Journals / Klinik Psikofarmakoloji Bülteni / 2016 / Cilt: 26 - Sayı: 4

The effect of intrauterine antipsychotic drug exposure on learning and memory in adult rats

Pages
364–373
Publication Date
2022-10-17
DOI
—
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AI Summary & Key Takeaways

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Thigmotaxis values of all groups were still higher except for the male group of thioridazine on fifth day.Conclusion: These results show that when prenatal exposure to antipsychotics occurs, it causes impairment in the realization of task of finding escape platform properly, rather than affecting learning and memory functions, specifically in their adulthood so that high thigmotaxis may be the reason for deterioration in escape latency parameter.

📌 3 Key Takeaways

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Objective & Hypothesis:Objective: The effects of antipsychotic drugs, of whose different classes can be used in the treatment of patients with resistant to schizophrenia, on the fetus and the benefits of the treatment to the mother should be taken into consideration before making a decision about initiating treatment.
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Key Findings & Data:This study aimed to examine the effects of prenatal exposure to various antipsychotic agents on learning and memory in adult rats.Method: In this study, antipsychotic drugs from different chemical classes (2 mg/kg haloperidol, 100 mg/kg thioridazine, 200 mg/kg sulpiride, 20 mg/kg chlorprothixene, 40 mg/kg clozapine, 10 mg/kg fluphenazine, 20 mg/kg chlorpromazine) and water for the control group were administered to pregnant Sprague-Dawley dams through gavage during the pregnancy period.
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Conclusion & Impact:Thigmotaxis values of all groups were still higher except for the male group of thioridazine on fifth day.Conclusion: These results show that when prenatal exposure to antipsychotics occurs, it causes impairment in the realization of task of finding escape platform properly, rather than affecting learning and memory functions, specifically in their adulthood so that high thigmotaxis may be the reason for deterioration in escape latency parameter.
🔬Design:Lab & Field Experiment
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Objective: The effects of antipsychotic drugs, of whose different classes can be used in the treatment of patients with resistant to schizophrenia, on the fetus and the benefits of the treatment to the mother should be taken into consideration before making a decision about initiating treatment. This study aimed to examine the effects of prenatal exposure to various antipsychotic agents on learning and memory in adult rats.Method: In this study, antipsychotic drugs from different chemical classes (2 mg/kg haloperidol, 100 mg/kg thioridazine, 200 mg/kg sulpiride, 20 mg/kg chlorprothixene, 40 mg/kg clozapine, 10 mg/kg fluphenazine, 20 mg/kg chlorpromazine) and water for the control group were administered to pregnant Sprague-Dawley dams through gavage during the pregnancy period. In total, 16 groups were created and tested in the Morris water maze by dividing offspring of eight mother rats into male and female rat groups (n=10) on postpartum day 60. Learning was tested with hidden platform task and memory was tested with probe test. Results: It has been observed that learning was impaired in the male and female groups that received haloperidol, sulpiride, chlorprothixene, clozapine, and chlorpromazine, as well as in the female groups receiving fluphenazine and thioridazine. Thigmotaxis is the time spent on 10 cm perimeter of the walls of the pool. Thigmotaxis values of all groups were still higher except for the male group of thioridazine on fifth day.Conclusion: These results show that when prenatal exposure to antipsychotics occurs, it causes impairment in the realization of task of finding escape platform properly, rather than affecting learning and memory functions, specifically in their adulthood so that high thigmotaxis may be the reason for deterioration in escape latency parameter.

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Cite This Article

KARADAG, C. H., OLTULU, Ç. (2022). The effect of intrauterine antipsychotic drug exposure on learning and memory in adult rats. Klinik Psikofarmakoloji Bülteni, Cilt: 26 - Sayı: 4, 364–373. https://ajindex.com/articles/573924

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References (14)

  1. Einarson A, Boskovic R. Use and safety of antipsychotic drugs during pregnancy. J Psychiatr Pract 2009
  2. 15(3):183-92. [CrossRef] 2. Coughlin CG, Blackwell KA, Bartley C, Hay M, Yonkers KA, Bloch MH. Obstetric and neonatal outcomes after antipsychotic medication exposure in pregnancy. Obstet Gynecol 2015
  3. 125(5):1224-35. [CrossRef] 3. Toh S, Li Q, Cheetham TC, Cooper WO, Davis RL, Dublin S, et al. Prevalence and trends in the use of antipsychotic medications during pregnancy in the U.S., 2001-2007: a population-based study of 585,615 deliveries. Arch Womens Ment Health 2013
  4. 16(2):149-57. [CrossRef] 4. Epstein RA, Bobo WV, Shelton RC, Arbogast PG, Morrow JA, Wang W. Increasing use of atypical antipsychotics and anticonvulsants during pregnancy. Pharmacoepidemiol Drug Saf 2013
  5. 22(7):794-801. [CrossRef] 5. Babu GN, Desai G, Chandra PS. Antipsychotics in pregnancy and lactation. Indian J Psychiatry 2015
  6. 57(Suppl. 2):S303-S7. [CrossRef] 6. Hammond JE, Toseland PA. Placental transfer of chlorpromazine. Case report. Arch Dis Child 1970
  7. 45(239):139-40. [CrossRef] 7. Newport DJ, Calamaras MR, DeVane CL, Donovan J, Beach AJ, Winn S, et al. Atypical antipsychotic administration during late pregnancy: placental passage and obstetrical outcomes. Am J Psychiatry 2007
  8. 164(8):1214-20. [CrossRef] 8. Barnas C, Bergant A, Hummer M, Saria A, Fleischhacker WW. Clozapine concentrations in maternal and fetal plasma, amniotic fluid, and breast milk. Am J Psychiatry 1994
  9. 151(6):945. [CrossRef] 9. Raha S, Taylor VH, Holloway AC. Effect of atypical antipsychotics on fetal growth: is the placenta involved? J Pregnancy 2012
  10. 315203. 10. Lauder JM. Ontogeny of the serotonergic system in the rat: serotonin as a developmental signal. Ann N Y Acad Sci 1990
  11. [CrossRef] 11. Zhang J, Wang L, Pitts DK. Prenatal haloperidol reduces the number of active midbrain dopamine neurons in rat offspring. Neurotoxicol Teratol 1996
  12. 18(1):49-57. [CrossRef] 12. Singh KP, Singh M. Effect of single prenatal haloperidol exposure on hippocampus and striatum of developing rat brain. Indian J Exp Biol 2001
  13. 39(3):223-9. 13. Singh KP, Tripathi N. Prenatal exposure to a novel antipsychotic quetiapine: impact on neuro-architecture, apoptotic neurodegeneration in fetal hippocampus and cognitive impairment in young rats. Int J Dev Neurosci 2015
  14. [CrossRef] 14. Law AJ, Hutchinson LJ, Burnet PW, Harrison PJ. Antipsychotics increase microtubule-associated protein 2 mRNA but not spinophilin mRNA i