Evidence map›Paper›PMID 17325649›Full record

ArticleBritish journal of pharmacology2007

5-HT4 receptor agonists increase sAPPalpha levels in the cortex and hippocampus of male C57BL/6j mice.

M Cachard-Chastel, F Lezoualc'h, I Dewachter, C Deloménie, S Croes, H Devijver, M Langlois, F Van Leuven, S Sicsic, A M Gardier

Open access · bronzeAbstract read
In one paragraph

Article in British journal of pharmacology, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 1 pooled it
1.9field-weighted citation impact, top 15% 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

24 citing papers in PubMed, 1 synthesis or guideline pooled it, 63 citations in OpenAlex.

  1. Prucalopride: For functional constipation only?Techniques in coloproctology · 2016
    Pooled it
  2. Review
  3. Review
  4. Combinatorial targeting of NMDARs and 5-HTAlzheimer's research & therapy · 2025
    Article
  5. Chronic, combinatorial targeting of NMDARs and 5-HTNeuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2025
    Article
  6. Article
  7. Review
  8. Review
  9. Article
  10. Review
  11. Memory Disorders Related to Hippocampal Function: The Interest of 5-HTInternational journal of molecular sciences · 2021
    Review
  12. Translating the promise of 5HTPsychological medicine · 2021
    Review
  13. Article
  14. Article
  15. Review
  16. Can Animal Models Inform on the Relationship between Depression and Alzheimer Disease?Canadian journal of psychiatry. Revue canadienne de psychiatrie · 2019
    Review
  17. Rapid anxiolytic effects of a 5-HT₄ receptor agonist are mediated by a neurogenesis-independent mechanism.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2014
    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

10 authors at 4 institutions in 2 countries.

M Cachard-ChastelEA3544, Sérotonine et Neuropharmacologie, Faculté de Pharmacie, Universite Paris-Sud, Châtenay-Malabry cedex, France.
F Lezoualc'h
I Dewachter
C Deloménie
S Croes
H Devijver
M Langlois
F Van Leuven
S Sicsic
A M Gardier
KU Leuven · BEUniversité Paris-Sud · FRInstitut Galien Paris-Saclay · FRLaboratoire d'Énergétique Moléculaire et Macroscopique, Combustion · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

background and purposeA strategy to treat Alzheimer's disease (AD) is to increase the soluble form of amyloid precursor protein (sAPPalpha), a promnesic protein, in the brain. Because strong evidence supports beneficial effects of 5-hydroxytryptamine 5-HT(4) receptor agonists in memory and learning, we investigated the role of 5-HT(4) receptors on APP processing in 8 weeks-old male C57BL/6j mice. EXPERIMENTAL APPROACH: Mice were given, subcutaneously, prucalopride or ML 10302 (s.c.), two highly selective 5-HT(4) receptor agonists and, up to 240 min later, the hippocampus and cortex were analysed by Western blot for sAPPalpha determination. KEY

resultsPrucalopride (5 or 10 mg kg(-1)) significantly increased sAPPalpha levels in the hippocampus and cortex, but did not modify the expression level of APP mRNA as detected by quantitative RT-PCR. A selective 5-HT(4) receptor antagonist, GR125487 (1 mg kg(-1), s.c.) inhibited prucalopride induced- increase in sAPPalpha levels. In addition, levels of sAPPalpha were increased by ML10302 only at 20 mg kg(-1) and was limited to the cortex. Also, prucalopride increased sAPPalpha levels in the cortex of a transgenic mouse model of AD, expressing the London mutation of APP. Furthermore, the combined injection of a selective acetylcholinesterase inhibitor, donepezil and prucalopride induced a synergic increase in sAPPalpha levels in the cortex and hippocampus. CONCLUSIONS AND IMPLICATIONS: Our results demonstrate that the 5-HT(4) receptor plays a key role in the non-amyloidogenic pathway of APP metabolism in vivo and give support to the beneficial use of 5-HT(4) agonists for AD treatment.

Indexed as

Serotonin 5-HT4 Receptor AgonistsAminobenzoatesAmyloid beta-Protein PrecursorAnimalsBenzofuransCerebral CortexCholinesterase InhibitorsDonepezilHippocampusIndansIndolesMaleMiceMice, Inbred C57BLMice, Transgenicpara-Aminobenzoates2-piperidinoethyl 4-amino-5-chloro-2-methoxybenzoateAminobenzoatesAmyloid beta-Protein PrecursorBenzofuransCholinesterase InhibitorsDonepezilGR 113808IndansIndolespara-AminobenzoatesPiperidinesprucaloprideRNA, MessengerSerotonin 5-HT4 Receptor AgonistsSerotonin 5-HT4 Receptor AntagonistsSerotonin AntagonistsSerotonin Receptor AgonistsSulfonamides

Identifiers

PMID17325649
PMCPMC2013878
OpenAlexW2151984407

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.