Evidence map›Paper›PMID 32717355›Full record

ArticleExperimental neurology2020

Reducing monocarboxylate transporter MCT1 worsens experimental diabetic peripheral neuropathy.

Mithilesh Kumar Jha, Xanthe H Ament, Fang Yang, Ying Liu, Michael J Polydefkis, Luc Pellerin, Brett M Morrison

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 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 1 pooled it
1.2field-weighted citation impact, top 21% 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

15 citing papers in PubMed, 1 synthesis or guideline pooled it, 18 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. [Research advances on the role of Schwann cells in diabetic peripheral neuropathy].Zhonghua shao shang yu chuang mian xiu fu za zhi · 2023
    Review
  8. Review
  9. Article
  10. Review
  11. Review
  12. Monocarboxylate Transporters: Role and Regulation in Corneal Diabetes.Analytical cellular pathology (Amsterdam) · 2022
    Article
  13. Metabolic Transporters in the Peripheral Nerve-What, Where, and Why?Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2021
    Review
  14. Article
  15. Review
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 2 countries.

Mithilesh Kumar JhaDepartment of Neurology, Johns Hopkins University School of Medicine, Baltimore, MD 21205, United States.
Xanthe H AmentDepartment of Neurology, Johns Hopkins University School of Medicine, Baltimore, MD 21205, United States.
Fang YangDepartment of Neurology, Johns Hopkins University School of Medicine, Baltimore, MD 21205, United States.
Ying LiuDepartment of Neurology, Johns Hopkins University School of Medicine, Baltimore, MD 21205, United States.
Michael J PolydefkisDepartment of Neurology, Johns Hopkins University School of Medicine, Baltimore, MD 21205, United States.
Luc PellerinInserm U1082, Universite de Poitiers, Poitiers Cedex 86021, France; Centre de Résonance Magnétique des Systèmes Biologiques, UMR5536 CNRS, LabEx TRAIL-IBIO, Université de Bordeaux, Bordeaux Cedex 33760, France.
Brett M MorrisonDepartment of Neurology, Johns Hopkins University School of Medicine, Baltimore, MD 21205, United States. Electronic address: bmorris7@jhmi.edu.
Johns Hopkins University · USCentre National de la Recherche Scientifique · FR

Funding

Oligodendroglial Dysfunction in C9orf72 ALS and FTDR01NS099320 · NINDS · JOHNS HOPKINS UNIVERSITY · PI MORRISON, BRETT M., ROTHSTEIN, JEFFREY D · 2017 to 2021
$3.0M
Role of Monocarboxylate Transporters in the Recovery from Peripheral Nerve InjuryR01NS086818 · NINDS · JOHNS HOPKINS UNIVERSITY · PI MORRISON, BRETT M. · 2015 to 2019
$1.8M
NINDS NIH HHS R01 NS086818NINDS NIH HHS R01 NS099320
6 · The paper itself

Abstract

Diabetic peripheral neuropathy (DPN) is one of the most common complications in diabetic patients. Though the exact mechanism for DPN is unknown, it clearly involves metabolic dysfunction and energy failure in multiple cells within the peripheral nervous system. Lactate is an alternate source of metabolic energy that is increasingly recognized for its role in supporting neurons. The primary transporter for lactate in the nervous system, monocarboxylate transporter-1 (MCT1), has been shown to be critical for peripheral nerve regeneration and metabolic support to neurons/axons. In this study, MCT1 was reduced in both sciatic nerve and dorsal root ganglia in wild-type mice treated with streptozotocin (STZ), a common model of type-1 diabetes. Heterozygous MCT1 null mice that developed hyperglycemia following STZ treatment developed a more severe DPN compared to wild-type mice, as measured by greater axonal demyelination, decreased peripheral nerve function, and increased numbness to innocuous low-threshold mechanical stimulation. Given that MCT1 inhibitors are being developed as both immunosuppressive and chemotherapeutic medications, our results suggest that clinical development in patients with diabetes should proceed with caution. Collectively, our findings uncover an important role for MCT1 in DPN and provide a potential lead toward developing novel treatments for this currently untreatable disease.

Indexed as

AnimalsAxonsBehavior, AnimalDemyelinating DiseasesDiabetes Mellitus, ExperimentalDiabetic NeuropathiesGanglia, SpinalHypesthesiaLactic AcidMaleMiceMice, Inbred C57BLMice, KnockoutMonocarboxylate Transport Protein 1Monocarboxylic Acid TransportersNeural ConductionLactic AcidMonocarboxylate Transport Protein 1Monocarboxylic Acid TransportersSymportersDiabetic peripheral neuropathyDorsal root ganglionMetabolismMonocarboxylate transporterPeripheral nerve

Identifiers

PMID32717355
PMCPMC7502508
OpenAlexW3045481993

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.