Evidence map›Paper›PMID 10381596›Full record

ArticleThe Journal of physiology1999

Serotonergic modulation of hyperpolarization-activated current in acutely isolated rat dorsal root ganglion neurons.

C G Cardenas, L P Mar, A V Vysokanov, P B Arnold, L M Cardenas, D J Surmeier, R S Scroggs

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of physiology, 1999. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
1.9field-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

38 citing papers in PubMed, 118 citations in OpenAlex.

  1. Article
  2. Serotonergic 5-HTCurrent neuropharmacology · 2023
    Review
  3. 5-HTFrontiers in molecular neuroscience · 2022
    Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Article
  9. Serotonergic regulation of excitability of principal cells of the dorsal cochlear nucleus.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2015
    Article
  10. HCN channels--modulators of cardiac and neuronal excitability.International journal of molecular sciences · 2015
    Review
  11. Article
  12. Review
  13. Review
  14. Article
  15. Article
  16. Article
  17. The cellular building blocks of breathing.Comprehensive Physiology · 2012
    Review
  18. Article
  19. Article
  20. 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

7 authors at 2 institutions in 1 country.

C G CardenasDepartment of Anatomy and Neurobiology, College of Medicine, University of Tennessee, Memphis, TN 38163, USA.
L P Mar
A V Vysokanov
P B Arnold
L M Cardenas
D J Surmeier
R S Scroggs
University of Tennessee Health Science Center · USNorthwestern University · US

Funding

SEROTONERGIC MODULATION OF SENSORY INFORMATIONR01NS037067 · NINDS · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI SCROGGS, REESE SCHILLER · 1998 to 2001
$231k
PRODUCTION OF OPTICALLY PURE 2 ARYLPROPIONIC ACIDSR43NS036496 · NINDS · TDA RESEARCH, INC. · PI DIETZ, STEVEN D · 1998 to 1998
–
NINDS NIH HHS NS 36496NINDS NIH HHS NS37067
6 · The paper itself

Abstract

1. The effect of serotonin (5-HT) on the hyperpolarization-activated cation current (IH) was studied in small-, medium- and large-diameter acutely isolated rat dorsal root ganglion (DRG) cells, including cells categorized as type 1, 2, 3 and 4 based on membrane properties. 5-HT increased IH in 91 % of medium-diameter DRG cells (including type 4) and in 67 % of large-diameter DRG cells, but not other DRG cell types. 2. The increase of IH by 5-HT was antagonized by spiperone but not cyanopindolol, and was mimicked by 5-carboxyamidotryptamine, but not (+)-8-hydroxydipropylaminotetralin (8-OH-DPAT) or cyanopindolol. These data suggested the involvement of 5-HT7 receptors, which were shown to be expressed by medium-diameter DRG cells using RT-PCR analysis. 3. 5-HT shifted the conductance-voltage relationship of IH by +6 mV without changing peak conductance. The effects of 5-HT on IH were mimicked and occluded by forskolin, but not by inactive 1,9-dideoxy forskolin. 4. At holding potentials negative to -50 mV, 5-HT increased steady-state inward current and instantaneous membrane conductance (fast current). The 5-HT-induced inward current and fast current were blocked by Cs+ but not Ba2+ and reversed at -23 mV, consistent with the properties of tonically activated IH. 5. In medium-diameter neurons recorded from in the current clamp mode, 5-HT depolarized the resting membrane potential, decreased input resistance and facilitated action potential generation by anode-break excitation. 6. The above data suggest that in distinct subpopulations of DRG neurons, 5-HT increases cAMP levels via activation of 5-HT7 receptors, which shifts the voltage dependence of IH to more depolarized potentials and increases neuronal excitability.

Indexed as

8-Hydroxy-2-(di-n-propylamino)tetralinAction PotentialsAnimalsCell SizeCyclic Nucleotide-Gated Cation ChannelsDopamine AntagonistsGanglia, SpinalHyperpolarization-Activated Cyclic Nucleotide-Gated ChannelsIn Vitro TechniquesIon ChannelsMaleMembrane PotentialsNeurons, AfferentPatch-Clamp TechniquesPindololPotassium Channels5-carboxamidotryptamine8-Hydroxy-2-(di-n-propylamino)tetralincyanopindololCyclic Nucleotide-Gated Cation ChannelsDopamine AntagonistsHyperpolarization-Activated Cyclic Nucleotide-Gated ChannelsIon ChannelsPindololPotassium ChannelsReceptors, SerotoninSerotoninserotonin 7 receptorSerotonin AntagonistsSerotonin Receptor AgonistsSpiperone

Identifiers

PMID10381596
PMCPMC2269436
OpenAlexW1984829646

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.