Evidence map›Paper›PMID 18945947›Full record

ArticleAmerican journal of physiology. Regulatory, integrative and comparative physiology2008

Sprouting of substance P-expressing primary afferent central terminals and spinal micturition reflex NK1 receptor dependence after spinal cord injury.

Xiaoyang Zhang, Kristy L Douglas, Huixia Jin, Bassem M Eldaif, Rashid Nassar, Matthew O Fraser, Paul C Dolber

Open access · greenAbstract read
In one paragraph

Article in American journal of physiology. Regulatory, integrative and comparative physiology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
0.8field-weighted citation impact, top 26% 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

19 citing papers in PubMed, 29 citations in OpenAlex.

  1. Review
  2. Sprouting of afferent and efferent inputs to pelvic organs after spinal cord injury.Journal of neuropathology and experimental neurology · 2023
    Article
  3. Upregulated 5-HTJournal of neurotrauma · 2023
    Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Neural control of the lower urinary tract.Comprehensive Physiology · 2015
    Review
  15. Review
  16. Article
  17. Review
  18. Article
  19. 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.

Xiaoyang ZhangDepartment of Surgery, Veterans Affairs Medical Center, Duke University Medical Center, Durham, NC 27710, USA.
Kristy L Douglas
Huixia Jin
Bassem M Eldaif
Rashid Nassar
Matthew O Fraser
Paul C Dolber
Duke Medical Center · USDuke University · US

Funding

Diabetic Urethral Pathophysiology and Afferent TherapyR01DK061391 · NIDDK · DUKE UNIVERSITY · PI FRASER, MATTHEW O · 2003 to 2006
$1.0M
NIDDK NIH HHS DK-61391NIDDK NIH HHS R01 DK061391
6 · The paper itself

Abstract

The primary afferent neurotransmitter triggering the spinal micturition reflex after complete spinal cord injury (SCI) in the rat is unknown. Substance P detected immunohistochemically in the sacral parasympathetic nucleus was significantly higher in 12 SCI rats than in 12 spinally intact rats (P = 0.008), suggesting substance P as a plausible candidate for the primary afferent neurotransmitter. The effects of the tachykinin NK1 receptor antagonist L-733060 on the spinal micturition reflex were then determined by performing conscious cystometry in an additional 14 intact rats and 14 SCI rats with L-733060 (0.1-100 microg) administered intrathecally at L6-S1. L-733060 was without effect in intact rats, but blocked the spinal micturition reflex in 10 of 14 SCI rats and increased the intermicturition interval in 2 of 4 others at doses ranging from 10 to 100 microg. Both phasic and nonphasic voiding contractions, differentiated according to the presence of phasic external urethral sphincter (EUS) activity, were present in most SCI rats. Both types of contractions were blocked by high doses of L-733060. Interestingly, there was a relative decline in phasic voiding contractions at high doses as well as a decline in contraction amplitude in nonphasic voiding contractions. In other respects, cystometric variables were largely unaffected in either spinally intact or SCI rats. L-733060 did not affect tonic EUS activity at any dose except when the spinal micturition reflex was blocked and tonic activity was consequently lost. These experiments show that tachykinin action at spinal NK1 receptors plays a major role in the spinal micturition reflex in SCI rats.

Indexed as

Cell ProliferationReflexUrinationAnimalsDisease Models, AnimalDose-Response Relationship, DrugElectromyographyFemaleInjections, SpinalMuscle ContractionNeurokinin-1 Receptor AntagonistsNeurons, AfferentPiperidinesPressureRatsRats, Sprague-Dawley3-((3,5-bis(trifluoromethyl)phenyl)methyloxy)-2-phenylpiperidineNeurokinin-1 Receptor AntagonistsPiperidinesReceptors, Neurokinin-1Substance P

Identifiers

PMID18945947
PMCPMC2685299
OpenAlexW2034556042

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.