Evidence map›Paper›PMID 42396171›Full record

ReviewFrontiers in molecular neuroscience2026

Neurotransmitter co-transmission: synaptic architectures, functional logic, and emerging tools.

Elif Tunc-Ozcan

Abstract readReview
In one paragraph

Review in Frontiers in molecular neuroscience, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

1 author.

Elif Tunc-OzcanDepartment of Neurosciences, University of New Mexico, Albuquerque, NM, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Neurotransmitter co-transmission has become recognized as a fundamental organizing principle of neural communication, challenging the traditional view that individual neurons operate through a single transmitter system. Current evidence demonstrates that many neurons utilize multiple transmitters via distinct synaptic architectures, such as co-packaging within the same vesicle, release from separate vesicle pools within the same terminal, and segregation of transmitters across different boutons or neuronal processes. These organizational modes are not simply structural variants; they impose distinct rules for release, target engagement, and short-term dynamics, thereby shaping circuit function in specific ways. Across neural systems, several common principles have emerged: co-transmission expands signaling across multiple timescales, enhances target specificity, and allows transmitter balance to shift according to firing patterns and circuit state. A major conceptual and technical challenge in the field is that no single method can definitively establish the release mechanism. Consequently, recent advances have relied on integrating molecular profiling, electrophysiology, high-resolution anatomy, optogenetics, and genetically encoded neurotransmitter sensors. Collectively, these approaches are beginning to clarify how multi-transmitter neurons are organized and how their signaling is regulated. Future progress will likely depend on multimodal strategies that connect synaptic architecture to release dynamics, circuit computation, and behavior

Indexed as

neurotransmissionneurotransmitter co-releaseneurotransmitter co-transmissionsynaptic architecturessynaptic plasticity

Identifiers

PMID42396171
PMCPMC13323446

What OpenQuestion holds

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Registered trials

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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.