Evidence map›Paper›PMID 28174689›Full record

ArticleFEBS open bio2017

Characterization of murine polyspecific monoamine transporters.

Yamato Miura, Takeo Yoshikawa, Fumito Naganuma, Tadaho Nakamura, Tomomitsu Iida, Anikó Kárpáti, Takuro Matsuzawa, Asuka Mogi, Ryuichi Harada, Kazuhiko Yanai

Open access · goldAbstract read
In one paragraph

Article in FEBS open bio, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.4field-weighted citation impact, top 17% 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

13 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
  2. Dopamine internalization via UptakeFrontiers in pharmacology · 2024
    Article
  3. Review
  4. Article
  5. Article
  6. Organic Cation Transporter Expression and Function in the CNS.Handbook of experimental pharmacology · 2021
    Article
  7. Review
  8. General Overview of Organic Cation Transporters in Brain.Handbook of experimental pharmacology · 2021
    Article
  9. Organic Cation Transporters in Psychiatric Disorders.Handbook of experimental pharmacology · 2021
    Article
  10. Article
  11. Review
  12. Article
  13. 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

10 authors at 2 institutions in 1 country.

Yamato MiuraDepartment of Pharmacology Tohoku University Graduate School of Medicine Sendai Miyagi Japan.
Takeo YoshikawaDepartment of Pharmacology Tohoku University Graduate School of Medicine Sendai Miyagi Japan.
Fumito NaganumaDepartment of Pharmacology Tohoku University Graduate School of Medicine Sendai Miyagi Japan; Division of Pharmacology Faculty of Medicine Tohoku Medical and Pharmaceutical University Sendai Miyagi Japan.
Tadaho NakamuraDepartment of Pharmacology Tohoku University Graduate School of Medicine Sendai Miyagi Japan; Division of Pharmacology Faculty of Medicine Tohoku Medical and Pharmaceutical University Sendai Miyagi Japan.
Tomomitsu IidaDepartment of Pharmacology Tohoku University Graduate School of Medicine Sendai Miyagi Japan.
Anikó KárpátiDepartment of Pharmacology Tohoku University Graduate School of Medicine Sendai Miyagi Japan.
Takuro MatsuzawaDepartment of Pharmacology Tohoku University Graduate School of Medicine Sendai Miyagi Japan.
Asuka MogiDepartment of Pharmacology Tohoku University Graduate School of Medicine Sendai Miyagi Japan.
Ryuichi HaradaDepartment of Pharmacology Tohoku University Graduate School of Medicine Sendai Miyagi Japan.
Kazuhiko YanaiDepartment of Pharmacology Tohoku University Graduate School of Medicine Sendai Miyagi Japan.
Tohoku University · JPTohoku Medical and Pharmaceutical University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The dysregulation of monoamine clearance in the central nervous system occurs in various neuropsychiatric disorders, and the role of polyspecific monoamine transporters in monoamine clearance is increasingly highlighted in recent studies. However, no study to date has properly characterized polyspecific monoamine transporters in the mouse brain. In the present study, we examined the kinetic properties of three mouse polyspecific monoamine transporters [organic cation transporter 2 (Oct2), Oct3, and plasma membrane monoamine transporter (Pmat)] and compared the absolute mRNA expression levels of these transporters in various brain areas. First, we evaluated the affinities of each transporter for noradrenaline, dopamine, serotonin, and histamine, and found that mouse ortholog substrate affinities were similar to those of human orthologs. Next, we performed drug inhibition assays and identified interspecies differences in the pharmacological properties of polyspecific monoamine transporters; in particular, corticosterone and decynium-22, which are widely recognized as typical inhibitors of human OCT3, enhanced the transport activity of mouse Oct3. Finally, we quantified absolute mRNA expression levels of each transporter in various regions of the mouse brain and found that while all three transporters were ubiquitously expressed, Pmat was the most highly expressed transporter. These results provide an important foundation for future translational research investigating the roles of polyspecific monoamine transporters in neurological and neuropsychiatric disease.

Indexed as

monoamine transporterpolyspecific transportersolute carrier family

Identifiers

PMID28174689
PMCPMC5292661
OpenAlexW2567347417

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.