Carthamin yellow improves cerebral ischemia‑reperfusion injury by attenuating inflammation and ferroptosis in rats.

Carthamin yellow (CY), a flavonoid compound extracted from safflower, has been reported to attenuate cardiac ischemia and reperfusion injury. However, whether CY could ameliorate ischemic stroke is not completely understood. In the present study, the preventive effects of CY on experimental ischemic stroke were investigated using middle cerebral artery occlusion (MCAO) model rats. Neurological scores, brain edema, infarct area and microtubule‑associated protein 2 (MAP‑2) immunoreactivity were assessed to evaluate the effects of CY on ischemic brain injury. The involvement of inflammation and ferroptosis were examined to investigate the mechanism underlying the effects of CY. The results demonstrated that 2‑week CY treatment attenuated the neurological deficit score, brain water content and infarct area, and increased MAP‑2 immunoreactivity in the cortex in MCAO model rats. CY administration also deactivated the cortex NF‑κB/NLR family pyrin domain containing 3 inflammasome signaling pathway, and decreased serum TNF‑α, IL‑1β and IL‑6 concentrations. Moreover, CY treatment inhibited Fe2+ and reactive oxygen species accumulation, and reversed acyl‑CoA synthetase long‑chain family member 4, transferrin receptor 1, glutathione peroxidase 4 and ferritin heavy chain 1 protein expression levels in the brain. The levels of glutathione, superoxide dismutase and malondialdehyde in the serum were also reversed by CY treatment. Collectively, the results of the present study demonstrated that CY protected rats against ischemic stroke, which was associated with mitigation of inflammation and ferroptosis.

Introduction

Ischemic stroke, which accounts for 85% of all stroke cases, is the leading cause of destructive cerebrovascular disease, and displays high mortality and morbidity rates (1). To date, pharmacological thrombolysis is the most effective treatment, but displays a golden treatment time, meaning only 3-8% of patients are eligible for this therapy. Therefore, novel therapies against ischemic stroke are required (2). Previous studies have indicated that inflammation and ferroptosis serve significant roles in the development of ischemic stroke (3,4).

The NLR family pyrin domain containing 3 (NLRP3) inflammasome, which consists of NLRP3, apoptosis-associated speck-like protein (ASC) and caspase-1, is an important component of the innate immune system (5). The NLRP3 inflammasome triggers the production of the proinflammatory cytokine, interleukin (IL)-1β, which facilitates the secretion of inflammatory mediators, including tumor necrosis factor (TNF)-α and IL-6 (6). NF-κB is a transcription factor that alters the formation of the NLRP3 inflammasome, and the NF-κB/NLRP3 inflammasome signaling is a key mechanism of ischemic stroke (7). Hippocampal NF-κB mRNA expression, and serum TNF-α and IL-1β levels were increased in response to ischemia stroke (8). Cerebral ischemia-reperfusion injury activated the NLRP3 inflammasome proteins in rats, which could be suppressed by electroacupuncture, leading to improvement of neurological deficit scores and infarct sizes in middle cerebral artery occlusion (MCAO) model rats (9).

Ferroptosis is a novel type of cell death driven by iron-dependent accumulation of lipid-based reactive oxygen species (ROS), which is regulated by the inactivation of glutathione peroxidase 4 (GPX4) that can reduce lipid peroxides at the expense of glutathione (GSH) (10). Numerous proteins are involved in ferroptosis, including acyl-CoA synthetase long-chain family member 4 (ACSL4), transferrin receptor 1 (TFR1) and ferritin heavy chain 1 (FTH1) (11,12). ACSL4 is a lipid metabolism enzyme that is required for ferroptosis, contributing to lipid peroxidation and ferroptosis (13). TFR1 transports iron from the extracellular environment into cells, facilitating the cellular iron pool essential for ferroptosis (14). FTH1 is a major iron storage protein responsible for maintaining the iron balance in cells (15). Ferroptosis is implicated in ischemic stroke (4,16). Increased ROS and iron levels were observed in the brain of ischemic stroke model rodents (17).

Carthamin yellow (CY) is a flavonoid compound isolated from safflower. In Traditional Chinese medicine, it is considered that CY improves blood circulation and alleviates pain; thus, CY is used for the treatment of coronary heart disease, cerebrovascular disease and angiitis in China (18). Antioxidant and anti-inflammatory properties of CY have been reported. CY inhibited lipopolysaccharide-induced activation of TNF-α (19). In vivo and in vitro studies demonstrated that CY protected against cardiac ischemia and reperfusion injury via decreasing ROS release and NLRP3 inflammasome-related inflammatory responses (18). The aforementioned studies indicated that whether CY could ameliorate ischemic stroke by attenuating inflammation and ferroptosis required further investigation. Therefore, the present study investigated the protective effect of CY in ischemic stroke by using MCAO model rats, and explored the involvement of inflammation and ferroptosis in CY-mediated effects to explore the possible underlying mechanisms.

Materials and methods

Animals

A total of 32 male Sprague-Dawley rats (aged 6-8 weeks; 250-280 g) were purchased from Shanghai Sipper-BK Lab Animal Co., Ltd. Animals were housed in an animal center at a controlled temperature (23±1°C) and humidity (60±2%) with 12-h light/dark cycles, and free access to food and water. All experiments were conducted in compliance with the Provision and General Recommendation of Chinese Experimental Animals Administration Legislation and approved by the Institutional Animal Care and Use Ethics Committee at Nanjing University of Chinese Medicine (approval no. 201907A544).

Materials

CY was obtained from Sigma-Aldrich (Merck KGaA; Fig. 1). All antibodies were purchased from Cell Signaling Technology, Inc., ProteinTech Group, ABclonal Technology, Inc. or Abcam.

Figure 1

Chemical structure of carthamin yellow.

Experimental protocol

Animals were randomly divided into the following four groups (n=8 per group): i) Sham; ii) MCAO; iii) CY (20 mg/kg); and iv) CY (40 mg/kg). CY was administered intragastrically to rats once daily for 2 weeks. At 60 min after the last administration, MCAO surgery was performed as previously described (20). At 24 h post-reperfusion, neurological scores, brain water content and infarct volume were determined. Immunofluorescence staining, western blotting and flow cytometry were performed to investigate the potential mechanisms. After neurological scoring, rats were euthanized with 400 mg/kg pentobarbital sodium. The brains were immediately removed, and the cortex and the serum were collected and stored at −80°C until further use.

Neurological scoring

For the evaluation of functional recovery, neurological scores were assessed at 24 h post-MCAO induction by an observer blinded to the treatments as previously reported (20). The neurological scoring ranged from 0 to 4 (normal score, 0; maximal deficit score, 4).

Infarct area assessment

Rats were sacrificed and the brains were rapidly removed. Coronal sections were cut into 2-mm thick slices and stained with 1% 2,3,5-triphenyltetrazolium chloride (TTC; Sigma-Aldrich; Merck KGaA) for 30 min at 37°C followed by fixation with 10% paraformaldehyde for 10 min. Infarction size was assessed using ImageJ software (version 1.52; National Institutes of Health). The size of infarct regions was calculated using the following equation: Infarct rate (%) = Infarct volume/total volume ×100.

Brain water content determination

The wet-dry method was applied to determine brain edema. The brains were immediately removed and weighed to obtain the wet weight. Following drying in an oven at 100°C for >24 h, the brains were weighed to obtain the dry weight. The percentage of brain water content was calculated using the following formula: Brain water content (%) = [(wet weight)−(dry weight)]/(wet weight) ×100.

Immunofluorescence staining

Immunofluorescence staining was performed to detect microtubule-associated protein 2 (MAP-2) and NF-κB expression as previously described (21). Briefly, brain tissues were obtained, fixed with 4% paraformaldehyde for 24 h at room temperature and transferred to 30% sucrose solution. Subsequently, the tissues were frozen in a cryostat machine and cut into frozen sections (10-µm thick) at -20°C. Slices were washed with 0.01 M PBS for 5 min, blocked with 5% goat serum (cat. no. SL038; Solarbio Life Sciences, Inc.) for 1 h at room temperature, and then incubated with rabbit anti-mouse primary antibodies targeted against MAP-2 (1:50; product no. 4542) and phosphorylated (p)-NF-κB p65 (1:500; product no. 3039; both from Cell Signaling Technology, Inc.) at 4°C overnight. After washing, samples were incubated with a goat anti-rabbit Alexa-Fluor IgG secondary antibody (1:100; cat. no. SA00003-2; ProteinTech Group, Inc.) for 1 h at room temperature. Nuclei were stained with DAPI for 10 min at room temperature. Images of the injured cortex were observed under high-power fields (magnification, ×200; Olympus BX53). The percentage of MAP-2- or p-NF-κB p65-positive staining was determined and analyzed using ImageJ software (version 1.52; National Institutes of Health).

Western blotting

Western blotting was performed as previously described (22). Total protein was isolated from samples using TRIzol® (Invitrogen; Thermo Fisher Scientific, Inc.). Nuclear proteins were extracted using Nuclear and Cytoplasmic Protein Extraction reagents (Thermo Fisher Scientific, Inc.) according to the manufacturer's protocol. Protein concentrations were measured using the BCA Protein Assay kit (Thermo Fisher Scientific, Inc.). Equal amounts of protein (50 µg) were separated via 10% or 12% SDS-PAGE and transferred to PVDF membranes. After blocking with 5% BSA (cat. no. A8020; Solarbio Life Sciences, Inc.) for 1 h at room temperature, the membranes were incubated at 4°C overnight with antibodies targeted against: p-NF-κB p65 (1:1,000; product no. 3039), NF-κB p65 (1:1,000; product no. 8242), p-IκBα (1:1,000; product no. 5209), IκBα (1:1,000; cat. no. 4812; all from Cell Signaling Technology, Inc.), NLRP3 (1:1,000; product code ab263899; Abcam), caspase-1 (1:1,000; cat. no. 22915-1-AP; ProteinTech Group, Inc.), IL-1β (1:1,000; cat. no. A1112; ABclonal Technology, Inc.), ACSL4 (1:1,000; cat. no. A14439; ABclonal Technology, Inc.), FTH1 (1:1,000; product no. 4393; Cell Signaling Technology, Inc.), GPX4 (1:1,000; cat. no. A1933; ABclonal Technology, Inc.), TFR1 (TFRC; 1:1,000; cat. no. A5865; ABclonal Technology, Inc.), β-tubulin (1:5,000; cat. no. 10068-1-AP; ProteinTech Group, Inc.) and Lamin A (1:1,000; cat. no. ab8980; Abcam). After washing with TBST (0.1% Tween-20), the membranes were incubated with appropriate secondary antibody (1:5,000; cat. no. SA00001-2; ProteinTech Group, Inc.) for 1 h at room temperature. Protein bands were visualized using an ECL kit (cat. no. 180-501; Tanon Science & Technology Co., Ltd.). Protein expression levels were semi-quantified using ImageJ software (version 1.52; National Institutes of Health) with β-tubulin or Lamin A as the loading control.

Determination of TNF-α, IL-1β, IL-6, malondialdehyde (MDA), GSH and superoxide dismutase (SOD) concentrations in serum

The levels of TNF-α (TNF-α ELISA Kit; cat. no. PT516), IL-1β (IL-1β ELISA Kit; cat. no. PI303), IL-6 (IL-6 ELISA Kit; cat. no. PI328), MDA (MDA detection kit; cat. no. S0131), GSH (GSH detection kit; cat. no. S0052) and SOD (SOD detection kit; cat. no. S0101) in serum were detected using different detection kits (Beyotime Institute of Biotechnology) according to the manufacturer's protocol.

ROS measurement

ROS content was assayed using 2,7-dichlorofluorescin diacetate (DCF), a ROS detection kit (cat. no. H131224; Shanghai Aladdin Bio-Chem Technology Co., Ltd.) according to the manufacturer's protocol.

Iron assay

Iron concentration was assessed using an Iron Assay kit (cat. no. MAK025-1KT; Sigma-Aldrich; Merck KGaA) according to the manufacturer's instructions.

Statistical analysis

Statistical analysis was performed using GraphPad Prism software (version 6; GraphPad Software, Inc.). Data are presented as the mean ± SEM. Comparisons among multiple groups were analyzed using one-way ANOVA followed by Bonferroni's post hoc test. P<0.05 was considered to indicate a statistically significant difference.

Results

CY improves neurological scores

To determine whether CY induced neurological function recovery in MCAO model rats, neurological scores were evaluated at 24 h post-reperfusion (Fig. 2A). MCAO model rats displayed increased neurological deficit scores compared with the Sham group, whereas MCAO model-induced neurological deficits were significantly relieved following treatment with CY. The results suggested that CY improved neurological performance in MCAO model rats.

Figure 2

Effects of CY on neurological deficit scores, brain water content and infarct area. (A) Neurological deficit score. (B) Brain water content. (C and D) Infarct area. Data are presented as the mean ± SEM. ##P<0.01 vs. Sham; *P<0.05 and **P<0.01 vs. MCAO. CY, carthamin yellow; MCAO, middle cerebral artery occlusion.

CY decreases infarction volume and brain water content

MCAO induced a noticeable increase in brain water content in the ischemic hemisphere at 24 h post-reperfusion, which was reduced following CY treatment (Fig. 2B). The infarct volume at 24 h post-reperfusion was determined by performing TTC staining. The results revealed that the infarct area percentage of the brain tissue in MCAO model rats was significantly higher compared with the Sham group, and lower in the CY administration groups compared with MCAO model rats (Fig. 2C and D). The results indicated that CY effectively attenuated the cerebral infarction area and brain water content in MCAO model rats.

CY increases MAP-2 expression in the cortex

To examine the protective effects of CY on neurons, immunofluorescence staining for MAP2 was performed. Obvious MAP-2 immunostaining was observed in the cortex of Sham rats (Fig. 3). However, MAP-2 expression in MCAO model rats at 24 h post-reperfusion was decreased compared with the Sham group. Interestingly, CY successfully enhanced MAP-2 expression following administration for 14 days. The results suggested that CY prevented neuronal damage in MCAO model rats.

Figure 3

MAP-2 expression in the cortex of MCAO model rats. (A) Representative images of immunofluorescence staining for MAP-2. Scale bar, 50 µm. (B) Quantification of MAP-2. Data are presented as the mean ± SEM. ##P<0.01 vs. Sham; *P<0.05 vs. MCAO. MAP-2, microtubule-associated protein 2; MCAO, middle cerebral artery occlusion; CY, carthamin yellow.

CY inhibits inflammation in the cortex

Subsequently, immunofluorescence staining, western blotting and ELISAs were performed to investigate the effects of CY on inflammation. The results demonstrated that in the cortex of MCAO model rats, p-NF-κB p65 expression detected via immunofluorescence staining, as well as the protein expression levels of p-NF-κB p65, p-IκBα, NLRP3, caspase-1 and IL-1β detected via western blotting were significantly increased compared with the Sham group (Figs. 4 and 5). Moreover, NF-κB p65 expression in the nucleus was significantly increased compared with the Sham group. Nonetheless, CY administration successfully reversed MCAO model-induced effects. In addition, the MCAO group displayed evidently higher serum levels of TNF-α, IL-1β and IL-6 (Fig. 6). Notably, following CY treatment, a marked decrease in TNF-α, IL-1β and IL-6 serum levels was observed. Collectively, the results demonstrated that CY treatment inhibited the inflammatory response in the cortex of MCAO model rats.

Figure 4

p-NF-κB expression in the cortex of MCAO model rats. (A) Representative images of immunofluorescence staining for p-NF-κB. Scale bar, 50 µm. (B) Quantification of p-NF-κB. Data are presented as the mean ± SEM. ##P<0.01 vs. Sham; *P<0.05 vs. MCAO. p, phosphorylated; MCAO, middle cerebral artery occlusion; CY, carthamin yellow.

Figure 5

Effects of CY on the NF-κB/NLRP3 inflammasome signaling pathway in the cortex. NF-κB/NLRP3 inflammasome signaling pathway-related protein expression levels were (A) determined via western blotting and (B) semi-quantified. Data are presented as the mean ± SEM. ##P<0.01 vs. Sham; *P<0.05 and **P<0.01 vs. MCAO. CY, carthamin yellow; NLRP3, NLR family pyrin domain containing 3; MCAO, middle cerebral artery occlusion; p, phosphorylated.

Figure 6

TNF-α, IL-1β and IL-6 concentrations in serum. (A) TNF-α, (B) IL-1β and (C) IL-6. Data are presented as the mean ± SEM. ##P<0.01 vs. Sham; *P<0.05 and **P<0.01 vs. MCAO. TNF, tumor-necrosis factor; IL, interleukin; MCAO, middle cerebral artery occlusion; CY, carthamin yellow.

CY attenuates ferroptosis

To determine the involvement of ferroptosis in MCAO model rats, iron and ROS accumulation, lipid peroxidation levels and the expression levels of ferroptosis-related proteins were assessed. MCAO model rats displayed obvious ROS and iron accumulation in the cortex compared with Sham rats (Fig. 7). In addition, increased MDA generation, but reduced GSH levels and SOD activities in the serum were observed in MCAO model rats (Fig. 8). The western blotting results indicated that MCAO challenge significantly increased the protein expression levels of ACSL4 and TFR1 in the cortex, but decreased the protein expression levels of FTH1 and GPX4 (Fig. 9). The aforementioned effects induced by MCAO modeling were significantly ameliorated by treatment with CY, indicating the antiferroptosis efficacy of CY in MCAO model rats.

Figure 7

ROS and iron accumulation in the cortex. (A and B) ROS generation. (C) Fe2+ production. Data are presented as the mean ± SEM. ##P<0.01 vs. Sham; **P<0.01 vs. MCAO. ROS, reactive oxygen species; MCAO, middle cerebral artery occlusion; CY, carthamin yellow; DCF, 2,7-dichlorofluorescin diacetate.

Figure 8

Lipid peroxidation level in serum. (A) GSH, (B) SOD and (C) MDA. Data are presented as the mean ± SEM. ##P<0.01 vs. Sham; *P<0.05 and **P<0.01 vs. MCAO. GSH, glutathione; SOD, superoxide dismutase; MDA, malondialdehyde; MCAO, middle cerebral artery occlusion; CY, carthamin yellow.

Figure 9

Expression levels of ferroptosis-related proteins in the cortex. Ferroptosis-related protein expression levels were (A) determined via western blotting and (B) semi-quantified. Data are presented as the mean ± SEM. ##P<0.01 vs. Sham; *P<0.05 and **P<0.01 vs. MCAO. MCAO, middle cerebral artery occlusion; CY, carthamin yellow; ACSL4, acyl-CoA synthetase long-chain family member 4; FTH1, ferritin heavy chain 1; GPX4, glutathione peroxidase 4; TFR1, transferrin receptor.

Discussion

In the present study, CY-mediated effects on experimental ischemic stroke were investigated. CY improved neurological deficit scores, brain water content, infarct area and MAP-2 expression in MCAO model rats. CY also deactivated the NF-κB/NLRP3 inflammasome signaling pathway in the cortex. In addition, CY treatment decreased the serum concentrations of TNF-α, IL-1β and IL-6. CY also alleviated MCAO-induced ferroptosis, as demonstrated by reduced iron and ROS accumulation, reduced lipid peroxidation level and restored ferroptosis-related protein expression levels.

The MCAO model is one of the models that most closely simulates human ischemic stroke (23). Animals that under-went cerebral ischemia and reperfusion displayed neurological movement disorders and pathological alterations, including brain edema and infarct area (24). In the present study, increased neurological deficit scores, brain water content and cerebra infarct areas were detected in MCAO model rats, suggesting the successful induction of ischemic stroke. However, CY alleviated MCAO-induced neurological deficit, brain edema and infarct area, indicating that CY pretreatment improved neurological function and ischemic brain injury in MCAO model rats.

Ischemic stroke has been reported to damage neurons (25). MAP-2, a protein expressed primarily in neuronal dendrites, is critical for numerous microtubule-related processes, including microtubule assembly, stabilization and cross-linking (26). MAP-2 deficiency following ischemic stroke has been documented in previous studies (27,28). In the present study, decreased MAP-2 immunofluorescence activity was observed in MCAO model rats, indicating MAP-2 defect in ischemic stroke. CY inhibited MCAO-induced reductions in MAP-2, suggesting that CY protected rats against MCAO-induced neuron injury.

Evidence suggests that the post-ischemic inflammatory responses alter the outcome of ischemic stroke (29). NF-κB is a pivotal regulator of inflammation-related gene transcription (30). Studies have revealed that NF-κB could serve as an upstream activator of the NLRP3 inflammasome, which consists of NLRP3, ASC and caspase-1, and contribute to the production of TNF-α, IL-1β and IL-6 (31,32). The NF-κB/NLRP3 inflammasome signaling pathway has been implicated in ischemic stroke (33). Terai et al (25) examined the distribution of NF-κB in brain samples obtained from patients who died following a stroke, and discovered that the immunoreactivity of NF-κB was enhanced in glial cells of infarcted areas compared with control cases. Arctigenin, a phenylpropanoid dibenzylbutyrolactone lignan derived from Arctium lappa L, has been reported to inhibit MCAO-induced neuronal deterioration, cerebral infarct and brain water content by inhibiting NLRP3 inflammasome activation and IL-1β secretion (34). In the present study, NF-κB/NLRP3 inflammasome signaling expression levels were upregulated in the cortex of MCAO model rats, which was accompanied by increased levels of TNF-α, IL-1β and IL-6 in the serum. Following CY administration, the aforementioned MCAO-induced effects were reversed, suggesting the involvement of NF-κB/NLRP3 inflammasome signaling in the pathology and treatment of ischemic stroke.

Ferroptosis is a newly defined cell death process that is characterized by iron-dependent accumulation of lipid peroxides to lethal levels (35). Increasing evidence has highlighted the role of ferroptosis in ischemic stroke (16). The content of free iron and MDA in brain tissues were significantly augmented, whereas levels of GPX4 and GSH were greatly decreased in MCAO model animals (36). Tau ablation protected mice against from MCAO-induced iron accumulation in the brain and inhibited ferroptosis, leading to the attenuation of the ischemia-reperfusion injury including neurological defects, infarct area, motor and cognitive dysfunctions (16). In the present study, MCAO challenge promoted cortex iron and ROS accumulation and serum lipid peroxidation levels, resulting in aberrant expression levels of ferroptosis-related proteins in the brain, whereas treatment with CY inhibited MCAO challenge-induced alterations. The aforementioned results suggested that ferroptosis may partially account for experimental ischemic stroke progression and CY-related treatment effects in MCAO model rats.

Collectively, the results of the present study suggested that CY treatment protected rats against ischemia-reperfusion injury by alleviating inflammation and ferroptosis (Fig. 10). The results indicated that CY may serve as a potential therapeutic agent for ischemic stroke.

Figure 10

Schematic illustration of the proposed mechanism underlying CY-mediated protection against cerebral ischemia-reperfusion injury. CY, carthamin yellow; ACSL4, acyl-CoA synthetase long-chain family member 4; NLRP3, NLR family pyrin domain containing 3; PUFA, polyunsaturated fatty acids; PL, phospholipid.