Mechanism of Xiezhuo Huayu Yiqi Tongluo Formula in the Treatment of Uric Acid Nephropathy Based on Network Pharmacology, Molecular Docking, and In Vivo Experiments

Background Xiezhuo Huayu Yiqi Tongluo Formula (XHYTF) consists of 14 Chinese herbal medicines. In this study, we investigated the potential mechanism of XHYTF in the treatment of uric acid nephropathy (UAN) through network pharmacology, molecular docking, and in vivo methods. Methods Using various pharmacological databases and analysis platforms, information on the active ingredients and targets of Chinese herbal medicine was collected, and UAN disease targets were retrieved using OMIM, Gene Cards, and NCBI. Then common target proteins were integrated. A Drug-Component-Target (D-C-T) map was constructed to screen core compounds and build a protein-protein interaction (PPI) network. Further, Gene Ontology (GO) enrichment analysis and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analysis were performed for common targets, and a Drug-Component-Target-Pathway (D-C-T-P) network diagram was constructed. The molecular docking simulation was performed to verify the binding affinity between core components and hub targets. Subsequently, the UAN rat model was established, followed by the collection of serum and renal tissues. The expression levels of indicators in the serum were determined using an enzyme-linked immunosorbent assay. The pathological changes of renal tissues were detected using H & E staining and Masson staining. The expression of related proteins in renal tissue was detected by western blot. Results In the study, 216 active ingredients and 439 targets in XHYTF were screened, and 868 targets were identified as being related to UAN. Among them, 115 were common targets. Based on the D-C-T network, quercetin, luteolin, β-sitosterol, and stigmasterol were observed to be the key active ingredients of XHYTF that were effective against UAN. The analysis of the PPI network revealed TNF, IL6, AKT1, PPARG, and IL1β as the 5 key targets. GO enrichment analysis revealed that the pathways were mainly concentrated in cell killing, regulation of signaling receptor activity, and other activities. Subsequently, KEGG pathway analysis revealed that multiple signaling pathways, including the HIF-1, PI3K-Akt, IL-17, and other signaling pathways, were closely related to the action of XHYTF. All 5 key targets were confirmed to interact with all core active ingredients. In vivo experiments indicated that XHYTF significantly reduced blood uric acid and creatinine levels, alleviated inflammatory cell infiltration in kidney tissues, reduced the levels of serum inflammatory factors such as TNF-α and IL1β, and ameliorated renal fibrosis in rats with UAN. Finally, western blot revealed decreased levels of PI3K and AKT1 proteins in the kidney, which confirmed the hypothesis. Conclusion Collectively, our observations demonstrated that XHYTF significantly protects kidney function, including alleviation of inflammation and renal fibrosis via multiple pathways. This study provided novel insights into the treatment of UAN using traditional Chinese medicines.


Introduction
Uric acid nephropathy (UAN) is caused by disrupted purine metabolism, resulting in excessive blood uric acid levels, excessive or reduced renal excretion, and supersaturated deposition of uric acid in the serum, resulting in deposits in the medulla, interstitium, or distal collecting duct, causing kidney damage. Patients with hyperuricemia had a 2.14-fold higher risk of developing chronic kidney disease (CKD) than patients with normal UA levels [1]. As observed in animal models of UAN and by studying the changes in human renal pathology, the main pathological manifestations of UAN were observed to be difuse tubulointerstitial lesions, renal arteriosclerosis, and tubular epithelial cell injury [2][3][4]. At present, the treatment of UAN mainly focuses on inhibiting uric acid production and promoting uric acid excretion using frst-line drugs such as allopurinol and benzbromarone. However, their clinical application is often limited because of their serious side efects. Terefore, it is here that various researchers' diferent studies converge to explore the intervention measures of UAN, which are crucial.
Traditional Chinese medicine (TCM) has its own unique understanding of the pathogenesis of UAN. Numerous studies indicated that TCM may be benefcial in treating UAN in a multitarget and multipathway manner [5][6][7]. . During the past decades, some extracts of traditional Chinese medicine in this formula have been proven to play an important role in the treatment of uric acid nephropathy. For example, studies have shown that the root extract of Rhizoma smilacis glabrae has antioxidant, anti-infammatory, and immune regulation properties, lowering uric acid levels, reducing infammatory cell infltration of kidney tissue, protecting kidneys, and so on [8]. Rhein, the active ingredient of Chinese rhubarb, can inhibit infammatory damage and has a protective efect on UAN [9]. Te therapeutic mechanism of XHYTF on UAN may involve a complex system of multiple components, multiple targets, and multiple pathways, which requires a more extensive study in accordance with the overall strategy.
Network pharmacology is an emerging research approach, which acts as a catalyst for revealing the biological basis of herbal formulations [10]. By integrating multidisciplinary information, a component-protein/gene-pathway network model can be obtained to systematically analyze the potential mechanisms of drugs, which can be used to understand the mechanism of action of TCM in the treatment of diseases. In this study, based on the network pharmacology research strategy, we assessed the interaction of XHYTF with the correlative molecular network of UAN through target prediction, network construction, pathway enrichment analysis, molecular docking, and other biological information technologies combined with animal experiments. Te predicted results were verifed to comprehensively explore the mechanism of action of XHYTF in UAN. Te detailed fow chart of the study design is given in Figure 1.  Te threshold was set to oral bioavailability (OB) ≥30% and drug likeness (DL) ≥0.18 for further fltering to obtain the active ingredients; this was supplemented by a literature search to continue including the active ingredients that had been deleted because of OB and DL thresholds but had research signifcance in the follow-up study. Pheretima could not be retrieved in TCMSP; therefore, the active ingredients could be collected by searching the CNKI database (https://www.cnki.net/) and using the PubChem database (https://Pubchem.ncbi.nlm.nih.gov/). SMILE structures of potential active ingredients were collected and imported into the SwissTargetPrediction database (https://www. swisstargetprediction.ch/) to predict potential targets. Selection probability >0 and TOP10 target genes were used as targets of the Pheretima. All targets were normalized to gene ID using the annotation fle of the UniProt database (https:// www.uniprot.org/). Te screened active ingredients and potential targets of XHYTF were imported into Cytoscape 3.7.1 (Institute of Systems Biology, US) to construct a network diagram of Drug-Component-Target (D-C-T).

Construction of a D-C-T Network.
Based on the above analyses, the compounds corresponding to common targets were matched with the drugs corresponding to the compounds. Further, Cytoscape 3.7.1 was used to construct a D-C-T network diagram, which was used for fshing the key active ingredients.

Construction of the Protein-Protein Interaction (PPI)
Network. Te obtained intersection targets were uploaded to the STRING database (https://string-db.org/). Te targets had the gene type Homo sapiens and selective PPI networks with a medium confdence level ≥0.400, and the free nodes were hidden. Te PPI network information was imported into Cytoscape 3.7.1, using "Network Analyzer" to calculate the topology parameters of the protein interaction network. Te node size and color refect degree value, and the edge thickness refects the combined score. Finally, the protein interaction network was obtained and visualized. Te targets with degree values in the top 5 were selected as the core targets.

Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) Pathway Enrichment Analyses.
Gene ontology (GO) functional annotation was conducted using the ClueGO plug of Cytoscape3.7.1, and the modules Biological Process (BP), Cell Compound (CC), and Molecular Function (MF) were selected. Te ClueGO network was created using Kappa statistics. Representative GO terms and pathways were selected using predefned flters. Te importance of these pathways and their similarity in related genes is automatically mapped onto the network and illustrated in diferent interchangeable visual styles [11]. Simultaneously, the common targets of XHYTF and UAN were added to Metascape (https://metascape.org/gp/index. html#/main/Step1) to perform KEGG pathway analysis. Te results with min overlap � 3, min enrichment � 1.5, and P < 0.01, were screened for the analysis of enrichment and sorted as per ascending P values. Te top 15 pathways ranked by KEGG were obtained. Additionally, the Omic-Share Tools online platform (https://www.omicshare.com/ tools/) was used to map the bubble chart of the KEGG enrichment analysis.

Construction of a Drug-Component-Target-Pathway
Network. Te 15 pathways obtained as mentioned in Section 2.1.5, their targets, corresponding compounds of the targets, and corresponding drugs of the compounds were collected to construct the network diagram of Drug-Component-Target-Pathway (D-C-T-P). Te nodes in the fgure represent drugs, components, targets, and pathways. Te bands represent the correlation between them, and the width of the bands refects the strength of the correlation.
2.1.7. Molecular Docking. 2D structures of the key active ingredients of XHYTF were downloaded from the PubChem database, and crystal structures corresponding to core targets were obtained from the RCSBPDB platform (https:// www1.rcsb.org/). Autodock Vina molecular docking was conducted on the SailVina platform. Molecular docking was performed by preparing the receptor, using Biopython functional correction, preparing the ligand, preparing the docking site, etc. Finally, docking scores were extracted. Te binding activity was evaluated from the docking score value, and the molecular docking results were obtained. Further, Open Babel software (Free Software Foundation, Inc., MA, USA) was used to convert "PDBQT" format to "PDB" format, and the results were visualized using PyMOL software (Schrodinger, the US). Simultaneously, the binding sites were determined on the PLIP website (https://projects. biotec.tu-dresden.de/plip-web/plip/index); the PyMOL results fle format was downloaded; and binding site residues were tagged and visually processed using PyMOL software.    Adenine + Ethambutol mixed suspension: frst, 500 mg sodium carboxymethylcellulose was dissolved in 100 mL distilled water and confgured into 5% sodium carboxymethyl cellulose solution for reserve. Te suspensions of adenine (100 mg/kg·d) and ethambutol (250 mg/kg·d) were prepared by suspending 100 mg adenine and 250 mg ethambutol in 5% carboxymethylcellulose sodium solution, stored at −20°C, and brought to room temperature before use. Allopurinol solution was prepared by mixing 50 mg with normal saline to obtain 100 mL solution (for use and storage, procedures followed were the same as those mentioned above).

Source and Preparation of XHYTF.
Te components of XHYTF used in the study were Coicis Semen 30 g, Smilacis Glabrae Rhizoma 30 g, Persicae Semen 10 g, Pseudobulbus Cremastrae seu Pleiones 9 g, Spatholobus suberectus Dunn 20 g, Hedysarum multijugum Maxim 30 g, Phellodendri chinensis cortex 12 g, Pheretima 15 g, Codonopsis Radix 15 g, Radix Salviae 20 g, Radix Rhei Et Rhizome 3 g, Cyathulae Radix 15 g, Plantaginis Semen 15 g, and Rhizoma Atractylodis 10 g (Te Tird People's Hospital of Fujian Province). To them, 10 times the volume of water was added, followed by soaking for 30 min. Te solutions were boiled twice, 1 h each time. Further, concentrations of 4.2 g/ mL (high dose solubility) were obtained using a rotary evaporator. Te samples were stored in a refrigerator at −20°C, brought to room temperature before use, and diluted as required.

Animals and Models.
A total of 30 male Sprague-Dawley (SD) rats were purchased from the Hangzhou Medical College (Certifcate No.: SCXK (Zhe) 2019-0002, Hangzhou, China). Te animals were reared in the SPF feeding room of the Fujian University of Traditional Chinese Medicine Experimental Animal Center (FJTCM IACUC-2021145). Te animals were group-housed with a 12 h light/ 12 h dark cycle, and the temperature was set at 22-25°C. Te rats were randomly divided into 6 groups: control, model, allopurinol, XHYTF low-dose (XHYTF-L), XHYTF medium-dose (XHYTF-M), and XHYTF high-dose (XHYTF-H) groups. Te rats were allowed to adapt to the environment for 1 week before experiments. Weighing and recording were done before each experiment. Te dosage was calculated based on the adult body weight of 70 kg. Hence, the dosage of XHYTF in rats was calculated according to body surface area [12]. Once a day in the morning for 21 consecutive days, rats in the control group were subjected to normal saline intragastric administration, and those in the other groups were administered with adenine (100 mg/kg·d) and ethambutol (250 mg/kg·d) suspension to establish the UAN model. Te control and model groups were intragastrically administered with equal volumes of normal saline; the allopurinol group was intragastrically administered with 5 mg/kg allopurinol. Te XHYTF-H, XHYTF-M, and XHYTF-L groups were intragastrically administered with 42.12, 21.06, and 10.53 g/kg XHYTF, respectively, once a day in the afternoon for 21 consecutive days.
After the last administration, the rats were fasted for 12 h and deprived from water of 4 h. Tey were anesthetized by intraperitoneal injection with ethyl carbamate solution. Blood was collected through the abdominal aorta, and serum samples were obtained by centrifugation at 3500 rpm for 10 min, which were stored at −80°C. Te bilateral kidneys of rats in each group were separated and weighed. Te right kidney tissue was quickly and carefully separated on an ice plate, and a part of the right kidney tissue was cut, frozen in liquid nitrogen, and stored at −80°C for western blot analysis. Furthermore, partial kidney tissue was cut and fxed with 4% bufered paraformaldehyde for morphological analysis. All the procedures were approved by the Experimental Animal Welfare Committee of the Fujian University of Traditional Chinese Medicine.

Serum Test.
Te levels of serum uric acid (SUA), serum creatinine (Scr), and blood urea nitrogen (BUN) in rats in each group were detected using an automatic biochemical analyzer. Te levels of TNF-α and IL-1β were detected using ELISA according to the manufacturer's protocol. 4 Evidence-Based Complementary and Alternative Medicine

Pathological Analysis of Renal Tissue.
Renal tissue was dehydrated and transparent with gradient ethanol and xylene, embedded in parafn, and stained with HE and Masson's trichrome staining. Te sections were sealed with neutral gum. Te renal tissue sections were carefully observed under a microscope, and images were taken. Tree visual felds in each section were randomly selected, the proportion of collagen-positive area (blue) in the kidney was measured, and the target area of tissue was selected for 200fold imaging. ImageJ analysis software was used to measure the collagen pixel area of Masson-stained sections, and the proportion of collagen deposition area was used to evaluate interstitial fbrosis.

Western Blot.
Renal tissues of each group were lysed with lysis bufer, and the supernatant was collected after centrifugation. A BCA protein concentration assay kit was used to determine the protein concentration. Te same amount of protein was separated by SDS-PAGE and transferred to a PVDF membrane, and the expression levels of target proteins were detected. Protein expression levels were normalized to GAPDH expression levels.

Statistical Analyses.
Relevant data were analyzed using SPSS 26.0 statistical software (SPSS, Chicago, USA). All results were presented as mean ± standard deviation (SD), and a univariate ANOVA was used to test the signifcance of diferences. When variance was not uniform, the rank sum test was used. For the nonparametric tests, the Kruskal-Wallis test was used for the analysis. P < 0.05 was considered signifcant.

UAN-Related Targets and D-C-T Network.
Overall, 358,428 and 36 UAN-related targets were respectively identifed through the GeneCards, OMIM, and NCBI databases. A total of 822 disease targets were obtained after all targets were integrated and repeated values were deleted. Te Venny 2.1 online tool was used to draw a Venn diagram for drug targets and disease targets (Figure 2(a)), and 115 intersection target genes of XHYTF and UAN were obtained. Cytoscape 3.7.1 was used to construct a "D-C-T" network ( Figure 2(b)), which contained 318 nodes and 1597 edges. Yellow triangles represented drugs, orange circles represented compounds, and green diamonds represented targets.
Notably, the size of the node represents the degree value of the node. Te darker the color and larger the area, the more edges sent out by the node. Te closer the correlation degree of D-C-T, the more likely it is to play a crucial role. According to network parameter analysis, the top 4 components by degree value were quercetin (B2), luteolin (D4), beta-sitosterol (B1), and stigmasterol (A2).

PPI Network Analysis.
A PPI network diagram was drawn according to degree and combine score values, with node area representing degree value and line thickness representing combine score value. Te PPI network consisted of 115 nodes with 1823 edges representing PPIs (Figure 2(c)). Te average number of neighbors of the PPT network was 31.704, and the clustering coefcient was 0.660. Moreover, the larger the node, the brighter the color, indicating a larger grade value. Te importance of the target is determined by the degree value. Finally, TNF (79), IL6 (78), AKT1 (77), PPARA (72), and IL1B (69) were defned as the key targets by degree sequencing.   Evidence-Based Complementary and Alternative Medicine

GO and KEGG Pathway Enrichment Analyses. Based on
ClueGO plugins of Cytoscape3.7.1 software, 115 common targets were annotated and analyzed in BP, MF, and CC for GO classifcation and functional annotation, and biological processes with P < 0.05 were screened. Te GO item with a smaller P value was more closely related to the XHYTF treatment UAN. GO analysis results revealed that 824 items were obtained from BP analysis. Te results were reclustered, and "Min Level: 0 and Max Level: 2" was selected for visualization. It mainly involved cell killing, regulation of growth, rhythmic processes, regulation of plasma lipoprotein particle levels, etc. (Figure 3(a)). MF analysis yielded 80 entries, which mainly included regulation signaling receptor activity, antioxidant activity, and positive regulation of DNA-binding transcription factor. "Min Level: 0 and Max Level: 2" were selected for visualization (Figure 3(b)). Overall, 9 items were obtained from CC analysis, mainly involving the GABA receptor complex, vesicle lumen, secretory granule lumen, platelet alpha granule lumen, etc. (Figure 3(c)). Each node represents a term. Te line refects the correlation between terms. Te color of the node refects its enrichment classifcation, and the size of the node indicates its enrichment degree. In total, 184 KEGG pathways were screened from the Metascape database. Te analysis revealed that it was mainly enriched in the AGE-RAGE signaling pathway in diabetic complications, the HIF-1 signaling pathway, the PI3K-Akt signaling pathway, and the TNF signaling pathway. Te top 15 pathways were visualized in the form of a bubble chart according to the P values (Figure 3(d)).

D-C-T-P Network.
Based on the top 15 KEGG enrichment results, the mechanism of action of XHYTF against UAN was comprehensively described by plotting the D-C-T-P Sankey diagram (Figure 4). Te diagram included 14 herbs and 159 compounds, which act on 15 pathways such as IL-17, TNF, and PI3K-Akt signaling pathways through 60 targets.   10 Evidence-Based Complementary and Alternative Medicine 3.6. Molecular Docking Verifcation. Te frst four key components obtained from D-C-T network analysis were docked with the fve potential core targets obtained from PPI network analysis. Te docking score represents the afnity between the protein receptor and the docking ligand. Te lower the docking score, the better the afnity and the more stable the binding of the component to the target (Figure 5(a)). Te docking fraction between 20 pairs of components and targets was lower than −5 (kcal/mol), indicating that better binding afnity existed between 4 compounds and 5 targets. Tis confrmed the scientifc effcacy of XHYTF in treating UAN. Among them, the binding energies of the core components, namely, stigmasterol and β-sitosterol, and the core target, namely, AKT1, were −14.9 kcal·mol −1 , which were the smallest among the 20 docking results. Tese results indicated that stigmasterol and β-sitosterol may exhibit therapeutic efects in UAN by acting on AKT1. We visualized the binding posture and binding site residues of the interaction between the three pairs of composite targets with the lowest docking scores (Figures 5(b)-5(d)).

Serological Observation.
Te levels of SUA, Scr, and BUN were detected. Compared with the control group, the levels of SUA, Scr, and BUN in the serum of rats in the model group were signifcantly increased (P < 0.01), indicating the successful establishment of the UAN rat model. Compared with the model group, SUA, Scr, and BUN levels were signifcantly decreased in the allopurinol and all XHYTF groups (P < 0.05 or P < 0.01) (Figures 6(a)-6(c)). Tese results suggested that XHYTF can reduce uric acid and improve renal insufciency in rats with UAN.
To study the relationship between infammation and UAN, serum TNF-α and IL-1β levels in rats were detected using ELISA. Compared with the control group, the expressions of proinfammatory factors TNF-α and IL-1β in the model group were high (P < 0.01), indicating that infammation was activated in UAN. Compared with the model group, TNF-α and IL-1β levels in the allopurinol and all XHYTF groups were decreased (P < 0.05 or P < 0.01), and the efect was more signifcant in the XHYTF-M group (Figures 6(d) and 6(e)).    Evidence-Based Complementary and Alternative Medicine 13

Renal Histological Observation.
To evaluate the efect of XHYTF on renal histology, the bilateral kidneys of rats in each group were isolated. HE staining was performed on the right kidney of each group to observe renal pathological changes, and Masson's trichrome staining was performed to evaluate extracellular matrix protein deposition in the kidneys. In the control group (P < 0.01), the renal tissue structure was normal without infammatory infltration and uric acid crystals, and no obvious connective tissue hyperplasia was observed in the interstitium. However, renal interstitium was widely observed in the model group, with renal tubular epithelial atrophy, small size or loss of structure, lymphocyte infltration, increased collagen fbers in the interstitium, mild interstitial fbrosis, uric acid crystals, and multinucleated giant cell phagocytosis. Compared with the model group (P < 0.05 or P < 0.01), the allopurinol and all XHYTF groups exhibited reduced renal tubular injury, uric acid crystal deposition, infammatory cell infltration, and interstitial fbrosis levels to varying degrees (Figure 7). Interstitial fbrosis is a common way of renal injury in UAN. We detected extracellular matrix protein deposition in the kidney using Masson trichromatic staining. Te results revealed that the proportion of collagen-positive renal tubule interstitial area increased in the model group and decreased in all other XHYTF groups.

Verifcation of Expression of Proteins Related to the XHYTF-Regulated Pathways.
To investigate whether XHYTF has a regulatory efect on the PI3K-Akt signaling pathway, western blotting was performed to detect the levels of proteins from the PI3K and Akt pathways according to the prediction results of network pharmacology and molecular docking. Compared with the control group, the protein expression of PI3K and AKT was signifcantly increased in the model group (P < 0.01), and it was signifcantly restored by XHYTF treatment (P < 0.05 or P < 0.01) (Figure 8).

Discussion
UAN is characterized by uric acid kidney stones, chronic interstitial nephritis, and interstitial fbrosis, which may eventually lead to chronic renal failure. Te potential role of uric acid in the progression of kidney disease has been demonstrated. Epidemiological studies have consistently reported that SUA is a risk factor for CKD [13]. Elevated SUA levels are associated with tubular injury, infammatory cell infltration, and subsequent tubular interstitial fbrosis [14,15]. Western therapies have focused on benzbromarone and other drugs to promote uric acid excretion by mediating reabsorption and xanthine oxidase inhibitors such as allopurinol and febuxostat to inhibit uric acid production. However, these drugs have limitations because of their low selectivity and toxicity [16][17][18]. TCMs have unique advantages in the treatment of UAN because of the combined characteristics of their multiple components, multiple targets, and multiple pathways. However, their complex pharmacological mechanism is difcult to explain. Network pharmacology is used to study the pathway model of "component-protein/gene-disease" and describe the complexity among biological systems, drugs, and diseases from the perspective of the network model, which is consistent with the overall philosophy of TCM [19]. XHYTF is an empirical prescription used by our research group in the clinical treatment of UAN, and its curative efect is significant. To the best of our knowledge, this is the frst study to use the network pharmacology method and molecular docking simulation to analyze the network molecular mechanism of XHYTF and perform relevant verifcation through in vivo experiments to further explore the potential mechanism of XHYTF in UAN treatment. Te results of network pharmacology and molecular docking revealed the multitarget and multipathway characteristics of XHYTF in treating UAN. Trough data mining, 216 potential bioactive ingredients and 115 UAN-related targets were identifed for XHYTF. Te "D-C-T" network identifed quercetin, β-sitosterol, stigmasterol, and luteolin as the key potential active ingredients. Furthermore, through PPI network analysis of UAN targets, we obtained 5 targets with the highest degree, including TNF, IL6, AKT1, PPARA, and IL-1β. GO functional enrichment and KEGG pathway analyses were performed to explore the biological mechanism of XHYTF. GO analysis suggested that the targets of XHYTF in treating UAN may be involved in cell killing, regulation of growth, rhythmic processes, regulation of signaling receptor activity, the GABA receptor complex, and other processes. KEGG enrichment analysis revealed that the targets were mainly enriched in the AGE-RAGE signaling pathway in diabetic complications, lipids, and atherosclerosis, the HIF-1 signaling pathway, the PI3K-Akt signaling pathway, the TNF signaling pathway, the IL-17 signaling pathway, etc. Among the predicted key compounds, quercetin was the most promising target. It has been reported that quercetin can inhibit renal infammation and fbrosis in UUO and LPS mouse models by decreasing expressions of IL-18, IL-1β, TNF-α, and fbrosis area in Masson staining and inhibiting collagen expression [20]. In addition, quercetin has a protective efect on renal tubular epithelial cell injury induced by oxidative stress in hyperoxaluria rats [21]. Terefore, we verifed the binding ability of the key compounds to the fve core genes through molecular docking simulation, and the docking results revealed that these compounds could stably bind to the active pocket of the core protein. Moreover, in vivo experimental results confrmed that XHYTF may reduce renal fbrosis and infammatory infltration in rats with UAN, release of proinfammatory cytokines (TNF-α and IL-1β) and uric acid levels, and play a role in improving renal function through the targeted regulation of the PI3k/Akt pathway, which verifed the accuracy of our analysis.
Network pharmacology suggested that some of the anti-UAN targets of XHYTF were involved in the above pathways, and molecular docking results revealed that XHYTF exhibited a high afnity for binding with the important targets in the above pathways. Collectively, we speculated that XHYTF may play an antifbrosis and anti-infammatory role in UAN through targeted regulation of the PI3K/AKT pathway. Among the pathological features of UAN, infammatory reaction and fbrinosis are the fundamental pathological mechanisms, whereas the SUA-induced infammatory mechanism pathway has been proven to be the main pathophysiological basis for the development of renal tubular injury and interstitial fbrosis and has been well-accepted as playing an important role in UAN injury [22]. Uric acid can trigger an infammatory cascade by inducing the production of proinfammatory cytokines such as TNF-α and IL-1β, which can cause local renal tubular injury and renal tubular interstitial fbrosis [23,24]. Indeed, in this study, we observed that serum TNF-α and IL-1β levels in rats with UAN were signifcantly increased and signifcantly decreased, respectively, after XHYTF treatment. In addition, renal pathological sections revealed that infammatory infltration and interstitial fbrosis were signifcantly reduced. Masson staining results revealed that the proportion of collagenpositive area in the kidney was signifcantly reduced. AKT1, whose full name is RAC-α serine/threonine protein kinase, has been reported to play a role in the regulation of multiple biological efects of activated AKT, including regulation of cell proliferation, survival, and metabolism, and is one of the key molecules activated downstream of the PI3K signaling pathway [25]. It has been reported that the PI3K/ AKT pathway can promote the occurrence of renal infammation, autophagy, and fbrosis [26][27][28]. To further investigate whether the PI3K/AKT signaling pathway is involved in the mechanism of action of XHYTF in UAN, we detected the expressions of PI3K and AKT. Te results revealed that XHYTF could reduce the expression of PI3K and AKT in rats with UAN, suggesting that XHYTF could regulate the PI3K/AKT signaling pathway while alleviating UAN. Terefore, the mechanism of action of XHYTF in treating UAN may be related to reducing the release of infammatory factors and alleviating renal fbrosis; however, the specifc molecular mechanism needs further study.

Conclusions
Tis study predicted, screened, analyzed, and verifed potential active ingredients, core genes, and signaling pathways for XHYTF that may play a key role in biological processes through network pharmacology, molecular docking, and in vivo experiments. Our results indicated that XHYTF could alleviate UAN by targeting the PI3K/AKT signaling pathway, downregulating the expression of infammatory cytokines, and reducing collagen fber deposition. Te mechanism of action of XHYTF in treating UAN might involve the synergistic efect of "multicomponents, multitargets, and multipathways." Although these preliminary fndings could not fully explain the potential mechanism of XHYTF in UAN, this study provided novel insights for further research. More studies are needed to explore the material basis and specifc molecular mechanism of XHYTF in treating UAN, and more clinical studies are needed to verify our conclusions. 16 Evidence-Based Complementary and Alternative Medicine

Data Availability
Te data supporting the fndings of this study will be made available from the corresponding author upon request.