» Articles » PMID: 30728768

General Principles of Neuronal Co-transmission: Insights From Multiple Model Systems

Overview
Date 2019 Feb 8
PMID 30728768
Citations 55
Authors
Affiliations
Soon will be listed here.
Abstract

It is now accepted that neurons contain and release multiple transmitter substances. However, we still have only limited insight into the regulation and functional effects of this co-transmission. Given that there are 200 or more neurotransmitters, the chemical complexity of the nervous system is daunting. This is made more-so by the fact that their interacting effects can generate diverse non-linear and novel consequences. The relatively poor history of pharmacological approaches likely reflects the fact that manipulating a transmitter system will not necessarily mimic its roles within the normal chemical environment of the nervous system (e.g., when it acts in parallel with co-transmitters). In this article, co-transmission is discussed in a range of systems [from invertebrate and lower vertebrate models, up to the mammalian peripheral and central nervous system (CNS)] to highlight approaches used, degree of understanding, and open questions and future directions. Finally, we offer some outlines of what we consider to be the general principles of co-transmission, as well as what we think are the most pressing general aspects that need to be addressed to move forward in our understanding of co-transmission.

Citing Articles

A high-performance GRAB sensor reveals differences in the dynamics and molecular regulation between neuropeptide and neurotransmitter release.

Xia X, Li Y Nat Commun. 2025; 16(1):819.

PMID: 39827209 PMC: 11743212. DOI: 10.1038/s41467-025-56129-w.


A brief history of insect neuropeptide and peptide hormone research.

Nassel D Cell Tissue Res. 2024; 399(2):129-159.

PMID: 39653844 PMC: 11787221. DOI: 10.1007/s00441-024-03936-0.


Cell type-specific driver lines targeting the central complex and their use to investigate neuropeptide expression and sleep regulation.

Wolff T, Eddison M, Chen N, Nern A, Sundaramurthi P, Sitaraman D bioRxiv. 2024; .

PMID: 39484527 PMC: 11526984. DOI: 10.1101/2024.10.21.619448.


UNC-30/PITX coordinates neurotransmitter identity with postsynaptic GABA receptor clustering.

Correa E, Mialon M, Cizeron M, Bessereau J, Pinan-Lucarre B, Kratsios P Development. 2024; 151(16).

PMID: 39190555 PMC: 11385328. DOI: 10.1242/dev.202733.


Arcuate dopaminergic/GABAergic neurons project within the hypothalamus and to the median eminence.

Mittal S, Arenkiel B, Lyons-Warren A J Neurophysiol. 2024; 132(3):943-952.

PMID: 39108212 PMC: 11427037. DOI: 10.1152/jn.00086.2024.


References
1.
Norton J, Bennett D, Knash M, Murray K, Gorassini M . Changes in sensory-evoked synaptic activation of motoneurons after spinal cord injury in man. Brain. 2008; 131(Pt 6):1478-91. PMC: 2566952. DOI: 10.1093/brain/awn050. View

2.
Qiu J, Nestor C, Zhang C, Padilla S, Palmiter R, Kelly M . High-frequency stimulation-induced peptide release synchronizes arcuate kisspeptin neurons and excites GnRH neurons. Elife. 2016; 5. PMC: 4995096. DOI: 10.7554/eLife.16246. View

3.
Henning R . Purinoceptors in neuromuscular transmission. Pharmacol Ther. 1997; 74(1):115-28. DOI: 10.1016/s0163-7258(97)00015-6. View

4.
Choi C, Cao G, Tanenhaus A, McCarthy E, Jung M, Schleyer W . Autoreceptor control of peptide/neurotransmitter corelease from PDF neurons determines allocation of circadian activity in drosophila. Cell Rep. 2012; 2(2):332-44. PMC: 3432947. DOI: 10.1016/j.celrep.2012.06.021. View

5.
Russell D, Hartline D . A multiaction synapse evoking both EPSPs and enhancement of endogenous bursting. Brain Res. 1981; 223(1):19-38. DOI: 10.1016/0006-8993(81)90803-9. View