Evidence map›Paper›PMID 27890817›Full record

ArticlePharmacological research2017

sec-Butylpropylacetamide (SPD), a new amide derivative of valproic acid for the treatment of neuropathic and inflammatory pain.

Dan Kaufmann, Peter J West, Misty D Smith, Boris Yagen, Meir Bialer, Marshall Devor, H Steve White, K C Brennan

Abstract read
In one paragraph

Article in Pharmacological research, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.4field-weighted citation impact, top 18% 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

7 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. sec-Butylpropylacetamide (SPD) has antimigraine properties.Cephalalgia : an international journal of headache · 2016
    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

8 authors at 2 institutions in 2 countries.

Dan KaufmannAnticonvulsant Drug Development Program, Department of Pharmacology and Toxicology, University of Utah, Salt Lake City, UT, USA.
Peter J WestAnticonvulsant Drug Development Program, Department of Pharmacology and Toxicology, University of Utah, Salt Lake City, UT, USA.
Misty D SmithAnticonvulsant Drug Development Program, Department of Pharmacology and Toxicology, University of Utah, Salt Lake City, UT, USA.
Boris YagenInstitute for Drug Research, School of Pharmacy, Faculty of Medicine, The Hebrew University of Jerusalem, Jerusalem, Israel; David R. Bloom Center for Pharmacy, Faculty of Medicine, The Hebrew University of Jerusalem, Jerusalem, Israel.
Meir BialerInstitute for Drug Research, School of Pharmacy, Faculty of Medicine, The Hebrew University of Jerusalem, Jerusalem, Israel; David R. Bloom Center for Pharmacy, Faculty of Medicine, The Hebrew University of Jerusalem, Jerusalem, Israel.
Marshall DevorDepartment of Cell and Animal Biology, Institute of Life Sciences, The Hebrew University of Jerusalem, Jerusalem, Israel.
H Steve WhiteAnticonvulsant Drug Development Program, Department of Pharmacology and Toxicology, University of Utah, Salt Lake City, UT, USA. Electronic address: hswhite@uw.edu.
K C BrennanDepartment of Neurology, University of Utah, Salt Lake City, UT, USA. Electronic address: K.C.Brennan@hsc.utah.edu.
University of Utah · USHebrew University of Jerusalem · IL

Funding

SCREENING FOR THE IDENTIFICATION, TREATMENT AND PREVENTION OF EPILEPSY AND NEURON01NS42359 · NINDS · UNIVERSITY OF UTAH · PI WHITE, H. STEVE WHITE · 2007 to 2010
$22.7M
Sensory plasticity in migraineR01NS085413 · NINDS · UNIVERSITY OF UTAH · PI BRENNAN, KEVIN CHRISTOPHER · 2013 to 2017
$1.7M
Natural History and Treatment Response of AVMsK08NS042359 · NINDS · UNIVERSITY OF CALIFORNIA SAN FRANCISCO · PI HALIM, ALEXANDER · 2002 to 2002
$131k
NINDS NIH HHS N01 NS042359NINDS NIH HHS N01NS42359NINDS NIH HHS R01 NS085413
6 · The paper itself

Abstract

Chronic pain is a multifactorial disease comprised of both inflammatory and neuropathic components that affect ∼20% of the world's population. sec-Butylpropylacetamide (SPD) is a novel amide analogue of valproic acid (VPA) previously shown to possess a broad spectrum of anticonvulsant activity. In this study, we defined the pharmacokinetic parameters of SPD in rat and mouse, and then evaluated its antinociceptive potential in neuropathic and acute inflammatory pain models. In the sciatic nerve ligation (SNL) model of neuropathic pain, SPD was equipotent to gabapentin and more potent than its parent compound VPA. SPD also showed either higher or equal potency to VPA in the formalin, carrageenan, and writhing tests of inflammatory pain. SPD showed no effects on compound action potential properties in a sciatic nerve preparation, suggesting that its mechanism of action is distinct from local anesthetics and membrane stabilizing drugs. SPD's activity in both neuropathic and inflammatory pain warrants its development as a potential broad-spectrum anti-nociceptive drug.

Indexed as

AmidesAminesAnalgesicsAnimalsCyclohexanecarboxylic AcidsDisease Models, AnimalGabapentingamma-Aminobutyric AcidInflammationMaleMiceNeuralgiaPainRatsRats, Sprague-DawleySciatic NerveAmidesAminesAnalgesicsCyclohexanecarboxylic AcidsGabapentingamma-Aminobutyric Acidsec-butyl-propylacetamideValproic AcidCarrageenan testChung modelCompound action potentialsFormalin testPharmacokineticssec-Butylpropylacetamide (SPD)Writhing test

Identifiers

PMID27890817
PMCPMC5352298
OpenAlexW2549762964

What OpenQuestion holds

Textmetadata
LicenceTDM
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.