Skip to main content
Download PDF

Gegen Qinlian decoction (GQD) inhibits ulcerative colitis by modulating ferroptosis-dependent pathway in mice and organoids

Chinese Medicine volume 18, Article number: 110 (2023) Cite this article

Abstract

Background

Gegen Qinlian decoction (GQD) is a classic prescription for treating ulcerative colitis (UC) in traditional Chinese medicine. However, the therapeutic mechanism has not been fully clarified.

Purpose

In the present study, we aimed to evaluate the role of ferroptosis-mediated IEC death in UC treated mice with GQD by using DSS-induced a colitis mouse model and RSL3-induced ferroptosis in intestinal organoids.

Methods

The effects of GQD on DSS-treated colitis were examined via daily body weight, DAI, colon length, HE staining, PAS staining, ZO-1 and Occludin immunohistochemical staining. Ferroptosis was determined by analysis of iron load, MDA, GSH, mitochondrial morphology, and expression of ferroptosis-associated proteins (GPX4, SLC7A11 and ACSL4).

Results

In vivo, GQD administration reduced body weight loss and DAI scores, increased colon length, and improved intestinal histological characteristics and epithelial barrier dysfunction. GQD administration obviously improved the levels of ferroptosis markers (iron load, MDA, GSH, and mitochondrial morphology) and the expression of ferroptosis-associated proteins (GPX4, SLC7A11 and ACSL4). Consistent with in vivo results, GQD administration partially reversed the levels of mtROS, Fe2+ and MDA in intestinal organoids induced by RSL3, and notably improved morphological destruction, histological damage and epithelial barrier dysfunction in organoids.

Conclusions

In this study, we demonstrated that ferroptosis was triggered in DSS-induced experimental colitis and that GQD adiministration could protect against colonic damage and intestinal epithelial barrier dysfunction by inhibiting ferroptosis.

Background

Ulcerative colitis (UC) is an inflammatory bowel disease characterized by long-lasting inflammation, and its typical symptoms include blood and/or mucus in the stool, increased frequency of diarrhea, feelings of incomplete defecation or urgency, and abdominal pain [1]. The incidence of UC is rising annually, with 24.3 per 100000 person-years in Europe, 19.2 per 100000 person-years in North America, and 6.3 per 100,000 person-years in Asia and the Middle East [2]. Multiple factors, such as genetic susceptibility, immune response disorder, microbiome imbalance and environmental stimulation, are considered to be possible causes, and intestinal epithelial barrier dysfunction also plays a vital role in the pathogenesis of UC [3, 4]. Intestinal epithelial cells (IEC) are part of the epithelial barrier, not only acting as the physical structure that separates the intestinal lumen from the body, but also actively participating in intestinal barrier functions [5, 6]. Complete regeneration of IEC promotes mucosal healing, helping to maintain long-term relief of symptoms in UC patients and reduce the risk of surgery [7]. Therefore, IEC play an important role in the pathogenesis and treatment of UC and deserve further research.

Excessive programmed death of IEC can lead to intestinal barrier dysfunction, causing pathogenic microbes to invade the intestinal mucosa and cause an abnormal immune response, which is the key mechanism of intestinal inflammation and ulcer formation [8]. Ferroptosis is a newly discovered type of programmed cell death characterized by iron dependence and lipid-based reactive oxygen species (ROS) accumulation, accompanied by severe oxidative stress and inflammatory reactions [9]. These cells secrete proinflammatory mediators such as high mobility group protein B1, arachidonic acid, leukotrienes and prostaglandins, strongly activating the innate immune system and leading to the release of inflammatory cytokines, leading to the destruction of IEC and intestinal hyperpermeability [10, 11]. Several studies have reported that ferroptosis is involved in IEC death and that ferrostatin-1, a ferroptosis inhibitor, can effectively alleviate the pathological phenotypes of DSS-induced UC [12,13,14,15]. Moreover, iron supplements increased the permeability of IECs and exacerbated UC symptoms in both patients and murine models [16, 17]. Thus, ferroptosis is considered an important contributor to IEC death, implying a potential therapeutic target for UC.

Gegen Qinlian decoction (GQD) originates from Treatise on Febrile Diseases and is composed of Puerariae Radix Lobatae, Glycyrrhizae Radix et Rhizoma, Scutellariae Radix, and Coptidis Rhizoma. It has the effect of relieving superficies and clearing interior, and is a classic prescription used to treat acute diarrhea. Previous studies have shown that GQD can effectively reduce intestinal oxidative stress, inhibit acute intestinal inflammation, and repair intestinal mucosal damage, which has therapeutic effect on UC [18,19,20]. In the present study, we found that GQD administration led to significant ferroptosis reduction and symptom improvements in a DSS-induced colitis mouse model. In vitro, GQD inhibited the injury caused by ferroptosis in intestinal organoids. Thus, it is intriguing to elucidate the possible role of ferroptosis inhibition in the protective effect of GQD on intestinal injury in UC.

Methods

Preparation and quality control of GQD

Four drugs, Puerariae Radix Lobatae, Glycyrrhizae Radix et Rhizoma, Scutellariae Radix, and Coptidis Rhizoma, were decocted twice. First, 8 times the amount of water was added to the decoction, which was boiled for 40 min under low heat, and the filtrate was collected. The second time, 6 times the amount of water was added to the decoction, which was boiled for another 30 min, and the filtrate was collected. Then, two filtrates were combined, and the liquid was concentrated with high heat until a thick paste was obtained. The thick paste was dried into powder (concentration of 3.40 g/g) by vacuum drying (80 ℃, −0.1 Mpa). According to pharmacopoeia, the four main compounds (Puerarin, Baicalin, Berberine, and Glycyrrhizic acid) of GQD were analyzed.

The HPLC experimental conditions were as follows: In baicalin detection, methanol-water-phosphoric acid (47:53:0.2) was used as the mobile phase, and the detection wavelength was 280 nm; in puerarin detection, methanol-water (25:75) was used as the mobile phase, and the detection wavelength was 250 nm; in glycyrrhizic acid detection, acetonitrile was used as mobile phase A, and 0.05% phosphoric acid solution was used as mobile phase B for gradient elution; in berberine detection, 12 mM ammonium acetate-0.5% glacial acetic acid was used as mobile phase A, and acetonitrile (0.1% formic acid) was used as mobile phase B for gradient elution, and the detection wavelength was 345 nm. The above detection column temperature was 35 ℃, and the injection volume was 10 µL. The analytical standards used in the experiment were as follows: puerarin (Cat No.RS00431120, purity ≥ 98%, NATURESTANDARD), baicalin (Cat No.RS01861120, purity ≥ 98%, NATURESTANDARD), berberine (Cat No.RS03071120, purity ≥ 98%, NATURESTANDARD), and glycyrrhizic acid (Cat No. RS01671120, purity ≥ 98%, NATURESTANDARD).

DSS-induced UC mouse model establishment and pharmaceutical treatment

Male C57BL/6 mice (6–8 weeks) were obtained from Beijing Vital River Laboratory Animal Technology Limited Company (Beijing, China). Mice were housed at a controlled temperature (25 °C) and photoperiod (12 h:12 h light-dark cycle). Mice were divided into different treatment groups after adaptation. All procedures were approved by the ethical committee of the Experimental Research Center, China Academy of Chinese Medicine Science (approval number: ERCCACMS21-2109-01).

For induction of the acute UC model, mice were administered 3% dextran sulfate sodium Salt (DSS) (MP Biomedicals) daily for one week. Mice were randomly divided into six groups: control, DSS, DSS + low dose of GQD (L-GQD), DSS + medium dose of GQD (L-GQD), DSS + high dose of GQD (L-GQD) and DSS + mesalazine group (MS). The GQD- and MS- treated groups were given GQD (0.86 g/kg/d, 1.72 g/kg/d and 3.44 g/kg/d) and MS (300 mg/kg/d) separately by gavage once a day for a week, and the doses were converted from clinically equivalent doses for humans. In the experiment, the dosage was calculated according to the ratio of Equivalent dose converted from the surface area between human and mouse (mice dose = 9.1 × mg/kg).

Disease activity index(DAI)

The body weight, fecal viscosity and fecal occult blood of mice were recorded daily. The DAI score was based on a combination of percentage of weight loss (0 for unchanged weight, 1 for 1–5% reduction, 2 for 6–10% reduction, 3 for 10–20%, and 4 for greater than 20% reduction), fecal viscosity (0 for normal, 1 for soft, 2 for mucus-like, and 3 for dilute), and fecal occult blood (0 for negative, 1 for light blue, 2 for blue, 3 for dark blue, and 4 for gross blood stool). The fecal occult blood was detected by the o-toluidine method, in which the color change was observed after collecting stools and adding o-toluidine and oxidant solution (Cat No.TC0511, LEAGENE).

Hematoxylin-eosin and peridic acid-schiff staining

Colonic tissue was fixed with 4% paraformaldehyde for 24 h, dehydrated, embedded in paraffin, and sliced (4 μm), followed by hematoxylin-eosin (HE) and peridic acid-schiff (PAS) staining. Organoids were fixed in Matrigel dome with 2% paraformaldehyde and 0.1% glutaraldehyde for 30 min at room temperature. Then, organoids were placed in 20% sucrose at 4 ℃ overnight. Carefully, the domes were removed from the sucrose solution and placed in an embedding mold containing OCT compound at -80℃. For HE staining, the tissue slices were dewaxed with xylene I and xylene II, followed by stepwise debenzene with a descending ethanol and rinsed with tap water. After nuclear staining, washing, differentiation and other experimental procedures, the slices were dehydrated, transparent, and mounted. For PAS staining, the dewaxed slices were placed in periodic acid solution for 10 min, followed by Schiff solution for 15 min. The slices were then subjected to Mayer hematoxylin restaining, differentiation and blue return. Finally, tissue slices were observed using an optical microscope (Olympus, Japan).

Immunohistochemical staining

After dewaxing the paraffin sections of colonic tissue, they were placed in xylene and anhydrous ethanol reagents in turn. Next, the slices were subjected to antigen retrieval, and the treated slices were drawn in circles. The primary antibodies against ZO-1 (1:200, Cat No. 21773-1-AP, Proteintech) and Occludin (1:200, Cat No. 66378-1-lg, Proteintech) were added dropwise to the circles and incubated overnight. The second day, secondary antibody was added, the sections were dehydrated after color development, and finally mounted on slides.

Transmission electron microscopy

Tissue blocks (1 mm3) were fixed with 2.5% glutaraldehyde, rinsed and dehydrated in ethanol. The tissues were then embedded and cut into 50–70 nm sections with an ultramicrotome and stained with 2% uranyl acetate and lead citrate. Morphological observations and pictures were taken using a transmission electron microscope (H7650, HITACHI).

MDA, GSH and iron level measurement

The malondialdehyde (MDA) content was detected according to the procedure of the lipid peroxidation (MDA) assay kit (Cat No. ab118970, Abcam). Tissue or organoids were homogenized in lysis solution on ice. Then, the sample was centrifuged at 13000 × g for 10 min to collect the supernatant which was incubated with TBA reagent at 95 ℃ for 60 min. After cooling to room temperature in an ice bath for 10 min, the absorbance of the sample was measured immediately on a microplate reader at OD 532 nm. Finally, the concentration of MDA in test samples was calibrated with tissue amount or protein quantification.

For glutathione (GSH) detection (Cat No. ab205811, Abcam), the tissue was resuspended and homogenized in 400 µl of ice-cold PBS/0.5% NP-40 (Cat No. P0013F, Beyotime). Then, the sample was centrifuged for 15 min at 4 ℃ at top speed to remove insoluble material. Next, 50 µl of GSH assay mixture and sample was added to a 96-well plate, followed by incubation at room temperature for 60 min protected from light. Fluorescence was monitored at Ex/Em = 490/520 nm with a fluorescence microplate reader.

Fe2+ was measured according to the procedure of the Iron Assay Kit (Cat No. ab83366, Abcam). Tissue was homogenized in Iron Assay Buffer and centrifuged at 16000 × g for 10 min to remove insoluble material. Five microliters of assays buffer was added to the sample and incubated at 37 ℃ for 30 min. Next, 100 µl of iron probe was added to each well containing the test samples and incubate at 37 ℃ for 60 min protected from light. Finally, output was measured immediately on colorimetric microplate reader at OD 593 nm.

Western blot analysis

Tissues were lysed with RIPA buffer and protease inhibitor. The protein concentrations were measured with the BCA method. Equivalent amounts of total protein were separated by SDS-PAGE and transferred to PVDF membranes. Nonspecific binding was blocked with 5% nonfat milk for 1 h and then incubated overnight at 4 °C with antibodies against glutathione peroxidase 4 (GPX4, 1:1000, Cat No. 67763-1-lg, Proteintech), solute carrier family 7, member 11 (SLC7A11, 1:1000, Cat No. 26864-1-AP, Proteintech), and acyl-CoA synthetase long-chain family member 4 (ACSL4, 1:5000, Cat No. ab155282, Abcam). All membranes were washed 3 times with TBST and incubated for 1 h at room temperature with secondary antibody (1:3000, ZSGB-BIO). The blots were then developed using an ECL detection kit (Cat No. WBKLS0100, Millipore). The developed blots were subjected to grayscale analysis by Image Lab 6.0.

Intestinal organoid culture and drug treatment

Separate the small intestine tissue from the proximal gastric end of C57BL/6 mice approximately 20 cm in length. The small intestine was cut into small segments of approximately 2 mm and transferred to centrifuge tubes, which were washed repeatedly with fresh cold PBS 15–20 times until the supernatant was clarified. Tissue fragments were resuspended in Gentle Cell Dissociation Reagent (Cat No. 07174, Stemcell) and incubated on a shaker for 15 min at room temperature. The tissue fragments were resuspended in cold PBS containing 0.1% BSA and filtered using a 70 μm filter 3 times. The filtrate was collected into a clean conical tube and the precipitate was collected by centrifugation at 290 × g for 5 min. The precipitate was resuspended in prechilled DMEM/F-12. The inoculum volume was counted and calculated at a density of 30 crypt foci per µl. Fifty microliters of the suspension containing 50% Matrigel (Cat No. 356,231, Corning) was inoculated into the center of the prewarmed plates to form droplets, and the inoculated plates were placed at 37 °C for 10 min. After the Matrigel was completely solidified, 750 µl of organoid complete medium (Cat No. 060051, Stemcell) was added. The plates were incubated at 37 °C and 5% CO2, and complete fluid changes were performed three times a week.

To observe the role of GQD in ferroptosis-induced intestinal injury in vitro, the intestinal organoids were randomly divided into 4 groups: (1) control group; (2) GQD group: 40 mg/L GQD was added to the organoids for 24 h; (3) RSL group: 10 µM RSL-3 was added to the organoids for 24 h; and (4) RSL + GQD group: 10 µM RSL-3 and 40 mg/L GQD were added to the organoids for 24 h.

Intestinal permeability determination

FITC-dextran (MW 4000) (Cat No. HY-128,868 A, MCE) is a fluorescent probe that can be used for cell permeability studies. Organoids were incubated with 5 ng/ml FITC-dextran working solution for 60 min at 37 °C in the dark. Then, organoids were washed gently 3 times with PBS buffer. Fluorescence intensity was measured with a fluorescent microscope.

Cell viability assays

The viability of organoids was measured by CellTiter-Glo 3D Cell Viability Assay (Cat No. G9681, Promega). Organoids were cultured in 96-well plates and 100 µl CellTiter-Glo 3D reagent was added to each well. The plate was shaken vigorously for 5 min to induce cell lysis and luminescence was recorded 30 min after reagent addition.

Mitochondrial ROS determination

The production of mitochondrial ROS was measured by MitoSOX Red mitochondrial superoxide indicator (Cat No. M36008, Invitrogen). Organoids were incubated with 5 µM MitoSOX working solution for 10 min at 37 °C in the dark. Then, organoids were washed gently 3 times with warm buffer. Red fluorescence was measured with a fluorescence microscope.

Intracellular ferrous ion (Fe2+) fluorescent probe detection

The organoids were cultured in fluorescent dishes. After treatment, the medium was removed and washed 3 times with HBSS or serum-free medium. FerroOrange working solution (Cat No. F374, DOJINDO) at a concentration of 1 µM was added and incubated for 30 min at 37 °C in a 5% CO2 incubator. After incubation, observations were made directly under a fluorescence microscope.

Whole tissue immunofluorescence detection of organoids

Whole tissue immunofluorescence staining of organoids was performed as previously described using the CytoVista 3D cell transparency/staining kit (Invitrogen, Cat No. V11325) [21]. Anti-ZO-1 antibody and anti-Occludin antibody (1:200) were used to detect protein expression in organoids. Images were captured at 400× with an ECHO immunofluorescence microscope.

Statistical analysis

All results were expressed as the means ± SE. Comparisons between two groups were calculated using Student’s t test. For comparisons involving more than two groups, one-way analysis of variance(ANOVA) with a post hoc Bonferroni multiple comparison test was used to assess the difference. All statistical analyses were performed with GraphPad Prism 7.0 software. <0.05 was considered statistically significant.

Results

Quality control of GQD

High performance liquid chromatography (HPLC) was applied to determine the main compounds of GQD: puerarin, baicalin, berberine and glycyrrhizic acid. Chromatographic analysis showed that the concentrations of puerarin, baicalin, berberine and glycyrrhizic acid were 2.66 mg/g, 5.96 mg/g, 2.37 mg/g and 0.39 mg/g respectively (Fig. 1).

Fig. 1
figure 1

HPLC chromatograms of main ingredients in GQD

Full size image

GQD alleviated DSS-induced colitis and intestinal epithelial barrier dysfunction in mice

To investigate the protective effect of GQD on UC, a mouse model was induced by administrating 3% DSS for 7 days. During the experiment, DSS treatment resulted in weight loss, diarrhea, and bloody stools. Clinical symptoms and pathological features were used to assess the severity of colitis injury. Compared to the DSS group, GQD treatment obviously alleviated symptoms of colitis in DSS-treated mice, as indicated by significantly reduced daily body weight loss and DAI and increased colon length (Fig. 2A and D). Meanwhile, there were no significant changes in the MS group. To further evaluate the protective role of GQD, HE staining, PAS staining, and immunohistochemistry were used to assess colonic damage. As shown, GQD treatment obviously attenuated the loss of crypt and epithelial cells, inflammatory cell infiltration and submucosal edema caused by DSS (Fig. 2E, F). Consistent with the above results, GQD treatment markedly increased the expression of ZO-1 and Occludin, indicators of the integrity of the intestinal mucosal barrier, in DSS-induced colitis. Taken together, these results indicated that GQD treatment improved DSS-induced colonic damage and intestinal epithelial barrier dysfunction in mice.

Fig. 2
figure 2

GQD alleviated DSS-induced colitis. A The change in daily body weight of mice. B The daily DAI scores of mice. C–D Representative pictures of colon tissue and colon length in all groups. E Representative pictures of HE staining, scale bar = 100 μm. F Representative pictures of PAS staining, scale bar = 100 μm. G–H Immunohistochemistry staining of ZO-1 and Occludin, scale bar = 50 μm. Compared with control group, #P < 0.05, ##P < 0.01; compared with DSS group, *P < 0.05, **P < 0.01

Full size image

GQD inhibited ferroptosis in mice with DSS-induced colitis

Ferroptosis is considered a potential therapeutic target for UC. To verify the existence of ferroptosis and its role in DSS-induced colitis, we determined the expression levels of ferroptosis markers. GSH exhaustion, lipid peroxidation, and iron overload are the initial steps of ferroptosis. Compared with the DSS group, the groups administered GQD showed decreased levels of iron load and MDA, and increased levels of GSH in mouse colons (Fig. 3A, C). The change in mitochondrial morphology is a characteristic indicator of ferroptosis [22]. Compared to the control group, we observed obviously shrunken mitochondria with disappearance of mitochondrial cristae and increased mitochondrial membrane density in the DSS group, while GQD and MS treatment improved the aforementioned changes in mitochondria (Fig. 3D). Furthermore, we determined several reported ferroptosis-associated proteins, namely, GPX4, SLC7A11 and ACSL4. GQD treatment increased the expression of GPX4 and SLC7A11, and reduced the expression of ACSL4 in the DSS-damaged colon, especially in the middle-dose group (Fig. 3E, H). On the basis of the findings described above, we concluded that ferroptosis was triggered by DSS and the GQD treatment could inhibit ferroptosis in the colonic IECs of UC.

Fig. 3
figure 3

GQD inhibited ferroptosis in DSS-induced colitic mice. A–C The level of Fe2+, GSH, and MDA in mouse colon tissue. D Electron microscope images of mouse colon tissue, enlarged image showing mitochondria, scale bar = 500 nm. E–H The protein levels of GPX4, SLC7A11 and ACSL4 in mouse colon tissue. Compared with control group, #P < 0.05, ##P < 0.01; compared with DSS group, *P < 0.05, **P < 0.01

Full size image

GQD suppressed RSL3-induced intestinal organoid ferroptosis in vitro

RSL3 is an activator of ferroptosis that binds to and inactivates GPX4, mediating ferroptosis regulated by GPX4. To further investigate the effect of GQD on ferroptosis in IEC, we utilized RSL3 to induce ferroptosis in vitro in intestinal organoids. As shown in Fig. 4A, RSL3 treatment destroyed the normal morphological structure and reduced the germination rate of organoids as observed under a light microscope with increasing dosage. Furthermore, RSL3 administration disrupted intestinal barrier homeostasis characterized by increased fluorescence intensity of fluorescein isothiocyanate (FITC) in organoids. In addition, the viability of organoids decreased with increasing concentrations of RSL3 and GQD (Fig. 4B, C). Based on the above results, we selected 10 μm RSL3 and 40 mg/L GQD for subsequent research. The levels of mitochondrial ROS (mtROS), Fe2+ and MDA were higher in the RSL group than in the control group, which indicates that RSL3 intervention for 24 h can induce ferroptosis in intestinal organoids. Meanwhile, GQD treatment partially reverted the levels of mtROS, Fe2+ and MDA in intestinal organoids induced by RSL3 (Fig. 5). These data suggest that GQD plays an inhibitory role in RSL3-induced ferroptosis in intestinal organoids.

Fig. 4
figure 4

RSL3 induced intestinal organoids injury and GQD treatment. A The morphological structure and FITC fluorescence intensity of intestinal organoids were induced at different concentrations of RSL3 for 24 h, scale bar = 200 μm. BFI is abbreviation for bright field imaging. B–C The viability of organoids at differen concentrations of RSL3 and GQD. Compared with control group, #P < 0.05, ##P < 0.01; compared with DSS group, *P < 0.05, **P < 0.01

Full size image
Fig. 5
figure 5

GQD suppressed RSL3-induced intestinal organoids ferroptosis. A and C Mitochondria ROS level of intestinal organoids, scale bar = 200 μm. B and D Fe2+ level of intestinal organoids, scale bar = 100 μm. E GSH level of intestinal organoids. F MDA level of intestinal organoids. Compared with control group, #P < 0.05, ##P < 0.01; compared with DSS group, *P < 0.05, **P < 0.01

Full size image

GQD treatment protects against ferroptosis-induced colonic damage in intestinal organoids

We next attempted to explore whether GQD treatment plays a role in colonic damage caused by ferroptosis. The results indicated that GQD treatment improved the morphological destruction and reduced the germination rate, and viability of organoids induced by RSL3 (Fig. 6A and B). Moreover, HE and PAS staining were applied to assess the changes in the basic organizational structure of intestinal organoids. As shown in Fig. 6C and D, RSL3 caused collapse of the monolayer structure of IEC and a reduction in goblet cells (shown by arrow), while GQD administration notably improved this histological damage in organoids. In addition, GQD administration restored intestinal barrier homeostasis by increasing the protein expression of tight junction ZO-1 and Occludin (Fig. 6E, F). Altogether, these results suggest that GQD treatment protects against ferroptosis-induced colonic damage in intestinal organoids.

Fig. 6
figure 6

GQD treatment protect against colonic damage in intestinal organoids. A Morphological structure of intestinal organoids, scale bar = 20 μm. B The viability of intestinal organoids. C–D HE and PAS staining of intestinal organoids, scale bar = 20 μm. E Mount organoids immunofluorescence of ZO-1 and Occludin, scale bar = 50 μm. Compared with control group, #P < 0.05, ##P < 0.01; compared with DSS group, *P < 0.05, **P < 0.01

Full size image

Discussion

Currently, the incidence and prevalence of UC continue to rise worldwide. UC patients have difficulty recovering due to prolonged and complex complications, resulting in a huge socioeconomic burden. The treatments for UC mainly include 5-aminosalicylic acid, steroids, immunosuppressants, and biological agents [4, 23]. These treatments have achieved significant progress, but for the majority of UC patients, there are still various issues, such as adverse reactions, lack of response, and susceptibility to tolerance [24]. UC is an advantageous disease in traditional Chinese medicine treatment, with remarkable effects in relieving symptoms, reducing complications, collaborating with Western medicine to alleviate reactions, and prolonging remission [25,26,27]. Recent studies have shown that GQD treatment could regulate the intestinal microbiota, inhibit the immune response, reconstruct damaged mucosa, and maintain intestinal homeostasis in UC [19, 28,29,30]. Similar to the above results, we found that GQD administration could improve DSS-induced experimental colitis in vivo, manifested in a reduction in body weight loss and DAI scores, increased colon length, and improvement in intestinal histological characteristics and epithelial barrier dysfunction. These findings encourage us to further explore the mechanism by which GQD alleviates UC.

Ferroptosis is a programmed cell death characterized by mitochondrial atrophy, elevated Fe2+, decreased intracellular synthesis of GSH, decreased GPX4 activity, increased ROS, and accumulation of lipid metabolites. Increasing evidence suggests that ferroptosis is implicated in the pathogenesis of UC. Dietary iron supplementation promotes DSS-induced colitis in mice, while selective iron chelators and antioxidants can alleviate clinical symptoms and improve colonoscopic manifestations [16, 31]. Xu et al. revealed that ferroptosis was significantly induced in IEC from UC patients and mice with colitis, as ferroptosis was mediated by endoplasmic reticulum (ER) stress signaling [12]. Moreover, NF-κBp65 phosphorylation markedly suppressed ER stress-mediated IEC ferroptosis to alleviate UC. Chen et al. showed that suppressing ferroptosis could effectively ameliorate DSS-induced UC by blocking the Nrf2/HO-1 pathway [14]. Thus, ferroptosis is a potential therapeutic target for UC.

Herein, we found that GQD administration obviously improved the levels of ferroptosis markers (iron load, MDA, GSH, and mitochondrial morphology) and the expression of ferroptosis-associated proteins (GPX4, SLC7A11 and ACSL4) in the colon after DSS challenge, which illustrated that GQD protects against DSS-induced colitis by inhibiting ferroptotic cell death in IECs. Indeed, the main components of GQD were shown to exert anti-ferroptosis effects in multiple diseases. Puerarin can inhibit ferroptosis and inflammation in myocardial and lung injury caused by sepsis [32, 33]. Puerarin also alleviated oxidative-stress-induced brain ferroptosis in rats by activating the AMPK/PGC1α/Nrf2 signaling pathway to exert neuroprotective effects [34]. Berberine is mainly extracted from the stem and root of Coptidis Rhizoma and has been widely used to treat intestinal inflammation [35, 36]. Song et al. indicated that berberine potentially protected against imatinib mesylate-induced cardiotoxicity by inhibiting Nrf2-dependent ferroptosis [37]. Berberine inhibited ferroptosis by reducing ROS generation and lipid peroxidation in cardiac cells [38]. As reported, the therapeutic efficacy of baicalin in various pathologic processes was achieved by suppressing ferroptosis [39,40,41]. Therefore, the main components of GQD have inhibitory effects on ferroptosis, which provides a pharmacological material basis for GQD to attenuate ferroptotic cell death in UC.

To further demonstrate the inhibitory effect of GQD on ferroptosis, we established an RSL3-induced organoid model in this experiment to simulate intestinal ferroptotic injury in UC. Compared with cell lines, organoids are three-dimensional structures with the majority of cell types in intestinal epithelial tissue, and exhibit functions similar to those in vivo. Compared with animal models, organoids avoid the interference of complex factors in vivo, making them more convenient and accurate [42,43,44]. Consistent with the in vivo results, GQD administration partially reverted the levels of mtROS, Fe2 + and MDA in intestinal organoids induced by RSL3 and notably improved morphological destruction, histological damage and epithelial barrier dysfunction in organoids. These data indicate that GQD is able to protect against ferroptosis-induced colonic damage. Contrary to expectations, we found that both RSL3 and GQD can increase the total GSH, which was different from the results in vivo and some studies [45, 46]. We speculated that this might be due to the accumulation of GSH, a synergistic factor of GPX4, caused by RSL3-mediated GPX4 inactivation, and GQD treatment can promote the synthesis of GSH during ferroptosis, which needs further experimental verification.

Nevertheless, some limitations should be acknowledged. First, ferroptotic inhibitors, ferrostatin-1 or deferoxamine, should be applied to demonstrate that ferroptosis is the prominent therapeutic target of IEC death in UC. Second, due to the inherent fate orientation and self-organization of stem cell-derived organoids, organoids are often heterogeneous in size, shape, and cellular composition, which results in some detection not being quantitatively analyzed. In the future, standardization and automation of organoid culture systems are needed. Finally, the specific mechanism by which GQD inhibits ferroptosis remains to be elucidated.

Conclusions

In summary, we demonstrated that ferroptosis was triggered in DSS-induced experimental colitis and that GQD administration could protect against colonic damage and intestinal epithelial barrier dysfunction by inhibiting ferroptosis. Thus, this study provides new insights to increase our understanding of GQD treatment in UC.

Availability of data and materials

The data in this study are available from the corresponding author upon reasonable request.

Abbreviations

DAI:

Disease activity index

DSS:

Dextran sulfate sodium salt

ER:

Endoplasmic reticulum

GQD:

Gegen Qinlian decoction

GSH:

Glutathione

HE:

Hematoxylin-eosin

HPLC:

High performance liquid chromatography

IEC:

Intestinal epithelial cells

MDA:

Malondialdehyde

PAS:

Periodic acid-schiff

ROS:

Reactive oxygen species

UC:

Ulcerative colitis

References

  1. Ordás IEL, Talamini M, Baumgart DC, Sandborn WJ. Ulcerative colitis. Lancet. 2012;380(9853):1606–19.

    PubMed  Google Scholar 

  2. Molodecky NA, Soon IS, Rabi DM, Ghali WA, Ferris M, Chernoff G, Benchimol EI, Panaccione R, Ghosh S, Barkema HW, Kaplan GG. Increasing incidence and prevalence of the inflammatory bowel diseases with time, based on systematic review. Gastroenterology. 2012;142(1):46–e30.

    PubMed  Google Scholar 

  3. Du L, Ha C. Epidemiology and pathogenesis of Ulcerative colitis. Gastroenterol Clin North Am. 2020;49(4):643–54.

    PubMed  Google Scholar 

  4. Kim DH, Cheon JH. Pathogenesis of inflammatory bowel disease and recent advances in biologic therapies. Immune Netw. 2017;17(1):25–40.

    PubMed  PubMed Central  Google Scholar 

  5. Peterson LW, Artis D. Intestinal epithelial cells: regulators of barrier function and immune homeostasis. Nat Rev Immunol. 2014;14(3):141–53.

    CAS  PubMed  Google Scholar 

  6. Nakamura T. Recent progress in organoid culture to model intestinal epithelial barrier functions. Int Immunol. 2019;31(1):13–21.

    CAS  PubMed  Google Scholar 

  7. Scheibe K, Backert I, Wirtz S, Hueber A, Schett G, Vieth M, Probst HC, Bopp T, Neurath MF, Neufert C. IL-36R signalling activates intestinal epithelial cells and fibroblasts and promotes mucosal healing in vivo. Gut. 2017;66(5):823–38.

    CAS  PubMed  Google Scholar 

  8. Patankar JV, Becker C. Cell death in the gut epithelium and implications for chronic inflammation. Nat Rev Gastroenterol Hepatol. 2020;17(9):543–56.

    PubMed  Google Scholar 

  9. Yu H, Guo P, Xie X, Wang Y, Chen G. Ferroptosis, a new form of cell death, and its relationships with tumourous diseases. J Cell Mol Med. 2017;21(4):648–57.

    CAS  PubMed  Google Scholar 

  10. Lewerenz J, Ates G, Methner A, Conrad M, Maher P. Oxytosis/Ferroptosis-(Re-) emerging roles for oxidative stress-dependent non-apoptotic cell death in diseases of the central nervous system. Front Neurosci. 2018;12:214.

    PubMed  PubMed Central  Google Scholar 

  11. Cao JY, Dixon SJ. Mechanisms of ferroptosis. Cell Mol Life Sci. 2016;73(11–12):2195–209.

    CAS  PubMed  PubMed Central  Google Scholar 

  12. Xu M, Tao J, Yang Y, Tan S, Liu H, Jiang J, Zheng F, Wu B. Ferroptosis involves in intestinal epithelial cell death in ulcerative colitis. Cell Death Dis. 2020;11(2):86.

    CAS  PubMed  PubMed Central  Google Scholar 

  13. Luo M, Wu L, Zhang K, Wang H, Zhang T, Gutierrez L, O’Connell D, Zhang P, Li Y, Gao T, Ren W, Yang Y. miR-137 regulates ferroptosis by targeting glutamine transporter SLC1A5 in melanoma. Cell Death Differ. 2018;25(8):1457–72.

    CAS  PubMed  PubMed Central  Google Scholar 

  14. Chen Y, Zhang P, Chen W, Chen G. Ferroptosis mediated DSS-induced ulcerative colitis associated with Nrf2/HO-1 signaling pathway. Immunol Lett. 2020;225:9–15.

    CAS  PubMed  Google Scholar 

  15. Xu J, Liu S, Cui Z, Wang X, Ning T, Wang T, Zhang N, Xie S, Min L, Zhang S, Liang C, Zhu S. Ferrostatin-1 alleviated TNBS induced colitis via the inhibition of ferroptosis. Biochem Biophys Res Commun. 2021;573:48–54.

    CAS  PubMed  Google Scholar 

  16. Seril DN, Liao J, Ho KL, Warsi A, Yang CS, Yang GY. Dietary iron supplementation enhances DSS-induced colitis and associated colorectal carcinoma development in mice. Dig Dis Sci. 2002;47(6):1266–78.

    CAS  PubMed  Google Scholar 

  17. Kobayashi Y, Ohfuji S, Kondo K, Fukushima W, Sasaki S, Kamata N, Yamagami H, Fujiwara Y, Suzuki Y, Hirota Y. Japanese case-control study group for Ulcerative colitis. Association between dietary iron and zinc intake and development of ulcerative colitis: a case-control study in Japan. J Gastroenterol Hepatol. 2019;34(10):1703–10.

    CAS  PubMed  Google Scholar 

  18. Li Q, Cui Y, Xu B, Wang Y, Lv F, Li Z, Li H, Chen X, Peng X, Chen Y, Wu E, Qu D, Jian Y, Si H. Main active components of Jiawei Gegen Qinlian decoction protects against ulcerative colitis under different dietary environments in a gut microbiota-dependent manner. Pharmacol Res. 2021;170:105694.

    CAS  PubMed  Google Scholar 

  19. Zhao Y, Luan H, Jiang H, Xu Y, Wu X, Zhang Y, Li R. Gegen Qinlian decoction relieved DSS-induced ulcerative colitis in mice by modulating Th17/Treg cell homeostasis via suppressing IL-6/JAK2/STAT3 signaling. Phytomedicine. 2021;84:153519.

    CAS  PubMed  Google Scholar 

  20. Zhang J, Wang X, Xu L, Zhang Z, Wang F, Tang X. Investigation of potential genetic biomarkers and molecular mechanism of Ulcerative colitis utilizing bioinformatics analysis. Biomed Res Int. 2020;2020:4921387.

    PubMed  PubMed Central  Google Scholar 

  21. Wang X, Zhang. J Q. Research progress and preliminary exploration of detection methods for gut organoid models chinese. J Cell Biol. 2022;44(02):326–31.

    CAS  Google Scholar 

  22. Xie Y, Hou W, Song X, Yu Y, Huang J, Sun X, Kang R, Tang D. Ferroptosis: process and function. Cell Death Differ. 2016;23(3):369–79.

    CAS  PubMed  PubMed Central  Google Scholar 

  23. Yan PG, Li JN. Standardized diagnosis and treatment of ulcerative colitis. Chin J Intern Med. 2021;60(6):567–70.

    CAS  Google Scholar 

  24. Segal JP, LeBlanc JF, Hart AL. Ulcerative colitis: an update. Clin Med. 2021;21(2):135–9.

    Google Scholar 

  25. Liu Y, Li BG, Su YH, Zhao RX, Song P, Li H, Cui XH, Gao HM, Zhai RX, Fu XJ, Ren X. Potential activity of traditional chinese medicine against Ulcerative colitis: a review. J Ethnopharmacol. 2022;289:115084.

    CAS  PubMed  Google Scholar 

  26. Zheng S, Xue T, Wang B, Guo H, Liu Q. Chinese medicine in the treatment of ulcerative colitis: the mechanisms of signaling pathway regulations. Am J Chin Med. 2022;50(7):1781–98.

    CAS  PubMed  Google Scholar 

  27. Shen H, Zhang L, Zhu L. Clinical thinking and experience of treating ulcerative colitis with classic formulas. Chin J Integr Traditional Western Med Digestion. 2023;31(04):250–4.

    Google Scholar 

  28. Lv J, Jia Y, Li J, Kuai W, Li Y, Guo F, Xu X, Zhao Z, Lv J, Li Z. Gegen Qinlian decoction enhances the effect of PD-1 blockade in colorectal cancer with microsatellite stability by remodelling the gut microbiota and the tumour microenvironment. Cell Death Dis. 2019;10(6):415.

    PubMed  PubMed Central  Google Scholar 

  29. Wang XHS, Zhang M, Su Y, Pan Z, Liang J, Xie X, Wang Q, Chen J, Zhou L, Luo X. Gegen Qinlian decoction activates AhR/IL-22 to repair intestinal barrier by modulating gut microbiota-related tryptophan metabolism in ulcerative colitis mice. J Ethnopharmacol. 2023;302(Pt B):115919.

    CAS  PubMed  Google Scholar 

  30. Yu YCJ, Zhang X, Wang Y, Wang S, Zhao L, Wang Y. Identification of anti-inflammatory compounds from Zhongjing formulae by knowledge mining and high-content screening in a zebrafish model of inflammatory bowel diseases. Chin Med. 2021;16(1):42.

    CAS  PubMed  PubMed Central  Google Scholar 

  31. Millar AD, Rampton DS, Blake DR. Effects of iron and iron chelation in vitro on mucosal oxidant activity in ulcerative colitis. Aliment Pharmacol Ther. 2000;14(9):1163–8.

    CAS  PubMed  Google Scholar 

  32. Xu B, Wang H, Chen Z. Puerarin inhibits ferroptosis and inflammation of Lung Injury caused by Sepsis in LPS Induced Lung epithelial cells. Front Pediatr. 2021;9:706327.

    PubMed  PubMed Central  Google Scholar 

  33. Zhou B, Zhang J, Chen Y, Liu Y, Tang X, Xia P, Yu P, Yu S. Puerarin protects against sepsis-induced myocardial injury through AMPK-mediated ferroptosis signaling. Aging. 2022;14(8):3617–32.

    CAS  PubMed  PubMed Central  Google Scholar 

  34. Huang Y, Wu H, Hu Y, Zhou C, Wu J, Wu Y, Wang H, Lenahan C, Huang L, Nie S, Gao X, Sun J. Puerarin attenuates oxidative stress and ferroptosis via AMPK/PGC1α/Nrf2 pathway after subarachnoid hemorrhage in rats. Antioxidants. 2022;11(7):1259.

    CAS  PubMed  PubMed Central  Google Scholar 

  35. Zhang W, Xu JH, Yu T, Chen QK. Effects of berberine and metformin on intestinal inflammation and gut microbiome composition in db/db mice. Biomed Pharmacother. 2019;118:109131.

    CAS  PubMed  Google Scholar 

  36. Li Y, Wen H, Ge X. Hormesis Effect of Berberine against Klebsiella pneumoniae is mediated by Up-Regulation of the Efflux Pump KmrA. J Nat Prod. 2021;84(11):2885–92.

    CAS  PubMed  Google Scholar 

  37. Song C, Li D, Zhang J, Zhao X. Berberine hydrochloride alleviates imatinib mesylate - induced cardiotoxicity through the inhibition of Nrf2-dependent ferroptosis. Food Funct. 2023;14(2):1087–98.

    CAS  PubMed  Google Scholar 

  38. Yang KT, Chao TH, Wang IC, Luo YP, Ting PC, Lin JH, Chang JC. Berberine protects cardiac cells against ferroptosis. Tzu Chi Med J. 2022;34(3):310–7.

    PubMed  PubMed Central  Google Scholar 

  39. Zhao S, Huang M, Yan L, Zhang H, Shi C, Liu J, Zhao S, Liu H, Wang B. Exosomes derived from baicalin-pretreated mesenchymal stem cells alleviate hepatocyte ferroptosis after acute liver injury via the Keap1-NRF2 pathway. Oxid Med Cell Longev. 2022;2022:8287227.

    PubMed  PubMed Central  Google Scholar 

  40. Zheng B, Zhou X, Pang L, Che Y, Qi X. Baicalin suppresses autophagy-dependent ferroptosis in early brain injury after subarachnoid hemorrhage. Bioengineered. 2021;12(1):7794–804.

    CAS  PubMed  PubMed Central  Google Scholar 

  41. Fan Z, Cai L, Wang S, Wang J, Chen B. Baicalin prevents myocardial ischemia/reperfusion injury through inhibiting ACSL4 mediated ferroptosis. Front Pharmacol. 2021;12:628988.

    CAS  PubMed  PubMed Central  Google Scholar 

  42. Sato T, Stange DE, Ferrante M, Vries RG, Van Es JH, Van den Brink S, Van Houdt WJ, Pronk A, Van Gorp J, Siersema PD, Clevers H. Long-term expansion of epithelial organoids from human colon, adenoma, adenocarcinoma, and Barrett’s epithelium. Gastroenterology. 2011;141(5):1762–72.

    CAS  PubMed  Google Scholar 

  43. Zur Bruegge TF, Liese A, Donath S, Kalies S, Kosanke M, Dittrich-Breiholz O, Czech S, Bauer VN, Bleich A, Buettner M. Intestinal organoids in colitis research: focusing on variability and cryopreservation. Stem Cells Int. 2021;2021:9041423.

    PubMed  PubMed Central  Google Scholar 

  44. Wu X, Li Z, Zhang H, He F, Qiao M, Luo H, Zhang J, Zhang M, Mao Y, Wagstaff W, Zhang Y, Niu C, Zhao X, Wang H, Huang L, Shi D, Liu Q, Ni N, Fu K, Haydon RC, …, Wang N. Modeling colorectal tumorigenesis using the organoids derived from conditionally immortalized mouse intestinal crypt cells (ciMICs). Genes Dis. 2021;8(6):814–26.

    CAS  PubMed  PubMed Central  Google Scholar 

  45. Hu J, Gu W, Ma N, Fan X, Ci X. Leonurine alleviates ferroptosis in cisplatin-induced acute kidney injury by activating the Nrf2 signalling pathway. Br J Pharmacol. 2022;179(15):3991–4009.

    CAS  PubMed  Google Scholar 

  46. Chen Y, Wang J, Li J, Zhu J, Wang R, Xi Q, Wu H, Shi T, Chen W. Astragalus polysaccharide prevents ferroptosis in a murine model of experimental colitis and human Caco-2 cells via inhibiting NRF2/HO-1 pathway. Eur J Pharmacol. 2021;911:174518.

    CAS  PubMed  Google Scholar 

Download references

Acknowledgements

Not applicable.

Funding

This work was funded by Special program for training outstanding young scientific and technological talents of Chinese Academy of traditional Chinese Medicine (No. ZZ14-YQ-040, ZZ15-YQ-002) and China Academy of Chinese Medical Sciences Innovation Fund (No. CI2021A01012).

Author information

Authors and Affiliations

  1. Beijing Key Laboratory of Research of Chinese Medicine on Preventional and Treatment for Major Diseases, Experimental Research Center, China Academy of Chinese Medical Sciences, Beijing, 100700, China

    Xue Wang, Jianye Quan, Chengkui Xiu & Jiali Wang

  2. Xiyuan Hospital, China Academy of Chinese Medical Sciences, No.1 Xiyuan Playground, Haidian District, Beijing, 100091, China

    Jiaqi Zhang

Authors
  1. Xue Wang
    View author publications

    You can also search for this author in PubMed Google Scholar

  2. Jianye Quan
    View author publications

    You can also search for this author in PubMed Google Scholar

  3. Chengkui Xiu
    View author publications

    You can also search for this author in PubMed Google Scholar

  4. Jiali Wang
    View author publications

    You can also search for this author in PubMed Google Scholar

  5. Jiaqi Zhang
    View author publications

    You can also search for this author in PubMed Google Scholar

Contributions

XW contributed to experiment performance and manuscript draft. JQ contributed to HPLC analysis of GQD; CX performed the statistical analysis; JW performed partial experiment; JZ contributed manuscript correcting.

Corresponding author

Correspondence to Jiaqi Zhang.

Ethics declarations

Ethics approval and consent to participate

Not applicable.

Consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

Additional information

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Wang, X., Quan, J., Xiu, C. et al. Gegen Qinlian decoction (GQD) inhibits ulcerative colitis by modulating ferroptosis-dependent pathway in mice and organoids. Chin Med 18, 110 (2023). https://doi.org/10.1186/s13020-023-00819-4

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/s13020-023-00819-4

Keywords

Chinese Medicine

ISSN: 1749-8546

Contact us