Evidence map›Paper›PMID 30022062›Full record

ReviewNeuropsychopharmacology : official publication of the American College of Neuropsychopharmacology2018

Regulation of monoamine transporters and receptors by lipid microdomains: implications for depression.

Joanne J Liu, Adrienne Hezghia, Saame Raza Shaikh, Joshua F Cenido, Ruth E Stark, J John Mann, M Elizabeth Sublette

Open access · bronzeAbstract readReview
In one paragraph

Review in Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

28 citing papers in PubMed, 45 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Review
  8. Article
  9. Article
  10. Review
  11. Serotonin Signaling through Lipid Membranes.ACS chemical neuroscience · 2024
    Review
  12. Review
  13. Oligomerization of Monoamine Transporters.Sub-cellular biochemistry · 2024
    Review
  14. Structures and membrane interactions of native serotonin transporter in complexes with psychostimulants.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  15. Article
  16. Article
  17. Phosphatidylinositol 4,5-bisphosphate (PIPCommunications biology · 2022
    Article
  18. Article
  19. Article
  20. 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

7 authors at 3 institutions in 1 country.

Joanne J LiuDepartment of Molecular Imaging & Neuropathology, New York State Psychiatric Institute, New York, NY, USA.
Adrienne HezghiaDepartment of Molecular Imaging & Neuropathology, New York State Psychiatric Institute, New York, NY, USA.
Saame Raza ShaikhDepartment of Nutrition, Gillings School of Global Public Health, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Joshua F CenidoDepartment of Molecular Imaging & Neuropathology, New York State Psychiatric Institute, New York, NY, USA.ORCID http://orcid.org/0000-0002-7137-6780
Ruth E StarkDepartment of Chemistry and Biochemistry and CUNY Institute for Macromolecular Assemblies, The City College of New York, New York, NY, USA.ORCID http://orcid.org/0000-0002-3132-4580
J John MannDepartment of Molecular Imaging & Neuropathology, New York State Psychiatric Institute, New York, NY, USA.
M Elizabeth SubletteDepartment of Molecular Imaging & Neuropathology, New York State Psychiatric Institute, New York, NY, USA. sublett@nyspi.columbia.edu.
New York Psychoanalytic Society and Institute · USThe Graduate Center, CUNY · USUniversity of North Carolina at Chapel Hill · US

Funding

Cellular/Molecular Basis of Development: Research CenterG12MD007603 · NIMHD · CITY COLLEGE OF NEW YORK · PI PEZZANO, MARK · 2012 to 2017
$11.5M
Suppressing inflammation and boosting humoral immunity with n-3 PUFAsR01AT008375 · NCCIH · UNIV OF NORTH CAROLINA CHAPEL HILL · PI SHAIKH, SAAME R · 2015 to 2019
$1.9M
Neuroimaging of Fatty Acids in Major DepressionK08MH079033 · NIMH · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI SUBLETTE, M ELIZABETH · 2008 to 2012
$887k
NCCIH NIH HHS R01 AT008375NIMHD NIH HHS G12 MD007603NIMH NIH HHS K08 MH079033U.S. Department of Health & Human Services | NIH | National Center for Complementary and Integrative Health (NCCIH) R01AT008375U.S. Department of Health & Human Services | NIH | National Institute on Minority Health and Health Disparities (NIMHD) 8G12 MD007603
6 · The paper itself

Abstract

Lipid microdomains ("rafts") are dynamic, nanoscale regions of the plasma membrane enriched in cholesterol and glycosphingolipids, that possess distinctive physicochemical properties including higher order than the surrounding membrane. Lipid microdomain integrity is thought to affect neurotransmitter signaling by regulating membrane-bound protein signaling. Among the proteins potentially affected are monoaminergic receptors and transporters. As dysfunction of monoaminergic neurotransmission is implicated in major depressive disorder and other neuropsychiatric conditions, interactions with lipid microdomains may be of clinical importance. This systematic review evaluates what is known about the molecular relationships of monoamine transporter and receptor regulation to lipid microdomains. The PubMed/MeSH database was searched for original studies published in English through August 2017 concerning relationships between lipid microdomains and serotonin, dopamine and norepinephrine transporters and receptors. Fifty-seven publications were identified and assessed. Strong evidence implicates lipid microdomains in the regulation of serotonin and norepinephrine transporters; serotonin 1A, 2A, 3A, and 7A receptors; and dopamine D1 and β2 adrenergic receptors. Results were conflicting or more complex regarding lipid microdomain associations with the dopamine transporter, D2, D3, and D5 receptors; and negative with respect to β1 adrenergic receptors. Indirect evidence suggests that antidepressants, lipid-lowering drugs, and polyunsaturated fatty acids may exert effects on depression and suicide by altering the lipid milieu, thereby affecting monoaminergic transporter and receptor signaling. The lipid composition of membrane subdomains is involved in localization and trafficking of specific monoaminergic receptors and transporters. Elucidating precise mechanisms whereby lipid microdomains modulate monoamine neurotransmission in clinical contexts can have critical implications for pharmacotherapeutic targeting.

Indexed as

AnimalsDopamine Plasma Membrane Transport ProteinsHumansLipid MetabolismMajor Depressive DisorderMembrane MicrodomainsNorepinephrine Plasma Membrane Transport ProteinsReceptors, Biogenic AmineVesicular Monoamine Transport ProteinsDopamine Plasma Membrane Transport ProteinsNorepinephrine Plasma Membrane Transport ProteinsReceptors, Biogenic AmineVesicular Monoamine Transport Proteins

Identifiers

PMID30022062
PMCPMC6135777
OpenAlexW2810748978

What OpenQuestion holds

Textmetadata
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.