Trigonelline alkaloid is effective in preventing doxorubicin-induced lung damage

被引:1
|
作者
Uslu, Hamit [1 ]
Uslu, Gozde Atila [1 ]
Cicek, Betuel [1 ]
Bolat, Ismail [2 ]
Yildirim, Serkan [2 ]
机构
[1] Erzincan Binali Yildirim Univ, Dept Physiol, Erzincan, Turkiye
[2] Ataturk Univ, Dept Pathol, Erzurum, Turkiye
关键词
Doxorubicin; trigonelline alkaloid; inflammation; apoptosis; NF-kappa B/MAPK; OXIDATIVE STRESS; TOXICITY; RAT;
D O I
10.1080/13813455.2024.2404097
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
BackgroundOne of the most popular chemotherapy medications is doxorubicin (DOX), however it can have non-negligible damage. When the underlying mechanisms of damage are investigated, the most prominent pathways are oxidative stress, inflammation and apoptosis.AimWe investigated the NF-kappa B/MAPK inflammatory pathway and cellular apoptosis to determine the efficacy of trigonelline alkaloid (TRIG) in preventing DOX-induced lung injury.MethodologyThe study consisted of C, TRIG, DOX and TRIG+DOX groups. TRIG and TRIG+DOX groups received 50 mg/kg TRIG for 7 days. On day 8, DOX and TRIG+DOX groups received a single dose of 15 mg/kg DOX.ResultsOur results showed that apoptosis markers and inflammation were higher in the DOX group. In contrast, TRIG pretreatment partially suppressed apoptosis and decreased inflammation by blocking the activation of the MAPK/NF-kappa B pathway, lowering IL-6 levels, and protecting the lung from apoptotic cell death.ConclusionAssessing TRIG's effectiveness in lung tissue injury, this study may be a crucial first step.
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页数:8
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