Evidence map›Paper›PMID 36674439›Full record

ArticleInternational journal of molecular sciences2023

Unique, Specific CART Receptor-Independent Regulatory Mechanism of CART(55-102) Peptide in Spinal Nociceptive Transmission and Its Relation to Dipeptidyl-Peptidase 4 (DDP4).

Márk Kozsurek, Kornél Király, Klára Gyimesi, Erika Lukácsi, Csaba Fekete, Balázs Gereben, Petra Mohácsik, Zsuzsanna Helyes, Kata Bölcskei, Valéria Tékus and 8 more

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.5field-weighted citation impact, top 36% 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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Review
  2. Molecular Links between Sensory Nerves, Inflammation, and Pain 2.0.International journal of molecular sciences · 2023
    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

18 authors at 9 institutions in 2 countries.

Márk KozsurekDepartment of Anatomy, Histology and Embryology, Semmelweis University, H-1094 Budapest, Hungary.ORCID 0000-0001-5465-2803
Kornél KirályDepartment of Pharmacology and Pharmacotherapy, Semmelweis University, H-1089 Budapest, Hungary.ORCID 0000-0002-7252-0422
Klára GyimesiDepartment of Anatomy, Histology and Embryology, Semmelweis University, H-1094 Budapest, Hungary.
Erika LukácsiDepartment of Anatomy, Histology and Embryology, Semmelweis University, H-1094 Budapest, Hungary.
Csaba FeketeLaboratory of Integrative Neuroendocrinology, Institute of Experimental Medicine, Eötvös Loránd Research Network, H-1083 Budapest, Hungary.
Balázs GerebenLaboratory of Integrative Neuroendocrinology, Institute of Experimental Medicine, Eötvös Loránd Research Network, H-1083 Budapest, Hungary.
Petra MohácsikLaboratory of Integrative Neuroendocrinology, Institute of Experimental Medicine, Eötvös Loránd Research Network, H-1083 Budapest, Hungary.
Zsuzsanna HelyesDepartment of Pharmacology and Pharmacotherapy, University of Pécs, H-7624 Pécs, Hungary.
Kata BölcskeiDepartment of Pharmacology and Pharmacotherapy, University of Pécs, H-7624 Pécs, Hungary.
Valéria TékusDepartment of Pharmacology and Pharmacotherapy, University of Pécs, H-7624 Pécs, Hungary.
Károly PapDepartment of Orthopaedics and Traumatology, Uzsoki Hospital, H-1145 Budapest, Hungary.
Edina SzűcsInstitute of Biochemistry, Biological Research Centre, Eötvös Loránd Research Network, H-6726 Szeged, Hungary.
Sándor BenyheInstitute of Biochemistry, Biological Research Centre, Eötvös Loránd Research Network, H-6726 Szeged, Hungary.
Tímea ImreMS Metabolomics Laboratory, Instrumentation Centre, Research Centre for Natural Sciences, Eötvös Loránd Research Network, H-1117 Budapest, Hungary.
Pál SzabóMS Metabolomics Laboratory, Instrumentation Centre, Research Centre for Natural Sciences, Eötvös Loránd Research Network, H-1117 Budapest, Hungary.ORCID 0000-0003-2260-4641
Andrea GajtkóDepartment of Anatomy, Histology and Embryology, Faculty of Medicine, University of Debrecen, H-4032 Debrecen, Hungary.
Krisztina HollóDepartment of Anatomy, Histology and Embryology, Faculty of Medicine, University of Debrecen, H-4032 Debrecen, Hungary.ORCID 0000-0001-5858-0296
Zita PuskárDepartment of Anatomy, Histology and Embryology, Semmelweis University, H-1094 Budapest, Hungary.
Semmelweis University · HUHUN-REN Institute of Experimental Medicine · HUHUN-REN Szegedi Biológiai Kutatóközpont · HUResearch Network (United States) · USUniversity of Debrecen · HUUniversity of Pecs · HUHungarian Research Network · HUTufts Medical Center · USUzsoki Hospital · HU

Funding

Eötvös Loránd Research Network (ELKH)Human Resource Development Operational Programme (EFOP) 3.6.2-17-2017-00008 N (2017-2019)National Research Development and Innovation (NKFI) Fund 2017-1.2.1-NKP-2017-00002National Research Development and Innovation (NKFI) Fund KTIA_NAP_13-2-2014-0005National Research Development and Innovation (NKFI) Fund OTKA-108518National Research Development and Innovation (NKFI) Fund OTKA-138046National Research Development and Innovation (NKFI) Fund PD-OTKA-101248National Research Development and Innovation (NKFI) Fund PharmaLab RRF-2.3.1-21-2022-00015National Research Development and Innovation (NKFI) Fund TKP2021-EGA-16ANational Research Development and Innovation (NKFI) Fund TKP2021-EGA-25
6 · The paper itself

Abstract

Cocaine- and amphetamine-regulated transcript (CART) peptides are involved in several physiological and pathological processes, but their mechanism of action is unrevealed due to the lack of identified receptor(s). We provided evidence for the antihyperalgesic effect of CART(55-102) by inhibiting dipeptidyl-peptidase 4 (DPP4) in astrocytes and consequently reducing neuroinflammation in the rat spinal dorsal horn in a carrageenan-evoked inflammation model. Both naturally occurring CART(55-102) and CART(62-102) peptides are present in the spinal cord. CART(55-102) is not involved in acute nociception but regulates spinal pain transmission during peripheral inflammation. While the full-length peptide with a globular motif contributes to hyperalgesia, its N-terminal inhibits this process. Although the anti-hyperalgesic effects of CART(55-102), CART(55-76), and CART(62-76) are blocked by opioid receptor antagonists in our inflammatory models, but not in neuropathic Seltzer model, none of them bind to any opioid or G-protein coupled receptors. DPP4 interacts with Toll-like receptor 4 (TLR4) signalling in spinal astrocytes and enhances the TLR4-induced expression of interleukin-6 and tumour necrosis factor alpha contributing to inflammatory pain. Depending on the state of inflammation, CART(55-102) is processed in the spinal cord, resulting in the generation of biologically active isoleucine-proline-isoleucine (IPI) tripeptide, which inhibits DPP4, leading to significantly decreased glia-derived cytokine production and hyperalgesia.

Indexed as

HyperalgesiaToll-Like Receptor 4AnimalsCocaine- and Amphetamine-Regulated Transcript ProteinDipeptidyl Peptidase 4InflammationIsoleucineNociceptionPainPeptide FragmentsRatsSpinal CordCocaine- and Amphetamine-Regulated Transcript Proteincocaine- and amphetamine-regulated transcript protein (55-102)Dipeptidyl Peptidase 4IsoleucinePeptide FragmentsToll-Like Receptor 4allodyniachronic paincocaine- and amphetamine-regulated transcript (CART) peptidedipeptidyl-peptidase-4 (DPP4)hyperalgesiaspinal cord

Identifiers

PMID36674439
PMCPMC9865214
OpenAlexW4313588193

What OpenQuestion holds

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LicenceCC BY
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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.