Journals / Turkish Journal of Veterinary and Animal Sciences / 2020 / Cilt: 44 - Sayı: 2

The effects of different doses of diclofenac sodium on newborn rat hippocampus exposed during the third trimester

Pages
404–417
Publication Date
2020-03-01
DOI
—
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

When the results are evaluated, it can be concluded that the use of diclofenac sodium during pregnancy may have teratogenic effects on the development of the nervous system.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:The main aim of the present study was to examine the neurotoxic effects of prenatal exposure to varying doses of diclofenac sodium DS on the rat hippocampus.
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Key Findings & Data:Twenty-eight Wistar albino adult female rats weighing 280-300 g were initially used for pregnancy.
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Conclusion & Impact:When the results are evaluated, it can be concluded that the use of diclofenac sodium during pregnancy may have teratogenic effects on the development of the nervous system.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Diclofenac sodium · hippocampus · prenatal

Abstract

The main aim of the present study was to examine the neurotoxic effects of prenatal exposure to varying doses of diclofenac sodium DS on the rat hippocampus. Twenty-eight Wistar albino adult female rats weighing 280-300 g were initially used for pregnancy. When vaginal plaques were seen in female rats, it was accepted as the 0th day of pregnancy. Female rats were divided into five main groups; pure control, saline, low dose DS 3.6 mg/kg , moderate dose DS 9 mg/kg , and high dose DS 18 mg/kg . They were exposed to these treatments during their gestation. After birth, all newborn male rats were euthanized by overdose anesthesia on the 7th postnatal day. Histological and stereological techniques were used for analyzing tissue samples. The stereological analyses in this study showed that the number of neurons in the hippocampus may be reduced due to the use of DS. Histological investigation of the drug-treated groups showed significant cell loss compared to the control. Darkly stained nuclei of the neurons in the high dose group compared to the other groups were also obvious. When the results are evaluated, it can be concluded that the use of diclofenac sodium during pregnancy may have teratogenic effects on the development of the nervous system.

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Cite This Article

ELİBOL, E., KAPLAN, S., ALTUN, G., AKSOY, A., ALTUNKAYNAK, B. Z. (2020). The effects of different doses of diclofenac sodium on newborn rat hippocampus exposed during the third trimester. Turkish Journal of Veterinary and Animal Sciences, Cilt: 44 - Sayı: 2, 404–417. https://ajindex.com/articles/116815

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References (11)

  1. Nettis E, Colanardi MC, Ferrannini A, Tursi A. Update on sensitivity to nonsteroidal antiinflammatory drugs. Current Drug Targets - Immune, Endocrine & Metabolic Disorders 2001
  2. doi: 10.2174/1568008013341235 2. Odacı E, Cihan OF, Aslan H, Rağbetli MÇ, Kaplan S. Prenatal diclofenac sodium administration increases the number of Purkinje cells in female rats: a stereological study. International Journal of Developmental Neuroscience 2009
  3. doi: 10.1016/j.ijdevneu.2009.12.004 3. Gökçimen A, Rağbetli MC, Baş O, Tunc AT, Aslan H et al. Effect of prenatal exposure to an anti-inflammatory drug on neuron number in cornu ammonis and dentate gyrus of the rat hippocampus: a stereological study. Brain Research 2007
  4. doi: 10.1016/j.brainres.2006.10.026 4. Cassina M, De Santis M, Cesari E, Eijkeren M, Berkovitch M et al. First trimester diclofenac exposure and pregnancy outcome. Reproductive Toxicology 2010
  5. doi: 10.1016/j. reprotox.2010.04.010 5. Smith SR, Deshpande BR, Collins JE, Katz JN, Losina E. Comparative pain reduction of oral non-steroidal antiinflammatory drugs and opioids for knee osteoarthritis: systematic analytic review. Osteoarthritis and Cartilage 2016
  6. doi: 10.1016/j.joca.2016.01.135 6. Beck A, Krischak G, Sorg T, Augat P, Farker K et al. Influence of diclofenac (group of nonsteroidal antiinflammatory drugs) on fracture healing. Archives of Orthopaedic and Trauma Surgery 2003
  7. doi: 10.1007/s00402-003-0537-5 7. Siu KL, Lee WH. Maternal diclofenac sodium ingestion and severe neonatal pulmonary hypertension. Journal of Paediatric and Child Health 2004
  8. doi: 10.1111/j.1440- 1754.2004.00319 8. Aygün D, Kaplan S, Odaci E, Onger ME, Altunkaynak ME. Toxicity of non-steroidal anti-inflammatory drugs: a review of melatonin and diclofenac sodium association. Histology and Histopathology 2012
  9. doi: 10.14670/HH-27.417 9. Nielsen GL, Sørensen HT, Larsen H, Pedersen L. Risk of adverse birth outcome and miscarriage in pregnant users of non-steroidal anti-inflammatory drugs: population based observational study and case-control study. British Medical Journal 2001
  10. doi: 10.1136/bmj.322.7281.266 10. Persaud TVN, Moore KL. Inhibitors of prostaglandin synthesis and fetal development. Lancet 1974
  11. doi: 10.1016/s0140- 6736(74)92312-5 11. Harris WH. The effects of repeated doses of indomethacin on fetal rabbit mortality and on the patency of the duct