BibTex RIS Cite

Effects of Psychostimulant Drugs on Developing Brain

Year 2013, Volume: 5 Issue: 4, 528 - 539, 01.12.2013
https://doi.org/10.5455/cap.20130532

Abstract

Although psychostimulants have been used for the treatment of attention deficit hyperactivity disorder for approximately 70 years, little is known about the long term effects of these drugs on developing brain. The observable effects of psychostimulants are influenced by the timing of exposure, the age of examination after drug exposure and sex. Preclinical studies point out that chronic psychostimulant exposure before adolescence cause reverse sensitization or tolerance and this leads to reduction in stimulant effectiveness in adolesecence and adulthood. Preclinical studies show the potential long term effects of psychostimulants. But it is necessary to investigate the relationship between preclinical effects and clinical practice. A developmental approach is needed to understand the impact of pediatric medications on the brain that includes assessment at multiple ages to completely characterize the long term effects of these medications. The aim of this paper is to review the effects of psychostimulants on developing brain.

References

  • Schachar RJ, Tannock R, Cunningham C, Corkum PV. Behavioral, situational, and temporal effects of treatment of ADHD with methylphenidate. J Am Acad Child Adolesc Psychiatry 1997; 36:754–763.
  • Pliszka SR. The use of psychostimulants in the pediatric patient. Pediatr Clin North Am 1998; 45:1085–1098.
  • Henry CA, Zamvil LS, Lam C, Rosenquist KJ, Ghaemi SN. Long-term outcome with divalproex in children and adolescents with bipolar disorder. J Child Adolesc Psychopharmacol 2003; 13:523–529.
  • Vaswani M, Linda FK, Ramesh S. Role of selective serotonin reuptake inhibitors in psychiatric disorders: a comprehensive review. Prog Neuropsychopharmacol Biol Psychiatry 2003: 27, 85–102.
  • Minde K. The use of psychotropic medication in preschoolers: some recent developments. Can J Psychiatry 1998; 43:571–575.
  • Zito JM, Safer DJ, dosReis S, Gardner JF, Boles M, Lynch F. Trends in the prescribing of psychotropic medications to preschoolers. J Am Med Assoc 2000; 283:1025–1030.
  • Goodwin R, Gould MS, Blanco C, Olfson M. Prescription of psychotropic medications to youths in office-based practice. Psychiatr Serv 2001; 52:1081–1087. Olfson M, Marcus SC, Weissman MM, Jensen PS. National trends in the use of psychotropic medications by children. J Am Acad Child Adolesc Psychiatry 2002; 41:514–521.
  • Costello EJ, Pine DS, Hammen C, March JS, Plotsky PM, Weissman MM et al. Development and natural history of mood disorders. Biol Psychiatry 2002; 52:529– 5
  • Greenfield B, Hechtman L, Weiss G. Two subgroups of hyperactives as adults: correlations of outcome. Can J Psychiatry 1988; 33:505–508.
  • Greene RW, Biederman J, Faraone SV, Wilens TE, Mick E, Blier HK. Further validation of social impairment as a predictor of substance use disorders: findings from a sample of siblings of boys with and without ADHD. J Clin Child Psychol 1999; 28:349–354.
  • Biederman J, Wilens T, Mick E, Spencer T, Faraone SV. Pharmacotherapy of attention deficit hyperactivity disorder reduces risk for substance use disorder. Pediatrics 1999; 104:e20.
  • Wilens TE, Biederman J, Millstein RB, Wozniak J, Hahesy AL, Spencer TJ. Risk for substance use disorders in youths with child- and adolescent-onset bipolar disorder. J Am Acad Child Adolesc Psychiatry 1999; 38:680–685.
  • Ryan ND. Child and adolescent depression: short-term treatment effectiveness and long-term opportunities. Int J Methods Psychiatr Res 2003; 12:44–53.
  • Spear L. The adolescent brain and age-related behavioral manifestations. Neurosci Bio-Behav Rev 2000; 24:417–463.
  • Slotkin TA, Tate CA, Cousins MM, Seidler FJ. Functional alterations in CNS catecholamine systems in adolescence and adulthood after neonatal chlorpyrifos exposure. Brain Res Dev Brain Res 2002: 133:163–173.
  • Andersen SL, Navalta CP. Altering the course of neurodevelopment: a framework for understanding the enduring effects of psychotropic drugs. Int J Dev Neurosci 2004; 22:423–440.
  • Swanson J. Compliance with stimulants for attention-deficit hyperactivity disorder. CNS Drugs 2003; 17:117-131.
  • Safer DJ, Zito JM, Fine EM. Increased methylphenidate usage for attention deficit disorder in the 1990s. Pediatrics 1996; 98:1084-1088.
  • Gillberg C, Melander H, von Knorring AL, Janols LO, Thernlund G, Hägglöf B et al. Long term stimulant treatment of children with attention-deficit hyperactivity disorder symptoms. A randomized, double-blind, placebo-controlled trial. Arch Gen Psychiatry 1997; 54:857-864.
  • MTA Cooperative Group. A 14-month randomized clinical trial of treatment strategies for attention-deficit/hyperactivity disorder. Arch Gen Psychiatry 1999; 56:1073-1086.
  • Jadad AR, Booker L, Gauld M, Kakuma R, Boyle M, Cunningham CE et al. The treatment of attention deficit hyperactivity disorder: an annotated bibliography and critical appraisal of published systematic reviews and metaanalyses. Can J Psychiatry 1999; 44:1025-1035.
  • American Academy of Pediatrics. Clinical practice guideline: treatment of the schoolaged child with attention-deficit/hyperactivity disorder. Pediatrics 2001;108:1033Andersen SL. Stimulants and the developing brain. Trends Pharmacol Sci 2005; 26:237-243.
  • Greenhill LL, Pliszka S, Dulcan MK, Bernet W, Arnold V, Beitchman J et al. Practice parameter for the use of stimulant medications in the treatment of children, adolescents, and adults. J Am Acad Child Adolesc Psychiatry 2002; 41:26S–49S.
  • Levitt P, Harvey JA, Friedman E, Simansky K, Murphy EH. New evidence for neurotransmitter influences on brain development. Trends Neurosci 1997; 20:269– 2
  • Lidow MS. Cocaine abuse and corticogenesis. Trends Neurosci 1998; 21:19–20.
  • Malanga III CJ, Kosofsky BE. Mechanisms of action of drugs of abuse on the developing fetal brain. Clin Perinatol 1999; 32:17–37.
  • Ernst M, Moolchan ET Robinson ML. Behavioral and neural consequences of prenatal exposure to nicotine. J Am Acad Child Adolesc Psychiatry 2001; 40:630– 6
  • Andersen S, Dumont N, Teicher MH. Differences in behavior and monoamine laterality following neonatal clomipramine treatment. Dev Psychobiol 2002; 41:50–
  • Andersen SL, Arvanitogiannis A, Pliakas AM, LeBlanc C, Carlezon WA Jr. Altered responsiveness to cocaine in rats exposed to methylphenidate during development. Nat Neurosci 2002; 5:13–14.
  • Andersen SL. Trajectories of brain development: point of vulnerability or window of opportunity? Neurosci Biobehav Rev 2003; 27: 3–18
  • Lidow MS, Song ZM. Primates exposed to cocaine in utero display reduced density and number of cerebral cortical neurons. J Comp Neurol 2001; 435:263–275.
  • Gelbard HA, Teicher MH, Baldessarini RJ, Gallitano A, Marsh ER, Zorc J. Dopamine D1 receptor development depends on endogenous dopamine. Brain Res Dev Brain Res 1990; 56:137–140.
  • Todd RD. Neural development is regulated by classical neurotransmitters: dopamine D2 receptor stimulation enhances neurite outgrowth. Biol Psychiatry 1992; 31:794– 80
  • Kline AE, Chen MJ, Tso-Olivas DY, Feeney DM. Methylphenidate treatment following ablation-induced hemiplegia in rat: experience during drug action alters effects on recovery of function. Pharmacol Biochem Behav 1994; 48:773–779.
  • Whitaker-Azmitia PM, Azmitia EC. Autoregulation of fetal serotonergic neuronal development: role of high affinity serotonin receptors. Neurosci Lett 1986; 67:307– 3
  • Insel TR. The development of brain and behavior. In Psychopharmacology: The Fourth Generation of Progress. New York, Raven Press, 1995.
  • Giedd JN, Blumenthal J, Jeffries NO, Castellanos FX, Liu H, Zijdenbos A et al. Brain development during childhood and adolescence: a longitudinal MRI study. Nat Neurosci 1999; 2:861–863.
  • Giedd JN, Jeffries NO, Blumenthal J, Castellanos FX, Vaituzis AC, Fernandez T et al. Childhood-onset schizophrenia: progressive brain changes during adolescence. Biol Psychiatry 1999; 46:892– 898.
  • Sowell ER, Thompson PM, Tessner KD, Toga AW. Mapping continued brain growth and gray matter density reduction in dorsal frontal cortex: Inverse relationships during postadolescent brain maturation. J Neurosci 2001; 21:8819– 88
  • Lidow MS, Goldman-Rakic PS, Rakic P. Synchronized overproduction of neurotransmitter receptors in diverse regions of the primate cerebral cortex. Proc Natl Acad Sci 1991; 88:10218-10221.
  • Andersen SL, Dumont NL, Teicher MH. Developmental differences in dopamine synthesis inhibition by 7-OHDPAT. Naunyn Schmiedeberg’s Arch Pharmacol 1997; 356:173–181.
  • Andersen SL, Rutstein M, Benzo JM, Hostetter JC, Teicher MH. Sex differences in dopamine receptor overproduction and elimination. Neuroreport 1997; 8:1495– 14
  • Andersen SL, Thompson AT, Rutstein M, Hostetter JC, Teicher MH. Dopamine receptor pruning in prefrontal cortex during the periadolescent period in rats. Synapse 2000; 37:167–169.
  • Shaw P, Sharp WS, Morrison M, Eckstrand K, Greenstein DK, Clasen LS et al. Psychostimulant treatment and the developnig cortex in attention deficit hyperactivity disorder. Am J Psychiatry 2009; 166:58-63.
  • Spear L. The adolescent brain and age-related behavioral manifestations. Neurosci Biobehav Rev 2000; 24:417–463.
  • Heyser CJ, Pelletier M, Ferris JS. The effects of methylphenidate on novel object exploration in weanling and periadolescent rats. Ann N Y Acad Sci 2004; 1021:465– 4
  • Andersen SL, LeBlanc CJ, Lyss PJ. Maturational increases in c-fos expression in the ascending dopamine systems. Synapse 2001; 41:345–350.
  • Casey BJ, Giedd JN, Thomas KM. Structural and functional brain development and its relation to cognitive development. Biol Psychol 2000; 54:241–257.
  • Durston S, Tottenham NT, Thomas KM, Davidson MC, Eigsti IM, Yang Y et al. Differential patterns of striatal activation in young children with and without ADHD. Biol Psychiatry 2003; 53:871–878.
  • Vaidya CJ Austin G, Kirkorian G, Ridlehuber HW, Desmond JE, Glover GH et al. Selective effects of methylphenidate in attention deficit hyperactivity disorder: a functional magnetic resonance study. Proc Natl Acad Sci USA 1998; 95:14494– 144
  • Bolanos CA, Barrot M, Berton O, Wallace-Black D, Nestler EJ. Methylphenidate treatment during pre- and periadolescence alters behavioral responses to emotional stimuli at adulthood. Biol Psychiatry 2003; 54:1317–1329.
  • Carlezon WA Jr, Mague SD, Andersen SL. Enduring behavioral effects of early exposure to methylphenidate in rats. Biol Psychiatry 2003; 54:1330– 1337.
  • Rosengarten H, Friedhoff AJ. Enduring changes in dopamine receptor cells of pups from drug administration to pregnant and nursing rats. Science 1979; 203:1133– Lerner P, Nose P, Gordon EK, Lovenberg W. Haloperidol: effect of long-term treatment on rat striatal dopamine synthesis and turnover. Science 1977; 197:181– 1
  • Laviola, G, Wood RD, Kuhn C, Francis R, Spear LP. Cocaine sensitization in periadolescent and adult rats. J Pharmacol Exp Ther 1995; 275:345–357.
  • McDougall S, Collins R, Karper PE, Watson JB, Crawford CA. Effects of repeated methylphenidate treatment in the young rat: sensitization of both locomotor activity and stereotyped sniffing. Exp Clin Psychopharmacol 1999; 7:208–218.
  • Gaytan O, Al-Rahim S, Swann A, Dafny N. Sensitization to locomotor effects of methylphenidate in the rat. Life Sci 1997; 61:101–107.
  • Schenk S, Partridge B. Cocaine-seeking produced by experimenter administered drug injections: dose-effect relationships in rats. Psychopharmacology (Berlin) 1999; 147:285–290.
  • Langley K, Fowler T, Ford T, Thapar AK, van der Bree M, Harold G et al. Adolescent clinical outcomes for young people with attention deficit hyperactivity disorder. Br J Psychiatry 2010;196:235-240.
  • Busidan Y, Dow-Edwards DL. Behavioral sensitization to apomorphine in adult rats exposed to cocaine during the preweaning period: a preliminary study. Pharmacol Biochem Behav 1999; 63:417–421.
  • Dow-Edwards DL, Busidan Y. Behavioral responses to dopamine agonists in adult rats exposed to cocaine during the preweaning period. Pharmacol Biochem Behav 2001; 70:23–30.
  • Moll G, Hause S, Rüther E, Rothenberger A, Huether G. Early methylphenidate adminstration to young rats causes a persistent reduction in the density of striatal transporters. J Child Adolesc Psychopharmacol 2001; 11:15–24
  • Howard SG, Fisher R, Landry CF. Alterations in the spontaneous release of dopamine and the density of the DA D2 receptor mRNA after chronic postnatal exposure to cocaine. Brain Res Bull 1997; 43:101–106.
  • Sproson EJ, Chantrey J, Hollis C, Marsden CA, Fonel KC. Effect of repeated methylphenidate administration on presynaptic dopamine and behaviour in young adult rats. J Psychopharmacol 2001; 15:67–75.
  • Cornish JL, Kalivas PW. Cocaine sensitization and craving: differing roles for dopamine and glutamate in the nucleus accumbens. J Addict Dis 2001; 20:43–54.
  • Soto PL, Wilcox KM, Zhou Y, Ator NA, Riddle MA,Wong DF et al. Long- term exposure to oral methyphenidate or dl-amphetamine mixture in peri-adolescent rhesus monkeys:effects on physiology, behavior, and dopamine system development. Neuropsychopharmacology 2012; 37:2566-2579.
  • Hilburn CR. The interaction of stimulant intake with brain aging:effects on behavioral capacity, oxidative defect and dopaminergic markers. Fort Worth, Tx: University of North Texas Health Science Center, 2009.
  • Derauf C, Lagasse LL, Smith LM, Newman E, Shah R, Neal CR et al. Prenatal methamphetamine exposure and inhibitory control among young school-age children. J Pediatr 2012; 161:452-459.
  • Wargin W, Patrick K, Kilts C, Gualtieri CT, Ellington K, Mueller RA et al. Pharmacokinetics of methylphenidate in man, rat and monkey. J Pharmacol Exp Ther 1983; 226:382–386.
  • Ding YS, Gatley SJ, Thanos PK. Brain kinetics of methylphenidate (Ritalin) enantiomers after oral administration. Synapse 2004; 53:168–175.
  • Elmas Ç, Bahçelioğlu M, Erdoğan D, Rabet G, Take G, Çalgüner G et al. Rat pineal ve hipofiz bezlerinde metilfenidata bağlı olarak oluşan immünohistokimyasal ve ince yapısal değişiklikler: doz bağımlı çalışma. Journal of Neurological Sciences-Turkish 2012; 29:476-493. İbrahim Durukan, Dr., GATA Çocuk ve Ergen Psikiyatrisi A.D, Ankara; Murat Erdem, Doç. Dr., GATA Psikiyatri A.D, Ankara; Koray Kara, Dr., GATA Çocuk ve Ergen Psikiyatrisi A.D, Ankara; Dursun Karaman, Dr., GATA Çocuk ve Ergen Psikiyatrisi A.D, Ankara. Yazışma Adresi/Correspondence: İbrahim Durukan, GATA Çocuk ve Ergen Psikiyatrisi A.D, Ankara, Turkey. E-mail: idurukan2003@yahoo.com Yazarlar bu makale ile ilgili herhangi bir çıkar çatışması bildirmemişlerdir. The authors reported no conflict of interest related to this article. Çevrimiçi adresi / Available online at: www.cappsy.org/archives/vol5/no4/ Çevrimiçi yayım / Published online 31 Aralık/December 31, 2013; doi:10.5455/cap.20130532

Psikostimülan İlaçların Gelişen Beyin Üzerindeki Etkileri

Year 2013, Volume: 5 Issue: 4, 528 - 539, 01.12.2013
https://doi.org/10.5455/cap.20130532

Abstract

Psikostimülanlar dikkat eksikliği hiperaktivite bozukluğu tedavisinde yaklaşık 70 yıldır kullanılmasına rağmen, bu ilaçların gelişen beyin üzerindeki uzun dönem etkileri hakkında çok az şey bilinmektedir. Psikostimülanların saptanan etkileri maruziyetin zamanı, yapılan değerlendirmenin zamanı ve cinsiyetten etkilenmektedir. Preklinik çalışmalar, ergenlik öncesinde kronik stimülan maruziyetinin ters duyarlılaşma veya tolerans oluşmasına yol açtığı ve bunun da ergenlik ve sonrasında stimulanların etkinliğinde azalmaya yol açacağına işaret etmektedir. Preklinik çalışmalar psikostimülanların uzun dönem etkileri olabileceğine işaret etmektedir. Ancak bu olası etkilerin klinik olarak hangi düzeyde olabileceğinin araştırılması gerekmektedir. Psikostimülan ilaçların beyin üzerindeki etkilerini daha iyi anlamak için farklı yaş gruplarında yapılacak çalışmalara gereksinim olduğu düşünülmektedir..

References

  • Schachar RJ, Tannock R, Cunningham C, Corkum PV. Behavioral, situational, and temporal effects of treatment of ADHD with methylphenidate. J Am Acad Child Adolesc Psychiatry 1997; 36:754–763.
  • Pliszka SR. The use of psychostimulants in the pediatric patient. Pediatr Clin North Am 1998; 45:1085–1098.
  • Henry CA, Zamvil LS, Lam C, Rosenquist KJ, Ghaemi SN. Long-term outcome with divalproex in children and adolescents with bipolar disorder. J Child Adolesc Psychopharmacol 2003; 13:523–529.
  • Vaswani M, Linda FK, Ramesh S. Role of selective serotonin reuptake inhibitors in psychiatric disorders: a comprehensive review. Prog Neuropsychopharmacol Biol Psychiatry 2003: 27, 85–102.
  • Minde K. The use of psychotropic medication in preschoolers: some recent developments. Can J Psychiatry 1998; 43:571–575.
  • Zito JM, Safer DJ, dosReis S, Gardner JF, Boles M, Lynch F. Trends in the prescribing of psychotropic medications to preschoolers. J Am Med Assoc 2000; 283:1025–1030.
  • Goodwin R, Gould MS, Blanco C, Olfson M. Prescription of psychotropic medications to youths in office-based practice. Psychiatr Serv 2001; 52:1081–1087. Olfson M, Marcus SC, Weissman MM, Jensen PS. National trends in the use of psychotropic medications by children. J Am Acad Child Adolesc Psychiatry 2002; 41:514–521.
  • Costello EJ, Pine DS, Hammen C, March JS, Plotsky PM, Weissman MM et al. Development and natural history of mood disorders. Biol Psychiatry 2002; 52:529– 5
  • Greenfield B, Hechtman L, Weiss G. Two subgroups of hyperactives as adults: correlations of outcome. Can J Psychiatry 1988; 33:505–508.
  • Greene RW, Biederman J, Faraone SV, Wilens TE, Mick E, Blier HK. Further validation of social impairment as a predictor of substance use disorders: findings from a sample of siblings of boys with and without ADHD. J Clin Child Psychol 1999; 28:349–354.
  • Biederman J, Wilens T, Mick E, Spencer T, Faraone SV. Pharmacotherapy of attention deficit hyperactivity disorder reduces risk for substance use disorder. Pediatrics 1999; 104:e20.
  • Wilens TE, Biederman J, Millstein RB, Wozniak J, Hahesy AL, Spencer TJ. Risk for substance use disorders in youths with child- and adolescent-onset bipolar disorder. J Am Acad Child Adolesc Psychiatry 1999; 38:680–685.
  • Ryan ND. Child and adolescent depression: short-term treatment effectiveness and long-term opportunities. Int J Methods Psychiatr Res 2003; 12:44–53.
  • Spear L. The adolescent brain and age-related behavioral manifestations. Neurosci Bio-Behav Rev 2000; 24:417–463.
  • Slotkin TA, Tate CA, Cousins MM, Seidler FJ. Functional alterations in CNS catecholamine systems in adolescence and adulthood after neonatal chlorpyrifos exposure. Brain Res Dev Brain Res 2002: 133:163–173.
  • Andersen SL, Navalta CP. Altering the course of neurodevelopment: a framework for understanding the enduring effects of psychotropic drugs. Int J Dev Neurosci 2004; 22:423–440.
  • Swanson J. Compliance with stimulants for attention-deficit hyperactivity disorder. CNS Drugs 2003; 17:117-131.
  • Safer DJ, Zito JM, Fine EM. Increased methylphenidate usage for attention deficit disorder in the 1990s. Pediatrics 1996; 98:1084-1088.
  • Gillberg C, Melander H, von Knorring AL, Janols LO, Thernlund G, Hägglöf B et al. Long term stimulant treatment of children with attention-deficit hyperactivity disorder symptoms. A randomized, double-blind, placebo-controlled trial. Arch Gen Psychiatry 1997; 54:857-864.
  • MTA Cooperative Group. A 14-month randomized clinical trial of treatment strategies for attention-deficit/hyperactivity disorder. Arch Gen Psychiatry 1999; 56:1073-1086.
  • Jadad AR, Booker L, Gauld M, Kakuma R, Boyle M, Cunningham CE et al. The treatment of attention deficit hyperactivity disorder: an annotated bibliography and critical appraisal of published systematic reviews and metaanalyses. Can J Psychiatry 1999; 44:1025-1035.
  • American Academy of Pediatrics. Clinical practice guideline: treatment of the schoolaged child with attention-deficit/hyperactivity disorder. Pediatrics 2001;108:1033Andersen SL. Stimulants and the developing brain. Trends Pharmacol Sci 2005; 26:237-243.
  • Greenhill LL, Pliszka S, Dulcan MK, Bernet W, Arnold V, Beitchman J et al. Practice parameter for the use of stimulant medications in the treatment of children, adolescents, and adults. J Am Acad Child Adolesc Psychiatry 2002; 41:26S–49S.
  • Levitt P, Harvey JA, Friedman E, Simansky K, Murphy EH. New evidence for neurotransmitter influences on brain development. Trends Neurosci 1997; 20:269– 2
  • Lidow MS. Cocaine abuse and corticogenesis. Trends Neurosci 1998; 21:19–20.
  • Malanga III CJ, Kosofsky BE. Mechanisms of action of drugs of abuse on the developing fetal brain. Clin Perinatol 1999; 32:17–37.
  • Ernst M, Moolchan ET Robinson ML. Behavioral and neural consequences of prenatal exposure to nicotine. J Am Acad Child Adolesc Psychiatry 2001; 40:630– 6
  • Andersen S, Dumont N, Teicher MH. Differences in behavior and monoamine laterality following neonatal clomipramine treatment. Dev Psychobiol 2002; 41:50–
  • Andersen SL, Arvanitogiannis A, Pliakas AM, LeBlanc C, Carlezon WA Jr. Altered responsiveness to cocaine in rats exposed to methylphenidate during development. Nat Neurosci 2002; 5:13–14.
  • Andersen SL. Trajectories of brain development: point of vulnerability or window of opportunity? Neurosci Biobehav Rev 2003; 27: 3–18
  • Lidow MS, Song ZM. Primates exposed to cocaine in utero display reduced density and number of cerebral cortical neurons. J Comp Neurol 2001; 435:263–275.
  • Gelbard HA, Teicher MH, Baldessarini RJ, Gallitano A, Marsh ER, Zorc J. Dopamine D1 receptor development depends on endogenous dopamine. Brain Res Dev Brain Res 1990; 56:137–140.
  • Todd RD. Neural development is regulated by classical neurotransmitters: dopamine D2 receptor stimulation enhances neurite outgrowth. Biol Psychiatry 1992; 31:794– 80
  • Kline AE, Chen MJ, Tso-Olivas DY, Feeney DM. Methylphenidate treatment following ablation-induced hemiplegia in rat: experience during drug action alters effects on recovery of function. Pharmacol Biochem Behav 1994; 48:773–779.
  • Whitaker-Azmitia PM, Azmitia EC. Autoregulation of fetal serotonergic neuronal development: role of high affinity serotonin receptors. Neurosci Lett 1986; 67:307– 3
  • Insel TR. The development of brain and behavior. In Psychopharmacology: The Fourth Generation of Progress. New York, Raven Press, 1995.
  • Giedd JN, Blumenthal J, Jeffries NO, Castellanos FX, Liu H, Zijdenbos A et al. Brain development during childhood and adolescence: a longitudinal MRI study. Nat Neurosci 1999; 2:861–863.
  • Giedd JN, Jeffries NO, Blumenthal J, Castellanos FX, Vaituzis AC, Fernandez T et al. Childhood-onset schizophrenia: progressive brain changes during adolescence. Biol Psychiatry 1999; 46:892– 898.
  • Sowell ER, Thompson PM, Tessner KD, Toga AW. Mapping continued brain growth and gray matter density reduction in dorsal frontal cortex: Inverse relationships during postadolescent brain maturation. J Neurosci 2001; 21:8819– 88
  • Lidow MS, Goldman-Rakic PS, Rakic P. Synchronized overproduction of neurotransmitter receptors in diverse regions of the primate cerebral cortex. Proc Natl Acad Sci 1991; 88:10218-10221.
  • Andersen SL, Dumont NL, Teicher MH. Developmental differences in dopamine synthesis inhibition by 7-OHDPAT. Naunyn Schmiedeberg’s Arch Pharmacol 1997; 356:173–181.
  • Andersen SL, Rutstein M, Benzo JM, Hostetter JC, Teicher MH. Sex differences in dopamine receptor overproduction and elimination. Neuroreport 1997; 8:1495– 14
  • Andersen SL, Thompson AT, Rutstein M, Hostetter JC, Teicher MH. Dopamine receptor pruning in prefrontal cortex during the periadolescent period in rats. Synapse 2000; 37:167–169.
  • Shaw P, Sharp WS, Morrison M, Eckstrand K, Greenstein DK, Clasen LS et al. Psychostimulant treatment and the developnig cortex in attention deficit hyperactivity disorder. Am J Psychiatry 2009; 166:58-63.
  • Spear L. The adolescent brain and age-related behavioral manifestations. Neurosci Biobehav Rev 2000; 24:417–463.
  • Heyser CJ, Pelletier M, Ferris JS. The effects of methylphenidate on novel object exploration in weanling and periadolescent rats. Ann N Y Acad Sci 2004; 1021:465– 4
  • Andersen SL, LeBlanc CJ, Lyss PJ. Maturational increases in c-fos expression in the ascending dopamine systems. Synapse 2001; 41:345–350.
  • Casey BJ, Giedd JN, Thomas KM. Structural and functional brain development and its relation to cognitive development. Biol Psychol 2000; 54:241–257.
  • Durston S, Tottenham NT, Thomas KM, Davidson MC, Eigsti IM, Yang Y et al. Differential patterns of striatal activation in young children with and without ADHD. Biol Psychiatry 2003; 53:871–878.
  • Vaidya CJ Austin G, Kirkorian G, Ridlehuber HW, Desmond JE, Glover GH et al. Selective effects of methylphenidate in attention deficit hyperactivity disorder: a functional magnetic resonance study. Proc Natl Acad Sci USA 1998; 95:14494– 144
  • Bolanos CA, Barrot M, Berton O, Wallace-Black D, Nestler EJ. Methylphenidate treatment during pre- and periadolescence alters behavioral responses to emotional stimuli at adulthood. Biol Psychiatry 2003; 54:1317–1329.
  • Carlezon WA Jr, Mague SD, Andersen SL. Enduring behavioral effects of early exposure to methylphenidate in rats. Biol Psychiatry 2003; 54:1330– 1337.
  • Rosengarten H, Friedhoff AJ. Enduring changes in dopamine receptor cells of pups from drug administration to pregnant and nursing rats. Science 1979; 203:1133– Lerner P, Nose P, Gordon EK, Lovenberg W. Haloperidol: effect of long-term treatment on rat striatal dopamine synthesis and turnover. Science 1977; 197:181– 1
  • Laviola, G, Wood RD, Kuhn C, Francis R, Spear LP. Cocaine sensitization in periadolescent and adult rats. J Pharmacol Exp Ther 1995; 275:345–357.
  • McDougall S, Collins R, Karper PE, Watson JB, Crawford CA. Effects of repeated methylphenidate treatment in the young rat: sensitization of both locomotor activity and stereotyped sniffing. Exp Clin Psychopharmacol 1999; 7:208–218.
  • Gaytan O, Al-Rahim S, Swann A, Dafny N. Sensitization to locomotor effects of methylphenidate in the rat. Life Sci 1997; 61:101–107.
  • Schenk S, Partridge B. Cocaine-seeking produced by experimenter administered drug injections: dose-effect relationships in rats. Psychopharmacology (Berlin) 1999; 147:285–290.
  • Langley K, Fowler T, Ford T, Thapar AK, van der Bree M, Harold G et al. Adolescent clinical outcomes for young people with attention deficit hyperactivity disorder. Br J Psychiatry 2010;196:235-240.
  • Busidan Y, Dow-Edwards DL. Behavioral sensitization to apomorphine in adult rats exposed to cocaine during the preweaning period: a preliminary study. Pharmacol Biochem Behav 1999; 63:417–421.
  • Dow-Edwards DL, Busidan Y. Behavioral responses to dopamine agonists in adult rats exposed to cocaine during the preweaning period. Pharmacol Biochem Behav 2001; 70:23–30.
  • Moll G, Hause S, Rüther E, Rothenberger A, Huether G. Early methylphenidate adminstration to young rats causes a persistent reduction in the density of striatal transporters. J Child Adolesc Psychopharmacol 2001; 11:15–24
  • Howard SG, Fisher R, Landry CF. Alterations in the spontaneous release of dopamine and the density of the DA D2 receptor mRNA after chronic postnatal exposure to cocaine. Brain Res Bull 1997; 43:101–106.
  • Sproson EJ, Chantrey J, Hollis C, Marsden CA, Fonel KC. Effect of repeated methylphenidate administration on presynaptic dopamine and behaviour in young adult rats. J Psychopharmacol 2001; 15:67–75.
  • Cornish JL, Kalivas PW. Cocaine sensitization and craving: differing roles for dopamine and glutamate in the nucleus accumbens. J Addict Dis 2001; 20:43–54.
  • Soto PL, Wilcox KM, Zhou Y, Ator NA, Riddle MA,Wong DF et al. Long- term exposure to oral methyphenidate or dl-amphetamine mixture in peri-adolescent rhesus monkeys:effects on physiology, behavior, and dopamine system development. Neuropsychopharmacology 2012; 37:2566-2579.
  • Hilburn CR. The interaction of stimulant intake with brain aging:effects on behavioral capacity, oxidative defect and dopaminergic markers. Fort Worth, Tx: University of North Texas Health Science Center, 2009.
  • Derauf C, Lagasse LL, Smith LM, Newman E, Shah R, Neal CR et al. Prenatal methamphetamine exposure and inhibitory control among young school-age children. J Pediatr 2012; 161:452-459.
  • Wargin W, Patrick K, Kilts C, Gualtieri CT, Ellington K, Mueller RA et al. Pharmacokinetics of methylphenidate in man, rat and monkey. J Pharmacol Exp Ther 1983; 226:382–386.
  • Ding YS, Gatley SJ, Thanos PK. Brain kinetics of methylphenidate (Ritalin) enantiomers after oral administration. Synapse 2004; 53:168–175.
  • Elmas Ç, Bahçelioğlu M, Erdoğan D, Rabet G, Take G, Çalgüner G et al. Rat pineal ve hipofiz bezlerinde metilfenidata bağlı olarak oluşan immünohistokimyasal ve ince yapısal değişiklikler: doz bağımlı çalışma. Journal of Neurological Sciences-Turkish 2012; 29:476-493. İbrahim Durukan, Dr., GATA Çocuk ve Ergen Psikiyatrisi A.D, Ankara; Murat Erdem, Doç. Dr., GATA Psikiyatri A.D, Ankara; Koray Kara, Dr., GATA Çocuk ve Ergen Psikiyatrisi A.D, Ankara; Dursun Karaman, Dr., GATA Çocuk ve Ergen Psikiyatrisi A.D, Ankara. Yazışma Adresi/Correspondence: İbrahim Durukan, GATA Çocuk ve Ergen Psikiyatrisi A.D, Ankara, Turkey. E-mail: idurukan2003@yahoo.com Yazarlar bu makale ile ilgili herhangi bir çıkar çatışması bildirmemişlerdir. The authors reported no conflict of interest related to this article. Çevrimiçi adresi / Available online at: www.cappsy.org/archives/vol5/no4/ Çevrimiçi yayım / Published online 31 Aralık/December 31, 2013; doi:10.5455/cap.20130532
There are 70 citations in total.

Details

Primary Language Turkish
Journal Section Review
Authors

İbrahim Durukan This is me

Murat Erdem This is me

Koray Kara This is me

Dursun Karaman This is me

Publication Date December 1, 2013
Published in Issue Year 2013 Volume: 5 Issue: 4

Cite

AMA Durukan İ, Erdem M, Kara K, Karaman D. Psikostimülan İlaçların Gelişen Beyin Üzerindeki Etkileri. Psikiyatride Güncel Yaklaşımlar - Current Approaches in Psychiatry. December 2013;5(4):528-539. doi:10.5455/cap.20130532

Creative Commons License
Psikiyatride Güncel Yaklaşımlar - Current Approaches in Psychiatry is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.