References
- Saboory E, Ebrahimi L, Roshan-Milani S, et al. Interaction of prenatal stress and morphine alters prolactin and seizure in rat pups. Physiol Behav. 2015;149:181–186. (15) 00339-X [pii].
- Saboory E, Gholami M, Zare S, et al. The long‐term effects of neonatal morphine administration on the pentylenetetrazol seizure model in rats: the role of hippocampal cholinergic receptors in adulthood. Dev Psychobiol. 2014;56(3):498–509.
- Schrott LM, Franklin L'M, Serrano PA. Prenatal opiate exposure impairs radial arm maze performance and reduces levels of BDNF precursor following training. Brain Res. 2008;1198:132–140.
- Vathy I. Prenatal opiate exposure: long-term CNS consequences in the stress system of the offspring. Psychoneuroendocrinology. 2002;27(1–2):273–283.
- Gholipoor P, Saboory E, Roshan-Milani S, et al. Effect of hyperthermia on histamine blood level and convulsive behavior in infant rats. Epilepsy Behav. 2013;29(2):269–274.
- Schmidt D, Schachter SC. Drug treatment of epilepsy in adults. BMJ. 2014;348:g254–g254.
- Gholipoor P, Saboory E, Ghazavi A, et al. Prenatal stress potentiates febrile seizure and leads to long-lasting increase in cortisol blood levels in children under 2 years old. Epilepsy Behav. 2017;72:22–27.
- Ravizza T, Terrone G, Salamone A, et al. High mobility group box 1 is a novel pathogenic factor and a mechanistic biomarker for epilepsy. Brain Behav Immun. 2017;72:14–21.
- Foote F, Gale K. Morphine potentiates seizures induced by GABA antagonists and attenuates seizures induced by electroshock in the rat. Eur J Pharmacol. 1983;95(3–4):259–264.
- Caspers H, Speckmann EJ. Cerebral pO2, pCO2 and pH: changes during convulsive activity and their significance for spontaneous arrest of seizures. Epilepsia. 1972;13(5):699–725.
- Gholami M, Saboory E, Zare S, et al. The effect of dorsal hippocampal administration of nicotinic and muscarinic cholinergic ligands on pentylenetetrazol-induced generalized seizures in rats. Epilepsy Behav. 2012;25(2):244–249.
- Ebrahimi L, Saboory E, Roshan-Milani S, et al. Effect of prenatal forced-swim stress and morphine co-administration on pentylentetrazol-induced epileptic behaviors in infant and prepubertal rats. Dev Psychobiol. 2014;56(6):1179–1186.
- Walsh LA, Li M, Zhao T-J, et al. Acute Pentylenetetrazol Injection Reduces Rat GABAA receptor mRNA levels and GABA stimulation of benzodiazepine binding with No effect on benzodiazepine binding site density. J Pharmacol Exp Ther. 1999;289(3):1626–1633.
- Kjernisted KD, Bleau P. Long-term goals in the management of acute and chronic anxiety disorders. Can J Psychiatry. 2004;49(1):51–63.
- Kandratavicius L, Balista PA, Lopes-Aguiar C, et al. Animal models of epilepsy: use and limitations. Neuropsychiatr Dis Treat. 2014;10:1693–1705.
- Heshmatian B, Roshan-Milani S, Saboory E. Prenatal acute stress attenuated epileptiform activities in neonate mice. Yakhteh Med J. 2009; 11(30):12.
- Gholami M, Saboory E, Khalkhali HR. Chronic morphine and tramadol re‐exposure induced an anti‐anxiety effect in prepubertal rats exposed neonatally to the same drugs. Clin Exp Pharmacol Physiol. 2014;41(10):838–843.
- Zagon IS, Wylie JD, Hurst WJ, et al. Transplacental transfer of the opioid growth factor,[Met5]-enkephalin, in rats. Brain Res Bull. 2001;55(3):341–346.
- Tavassoli E, Saboory E, Teshfam M, et al. Effect of prenatal stress on density of NMDA receptors in rat brain. Int J Dev Neurosci. 2013;31(8):790–795. Dec
- Mei B, Niu L, Cao B, et al. Prenatal morphine exposure alters the layer II/III pyramidal neurons morphology in lateral secondary visual cortex of juvenile rats. Synapse. 2009;63(12):1154–1161.
- Shin I-C, Kim H-C, Swanson J, et al. Anxiolytic effects of acute morphine can be modulated by nitric oxide systems. Pharmacology. 2003;68(4):183–189.
- Zarrindast MR, Rostami P, Zarei M, et al. Intracerebroventricular effects of histaminergic agents on morphine‐induced anxiolysis in the elevated plus‐maze in rats. Basic Clin Pharmacol Toxicol. 2005;97(5):276–281.
- Saboory E, Derchansky M, Ismaili M, et al. Mechanisms of morphine enhancement of spontaneous seizure activity. Anesth Analg. 2007;105(6):1729–1735.
- Shafaroodi H, Asadi S, Sadeghipour H, et al. Role of ATP-sensitive potassium channels in the biphasic effects of morphine on pentylenetetrazole-induced seizure threshold in mice. Epilepsy Res. 2007;75(1):63–69.
- Barber J. Examining the use of tramadol hydrochloride as an antidepressant. Exp Clin Psychopharmacol. 2011;19(2):123–130.
- Hosseini-Sharifabad A, Rabbani M, Sharifzadeh M, et al. Acute and chronic tramadol administration impair spatial memory in rat. Res Pharm Sci. 2016;11(1):49–57.
- Willaschek C, Wolter E, Buchhorn R. Tramadol withdrawal in a neonate after long-term analgesic treatment of the mother. Eur J Clin Pharmacol. 2009;65(4):429–430.
- Gasse MC, Derby L, Vasilakis‐Scaramozza C, et al. Incidence of first‐time idiopathic seizures in users of tramadol. Pharmacotherapy. 2000;20(6):629–634.
- Mammen K, Bell J. The clinical efficacy and abuse potential of combination buprenorphine–naloxone in the treatment of opioid dependence. Expert Opin Pharmacother. 2009;10(15):2537–2544.
- A Yokell M, D Zaller N, C Green T, et al. Buprenorphine and buprenorphine/naloxone diversion, misuse, and illicit use: an international review. Curr Drug Abuse Rev. 2011;4(1):28–41.
- Petri W, editor. Goodman and Gilman’s the pharmacological basis of therapeutics. Boston (MA): McGraw Hill; 2001.
- Yanai J, Huleihel R, Izrael M, et al. Functional changes after prenatal opiate exposure related to opiate receptors' regulated alterations in cholinergic innervation. Int J Neuropsychopharm. 2003;6(3):253–265.
- Mannino RA, Wolf HH. Opiate receptor phenomenon: proconvulsant action of morphine in the mouse. Life Sci. 1974;15(12):2089–2096.
- Ling W, Jacobs P, Hillhouse M, et al. From research to the real world: buprenorphine in the decade of the clinical trials network. J Subst Abuse Treat. 2010;38:S53–S60.
- Mattick RP, Breen C, Kimber J, et al. Methadone maintenance therapy versus no opioid replacement therapy for opioid dependence. Cochrane Database Syst Rev. 2009;(3):CD002209.
- Boyer EW, McCance‐Katz EF, Marcus S. Methadone and buprenorphine toxicity in children. Am J Addict. 2010;19(1):89–95.
- Patrick SW, Schumacher RE, Benneyworth BD, et al. Neonatal abstinence syndrome and associated health care expenditures: United States, 2000–2009. JAMA. 2012;307(18):1934–1940.
- Vazquez B, Devinsky O. Epilepsy and anxiety. Epilepsy Behav. 2003;4:20–25.
- Gholami M, Saboory E. Morphine exposure induces age‐dependent alterations in pentylenetetrazole‐induced epileptic behaviors in prepubertal rats. Dev Psychobiol. 2013;55(8):881–887.
- Jayasree D, Rajeswaramma G. Effect of tramadol in elevated plus maze apparatus–A rodent model of anxiety. J Drug Discovery Ther. 2015;3(27):3–7.
- Vathy I. Prenatal morphine exposure induces age-and sex-dependent changes in seizure susceptibility. Prog Neuropsychopharmacol Biol Psychiatry. 2001;25(6):1203–1226.
- Sperber E, Veliskova J, Germano I, et al. Age-dependent vulnerability to seizures. Adv Neurol. 1999;79:161–169.
- Stefano GB, Salzet B, Rialas CM, et al. Morphine-and anadamide-stimulated nitric oxide production inhibits presynaptic dopamine release. Brain Res. 1997;763(1):63–68.
- Bahremand A, Nasrabady SE, Shafaroodi H, et al. Involvement of nitrergic system in the anticonvulsant effect of the cannabinoid CB1 agonist ACEA in the pentylenetetrazole-induced seizure in mice. Epilepsy Res. 2009;84(2–3):110–119.
- Brown MJ, Bristow DR. Molecular mechanisms of benzodiazepine‐induced down‐regulation of GABAA receptor α1 subunit protein in rat cerebellar granule cells. Br J Pharmacol. 1996;118(5):1103–1110.
- Hong J. Hippocampal opioid peptides and seizures. Epilepsy Res Suppl. 1992;7:187–195.
- Vathy I, Velı́ J, Moshé SL. Prenatal morphine exposure induces age-related changes in seizure susceptibility in male rats. Pharmacol Biochem Behav. 1998;60((3):635–638.
- Rehni AK, Singh TG, Singh N, et al. Tramadol-induced seizurogenic effect: a possible role of opioid-dependent histamine (H 1) receptor activation-linked mechanism. Naunyn-Schmied Arch Pharmacol. 2010;381(1):11–19.
- Rehni AK, Singh I, Kumar M. Tramadol‐induced seizurogenic effect: a possible role of opioid‐dependent γ‐aminobutyric acid inhibitory pathway. Basic Clin Pharmacol Toxicol. 2008;103(3):262–266.
- Engin E, Treit D, Dickson C. Anxiolytic-and antidepressant-like properties of ketamine in behavioral and neurophysiological animal models. Neuroscience. 2009;161(2):359–369.
- Wiley JL, Cristello AF, Balster RL. Effects of site-selective NMDA receptor antagonists in an elevated plus-maze model of anxiety in mice. Eur J Pharmacol. 1995; 294 (1):101–107.
- Lingford-Hughes A, Nutt D. Neurobiology of addiction and implications for treatment. Br J Psychiatry. 2003;182(2):97–100.
- Oliveira J, Lopes P, Gamito P, et al. Neuropsychological Status of Heroin Users Undergoing Methadone Maintenance in Harm Reduction Program and Therapeutic Community. Int J Ment Health Addiction. 2016;14(2):141–148.
- Dryden C, Young D, Hepburn M, et al. Maternal methadone use in pregnancy: factors associated with the development of neonatal abstinence syndrome and implications for healthcare resources. BJOG. 2009;116(5):665–671.
- Baamonde AI, Hidalgo A, Andres-Trelles F. Sex-related differences in the effects of morphine and stress on visceral pain. Neuropharmacology. 1989;28(9):967–970.
- Dahan A, Kest B, Waxman AR, et al. Sex-specific responses to opiates: animal and human studies. Anesth Analg. 2008;107(1):83–95.
- Lee C-S, Ho K. Sex differences in opioid analgesia and addiction: interactions among opioid receptors and estrogen receptors. Mol Pain. 2013;9(1):1744-8069-9-45.
- Kim EU, Spear LP. Sex-dependent consequences of pre-pubertal gonadectomy: social behavior, stress and ethanol responsivity. Behav Brain Res. 2016;296:260–269.
- Collins D, Reed B, Zhang Y, et al. Sex differences in responsiveness to the prescription opioid oxycodone in mice. Pharmacol Biochem Behav. 2016;148:99–105.