Therapeutic potential of young plasma in reversing age-related liver inflammation via modulation of NLRP3 inflammasome and necroptosis
 
Yazarlar (7)
Burcu Baba Yüksek İhtisas Üniversitesi, Türkiye
Taha Ceylani Muş Alparslan Üniversitesi, Türkiye
Hikmet Taner Teker Ankara Medipol University, Türkiye
Seda Keskin Van Yüzüncü Yıl Üniversitesi, Türkiye
Arş. Gör. Dr. Aysun İNAN GENÇ Kastamonu Üniversitesi, Türkiye
Rafig Gurbanov Bilecik Şeyh Edebali Üniversitesi, Türkiye
Eda Açıkgöz Van Yüzüncü Yıl Üniversitesi, Türkiye
Makale Türü Açık Erişim Özgün Makale (SSCI, AHCI, SCI, SCI-Exp dergilerinde yayınlanan tam makale)
Dergi Adı Biogerontology (Q2)
Dergi ISSN 1389-5729 Wos Dergi Scopus Dergi
Dergi Tarandığı Indeksler SCI-Expanded
Makale Dili Türkçe Basım Tarihi 05-2025
Cilt / Sayı / Sayfa 26 / 3 / 117–0 DOI 10.1007/s10522-025-10260-9
Makale Linki https://doi.org/10.1007/s10522-025-10260-9
Özet
The phenomenon of inflammaging, characterized by an increase in low-grade chronic inflammation, is closely associated with diseases related to liver dysfunction. This study investigated daily plasma exchange between 5-week-old and 24-month-old Sprague Dawley rats for 30 days, focusing on protein secondary structures, NLRP3 inflammasome, and necroptosis. Conformation changes in protein secondary structures were identified by infrared spectroscopy-based pattern recognition analysis. Liver biopsies with histochemical and immunohistochemical staining were used to assess molecules associated with inflammation, necroptosis and NLRP3 inflammasome complex. Expression levels of NLRP3 components were determined by qPCR. Enhanced random coils, 310 helices, β-turns, and loop structures were identified in old rats and young rats with old plasma. Young rats and old rats with young plasma …
Anahtar Kelimeler
Inflammaging | Infrared spectroscopy | Necroptosis | NLRP3 Inflammasome | Plasma exchange
BM Sürdürülebilir Kalkınma Amaçları
Atıf Sayıları
Web of Science 4
Scopus 4
Google Scholar 4
Therapeutic potential of young plasma in reversing age-related liver inflammation via modulation of NLRP3 inflammasome and necroptosis

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