Coloboma hyperactive mutant mice exhibit regional and transmitter- specific deficits in neurotransmission

Jacob Raber, Prashant P. Mehta, Max Kreifeldt, Loren H. Parsons, Friebert Weiss, Floyd E. Bloom, Michael C. Wilson

Research output: Contribution to journalArticle

80 Citations (Scopus)

Abstract

The mouse mutant coloboma (Cm/+), which exhibits profound spontaneous hyperactivity and bears a deletion mutation on chromosome 2, including the gene encoding synaptosomal protein SNAP-25, has been proposed to model aspects of attention-deficit hyperactivity disorder. Increasing evidence suggests a crucial role for SNAP-25 in the release of both classical neurotransmitters and neuropeptides. In the present study, we compared the release of specific naurotransmitters in vitro from synaptosomes and slices of selected brain regions from Cm/+ mice with that of +/+ mice. The release of dopamine (DA) and serotonin (5-HT) from striatum, and of arginine vasopressin and corticotropin-releasing factor from hypothalamus and amygdala is calcium-dependent. Glutamate release from and content in cortical synaptosomes of Cm/+ mice are greatly reduced, which might contribute to the learning deficits in these mutants. In dorsal striatum of Cm/+ mutants, but not ventral striatum, KCl-induced release of DA is completely blocked and that of 5-HT is significantly attenuated, suggesting that striatal DA and 5- HT deficiencies may be involved in hyperactivity. Further, although acetylcholine failed to induce hypothalamic corticotropin-releasing factor release from Cm/+ slices, restraint stress increased plasma corticosterone levels in Cm/+ mice to a significantly higher level than in +/+ mice, suggesting an important role for arginine vasopressin in hypothalamic- pituitary-adrenal axis activation. These results suggest that reduced SNAP- 25 expression may contribute to a region-specific and neurotransmitter- specific deficiency in neurotransmitter release.

Original languageEnglish (US)
Pages (from-to)176-186
Number of pages11
JournalJournal of Neurochemistry
Volume68
Issue number1
StatePublished - Jan 1997
Externally publishedYes

Fingerprint

Coloboma
Synaptic Transmission
Transmitters
Serotonin
Neurotransmitter Agents
Dopamine
Arginine Vasopressin
Corticotropin-Releasing Hormone
Synaptosomal-Associated Protein 25
Synaptosomes
Gene encoding
Chromosomes
Corticosterone
Neuropeptides
Pituitary Hormone-Releasing Hormones
Acetylcholine
Corpus Striatum
Glutamic Acid
Brain
Chromosomes, Human, Pair 2

Keywords

  • Cortex
  • Dopamine
  • Glutamate
  • Serotonin
  • SNAP-25
  • Striatum

ASJC Scopus subject areas

  • Biochemistry
  • Cellular and Molecular Neuroscience

Cite this

Raber, J., Mehta, P. P., Kreifeldt, M., Parsons, L. H., Weiss, F., Bloom, F. E., & Wilson, M. C. (1997). Coloboma hyperactive mutant mice exhibit regional and transmitter- specific deficits in neurotransmission. Journal of Neurochemistry, 68(1), 176-186.

Coloboma hyperactive mutant mice exhibit regional and transmitter- specific deficits in neurotransmission. / Raber, Jacob; Mehta, Prashant P.; Kreifeldt, Max; Parsons, Loren H.; Weiss, Friebert; Bloom, Floyd E.; Wilson, Michael C.

In: Journal of Neurochemistry, Vol. 68, No. 1, 01.1997, p. 176-186.

Research output: Contribution to journalArticle

Raber, J, Mehta, PP, Kreifeldt, M, Parsons, LH, Weiss, F, Bloom, FE & Wilson, MC 1997, 'Coloboma hyperactive mutant mice exhibit regional and transmitter- specific deficits in neurotransmission', Journal of Neurochemistry, vol. 68, no. 1, pp. 176-186.
Raber, Jacob ; Mehta, Prashant P. ; Kreifeldt, Max ; Parsons, Loren H. ; Weiss, Friebert ; Bloom, Floyd E. ; Wilson, Michael C. / Coloboma hyperactive mutant mice exhibit regional and transmitter- specific deficits in neurotransmission. In: Journal of Neurochemistry. 1997 ; Vol. 68, No. 1. pp. 176-186.
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