Evidence map›Paper›PMID 19407249›Full record

ArticleJournal of applied physiology (Bethesda, Md. : 1985)2009

Aging and muscle fiber type alter K+ channel contributions to the myogenic response in skeletal muscle arterioles.

Lori S Kang, SeJeong Kim, James M Dominguez, Amy L Sindler, Gregory M Dick, Judy M Muller-Delp

Abstract read
In one paragraph

Article in Journal of applied physiology (Bethesda, Md. : 1985), 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
0.8field-weighted citation impact, top 27% 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

34 citing papers in PubMed, 56 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. The BKPhysiological reports · 2024
    Article
  5. Review
  6. Article
  7. Impact of aging on vascular ion channels: perspectives and knowledge gaps across major organ systems.American journal of physiology. Heart and circulatory physiology · 2023
    Review
  8. Effects of Atmospheric Ammonia on Skeletal Muscle Growth in Broilers.Animals : an open access journal from MDPI · 2023
    Article
  9. Inhibition of BKCell death discovery · 2022
    Article
  10. Article
  11. Review
  12. Review
  13. AlphaPhysiological reports · 2018
    Article
  14. KMicrocirculation (New York, N.Y. : 1994) · 2018
    Review
  15. The yin and yang of KMicrocirculation (New York, N.Y. : 1994) · 2018
    Review
  16. Article
  17. Article
  18. Article
  19. Review
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 1 institution in 1 country.

Lori S KangDepartment of Physiology and Pharmacology, West Virginia University School of Medicine, Morgantown, WV, USA.
SeJeong Kim
James M Dominguez
Amy L Sindler
Gregory M Dick
Judy M Muller-Delp
West Virginia University · US

Funding

Aging, Estrogen, and Coronary Endothelial FunctionR01HL077224 · NHLBI · WEST VIRGINIA UNIVERSITY · PI DELP, JUDY M · 2005 to 2008
$1.4M
NHLBI NIH HHS HL077224-01NHLBI NIH HHS R01 HL077224
6 · The paper itself

Abstract

Aging diminishes myogenic tone in arterioles from skeletal muscle. Recent evidence indicates that both large-conductance Ca2+-activated (BKCa) and voltage-dependent (KV) K+ channels mediate negative feedback control of the myogenic response. Thus we tested the hypothesis that aging increases the contributions of KV and BKCa channels to myogenic regulation of vascular tone. Because myogenic responsiveness differs between oxidative and glycolytic muscles, we predicted that KV and BKCa channel contributions to myogenic responsiveness vary with fiber type. Myogenic responses of first-order arterioles from the gastrocnemius and soleus muscles of 4- and 24-mo-old Fischer 344 rats were evaluated in the presence and absence of 4-aminopyridine (5 mM) or iberiotoxin (30 nM), inhibitors of KV and BKCa, respectively. 4-Aminopyridine enhanced myogenic tone with aging and normalized age-related differences in both muscle types. By contrast, iberiotoxin eliminated age-related differences in soleus arterioles and had no effect in gastrocnemius vessels. KV1.5 is an integral component of KV channels in vascular smooth muscle; therefore, we determined the relative protein expression of KV1.5, as well as BKCa, in soleus and gastrocnemius arterioles. Immunoblot analysis revealed no differences in KV1.5 protein with aging or between variant fiber types, whereas BKCa protein levels declined with age in arterioles from both muscle groups. Collectively, these results suggest that the contribution of BKCa to myogenic regulation of vascular tone changes with age in soleus muscle arterioles, whereas increased KV channel expression and negative feedback regulation of myogenic tone increases with advancing age in arterioles from both oxidative and glycolytic muscles.

Indexed as

VasoconstrictionAge FactorsAgingAnimalsArteriolesDose-Response Relationship, DrugFeedback, PhysiologicalGlycolysisIn Vitro TechniquesKv1.5 Potassium ChannelLarge-Conductance Calcium-Activated Potassium ChannelsMaleMuscle Fibers, SkeletalMuscle, SkeletalMuscle, Smooth, VascularOxidation-ReductionKcna5 protein, ratKv1.5 Potassium ChannelLarge-Conductance Calcium-Activated Potassium ChannelsPotassiumPotassium Channel BlockersPotassium Channels, Voltage-Gated

Identifiers

PMID19407249
PMCPMC2724325
OpenAlexW2170250797

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.