Evidence map›Paper›PMID 17761778›Full record

ArticleThe Journal of physiology2007

Differences in sympathetic neuroeffector transmission to rat mesenteric arteries and veins as probed by in vitro continuous amperometry and video imaging.

Jinwoo Park, James J Galligan, Gregory D Fink, Greg M Swain

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of physiology, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.3field-weighted citation impact, top 14% 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

21 citing papers in PubMed, 41 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. The Analyst · 2022
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  7. Spinal cord injury alters purinergic neurotransmission to mesenteric arteries in rats.American journal of physiology. Heart and circulatory physiology · 2020
    Article
  8. Article
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  11. Macrophage-dependent impairment of αAmerican journal of physiology. Heart and circulatory physiology · 2018
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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

4 authors at 1 institution in 1 country.

Jinwoo ParkDepartment of Chemistry and the Neuroscience Program, Michigan State University, East Lansing, MI 48824, USA.
James J Galligan
Gregory D Fink
Greg M Swain
Michigan State University · US

Funding

SIGNALING MECHANISMS IN ARTERIES AND VEINS IN HYPERTENSIONP01HL070687 · NHLBI · MICHIGAN STATE UNIVERSITY · PI WATTS, STEPHANIE W · 2003 to 2019
$22.8M
ENDOTHELIN AND NEURAL CONTROL OF VEINS IN HYPERTENSIONR01HL063973 · NHLBI · MICHIGAN STATE UNIVERSITY · PI FINK, GREGORY D · 2000 to 2002
$627k
Sympathetic Neural Control Mechanisms in HypertensionR01HL084258 · NHLBI · MICHIGAN STATE UNIVERSITY · PI SWAIN, GREG M · 2005 to 2007
$469k
NHLBI NIH HHS HL63973NHLBI NIH HHS HL70687NHLBI NIH HHS HL84258NHLBI NIH HHS P01 HL070687NHLBI NIH HHS R01 HL084258
6 · The paper itself

Abstract

As arteries are resistance blood vessels while veins perform a capacitance function, it might be expected that sympathetic neural control of arteries and veins would differ. The function of sympathetic nerves supplying mesenteric arteries (MA) and veins (MV) in rats was investigated using in vitro continuous amperometry with a carbon fibre microelectrode and video imaging. We simultaneously measured noradrenaline (NA) overflow at the blood vessel adventitial surface and vasoconstriction evoked by electrical stimulation of perivascular sympathetic nerves. Sympathetic nerve arrangement was studied using glyoxylic acid-induced fluorescence of NA. We found that: (i) there were significant differences between MA and MV in the arrangement of sympathetic nerves; (ii) frequency-response curves for NA overflow and vasoconstriction for MV were left-shifted compared to MA; (iii) the P2X receptor antagonist, pyridoxal-phosphate-6-azophenyl-2',4'-disulphonic acid (PPADS, 10 microm), reduced constrictions in MA but not in MV while the alpha(1)-adrenergic receptor antagonist, prazosin (0.1 microm), blocked constrictions in MV but not in MA; (iv) NA overflow for MA was enhanced by the alpha(2)-adrenergic receptor antagonist, yohimbine (1.0 microm), and attenuated by the alpha(2)-adrenergic receptor agonist, UK 14,304 (1.0 microm), while yohimbine and UK 14,304 had little effect in MV; (v) cocaine (10 microm) produced larger increases in NA overflow in MA than in MV; (vi) UK 14,304 constricted MV but not MA while yohimbine reduced constrictions in MV but not MA. We conclude that there are fundamental differences in sympathetic neuroeffector mechanisms in MA and MV, which are likely to contribute to their different haemodynamic functions.

Indexed as

AnimalsCocaineElectrophysiologyGlyoxylatesMesenteric ArteriesMesenteric VeinsOxidation-ReductionPrazosinPyridoxal PhosphateRatsSympathetic Nervous SystemVasoconstrictionVideo RecordingYohimbineCocaineGlyoxylatesglyoxylic acidPrazosinPyridoxal Phosphatepyridoxal phosphate-6-azophenyl-2',4'-disulfonic acidYohimbine

Identifiers

PMID17761778
PMCPMC2276997
OpenAlexW1546379901

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.