Evidence map›Paper›PMID 24907493›Full record

ArticleNeurobiology of disease2014

Mechanism underlying unaltered cortical inhibitory synaptic transmission in contrast with enhanced excitatory transmission in CaV2.1 knockin migraine mice.

Dania Vecchia, Angelita Tottene, Arn M J M van den Maagdenberg, Daniela Pietrobon

Open access · hybridAbstract read
In one paragraph

Article in Neurobiology of disease, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
3.5field-weighted citation impact, top 8% 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

36 citing papers in PubMed, 60 citations in OpenAlex.

  1. Hemiplegic migraine: genetics and pathophysiology.The Journal of clinical investigation · 2026
    Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Review
  7. Review
  8. Article
  9. Article
  10. Article
  11. Headache in people with epilepsy.Nature reviews. Neurology · 2021
    Review
  12. Article
  13. Review
  14. Article
  15. Article
  16. Rare CACNA1A mutations leading to congenital ataxia.Pflugers Archiv : European journal of physiology · 2020
    Review
  17. Article
  18. Genetics of migraine aura: an update.The journal of headache and pain · 2020
    Review
  19. Review
  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

4 authors at 2 institutions in 2 countries.

Dania VecchiaDepartment of Biomedical Sciences, University of Padova and CNR Institute of Neuroscience, 35121 Padova, Italy.
Angelita TotteneDepartment of Biomedical Sciences, University of Padova and CNR Institute of Neuroscience, 35121 Padova, Italy.
Arn M J M van den MaagdenbergDepartment of Human Genetics and Neurology, Leiden University Medical Centre, Leiden, The Netherlands.
Daniela PietrobonDepartment of Biomedical Sciences, University of Padova and CNR Institute of Neuroscience, 35121 Padova, Italy. Electronic address: daniela.pietrobon@unipd.it.
University of Padua · ITLeiden University Medical Center · NL

Funding

Telethon GGP06234
6 · The paper itself

Abstract

Familial hemiplegic migraine type 1 (FHM1), a monogenic subtype of migraine with aura, is caused by gain-of-function mutations in CaV2.1 (P/Q-type) calcium channels. In FHM1 knockin mice, excitatory neurotransmission at cortical pyramidal cell synapses is enhanced, but inhibitory neurotransmission at connected pairs of fast-spiking (FS) interneurons and pyramidal cells is unaltered, despite being initiated by CaV2.1 channels. The mechanism underlying the unaltered GABA release at cortical FS interneuron synapses remains unknown. Here, we show that the FHM1 R192Q mutation does not affect inhibitory transmission at autapses of cortical FS and other types of multipolar interneurons in microculture from R192Q knockin mice, and investigate the underlying mechanism. Lowering the extracellular [Ca(2+)] did not reveal gain-of-function of evoked transmission neither in control nor after prolongation of the action potential (AP) with tetraethylammonium, indicating unaltered AP-evoked presynaptic calcium influx at inhibitory autapses in FHM1 KI mice. Neither saturation of the presynaptic calcium sensor nor short duration of the AP can explain the unaltered inhibitory transmission in the mutant mice. Recordings of the P/Q-type calcium current in multipolar interneurons in microculture revealed that the current density and the gating properties of the CaV2.1 channels expressed in these interneurons are barely affected by the FHM1 mutation, in contrast with the enhanced current density and left-shifted activation gating of mutant CaV2.1 channels in cortical pyramidal cells. Our findings suggest that expression of specific CaV2.1 channels differentially sensitive to modulation by FHM1 mutations in inhibitory and excitatory cortical neurons underlies the gain-of-function of excitatory but unaltered inhibitory synaptic transmission and the likely consequent dysregulation of the cortical excitatory-inhibitory balance in FHM1.

Indexed as

Action PotentialsAnimalsCalciumCalcium ChannelsCalcium Channels, N-TypeCell Culture TechniquesCerebral CortexDisease Models, Animalgamma-Aminobutyric AcidGene Knock-In TechniquesHumansInhibitory Postsynaptic PotentialsInterneuronsMice, Inbred C57BLMice, TransgenicMigraine with AuraCACNA1A protein, humanCalciumCalcium ChannelsCalcium Channels, N-Typegamma-Aminobutyric Acidcalcium channel, inhibitory synaptic transmissionChannelopathyExcitatory–inhibitory balanceFast-spiking interneuronKnockin mouse modelMigraine

Identifiers

PMID24907493
PMCPMC4107271
OpenAlexW2044444729

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.