Skip to main content Accessibility help
×
Hostname: page-component-8448b6f56d-42gr6 Total loading time: 0 Render date: 2024-04-23T12:17:56.068Z Has data issue: false hasContentIssue false

Chapter 25 - Using Pharmacotherapy to Enhance Stroke Recovery

from Part VI - Stroke Rehabilitation and Recovery

Published online by Cambridge University Press:  15 December 2020

Jeffrey L. Saver
Affiliation:
David Geffen School of Medicine, University of Ca
Graeme J. Hankey
Affiliation:
University of Western Australia, Perth
Get access

Summary

Pre-clinical studies provide clear and consistent evidence that a variety of centrally acting drugs affecting specific neurotransmitters can either facilitate or interfere with functional recovery after brain injury. Although at least some clinical trials suggest similar effects in humans, results have been inconsistent. The impact of important factors such as drug dose, duration, and intensity of physiotherapy, and timing between injury and treatment are difficult to translate from preclinical studies. Issues related to variability in stroke severity, location of injury, and comorbid conditions further complicate trial design and could obscure a true treatment effect. Because of these and other issues, the design of efficacy trials assessing putative neuro-restorative interventions is not trivial. Although a proven pharmacological approach resulting in a clinically meaningful improvement in post-stroke recovery remains elusive, it is reasonable to avoid medications that may have harmful effects in patients who have had a stroke. It is also important to control for these possible harmful effects in future clinical trials assessing the outcomes of stroke patients after the acute period.

Type
Chapter
Information
Stroke Prevention and Treatment
An Evidence-based Approach
, pp. 517 - 531
Publisher: Cambridge University Press
Print publication year: 2020

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Adkins, DL, Jones, TA. (2005). D-amphetamine enhances skilled reaching after ischemic cortical lesions in rats. Neurosci Lett, 380, 214–18.CrossRefGoogle ScholarPubMed
Alaverdashvili, M, Lim, DH, Whishaw, IQ. (2007). No improvement by amphetamine on learned non-use, attempts, success or movement in skilled reaching by the rat after motor cortex stroke. Eur J Neurosci, 25, 3442–52.CrossRefGoogle ScholarPubMed
Albert, ML, Bachman, DL, Morgan, A, Helm-Estabrooks, N. (1988). Pharmacotherapy for aphasia. Neurology, 38, 877–9.Google Scholar
Aroniadou, VA, Teyler, TJ. (1991). The role of NMDA receptors in long-term potentiation (LTP) and depression (LTD) in rat visual cortex. Brain Res, 562, 136–43.Google Scholar
Artola, A, Singer, W. (1989). NMDA receptors and developmental plasticity in visual neocortex. In Collingridge, GL Watkins, JC, eds., The NMDA Receptor. Oxford: Oxford University Press, pp. 153–66.Google Scholar
Bachman, DL, Morgan, A. (1988). The role of pharmacotherapy in the treatment of aphasia. Aphasiology, 3–4, 225–8.Google Scholar
Barbay, S, Zoubina, EV, Dancause, N, Frost, SB, Eisner-Janowicz, I, Stowe, AM, et al. (2006). A single injection of D-amphetamine facilitates improvements in motor training following a focal cortical infarct in squirrel monkeys. Neurorehabil Neural Repair, 20, 455–8.CrossRefGoogle ScholarPubMed
Blandina, P, Goldfarb, J, Walcott, J, Green, JP. (1991). Serotonergic modulation of the release of endogenous norepinephrine from rat hypothalamic slices. J Pharmacol Exp Ther, 256, 341–7.Google Scholar
Bliss, TV, Collingridge, GL. (1993). A synaptic model of memory: long-term potentiation in the hippocampus. Nature, 361, 31–9.Google Scholar
Boyeson, MG, Callister, TR, Cavazos, JE. (1992a). Biochemical and behavioral effects of a sensorimotor cortex injury in rats pretreated with the noradrenergic neurotoxin DSP-4. BehavNeurosci, 106, 964–73.Google Scholar
Boyeson, MG, Feeney, DM. (1990). Intraventricular norepinephrine facilitates motor recovery following sensorimotor cortex injury. Pharmacol BiochemBehav, 35, 497501.Google Scholar
Boyeson, MG, Harmon, RL. (1993). Effects of trazodone and desipramine on motor recovery in brain-injured rats. Am J Phys Med Rehabil, 72, 286–93.CrossRefGoogle ScholarPubMed
Boyeson, MG, Harmon, RL, Jones, JL. (1994). Comparative effects of fluoxetine, amitriptyline and serotonin on functional motor recovery after sensorimotor cortex injury. Am J Phys Med Rehabil, 73, 7683.Google Scholar
Boyeson, MG, Krobert, KA, Grade, CM, Scherer, PJ. (1992b). Unilateral, but not bilateral, locus coeruleus lesions facilitate recovery from sensorimotor cortex injury. Pharmacol Biochem Behav, 43, 771–7.CrossRefGoogle Scholar
Boyeson, MG, Scherer, PJ, Grade, CM, Krobert, KA. (1993). Unilateral locus coeruleus lesions facilitate motor recovery from cortical injury through supersensitivity mechanisms. Pharmacol Biochem Behav, 44, 297305.Google Scholar
Brailowsky, S, Knight, RT, Efron, R. (1986). Phenytoin increases the severity of cortical hemiplegia in rats. Brain Res, 376, 71–7.Google Scholar
Bröcher, S, Artola, A, Singer, W. (1992). Agonists of cholinergic and noradrenergic receptors facilitate synergistically the induction of long-term potentiation in slices of rat visual cortex. Brain Res, 573, 2736.CrossRefGoogle ScholarPubMed
Brown, AW, Bjelke, B, Fuxe, K. (2004). Motor response to amphetamine treatment, task-specific training, and limited motor experience in a postacute animal stroke model. Exp Neurol, 190, 102–08.CrossRefGoogle Scholar
Burgard, EC, Decker, G, Sarvey, JM. (1989). NMDA receptor antagonists block norepinephrine-induced long- lasting potentiation and long-term potentiation in rat dentate gyrus. Brain Res, 482, 351–5.Google Scholar
Burgard, EC, Sarvey, JM. (1990). Muscarinic receptor activation facilitates the induction of long-term potentiation (LTP) in the rat dentate gyrus. Neurosci Lett, 116, 3439.Google Scholar
Bütefisch, CM, Kleiser, R, Körber, B, Müller, K, Wittsack, HJ, Hömberg, V, et al. (2005). Recruitment of contralesional motor cortex in stroke patients with recovery of hand function. Neurology, 64, 1067–9.Google Scholar
Chen, MJ, Sutton, RL, Feeney, DM. (1986). Recovery of function after brain injury in rat and cat: beneficial effects of phenylpropanolamine. Abstracts Soc Neurosci, 12, 881.Google Scholar
Chollet, F, Tardy, J, Albucher, JF, Thalamas, C, Berard, E, Lamy, C, et al. (2011). Fluoxetine for motor recovery after acute ischaemic stroke (FLAME): a randomised placebo-controlled trial. Lancet Neurol, 10, 123–30.Google Scholar
Cohen, BM, Lipinski, JF. (1986). In vivo potencies of antipsychotic drugs in blocking alpha 1 noradrenergic and dopamine D2 receptors: implications for drug mechanisms of action. Life Sci, 39, 2571–80.Google Scholar
Cramer, SC. (2011). An overview of therapies to promote repair of the brain after stroke. Head Neck, 33, (Suppl 1), S57.Google Scholar
Cramer, SC, Nelles, G, Benson, RR, Kaplan, JD, Parker, RA, Kwong, KK, et al. (1997). A functional MRI study of subjects recovered from hemiparetic stroke. Stroke, 28, 2518–27.Google Scholar
Crisostomo, EA, Duncan, PW, Propst, MA, Dawson, DB, Davis, JN. (1988). Evidence that amphetamine with physical therapy promotes recovery of motor function in stroke patients. Ann Neurol, 23, 94–7.Google Scholar
Dahl, D, Sarvey, JM. (1989). Norepinephrine induces pathway-specific long-lasting potentiation and depression in the hippocampal dentate gyrus. Proc Natl Acad Sci USA, 86, 4776–80.CrossRefGoogle ScholarPubMed
Dam, M, Tonin, P, De Boni, A, Pizzolato, G, Casson, S, Ermani, M, et al. (1996). Effects of fluoxetine and maprotiline on functional recovery in poststroke hemiplegic patients undergoing rehabilitation therapy. Stroke, 27, 1211–14.Google Scholar
Delanoy, RL, Tucci, DL, Gold, PE. (1983). Amphetamine effects on long term potentiation in dentate granule cells. Pharmacol Biochem Behav, 18, 137–9.CrossRefGoogle ScholarPubMed
Dietrich, WD, Alonso, O, Busto, R, Ginsberg, MD. (1990). Influence of amphetamine treatment on somatosensory function of the normal and infarcted rat brain. Stroke, 21 (Suppl. III), III-147-III–150.Google Scholar
Dose, JM, Dhillon, HS, Maki, A, Kraemer, PJ, Prasad, RM. (1997). Lack of delayed effects of amphetamine, methoxamine, and prazosin (adrenergic drugs) on behavioral outcome after lateral fluid percussion brain injury in the rat. J Neurotrauma, 14, 327–37.Google Scholar
Dunbar, GL, Smith, GA, Look, SK, Whalen, RJ. (1989). d-Amphetamine attenuates learning and motor deficits following cortical injury in rats. Abstracts Soc Neurosci, 15, 132.Google Scholar
Dunwiddie, TV, Roberson, NL, Worth, T. (1982). Modulation of long-term potentiation: effects of adrenergic and neuroleptic drugs. Pharmacol Biochem Behav, 17, 1257–64.Google Scholar
El Husseini, N, Goldstein, LB, Peterson, ED, Zhao, X, Pan, W, Olson, D.M, et al. (2012). Depression and antidepressant use after stroke and transient ischemic attack. Stroke, 43, 1609–16.Google Scholar
Enderby, P, Broeckx, J, Hospers, W, Schildermans, F, Deberdt, W. (1994). Effect of piracetam on recovery and rehabilitation after stroke: a double-blind, placebo-controlled study. Clin Neuropharmacol, 17, 320–31.Google Scholar
Feeney, DM. (1991). Pharmacologic modulation of recovery after brain injury: a reconsideration of diaschisis. J Neurol Rehabil, 5, 113–28.Google Scholar
Feeney, DM, Gonzalez, A, Law, WA. (1981). Amphetamine restores locomotor function after motor cortex injury in the rat. Proc West Pharmacol Soc, 24, 1517.Google Scholar
Feeney, DM, Gonzalez, A, Law, WA. (1982). Amphetamine, haloperidol, and experience interact to affect the rate of recovery after motor cortex injury. Science, 217, 855–7.Google Scholar
Feeney, DM, Hovda, DA. (1983). Amphetamine and apomorphine restore tactile placing after motor cortex injury in the cat. Psychopharmacology, 79, 6771.Google Scholar
Feeney, DM, Hovda, DA. (1985). Reinstatement of binocular depth perception by amphetamine and visual experience after visual cortex ablation. Brain Res, 342, 352–6.Google Scholar
Feeney, DM, Westerberg, VS. (1990). Norepinephrine and brain damage: alpha noradrenergic pharmacology alters functional recovery after cortical trauma. Can J Psychol, 44, 233–52.Google Scholar
Fiorelli, M, Blin, J, Bakchine, S, Laplane, D, Baron, JC. (1991). PET studies of cortical diaschisis in patients with motor hemi-neglect. J Neurol Sci, 104, 135–42.CrossRefGoogle ScholarPubMed
FOCUS Trial Collaboration. (2019). Effects of fluoxetine on functional outcomes after acute stroke (FOCU): a pragmatic, double-blind, randomized, controlled trial. Lancet, 393, 265–74.Google Scholar
Fuxe, K, Ungerstedt, U. (1970). Histochemical, biochemical and functional studies on central monoamine neurons after acute and chronic amphetamine administration. In Costa, E, Garattini, S, eds., Amphetamines and Related Compounds. New York: Raven Press, pp. 257288.Google Scholar
Gladstone, DJ, Danells, CJ, Armesto, A, Mcllroy, WE, Staines, WR, Graham, SJ, et al. (2006). Physiotherapy coupled with dextroamphetamine for motor rehabilitation after hemiparetic stroke: a randomized, double-blind, placbo-controlled trial. Stroke, 37, 179–85.Google Scholar
Gold, PE, Delanoy, RL, Merrin, J. (1984). Modulation of long-term potentiation by peripherally administered amphetamine and epinephrine. Brain Res, 305, 103–07.Google Scholar
Goldstein, LB. (1990). Pharmacology of recovery after stroke. Stroke, 21 (Suppl. III), III-139–III-142.Google Scholar
Goldstein, LB. (1995). Right vs. left sensorimotor cortex suction-ablation in the rat: no difference in beam-walking recovery. Brain Res, 674, 167–70.Google Scholar
Goldstein, LB. (1997). Effects of bilateral and unilateral locus coeruleus lesions on beam-walking recovery after subsequent unilateral sensorimotor cortex suction-ablation in the rat. Restor Neurol Neurosci, 11, 5563.Google ScholarPubMed
Goldstein, LB. (1998). Potential effects of common drugs on stroke recovery. Arch Neurol, 55, 454–6.Google Scholar
Goldstein, LB. (2000). Effects of amphetamines and small related molecules on recovery after stroke in animals and man. Neuropharmacology, 39, 852–9.Google Scholar
Goldstein, LB. (2006). Neurotransmitters and motor activity: effects on functional recovery after brain injury. NeuroRx, 3, 451–7.Google Scholar
Goldstein, LB. (2009). Amphetamine trials and tribulations. Stroke, 40 (Suppl. 1), S133S135.Google Scholar
Goldstein, LB, Bullman, S. (1997). Effects of dorsal noradrenergic bundle lesions on recovery after sensorimotor cortex injury. Pharmacol Biochem Behav, 58, 1151–7.Google Scholar
Goldstein, LB, Bullman, S. (1999). Age but not sex affects motor recovery after unilateral sensorimotor cortex suction-ablation in the rat. Restor Neurol Neurosci, 15, 3943.Google Scholar
Goldstein, LB, Bullman, S. (2002). Differential effects of haloperidol and clozapine on motor recovery after sensorimotor cortex injury in the rat. Neurorehabil Neural Repair, 16, 321–5.Google Scholar
Goldstein, LB, Coviello, A, Miller, GD, Davis, JN. (1991). Norepinephrine depletion impairs motor recovery following sensorimotor cortex injury in the rat. Restor Neurol Neurosci, 3, 41–7.Google Scholar
Goldstein, LB, Davis, JN. (1988). Physician prescribing patterns following hospital admission for ischemic cerebrovascular disease. Neurology, 38, 1806–09.CrossRefGoogle ScholarPubMed
Goldstein, LB, Davis, JN. (1990a). Clonidine impairs recovery of beam-walking in rats. Brain Res, 508, 305–09.Google Scholar
Goldstein, LB, Davis, JN. (1990b). Influence of lesion size and location on amphetamine-facilitated recovery of beam-walking in rats. Behav Neurosci, 104, 318–25.Google Scholar
Goldstein, LB, Davis, J.N. (1990c). Post-lesion practice and amphetamine-facilitated recovery of beam-walking in the rat. Restor Neurol Neurosci, 1, 311–14.Google Scholar
Goldstein, LB, Hasselblad, V, McCrory, DC, Matchar, DB. (1995). Meta-analysis and comparison of randomized trials of endarterectomy for symptomatic carotid stenosis. Neurology, 45 (Suppl 4), A375.Google Scholar
Goldstein, LB, Matchar, DB, Morgenlander, JC, Davis, JN. (1990). Influence of drugs on the recovery of sensorimotor function after stroke. J NeuroloRehabi, 4, 137–44.Google Scholar
Goldstein, LB, Poe, HV, Davis, JN. (1989). An animal model of recovery of function after stroke: Facilitation of recovery by an a2-adrenergic receptor antagonist. Ann Neurol, 26, 157.Google Scholar
Grade, C, Redford, B, Chrostowski, J, Toussaint, L, Blackwell, B. (1998). Methylphenidate in early poststroke recovery: a double-blind, placebo-controlled study. Arch Phys Med Rehabil, 79, 1047–50.Google Scholar
Green, J, Forster, A, Bogle, S, Young, J. (2002). Physiotherapy for patients with mobility problems more than 1 year after stroke: a randomised controlled trial. Lancet, 359, 199203.Google Scholar
Gupta, SR, Mlcoch, AG, Scolaro, C, Moritz, T. (1995). Bromocriptine treatment of nonfluent aphasia. Neurology, 45, 2170–3.CrossRefGoogle ScholarPubMed
Hernandez, TD, Holling, LC. (1994). Disruption of behavioral recovery by the anti-convulsant phenobarbital. Brain Res, 635, 300–06.Google Scholar
Hernandez, TD, Jones, GH, Schallert, T. (1989). Co-administration of Ro 15–1788 prevents diazepam-induced retardation of recovery of function. Brain Res, 487, 8995.Google Scholar
Hovda, DA, Bailey, B, Montoya, S, Salo, AA, Feeney, DM. (1983). Phentermine accelerates recovery of function after motor cortex injury in rats and cats. FASEB J, 42, 1157.Google Scholar
Hovda, DA, Feeney, DM. (1984). Amphetamine with experience promotes recovery of locomotor function after unilateral frontal cortex injury in the cat. Brain Res, 298, 358–61.Google Scholar
Hovda, DA, Sutton, RL, Feeney, DM. (1987). Recovery of tactile placing after visual cortex ablation in cat: a behavioral and metabolic study of diaschisis. Exp Neurol, 97, 391402.CrossRefGoogle Scholar
Hovda, DA, Sutton, RL, Feeney, DM. (1989). Amphetamine-induced recovery of visual cliff performance after bilateral visual cortex ablation in cats: measurements of depth perception thresholds. Behav Neurosci, 103, 574–84.Google Scholar
Huber, W, Willmes, K, Poeck, K, Van Vleymen, B, Deberdt, W. (1997). Piracetam as an adjuvant to language therapy for aphasia: a randomized double-blind placebo-controlled pilot study. Arch Phys Med Rehabil, 78, 245–50.Google Scholar
Hurwitz, BE, Dietrich, WD, McCabe, PM, Watson, BD, Ginsberg, MD, Schneiderman, N. (1989). Amphetamine-accelerated recovery from cortical barrel-field infarction: pharmacological treatment of stroke. In Ginsberg, MD, Dietrich, WD, eds., Cerebrovascular Diseases. The Sixteenth Research (Princeton) Conference. New York: Raven Press, pp. 309318.Google Scholar
Infeld, B, Davis, SM, Lichtenstein, M, Mitchell, PJ, Hopper, JL. (1995). Crossed cerebellar diaschisis and brain recovery after stroke. Stroke, 26, 90–5.Google Scholar
Iriki, A, Pavlides, C, Keller, A, Asanuma, H. (1989). Long-term potentiation in the motor cortex. Science, 245, 1385–7.Google Scholar
Ito, T, Miura, Y, Kadokawa, T. (1988). Effects of physostigmine and scopolamine on long-term potentiation of hippocampal population spikes in rats. Can J Physiol Pharmacol, 66, 1010–16.Google Scholar
Jaspers, RMA, Van Der Sprenkel, JWB, Tulleken, CAF, Cools, AR. (1990). Local as well as remote functional and metabolic changes after focal ischemia in cats. Brain Res Bull, 24, 2332.Google Scholar
Johnson, ML, Roberts, MD, Ross, AR, Witten, CM. (1992). Methylphenidate in stroke patients with depression. Am J Phys Med Rehabil, 71, 239–41.Google Scholar
Jones, TA, Schallert, T. (1992). Subcortical deterioration after cortical damage: effects of diazepam and relation to recovery of function. Behav Brain Res, 51, 113.Google Scholar
Kaplitz, SE. (1975). Withdrawn, apathetic geriatric patients responsive to methylphenidate. J Am Geriatr Soc, 23, 271–6.Google Scholar
Keith, JR, Wu, Y, Epp, JR, Sutherland, RJ. (2007). Fluoxetine and the dentate gyrus: memory, recovery of function, and electrophysiology. Behav Pharmacol, 18, 521–31.Google Scholar
Keller, A, Iriki, A, Asanuma, H. (1990). Identification of neurons producing long-term potentiation in the cat motor cortex: intracellular recordings and labeling. J Comp Neurol, 300, 4760.Google Scholar
Kessler, J, Thiel, A, Karbe, H, Heiss, WD. (2000). Piracetam improves activated blood flow and facilitates rehabilitation of poststroke aphasic patients. Stroke, 31, 2112–16.Google Scholar
Kikuchi, K, Nishino, K, Ohyu, H. (1999). L-DOPS-Accelerated recovery of locomotor function in rats subjected to sensorimotor cortex ablation injury: pharmacobehavioral studies. Tohoku J Exp Med, 188, 203–15.Google Scholar
Kikuchi, K, Nishino, K, Ohyu, H. (2000). Increasing CNS norepinephrine levels by the precursor L-DOPS facilitates beam-walking recovery after sensorimotor cortex ablation in rats. Brain Res, 860, 130–5.Google Scholar
Kline, AE, Chen, MJ, Tso-Olivas, DY, Feeney, DM. (1994). Methylphenidate treatment following ablation-induced hemiplegia in rat: experience during drug action alters effects on recovery of function. Pharmacol Biochem Behav, 48, 773–9.Google Scholar
Kraglund, KL, Mortensen, JK, Damsbo, AG, Modrau, B, Simonsen, SA, Iversen, HK, et al. (2018). Neuroregeneration and Vascular Protection by Citalopram in Acute Ischemic Stroke (TALOS). Stroke, 49(11), 2568–76. doi:10.1161/STROKEAHA.Google Scholar
Kulla, A, Manahan-Vaughan, D. (2002). Modulation by serotonin 5-HT(4) receptors of long-term potentiation and depotentiation in the dentate gyrus of freely moving rats. Cereb Cortex, 12, 150–62.Google Scholar
Larsson, M, Ervik, M, Lundborg, P, Sundh, V, Svanborg, A. (1988). Comparison between methylphenidate and placebo as adjuvant in care and rehabilitation of geriatric patients. Comp Gerontol, 2, 53–9.Google Scholar
Lenzi, GL, Frackowiak, RSJ, Jones, T. (1982). Cerebral oxygen metabolism and blood flow in human cerebral infarction. J Cereb Blood Flow Metab, 2, 321–35.Google Scholar
Lipsey, JR, Pearlson, GD, Robinson, RG, Rao, K, Price, TR. (1984). Nortriptyline treatment of post-stroke depression: a double-blind study. Lancet, 1, 297300.Google Scholar
Maling, HM, Acheson, GH. (1946). Righting and other postural activity in low-decerebrate and in spinal cats after d-amphetamine. J Neurophysiol, 9, 379–86.Google Scholar
Manahan-Vaughan, D, Kulla, A. (2003). Regulation of depotentiation and long-term potentiation in the dentate gyrus of freely moving rats by dopamine D2-like receptors. Cereb Cortex, 13, 123–35.Google Scholar
Martin, WRW, Raichle, ME. (1983). Cerebellar blood flow and metabolism in cerebral hemisphere infarction. Ann Neurol, 14, 168–76.Google Scholar
Martinsson, L, Eksborg, S, Wahlgren, NG. (2003). Intensive early physiotherapy combined with dexamphetamine treatment in severe stroke: a randomized, controlled pilot study. Cerebrovasc Dis, 16, 338–45.CrossRefGoogle ScholarPubMed
Martinsson, L, Hardemark, H, Eksborg, S. (2007). Amphetamines for improving recovery after stroke. Cochrane Database Syst Rev, 1. CD002090.Google ScholarPubMed
Marzo, A, Bai, J, Otani, S. (2009). Neuroplasticity regulation by noradrenaline in mammalian brain. Curr Neuropharmacol, 7, 286–95.CrossRefGoogle ScholarPubMed
Masotto, C., Apud, J. A., & Racagni, G. (1985). Neurochemical studies on GABAergic and aminergic systems in the rat brain following acute and chronic piracetam administration. Pharmacol Res Commun, 17, 749–72.Google Scholar
Mead, GE, Hsieh, CF, Hackett, M. (2013). Selective serotonin reuptake inhibitors for stroke recovery. JAMA, 310, 1066–7.Google Scholar
Meyer, PM, Horel, JA, Meyer, DR. (1963). Effects of dl-amphetamine upon placing responses in neodecorticate cats. J Comp PhysiolPsychol, 56, 402–04.Google Scholar
Nishino, K, Sasaki, T, Takahashi, K, Chiba, M, Ito, T. (2001). The norepinephrine precursor L-threo-3, 4-dihydroxyphenylserine facilitates motor recovery in chronic stroke patients. J Clin Neurosci, 8, 547–50.Google Scholar
Olpe, HR, Karlsson, G. (1990). The effects of baclofen and two GABA B-receptor antagonists on long-term potentiation. Naunyn Schmiedeberg Arch Pharmacol, 342, 194–7.Google Scholar
Peroutka, SJ, U’Pritchard, DC, Greenberg, DA, Snyder, SH. (1977). Neuroleptic drug interactions with norepinephrine alpha receptor binding sites in rat brain. Neuropharmacology, 16, 549–56.Google Scholar
Prasad, RM, Dose, JM, Dhillon, HS, Carbary, T, Kraemer, PJ. (1995). Amphetamine affects the behavioral outcome of lateral fluid percussion brain injury in the rat. Restor Neurol Neurosci, 9, 6575.Google Scholar
Ramic, M, Emerick, AJ, Bollnow, MR, O’Brien, TE, Tsai, SY, Kartje, GL. (2006). Axonal plasticity is associated with motor recovery following amphetamine treatment combined with rehabilitation after brain injury in the adult rat. Brain Res, 1111, 176–86.Google Scholar
Reding, MJ, Orto, LA, Winter, SW, Fortuna, IM, Di Ponte, P, McDowell, FH. (1986). Antidepressant therapy after stroke. A double-blind trial. Arch Neurol, 43, 763–5.Google Scholar
Reding, MJ, Solomon, B, Borucki, SJ. (1995). Effect of dextroamphetamine on motor recovery after stroke. Neurology, 45 (Suppl. 4), A222.Google Scholar
Roffler-Tarlov, S, Schildkraut, JJ, Draskoczy, PR. (1973). Effects of acute and chronic administration of desmethylimipramine on the content of norepinephrine and other monamines in the rat brain. Biochem Pharmacol, 22, 2923–6.Google Scholar
Sabe, L, Salvarezza, F, Cuerva, AG, Leiguarda, R, Starkstein, S. (1995). A randomized, double-blind, placebo-controlled study of bromocriptine in nonfluent aphasia. Neurology, 45, 2272–4.Google Scholar
Santarelli, L, Saxe, M, Gross, C, Surget, A, Battaglia, F, Dulawa, S, et al. (2003). Requirement of hippocampal neurogenesis for the behavioral effects of antidepressants. Science, 301, 805–09.Google Scholar
Satoh, M, Ishihara, K, Iwama, T, Takagi, H. (1986). Aniracetam augments, and midazolam inhibits, the long-term potentiation in guinea-pig hippocampal slices. Neurosci Lett, 68, 216–20.Google Scholar
Schallert, T, Hernandez, TD, Barth, TM. (1986). Recovery of function after brain damage: Severe and chronic disruption by diazepam. Brain Res, 379, 104–11.Google Scholar
Schallert, T, Jones, TA, Weaver, MS, Shapiro, LE, Crippens, D, Fulton, R. (1992). Pharmacologic and anatomic considerations in recovery of function. Phys Med Rehabil, 6, 375–93.Google Scholar
Schmanke, TD, Avery, RA, Barth, TM. (1996). The effects of amphetamine on recovery of function after cortical damage in the rat depend on the behavioral requirements of the task. J Neurotrauma, 13, 293307.Google Scholar
Sonde, L, Nordström, M, Nilsson, C-G, Lökk, J, Viitanen, M. (2001). A double-blind placebo-controlled study of the effects of amphetamine and physiotherapy after stroke. Cerebrovasc Dis, 12, 253–7.Google Scholar
Stanton, PK, Sarvey, JM. (1985). Blockade of norepinephrine-induced long-lasting potentiation in the hippocampal dentate gyrus by an inhibitor of protein synthesis. Brain Res, 361, 276–83.Google Scholar
Stroemer, RP, Kent, TA, Hulsebosch, CE. (1994). Amphetamines permanently promote recovery following cortical infarction. Abstracts Soci Neurosci, 20, 186.Google Scholar
Stroemer, RP, Kent, TA, Hulsebosch, CE. (1995). Neocortical neural sprouting, synaptogenesis, and behavioral recovery after neocortical infarction in rats. Stroke, 26, 2135–44.Google Scholar
Sutton, RL, Feeney, DM. (1992). α-Noradrenergic agonists and antagonists affect recovery and maintenance of beam-walking ability after sensorimotor cortex ablation in the rat. Restor Neurol Neurosci, 4, 111.Google Scholar
Sutton, RL, Hovda, DA, Feeney, DM. (1989). Amphetamine accelerates recovery of locomotor function following bilateral frontal cortex ablation in cats. Behav Neurosci, 103, 837–41.Google Scholar
Tanaka, M, Kondo, S, Hirai, S. Ishiguro, K, Ishihara, T, Morimatsu, M. (1992). Crossed cerebellar diaschisis accompanied by hemiataxia: a PET study. J Neurol Neurosurg Psychiatry, 55, 121–5.Google Scholar
Theodore, DR, Meier-Ruge, W, Abraham, J. (1992). Microvascular morphometry in primate diaschisis. Microvasc Res, 43, 147–55.Google Scholar
Treig, T, Werner, C, Sachse, M, Hesse, S. (2003). No benefit from D-amphetamine when added to physiotherapy after stroke: a randomized, placebo-controlled study. Clin Rehabil, 17, 590–9.Google Scholar
Troisi, E, Paolucci, S, Silvestrini, M, Matteis, M, Vernieri, F, Grasso, MG., et al (2002). Prognostic factors in stroke rehabilitation: the possible role of pharmacological treatment. Acta Neurol Scand, 105, 100–06.Google Scholar
Van Hasselt, P. (1973). Effect of butyrophenones on motor function in rats after recovery from brain damage. Neuropharmacology, 12, 245–7.Google Scholar
Wade, DT, Collen, FM, Robb, GF, Warlow, CP. (1992). Physiotherapy intervention late after stroke and mobility. Br Med J, 304, 609–13.Google Scholar
Walker-Batson, D, Curtis, S, Natarajan, R, Ford, J, Dronkers, N, Salmeron, E, et al. (2001). A double-blind, placebo-controlled study of the use of amphetamine in the treatment of aphasia. Stroke, 32, 2093–8.Google Scholar
Walker-Batson, D, Smith, P, Curtis, S, Unwin, H, Greenlee, R. (1995). Amphetamine paired with physical therapy accelerates motor recovery after stroke – further evidence. Stroke, 26, 2254–9.Google Scholar
Weaver, MS, Chen, MJ, Westerberg, VS, Feeney, DM. (1988). Locus coeruleus lesions facilitate recovery of locomotor function after sensorimotor cortex contusion in the rat. Abstracts Soc Neurosci, 14, 405.Google Scholar
Wigstrom, H, Gustafsson, B. (1985). Facilitation of hippocampal long-lasting potentiation by GABA antagonists. Acta Physiol Scand, 125, 159–72.Google Scholar
Williams, S, Johnston, D. (1988). Muscarinic depression of long-term potentiation in CA3 hippocampal neurons. Science, 242, 84–7.Google Scholar
Wilson, MS, Hamm, RJ. (2002). Effects of fluoxetine on the 5-HT1A receptor and recovery of cognitive function after traumatic brain injury in rats. Am J Phys Med Rehabil, 81, 364–72.Google Scholar

Save book to Kindle

To save this book to your Kindle, first ensure coreplatform@cambridge.org is added to your Approved Personal Document E-mail List under your Personal Document Settings on the Manage Your Content and Devices page of your Amazon account. Then enter the ‘name’ part of your Kindle email address below. Find out more about saving to your Kindle.

Note you can select to save to either the @free.kindle.com or @kindle.com variations. ‘@free.kindle.com’ emails are free but can only be saved to your device when it is connected to wi-fi. ‘@kindle.com’ emails can be delivered even when you are not connected to wi-fi, but note that service fees apply.

Find out more about the Kindle Personal Document Service.

Available formats
×

Save book to Dropbox

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Dropbox.

Available formats
×

Save book to Google Drive

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Google Drive.

Available formats
×