Receptor binding and drug modulation in anxiety
Abstract
Anxiety is an emotion that allows an individual to prepare for, or respond to, changes in the environment. For many people, however, this emotion is expressed inappropriately and impairs their lives causing considerable distress and disability. These disorders cause a great deal of personal distress, result in reduced life expectancy and, in the UK alone, have an estimated cost of approximately pound 5 billion per year. Despite a great deal of research, an adequate account of the mechanisms that underlie these human disorders is still lacking. An understanding of the brain substrates underlying these disorders is likely to provide such adequate explanations, but one of the principal challenges facing the investigators has been the reciprocal mapping of pre-clinical and clinical knowledge. Altogether, the last 10 years have seen a consolidation of imaging techniques. These are now mature in many areas and are likely to provide fundamental contributions in our understanding of human psychopharmacology.
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Antidepressant effects of low-dose ketamine and transcranial magnetic stimulation can improve cerebral glucose metabolism in these regions.
“Antidepressant effects of low-dose ketamine [56] and transcranial magnetic stimulation can improve the cerebral glucose metabolism in these regions [57–60].”
From APOE4 genotype exacerbates the depression-like behavior of mice during aging through ATP decline (2021) · cites this paper as [60]
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Nutt, D. J. (1990) · Archives of General Psychiatry · doi:10.1001/archpsyc.1990.01810220033004 · Cited by 272 · see citing works
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Regulating anxiety with extrasynaptic inhibition
Botta, P., Demmou, L., Kasugai, Y., Markovic, M., Xu, C., Fadok, J. P., Lu, T., Poe, M. M., Xu, L., Cook, J. M., et al. (2015) · Nature Neuroscience · doi:10.1038/nn.4102 · Cited by 192 · see citing works
“Generalized anxiety disorders, panic anxiety, but also sleep disturbances and epilepsy, including status epilepticus, are pathologies ameliorated by enhancing inhibitory neurotransmission largely mediated by γ-aminobutyric acid (GABA), acting through GABA type A receptors (GABAARs) in the central nervous system (Maliz…”
APOE4 genotype exacerbates the depression-like behavior of mice during aging through ATP decline
Fang, W., Xiao, N., Zeng, G., Bi, D., Dai, X., Mi, X., Ye, Q., Chen, X., & Zhang, J. (2021) · Translational Psychiatry · doi:10.1038/s41398-021-01631-0 · Cited by 42 · see citing works
- Authors
- Malizia, A.
- Affiliations
- University of Bristol (GB)
- Corresponding author
- Malizia, A
- Venue
- European Neuropsychopharmacology
- Publisher
- Elsevier BV
- Published
- 2002-12
- Volume
- 12
- Issue
- 6
- Pages
- 567-574
- ISSN
- 0924-977X (ISSN-L)
- OpenAlex
- W2081713978
- Cited by
- 13
- References
- 1
- Citations by year
- 2021: 1 · 2015: 1 · 2012: 1
- FWCI
- 0.44
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- European Neuropsychopharmacology (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Social Sciences › Psychology › Experimental and Cognitive Psychology › Anxiety, Depression, Psychometrics, Treatment, Cognitive Processes
- Keywords
- anxiety disorders, receptor binding, drug modulation, brain substrates, neuroimaging, psychopharmacology
- MeSH terms
- Animals, Anxiety, Anxiety Disorders, Binding, Competitive, Brain, Humans, Radioligand Assay, Receptors, GABA-A, Tomography, Emission-Computed
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