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Exploring the mechanism of Qihuang Jiedu Huayu Yin in treating acute kidney injury in sepsis based on TLR4/MyD88/NF-κB signal pathway
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DOI   10.11656/j.issn.1672-1519.2025.02.16
Key Words   sepsis;acute kidney injury;Qihuang Jiedu Huayu Yin;TLR4/MyD88/NF-κB signal pathway
Author NameAffiliationE-mail
SHI Yuexin Dongzhimen Hospital of Beijing University of Chinese Medicine, Beijing 100700, China
Beijing University of Chinese Medicine, Beijing 100029, China 
 
YAO Zhi Dongzhimen Hospital of Beijing University of Chinese Medicine, Beijing 100700, China
Beijing University of Chinese Medicine, Beijing 100029, China 
 
LI Li Dongzhimen Hospital of Beijing University of Chinese Medicine, Beijing 100700, China  
ZHU Rui Dongzhimen Hospital of Beijing University of Chinese Medicine, Beijing 100700, China
Beijing University of Chinese Medicine, Beijing 100029, China 
 
YAN Jun Dongzhimen Hospital of Beijing University of Chinese Medicine, Beijing 100700, China dzmyyyj@126.com 
WU Caijun Dongzhimen Hospital of Beijing University of Chinese Medicine, Beijing 100700, China  
Abstract
    [Objective] To explore the mechanism of Qihuang Jiedu Huayu Yin in treating sepsis-induced acute kidney injury(AKI) based on TLR4/MyD88/NF-κB signal pathway. [Methods] SD rats were randomly divided into sham group,model group,and low,medium,and high dose groups of Qihuang Jiedu Huayu Yin,with 10 rats in each group. The sepsis-induced AKI rat model was constructed by cecal ligation and puncture. Each group was orally administered every 12 hours before modeling for 3 consecutive days,and 12 hours after modeling. Record the general status of each group of rats,and use an ELISA kit to detect serum creatinine(Scr),urea nitrogen(BUN),neutrophil gelatinase-associated lipid releasing hormone(NGAL),kidney injury molecule-1(KIM-1),and interleukin-1β(IL-1β)、IL-6,IL-10,tumor necrosis factor(TNF)-α,catalase(CAT),glutathione peroxidase(GSH-PX),malondialdehyde(MDA),and total superoxide dismutase(T-SOD). Observation of pathological morphological changes in rat kidney tissue using hematoxylin-eosin(HE) staining. The expression levels TLR4,MyD88,NF-κB in rat kidney tissue protein were detected by Western blot. [Results] ACompared with the model group,the general state of rats in the low,medium,and high-dose groups of Qihuang Jiedu Huayu Yin was improved. The serum levels of Scr and BUN were significantly reduced in the high-dose group(P<0.05),while the levels of NGAL and KIM-1 were significantly reduced in the medium and high-dose groups(P<0.05 or P<0.01). The pathological damage of renal tissue in low,medium,and high dose groups of Qihuang Jiedu Huayu Yin was significantly improved;the level of IL-1β,IL-6,TNF-α in Low,medium,and high-dose groups of Qihuang Jiedu Huayu Yin were decreased(P<0.01 or P<0.05),while the level of IL-10 was increased(P<0.01). The levels of MDA in the low,medium,and high dose groups of Qihuang Jiedu Huayu Yin were significantly reduced(P<0.01),while the level of CAT was significantly increased(P<0.05 or P<0.01). The levels of GSH-PX significantly increased in the medium and high dose groups(P<0.05). The T-SOD level in the high-dose group significantly increased(P<0.05). In low,medium,and high-dose groups of Qihuang Jiedu Huayu Yin,the expression level of TLR4,MyD88,and NF-κB were significantly reduced(P<0.01 or P<0.05). [Conclusion] Qihuang Jiedu Huayu Yin can improve the general state of sepsis-induced AKI rats,improve renal dysfunction and pathological damage,reduce inflammation levels and oxidative stress response,and its mechanism of action may be related to the inhibition of TLR4/MyD88/NF-κB signal pathway.

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