Neuroprotective Effect of Chitosan Nanoparticle–Delivered Orientin Against Hypoxia-Induced Brain Injury in Rats
 
Yazarlar (9)
İhsan Topaloğlu Kafkas Üniversitesi, Türkiye
Çağrı Atasoy Kafkas Üniversitesi, Türkiye
Gülfem Özduygu
University of Health Sciences, Türkiye
Eren Erdoğdu
İstanbul Tıp Fakültesi, Türkiye
Doç. Dr. Guntug Batihan Kafkas Üniversitesi, Türkiye
Volkan Gelen Kafkas Üniversitesi, Türkiye
Doç. Dr. Ali YEŞİLDAĞ Kafkas Üniversitesi, Türkiye
Prof. Dr. Adem Kara Erzurum Technical University, Türkiye
Doç. Dr. Elif Erbaş Atatürk Üniversitesi, Türkiye
Makale Türü Özgün Makale (SSCI, AHCI, SCI, SCI-Exp dergilerinde yayınlanan tam makale)
Dergi Adı Molecular Neurobiology (Q1)
Dergi ISSN 0893-7648 Dergi Bilgileri (2026)
Makale Dili İngilizce Basım Tarihi 01-2026
Cilt / Sayı / Sayfa 63 / 1 / – DOI 10.1007/s12035-026-06076-4
Makale Linki https://link.springer.com/article/10.1007/s12035-026-06076-4
UAK Araştırma Alanları
Özet
Reduced brain oxygenation rapidly amplifies oxidative and inflammatory injury, creating a self-perpetuating cascade that can end in neuronal loss. Orientin can activate Nrf2/ARE-dependent antioxidant responses and suppress NF-κB–mediated inflammation, but poor solubility and limited bioavailability weaken its therapeutic impact. Here, we used chitosan nanoparticles (CNPs) to improve Orientin delivery and evaluated the protective effects of CNPs/Orientin on oxidative stress, inflammation, and apoptosis in hypoxia-induced brain injury. Forty-eight male Wistar albino rats were split into eight groups: (Control, Orientin, CNPs, CNPs/Orientin, Hypoxia, Hypoxia+Orientin, Hypoxia+CNPs, Hypoxia+CNPs/Orientin). The hypoxia model was applied with an 8% O₂+92% N₂ gas mixture for 8 h per day for 7 days. Orientin (40 mg/kg/day, i.p.) was administered simultaneously with the hypoxia period. MDA, SOD, GSH …
Anahtar Kelimeler
Chitosan nanoparticle | Hypoxia | Inflammation | Neuroprotection | Orientin | Oxidative stress
BM Sürdürülebilir Kalkınma Amaçları
Atıf Sayıları
Scopus 2
Google Scholar 2
Neuroprotective Effect of Chitosan Nanoparticle–Delivered Orientin Against Hypoxia-Induced Brain Injury in Rats

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