Korean J Physiol Pharmacol 2025; 29(2): 165-178
Published online March 1, 2025 https://doi.org/10.4196/kjpp.24.121
Copyright © Korean J Physiol Pharmacol.
Enhui Cui1, Qijing Wu2,*, Haiyan Zhu2, and Weiqian Tian1,*
1Department of Anesthesiology, The Affiliated Hospital of Nanjing University of Chinese Medicine, Nanjing 210023, 2Department of Anesthesiology, The Affiliated Huaian No.1 People’s Hospital of Nanjing Medical University, Huaian 223001, Jiangsu, China
Correspondence to:Weiqian Tian
E-mail: yfy0066@njucm.edu.cn
Qijing Wu
E-mail: wuqijing1948@njmu.edu.cn
Author contributions: The study was designed by W.T. The research was conducted by E.C. and Q.W. Q.W. and H.Z. analyzed the data. All authors participated in intellectual discussions. Q.W. wrote the manuscript, and the final version was approved by all authors.
Sepsis is a potentially fatal infectious disease that easily causes shock and numerous organ failures. The kidney is one of the most susceptible to injury. Early intervention and renal protection significantly minimize patient mortality. Oligomeric proanthocyanidin (OPC), a naturally occurring plant compound, has a high potential for renal protection. This study was aimed at exploring the potential renoprotective role of OPC in sepsis-related renal tubular injury. C57/B6 mice were intraperitoneally injected with lipopolysaccharide (LPS) to simulate sepsis-related acute kidney injury in vivo. Renal function and pathology were assessed. RNA sequencing examined OPC mechanisms against LPS-induced renal injury. Oxidative stress indicators and inflammatory cytokines in blood serum and renal tissues were evaluated. In vitro, MTT assays assess cell viability. Apoptosis cells were detected using Hoechst 33342 and propidium iodide staining. Western blot assessed PI3K/AKT and NFκB signaling pathway proteins. OPC reduced LPS-induced renal tubular injury, improved renal functions and pathological changes, restored glutathione content, superoxide dismutase activity, and catalase activity, inhibited malondialdehyde overproduction, and suppressed LPS-induced overproduction of pro-inflammatory cytokines and the decline of anti-inflammatory cytokines. OPC attenuated LPS-induced cell morphological injury, reduced cell viability loss, and recovered the changes in proteins involved in PI3K/AKT and NFκB signaling pathways in MTEC cells. OPC protects against LPSinduced renal tubular injury by counteracting oxidative stress, inhibiting inflammatory responses, activating the PI3K/AKT signaling pathway, and inhibiting the NFκB signaling pathway. It may provide a viable solution to lessen renal injury in patients with sepsis.
Keywords: Inflammation, NFκB, Oligomeric proanthocyanidin, Oxidative stress, PI3K-AKT, Sepsis-associated renal tubular injury
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