水飞蓟宾
化学
黄芩素
纤维化
药理学
柚皮苷
肾脏疾病
氧化应激
黄芩苷
炎症
生物化学
医学
内科学
高效液相色谱法
色谱法
作者
Haitham Amin,Hanan S. Althagafy,Mostafa S. Abd El‐Maksoud,Islam M. Ibrahim,Emad H.M. Hassanein
标识
DOI:10.1002/cbdv.202403022
摘要
Chronic kidney disease (CKD) is an overriding concern for many researchers, as it causes unspeakable suffering among patients. Renal fibrosis is the hallmark of end‐stage kidney disease (ESKD), which can progress to death. The super‐fuels for renal fibrosis are oxidative stress and inflammation. It occurs in all CKD patients, but how it develops is still ambiguous. Flavonoids demonstrate tremendous fighting power against inflammation and oxidative stress in many diseases. NF‐κB suppression has been deeply investigated in renal fibrosis, with phenomenally good outcomes. This review shed light on flavonoids’ ability to beat renal fibrosis associated with NF‐κB activation. Flavonoids exhibit a promising antifibrotic effects through targeting NF‐κB such as Apigenin, Baicalin, Diosmin, Epigallocatechin 3‐Gallate, Genistein, Isoliquiritigenin, Naringin, Puerarin, Quercetin, Silibinin, Wogonin, Biochanin A, and Cardamonin. Moreover, in silico studies showed that flavonoids displayed an outstanding inhibitory effect on NF‐κB based on the energy of binding. They are well‐fitted to the binding pocket of the target protein by forming hydrogen bonds, hydrophobic and ionic interactions with the key amino acid residues. The outcomes revealed that silibinin, baicalin, and baicalein are the most powerful NF‐κB inhibitors. In conclusion, through suppressing NF‐κB signal, flavonoids display a dynamite performance in combating CKD and renal fibrosis.
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