA (MCG) · PI MCCLUSKEY, LYNNETTE MARIE · 2003 to 2013
$2.8M
NIDCD NIH HHS R01 DC005811
6 · The paper itself

Abstract

Inflammation-mediated changes in taste perception can affect health outcomes in patients, but little is known about the underlying mechanisms. In the present work, we hypothesized that proinflammatory cytokines directly modulate Na(+) transport in taste buds. To test this, we measured acute changes in Na(+) flux in polarized fungiform taste buds loaded with a Na(+) indicator dye. IL-1β elicited an amiloride-sensitive increase in Na(+) transport in taste buds. In contrast, TNF-α dramatically and reversibly decreased Na(+) flux in polarized taste buds via amiloride-sensitive and amiloride-insensitive Na(+) transport systems. The speed and partial amiloride sensitivity of these changes in Na(+) flux indicate that IL-1β and TNF-α modulate epithelial Na(+) channel (ENaC) function. A portion of the TNF-mediated decrease in Na(+) flux is also blocked by the TRPV1 antagonist capsazepine, although TNF-α further reduced Na(+) transport independently of both amiloride and capsazepine. We also assessed taste function in vivo in a model of infection and inflammation that elevates these and additional cytokines. In rats administered systemic lipopolysaccharide (LPS), CT responses to Na(+) were significantly elevated between 1 and 2 h after LPS treatment. Low, normally preferred concentrations of NaCl and sodium acetate elicited high response magnitudes. Consistent with this outcome, codelivery of IL-1β and TNF-α enhanced Na(+) flux in polarized taste buds. These results demonstrate that inflammation elicits swift changes in Na(+) taste function, which may limit salt consumption during illness.

Indexed as

AmilorideAnalgesics, Non-NarcoticAnalysis of VarianceAnimalsBody WeightCapsaicinChorda Tympani NerveDose-Response Relationship, DrugEpithelial Sodium Channel BlockersFemaleFunctional LateralityInterleukin-6LipopolysaccharidesQuinineRatsSensory Receptor CellsAmilorideAnalgesics, Non-NarcoticCapsaicincapsazepineEpithelial Sodium Channel BlockersInterleukin-6LipopolysaccharidesQuinineSodiumSodium AcetateSodium ChlorideTumor Necrosis Factor-alphaepithelial sodium channelinterleukin-1βneuroimmunologytaste budtumor necrosis factor-α

Identifiers

PMID27009163
PMCPMC4922616

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.