Honokiol Protects the Kidney from Renal Ischemia and Reperfusion Injury by Upregulating the Glutathione Biosynthetic Enzymes.
Eun Jung ParkTheodomir DusabimanaJihyun JeKyuho JeongSeung Pil YunHye Jung KimHyun Joon KimSang-Won ParkPublished in: Biomedicines (2020)
Glutathione (GSH) is an endogenous antioxidant found in plants, animals, fungi, and some microorganisms that protects cells by neutralizing hydrogen peroxide. Honokiol, an active ingredient of Magnolia officinalis, is known for antioxidant, anti-inflammatory, and anti-bacterial properties. We investigated the protective mechanism of honokiol through regulating cellular GSH in renal proximal tubules against acute kidney injury (AKI). First, we measured cellular GSH levels and correlated them with the expression of GSH biosynthetic enzymes after honokiol treatment in human kidney-2 (HK-2) cells. Second, we used pharmacological inhibitors or siRNA-mediated gene silencing approach to determine the signaling pathway induced by honokiol. Third, the protective effect of honokiol via de novo GSH biosynthesis was investigated in renal ischemia-reperfusion (IR) mice. Honokiol significantly increased cellular GSH levels by upregulating the subunits of glutamate-cysteine ligase (Gcl)-Gclc and Gclm. These increases were mediated by activation of nuclear factor erythroid 2-related factor 2, via PI3K/Akt and protein kinase C signaling. Consistently, honokiol treatment reduced the plasma creatinine, tubular cell death, neutrophil infiltration and lipid peroxidation in IR mice and the effect was correlated with upregulation of Gclc and Gclm. Conclusively, honokiol may benefit to patients with AKI by increasing antioxidant GSH via transcriptional activation of the biosynthetic enzymes.
Keyphrases
- cell cycle arrest
- signaling pathway
- pi k akt
- fluorescent probe
- acute kidney injury
- induced apoptosis
- anti inflammatory
- cell death
- hydrogen peroxide
- oxidative stress
- nuclear factor
- cell proliferation
- living cells
- poor prognosis
- endothelial cells
- nitric oxide
- type diabetes
- gene expression
- drug delivery
- heart failure
- epithelial mesenchymal transition
- endoplasmic reticulum stress
- high fat diet induced
- left ventricular
- skeletal muscle
- coronary artery disease
- mass spectrometry
- long non coding rna
- high glucose
- uric acid