Through Genecards database (https://www.genecards.org/) CIRI-related genes were investigated. Using Prediction database (https://prediction.charite.de/index.php), search for downstream targets of Res. Human transcription factor database (TFDB) (http://bioinfo.life.hust.edu.cn/HumanTFDB#!/) was used to query human transcription factors. On the jvenn website (https://bioinfogp.cnb.csic.es/tools/venny/index.html), perform intersection analysis on different datasets to generate Venn graphs. In the hTFtarget database (https://guolab.wchscu.cn/hTFtarget//#!/Tf), obtain downstream targets of NR3C2.

Seventy 7-week-old male Sprague-Dawley rats (weighing 230–270 g) were purchased from Hunan SJA Laboratory Animal Co., Ltd. (Hunan, China). All rats were housed under the following conditions: a room temperature of 25 $\pm$ 5 °C, relative humidity of 60 $\pm$ 5%, free access to food and water, a constant 12-hour light/dark cycle, and an adaptation period of 7 days.

Rats were randomly assigned to the following groups: sham, middle cerebral artery occlusion/reperfusion (MCAO/R), Res, overexpression-negative control (OE-NC), OE-NR3C2, OE-NR3C2+sh-NC, and OE-NR3C2+sh-TRIM28, with 10 rats in each group. Rats were anesthetized with 2% isoflurane (HY-A0134, Medchemexpress, Monmouth Junction, NJ, USA), and the left carotid artery, internal carotid artery (ICA), and external carotid artery (ECA) were carefully dissected. Insert a silicone-coated 3-0 monofilament nylon round head suture (Ethicon, Somerville, NJ, USA) into the ICA to close the middle cerebral artery (MCA). After 120 minutes of MCAO, the suture was removed to induce reperfusion and establish a CIRI rat model [18]. Rats in the sham group underwent the same procedure but without carotid artery ligation. All groups, except the Sham and Model groups, received intravenous injection of 30 mg/kg Res (53271ES70, Yeasen, Shanghai, China) at the start of reperfusion [19]. Rats in the OE-NC, OE-NR3C2, OE-NR3C2+sh-NC (sh-NC: 5^′-TTCTCCGAACGTGTCACGTTT-3^′), and OE-NR3C2+sh-TRIM28 (sh-TRIM28: 5^′-ATCATGAAGGAGCTGAATAAA-3^′) groups were injected with adeno-associated virus (AAV). Seven days before MCAO surgery, 4 µL of concentrated virus solution (overexpressed adeno-associated virus (VB900166-4386vrw, Vectorbuilder, Guangzhou, China), interfering adeno-associated virus (VB900185-3370auz, Vectorbuilder)) was stereotactically injected into the ipsilateral ventricle (coordinates: anterior fontanelle: anterior-posterior (AP) 1.1 mm, medial-lateral (ML) 0.8 mm, dorsal-ventral (DV) 4.2 mm). Twenty-four hours after MCAO, rats were euthanized via intraperitoneal injection of 2% pentobarbital sodium (P3761, Sigma-Aldrich, St. Louis, MO, USA) (150 mg/kg), and tissues were collected for subsequent experiments. This study was approved by the Animal Committee of Hunan Evidence-based Biotechnology Co., Ltd. (Hunan, China) (No: 202310007).

The rat PC12 cell line (MZ-2620, Mingzhoubio, Ningbo, China) was validated by short tandem repeats (STR) analysis and was cultured in DMEM (D5796, Sigma-Aldrich, St. Louis, MO, USA) supplemented with 10% FBS (HY-T1000, Medchemexpress, Monmouth Junction, NJ, USA) at 37 °C in a 5% CO₂ humidified incubator until the cells reached 80% confluency [20]. Detect cells for mycoplasma contamination using mycoplasma polymerase chain reaction (PCR) Detection Kit (C0301S, Beyotime, Shanghai, China), and the result were negative. For the oxygen-glucose deprivation/reperfusion (OGD/R) treatment, the PC12 cells were first cultured in Earle’s Balanced Salt Solution (24010043, Thermo Fisher Scientific, Waltham, MA, USA) without glucose and FBS for 24 hours under hypoxic conditions (95% N₂, 5% CO₂, 37 °C). Subsequently, the cells were transferred to DMEM containing normal serum and cultured for an additional 24 hours. During the reoxygenation and re-glucose period, the cells were treated with Res (10 µM) for 24 hours [21].

For lentiviral infection, we utilized lentivirus containing either overexpression of NR3C2 or a negative control, along with sh-TRIM28 (5^′-ATCATGAAGGAGCTGAATAAA-3^′) and its corresponding negative control short hairpin RNA (shRNA) lentivirus (22917-1, Genechem, Shanghai, China). Cells were inoculated at a concentration of 1 $\times$ 10⁵ cells per well in a 24-well plate. Once the cell density reached 60%, the lentivirus solution was added for infection. Cells were harvested 48 hours post-infection for subsequent experimental analysis.

To evaluate the learning ability of rats, they were tested in a circular water pool with a diameter of 1.5 meters, and an external maze was set up in the laboratory to provide visual cues. The platform (with a diameter of 120 centimeters) was submerged 30 cm below the water surface, and the water temperature was maintained between 23 °C and 25 °C. The experiments included positioning and navigation tasks as well as space exploration trials. The positioning and navigation experiment lasted for 5 days, during which rats were placed in the first, second, and fourth quadrants of the pool, and their swimming trajectories were recorded within 120 seconds, with the escape latency defined as the time taken to find the platform. In the space exploration trials, the platform was removed, and rats were placed in the first quadrant, with data collected on the time to swim to the original platform location, the number of platform crossings, and the time spent in the target quadrant. To minimize the effects of circadian rhythm, experiments were conducted at 8 AM and 3 PM in a quiet laboratory with controlled temperature and light intensity [22]. Metrics such as escape latency, time spent in the target quadrant, and platform crossings were tracked and analyzed using ANY-maze video tracking software (DigBehv 4.1.9&1.0.29, YAN-MWMR, Yuyanbio, Shanghai, China).

The Longa scoring system and Bederson rating criteria were used to assess neurological deficits in rats. In the Longa system, 0 points indicate no deficits; 1 point reflects an inability to fully extend the left forepaw with mild deficits; 2 points signify left circling and moderate deficits; 3 points represent severe focal deficits with constant left turning; and 4 points indicate an inability to walk spontaneously and reduced consciousness. In the Bederson criteria, 0 points indicate no deficits; 1 point reflects loss of forelimb flexion; 2 points include loss of forelimb flexion with increased resistance to lateral thrust and reduced postural stability; 3 points signify unidirectional circling; 4 points represent longitudinal rolling or epileptic activity; and 5 points indicate a complete lack of spontaneous activity.

The brain tissue was sectioned into 5–6 consecutive coronal slices and placed in 1% 2,3,5-triphenyl tetrazolium chloride (TTC) buffer (298-96-4, Yeasen, Shanghai, China), followed by incubation at 37 °C for 20 minutes. After incubation, the slices were postfixed in 4% paraformaldehyde (MA0192, Meilune, Dalian, China) for 24 hours and then photographed. The red area represents the non-infarcted tissue portion, while the light white area shows the infarcted tissue portion. The morphometric analysis of the infarcted area was performed using Image (V1.8.0.112, NIH, Madison, WI, USA).

Collect rat brain tissue and fix it with 4% paraformaldehyde for 24 hours. Then the brain tissue was processed into paraffin blocks, sliced into paraffin sections of 4 µm thickness, stained with H&E dye, and observed for cell morphology under a light microscope (CX43, Olympus, Tokyo, Japan).

The preparation of tissue slices is the same as described above. The tissue was stained in 0.1% toluidine blue solution (BL1138A, biosharp, Hefei, China) for 20 minutes, washed with distilled water, and differentiated in 95% ethanol (A507050-0005, Sangon, Shanghai, China) for 15 minutes. Observe the morphological changes of Nissl bodies under an optical microscope (CX43, Olympus, Tokyo, Japan).

The terminal deoxynucleotidyl transferase-mediated deoxyuridine triphosphate nick end labeling (TUNEL) assay kit (C1089, Beyotime, Shanghai, China) was employed to assess cell apoptosis. Cells were fixed in 4% paraformaldehyde for 30 minutes, followed by washing with PBS (P3813, Sigma-Aldrich, St. Louis, MO, USA). To permeabilize the cell membrane, immunostaining permeabilization solution (P0097, Beyotime, Shanghai, China) was applied for 5 minutes at room temperature, then rinsed twice with PBS. TUNEL detection solution was added to the cells, and incubation proceeded at 37 °C in the dark for 60 minutes. After three PBS washes, the cells were mounted with anti-fluorescence quenching mounting medium (HY-K1042, Medchemexpress, Monmouth Junction, NJ, USA) and visualized under a fluorescence microscope. For nuclear staining DAPI (Solarbio, Beijing, China) was applied and incubated in the dark for 10 minutes. Fluorescence intensity was quantified using ImageJ software (V1.8.0.112, NIH, Madison, WI, USA).

Enzyme linked immunosorbent assay (ELISA) kits for TNF-$\alpha$ (PT516, Beyotime, Shanghai, China), IL-6 (PI328, Beyotime, Shanghai, China), and IL-1$\beta$ (88-6010A-22, Thermo Fisher Scientific, Waltham, MA, USA) were employed following the manufacturer’s protocols to measure the expression level of them in tissue homogenates and cell culture supernatants.

Total RNA was isolated from rat brain tissue and PC12 cells from each group using a rapid RNA extraction kit (DP419, Tiangen, Beijing, China), followed by real time quantitative polymerase chain reaction (RT-qPCR) using a fluorescence quantification kit (QR0100, Sigma-Aldrich, St. Louis, MO, USA). GAPDH was used as the internal reference gene, and relative messenger RNA (mRNA) levels were calculated using the 2^{-Δ⁢Δ⁢Ct} method (Table 1).

Total protein from tissues and cells was extracted using radioimmunoprecipitation assay (RIPA) lysis buffer (ab170197, Abcam, Cambridge, UK). Protein concentrations were determined using a bicinchoninic acid (BCA) protein quantification kit (P0010, Beyotime, Shanghai, China). Equal amounts of protein (10 µg) were separated by sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) and transferred onto polyvinylidene fluoride (PVDF) membranes using the wet transfer method (ab133411, Abcam, Cambridge, UK). Seal the membrane with 5% skim milk powder (P0216, Beyotime, Shanghai, China) for 1 hour, then incubate the membrane overnight at 4 °C with the following primary antibodies: NR3C2 (0.1 µg/mL, PA5-79761, Thermo Fisher Scientific, Waltham, MA, USA), B-cell lymphoma 2 (Bcl-2) associated X (Bax) (1:1000, ab32503, Abcam, Cambridge, UK), Bcl-2 (1:500, ab194583, Abcam, Cambridge, UK), Cleaved-caspase-3 (1:500, PA5-114687, Thermo Fisher Scientific, Waltham, MA, USA), microtubule-associated protein 1A/1B-light chain 3 (LC3) (1:500, ab62721, Abcam, Cambridge, UK), Beclin-1 (1:2000, ab207612, Abcam, Cambridge, UK), sequestosome 1/p62 (p62) (1:1000, SAB5701338, Sigma-Aldrich, St. Louis, MO, USA), TRIM28 (1:500, SAB5701273, Sigma-Aldrich, St. Louis, MO, USA), GAPDH (1:2000, ab181602, Abcam, Cambridge, UK). After washing the membrane with TBST (ZS405-3, Zomanbio, Beijing, China), it was incubated with Goat Anti-Rabbit IgG H&L secondary antibody (1:1000, ab6702, Abcam, Cambridge, UK) for 2 hours. Develop using enhanced chemiluminescence (ECL) (A38554, Thermo Fisher Scientific, Waltham, MA, USA) and analyze the bands using ImageJ software (V1.8.0.112, NIH, Madison, WI, USA).

Cell viability experiments were conducted using cell counting kit-8 (CCK-8) assay kit (C0037, Beyotime, Shanghai, China). Inoculate PC12 cells onto a 96 well plate with a cell count of 1 $\times$ 10⁴ per well. After various treatments, 10 µL of CCK-8 reagent and 90 µL of complete culture medium were added to each well, followed by incubation at 37 °C for 2 hours. Absorbance was measured at 450 nm using a Gen5 ELISA reader (BioTek, Winooski, VT, USA).

Binding sites for NR3C2 on the TRIM28 promoter were predicted using JASPAR (https://jaspar.elixir.no/search?q=HLAA&collection=CORE&tax_group=vertebrates&tax_id=9606&type=all&class=all&family=all&version=all). The top three binding sites with the highest scores were mutated. Wild-type (WT) TRIM28 promoter sequences and binding site-mutated (MUT) TRIM28 promoter sequences were cloned into the pGL3 luciferase vector (Promega, Madison, WI, USA) to construct the TRIM28-WT and TRIM28-MUT vectors, respectively. Site-directed mutagenesis to generate TRIM28-MUT was performed using a site-directed mutagenesis kit (Agilent, Roseville, CA, USA). PC12 cells were co-transfected with TRIM28-WT or TRIM28-MUT reporter vectors along with NR3C2 mimetics or NC mimetics using Lipofectamine 2000 (11668030, Thermo Fisher Scientific, Waltham, MA, USA). After 48 hours, luciferase activity was measured using the Dual-Luciferase® Reporter Assay System (Promega, Madison, WI, USA).

According to the instructions of the Simple ChIP® Enzymatic Chromatin IP Kit (9003, Cell Signaling Technology, Danvers, MA, USA), PC12 cells were treated with formaldehyde for 15 minutes. The protein-chromatin cross-linking reaction was terminated with glycine. Chromatin was digested using Micrococcus nuclease and resuspended in chromatin immunoprecipitation (ChIP) buffer. Subsequently, NR3C2 antibody (4 µL/mg of lysate, PA5-81527, Thermo Fisher Scientific, Waltham, MA, USA) or IgG antibody (SAB5600195, Sigma-Aldrich, St. Louis, MO, USA) was added, and the immunoprecipitation (IP) reaction was performed overnight at 4 °C. After washing to remove unbound chromatin and reversing the cross-links, the DNA was purified for qPCR analysis.

Statistical analyses were performed using GraphPad Prism 9.0 software (Dotmatics, Boston, MA, USA). Student t-test was used between two groups. For comparisons among three or more groups, one-way analysis of variance (ANOVA) was used, followed by Tukey’s post-hoc test for pairwise group comparisons. A p-value of 0.05 was considered statistically significant. All experiments were conducted in triplicate or more.

To investigate the effects of Res on cognitive behavior, brain injury, and NR3C2 in MCAO/R rats, we assessed neurological and cognitive functions alongside NR3C2 expression. The morris water maze (MWM) test revealed significant cognitive impairment in the Model group compared to the Sham group, characterized by prolonged escape latency, decreased platform crossings, and reduced target quadrant dwell time. In contrast, the Res group exhibited improved cognitive function, evidenced by shorter escape latency and increased platform crossings and target quadrant dwell time (Fig. 1A). Neurological assessments indicated that the Longa and Bederson scores in the Model group were elevated compared to the Sham group; however, these scores significantly decreased in the Res-treated rats (Fig. 1B), suggesting that Res effectively mitigates neurological dysfunction. Additionally, TTC staining demonstrated larger cerebral infarction areas in the Model group relative to the Sham group, with the Res group showing a notable reduction in infarction size compared to the Model group (Fig. 1C). The expression levels of inflammatory factors TNF-$\alpha$, IL-6, and IL-1$\beta$ were significantly elevated in the Model group but reversed following Res treatment (Fig. 1D). HE staining revealed widespread tissue disorganization, nuclear condensation, and necrosis in the Model group’s brain tissue. Conversely, Res treatment resulted in significantly reduced brain tissue damage, improved structural integrity, and diminished inflammatory cell infiltration (Fig. 1E). Nissl staining confirmed a marked reduction in Nissl bodies in the Model group compared to the Sham group, whereas the Res group exhibited restoration in both the number and structure of Nissl bodies, indicating more intact neuronal morphology (Fig. 1E). To identify downstream targets of Res related to cerebral CIRI, we utilized the GeneCards database to extract relevant genes and the Prediction database to pinpoint transcription factors. Subsequent intersection analysis via Jvenn revealed five overlapping transcription factors: nuclear factor, erythroid 2 like 2 (NFE2L2), signal transducer and activator of transcription 1 (STAT1), nuclear factor kappa B subunit 1 (NFKB1), NR3C2, and thyroid hormone receptor alpha (THRA) (Fig. 1F). NR3C2 is known to play multiple roles in neural regulation, including stress response, neuroplasticity, emotion and behavior regulation, electrolyte balance, and neuroinflammation [23]. However, it remains unclear whether Res exerts its effects on CIRI through NR3C2. Our experimental findings demonstrated a significant upregulation of NR3C2 expression in the MCAO/R rat brain tissue (Fig. 1G,H), which was notably decreased following Res treatment. These results suggest that Res exerts a neuroprotective effect in MCAO/R rats by downregulating NR3C2 expression.

Fig. 1.

Res can alleviate nerve damage in middle cerebral artery occlusion/reperfusion (MCAO/R) rats and downregulate nuclear receptor subfamily 3 group C member 2 (NR3C2). (A) In the Morris water maze test, the rats’ escape latency was recorded. The probe trial recorded the time spent in the goal quadrant within 120 seconds and the number of platform crossings. N = 10. (B) Longa and Bederson scores. N = 10. (C) 2,3,5-triphenyl tetrazolium chloride (TTC) staining was used to evaluate the size of cerebral infarction in rats. N = 5. Scale bar = 5 mm. (D) Enzyme linked immunosorbent assay (ELISA) was used to detect the expression of inflammatory factors. N = 5. (E) H&E and Nissl staining were used to observe the pathological conditions of hippocampal tissue and the changes of Nissl bodies. N = 5. Scale bar = 100 µm. (F) Venn diagram of the intersection of direct targets and transcription factors of Cerebral ischemia-reperfusion injury (CIRI) and resveratrol (Res). (G) Reverse transcription quantitative real-time PCR (RT-qPCR) was used to detect the messenger RNA (mRNA) expression of NR3C2 in rats in each group. N = 5. (H) Western blot (WB) was used to detect the expression of NR3C2 protein in rats in each group. N = 5. The data was analyzed using one-way ANOVA, and the post hoc test was conducted using Tukey’s. *p 0.05, **p 0.01, ***p 0.001, ****p 0.0001. TF, transcription factor.

To explore the specific mechanism by which Res protects against CIRI, we constructed NR3C2 overexpressing cells and established in vitro model. The results showed that compared with the Control group, the expression of NR3C2 was significantly increased (Fig. 2A,B), while cell viability was significantly decreased (Fig. 2C) in the Model group. The expression levels of inflammatory factors TNF-$\alpha$, IL-6, and IL-1$\beta$ were elevated (Fig. 2D). TUNEL staining revealed an increase in cell apoptosis (Fig. 2E), and the expression of apoptosis-related proteins Bax and Cleaved caspase-3 was increased, while Bcl-2 expression was decreased (Fig. 2F). Additionally, the ratio of autophagy-related protein LC3II/I was elevated, Beclin-1 expression was upregulated, and P62 was significantly reduced (Fig. 2G), indicating a marked increase in autophagy. Following Res treatment, NR3C2 expression was downregulated (Fig. 2A,B), cell viability increased (Fig. 2C), inflammatory factor expression decreased (Fig. 2D), and apoptosis, along with apoptosis-related proteins Bax and Cleaved caspase-3, was reduced, while Bcl-2 expression was increased (Fig. 2E,F). Moreover, autophagy-related proteins LC3II/I and Beclin-3 decreased, and P62 was significantly increased (Fig. 2G), suggesting that autophagy was inhibited. However, overexpression of NR3C2 inhibited the protective effects of Res on OGD/R-induced cell apoptosis and autophagy. These results demonstrate that Res inhibits NR3C2 and alleviates apoptosis and autophagy in PC12 cells during OGD/R treatment.

Fig. 2.

Res protects against oxygen-glucose deprivation/reperfusion (OGD/R)-induced cell damage by inhibiting NR3C2. (A) The expression of NR3C2 mRNA was detected by RT-qPCR. (B) WB was used to detect the expression of NR3C2 protein. (C) CCK-8 was used to detect cell viability. (D) ELISA was used to detect the content of inflammatory factors. (E) Terminal deoxynucleotidyl transferase–mediated dUTP nick end labeling (TUNEL) was used to detect apoptosis. Scale bar = 200 µm. (F) WB was used to detect the expression of apoptosis-related proteins. (G) WB was used to detect the expression of autophagy-related proteins. The data was analyzed using one-way ANOVA, and the post hoc test was conducted using Tukey’s. N = 3, *p 0.05, **p 0.01, ***p 0.001, ****p 0.0001. OE, overexpression; NC, negative control; Bax, Bcl-2 associated X; Bcl-2, B-cell lymphoma 2; LC3, microtubule-associated protein 1A/1B-light chain 3.

To further elucidate the mechanism by which Res protects nerve cells, we identified downstream target genes of NR3C2 using the hTFtarget database and intersected these targets with CIRI-related genes via the Jvenn website. This analysis revealed nine downstream targets: peptidylprolyl isomerase A (PPIA), DNA damage-inducible transcript 3 (DDIT3), metastasis associated lung adenocarcinoma transcript 1 (MALAT1), small nucleolar RNA host gene 12 (SNHG12), alpha-enolase (ENO1), sequestosome 1 (p62/SQSTM1), TRIM28, interferon regulatory factor 9 (IRF9), and long non-coding RNA (lncRNA) THUMPD3-AS1 (Fig. 3A). Notably, while TRIM28 is known to play a role in autophagy regulation [24], its significance in the context of CIRI remains unexplored, warranting further investigation into its functional role. Our findings demonstrated that TRIM28 expression was elevated in OGD/R PC12 cells and subsequently decreased following Res treatment. However, this downregulation was inhibited by NR3C2 overexpression (Fig. 3B,C). To validate the predicted interaction between NR3C2 and TRIM28, we conducted dual luciferase assays. The results showed that NR3C2 overexpression positively regulated the wild-type TRIM28 promoter, while it had no effect on the mutant TRIM28 promoter (Fig. 3D). Additionally, ChIP quantitative PCR results revealed a significant enrichment of the TRIM28 promoter with NR3C2 compared to the IgG isotype control (Fig. 3E). These findings collectively suggest that NR3C2 regulates TRIM28 expression, positioning TRIM28 as a potential therapeutic target for Res in the treatment of CIRI.

Fig. 3.

NR3C2 regulates the expression of TRIM28 in OGD/R model. (A) Venn diagram of the intersection of NR3C2 downstream targets and CIRI-related genes. (B) RT-qPCR was used to detect the expression of TRIM28 mRNA. (C) WB was used to detect the expression of TRIM28 protein. (D) Dual luciferase analysis of the regulatory relationship between NR3C2 and TRIM28. (E) ChIP qPCR was used to detect the enrichment of the TRIM28 promoter in NR3C2. The data was analyzed using one-way ANOVA, and the post hoc test was conducted using Tukey’s. N = 3, ns, p $>$ 0.05, *p 0.05, ****p 0.0001. WT, wild-type; MUT, mutated; TRIM28, tripartite motif containing; ChIP, chromatin immunoprecipitation.

To validate the hypothesis that Res alleviates neuronal apoptosis and autophagy by inhibiting NR3C2, specifically targeting TRIM28, we conducted an in vitro experiment involving NR3C2 overexpression combined with TRIM28 knockdown. WB results showed that TRIM28 protein expression significantly decreased following knockdown (Fig. 4A), while NR3C2 protein levels remained unaffected. CCK-8 assay results indicated that cell viability increased after TRIM28 silencing (Fig. 4B). Furthermore, the expression levels of inflammatory factors were relatively reduced upon TRIM28 knockdown (Fig. 4C). Using the TUNEL assay, we observed that TRIM28 knockdown rescued apoptosis induced by NR3C2 overexpression (Fig. 4D). WB analysis was employed to evaluate protein expression levels. Results revealed that in the Res+OE-NR3C2+sh-TRIM28 group, compared to the Res+OE-NR3C2+sh-NC group, the expression of pro-apoptotic proteins Bax and cleaved caspase-3 was reduced, while Bcl-2 levels increased. Additionally, analysis of autophagy markers demonstrated a decrease in the LC3-II/LC3-I ratio and Beclin-1 expression, accompanied by an increase in P62 levels (Fig. 4E). These findings collectively suggest that Res alleviates neuronal apoptosis and excessive autophagy by directly targeting TRIM28 through the inhibition of NR3C2.

Fig. 4.

Res can protect OGD/R-induced cell damage by inhibiting NR3C2 targeting TRIM28. (A) WB was used to detect the expression of NR3C2 and TRIM28 protein. (B) CCK-8 was used to detect cell viability. (C) ELISA was used to detect the content of inflammatory factors. (D) TUNEL was used to detect apoptosis. Scale bar = 200 µm. (E) WB was used to detect the expression of apoptosis-related proteins and autophagy-related proteins. Statistical analysis was performed using student’s t-test. N = 3, ns, p $>$ 0.05, **p 0.01, ***p 0.001, ****p 0.0001. CCK8, cell counting kit-8.

We further investigated the therapeutic effects of Res on CIRI through in vivo experiments, specifically evaluating whether Res alleviates CIRI by regulating NR3C2 and targeting TRIM28 expression, as well as modulating neuronal cell apoptosis and autophagy. Our findings were consistent with those from in vitro studies. Overexpression of NR3C2 resulted in an increase in both NR3C2 and TRIM28 expression. In contrast, silencing TRIM28 did not lead to significant alteration in NR3C2 levels while downregulating TRIM28 expression (Fig. 5A). Behavioral assessments indicated that NR3C2 overexpression significantly prolonged escape latency in rats, accompanied by a reduction in the number of platform crossings and target quadrant dwell time. Conversely, knockdown of TRIM28 resulted in shorter escape latency along with an increase in both the number of platform crossings and target quadrant dwell time (Fig. 5B). Additionally, NR3C2 overexpression was associated with elevated Longa and Bederson scores, indicative of neurological impairment, while TRIM28 knockdown resulted in decreased scores, although these changes were not statistically significant (Fig. 5C). Further histopathological analysis demonstrated that NR3C2 overexpression was associated with an increased cerebral infarction area, whereas TRIM28 knockdown led to a reduction in this area (Fig. 5D). Tissue structural changes included a tendency towards nuclear condensation and necrosis with diminished Nissl bodies and cell volume following NR3C2 overexpression; these effects were reversed upon TRIM28 silencing (Fig. 5E). Moreover, NR3C2 overexpression resulted in elevated levels of inflammatory markers TNF-$\alpha$, IL-6, and IL-1$\beta$ in rat brain tissue, while TRIM28 knockdown led to downregulation of these inflammatory factors (Fig. 5F). In terms of apoptosis and autophagy markers, NR3C2 overexpression was associated with increased levels of pro-apoptotic proteins Bax and cleaved caspase-3, decreased anti-apoptotic protein Bcl-2, and an elevation of autophagy-related proteins LC3-II/LC3-I and Beclin-1, alongside a reduction in P62. These molecular changes were reversed following TRIM28 knockdown (Fig. 5G). Collectively, these findings indicate that Res exerts protective effects against CIRI-induced neurological dysfunction, neuronal cell apoptosis, and excessive autophagy by inhibiting NR3C2 and targeting TRIM28 to suppress its transcription.

Fig. 5.

Res can alleviate neuronal apoptosis and autophagy by inhibiting NR3C2 and reducing TRIM28 expression in MCAO/R rat brain tissue. (A) WB was used to detect the protein expression of NR3C2 and TRIM28. N = 5. (B) In the Morris water maze test, the rats’ escape latency was recorded. The probe trial recorded the time spent in the goal quadrant within 120 seconds and the number of platform crossings. N = 10. (C) Longa and Bederson scores. N = 10. (D) TTC staining was used to evaluate the size of cerebral infarction in rats. N = 5. Scale bar = 5 mm. (E) H&E and Nissl staining were used to observe the pathological conditions of hippocampal tissue and the changes of Nissl bodies. N = 5. Scale bar = 100 µm. (F) ELISA was used to detect the expression of inflammatory factors. N = 5. (G) WB was used to detect the expression of apoptosis-related proteins and autophagy-related proteins. N = 5. The data was analyzed using one-way ANOVA, and the post hoc test was conducted using Tukey’s. ns, p $>$ 0.05, *p 0.05, **p 0.01, ***p 0.001, ****p 0.0001.