Journals / Genel Tıp Dergisi / 2020 / Cilt: 30 - Sayı: 1

Dentate gyrus T4 infused into activation response effect of long-term, and mitogen-activated protein kinase role

Dentat girus içerisine infüze edilen T4'ün uzun dönemli etkinleşme yanıtları üzerine etkisi ve mitojen ile aktive olan protein kinazın rolü

Pages
16–23
DOI
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⚡ TL;DR(Too Long; Didn't Read)

Conclusion: The findings of the study provide evidence that the infusion of thyroxine inhibits synaptic plasticity and that this inhibition is mediated by changes in NR2B and P38 MAPK expression.

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Objective & Hypothesis:Objective: In the present study, it was aimed to investigate the effect of the L-thyroxine hormone on long-term potentiation (LTP) responses, N-methyl-D aspartate (NMDA) receptor and P38-mitogen-activated protein kinase (P38 MAPK).
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Key Findings & Data:Material and Method: The study was performed on 2-4 month old male and female Wistar albino rats.
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Conclusion & Impact:Conclusion: The findings of the study provide evidence that the infusion of thyroxine inhibits synaptic plasticity and that this inhibition is mediated by changes in NR2B and P38 MAPK expression.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Objective: In the present study, it was aimed to investigate the effect of the L-thyroxine hormone on long-term potentiation (LTP) responses, N-methyl-D aspartate (NMDA) receptor and P38-mitogen-activated protein kinase (P38 MAPK). Material and Method: The study was performed on 2-4 month old male and female Wistar albino rats. Rats were placed onto stereotaxic roof under anesthesia. Field potentials were recorded in dentate gyrus in response to perforant pathway stimulation. Hippocampal thyroxine infusion was performed for 15 min following basal field potentials. Following infusion, 100 Hz frequency stimulation was applied 4 times with 5 min intervals. After 60 minutes from the last tetanic stimulation, the hippocampus of the rats was removed. Examination of gene expression of NR1, NR2A, NR2B and P38 MAPK from hippocampal samples was performed by real-time quantitative polymerase chain reaction (RT-qPCR) method. Results: It has been determined that the population spike (PS) amplitude and the excitatory post synaptic potential (EPSP) triggered during high frequency stimulation are reduced in both sexes by hippocampal infusion of thyroxine. Conclusion: The findings of the study provide evidence that the infusion of thyroxine inhibits synaptic plasticity and that this inhibition is mediated by changes in NR2B and P38 MAPK expression.

Özet

Amaç: Bu çalışmada tiroksin hormonunun uzun dönemli güçlenme (UDG) yanıtları, N-metil-D aspartat (NMDA) reseptörü ve P38-Mitojenle Aktive Olan Protein Kinaz (P38 MAPK) üzerine olan etkisinin araştırılması amaçlanmıştır. Gereç ve Yöntem: Çalışma, 2-4 aylık erkek ve dişi Wistar albino sıçanlar üzerinde yapıldı. Sıçanlar üretan anestezisi altında stereotaksik çatıya yerleştirildi. Alan potansiyelleri perforan yolun uyarılmasına yanıt olarak dentat girustan kaydedildi. Bazal alan potansiyellerini takiben 15 dk süre ile hipokampüse tiroksin infüzyonu yapıldı. İnfüzyonu takiben 100 Hz frekanslı uyarım 5 dakika ara ile 4 kez uygulandı. Son tetanik uyarımdan 60 dakika sonra sıçanların hipokampüsleri çıkarıldı. Hipokampüs örneklerinden NR1, NR2A, NR2B ve P38 MAPK'a ait gen anlatımlarının incelenmesi gerçek zamanlı kantitatif polimeraz zincir reaksiyonu (RT-qPCR) yöntemi ile yapıldı. Bulgular: Yüksek frekanslı uyarım verilmesi esnasında tetiklenen populasyon spike (PS) genliği ve eksitatör post sinaptik potansiyel (EPSP) eğiminin, tiroksinin hipokampüse infüze edilmesiyle her iki cinsiyette kontrole göre azaldığı belirlendi. Bununla uyumlu olarak, NR2B ve P38 MAPK düzeyleri için her iki cinsiyette kontrole göre artış olduğu belirlendi. Sonuç: Çalışma bulguları, tiroksin infüzyonunun sinaptik plastisiteyi inhibe ettiği ve bu inhibisyona NR2B ve P38 MAPK ekspresyonundaki değişimlerin aracılık ettiğine dair kanıtlar sunmaktadır.

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Cite This Article

TAN, B., BABUR, E., GÜLER, A. D., SÜER, C., DURSUN, N. (2020). Dentate gyrus T4 infused into activation response effect of long-term, and mitogen-activated protein kinase role. Genel Tıp Dergisi, Cilt: 30 - Sayı: 1, 16–23. https://ajindex.com/articles/157123

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References (16)

  1. Herron CE, Lester RA, Coan EJ, et al. Frequency-dependent involvement of NMDA receptors in the hippocampus: a novel synaptic mechanism. Nature 1986; 322: 265-8
  2. Blitzer RD, Connor JH, Brown GP, et al. Gating of CaMKII by cAMP-regulated protein phosphatase activity during LTP. Science 1998; 280: 1940-3
  3. Castro-Alamancos MA, Calcagnotto ME. Presynaptic longterm potentiation in corticothalamic synapses. J Neuroscience 1999; 19: 9090-7
  4. Andersen P, Bliss TV, Skrede KK. Lamellar organization of hippocampal pathways. Exp Brain Res 1971; 13: 222-38
  5. McNaughton B. Evidence for two physiologically distinct perforant pathways to the fascia dentata. Brain Res 1980; 199: 1-19
  6. Bramham CR, Milgram NW, Srebro B. Activation of AP5‐ sensitive NMDA receptors is not required to induce LTP of synaptic transmission in the lateral perforant path. Eur J Neurosci 1991; 3: 1300-8
  7. Colino A, Malenka RC. Mechanisms underlying induction of long-term potentiation in rat medial and lateral perforant paths in vitro. J Neurophysiol 1993; 69: 1150-9
  8. Bliss TV, Lømo T. Long‐lasting potentiation of synaptic transmission in the dentate area of the anaesthetized rabbit following stimulation of the perforant path. J Physiol 1973; 232: 331-56
  9. Rygh LJ, Tjølsen A, Hole K, et al. Cellular memory in spinal nociceptive circuitry. Scandinavian journal of psychology 2002; 43: 153-9
  10. Jones M, Errington M, French P, et al. A requirement for the immediate early gene Zif268 in the expression of late LTP and long-term memories. Nature neuroscience 2001; 4: 289-96
  11. Plátenıik J, Kuramoto N, Yoneda Y. Molecular mechanisms associated with long-term consolidation of the NMDA signals. Life sciences 2000; 67: 335-64
  12. Soderling TR, Derkach VA. Postsynaptic protein phosphorylation and LTP. Trends in neurosciences 2000; 23: 75-80
  13. Arnsten AFT, Ramos BP, Birnbaum SG, et al. Protein kinase A as a therapeutic target for memory disorders: rationale and challenges. Trends in molecular medicine 2005; 11: 121-8
  14. Songur A, Özen OA, Sarsılmaz M. Hipokampus. Turkiye Klinikleri Tıp Bilimleri Dergisi 2001; 21: 427-31
  15. Pavlides C, Westlind-Danielsson A, Nyborg H, et al. Neonatal hyperthyroidism disrupts hippocampal LTP and spatial learning. Experimental brain research 1991; 85: 559-64
  16. Colicos MA, Dash PK. Apoptotic morphology of dentate gyrus granule cells following experimental cortical impact injury in rats: possible role in spatial memory deficits. Brain research 1996;