Protective mechanism of kaempferol against adriamycin-induced renal injury in rats

ObjectiveThe aim of this study was to explore the protective effect of kaempferol against adriamycin-induced renal injury in rats and its underlying mechanism.MethodsA rat model of renal injury was established by adriamycin injection. The rats were divided into the model group; the low-, medium-, an...

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Main Authors: ZUO Xiaoli, BI Lingyun, CAO Hongmin
Format: Article
Language:zho
Published: The Editorial Office of Chinese Journal of Food Hygiene 2023-10-01
Series:Zhongguo shipin weisheng zazhi
Subjects:
Online Access:https://www.zgspws.com/zgspwszz/article/abstract/202310003?st=article_issue
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author ZUO Xiaoli
BI Lingyun
CAO Hongmin
author_facet ZUO Xiaoli
BI Lingyun
CAO Hongmin
author_sort ZUO Xiaoli
collection DOAJ
description ObjectiveThe aim of this study was to explore the protective effect of kaempferol against adriamycin-induced renal injury in rats and its underlying mechanism.MethodsA rat model of renal injury was established by adriamycin injection. The rats were divided into the model group; the low-, medium-, and high-dose kaempferol groups; and the high-dose kaempferol + EX527 (silence information regulator 1 [SIRT1]-specific inhibitor) group. A blank control group was also used (n = 10). Twenty-four-hour urine protein levels were measured on the day of modeling and at 1, 2, and 4 weeks after modeling. Serum creatinine and blood urea nitrogen concentrations were measured using an automatic biochemical analyzer. The levels of tumor necrosis factor-α (TNF-α) and interleukin-1β (IL-1β) were measured by enzyme-linked immunosorbent assay. Hematoxylin and eosin staining was used to detect pathological changes in renal tissues. The ultrastructure of the kidneys was observed using transmission electron microscopy. Flow cytometry was used to observe renal cell apoptosis. Western blotting was used to detect the protein levels of SIRT1, p38-mitogen activated protein kinase (p38MAPK), phosphorylated (p)-p38MAPK, nuclear factor-κB p65 (NF-κB p65), p-NF-κB p65, B lymphocytoma-2 protein (Bcl-2), Bcl-2-related X protein (Bax), and caspase-3 in renal tissue.ResultsIn the first week, the 24 h urine protein level increased in the model group compared to that in the blank control group. In the second and fourth weeks, the levels of serum creatinine, blood urea nitrogen, TNF-α, and IL-1β increased. The renal tissue injury score and the apoptotic rate also increased. The protein levels of p-p38MAPK/p38MAPK, p-NF-κB p65/NF-κB p65, Bax, and caspase-3 increased. SIRT1 and Bcl-2 protein expression levels significantly decreased (P < 0.05). After intervention with low, medium, and high doses of kaempferol in the model rats, the aforementioned changes were significantly reversed (P < 0.05). The SIRT1-specific inhibitor EX527 significantly downregulated the expression level of SIRT1 and significantly weakened the protective effect of kaempferol against kidney injury (P < 0.05).ConclusionKaempferol has a protective effect against adriamycin-induced renal injury, and the mechanism may be related to the upregulation of SIRT1 expression, the inhibition of p38MAPK signal pathway activation, and a reduction in renal cell apoptosis.
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spelling doaj.art-3f550f3a930d40329c55dc6f92db24922024-02-20T07:51:14ZzhoThe Editorial Office of Chinese Journal of Food HygieneZhongguo shipin weisheng zazhi1004-84562023-10-0135101416142310.13590/j.cjfh.2023.10.0031004-8456(2023)10-1416-08Protective mechanism of kaempferol against adriamycin-induced renal injury in ratsZUO Xiaoli0BI Lingyun1CAO Hongmin2School of Medical Technology, Anyang Vocational and Technical College, He’nan Anyang 455000, ChinaThe Second Department of Pediatrics, The First Affiliated Hospital of Xinxiang Medical College, He’nan Weihui 453100, ChinaDepartment of Nephrology, The First People’s Hospital of Anyang City, He’nan Anyang 455000, ChinaObjectiveThe aim of this study was to explore the protective effect of kaempferol against adriamycin-induced renal injury in rats and its underlying mechanism.MethodsA rat model of renal injury was established by adriamycin injection. The rats were divided into the model group; the low-, medium-, and high-dose kaempferol groups; and the high-dose kaempferol + EX527 (silence information regulator 1 [SIRT1]-specific inhibitor) group. A blank control group was also used (n = 10). Twenty-four-hour urine protein levels were measured on the day of modeling and at 1, 2, and 4 weeks after modeling. Serum creatinine and blood urea nitrogen concentrations were measured using an automatic biochemical analyzer. The levels of tumor necrosis factor-α (TNF-α) and interleukin-1β (IL-1β) were measured by enzyme-linked immunosorbent assay. Hematoxylin and eosin staining was used to detect pathological changes in renal tissues. The ultrastructure of the kidneys was observed using transmission electron microscopy. Flow cytometry was used to observe renal cell apoptosis. Western blotting was used to detect the protein levels of SIRT1, p38-mitogen activated protein kinase (p38MAPK), phosphorylated (p)-p38MAPK, nuclear factor-κB p65 (NF-κB p65), p-NF-κB p65, B lymphocytoma-2 protein (Bcl-2), Bcl-2-related X protein (Bax), and caspase-3 in renal tissue.ResultsIn the first week, the 24 h urine protein level increased in the model group compared to that in the blank control group. In the second and fourth weeks, the levels of serum creatinine, blood urea nitrogen, TNF-α, and IL-1β increased. The renal tissue injury score and the apoptotic rate also increased. The protein levels of p-p38MAPK/p38MAPK, p-NF-κB p65/NF-κB p65, Bax, and caspase-3 increased. SIRT1 and Bcl-2 protein expression levels significantly decreased (P < 0.05). After intervention with low, medium, and high doses of kaempferol in the model rats, the aforementioned changes were significantly reversed (P < 0.05). The SIRT1-specific inhibitor EX527 significantly downregulated the expression level of SIRT1 and significantly weakened the protective effect of kaempferol against kidney injury (P < 0.05).ConclusionKaempferol has a protective effect against adriamycin-induced renal injury, and the mechanism may be related to the upregulation of SIRT1 expression, the inhibition of p38MAPK signal pathway activation, and a reduction in renal cell apoptosis.https://www.zgspws.com/zgspwszz/article/abstract/202310003?st=article_issuekaempferoladriamycinrenal injuryp38-mitogen activated protein kinaseapoptosis
spellingShingle ZUO Xiaoli
BI Lingyun
CAO Hongmin
Protective mechanism of kaempferol against adriamycin-induced renal injury in rats
Zhongguo shipin weisheng zazhi
kaempferol
adriamycin
renal injury
p38-mitogen activated protein kinase
apoptosis
title Protective mechanism of kaempferol against adriamycin-induced renal injury in rats
title_full Protective mechanism of kaempferol against adriamycin-induced renal injury in rats
title_fullStr Protective mechanism of kaempferol against adriamycin-induced renal injury in rats
title_full_unstemmed Protective mechanism of kaempferol against adriamycin-induced renal injury in rats
title_short Protective mechanism of kaempferol against adriamycin-induced renal injury in rats
title_sort protective mechanism of kaempferol against adriamycin induced renal injury in rats
topic kaempferol
adriamycin
renal injury
p38-mitogen activated protein kinase
apoptosis
url https://www.zgspws.com/zgspwszz/article/abstract/202310003?st=article_issue
work_keys_str_mv AT zuoxiaoli protectivemechanismofkaempferolagainstadriamycininducedrenalinjuryinrats
AT bilingyun protectivemechanismofkaempferolagainstadriamycininducedrenalinjuryinrats
AT caohongmin protectivemechanismofkaempferolagainstadriamycininducedrenalinjuryinrats