Male C57BL/6J mice (6-8 weeks old; 20-22 g) were purchased from Jilin Qianhe Model Biotechnology Co., Ltd. During the study period, mice were maintained under specific pathogen-free (SPF) conditions with controlled temperature (20-22°C) and humidity (45-50%), under a 12-h light/12-h dark cycle. Mice had free access to food and water. All animal experiments were approved by the Institutional Ethics Committee of the School of Basic Medical Sciences, Jilin University (Jilin, China; approval nos. 2025-597 and 2026-491). All procedures were conducted in accordance with the institution's guidelines for the care and use of laboratory animals. To eliminate potential sex-related variability and hormonal fluctuations associated with the estrous cycle, only male mice were included in the present study.

A total of 24 mice were randomly divided into four groups (n=6 per group): Control, control+myonectin, lipopolysaccharide (LPS) and LPS+myonectin groups. Mice in the LPS group received an intraperitoneal injection of LPS (from E. coli O111:B4; L2630; MilliporeSigma) at 10 mg/kg to establish a SIC model (20,21). The LPS+myonectin group received a tail vein injection of recombinant mouse myonectin (rMyonectin; cat.no. 00393-06-100; Aviscera Bioscience, Inc.) at 200 ng/g, a dose based on previous literature (17), 2 h before LPS administration. The control group received equal volumes of PBS via tail vein and intraperitoneal injections, separately. The control+myonectin group received rMyonectin at 200 ng/g via tail vein injection, followed by an equal volume of PBS via intraperitoneal injection 2 h later. Cardiac function was assessed by echocardiography 24 h after LPS injection. Subsequently, mice remained deeply anesthetized with an overdose of 5% isoflurane. After the disappearance of corneal reflexes and pedal withdrawal reflexes, which indicated a deep unconscious state, blood was collected via intracardiac puncture, and heart tissues were harvested as an adjunctive means to confirm death. This procedure ensured euthanasia while the animals were unconscious. The total experimental duration was 26 h. Humane endpoints were predefined as meeting any one of the following conditions: Severe respiratory distress evidenced by open-mouth breathing, a decline in body weight >20% relative to baseline, hypothermia (<32°C), lateral recumbency or loss of responsiveness to external stimuli.

For the cecal ligation and puncture (CLP) model, a total of 24 mice were randomly divided into four groups (n=6 per group): Sham, sham+myonectin, CLP and CLP+myonectin groups. The experimental procedure for CLP was based on previously published literature (22,23). Mice were anesthetized with isoflurane (4% for induction and 2% for maintenance). Following disinfection of the lower abdomen with 75% ethanol, a 1.5 cm midline longitudinal incision was made to expose the cecum. The distal three-quarters of the cecum was ligated. A total of two holes were then punctured in the ligated segment using a 22-gauge needle, and a small amount of fecal content was gently expressed. The cecum was subsequently returned to the peritoneal cavity, and the abdominal incision was closed in layers with sutures. Immediately after surgery, 1 ml sterile saline was administered intraperitoneally to compensate for fluid loss. Sham-operated mice were subjected to the identical surgical procedure except that CLP was omitted. No antibiotics were administered during the experimental period. The sham+myonectin and the CLP+myonectin groups were pretreated with rMyonectin (200 ng/g) via tail vein injection 2 h prior to the procedure. Cardiac function was assessed by echocardiography 24 h after surgery. The total experimental duration was 26 h. The procedures for anesthesia, euthanasia and blood and tissue collection, as well as the humane endpoints, were identical to those described for the LPS model.

To determine the survival rate, separate experiments were conducted. For the LPS model, mice were randomly divided into four groups (n=10 per group): Control, control+myonectin, LPS and LPS+myonectin groups. For the CLP model, mice were randomly divided into four groups (n=10 per group): Sham, sham+myonectin, CLP and CLP+myonectin groups. Mice were pretreated via tail vein injection with either rMyonectin (200 ng/g) or PBS 2 h prior to an intraperitoneal dose of LPS (15 mg/kg) or CLP surgery. Survival was monitored every 12 h for 3 days as described previously (24,25).

A total of 128 mice were used in the present study, of which 123 were euthanized, while 5 were found dead (attributed to SIC-mediated cardiac emergencies). Of the 123 mice that were euthanized, 24 were euthanized upon reaching humane endpoints, and the remaining 99 were euthanized at the scheduled end of the study.

Echocardiography was performed under isoflurane anesthesia (4% for induction and 2% for maintenance) in mice from each group using a GE Vivid E95 ultrasound system (GE Healthcare Technologies, Inc.) to non-invasively evaluate changes in cardiac structure and function. M-mode images were acquired from the left ventricular long-axis view, and left ventricular parameters including left ventricular ejection fraction (LVEF), left ventricular fractional shortening (LVFS), left ventricular internal diameter at end-systole (LVIDs), left ventricular internal diameter at end-diastole (LVIDd) and heart rate (HR) were measured. The echocardiographer was blinded to the treatment groups.

Cardiac tissues were fixed in 4% paraformaldehyde at 4°C for 48 h, embedded in paraffin and sectioned at 4-μm thickness. Sections were deparaffinized with dimethylbenzene and rehydrated through a graded ethanol series (100, 95, 80 and 70%). Subsequently, parallel sections were processed for hematoxylin and eosin (H&E) staining and terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) assay. The stained sections were observed and imaged under the microscope (OLYMPUS BX53), and the images were analyzed using ImageJ software (National Institutes of Health; v1.54f). The apoptotic index was calculated as the integrated density of TUNEL-positive cells divided by the total DAPI-stained nuclear area.

The relative levels of ATP were determined using the ATP assay kit (cat. no. S0027; Beyotime Biotechnology) according to the manufacturer's instructions. Samples (20 mg cardiac tissue or cells from one well of a 6-well plate) were homogenized with ATP lysis buffer (200 μl). Cell lysates or tissue homogenates were centrifuged at 12,000 × g for 5 min at 4°C, and the supernatants were collected and kept on ice. ATP working solution (100 μl) was added to each well of 96-well plates and allowed to equilibrate at room temperature for 3-5 min. Subsequently, 20 μl sample or standard solution was added to each well and mixed thoroughly. The values, relative light unit (RLU), were measured using the multimode microplate reader (CLARIOSTAR, BMG Labtech GmbH).

Serum was obtained by centrifugation (1,000 × g; 15 min; 4°C) of blood samples after allowing them to clot at room temperature for 2 h. The levels of cardiac troponin I (cTn-I) and brain natriuretic peptide (BNP) in the serum were measured using the commercial ELISA kits (cat. nos. CSB-E08421m and CSB-E07971m; Cusabio Technology, LLC) according to the manufacturer's instructions.

Mitochondrial ultrastructure was observed using TEM. Heart tissue was initially fixed in 3% glutaraldehyde overnight at 4°C, post-fixed in 1% osmium tetroxide for 2 h at 4°C and rinsed with PBS. Following dehydration through a graded ethanol series, the samples were embedded in Epon resin. Ultrathin sections (50 nm) were cut using a diamond knife and mounted on copper grids. The sections were then stained with uranyl acetate for 15 min at room temperature and lead citrate for 10 min at room temperature. Images were acquired using the TEM (Hitachi H600 Electron Microscope, Hitachi, Ltd.) at magnifications of ×3,000, ×7,000 and ×20,000 to assess overall morphology and detailed structures.

The isolation and culture of NMCMs were performed based on a previously described method (26). Neonatal C57BL/6J mice (1-3 days old) were derived from an in-house SPF breeding colony established by mating male and female mice purchased from Jilin Qianhe Model Biotechnology Co., Ltd. Following anesthesia induction with 2% isoflurane (on a thermostatic heating pad at 37°C for ~2 min) and confirmation of loss of consciousness and reflexes, mice were euthanized by rapid decapitation with sterile scissors, and hearts were aseptically harvested, promptly chilled, washed, and minced in cold Ca²⁺- and Mg²⁺-free Hank's Balanced Salt Solution (cat. no. 14175095; Gibco; Thermo Fisher Scientific, Inc.). The tissue fragments were then digested in a solution of 1 mg/ml trypsin (cat. no. T4799; MilliporeSigma) at 4°C for 7 h. The trypsin solution was then removed. The tissue fragments were subjected to sequential digestions with 0.8 mg/ml Collagenase Type II (cat. no. C6885; MilliporeSigma) in a 37°C water bath for 5 min per cycle, until no visible tissue fragments remained. The released cell suspension from each digestion was collected and kept on ice. The cell suspension was centrifuged at 200 × g for 5 min at 4°C. The pellet was resuspended in Dulbecco's modified Eagle medium/F12 Ham medium (DMEM/F12; cat. no. C11330500BT; Gibco; Thermo Fisher Scientific, Inc.) supplemented with 10% Fetal Bovine Serum (FBS; cat. no. A5256701; Gibco; Thermo Fisher Scientific, Inc.) and 1% penicillin-streptomycin solution. The cell suspension was filtered through a cell strainer and cultured for 90 min under standard culture conditions (37°C, 5% CO₂) to remove fibroblasts. Cardiomyocytes were then collected, plated onto culture dishes pre-coated with 0.01% poly-L-lysine (cat. no. ST508; Beyotime Biotechnology) and cultured until a synchronous, spontaneous beating rhythm was observed, after which they were ready for subsequent treatments. NMCMs were pretreated for 2 h with rMyonectin or with the AMPK inhibitor Compound C (CC; 10 μM; cat. no. HY-13418A; MedChemExpress) (27,28), followed by stimulation with 10 μg/ml LPS for 24 h (29).

The AdipoR1-targeting siRNA was designed and synthesized by GenCefe Biotech and had the following sequences: Sense strand, 5'-GGCUCUUCCACACUGUCUTT-3'; antisense strand, 5'-UAGACAGUGUGGAAGAGCCTT-3'. The negative control siRNA sequences were: Sense strand, 5'-UUCUCCGAACGUGUCACGUTT-3'; antisense strand, 5'-ACGUGACACGUUCGGAGAATT-3'. Cells were transfected with 150 pmol siRNA per well in a 6-well plate using 7.5 μl GP-transfect-Mate reagent (cat. no. G04008; Shanghai GenePharma Co., Ltd.). After 6 h incubation at 37°C, the medium was replaced with fresh culture medium, and the cells were further cultured. The levels of mRNA and protein were assessed at 24 and 48 h, respectively.

Cell viability of NMCMs was assessed using the CCK-8 assay (cat. no. BA00208; Bioss) according to the manufacturer's instructions. Absorbance was measured at 450 nm.

The activity of intracellular LDH was determined with the commercial assay kit (cat. no. BC0685; Beijing Solarbio Science & Technology Co., Ltd.) per the manufacturer's instructions. Cells were lysed in the provided extraction buffer and sonicated on ice. After centrifugation of the lysates (8,000 × g; 10 min; 4°C), the absorbance of the supernatant was measured at 450 nm. The protein concentration of the supernatant was determined using a BCA Protein Assay Kit (cat. no. C05-02001; Bioss) to normalize the LDH activity. Finally, the specific activity of LDH was calculated and expressed as units per milligram of protein.

MMP was evaluated using a JC-1 assay kit (cat. no. C2003S; Beyotime Biotechnology) following the manufacturer's instructions. NMCMs were plated on glass-bottom confocal culture dishes and stained with 1 μM JC-1 probes for 20 min at 37°C in the dark. After washing twice with PBS, fluorescent images were immediately acquired using the confocal microscope (Nikon Corporation). The fluorescent signals of JC-1 aggregates (red) and monomers (green) were recorded. The ratio of red-to-green fluorescence intensity was quantified using ImageJ software (National Institutes of Health, v1.54f) to evaluate MMP.

The activities of mitochondrial respiratory chain complexes I and III were assessed using the Cell Mitochondrial Complex I (NADH-CoQ Reductase) Activity Assay Kit (cat. no. E-BC-K834-M; Wuhan Elabscience Biotechnology Co., Ltd.) and the Cell Mitochondrial Complex III (Coenzyme Q-Cytochrome C Reductase) Activity Assay Kit (cat. no. E-BC-K836-M; Wuhan Elabscience Biotechnology Co., Ltd.), respectively. Cardiomyocytes were harvested, resuspended in the provided extraction solution and processed according to the manufacturer's instructions for mitochondrial respiratory chain complex extraction. The absorbance was measured at 340 nm (for complex I) and 550 nm (for complex III).

After treatment according to the experimental groups, cells were cultured for 24 h. OCR was evaluated using the Enhanced Oxygen Consumption Rate Fluorometric Assay Kit (cat. no. E-BC-F070; Wuhan Elabscience Biotechnology Co., Ltd.). The microplate was placed in the multifunctional microplate reader (Synergy H1, BioTek; Agilent Technologies, Inc.) set at 37°C in dynamic reading mode. The excitation wavelength was set at 405 nm, the emission wavelength at 675 nm, and measurements were taken every 2 min for 100 min. Finally, the fluorescence values were plotted against time, and OCR was represented by the slopes of the curves.

Cell apoptosis was analyzed using flow cytometry. Following harvest by trypsinization, cells were stained with Annexin V-FITC and propidium iodide (PI), and then immediately analyzed by a DxFLEX flow cytometer (Beckman Coulter, Inc.). The data were analyzed using FlowJo software (v10.8.1; BD Biosciences) to quantify the percentage of apoptotic cells in each group.

Proteins were extracted from cardiac tissue and NMCMs using RIPA lysis buffer (cat. no. PC101; Shanghai Epizyme Biopharmaceutical Technology Co., Ltd.) supplemented with protease and phosphatase inhibitors. The protein concentration was quantified with the BCA Protein Assay Kit (cat. no. C05-02001; Bioss). Equal amounts of proteins (20 μg per lane) were denatured in SDS-PAGE loading buffer (cat. no. P1040; Beijing Solarbio Science & Technology Co., Ltd.) at 100°C for 5 min, separated by 8-12% SDS-PAGE and transferred to PVDF membranes. The membranes were blocked with 5% skim milk for 1 h at room temperature and then incubated overnight at 4°C with the following primary antibodies: Bax (1:1,000; cat. no. ab32503; Abcam), Bcl-2 (1:1,000; cat. no. A19693; ABclonal Biotech Co., Ltd.), cleaved caspase-3 (1:600; cat. no. WL02117; Wanleibio Co., Ltd.), caspase-3 (1:500; cat. no. T40044; Abmart Pharmaceutical Technology Co., Ltd.), PGC-1α (1:2,000; cat. no. ab313559; Abcam), nuclear respiratory factor 1 (NRF1; 1:1,000; cat. no. A3252; ABclonal Biotech Co., Ltd.), mitochondrial transcription factor A (TFAM; 1:1,000; cat. no. 15218; Cell Signaling Technology, Inc.), mitofusin 2 (Mfn2; 1:3,000; cat. no. ab124773; Abcam), optic atrophy 1 (OPA1; 1:1,000; cat. no. ab157457; Abcam), phosphorylated (p)-dynamin-related protein 1 (Drp1; Ser616; 1:1,000; cat. no. ab314755; Abcam), Drp1 (1:4,000; cat. no. ab184247; Abcam), p-AMPK (1:1,000; cat. no. ab133448; Abcam), AMPK (1:1,000; cat. no. ab207442; Abcam), AdipoR1 (1:4,000; cat. no. bs-0610R; Bioss), β-actin (1:8,000; cat. no. P30002; Abmart Pharmaceutical Technology Co., Ltd.) and β-tubulin (1:10,000; cat. no. A12289; ABclonal Biotech Co., Ltd.). After washing, the membranes were incubated with HRP-conjugated Goat Anti-Rabbit secondary antibody (1:10,000; cat. no. ab6721; Abcam) for 1 h at room temperature. After incubation with an enhanced chemiluminescence (ECL) substrate, the bands were visualized using MiniChemi 610 System (SinSage Technology, Co., Ltd.) and SageCapture™ software. Band intensities were quantified using ImageJ software (National Institutes of Health, v1.54f) and normalized to β-actin or β-tubulin.

Total RNA was extracted using the Fast Total RNA Extraction Kit (cat. no. RP1201; BioTeke Corporation). cDNA was synthesized from the extracted RNA with the ToloScript All-in-One RT EasyMix for qPCR (cat. no. 22107-01; Tolo Biotech Co., Ltd.) according to the manufacturer's instructions. The primers were synthesized by Comate Bioscience. The primer sequences used in the present study were as follows: AdipoR1: Forward 5'-GAGAAGATGGAGGAGTTCGTGTA-3', reverse 5'-AGCAGGTAGTCGTTGTCTTTCAG-3'; β-actin: Forward 5'-GTACTCTGTGTGGATCGGTGG-3', reverse 5'-GCAGCTCAGTAACAGTCCG-3'. Following the mixture of cDNA, primers, and the 2X Q3 SYBR qPCR Master Mix (cat. no. 22204; Tolo Biotech Co., Ltd.), qPCR was performed using the Real-Time PCR system (ABI 7500 DX). The thermocycling protocol was as follows: Initial denaturation at 95°C for 30 sec, followed by 40 cycles of 95°C for 10 sec and 60°C for 30 sec. A melt curve analysis was performed to verify amplification specificity. Relative gene expression was quantified via the 2^−ΔΔCq method (30), where β-actin served as internal control.

Data from three or more independent experiments are presented as the mean±SEM. Statistical analyses were performed using GraphPad Prism software (version 10.0; Dotmatics). Comparisons among multiple groups were performed using one-way ANOVA followed by Tukey's multiple comparison test. Survival was assessed using the Kaplan-Meier method, and differences between groups were compared with the Gehan-Breslow-Wilcoxon test. P<0.05 was considered to indicate a statistically significant difference.

Following pretreatment with rMyonectin via tail vein injection, SIC was induced in mice by intraperitoneal injection of LPS after a 2-h interval. Cardiac function was evaluated by echocardiography 24 h post-induction. Subsequently, blood samples and heart tissue were collected under anesthesia for analysis (Fig. 1A). The results showed that rMyonectin administration significantly improved the survival rate of mice challenged with LPS (Fig. 1B). Echocardiographic assessment revealed that LPS-challenged mice displayed significant impairments in cardiac systolic function compared with controls, characterized by reduced LVEF and LVFS, alongside increased LVIDs (Fig. 1C-F). Consistent with these functional deficits, serum levels of BNP and cTn-I were markedly elevated in LPS-challenged mice (Fig. 1G and H), confirming the successful induction of SIC. Notably, pretreatment with rMyonectin effectively attenuated these pathophysiological alterations, improving systolic performance and reducing myocardial injury (Fig. 1C-H). Histopathological analysis revealed that myocardial fibers in the control group were orderly arranged with preserved interstitial integrity. rMyonectin treatment alone induced no structural alterations. By contrast, LPS challenge induced distinct pathological changes, including cardiomyocyte disarray, interstitial edema and vacuolar degeneration. Importantly, rMyonectin pretreatment significantly attenuated these LPS-induced structural abnormalities (Fig. 1I). Furthermore, rMyonectin significantly attenuated LPS-induced cardiomyocyte apoptosis, as shown by a reduced apoptosis index (Fig. 1J and K), downregulated cleaved caspase-3 and Bax, and upregulated Bcl-2 in myocardial tissue (Fig. 1L).

Moreover, a CLP-induced model was established in C57BL/6J mice to further evaluate the effects of rMyonectin on SIC (Fig. 2A). The results showed that rMyonectin significantly improved the survival rate (Fig. 2B), ameliorated cardiac dysfunction (Fig. 2C-G) and myocardial injury (Fig. 2H and I), and inhibited cardiomyocyte apoptosis (Fig. 2J-L) in CLP-induced SIC mice. These results demonstrate that rMyonectin protects against SIC irrespective of the sepsis model, whether endotoxemic or polymicrobial.

The present study revealed that rMyonectin attenuated the LPS-induced decrease in myocardial ATP levels (Fig. 3A). This indicated a beneficial role for myonectin in cardiac energy metabolism during SIC. Due to the central role of mitochondria in cardiac energetics, their morphology was assessed using TEM. Results revealed that LPS challenge induced mitochondrial shortening, swelling, cristae disruption and increased vacuolation. These structural defects were mitigated by rMyonectin pretreatment (Fig. 3B). At the molecular level, relative to LPS administration alone, pretreatment with rMyonectin upregulated the expression of PGC-1α, NRF1, TFAM, OPA1 and Mfn2 while reducing the p-Drp1(Ser616)/Drp1 ratio, thereby promoting mitochondrial biogenesis and restoring the balance of mitochondrial fusion-fission dynamics (Fig. 3C). Consistently, in CLP-induced SIC mice, rMyonectin pretreatment also attenuated myocardial ATP depletion (Fig. 4A), improved mitochondrial ultrastructure (Fig. 4B), promoted mitochondrial biogenesis and restored the balance of mitochondrial fusion-fission dynamics (Fig. 4C).

NMCMs were isolated from 1-3-day-old C57BL/6J mice and treated with LPS to establish an in vitro model of SIC (Fig. 5A). To evaluate the cellular safety of rMyonectin, NMCMs were treated with increasing concentrations of rMyonectin (1, 2, 5 and 8 μg/ml). The CCK-8 assay showed that rMyonectin at these concentrations had no significant effect on cell viability (Fig. 5B). To assess its protective effect, NMCMs were pretreated with the same concentrations of rMyonectin prior to LPS challenge. Analysis revealed that rMyonectin reduced the activity of LPS-induced intracellular LDH. Notably, LDH activity was significantly reduced at a concentration of 5 μg/ml, but no further reduction was observed at 8 μg/ml (Fig. 5C). Therefore, 5 μg/ml rMyonectin was selected for subsequent experiments. At this optimal concentration, rMyonectin pretreatment reduced LPS-induced apoptosis (Fig. 5D and E) and downregulated cleaved caspase-3 and Bax, while upregulating Bcl-2 expression (Fig. 5F). Taken together, these data indicate that rMyonectin attenuates LPS-induced cardiomyocyte injury and inhibits apoptosis.

In cardiomyocytes, rMyonectin reversed the LPS-induced decrease in ATP levels (Fig. 6A), ameliorated the reductions in OCR (Fig. 6B) and in the activities of mitochondrial respiratory chain complexes I and III (Fig. 6C), and stabilized MMP (Fig. 6D). Consistent with the in vivo observations, LPS challenge downregulated PGC-1α, NRF1, TFAM, OPA1 and Mfn2 while increasing the p-Drp1(Ser616)/Drp1 ratio, all of which were reversed by rMyonectin (Fig. 6E). These results indicate that rMyonectin ameliorates LPS-induced mitochondrial dysfunction, as evidenced by enhanced mitochondrial respiratory function, stabilized membrane potential, and restored mitochondrial dynamics and biogenesis.

Due to the key role of AMPK in energy metabolism, the present study first assessed AMPK activation. Analysis revealed that rMyonectin effectively attenuated the LPS-induced reduction in AMPK phosphorylation in both myocardial tissue and NMCMs (Fig. 7A and B). To determine whether AMPK activation mediates the protective effects of rMyonectin, the present study inhibited AMPK in cardiomyocytes using CC in addition to rMyonectin pretreatment (Fig. 7C). CC abolished the protective effects of rMyonectin against cardiomyocyte injury (Fig. 7D) and apoptosis (Fig. 7E-G). Furthermore, CC attenuated the ability of rMyonectin to elevate intracellular ATP levels (Fig. 8A), to increase OCR (Fig. 8B) and activities of mitochondrial respiratory chain complexes I and III (Fig. 8C), and to preserve MMP (Fig. 8D). Western blot analysis further demonstrated that the rMyonectin-induced upregulation of PGC-1α, NRF1, TFAM, OPA1 and Mfn2, as well as the downregulation of the p-Drp1(Ser616)/Drp1 ratio, was abolished upon AMPK inhibition (Fig. 8E). These results demonstrate that the anti-apoptotic and mitochondrial-protective effects of rMyonectin are mediated by AMPK activation.

Myonectin is a paralog of adiponectin, sharing similar structural and functional characteristics. Adiponectin mediates its cardioprotective effects primarily through activating the adiponectin receptors. Notably, AdipoR1 has been established as an upstream activator in the AMPK signaling pathway (31,32). To determine whether myonectin protected cardiomyocytes through the AdipoR1/AMPK pathway, the present study measured AdipoR1 protein levels in myocardial tissue and NMCMs. The results indicated that rMyonectin treatment reversed the LPS-induced downregulation of AdipoR1 expression in these models (Fig. 9A and B). Following siRNA-mediated knockdown of AdipoR1 in NMCMs (with transfection efficiency validated in Figs. S1 and S2), AMPK phosphorylation was reduced (Fig. 9C and D), and the protective effects of rMyonectin were abolished. Specifically, AdipoR1 knockdown reversed the protective effects of rMyonectin against cardiomyocyte injury (Fig. 9E) and apoptosis (Fig. 9F-H). Moreover, it eliminated the rMyonectin-induced enhancements in intracellular ATP levels (Fig. 10A), OCR (Fig. 10B), the activities of mitochondrial respiratory chain complexes I and III (Fig. 10C), as well as the restoration of MMP (Fig. 10D). Western blot analysis further demonstrated that the rMyonectin-induced upregulation of PGC-1α, NRF1, TFAM, OPA1 and Mfn2, as well as the downregulation of the p-Drp1(Ser616)/Drp1 ratio, was abolished by AdipoR1 knockdown (Fig. 10E). Collectively, these results demonstrate that rMyonectin protects cardiomyocytes from LPS-induced injury via the AdipoR1/AMPK pathway.