Jian-Pi-Gu-Shen-Hua-Yu Decoction Alleviated Diabetic Nephropathy in Mice through Reducing Ferroptosis

Lv, Shuquan; Fan, Lirong; Chen, Xiaoting; Su, Xiuhai; Dong, Li; Wang, Qinghai; Wang, Yuansong; Zhang, Hui; Cui, Huantian; Zhang, Shufang; Wang, Lixin

doi:https://doi.org/10.1155/2024/9990304

Journal of Diabetes Research

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Abstract Introduction Methods Results Discussion Conclusion Abbreviations Data Availability Conflicts of Interest Authors’ Contributions Acknowledgments Supplementary Materials References Copyright Related Articles

Research Article | Open Access

Volume 2024 | Article ID 9990304 | https://doi.org/10.1155/2024/9990304

Jian-Pi-Gu-Shen-Hua-Yu Decoction Alleviated Diabetic Nephropathy in Mice through Reducing Ferroptosis

Shuquan Lv,¹Lirong Fan,²Xiaoting Chen,¹Xiuhai Su,¹Li Dong,¹Qinghai Wang,¹Yuansong Wang,¹Hui Zhang,¹Huantian Cui,³Shufang Zhang,¹and Lixin Wang¹

Academic Editor: Abdelaziz Amrani

Received26 Oct 2023

Revised06 Feb 2024

Accepted22 Feb 2024

Published16 Mar 2024

Abstract

Background. Diabetic nephropathy (DN), one of the most frequent complications of diabetes mellitus, is a leading cause of end-stage renal disease. However, the current treatment methods still cannot effectively halt the progression of DN. Jian-Pi-Gu-Shen-Hua-Yu (JPGS) decoction can be used for the treatment of chronic kidney diseases such as DN, but the specific mechanism of action has not been fully elucidated yet. Purpose. The aim of this study is to clarify whether JPGS alleviates the progression of diabetic nephropathy by inhibiting ferroptosis. Materials and Methods. We established a DN mouse model to investigate the therapeutic effect of JPGS in a DN mouse model. Subsequently, we examined the effects of JPGS on ferroptosis- and glutathione peroxidase 4 (GPX4) pathway-related indices. Finally, we validated whether JPGS inhibited ferroptosis in DN mice via the GPX4 pathway using GPX4 inhibitor and ferroptosis inhibitors. Results. The results indicate that JPGS has a therapeutic effect on DN mice by improving kidney function and reducing inflammation. Additionally, JPGS treatment decreased iron overload and oxidative stress levels while upregulating the expression of GPX4 pathway-related proteins. Moreover, JPGS demonstrated a similar therapeutic effect as Fer-1 in the context of DN treatment, and RSL3 was able to counteract the therapeutic effect of JPGS and antiferroptotic effect. Conclusion. JPGS has significant therapeutic and anti-inflammatory effects on DN mice, and its mechanism is mainly achieved by upregulating the expression of GPX4 pathway-related proteins, thereby alleviating iron overload and ultimately reducing ferroptosis.

1. Introduction

Diabetic nephropathy (DN), a prevalent complication of diabetes mellitus (DM), stands as a prominent contributor to end-stage renal disease. In 2019, there were 460 million DM patients worldwide, of whom 30%–40% developed DN [1]. The pathogenesis of DN primarily involves inflammation, oxidative stress, renal hemodynamic changes, and dysregulated metabolism [2–5]. Medications that control blood glucose and lipids levels as well as blood pressure cannot impede the progression of DN [6]. Therefore, developing novel drugs to treat DN contributes significantly to prevention.

Ferroptosis, characterized by increased iron-dependent production of reactive oxygen species (ROS) and lipid peroxide, is a newly discovered form of regulated cell death [7]. Regulated by multiple genes with a complex mechanism involving iron homeostasis, lipid peroxidation, and metabolism, ferroptosis plays a pivotal role in the progression of renal diseases [8]. Ferroptosis contributes to DN through triggering renal tubular injury [9], glomerular injury [10], and renal fibrosis [11, 12]. A significant characteristic of DN is renal tubular injury, which emerges due to hyperglycemia-induced iron overload, diminished antioxidant, heightened ROS production, and escalated lipid peroxidation within renal tubular cells [13]. A novel approach to investigating the progression and treatment of DN may involve inhibiting ferroptosis, as indicated by recent studies [14, 15]. Thus, inhibiting ferroptosis in a targeted manner is expected to be an emerging strategy for improving DN-related renal injury.

Traditional Chinese medicine is efficacious in improving renal injury. Tang-Shen-Wei-Ning formula reduced podocyte injury in DN mice via SIRT1/HIF-1α pathway [16]. Gandi capsules can protect kidney function in DN mice via SIRT1/AMPK/HNF4A pathway [17]. The latest study revealed that renal injury mitigation through ferroptosis inhibition is a mechanism of action for traditional Chinese medicine. Tao-Hong-Si-Wu decoction alleviates high salt diet-induced renal inflammation and fibrosis by inhibiting ferroptosis [18]. Glabridin protects against DN by inhibiting oxidative stress and ferroptosis in vivo and in vitro [19]. Quercetin protects kidney function by inhibiting ferroptosis in renal tubular epithelial cells by regulating NRF2/HO-1 signaling pathway [20].

Jian-Pi-Gu-Shen-Hua-Yu (JPGS) decoction, consisting of Astragalus membranaceus Bunge, Panax ginseng C.A.Mey., Rosa laevigata Michx., Euryale ferox Salisb., Cornus officinalis Siebold & Zucc., Dioscorea opposita L., Atractylodes macrocephala Koidz., Angelica sinensis (Oliv.) Diels, Salvia miltiorrhiza Bunge, Conioselinum anthriscoides “Chuanxiong,” leeches, and Rheum officinale Baill., is commonly used in clinical practice to treat chronic kidney diseases, such as DN [21]. In this study, we established a DN mouse model to investigate the therapeutic effect of JPGS in a DN mouse model. Subsequently, we examined the effects of JPGS on ferroptosis- and GPX4 pathway-related indices. Finally, we validated whether JPGS inhibited ferroptosis in DN mice via the GPX4 pathway using GPX4 inhibitor and ferroptosis inhibitors.

2. Methods

2.1. Animals and Reagents

Specific pathogen-free grade healthy male C57BL/6J mice (6–8 weeks, g) were purchased from HFK Bioscience Co., Ltd. (Beijing, China). Detailed information on reagents, kits, and antibodies is provided in the supplemental material (available here). JPGS was acquired from Cangzhou Hospital of Integrated Traditional Chinese Medicine and Western Medicine. Quality control of JPGS was performed using ultra performance liquid chromatography coupled with mass spectrometer. Further information on JPGS can be found in the supplementary material.

2.2. DN Mouse Models

All experiments were conducted in an SPF environment. Each cage housed five mice with free access to food and water. This study was approved by Cangzhou Hospital of Integrated Traditional Chinese Medicine and Western Medicine of Hebei Province (approval no. CZX2023-KY-065), and all animal experiments were conducted in compliance with the “Guide for the Care and Use of Laboratory Animals” published by National Institutes of Health.

Prior to establishment of the DN mouse models, all mice underwent 1 week of adaptive feeding and then received a high-sugar high-fat diet (HFD) for 8 weeks. At the end of week 8, all mice were fasted for 12 h with unrestricted access to water and then were intraperitoneally injected with 30 mg/kg of streptozotocin (STZ). The random blood glucose levels were detected after 72 h. A blood glucose mmol/L was considered as the modeling criterion for type 2 diabetes mellitus (T2DM). The mice were tested weekly for 24 h urinary total protein (UTP). A blood glucose mmol/L and positive results for glucose and protein in the urine were considered as the modeling criteria for DN.

2.3. Animal Experiment

For the investigation of JPGS’s therapeutic impact on DN mice and its potential antiferroptosis mechanism, a total of 60 mice were categorized into different groups, control, DN, irbesartan (IRB), low-dose JPGS (JPGS-L), medium-dose JPGS (JPGS-M), and high-dose JPGS (JPGS-H), each containing 10 mice. While the control group was given a regular diet, DN mouse models were established in all groups except the control. Subsequently, mice in the control and DN groups received 0.2 mL of the vehicle daily through gavage. In the IRB group, mice were administered 30 mg/kg of IRB daily via gavage. Meanwhile, the JPGS-L, JPGS-M, and JPGS-H groups received 2.4 g/kg, 4.8 g/kg, and 9.6 g/kg of JPGS daily through gavage, respectively. The duration of administration in each group was 8 consecutive weeks.

To validate whether JPGS inhibited ferroptosis in DN mice via the GPX4 pathway based on GPX4 and ferroptosis inhibitors, 60 mice were divided into groups of 10 for the control, DN, JPGS, Fer-1 (ferrostatin-1, a ferroptosis inhibitor), RSL-3 (Ras-selective lethal small molecule 3, a GPX4 inhibitor), and RSL-3+JPGS groups. The duration of administration for each group was eight consecutive weeks according to the following regimen. The mice in the control group accepted normal diets, and DN mouse model was established in all groups except for the control group. Subsequently, mice in the control and model groups received vehicle both via gavage and intraperitoneal (IP) injection. Mice in the JPGS group received 9.6 g/kg JPGS daily via gavage and vehicle via IP injection. Mice in the Fer-1 group received 10 mg/kg Fer-1 via IP injection and vehicle daily via gavage [22]. Mice in the RSL-3 group received 10 mg/kg RSL-3 via IP injection and vehicle daily via gavage [22]. Mice in the RSL-3+JPGS group received 10 mg/kg RSL-3 via IP injection and 9.6 g/kg JPGS daily via gavage.

At weeks 0, 2, 4, 6, and 8 after drug administration and fasting, the fasting blood glucose (FBG) levels and body weights of mice in each group were measured. At week 8, 24 h UTP was tested again in each group. Then, blood was collected via inner canthus, and serums were separated. After blood collection, mice were euthanized and the kidneys were removed. The left one was frozen, and the right one was immobilized in a 4% paraformaldehyde solution for later use.

2.4. Biochemical Experiment

Serum creatinine (Cr) and blood urea nitrogen (BUN) levels from each group were measured using corresponding assay kits.

The left kidneys were analyzed to measure the levels of malondialdehyde (MDA), ROS, iron (Fe), and the reduced glutathione (GSH) to oxidized glutathione (GSSG, glutathione disulfide) ratio (GSH/GSSG ratio) using MDA, ROS, and Fe assay kits, respectively. The remaining left kidneys were cryopreserved in an ultradeep freezer at -80°C for later use.

2.5. Enzyme-Linked Immunosorbent Assay (ELISA)

The levels of interleukin-1β (IL-1β), interleukin-6 (IL-6), tumor necrosis factor alpha (TNF-α), and 4-hydroxynonenal (4-HNE) in the kidney were measured using specific assay kits. All procedures were carried out in accordance with instructions provided by the manufacturer.

2.6. Morphological Observation of Pathological Changes in Kidney Tissues

The kidneys immobilized in 4% paraformaldehyde solution were sliced, sealed, and microscopically analyzed. The pathological morphology was observed using hematoxylin and eosin (HE) staining. Periodic acid Schiff (PAS) staining-positive area indicated glycogen deposition, and TUNEL (TdT-mediated dUTP nick-end labeling) staining-positive cells indicated cellular apoptosis.

2.7. Quantitative Reverse Transcription Polymerase Chain Reaction (RT-qPCR)

Total RNA was extracted from the kidney and reverse transcribed into cDNA. Gene expression analysis was performed using a real-time PCR detection system and the SuperReal PreMix Plus kit. Cycle thresholds (Ct) were determined, and the relative expression quantities of the genes of interest were calculated by the 2^-ΔΔCt method [23]. The primer sequences were included in the supplementary material.

2.8. Western Blot

Total protein was extracted from the kidney, and the concentration of protein was measured using bicinchoninic acid assay method. The protein was fully denatured in 99°C for 5 min. The protein samples were separated by SDS-PAGE and transferred to PVDF membranes. After blocking for 2 h in 5% skim milk, a suitable concentration of primary antibody was added and incubated overnight. After washing, the corresponding secondary antibodies were added and incubated for 2 h. Finally, membranes were washed and the bands visualized by enhanced chemiluminescence. ImageJ was utilized to quantitate the optical density of each protein band.

2.9. Statistics

The statistical analysis was performed using the SPSS v26.0, and all data were described in (SD). The multigroup comparisons were performed by one-way analysis of variance. The intergroup pairwise comparisons were performed using the least significant difference test in the case of homogeneity of variance and the Tamhane’s T2 test in the case of heterogeneity of variance. indicated statistically significant differences.

3. Results

3.1. Therapeutic Effect of JPGS in DN Mice

Compared to the control group, the body weight of mice in the DN group significantly decreased. The body weight increased to varying degrees in the IRB and JPGS groups compared with the DN group (Figure 1(a)). FBG levels were elevated in the DN group compared with the control group but decreased in the IRB and JPGS groups (Figure 1(b)).

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Figure 1

The administration of JPGS showed a therapeutic effect in mice with DN. The administration of JPGS controlled body weight, fasting blood glucose levels, and kidney function in DN mice. The changes in (a) body weight and (b) fasting blood glucose levels for each group are shown in the curve graphs. After JPGS treatment, there were improvements in kidney function, as seen in the changes in (c) 24 h UTP, (d) Cr, and (e) BUN. Kidney tissue samples stained with (f) HE and (g) PAS were also analyzed. JPGS treatment resulted in a reduction of proinflammatory cytokines (h) IL-1β, (i) IL-6, and (j) TNF-α in the kidney. Control, model, IRB, JPGS-L, JPGS-M, and JPGS-H ( per group) groups. Data are presented as . ^## vs. control group. and vs. model group.

The renal function test results revealed that 24 h UTP concentration, serum Cr, and BUN levels increased in the DN group compared with the control group and decreased in the IRB, JPGS-M, and JPGS-H groups as compared to the DN group (Figures 1(c)–1(e)).

The HE staining revealed clearly visible and intact renal structures in the control group. However, severe pathological changes like glomerular mesangial cell proliferation, thickened basement membrane, tubular atrophy, and tubulointerstitial inflammatory cell infiltration were present in the DN group. The glomerular and renal tubular lesions were reduced with the most noticeable reduction in the IRB, JPGS-M, and JPGS-H groups compared with the DN group (Figure 1(f)). The results of PAS staining showed that the positive area in the control group was mainly scattered along the walls of glomerular capillaries and renal tubules, and there was no positive area in between. Excessive PAS-positive area was observed in glomerular basement membrane and mesangial area in DN mice, with the most noticeable reduction occurring in the IRB, JPGS-M, and JPGS-H groups as compared to the DN group (Figure 1(g)). Collectively, the results signified that JPGS effectively reduced pathological changes in the kidneys of DN mice.

The inflammatory factor test results revealed that IL-1β, IL-6, and TNFα concentrations increased in the DN group as compared to the control group and decreased to varying degrees in the IRB, JPGS-L, JPGS-M, and JPGS-H groups as compared to the DN group (Figures 1(h)–1(j)).

3.2. Effects of JPGS on Ferroptosis-Related Expression Factors in DN Mice

The TUNEL staining revealed green fluorescence in the DN group as compared to the control group signaling that apoptosis had occurred in the kidneys. Positive fluorescence was markedly diminished in the IRB, JPGS-L, JPGS-M, and JPGS-H groups as compared to the DN group (Figures 2(a) and 2(b)). The oxidative stress test results revealed that ROS, MDA, and 4-HNE levels were markedly elevated in the DN group as compared to the control group. ROS, MDA, and 4-HNE levels decreased significantly in the IRB and JPGS groups as compared to the DN group (Figures 2(c)–2(e)). The changes in total iron levels were measured revealing that the Fe levels increased in the DN group as compared to the control group but decreased in the IRB, JPGS-L, JPGS-M, and JPGS-H groups as compared to the DN group (Figure 2(f)).

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3.3. Effects of JPGS on GPX4 Pathway-Related Factors in DN Mice

Lipid peroxidation regulated via the GPX4 pathway is vital for activating ferroptosis. The changes in GSH/GSSG ratio in the kidneys from each group were measured. The GSH/GSSG ratio decreased in the DN group as compared to the control group suggesting that the antioxidant capacity decreased and lipid peroxides accumulated in the DN mice, potentially causing ferroptosis. GSH/GSSG ratio increased in the IRB, JPGS-L, JPGS-M, and JPGS-H groups as compared to the DN group, indicating that the antioxidant capacity increased in the DN mice after drug administration (Figures 3(a)–3(c)).

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The alterations in GPX4 pathway-related components were assessed using both qPCR and western blotting methods. Specifically, the solute carrier family 7A11 (SLC7A11), SLC3A2, glutamate-cysteine ligase (GCLC), GPX4 mRNA, and protein levels decreased in the DN group as compared to the control group and increased in the IRB, JPGS-L, JPGS-M, and JPGS-H groups as compared to the DN group, indicating that IRB and JPGS reduced lipid peroxide accumulation in the DN mice by activating the GPX4 pathway, and the protective effect may be associated with ferroptosis inhibition (Figure 3(d)–3(i)).

Overall, because the JPGS-H group showed the most significant effect on DN mice by activating the GPX4 pathway and reducing inflammation, oxidative stress, apoptosis, and ferroptosis, JPGS-H was selected for all subsequent experiments.

3.4. Therapeutic Effect of JPGS in DN Mice after Ferroptosis Inhibition

The previous results demonstrated that ferroptosis participated in DN progression and that the accumulation of lipid peroxides was reduced by activating the GPX4 pathway. To further investigate ferroptosis inhibition via the GPX4 pathway activation, the therapeutic effects of JPGS on DN mice treated with ferroptosis inhibitor Fer-1 and GPX4 inhibitor RSL3, respectively, were observed.

Weekly observations were made on changes in body weight and FBG levels of all mice following the initiation of drug administration. In comparison to the control group, the DN group exhibited a decline in body weight, while the JPGS and Fer-1 groups demonstrated an increase relative to the DN group. However, no significant variation in body weights was observed between the RSL3 and RSL3+JPGS groups (Figure 4(a)). Similarly, FBG levels were higher in the DN group compared to the control group but notably reduced in the JPGS and Fer-1 groups compared to the DN group. Again, no marked distinction in FBG levels was noted between the RSL3 and RSL3+JPGS groups (Figure 4(b)).

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Figure 4

The therapeutic effect of JPGS on DN mice was abolished by GPX4 inhibitor. The administration of RSL3 completely nullified the beneficial effect of JPGS treatment on DN mice. (a, b) RSL-3 cancelled the effects of JPGS on body weight and FBG. (c–e) The levels of 24 h UTP, Cr, and BUN after treatment with JPGS. (f, g) Kidney tissue was stained with HE and PAS to evaluate histopathological changes. (h–j) RSL-3 cancelled the effect of JPSG on reducing proinflammatory cytokines in the kidney. Control, model, JPGS, Fer-1, RSL3, and JPGS+RSL3 ( per group) groups. Data are presented as . ^## vs. control group. and vs. model group.

Analysis of renal function tests indicated a rise in 24 h UTP concentration, as well as Cr and BUN levels in the DN group relative to the control group. However, these levels demonstrated a decrease in the JPGS and Fer-1 groups when compared to the DN group. Notably, no substantial disparity was observed in 24 h UTP concentration, serum Cr, or BUN levels among the DN, RSL3, or RSL3+JPGS groups (Figures 4(c)–4(e)).

The HE staining revealed that the renal structures were clearly visible and intact in the control group and that the kidneys suffered severe pathological changes like the previous study in the DN group. The renal pathological changes were relieved in the JPGS and Fer-1 groups and were not reduced in the RSL3 and RSL3+JPGS group as compared to the DN group (Figure 4(f)). PAS-positive staining was primarily distributed along the glomerular capillary wall and renal tubular wall. No PAS-positive staining was detected in the control group. PAS-positive staining was deposited in glomerular basement membrane and mesangial area in the DN group. Less PAS-positive area was observed in the glomerulus, and the thickened basement membranes were reduced in the JPGS and Fer-1 groups as compared to the DN group. The pathological changes were more severe in the RSL3 group, and no reduction was observed in the RSL3+JPGS group as compared to the DN group (Figure 4(g)).

The inflammation test results revealed that IL-1β, IL-6, and TNFα concentrations were increased significantly in the DN group as compared to the control group but decreased in the JPGS and Fer-1 groups. There was no reduction in the RSL3 and RSL3+JPGS groups as compared to the DN group (Figures 4(h)–4(j)).

3.5. Effects of JPGS on Ferroptosis-Related Expression Factors in DN Mice after Ferroptosis Inhibition

Positive TUNEL staining indicated by green fluorescence in the DN group as compared to the control group revealed that apoptosis had occurred. Positive fluorescence was diminished in the JPGS and Fer-1 groups. No significant difference was found in the RSL3 and RSL3+JPGS groups compared with the DN group (Figures 5(a) and 5(b)). The oxidative stress test results indicated that ROS and lipid peroxide levels increased in the DN group as compared to the control group. The levels of oxidative stress-related indicators decreased in the JPGS and Fer-1 groups as compared to the DN group. All these levels were not reduced in the RSL3 and RSL3+JPGS groups (Figures 5(c)–5(e)). Measurement of Fe level changes indicated that Fe levels were elevated in the DN group as compared to the control group and decreased in the JPGS and Fer-1 groups. No significant reduction in the RSL3 and RSL3+JPGS groups as compared to the DN group (Figure 5(f)).

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3.6. Effects of JPGS on the GPX4 Pathway in DN Mice after Ferroptosis Inhibition

The GSH/GSSG ratio decreased in the DN group as compared to the control group and increased in the JPGS and Fer-1 groups. No reduction was found in the RSL3 and RSL3+JPGS groups as compared to the DN group. The changes in GPX4 pathway were also evaluated, and the results demonstrated that SLC7A11, SLC3A2, GCLC, GPX4, mRNA, and protein levels decreased in the DN group as compared to the control group and increased in the JPGS and Fer-1 groups. No reduction was found in the RSL3 and RSL3+JPGS groups when compared to the DN group (Figure 6).

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Figure 6

The inhibitory effect of GPX4 abolished effect of JPGS on GPX4 pathway in the kidneys. (a–c) The ameliorated GSH/GSSG ratio in DN kidney by JPGS was cancelled by RSL3 treatment. (d–g) RSL-3 cancelled the effects of JPGS on mRNA related to GPX4 pathway in DN kidney. (h–l) Western blotting revealed the expressions of GPX4 pathway-related proteins in DN kidney. Control, model, JPGS, Fer-1, RSL3, and JPGS+RSL3 ( per group) groups. Data are presented as . ^# and ^## vs. control group. and vs. model group.

4. Discussion

STZ combined with HFD is commonly used to induce DN. HFD causes insulin resistance and pancreatic β cell dysfunction, whereas STZ destroys the remaining pancreatic β cells and exacerbates hypoinsulinism inducing overt hyperglycemia [24]. Long-term hyperglycemia damages the glomerular capillary wall causing pathological changes which results in increased permeability of the glomerular filtration membrane, the infiltration of macromolecular proteins and cell constituents in the urine, the occurrence of proteinuria, and renal tubulointerstitial fibrosis and interstitial inflammation [25]. 24 h UTP is the most sensitive indicator of early-stage DN-related renal injury [26]. Because Cr and BUN are metabolized and excreted via the kidneys, an increase in Cr and BUN levels is indicative of diminished renal function [27]. In this study, JPGS improved the body weight, blood glucose, 24 h urinary protein content, and Cr and BUN levels in DN mice. In addition, pathological staining revealed that JPGS reduced the pathological changes like glomerular mesangial matrix hyperplasia and thickened basement membrane. Long-term hyperglycemia led to the formation of an inflammatory microenvironment in the kidneys with elevated inflammatory factor levels causing further damage to kidney tissues [28]. IL-1β, IL-6, and TNF-α levels were closely associated with DN progression [29]. Furthermore, JPGS reduced IL-1β, IL-6, and TNF-α levels in the kidneys of DN mice. These results indicate that JPGS reduced disease symptoms in DN mice [30, 31].

Cell apoptosis remained fundamental to DN progression, and hyperglycemia facilitated apoptosis in various cells such as proximal renal tubular epithelial cells in DN mice [32]. The renal biopsy in patients with DN has shown that renal tubular epithelial cells, endothelial cells, and interstitial cells suffer apoptosis [33]. The protective effect against DN is demonstrated by inhibiting glucose-induced apoptosis of endothelial and capsular cells [34]. TUNEL staining is frequently used to observe cell apoptosis. In this study, TUNEL staining indicated that JPGS effectively reduced apoptosis in the kidneys of DN mice. Oxidative stress is considered a major feature of diabetic renal injury in the presence of abnormal metabolism and hemodynamics [35]. If excessive ROS is not regulated by the intrinsic antioxidant system, oxidative stress occurs. As a result, bioactive molecules (carbohydrates, proteins, lipids, and DNA) are oxidized leading to cell injuries [36]. MDA and 4-HNE, which are final products of the reaction between ROS and lipids, are highly cytotoxic, and their levels directly indicate oxidative stress levels [37]. In this study, the levels of ROS and lipid peroxide increased in the DN group as compared to the control group. JPGS effectively reduced oxidative stress and MDA, ROS, and 4-HNE levels. The above results further demonstrate that JPGS may significantly treat DN.

Iron is a metal that partakes in redox reactions in the human body. Normally, iron homeostasis is coordinated and maintained via iron metabolism involving iron absorption, utilization, recirculation, and storage, through the coordination of multiple proteins. To avoid intracellular iron accumulation and maintain intracellular iron homeostasis, normal histiocytes discharge excess iron via ferroportin, which is the only free iron exporter on the cell membrane [38]. A change in the expression of proteins involved in iron metabolism potentially induces iron metabolism disorders, rendering it impossible to discharge free intracellular iron and leading to an aberrant increase in the labile iron pool, iron overload, and the production of ROS via the Fenton reaction. The accumulation of ROS leads to GSH depletion and GPX4 inactivation. Consequently, lipids are peroxidized, and eventually, ferroptosis is induced [39, 40]. Clinical studies have shown that when cell ferroptosis occurred, SLC7A11 and GPX4 levels decreased significantly in the renal tubules of patients with DM, while the ferroptosis inhibitor effectively reduced renal tubular injuries [41]. Animal experiments in the STZ-induced DN mice model have also shown that GPX4 expression levels decreased, while lipid peroxide and iron concentrations increased [42]. Our findings suggest that JPGS reduced the total iron concentration in DN mice kidneys, signaling that iron overload was reduced.

The GPX4 pathway serves as a major defense against lipid peroxidation because GPX4 is the only known enzyme to reduce phospholipid hydroperoxides [43]. Normally, extracellular cysteine is transported into cells by system xc⁻, a cystine/glutamate antiporter consisting of SLC7A11 and SLC3A2 located on the cell membrane [44]. It is transformed into GSH by a series of enzymatic reactions including glutamate-cysteine ligase and glutathione synthetase. GSH, a reducing agent, is catalyzed by GPX4 and reduces lipid peroxides eliminating their cytotoxicity [45]. N-Acetylcysteine may activate the expression of GPX4 to reduce high glucose-induced ferroptosis in Madin-Darby canine kidney cells, and this effect may be abolished by the GPX4 inhibitor, FIN56 [46]. The results demonstrate that JPGS considerably increased GSH/GSSG ratio in DN mice kidneys, signifying that GSH depletion was reduced. Additionally, mRNA and proteins in the GPX4 pathway were elevated suggesting that JPGS promotes the expression of GPX4 in DN mice kidneys. Irbesartan, serving as a positive control, is widely utilized in the treatment of DN [47]. Our findings demonstrate that JPGS-H and irbesartan have similar effects in treating DN and in inhibiting ferroptosis. However, detailed research into irbesartan’s specific action during the ferroptosis process is lacking. Studies have suggested that irbesartan may affect pathways related to oxidative stress and iron metabolism [48, 49], which aligns with the outcomes observed in our research. This lays a new groundwork for further in-depth investigation into irbesartan’s role in ferroptosis-related pathways and mechanisms.

To further analyze the JPGS mechanism of action to reduce renal injury in DN, Fer-1 and RSL3 were used to verify the effects of JPGS after inhibition of GPX4 expression. Fer-1, a ferroptosis inhibitor, inhibits ferroptosis by scavenging lipid peroxides, thereby preventing their accumulation. Animal experiments showed that Fer-1 significantly reduced ROS and increased the GPX4 level in DN mice kidneys [50]. RSL3, a GPX4 inhibitor, reduced the expression and activity of GPX4 and induced ferroptosis. RSL3 has been verified to induce ferroptosis in mice [21]. The results of this study suggest that the effect of JPGS and Fer-1 alone has no significant difference in DN mice and that RSL3 abolished the therapeutic effect of JPGS, suggesting that JPGS treats DN via upregulating the expression of GPX4 pathway-related proteins, regulating iron intake, and relieving iron overload to reduce ferroptosis and improve renal injury. However, as a preliminary study, our experiment has some limitations. In future research, we plan to set up a combined treatment group with FER-1 and JPGS to more comprehensively explore the mechanism of action of JPGS on ferroptosis.

5. Conclusion

In summary, JPGS has significant therapeutic and anti-inflammatory effects on DN mice, and its mechanism is mainly achieved by upregulating the expression of GPX4 pathway-related proteins, thereby alleviating iron overload and ultimately reducing ferroptosis.

Abbreviations

DN:	Diabetic nephropathy
GPX4:	Glutathione peroxidase 4
ROS:	Reactive oxygen species
JPGS:	Jian-Pi-Gu-Shen-Hua-Yu decoction
24 h UTP:	24 h urinary total protein
Cr:	Creatinine
BUN:	Blood urea nitrogen
MDA:	Malondialdehyde
GSH:	Glutathione
GSSG:	Oxidized glutathione
IL-1β:	Interleukin-1β
IL-6:	Interleukin-6
TNF-α:	Tumor necrosis factor alpha
4-HNE:	4-Hydroxynonenal
SLC7A11:	Solute carrier family 7A11
GCLC:	Glutamate-cysteine ligase.

Data Availability

The data used to support the findings of this study are available from the corresponding author upon reasonable request.

Conflicts of Interest

All authors declare no conflict of interests.

Authors’ Contributions

SQL wrote the original draft and was responsible for the investigation and funding acquisition. LRF wrote the original draft and was responsible for the investigation, validation, and data curation. XTC and XHS wrote the original draft and were responsible for the investigation, validation, and data curation. LD, QGW, and HZ wrote the original draft and were responsible for the formal analysis and visualization. HTC and YSW wrote the original draft and were responsible for the investigation, data curation, validation, and conceptualization. LXW wrote, reviewed, and edited the manuscript and was responsible for the conceptualization.

Acknowledgments

This work was supported by the Hebei Province Science and Technology Project (grant no. 2023257).

Supplementary Materials

The details of the materials, reagents, primers, and UPLC-MS analysis protocol can be found in the supplementary materials. (Supplementary Materials)

References

Y. Zhang, X. Le, S. Zheng et al., “MicroRNA-146a-5p-modified human umbilical cord mesenchymal stem cells enhance protection against diabetic nephropathy in rats through facilitating M2 macrophage polarization,” Stem Cell Research and Therapy, vol. 13, no. 1, 2022.
View at: Publisher Site | Google Scholar
N. Samsu, “Diabetic nephropathy: challenges in pathogenesis, diagnosis, and treatment,” BioMed Research International, vol. 2021, Article ID 1497449, 17 pages, 2021.
View at: Publisher Site | Google Scholar
X. Li, L. Lu, W. Hou et al., “Epigenetics in the pathogenesis of diabetic nephropathy,” Acta Biochimica et Biophysica Sinica, vol. 54, no. 2, pp. 163–172, 2022.
View at: Publisher Site | Google Scholar
L. Liu, F. Bai, H. Song et al., “Upregulation of TIPE1 in tubular epithelial cell aggravates diabetic nephropathy by disrupting PHB2 mediated mitophagy,” Redox Biology, vol. 50, article 102260, 2022.
View at: Publisher Site | Google Scholar
A. Roointan, Y. Gheisari, K. L. Hudkins, and A. Gholaminejad, “Non-invasive metabolic biomarkers for early diagnosis of diabetic nephropathy: meta-analysis of profiling metabolomics studies,” Nutrition, Metabolism and Cardiovascular Diseases, vol. 31, no. 8, pp. 2253–2272, 2021.
View at: Publisher Site | Google Scholar
R. Alicic, “Diabetic kidney disease: challenges, progress, and possibilities,” Clinical Journal of the American Society of Nephrology, vol. 12, no. 12, pp. 2032–2045, 2017.
View at: Publisher Site | Google Scholar
M. Gao and X. Jiang, “To eat or not to eat — the metabolic flavor of ferroptosis,” Current Opinion in Cell Biology, vol. 51, pp. 58–64, 2018.
View at: Publisher Site | Google Scholar
J. Y. Duan, X. Lin, F. Xu et al., “Ferroptosis and its potential role in metabolic diseases: a curse or revitalization?” Frontiers in Cell and Developmental Biology, vol. 9, article 701788, 2021.
View at: Publisher Site | Google Scholar
L. Zhao, Y. Zou, J. Zhang et al., “Serum transferrin predicts end-stage Renal Disease in Type 2 Diabetes Mellitus patients,” International Journal of Medical Sciences, vol. 17, no. 14, pp. 2113–2124, 2020.
View at: Publisher Site | Google Scholar
J. Lu, P. P. Chen, J. X. Zhang et al., “GPR43 deficiency protects against podocyte insulin resistance in diabetic nephropathy through the restoration of AMPKα activity,” Theranostics, vol. 11, no. 10, pp. 4728–4742, 2021.
View at: Publisher Site | Google Scholar
Y. Ikeda, I. Ozono, S. Tajima et al., “Iron chelation by deferoxamine prevents renal interstitial fibrosis in mice with unilateral ureteral obstruction,” PLoS One, vol. 9, no. 2, article e89355, 2014.
View at: Publisher Site | Google Scholar
L. Zhou, X. Xue, Q. Hou, and C. Dai, “Targeting ferroptosis attenuates interstitial inflammation and kidney fibrosis,” Kidney Diseases, vol. 8, no. 1, pp. 57–71, 2022.
View at: Publisher Site | Google Scholar
W. J. Wang, X. Jiang, C. C. Gao, and Z. W. Chen, “Salusin-β participates in high glucose-induced HK-2 cell ferroptosis in a Nrf-2-dependent manner,” Molecular Medicine Reports, vol. 24, no. 3, 2021.
View at: Publisher Site | Google Scholar
M. Matsumoto, N. Sasaki, T. Tsujino, H. Akahori, Y. Naito, and T. Masuyama, “Iron restriction prevents diabetic nephropathy in Otsuka Long-Evans Tokushima fatty rat,” Renal Failure, vol. 35, no. 8, pp. 1156–1162, 2013.
View at: Publisher Site | Google Scholar
R. Miao, X. Fang, Y. Zhang, J. Wei, Y. Zhang, and J. Tian, “Iron metabolism and ferroptosis in type 2 diabetes mellitus and complications: mechanisms and therapeutic opportunities,” Cell Death & Disease, vol. 14, no. 3, 2023.
View at: Publisher Site | Google Scholar
J. Chang, J. Zheng, X. Gao et al., “TangShenWeiNing formula prevents diabetic nephropathy by protecting podocytes through the SIRT1/HIF-1α pathway,” Frontiers in Endocrinology, vol. 13, article 888611, 2022.
View at: Publisher Site | Google Scholar
Y. Zhang, H. Yao, C. Li et al., “Gandi capsule improved podocyte lipid metabolism of diabetic nephropathy mice through SIRT1/AMPK/HNF4A pathway,” Oxidative Medicine and Cellular Longevity, vol. 2022, Article ID 6275505, 17 pages, 2022.
View at: Publisher Site | Google Scholar
T. Xie, Z. Bai, Z. Chen et al., “Inhibition of ferroptosis ameliorates hypertensive nephropathy through P53/Nrf2/P21 pathway by Taohongsiwu decoction: based on network pharmacology and experimental validation,” Journal of Ethnopharmacology, vol. 312, article 116506, 2023.
View at: Publisher Site | Google Scholar
H. Tan, J. Chen, Y. Li et al., “Glabridin, a bioactive component of licorice, ameliorates diabetic nephropathy by regulating ferroptosis and the VEGF/Akt/ERK pathways,” Molecular Medicine, vol. 28, no. 1, p. 58, 2022.
View at: Publisher Site | Google Scholar
Q. Feng, Y. Yang, Y. Qiao et al., “Quercetin ameliorates diabetic kidney injury by inhibiting ferroptosis via activating Nrf2/HO-1 signaling pathway,” The American Journal of Chinese Medicine, vol. 51, no. 4, pp. 997–1018, 2023.
View at: Publisher Site | Google Scholar
L. Shuquan, S. Huili, and H. Zhongqian, “Study on the clinical effects of Jianpi Gushen Huayu formula combined with Tripterygium glycosides tablets on clinical diabetic nephropathy treated and influences on renal fibrosis indexes,” World Chinese Medicine, vol. 14, pp. 174–177, 2019.
View at: Google Scholar
J. Qi, J. W. Kim, Z. Zhou, C. W. Lim, and B. Kim, “Ferroptosis affects the progression of nonalcoholic steatohepatitis via the modulation of lipid peroxidation–mediated cell death in mice,” The American Journal of Pathology, vol. 190, no. 1, pp. 68–81, 2020.
View at: Publisher Site | Google Scholar
S. Lv, Z. Zhang, X. Su et al., “Qingrequzhuo capsule alleviated methionine and choline deficient diet-induced nonalcoholic steatohepatitis in mice through regulating gut microbiota, enhancing gut tight junction and inhibiting the activation of TLR4/NF-κB signaling pathway,” Frontiers in Endocrinology, vol. 13, article 1106875, 2022.
View at: Publisher Site | Google Scholar
B. L. Furman, “Streptozotocin-induced diabetic models in mice and rats,” Current Protocols in Pharmacology, vol. 70, no. 1, 2015.
View at: Publisher Site | Google Scholar
A. S. O’Connor and J. R. Schelling, “Diabetes and the kidney,” American Journal of Kidney Diseases, vol. 46, no. 4, pp. 766–773, 2005.
View at: Publisher Site | Google Scholar
H. H. Parving, B. Oxenbøll, P. A. Svendsen, J. S. Christiansen, and A. R. Andersen, “Early detection of patients at risk of developing diabetic nephropathy. A longitudinal study of urinary albumin excretion,” Acta Endocrinologica, vol. 100, no. 4, pp. 550–555, 1982.
View at: Publisher Site | Google Scholar
M. J. Kussman, “The clinical course of diabetic nephropathy. JAMA: The,” Journal of the American Medical Association, vol. 236, no. 16, p. 1861, 1976.
View at: Publisher Site | Google Scholar
M. B. Duran-Salgado, “Diabetic nephropathy and inflammation,” World Journal of Diabetes, vol. 5, no. 3, p. 393, 2014.
View at: Publisher Site | Google Scholar
J. Navarro-González, “Inflammatory molecules and pathways in the pathogenesis of diabetic nephropathy,” Nature Reviews Nephrology, vol. 7, no. 6, pp. 327–340, 2011.
View at: Publisher Site | Google Scholar
B. Najafian, C. E. Alpers, and A. B. Fogo, “Pathology of human diabetic nephropathy,” Diabetes and the Kidney, vol. 170, pp. 36–47, 2011.
View at: Publisher Site | Google Scholar
K. Azushima, S. B. Gurley, and T. M. Coffman, “Modelling diabetic nephropathy in mice,” Nature Reviews Nephrology, vol. 14, no. 1, pp. 48–56, 2018.
View at: Publisher Site | Google Scholar
D. A. Allen, S. M. Harwood, M. Varagunam, M. J. Raftery, and M. M. Yaqoob, “High glucose‐induced oxidative stress causes apoptosis in proximal tubular epithelial cells and is mediated by multiple caspases,” The FASEB Journal, vol. 17, no. 8, pp. 1–21, 2003.
View at: Publisher Site | Google Scholar
D. Kumar, S. Robertson, and K. D. Burns, “Evidence of apoptosis in human diabetic kidney,” Molecular and Cellular Biochemistry, vol. 259, no. 1/2, pp. 67–70, 2004.
View at: Publisher Site | Google Scholar
B. Isermann, I. A. Vinnikov, T. Madhusudhan et al., “Activated protein C protects against diabetic nephropathy by inhibiting endothelial and podocyte apoptosis,” Nature Medicine, vol. 13, no. 11, pp. 1349–1358, 2007.
View at: Publisher Site | Google Scholar
S. Badal, “New insights into molecular mechanisms of diabetic kidney disease,” American Journal of Kidney Diseases, vol. 63, no. 2, pp. S63–S83, 2014.
View at: Publisher Site | Google Scholar
H. Ha, I. A. Hwang, J. H. Park, and H. B. Lee, “Role of reactive oxygen species in the pathogenesis of diabetic nephropathy,” Diabetes Research and Clinical Practice, vol. 82, pp. S42–S45, 2008.
View at: Publisher Site | Google Scholar
S. Li, L. Zheng, J. Zhang, X. Liu, and Z. Wu, “Inhibition of ferroptosis by up-regulating Nrf2 delayed the progression of diabetic nephropathy,” Free Radical Biology and Medicine, vol. 162, pp. 435–449, 2021.
View at: Publisher Site | Google Scholar
D. L. Zhang, J. Wu, B. N. Shah et al., “Erythrocytic ferroportin reduces intracellular iron accumulation, hemolysis, and malaria risk,” Science, vol. 359, no. 6383, pp. 1520–1523, 2018.
View at: Publisher Site | Google Scholar
S. Zhang, W. Xin, G. J. Anderson et al., “Double-edge sword roles of iron in driving energy production versus instigating ferroptosis,” Cell Death & Disease, vol. 13, no. 1, 2022.
View at: Publisher Site | Google Scholar
S. Dixon, “Ferroptosis: an iron-dependent form of nonapoptotic cell death,” Cell, vol. 149, no. 5, pp. 1060–1072, 2012.
View at: Publisher Site | Google Scholar
S. Kim, S. W. Kang, J. Joo et al., “Characterization of ferroptosis in kidney tubular cell death under diabetic conditions,” Cell Death & Disease, vol. 12, no. 2, 2021.
View at: Publisher Site | Google Scholar
Y. Wang, R. Bi, F. Quan et al., “Ferroptosis involves in renal tubular cell death in diabetic nephropathy,” European Journal of Pharmacology, vol. 888, article 173574, 2020.
View at: Publisher Site | Google Scholar
R. Brigelius-FlohÉ and M. Maiorino, “Glutathione peroxidases,” Biochimica et Biophysica Acta (BBA) - General Subjects, vol. 1830, no. 5, pp. 3289–3303, 2013.
View at: Publisher Site | Google Scholar
M. Liu, W. Zhu, and D. Pei, “System xc−: a key regulatory target of ferroptosis in cancer,” Investigational New Drugs, vol. 39, no. 4, pp. 1123–1131, 2021.
View at: Publisher Site | Google Scholar
F. Ursini and M. Maiorino, “Lipid peroxidation and ferroptosis: the role of GSH and GPx4,” Free Radical Biology and Medicine, vol. 152, pp. 175–185, 2020.
View at: Publisher Site | Google Scholar
Q. Li, J. Liao, W. Chen et al., “NAC alleviative ferroptosis in diabetic nephropathy via maintaining mitochondrial redox homeostasis through activating SIRT3-SOD2/Gpx4 pathway,” Free Radical Biology and Medicine, vol. 187, pp. 158–170, 2022.
View at: Publisher Site | Google Scholar
J. Zhao, I. Tostivint, L. Xu et al., “Efficacy of combined Abelmoschus manihot and irbesartan for reduction of albuminuria in patients with type 2 diabetes and diabetic kidney disease: a multicenter randomized double-blind parallel controlled clinical trial,” Diabetes Care, vol. 45, no. 7, pp. e113–e115, 2022.
View at: Publisher Site | Google Scholar
Y. Liu, S. Wang, G. Jin et al., “Network pharmacology-based study on the mechanism of ShenKang injection in diabetic kidney disease through Keap1/Nrf2/Ho-1 signaling pathway,” Phytomedicine, vol. 118, article 154915, 2023.
View at: Publisher Site | Google Scholar
T. Zhou, Y. Xie, X. Hou et al., “Irbesartan overcomes gemcitabine resistance in pancreatic cancer by suppressing stemness and iron metabolism via inhibition of the Hippo/YAP1/c-Jun axis,” Journal of Experimental & Clinical Cancer Research, vol. 42, no. 1, pp. 1–27, 2023.
View at: Publisher Site | Google Scholar
X. Feng, S. Wang, Z. Sun et al., “Ferroptosis enhanced diabetic renal tubular injury via HIF-1α/HO-1 pathway in db/db mice,” Frontiers in Endocrinology, vol. 12, 2021.
View at: Publisher Site | Google Scholar

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