The DOI matches its Crossref record; 36 of the 36 references it cites were found in a registry or an index.
Methylphenidate Increases Cortical Excitability via Activation of Alpha-2 Noradrenergic Receptors
Open accessAbstract
Although methylphenidate (MPH), a catecholaminergic reuptake blocker, is prescribed for attention-deficit/hyperactivity disorder, there is a dearth of information regarding the cellular basis of its actions. To address this issue, we used whole-cell patch-clamp recordings to investigate the roles of various catecholamine receptors in MPH-induced changes in cortical neuron excitability. We bath-applied dopamine or noradrenaline receptor antagonists in combination with MPH to pyramidal cells located in deep layers of the infralimbic and prelimbic prefrontal cortices. Application of MPH (10 microM) by itself increased cortical cell excitability in slices obtained from juvenile rats. This MPH-mediated increase in excitability was lost when catecholamines were depleted with reserpine prior to recording, demonstrating the requirement for a presynaptic monoamine component. Antagonist studies further revealed that stimulation of alpha-2 noradrenergic receptors mediates the MPH-induced increase in intrinsic excitability. Dopamine D1 receptors played no observable role in the actions of MPH. We therefore propose that MPH is acting to increase catecholaminergic tone in the PFC, and thereby increases cortical excitability by mediating the disinhibition of pyramidal cells through mechanisms that may include activation of alpha-2 adrenoreceptors located in interneurons.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“Multiple studies have demonstrated that MPH also directly interacts with adrenergic receptors (109, 115, 119, 120). Through activation of α2 adrenergic receptors, MPH has been demonstrated to stimulate cortical excitability (109).”
In the citing paper
“Moreover, it has been shown that MPH exerts excitatory actions on PFC neurons by activating ADRA2 [175, 176].”
From Molecular Characterisation of the Mechanism of Action of Stimulant Drugs Lisdexamfetamine and Methylphenidate on ADHD Neurobiology: A Review (2022) · cites this paper as [176]
Citations
Cites
Regional and cellular fractionation of working memory
Goldman‐Rakic, P. S. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.24.13473 · Cited by 826
Solanto, M. V. (1998) · Behavioural Brain Research · doi:10.1016/s0166-4328(97)00175-7 · Cited by 677
Mehta, M. A., Owen, A. M., Sahakian, B. J., Mavaddat, N., Pickard, J. D., & Robbins, T. W. (2000) · The Journal of Neuroscience · doi:10.1523/jneurosci.20-06-j0004.2000 · Cited by 608 · cited 1×
“Moreover, MPH improves WM performance in healthy subjects (Elliot et al, 1997; Mehta et al, 2000) and several studies have shown that MPH increases overall speed and accuracy of attentional process in normal adults (Strauss et al, 1984; Solanto, 1998).”
BackgroundDopamine D1 receptor mechanisms in the cognitive performance of young adult and aged monkeys
Arnsten, A. F. T., Cai, J. X., Murphy, B. L., & Goldman-Rakic, P. S. (1994) · Psychopharmacology · doi:10.1007/bf02245056 · Cited by 566
Sonders, M. S., Zhu, S.-J., Zahniser, N. R., Kavanaugh, M. P., & Amara, S. G. (1997) · Journal of Neuroscience · doi:10.1523/jneurosci.17-03-00960.1997 · Cited by 446
Carlsson, A., Fuxé, K., Hamberger, B., & Lindqvist, M. (1966) · Acta Physiologica Scandinavica · doi:10.1111/j.1748-1716.1966.tb03334.x · Cited by 412
Effects of methylphenidate on spatial working memory and planning in healthy young adults
Elliott, R., Sahakian, B. J., Matthews, K., Bannerjea, A., Rimmer, J., & Robbins, T. W. (1997) · Psychopharmacology · doi:10.1007/s002130050284 · Cited by 389
Yang, C., & Seamans, J. K. (1996) · Journal of Neuroscience · doi:10.1523/jneurosci.16-05-01922.1996 · Cited by 369
Porrino, L. J., & Goldman, P. S. (1982) · The Journal of Comparative Neurology · doi:10.1002/cne.902050107 · Cited by 357
Amphetamine and Related Compounds
Cole, M. (2003) · Analytical techniques in the sciences · doi:10.1002/0470868007.ch2 · Cited by 326
Lewis, D., Campbell, M., Foote, S., Goldstein, M., & Morrison, J. (1987) · The Journal of Neuroscience · doi:10.1523/jneurosci.07-01-00279.1987 · Cited by 325
Ferris, R. M., Tang, F. L. M., & Maxwell, R. A. (1972) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1016/s0022-3565(25)29222-9 · Cited by 302
Lewis, B. L. (2000) · Cerebral Cortex · doi:10.1093/cercor/10.12.1168 · Cited by 287
Williams, J., Henderson, G., & North, R. A. (1985) · Neuroscience · doi:10.1016/0306-4522(85)90166-6 · Cited by 262
Arnsten, A. F. T., Cai, J., Steere, J. C., & Goldman-Rakic, P. S. (1995) · Journal of Neuroscience · doi:10.1523/jneurosci.15-05-03429.1995 · Cited by 252
Anti-hyperactivity medication: methylphenidate and amphetamine
Seeman, P., & Madras, B. K. (1998) · Molecular Psychiatry · doi:10.1038/sj.mp.4000421 · Cited by 252
A Neurocomputational Theory of the Dopaminergic Modulation of Working Memory Functions
Durstewitz, D., Kelc, M., & Güntürkün, O. (1999) · Journal of Neuroscience · doi:10.1523/jneurosci.19-07-02807.1999 · Cited by 229
Perikaryal and synaptic localization ofα2A-adrenergic receptor-like immunoreactivity
Aoki, C. J., Go, C.-G., Venkatesan, C., & Kurose, H. (1994) · Brain Research · doi:10.1016/0006-8993(94)91782-5 · Cited by 221
The dopamine mesocorticolimbic pathway is affected by deficiency in n−3 polyunsaturated fatty acids
Zimmer, L., Vancassel, S., Cantagrel, S., Breton, P., Delamanche, S., Guilloteau, D., Durand, G., & Chalon, S. (2002) · American Journal of Clinical Nutrition · doi:10.1093/ajcn/75.4.662 · Cited by 218
Noradrenaline‐mediated synaptic inhibition in rat locus coeruleus neurones.
Egan, T. M., Henderson, G., North, R. A., & Williams, J. T. (1983) · The Journal of Physiology · doi:10.1113/jphysiol.1983.sp014990 · Cited by 199
Sawaguchi, T., Matsumura, M., & Kubota, K. (1990) · Journal of Neurophysiology · doi:10.1152/jn.1990.63.6.1401 · Cited by 193
Levitt, P. R., RAKIC, P. T., & Goldman, P. S. (1984) · The Journal of Comparative Neurology · doi:10.1002/cne.902270105 · Cited by 190
Prefrontal neurons in networks of executive memory
Fuster, J. M. (2000) · Brain Research Bulletin · doi:10.1016/s0361-9230(99)00258-0 · Cited by 166
Miner, L. H., Schroeter, S., Blakely, R., & Sesack, S. R. (2000) · The Journal of Comparative Neurology · doi:10.1002/1096-9861(20001113)427:2 · Cited by 148
Heeringa, M. J., & Abercrombie, E. D. (1995) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.1995.65010192.x · Cited by 144
Lewis, D. A., & Morrison, J. H. (1989) · The Journal of Comparative Neurology · doi:10.1002/cne.902820302 · Cited by 131
Andrade, R., & Aghajanian, G. K. (1985) · Journal of Neuroscience · doi:10.1523/jneurosci.05-09-02359.1985 · Cited by 130
Miner, L. H., Schroeter, S., Blakely, R., & Sesack, S. R. (2003) · The Journal of Comparative Neurology · doi:10.1002/cne.10898 · Cited by 112
Strauss, J., Lewis, J. L., Klorman, R., Peloquin, L., Perlmutter, R. A., & Salzman, L. F. (1984) · Psychophysiology · doi:10.1111/j.1469-8986.1984.tb00247.x · Cited by 90
Lavı́n, A., & Grace, A. A. (2001) · Neuroscience · doi:10.1016/s0306-4522(01)00096-3 · Cited by 87
Rd, H. (1987) · PubMed · Cited by 84
Hunt, R. D., Cohen, D. J., Anderson, G. M., & Clark, L. R. (1984) · Life Sciences · doi:10.1016/0024-3205(84)90415-6 · Cited by 60
Hendley, E. D., Snyder, S. H., Fauley, J. J., & LaPidus, J. B. (1972) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1016/s0022-3565(25)29320-x · Cited by 37
Ross, S. B. (1978) · Journal of Pharmacy and Pharmacology · doi:10.1111/j.2042-7158.1978.tb13218.x · Cited by 29
Lacroix, D., & Ferron, A. (1988) · European Journal of Pharmacology · doi:10.1016/0014-2999(88)90658-9 · Cited by 23
Cited by
Sorted by citations
Candidate gene studies of ADHD: a meta-analytic review
Gizer, I. R., Ficks, C., & Waldman, I. D. (2009) · Human Genetics · doi:10.1007/s00439-009-0694-x · Cited by 1,020
Samuels, E., & Szabadi, E. (2008) · Current Neuropharmacology · doi:10.2174/157015908785777229 · Cited by 766
Faraone, S. V. (2018) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2018.02.001 · Cited by 631
Functional neuroanatomy of the central noradrenergic system
Szabadi, E. (2013) · Journal of Psychopharmacology · doi:10.1177/0269881113490326 · Cited by 366
Wilens, T. E. (2008) · Journal of Clinical Psychopharmacology · doi:10.1097/jcp.0b013e318173312f · Cited by 269
Metadata
- Authors
- Andrews, G. D., & Lavin, A.
- Affiliations
- Medical University of South Carolina (US)
- Venue
- Neuropsychopharmacology
- Published
- 2005-07-06
- Volume
- 31
- Issue
- 3
- Pages
- 594-601
- ISSN
- 0893-133X (ISSN-L)
- 1740-634X
- PMC
- PMC5509071
- OpenAlex
- W2018418849
- Cited by
- 101
- References
- 36
- Citations by year
- 2026: 1 · 2024: 2 · 2023: 4 · 2022: 5 · 2021: 7 · 2020: 6 · 2019: 4 · 2018: 3 · 2017: 6 · 2016: 7 · 2015: 4 · 2014: 8 · 2013: 4 · 2012: 9
- FWCI
- 2.82
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Neuropsychopharmacology (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institutes of Health (14698)
- National Institute on Drug Abuse (R01DA014698, R56DA014698, DA 14698)
- Topics
- Health Sciences › Medicine › Psychiatry and Mental health › Attention Deficit Hyperactivity Disorder
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
- Keywords
- methylphenidate, alpha2-adrenoceptors, cortical excitability, prefrontal cortex, pyramidal neurons, catecholamine depletion, reserpine, dopamine D1 receptor, norepinephrine, attention deficit hyperactivity disorder, disinhibition, interneurons
- MeSH terms
- Adrenergic alpha-Agonists, Adrenergic alpha-Antagonists, Central Nervous System Stimulants, Animals, Catecholamines, Cerebral Cortex, Dopamine, Electrophysiology, Male, Methylphenidate, Nerve Net, Norepinephrine, Prefrontal Cortex, Pyramidal Cells, Receptors, Adrenergic, alpha-2, Dopamine Agonists, Rats, In Vitro Techniques
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review