Evidence map›Paper›PMID 31678138›Full record

ArticleExperimental neurology2020

Paradoxical effects of continuous high dose gabapentin treatment on autonomic dysreflexia after complete spinal cord injury.

Khalid C Eldahan, Hannah C Williams, David H Cox, Jenna L Gollihue, Samir P Patel, Alexander G Rabchevsky

Open access · greenAbstract read
In one paragraph

Article in Experimental neurology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.8field-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

9 citing papers in PubMed, 17 citations in OpenAlex.

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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

6 authors at 1 institution in 1 country.

Khalid C EldahanDepartment of Physiology, University of Kentucky, Lexington, KY 40536, USA; Spinal Cord and Brain Injury Research Center (SCoBIRC), University of Kentucky, B 436 Biomedical & Biological Research Building (BBSRB), 741 South Limestone Street, Lexington, KY 40536-0509, USA. Electronic address: khalid.eldahan@uky.edu.
Hannah C WilliamsSpinal Cord and Brain Injury Research Center (SCoBIRC), University of Kentucky, B 436 Biomedical & Biological Research Building (BBSRB), 741 South Limestone Street, Lexington, KY 40536-0509, USA. Electronic address: hannahwilliams@uky.edu.
David H CoxSpinal Cord and Brain Injury Research Center (SCoBIRC), University of Kentucky, B 436 Biomedical & Biological Research Building (BBSRB), 741 South Limestone Street, Lexington, KY 40536-0509, USA. Electronic address: davidhcox@uky.edu.
Jenna L GollihueDepartment of Physiology, University of Kentucky, Lexington, KY 40536, USA; Spinal Cord and Brain Injury Research Center (SCoBIRC), University of Kentucky, B 436 Biomedical & Biological Research Building (BBSRB), 741 South Limestone Street, Lexington, KY 40536-0509, USA. Electronic address: jlva227@uky.edu.
Samir P PatelDepartment of Physiology, University of Kentucky, Lexington, KY 40536, USA; Spinal Cord & Brain Injury Research Center (SCoBIRC), University of Kentucky, B 461 Biomedical & Biological Research Building (BBSRB), 741 South Limestone Street, Lexington, KY 40536-0509, USA. Electronic address: skpate2@uky.edu.
Alexander G RabchevskyDepartment of Physiology, University of Kentucky, Lexington, KY 40536, USA; Spinal Cord and Brain Injury Research Center (SCoBIRC), University of Kentucky, B 471 Biomedical & Biological Research Building (BBSRB), 741 South Limestone Street, Lexington, KY 40536-0509, USA. Electronic address: agrab@uky.edu.
University of Kentucky · US

Funding

UK Spinal Cord &Brain Injury Research Center Core GrantP30NS051220 · NINDS · UNIVERSITY OF KENTUCKY · PI HALL, EDWARD D. · 2005 to 2015
$6.4M
Neurobiology of CNS Injury and RepairT32NS077889 · NINDS · UNIVERSITY OF KENTUCKY · PI Warren Joseph Alilain, JOHN C GENSEL · 2012 to 2026
$2.4M
Role of Intraspinal Plasticity in Autonomic DysreflexiaR01NS049901 · NINDS · UNIVERSITY OF KENTUCKY · PI RABCHEVSKY, ALEXANDER GEORGE · 2004 to 2008
$1.7M
Changing serotonin receptor 2C splice variants to combat spasticity after spinal cord injuryR21NS098186 · NINDS · UNIVERSITY OF KENTUCKY · PI RABCHEVSKY, ALEXANDER GEORGE, STAMM, STEFAN · 2017 to 2018
$414k
NINDS NIH HHS P30 NS051220NINDS NIH HHS R01 NS049901NINDS NIH HHS R21 NS098186NINDS NIH HHS T32 NS077889
6 · The paper itself

Abstract

Spinal cord injury (SCI) can have profound effects on the autonomic and cardiovascular systems, notably with injuries above high-thoracic levels that result in the development of autonomic dysreflexia (AD) characterized by volatile hypertension in response to exaggerated sympathetic reflexes triggered by afferent stimulation below the injury level. Pathophysiological changes associated with the development of AD include sprouting of both nociceptive afferents and ascending propriospinal 'relay' neurons below the injury, as well as dynamic changes in synaptic inputs onto sympathetic preganglionic neurons. However, it remains uncertain whether synapse formation between sprouted c-fibers and propriospinal neurons contributes to the development of exaggerated sympathetic reflexes produced during AD. We previously reported that once daily treatment with the anti-epileptic and neuropathic pain medication, gabapentin (GBP), at low dosage (50 mg/kg) mitigates experimentally induced AD soon after injections, likely by impeding glutamatergic signaling. Since much higher doses of GBP are reported to block the formation of excitatory synapses, we hypothesized that continuous, high dosage GBP treatment after SCI might prevent the formation of aforementioned aberrant synapses and, accordingly, reduce the incidence and severity of AD. Adult female rats implanted with aortic telemetry probes for hemodynamic monitoring underwent T4-transection SCI and immediately received 100 mg/kg (i.p.) of GBP and then every six hours (400 mg/kg/day) for 4-weeks after injury. We assessed daily body weight, mean arterial pressure, heart rate, frequency of spontaneous AD, and hemodynamic changes during colorectal distension (CRD) to establish whether high dose GBP treatment prophylactically mitigates both AD and associated aberrant synaptic plasticity. This regimen significantly reduced both the absolute blood pressure reached during experimentally induced AD and the time required to return to baseline afterwards. Conversely, GBP prevented return to pre-injury body weights and paradoxically increased the frequency of spontaneously occurring AD. While there were significant decreases in the densities of excitatory and inhibitory pre-synaptic markers in the lumbosacral dorsal horn following injury alone, they were unaltered by continuous GBP treatment. This indicates distinct mechanisms of action for acute GBP to mitigate induced AD whereas chronic GBP increases non-induced AD frequencies. While high dose prophylactic GBP is not recommended to treat AD, acute low dose GBP may hold therapeutic value to mitigate evoked AD, notably during iatrogenic procedures under controlled clinical conditions.

Indexed as

AnimalsAutonomic DysreflexiaDose-Response Relationship, DrugExcitatory Amino Acid AntagonistsFemaleGabapentinNeuronal PlasticityRatsRats, WistarSpinal CordSpinal Cord InjuriesExcitatory Amino Acid AntagonistsGabapentinAutonomicNeurontinPlasticitySympatheticSynapse

Identifiers

PMID31678138
PMCPMC9204647
OpenAlexW2988398488

What OpenQuestion holds

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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.