Anxiolytic-like effect of noradrenaline microinjection into the dorsal periaqueductal gray of rats
- PMID: 19407657
- DOI: 10.1097/FBP.0b013e32832c7098
Anxiolytic-like effect of noradrenaline microinjection into the dorsal periaqueductal gray of rats
Abstract
The brain noradrenergic system has been implicated in the expression of defensive behaviors elicited by acute stress. The dorsal periaqueductal gray area (dPAG) is a key structure involved in the behavioral and cardiovascular responses elicited by fear and anxiety situations. Although there are noradrenergic terminals in the dPAG, few studies have investigated the role of noradrenaline (NA) in the dPAG on anxiety modulation. The aim of this study was to evaluate the effect of NA microinjection into the dPAG of rats subjected to two animal models of anxiety, the elevated plus-maze and the Vogel conflict test. Male Wistar rats implanted with a guide cannula aimed at the dPAG received microinjections of NA (3, 15, or 45 nmol/0.05 microl) or artificial cerebral spinal fluid into the dPAG immediately before being exposed to the elevated plus-maze or the Vogel conflict test. NA increased the exploration of the open arms and the number of enclosed arm entries in the elevated plus-maze. The increase in open arm exploration remained significant after being subjected to an analysis of covariance using the latter variable as covariate. Moreover, the NA microinjection into the dPAG did not increase general exploratory activity of animals subjected to the open-field test, indicating that the increase in open arm exploration cannot be attributed to a nonspecific increase in exploratory activity. In the Vogel test, the NA microinjection into the dPAG increased the number of punished licks without changing the number of nonpunished licks or interfering with the tail-flick test. The results, therefore, indicate that the NA microinjection into the dPAG produces anxiolytic-like effects, suggesting its possible involvement in the anxiety modulation.
Similar articles
-
Noradrenaline microinjected into the dorsal periaqueductal gray matter causes anxiolytic-like effects in rats tested in the elevated T-maze.Life Sci. 2016 May 1;152:94-8. doi: 10.1016/j.lfs.2016.03.011. Epub 2016 Mar 9. Life Sci. 2016. PMID: 26968783
-
The dorsal periaqueductal gray modulates the increased fear-like behavior exhibited by experienced rats in the elevated plus-maze.Behav Brain Res. 2010 Jan 5;206(1):120-6. doi: 10.1016/j.bbr.2009.09.001. Epub 2009 Sep 6. Behav Brain Res. 2010. PMID: 19737580
-
Anxiolytic effect of a CRH receptor antagonist in the dorsal periaqueductal gray.Depress Anxiety. 2000;12(2):99-101. doi: 10.1002/1520-6394(2000)12:2<99::AID-DA6>3.0.CO;2-Q. Depress Anxiety. 2000. PMID: 11091933
-
Role of brain norepinephrine in the behavioral response to stress.Prog Neuropsychopharmacol Biol Psychiatry. 2005 Dec;29(8):1214-24. doi: 10.1016/j.pnpbp.2005.08.007. Epub 2005 Oct 13. Prog Neuropsychopharmacol Biol Psychiatry. 2005. PMID: 16226365 Review.
-
Serotonin, the periaqueductal gray and panic.Neurosci Biobehav Rev. 2004 May;28(3):239-59. doi: 10.1016/j.neubiorev.2003.12.004. Neurosci Biobehav Rev. 2004. PMID: 15225969 Review.
Cited by
-
The Antidepressant Effect of L-Tyrosine-Loaded Nanoparticles: Behavioral Aspects.Ann Neurosci. 2016 Jul;23(2):89-99. doi: 10.1159/000443575. Epub 2016 Jul 7. Ann Neurosci. 2016. PMID: 27647959 Free PMC article.
-
Identification of neural networks that contribute to motion sickness through principal components analysis of fos labeling induced by galvanic vestibular stimulation.PLoS One. 2014 Jan 23;9(1):e86730. doi: 10.1371/journal.pone.0086730. eCollection 2014. PLoS One. 2014. PMID: 24466215 Free PMC article.
-
Gene Expression Changes in Glutamate and GABA-A Receptors, Neuropeptides, Ion Channels, and Cholesterol Synthesis in the Periaqueductal Gray Following Binge-Like Alcohol Drinking by Adolescent Alcohol-Preferring (P) Rats.Alcohol Clin Exp Res. 2016 May;40(5):955-68. doi: 10.1111/acer.13056. Epub 2016 Apr 8. Alcohol Clin Exp Res. 2016. PMID: 27061086 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical