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Yıl 2023, Cilt: 9 Sayı: 3, 288 - 295, 30.09.2023

Öz

Kaynakça

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Edaravone ameliorates memory, hippocampal morphology, and inflammation in a rat model of Alzheimer’s disease

Yıl 2023, Cilt: 9 Sayı: 3, 288 - 295, 30.09.2023

Öz

Oxidative stress and neural inflammation play a role in the pathogenesis of Alzheimer's disease (AD). Edaravone (EDA) has an antioxidant-free radical scavenger property. The purpose of this study to evaluate the effect of EDA on memory, hippocampal morphology, and inflammation in a streptozocin (STZ)-induced AD model. This study used 18 Wistar albino adult rats, weighing 200-220 g. Following general anesthesia, 3 mg/kg STZ was dissolved in 0.9% NaCl and administered intracerebroventricularly (ICV) in both lateral ventricles to 12 rats in a total of 5 µl. The animals were allowed to recover for two weeks and then divided into two groups. Six rats were given 0.9% NaCl i.p. for 15 days, and the other six were administered EDA 40 mg/kg i.p. for 15 days, once a day. The control group of six rats did not undergo any surgical procedures or medications. After treatment, a passive avoidance learning (PAL) test was used, followed by the removal of the brain tissue in all animals. Nissl staining was used to count neurons in the hippocampal CA1 and CA3 regions, and TNF-α and IL-6 levels in the brain were measured. In the STZ group, significantly shorter latency time, and decreased number of neurons in the CA1 and CA3 hippocampal regions compared to the control group were observed. EDA significantly prolonged the latency time and increased hippocampal CA1 and CA3 neuron counts compared to the STZ group. TNF-α and IL-6 levels were higher in the STZ+saline group than in the control group. Similarly, EDA treatment reduced TNF-α and IL-6 levels when compared to the STZ+saline and control groups. For the first time, we demonstrated the neuroprotective and anti-inflammatory potential of EDA in an experimental AD model. Our results may provide evidence for EDA therapy in addition to the standard regimen in patients with cognitive decline.

Kaynakça

  • [1] Chan, S. W. C. (2011). Family caregiving in dementia: the asian perspective of a global problem. Dementia and Geriatric Cognitive Disorders. 30(6):469-478. DOI: 10.1159/000322086
  • [2] Khan, S., Barve, K. H., & Kumar, M. S. (2020). Recent Advancements in Pathogenesis, Diagnostics and Treatment of Alzheimer’s Disease. Curr Neuropharmacol. 18(11):1106-1125. DOI: 10.2174/1570159X18666200528142429.
  • [3] Lashley, T., Schott, J.M., Weston, P., Murray, C.E., Wellington, H., Keshavan, A., Foti, S. C., Foiani, M., Toombs, J., Rohrer, J.D., Heslegrave, A., & Zetterberg, H. (2018). Molecular biomarkers of Alzheimer's disease: progress and prospects. Dis Model Mech. 2018; 11(5):dmm031781. DOI: 10.1242/dmm.031781.
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  • [7] Cameron, B., & Landreth, G. E. (2010). Inflammation, microglia and Alzheimer's disease. Neurobiol Dis. 37(3):503-509. DOI: 10.1016/j.nbd.2009.10.006.
  • [8] Wang, W. Y., Tan, M. S., Yu, J. T., & Tan, L. (2015). Role of pro-inflammatory cytokines released from microglia in Alzheimer's disease. Ann Transl Med. 3(10):136. DOI: 10.3978/j.issn.2305-5839.2015.03.49.
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  • [12] Liu, J., Jiang, Y., Zhang, G., Lin, Z., & Du, S. (2019). Protective effect of edaravone on blood-brain barrier by affecting NRF-2/HO-1 signaling pathway. Exp Ther Med. 18(4):2437-2442. DOI: 10.3892/etm.2019.7859.
  • [13] Okuyama, S., Morita, M., Sawamoto, A., Terugo, T., Nakajima, M., & Furukawa, Y. (2015). Edaravone enhances brain-derived neurotrophic factor production in the ischemic mouse brain. Pharmaceuticals (Basel, Switzerland). 8:176-185. DOI: 10.3390/ph8020176.
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  • [16] Yuan, Y., Zha, H., Rangarajan, P., Ling, E. A., & Wu, C. (2014). Anti-inflammatory effects of Edaravone and Scutellarin in activated microglia in experimentally induced ischemia injury in rats and in BV-2 microglia. BMC Neurosci. 15:125. DOI: 10.1186/s12868-014-0125-3.
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  • [22] Gómez-Ramos, A., Díaz-Nido, J., Smith, M. A., Perry, G., & Avila, J. (2003). Effect of the lipid peroxidation product acrolein on tau phosphorylation in neural cells. J Neurosci Res. 71:863-870. DOI: 10.1002/jnr.10525.
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  • [36] Erta, M., Quintana, A., & Hidalgo, J. (2012). Interleukin-6, a Major Cytokine in the Central Nervous System. Int J Biol. Sci. 8:1254-1266. DOI: 10.7150/ijbs.4679.
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  • [46] Wu, S., Sena, E., Egan, K., Macleod, M., & Mead, G. (2014). Edaravone improves functional and structural outcomes in animal models of focal cerebral ischemia: a systematic review. Int J Stroke. 9(1):101-6. DOI: 10.1111/ijs.12163.
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Toplam 50 adet kaynakça vardır.

Ayrıntılar

Birincil Dil İngilizce
Konular Cerrahi (Diğer)
Bölüm Araştırma Makalesi
Yazarlar

Şeyma Özsoy 0000-0003-1783-3618

Elif Azize Özşahin Delibaş 0000-0002-4195-0884

Gürkan Yiğittürk 0000-0002-5315-253X

Erken Görünüm Tarihi 24 Eylül 2023
Yayımlanma Tarihi 30 Eylül 2023
Gönderilme Tarihi 6 Eylül 2023
Kabul Tarihi 20 Eylül 2023
Yayımlandığı Sayı Yıl 2023 Cilt: 9 Sayı: 3

Kaynak Göster

APA Özsoy, Ş., Özşahin Delibaş, E. A., & Yiğittürk, G. (2023). Edaravone ameliorates memory, hippocampal morphology, and inflammation in a rat model of Alzheimer’s disease. International Journal of Computational and Experimental Science and Engineering, 9(3), 288-295.