Hispidulin Ameliorates Endotoxin-Induced Acute Kidney Injury in Mice.
Kiryeong KimJaechan LeemPublished in: Molecules (Basel, Switzerland) (2022)
Lipopolysaccharide (LPS) is an endotoxin that plays a crucial role in septic acute kidney injury (AKI). Hispidulin is a natural flavonoid that possesses various biological activities. Recent studies have shown that hispidulin administration alleviates various inflammatory diseases in animal models. This study aimed to investigate the renoprotective effect of hispidulin on LPS-induced AKI. Male C57BL/6 mice were administered LPS (10 mg/kg) with or without hispidulin (50 mg/kg). Hispidulin administration attenuated renal dysfunction, histological alterations, and the upregulation of neutrophil gelatinase-associated lipocalin. This flavonoid also reduced cytokine production and Toll-like receptor 4 expression, inhibited nuclear factor-κB and mitogen-activated protein kinase cascades, and alleviated immune cell infiltration. The oxidation of lipids and DNA was also inhibited by hispidulin administration. This antioxidant effect of hispidulin was associated with the downregulation of NADPH oxidase 4, the activation of catalase and superoxide dismutase activities, and the restoration of glutathione levels. Moreover, hispidulin administration attenuated tubular cell apoptosis by inhibiting caspase-3 pathway. These data suggest that hispidulin ameliorates endotoxin-induced kidney injury by suppressing inflammation, oxidative stress, and tubular cell death.
Keyphrases
- toll like receptor
- oxidative stress
- acute kidney injury
- inflammatory response
- nuclear factor
- lps induced
- cell death
- diabetic rats
- high glucose
- signaling pathway
- cell proliferation
- poor prognosis
- induced apoptosis
- dna damage
- anti inflammatory
- drug induced
- machine learning
- endothelial cells
- high fat diet induced
- adipose tissue
- endoplasmic reticulum stress
- long non coding rna
- insulin resistance
- single molecule
- fatty acid
- diabetic nephropathy
- circulating tumor cells
- cell cycle arrest