Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2012 Jan;139(1):93-6.
doi: 10.1085/jgp.201110659.

Co-transmission of dopamine and glutamate

Affiliations

Co-transmission of dopamine and glutamate

John I Broussard. J Gen Physiol. 2012 Jan.
No abstract available

PubMed Disclaimer

Figures

Figure 1.
Figure 1.
Two models of dopamine/glutamate co-transmission. Glutamate is green, dopamine is blue, and VGLUT2 in A10 neurons is labeled red. Bursting activity of mesolimbic dopaminergic neurons has been shown to activate AMPA and NMDA receptors on medium spiny neurons (as shown in Tecuapetla et al., 2010), possibly promoting the insertion of AMPA receptors, whereas activation of D1-like receptors promotes intracellular postsynaptic changes through G-coupled activation of adenylyl cyclase (AC). (A) Co-transmission from the same presynaptic terminal. Evidence from Hnasko et al. (2010) indicates that VGLUT2 may promote loading of dopamine into vesicles. This is evidence that glutamate and dopamine are packaged and released from the same vesicle at all structures. (B) Co-transmission by the same neuron at separate structures. Although medial mesolimbic neurons express both TH and VGLUT2 mRNA, NAc sections show VGLUT2+ staining sequestered in varicosities sprouting from the axons of TH+ neurons (Kawano et al., 2006; Yamaguchi et al., 2011). This suggests that the same neuron releases different neurotransmitters at different structures. Either model may explain the physiological results now presented by three studies (Hnasko et al., 2010; Stuber et al., 2010; Tecuapetla et al., 2010).

References

    1. Bérubé-Carrière N., Riad M., Dal Bo G., Lévesque D., Trudeau L.E., Descarries L. 2009. The dual dopamine-glutamate phenotype of growing mesencephalic neurons regresses in mature rat brain. J. Comp. Neurol. 517:873–891 10.1002/cne.22194 - DOI - PubMed
    1. Chuhma N., Zhang H., Masson J., Zhuang X., Sulzer D., Hen R., Rayport S. 2004. Dopamine neurons mediate a fast excitatory signal via their glutamatergic synapses. J. Neurosci. 24:972–981 10.1523/JNEUROSCI.4317-03.2004 - DOI - PMC - PubMed
    1. Dal Bo G., Bérubé-Carrière N., Mendez J.A., Leo D., Riad M., Descarries L., Lévesque D., Trudeau L.E. 2008. Enhanced glutamatergic phenotype of mesencephalic dopamine neurons after neonatal 6-hydroxydopamine lesion. Neuroscience. 156:59–70 10.1016/j.neuroscience.2008.07.032 - DOI - PubMed
    1. Dale H. 1935. Pharmacology and nerve-endings (Walter Ernest Dixon Memorial Lecture): (Section of Therapeutics and Pharmacology). Proc. R. Soc. Med. 28:319–332 - PMC - PubMed
    1. Dobi A., Margolis E.B., Wang H.L., Harvey B.K., Morales M. 2010. Glutamatergic and nonglutamatergic neurons of the ventral tegmental area establish local synaptic contacts with dopaminergic and nondopaminergic neurons. J. Neurosci. 30:218–229 10.1523/JNEUROSCI.3884-09.2010 - DOI - PMC - PubMed