DOI QR코드

DOI QR Code

Long-term prenatal stress increases susceptibility of N-methyl-D-aspartic acid-induced spasms in infant rats

  • Kwon, Hyeok Hee (Department of Medical Science, College of Medicine, Chungnam National University) ;
  • Lee, Taekwan (Department of Pediatrics, Chungnam National University Hospital, Chungnam National University School of Medicine) ;
  • Hong, Jinpyo (Department of Anatomy, College of Medicine, Chungnam National University) ;
  • Kim, Dong Woon (Department of Medical Science, College of Medicine, Chungnam National University) ;
  • Kang, Joon Won (Department of Medical Science, College of Medicine, Chungnam National University)
  • Received : 2017.07.10
  • Accepted : 2017.11.09
  • Published : 2018.05.15

Abstract

Purpose: Infantile spasms, also known as West syndrome, is an age-specific epileptic seizure. Most patients with this condition also exhibit delayed development. This study aimed to determine the effect of long-term prenatal stress on susceptibility to infantile spasms. Methods: We subjected pregnant rats to acute or chronic immobilization stress. Resulting offspring received N-methyl-D-aspartic acid (15 mg/kg, intraperitoneally) on postnatal day 15, and their behaviors were observed 75 minutes after injection. The expression of KCC2 and GAD67 was also determined using immunohistochemistry. Results: Exposure to long-term prenatal stress increased the frequency of spasms and decreased the latency to onset of spasms compared with offspring exposed to short-term prenatal stress. Expression of KCC2 and GAD67 also decreased in the group exposed to long-term prenatal stress compared with the group exposed to short-term prenatal stress. Conclusion: Our study suggests that exposure to long-term prenatal stress results in increased susceptibility to seizures.

Keywords

References

  1. Dulac O. What is West syndrome? Brain Dev 2001;23:447-52. https://doi.org/10.1016/S0387-7604(01)00268-6
  2. Dulac O. Infantile spasms and West syndrome. London: W.B. Saunders, 1994.
  3. Weinstock M. The long-term behavioural consequences of prenatal stress. Neurosci Biobehav Rev 2008;32:1073-86. https://doi.org/10.1016/j.neubiorev.2008.03.002
  4. Edwards HE, Dortok D, Tam J, Won D, Burnham WM. Prenatal stress alters seizure thresholds and the development of kindled seizures in infant and adult rats. Horm Behav 2002;42:437-47. https://doi.org/10.1006/hbeh.2002.1839
  5. Coghlan S, Horder J, Inkster B, Mendez MA, Murphy DG, Nutt DJ. GABA system dysfunction in autism and related disorders: from synapse to symptoms. Neurosci Biobehav Rev 2012;36:2044-55. https://doi.org/10.1016/j.neubiorev.2012.07.005
  6. Malaspina D, Corcoran C, Kleinhaus KR, Perrin MC, Fennig S, Nahon D, et al. Acute maternal stress in pregnancy and schizophrenia in offspring: a cohort prospective study. BMC Psychiatry 2008;8:71. https://doi.org/10.1186/1471-244X-8-71
  7. Treiman DM. GABAergic mechanisms in epilepsy. Epilepsia 2001;42 Suppl 3:8-12. https://doi.org/10.1046/j.1528-1157.2001.042suppl.3008.x
  8. Baek H, Yi MH, Pandit S, Park JB, Kwon HH, Zhang E, et al. Altered expression of KCC2 in GABAergic interneuron contributes prenatal stress-induced epileptic spasms in infant rat. Neurochem Int 2016;97: 57-64. https://doi.org/10.1016/j.neuint.2016.05.006
  9. McMahon A, Kvetnanský R, Fukuhara K, Weise VK, Kopin IJ, Sabban EL. Regulation of tyrosine hydroxylase and dopamine beta-hydroxy- lase mRNA levels in rat adrenals by a single and repeated immo- bilization stress. J Neurochem 1992;58:2124-30. https://doi.org/10.1111/j.1471-4159.1992.tb10954.x
  10. Jeong HJ, Jeong HW, Song SS, Kang JW, Seo JH, Lee YH, et al. Upregulation of peroxiredeoxin III in the hippocampus of acute immobilization stress model rats and the Foxo3a-dependent expression in PC12 cells. Cell Mol Neurobiol 2011;31:1041-6. https://doi.org/10.1007/s10571-011-9703-4
  11. Wang CT, Shui HA, Huang RL, Tai MY, Peng MT, Tsai YF. Sexual motivation is demasculinized, but not feminized, in prenatally stressed male rats. Neuroscience 2006;138:357-64. https://doi.org/10.1016/j.neuroscience.2005.11.026
  12. Oh SH, Lee EH, Joung MH, Yum MS, Ko TS. Long-term outcomes of infantile spasms. Korean J Pediatr 2010;53:80-4. https://doi.org/10.3345/kjp.2010.53.1.80
  13. Yum MS, Chachua T, Veliskova J, Velisek L. Prenatal stress promotes development of spasms in infant rats. Epilepsia 2012;53:e46-9. https://doi.org/10.1111/j.1528-1167.2011.03357.x
  14. Li J, Vestergaard M, Obel C, Precht DH, Christensen J, Lu M, et al. Prenatal stress and epilepsy in later life: a nationwide follow-up study in Denmark. Epilepsy Res 2008;81:52-7. https://doi.org/10.1016/j.eplepsyres.2008.04.014
  15. Ahmadzadeh R, Saboory E, Roshan-Milani S, Pilehvarian AA. Predator and restraint stress during gestation facilitates pilocarpine- induced seizures in prepubertal rats. Dev Psychobiol 2011;53:806-12. https://doi.org/10.1002/dev.20555
  16. Fatima M, Srivastav S, Mondal AC. Prenatal stress and depression associated neuronal development in neonates. Int J Dev Neurosci 2017;60:1-7. https://doi.org/10.1016/j.ijdevneu.2017.04.001
  17. Shaikh K, Premji SS, Ali Khowaja KZ, Tough S, Kazi AM, Khowaja SS. The relationship between prenatal stress, depression, cortisol and preterm birth: a review. Open J Depression 2013;2:24-31. https://doi.org/10.4236/ojd.2013.23006
  18. Cherian SB, Bairy KL, Rao MS. Chronic prenatal restraint stress induced memory impairment in passive avoidance task in post wean- ed male and female Wistar rats. Indian J Exp Biol 2009;47:893-9.
  19. Charil A, Laplante DP, Vaillancourt C, King S. Prenatal stress and brain development. Brain Res Rev 2010;65:56-79. https://doi.org/10.1016/j.brainresrev.2010.06.002