The animal study was conducted according to a protocol approved by the Institutional Animal Care and Use Committee of Guilin Medical University, Guilin, China (approval no. IACUC-202510137) and adhered to the National Institutes of Health guidelines for laboratory animal welfare. A total of 12 male C57BL/6J mice (aged 4 weeks; body weight 12–15 g at arrival) were obtained from Cyagen Biosciences, Inc. Male mice were selected to minimize the potential confounding effects of estrous cycle-associated hormonal fluctuations on metabolic parameters, including body weight, insulin sensitivity and AT inflammation, thereby ensuring more stable and reproducible readouts for the assessment of LIC-A efficacy. The experimental mice were housed under standard specific-pathogen-free conditions, with a 12 h light-dark cycle, at a temperature of 24±2°C and a humidity of 50±10°C, and were allowed ad libitum access to a HFD (manufactured by Biotech HD Biotechnology Co., Ltd.). This purified diet was specifically formulated for diet-induced obesity studies with the following approximate composition: 34.9% fat (primarily lard), 23.5% protein (casein) and 26.2% carbohydrates (maltodextrin and sucrose), providing 60% of the total calories from fat, 20% from protein and 20% from carbohydrates, with an energy density of 5.24 kcal/g.

Throughout the experimental period, all mice were monitored daily for general health status, behavioral changes and body weight. To minimize animal suffering and ensure compliance with ethical guidelines, the following humane endpoints were predefined in accordance with the IACUC-approved protocol (approval no. GLMU-IACUC-202510137): i) Body weight loss exceeding 20% of baseline body weight (measured at the start of dietary intervention); ii) persistent clinical signs of severe illness or distress lasting >48 h, including but not limited to hunched posture, piloerection, lethargy, immobility or markedly reduced responsiveness to external stimuli; iii) severe neurological symptoms (for example convulsions, circling behavior and/or paralysis) or persistent respiratory distress (for example labored breathing and/or cyanosis) that did not resolve spontaneously within 2 h; and iv) severe abdominal distension or ulcerative dermatitis that interfered with normal movement or caused visible bleeding. Animals meeting any of these criteria would be immediately euthanized under deep anesthesia (sodium pentobarbital, 100 mg/kg, intraperitoneal injection) prior to the scheduled endpoint to prevent unnecessary suffering. During the entire study, no animals in either the control group or the LIC-A treatment group reached any of these predefined humane endpoints, confirming that the experimental interventions were well tolerated. All animals were therefore maintained until the scheduled termination at week 16, at which point they were euthanized for tissue collection as described below.

At week 4 after the start of the HFD intervention, the mice were randomly divided into two groups (n=6 per group): i) Control group (0.5% carboxymethyl cellulose sodium by oral gavage); and ii) LIC-A treatment group (60 mg/kg body weight LIC-A dissolved in 0.5% carboxymethyl cellulose sodium by oral gavage). From week 4 to 16 after the start of the dietary intervention, treatment was administered twice weekly (for a total of 24 doses). Body weight was recorded weekly. At week 15, metabolic assessments including glucose tolerance tests (GTT) and insulin tolerance tests (ITT) were performed with a 3-day recovery interval between tests. After the metabolic assessments, the mice were allowed to recover and continued to receive the respective treatments until the end of week 16. At the end of week 16, mice were deeply anesthetized by intraperitoneal injection of 1% sodium pentobarbital (50 mg/kg body weight). Blood was collected from the retro-orbital venous plexus using a heparinized glass capillary tube (inner diameter 0.9–1.0 mm) and immediately transferred to a sterile tube without anticoagulant. In total, 0.6–0.8 ml of blood was obtained and after blood collection, gentle pressure was applied to the orbit to ensure hemostasis. Mice were then euthanized by cervical dislocation while still under deep anesthesia. The blood samples were allowed to clot at room temperature for 30 min and subsequently centrifuged at 1,500 × g for 15 min at 4°C. The resulting serum supernatant was carefully aspirated, aliquoted and stored at −80°C for subsequent biochemical and ELISA analyses. Epididymal WAT (eWAT) and inguinal WAT (iWAT) were rapidly dissected and collected for subsequent analysis.

To identify potential upstream regulators of METTL3 in FJHQT, a multistep virtual screening strategy was employed. First, using the Traditional Chinese Medicine Systems Pharmacology Database and Analysis Platform (TCMSP), compounds were screened from the chemical constituents of four herbal ingredients: Stephaniae Tetrandrae Radix (Fangji), Astragali Radix (Huangqi), Atractylodis macrocephalae Rhizoma (Baizhu) and Glycyrrhizae Radix (Gancao), to construct a compound library. The initial library comprised 528 compounds.

Second, to identify compounds with favorable pharmacokinetic properties and drug-like characteristics, the compound library was screened using Lipinski's rule of five, which comprises four criteria related to oral bioavailability: Molecular weight <500 Da, ≤5 hydrogen bond donors, ≤10 hydrogen bond acceptors and a calculated logP value <5. Compounds that did not meet any of these criteria were excluded. This step ensured that the selected compounds possessed sufficient oral absorption and bioavailability to meet the requirements for subsequent in vivo evaluation.

Third, the three-dimensional (3D) structure of METTL3 was retrieved from the Protein Data Bank (PDB; https://www.rcsb.org; PDB ID: 5TEY) and processed using Discovery Studio 2021 software (Dassault Systèmes Americas Corp.). The binding pocket was defined within a 5 Å radius around the native ligand. Flexible docking analysis was performed using the LibDock module and the ligand-protein binding affinities were ranked based on LibDock score values. Ultimately, the 16 compounds with the highest docking scores were selected for further experimental validation (Table SI). LIC-A exhibited the strongest METTL3 expression-promoting activity in the subsequent experiments.

3T3-L1 cells (Wuhan Pricella Biotechnology Co., Ltd.) were maintained in DMEM (Beijing Solarbio Science & Technology Co., Ltd.) supplemented with 10% heat-inactivated fetal bovine serum (FBS: Sangon Biotech Co., Ltd.) and 1% penicillin-streptomycin (MilliporeSigma) at 37°C in a humidified atmosphere containing 5% CO₂.

For experimental assays, 3T3-L1 cells were seeded at the following densities: i) 5×10³ cells/well in 96-well plates; ii) 2×10⁵ cells/well in 6-well plates; and iii) 1×10⁶ cells per T25 flask. The cells were allowed to adhere overnight prior to treatment.

To induce adipogenic differentiation, 3T3-L1 cells were cultured in T25 flasks or 6-well plates at 37°C in a humidified atmosphere with 5% CO₂ until they reached 100% confluency. The standard medium was then replaced with adipogenic differentiation medium supplemented with 0.5 mM 3-isobutyl-1-methylxanthine (IBMX; Beijing Solarbio Science & Technology Co., Ltd.), 1 µM dexamethasone (Beyotime Biotechnology) and 1 µg/ml insulin (Wuhan Pricella Biotechnology Co., Ltd.), and the cells were incubated under the same conditions. After 3 days of induction, the medium was switched to maintenance medium (DMEM containing 10% FBS and 1 µg/ml insulin). Subsequently, the maintenance medium was refreshed every 2 days until day 8 to support complete differentiation.

After differentiation, 3T3-L1 adipocytes were treated in the presence or absence of TNF-α (10 ng/ml; Wuhan Pricella Biotechnology Co., Ltd.) or LPS (100 ng/ml; Wuhan Pricella Biotechnology Co., Ltd.), with or without LIC-A (Beijing Kangrun Chengye Biotechnology Co., Ltd.). Based on the optimal concentrations determined by MTT assay, LIC-A was used at 8 µmol/l for TNF-α-stimulated experiments and 6 µmol/l for LPS-stimulated experiments. Cells were pretreated with LIC-A for 6 h, followed by 24 h of co-culture with TNF-α or LPS. The control group was treated with an equal volume of vehicle (0.1% DMSO, the solvent for LIC-A) and maintained under the same culture conditions without any drug exposure. The experimental groups included: i) Control group; ii) group treated with LIC-A alone; iii) group treated with TNF-α alone; iv) group treated with LPS alone; v) group treated with the combination of TNF-α and LIC-A; and vi) group treated with the combination of LPS and LIC-A. In the METTL3 knockdown experiment, cells transduced with short hairpin (sh) METTL3 were subjected to the same treatment protocol and compared with the sh negative control (NC) group. Each experiment was performed at least three times to ensure reproducibility.

Cells were treated with 5 mg/ml MTT solution (MedChemExpress; cat. no. HY-15924) and incubated for 4 h at 37°C. After removing the supernatant, the resulting formazan crystals were solubilized by adding DMSO and agitating the plates for 10 min. The optical density (OD) of each well was subsequently measured at 490 nm using a microplate reader.

Total RNA was extracted from cultured 3T3-L1 or AT cells using the TRIzol reagent (Invitrogen; Thermo Fisher Scientific, Inc.) according to the manufacturer's instructions. After extraction, the RNA concentration and purity were determined using a multifunctional microplate reader (BioTek; Agilent Technologies, Inc.), and the RNA purity was assessed by calculating the absorbance ratios, A260/A280 and A260/A230. Only samples with an A260/A280 ratio between 1.8 and 2.0 and an A260/A230 ratio >2.0 were selected as purified samples for subsequent experiments. The RNA concentration was then adjusted to 1 µg/µl using RNase-free water and the samples were stored at −80°C until use.

Total RNA was extracted and quantified as described in the RNA extraction and quantification subsection. Relative m6A levels in total RNA were measured using an m⁶A RNA Methylation Quantification Kit (Wuhan Aimeijie Technology Co., Ltd.; cat. no. P-9008-48) according to the manufacturer's instructions. For the assay, 200 ng of extracted RNA was added to each well and incubated in the provided binding solution at 37°C for 90 min to facilitate RNA immobilization. Following the washing steps, the captured RNA was incubated sequentially with capture and detection antibodies. Colorimetric signals were developed and quantified by measuring the OD at 450 nm. Each reaction was performed in triplicate to calculate relative m⁶A levels.

The total RNA was harvested as described in the RNA extraction and quantification subsection. Equal amounts of total RNA (concentration determined by spectrophotometry) were heat-denatured at 95°C for 10 min and then snap-cooled on ice. Samples were blotted onto an N+ nylon membrane. The RNA was immobilized by UV cross-linking. The membrane was blocked with 5% (w/v) non-fat dry milk in PBST [phosphate-buffered saline containing 0.1% (v/v) Tween-20] for 1 h at room temperature, followed by overnight incubation at 4°C with a primary antibody against m⁶A (1:2,000; Proteintech Group, Inc.; cat. no. 68055-1-Ig). After extensive washing with PBST, the membrane was probed with a horseradish peroxidase (HRP)-conjugated goat anti-rabbit IgG secondary antibody (1:5,000; Proteintech Group, Inc.; cat. no. RGAR001-50ul)) for 1 h at room temperature on a shaker. Signals were developed using an enhanced chemiluminescence (ECL) kit (Shanghai Epizyme Biomedical Technology Co., Ltd.; cat. no. SQ201) and captured using a chemiluminescence imaging system.

The levels of inflammatory cytokines (IL-6 and IL-1β) and adipokines (adiponectin, resistin and leptin) secreted into the culture medium by 3T3-L1 cells following LIC-A treatment were determined by ELISA. The following ELISA kits were purchased from Wuhan Elabscience Biotechnology Co., Ltd.: IL-6 (cat. no. E-AB-F1207D), IL-1β (cat. no. E-EL-M0037), leptin (cat. no. E-EL-M3008-96T), adiponectin (cat. no. E-EL-M0002-96T) and resistin (cat. no. E-EL-M3056-96T). The assays were performed strictly following the manufacturer's instructions and the OD was measured at 450 nm on a microplate reader. All measurements were performed in triplicate for each sample.

Total RNA was extracted from 3T3-L1 cells or AT and quantified as described in the RNA extraction and quantification subsection. RT was performed using PrimeScript II RT Mix with gDNA Remover (Beijing Kangrun Chengye Biotechnology Co., Ltd.; cat. no. A224) according to the manufacturer's instructions. Briefly, 1 µg of total RNA was mixed with 2 µl of 5X gDNA Remover Reaction buffer and 1 µl of gDNA Remover in DEPC-treated water (total volume 10 µl), then incubated at 37°C for 5 min to remove genomic DNA. Subsequently, 10 µl of the gDNA-removed RNA sample was added to a mixture containing 4 µl of 5X RT Reaction Mix, 1 µl of PrimeScript II RT and DEPC-treated water to a final volume of 20 µl. The RT reaction was carried out at 42°C for 15 min, followed by inactivation at 85°C for 5 min. The resulting cDNA was placed on ice for immediate use or stored at −20°C for subsequent experiments.

Following RT, the resulting cDNA was subjected to qPCR with 2X Taq PCR Master Mix (Wuhan Huarui Kang Biotechnology Co., Ltd.) using a real-time PCR system (Thermo Fisher Scientific, Inc.). The thermal cycling program was as follows: Initial denaturation at 95°C for 3 min, followed by 40 cycles of denaturation at 95°C for 15 sec, annealing at 54°C for 30 sec and extension at 72°C for 30 sec. To verify amplification specificity, melting curve analysis was performed from 65°C to 95°C in 0.5°C increments. Gene expression levels were normalized to β-actin and calculated using the 2^−ΔΔCq method (44). Primer sequences and their corresponding annealing temperatures are listed in Table SII.

Total protein was extracted from 3T3-L1 cells or AT using precooled RIPA lysis buffer (Beijing Solarbio Science & Technology Co., Ltd.) supplemented with a 1% protease inhibitor cocktail (MilliporeSigma). After centrifugation at 12,000 × g for 15 min at 4°C, the supernatant was collected. Protein concentration was determined using a BCA protein assay kit (Beyotime Biotechnology) according to the manufacturer's instructions. Briefly, the working reagent was prepared by mixing solutions A and B at a 50:1 ratio (v/v). A 25 µl aliquot of either the bovine serum albumin (BSA) standard or the diluted protein sample (the original sample was diluted 10-fold with ultrapure water) was added to individual wells of a 96-well plate. Subsequently, 200 µl of the working reagent was added to each well and the plate was incubated at 37°C for 30 min with gentle shaking. The absorbance was measured at 562 nm using a microplate reader. Following quantification, equal aliquots of protein (25–30 µg per lane) were resolved by 10% sodium dodecyl sulfate-polyacrylamide gel electrophoresis and electrotransferred onto 0.45 µm PVDF membranes (Merck KGaA). The membranes were blocked with 5% non-fat milk in Tris-buffered saline containing 0.1% (v/v) Tween-20 (TBST) for 2 h at room temperature and then probed overnight at 4°C with primary antibodies targeting METTL3 (1:10,000; Proteintech Group, Inc.; cat. no. 15073-1-AP), monocyte chemoattractant protein-1 (1:2,000; Proteintech Group, Inc.; cat. no. HZ-1334), IL-6 (1:2,000; Proteintech Group, Inc.; cat. no. 83747-5-RR) and β-actin (1:5,000; Proteintech Group, Inc.; cat. no. 66009-1-Ig). After extensive washing with TBST, the membranes were incubated with appropriate HRP-conjugated secondary antibodies (goat anti-mouse or goat anti-rabbit IgG; 1:4,000; OriGene Technologies, Inc.) for 2 h at 4°C. Immunoreactive bands were detected using an ECL substrate (Shanghai Epizyme Biomedical Technology Co., Ltd.; cat. no. SQ201) and imaged using a Tanon-5200SF chemiluminescence imaging system (Tanon Science and Technology Co., Ltd.). Densitometric analysis was performed using the Tanon-5200SF system software (version ALLDOC; Tanon Science & Technology Co., Ltd.).

Mouse AT samples were fixed with 4% paraformaldehyde at 4°C for 2 h, dehydrated, embedded in paraffin and cut into 7 µm-thick sections. The sections were deparaffinized, rehydrated and then permeabilized with 0.5% Triton X-100 in PBS and blocked overnight with 2% BSA in PBS at 4°C. The tissues were then incubated overnight at 4°C with primary antibodies against METTL3 (1:200; Proteintech Group, Inc.; cat. no. 15073-1-AP), F4/80 (1:200; Proteintech Group, Inc.; cat. no. 28463-1-AP) and Plin1 (1:300; Proteintech Group, Inc.; cat. no. 83905-4-RR). After washing, the sections were incubated with fluorophore-conjugated secondary antibodies for 1 h at room temperature as follows: Cy3-conjugated goat anti-rabbit IgG (1:400; Proteintech Group, Inc.) for METTL3, Cy3-conjugated goat anti-rabbit IgG (1:400; Proteintech Group, Inc.) for F4/80 and FITC-conjugated goat anti-rabbit IgG (1:400; Proteintech Group, Inc.) for Plin1. Nuclei were counterstained with a DAPI-containing antifade mounting medium (Beijing Solarbio Science & Technology Co., Ltd.) at room temperature for 5 min. Fluorescent images were acquired using a confocal microscope.

Three independent shRNA sequences targeting mouse METTL3 (NM_019721; CDS region 138-1,880 bp) were designed and inserted into the GV493 lentiviral vector (Shanghai GeneChem Co., Ltd.). The resulting plasmids were designated as follows: LV-METTL3-RNAi (cat. no. 112185-1; shMETTL3-1), LV-METTL3-RNAi (cat. no. 112186-1; shMETTL3-2) and LV-METTL3-RNAi (cat. no. 112187-1; shMETTL3-3). The core targeting sequences (guide strand, 5′-3′) were: shMETTL3-1, GAAGGAACACTGCTTGGTTGG; shMETTL3-2, GAACCAACAGTCAACGAAAGA; and shMETTL3-3, GCCAAGGAACAGTCCATTGTT. A non-targeting shRNA with the sequence 5′-TTCTCCGAACGTGTCACGT-3′ (cat. no. CON313; Shanghai GeneChem Co., Ltd.) was used as a negative control (shNC). Seed-region BLAST analysis (nucleotides 2–8 of the guide strand) confirmed that these sequences specifically target METTL3 with no perfect matches to other known mouse genes.

Lentiviral particles were generated using a second-generation self-inactivating packaging system. Briefly, 293T cells (Chinese Academy of Sciences) were co-transfected with the GV493 vector plasmid (20 µg per 10 cm dish), the packaging plasmid pHelper 1.0 (15 µg; containing gag, pol and rev genes), and the envelope plasmid pHelper 2.0 (10 µg; encoding VSV-G), at a ratio of ~4:3:2. Transfection was performed at 37°C for 6 h, after which the medium was replaced with fresh complete medium. Cells were further cultured at 37°C for 48–72 h, and lentiviral supernatants were collected. Among the three shRNAs, shMETTL3-1 was selected for all functional experiments based on its validated knockdown efficiency.

To establish stable knockdown cell lines, 3T3-L1 cells at ~60% confluency were transduced with shMETTL3-1 or shNC lentivirus at a multiplicity of infection of 8 for 16 h, after which the virus-containing medium was replaced with fresh complete medium. At 48 h post-transduction, stably transduced cells were selected with 3 µg/ml puromycin for 24 h. Following selection, the puromycin concentration was reduced to 1 µg/ml for maintenance culture. Cells were used for subsequent experiments after stable knockdown was confirmed.

At the 16-week time point, metabolic phenotyping of the mice was performed using glucose and insulin tolerance tests. For the GTT, mice were subjected to a 12 h fast, followed by an intraperitoneal injection of D-glucose (2 g/kg body weight) prepared as a 400 mg/ml solution. Blood glucose levels were measured using blood collected from the tail vein using a glucose meter (Kefu Industrial Co., Ltd.) at 0, 15, 30, 60, 90 and 120 min after injection.

An ITT was conducted after a 3-day recovery period following the GTT. Mice were fasted for 4 h and then intraperitoneally injected with insulin at a dose of 0.75 U/kg body weight. Blood glucose concentrations were monitored at 0, 15, 30, 60, 90 and 120 min after insulin administration. All glucose measurements were recorded and subjected to statistical analysis.

Mouse adipose tissue (eWAT and iWAT) samples were fixed with 4% paraformaldehyde at 4°C for 2 h, then dehydrated through a graded ethanol series (70, 80, 95 and 100%), cleared in xylene and embedded in paraffin wax. The paraffin-embedded tissues were sectioned at 7 µm thickness using a microtome. For H&E staining, the sections were dewaxed in xylene and rehydrated through a descending ethanol series to distilled water. The sections were then stained with Harris hematoxylin solution (Beijing Solarbio Science & Technology Co., Ltd.) for 8 min at room temperature (25°C), followed by washing in running tap water for 5 min to allow blueing. Subsequently, the sections were counterstained with eosin Y solution (0.5%, w/v) for 2 min at room temperature. After dehydration through graded ethanol and clearing in xylene, the sections were mounted with neutral balsam mounting medium. Images were captured using a light microscope (Olympus Corporation) at ×200 magnification. For adipocyte size quantification, at least three randomly selected non-overlapping fields per section and six mice per group were analyzed using ImageJ software (version 1.54p; National Institutes of Health), and the cross-sectional area of adipocytes was measured.

Data are presented as mean ± SD. Normality and variance homogeneity were verified. For multi-group comparisons, one-way or repeated-measures ANOVA was applied as appropriate, followed by Tukey's post hoc test for all pairwise comparisons. For direct two-group comparisons, an unpaired two-tailed Student's t-test was used. All analyses were performed using GraphPad Prism 10 (Dotmatics). P<0.05 was considered statistically significant.

To identify candidate compounds that regulate METTL3 expression and AT homeostasis, compounds from FJHQT were retrieved using the TCMSP, and molecular docking was performed against METTL3 (PDB ID: 5TEY) using Discovery Studio. LibDock was used to sort the docking scores into binding free energies and molecular affinities (Table SII) to select 16 drug-like monomers (Fig. S1).

The optimal non-cytotoxic treatment concentration for each monomer in adipogenic 3T3-L1 cells was first determined using MTT assays across a range of concentrations (Fig. 1A). The cells were then treated with each monomer at the selected concentrations for 48 h. Western blot analysis revealed that, among all candidates, LIC-A significantly upregulated METTL3 protein expression compared with other drug monomers and the DMSO control (Fig. 1B and C). Moreover, dot blotting and colorimetric assays showed that LIC-A treatment markedly increased global RNA m6A modification levels (Fig. 1D and E). Together, these results indicated that LIC-A enhanced METTL3-mediated m6A modification in 3T3-L1 preadipocytes.

To explore the effects of LIC-A on adipocyte function, adipokine and inflammatory factor expression in TNF-α- or LPS-stimulated adipogenic 3T3-L1 adipocytes was examined. The optimal LIC-A concentration was first determined under acute TNF-α stimulation (Fig. 2A) and 8 µmol/l was used in all subsequent cotreatment experiments (Fig. 2B-H). Differentiated adipogenic 3T3-L1 cells were challenged with the obesity-mimicking cocktail and followed by TNF-α treatment. ELISA showed that LIC-A treatment could significantly enhance adiponectin secretion and inhibit leukin secretion (leptin and resistin) when compared with the group treated by TNF-α alone (Fig. 2B and C). LIC-A also inhibited the release of inflammatory cytokines, such as IL-6 and IL-1β, induced by TNF-α (Fig. 2D) and elevated expression of insulin-sensitizing genes (Fig. 2E). At the transcriptional level, LIC-A significantly promoted the expression of adiponectin mRNA while suppressing leptin and resistin mRNA compared with the TNF-α group (Fig. 2F). Consistent with these findings, LIC-A significantly decreased the mRNA and protein levels of TNF-α-induced inflammatory factors (Fig. 2G and H).

Whether LIC-A exerts similar regulatory effects under acute LPS stimulation was further evaluated. The optimal LIC-A concentration under LPS stimulation was determined (Fig. 2I) and this concentration was used consistently (6 µmol/l) in all subsequent co-treatment experiments (Fig. 2J-O). It was observed that LIC-A treatment notably ameliorated LPS-induced alterations in adipokine secretion and inflammatory cytokine production (Fig. 2J-L). Moreover, LIC-A regulated mRNA and protein expression of adipokines and inflammatory factors in a manner highly consistent with its effects under TNF-α stimulation (Fig. 2M-O). Together, these data indicated that LIC-A alleviated TNF-α- and LPS-induced dysregulation of adipokine expression and inflammatory responses in adipogenic 3T3-L1 cells.

Since METTL3 upregulation may mediate the effects of LIC-A on TNF-α- and LPS-induced adipokine dysregulation and inflammatory responses, METTL3 protein levels in adipogenic 3T3-L1 cells were examined. Acute stimulation with TNF-α or LPS markedly decreased METTL3 levels, whereas LIC-A treatment restored them (Fig. 3A). Next, adipogenic 3T3-L1 cells were transduced with a METTL3-knockdown lentivirus. Knockdown efficiency was confirmed at the protein and mRNA levels (Fig. 3B and C). ELISA revealed that, in response to acute TNF-α stimulation, METTL3 knockdown abolished the beneficial effects of LIC-A. This was supported by the lack of increase in adiponectin secretion, lack of a significant decrease in leptin and resistin expression and lack of an effect on the secreted levels of key proinflammatory cytokines in comparison to the empty vector group (Fig. 3D-F). In accordance with these changes, METTL3 knockdown blocked the LIC-A upregulation of adiponectin mRNA and the downregulation of leptin, resistin and proinflammatory factor transcripts (Fig. 3G and H). Whether LIC-A could ameliorate secretory dysfunction under LPS challenge in METTL3 deficient cells was also investigated.

ELISA confirmed that METTL3 knockdown abrogated the protective effects of LIC-A under LPS challenge, as shown by the persistently low adiponectin secretion alongside unabated levels of leptin, resistin and inflammatory mediators. Consistent with this profile, qPCR analysis further revealed a parallel failure in the transcriptional regulation of these key metabolic and inflammatory genes (Fig. 3I-M). Collectively, these results indicated that the ability of LIC-A to counteract TNF-α- and LPS-induced adipokine dysregulation and inflammation depends on its promotion of METTL3 expression.

To assess the in vivo anti-obesity effects of LIC-A, obesity was induced in C57BL/6J mice who were fed a HFD over a 12-week period. Experimental animals (4–16 weeks of age) were treated with LIC-A (60 mg/kg) by oral gavage (twice a week) (Fig. 4A). The body weight of the experimental group treated with LIC-A decreased compared with that of the HFD control group (Fig. 4B and C). These changes were associated with improved insulin sensitivity and glucose homeostasis (Fig. S2A and B) and reduced hyperglycemia and dyslipidemia (Fig. S2C). In addition, LIC-A efficiently attenuated WAT mass enlargement and impeded the pathological remodeling of this tissue (Fig. 4D and E). A notable reduction in the size of adipocytes in the eWAT of LIC-A-treated animals was observed (Fig. 4F, 4G and S2D), which reflects the inhibition of adipocyte hypertrophy, a hallmark of dysfunctional eWAT in obesity.

Notably, LIC-A treatment markedly attenuated eWAT inflammation. Immunofluorescence staining for the macrophage marker F4/80 revealed a significant reduction in macrophage infiltration (quantified as F4/80-positive area) in the eWAT of LIC-A-treated mice compared with HFD controls (Fig. 4H). Consistently, the entire panel of adipokines showed a metabolically favorable shift. ELISA of eWAT homogenates further showed increased adiponectin levels and decreased levels of leptin, resistin and inflammatory factors. Furthermore, qPCR analysis of inflammatory gene expression at the transcript level confirmed the downregulation of proinflammatory genes (Fig. S2E-H).

Notably, LIC-A treatment also elevated METTL3 expression in the AT of mice, thereby recapitulating the in vitro findings and confirming that LIC-A promotes METTL3 expression in both physiological and experimental settings (Fig. 4I and J). Taken together, these results demonstrated that LIC-A supplementation effectively alleviated metabolic dysregulation and pathological AT changes in diet-induced obese mice, suggesting that the beneficial effects of LIC-A may be mediated, at least in part, through METTL3 upregulation in AT.