1. Introduction
Sepsis, a major international health challenge, refers to a life-threatening pathological condition characterised by organ impairment induced by a dysregulated immune system [
1,
2]. The physiopathology by which the dysregulations of acute inflammatory response and associated organ injury occur in sepsis is yet to be investigated in depth [
3].
Substance P (SP) is an undecapeptide encoded by the
Tac1 gene in rodents [
4]. It has been implicated in diverse biological processes and pathological settings, predominantly by activating its functional receptor, named neurokinin 1 receptor (NK1R) [
5]. Increased SP-NK1R signalling has been shown to contribute to aberrant systemic inflammatory response, leading to acute inflammatory injury in multiple organs, including the liver, lungs, and kidney in sepsis [
5,
6,
7]. However, the precise mechanism still needs to be fully understood.
Emerging evidence has highlighted the involvement of unorganized programmed cell death in the host acute inflammatory response in sepsis [
8]. Ferroptosis is a newly identified programmed cell death triggered by intracellular iron-overload-mediated lipid peroxidation [
9,
10,
11]. Ferroptosis is closely related to damage-associated molecular patterns and the release of pro-inflammatory mediators, which further results in increased host acute inflammatory responses [
11,
12,
13]. It has been recognized as a significant contributor to the pathogenesis of host-dysregulated acute inflammatory response in sepsis and associated organ injury [
14,
15,
16]. The process of ferroptosis is modulated by multiple signalling cascades [
9,
10,
11]. Glutathione peroxidase 4 (Gpx4) is an important inhibitor of ferroptosis that uses glutathione (GSH) as a reducing substrate to inhibit lipid peroxidation and maintain lipid homeostasis [
17,
18]. The transcription factor nuclear factor erythroid 2-related factor 2 (Nrf2) has also been recognized as a versatile negative regulator of ferroptosis [
19,
20]. Nrf2 can modulate iron recycling, storage, and usage and is therefore central to iron homeostasis. Nrf2 can also increase the biosynthesis of GSH and enhance the expression and activity of Gpx4 in repressing lipid peroxidation [
19,
20]. Consequently, the dysregulation of the Nrf2-Gpx4 cascade has been recognized as an important mechanism of ferroptosis in a wide range of disorders [
21,
22,
23]. Under pathological conditions, ferroptosis and host acute inflammatory response can lead to each other, thus driving an auto-amplification loop and further exaggerating ferroptosis and the host acute inflammatory response [
12,
24,
25]. Therefore, the dysregulated activation of pro-inflammatory signalling pathways, such as the NF-κB signalling pathway and MAPK signalling pathway, leading to increased acute inflammatory response, has also been recognised as a significant mechanism of aberrant ferroptosis in various diseases [
12,
24,
25].
The activation of the ERK1/2-NF-κB cascade promotes the pro-inflammatory role of SP in CLP-induced sepsis and organ damage [
26]. Moreover, previous studies have shown that SP upregulated the expression of cyclooxygenase-2 (COX-2), a well-recognized driver and marker of ferroptosis [
11], in various pathological conditions [
27,
28,
29]. Noteworthily, increased SP-NK1R signalling has been shown to increase the expression of COX-2 in the lungs of mice following local burn injury via the activation of the ERK1/2-NF-κB cascade [
27]. Considering the roles of the ERK1/2-NF-κB cascade and COX-2 in ferroptosis and that of the SP-NK1R axis in activating the ERK1/2-NF-κB cascade and promoting the expression of COX-2, increased SP-NK1R signalling may also promote ferroptosis in sepsis.
However, whether the SP-NK1R axis contributes to sepsis and associated organ injury via the promotion of ferroptosis remains to be investigated in depth. Likewise, whether dysregulated ferroptosis is involved in the impacts of the SP-NK1R axis on acute inflammatory response and organ injury in mice with sepsis is not fully understood. Therefore, this study aimed to investigate the potential impact and underlying mechanism of endogenous SP on ferroptosis and associated acute inflammatory injury in the liver and lungs in mice following caecal ligation puncture (CLP)-surgery-induced sepsis. To achieve this aim, the genetic deletion of the Tac1 gene, the pharmacological blockade of NK1R using L703606, and the combination of these two approaches were employed in this study.
2. Materials and Methods
2.1. Group Setting
This in vivo study is regulated by the Animal Welfare Act and was approved by the University of Otago Animal Ethics Committee (AUP-19-104). The protocol used in this in vivo study is presented in
Figure 1. Twenty-four
Tac1+/+ (Balb/c, male) and twenty-four
Tac1−/− (Male) mice aged between 8 and 10 weeks with body weights ranging from 20 to 30 g were randomly divided into three groups of eight mice: the sham-saline group, the CLP-saline group, and the CLP-L703606 group, respectively (n = 8 each).
Tac1+/+ mice were acquired from the Christchurch Animal Research Area.
Tac1−/− mice were a gift from Prof. AI Basbaum (University of California, San Francisco, CA, USA) and bred as described previously [
30,
31].
2.2. Sepsis Establishment, Manipulations, and Sample Collection in Mice
CLP-surgery-induced sepsis was induced according to a previously reported protocol with minor modifications [
32]. L703606, a specific antagonist of NK1R widely used to block the interaction between SP and NK1R, was dissolved in DMSO and then diluted in sterile saline before experiments. Then, 0.2 mL of saline or L703606 (4 mg/kg) was peritoneally injected into all mice 30 min before the sham or CLP surgery. Prior to surgery, mice were anesthetized by inhaling 2% isoflurane. During the operation, inhaled isoflurane was reduced to 1%. Aseptic surgical techniques were applied during surgery. Firstly, the abdominal area was disinfected after the abdominal fur was shaved. Secondly, a small midline incision was made through the skin and peritoneum of the abdomen to expose the caecum. Thirdly, the cecum was ligated at the designated position (1 cm from the tip of the cecum) without occluding the bowel passage with silkam 5.0. Subsequently, the cecum was perforated at the distal end using a 22-gauge needle to make a through-and-through puncture. Afterwards, a small amount of stool was squeezed out through both holes. Thereafter, the bowel contents were repositioned and the abdomen was sutured using permilene 5.0 thread. Mice in the sham operation group underwent the same operation without CLP procedure. All mice received saline at the end of the operation by the subcutaneous route. Buprenorphine (Temgesic, 0.2 mg/kg) was subcutaneously injected into all mice 45 min before and 3 h after surgery for analgesia. Eight hours after the sham or CLP surgery, mice were euthanized by intraperitoneally injecting a lethal dose of sodium pentobarbital (150 mg/kg). Blood was withdrawn from the right ventricle using heparinized syringes via cardiac puncture and then spun for 5 min at 4 °C (1000 g). Then, the plasma was carefully pipetted into chilled microtubes and then kept in a −80 °C freezer. The liver tissues were either fixed in 10% neutral phosphate-buffered formalin or frozen in liquid nitrogen and further transferred to a −80 °C freezer. The cranial lobe of the right lung was used for the wet-to-dry (W/D) ratio measurement. The remaining lung tissues were processed and stored as for the protocol applied to the liver tissues.
2.3. Evaluation of Sepsis Severity in Mice
The physical condition of mice after the sham or CLP operation was recorded hourly for eight hours. The body temperature was detected in four randomly selected mice in each group through a rectal probe every two hours for eight hours. The severity of sepsis was evaluated according to a previously reported murine sepsis scoring system with minor modifications [
33].
2.4. Measurement of Lung W/D Ratio
The cranial lobe of the right lung from every mouse was dissected and weighed immediately (wet weight). Every collected lobe was kept in a small cassette and placed in a 60 °C oven for 24 h. On the second day, these lobes were weighed again (dry weight). The lung W/D ratio was calculated as lung W/D ratio = wet weight/dry weight.
2.5. Determination of SP in Tissues
Tissue samples were weighted (~20 mg), thawed, snipped, homogenized in 20 mM phosphate buffer (pH 7.4), and spun (4 °C, 10,000× g, 10 min). Supernatants were transferred to fresh chilled microtubes. The concentrations of SP in the supernatants were measured using the competitive ELISA method according to the instruction of the SP ELISA kit (Cayman Chemical, Ann Arbor, MI, USA). The concentration of protein in tissues was determined by the Bradford assay. The concentration of SP was corrected for the total protein content of tissues and expressed as ng per mg protein.
2.6. Measurement of Pro-Inflammatory Cytokines and Chemokines in Tissues
The concentrations of cytokines (IL-1β, IL-6, and TNF-α) and chemokines (MCP-1 and MIP-2) in the liver and lungs were measured using the sandwich ELISA method according to the instructions of the DuoSet ELISA kits (R&D System, Minneapolis, MN, USA). The concentrations of these mediators in tissues were corrected for the total protein content of the tissues. The results were presented as pg or ng per mg protein.
2.7. Western Blotting
Tissues were homogenized in chilled RIPA buffer supplemented with protease and phosphatase inhibitors on ice. Homogenates were then centrifuged for 10 min (4 °C, 15,000×
g) and the resulting supernatants contained the total protein of tissues. Protein samples were mixed with 4X loading buffer supplemented with 2-mercaptoethanol and then boiled at 100 °C for 5 min. Then, 20~40 µg protein was separated by electrophoresis using a 10% sodium dodecyl sulphate-polyacrylamide gel along with a molecular weight marker (100 V, 120 min) and then transferred to a methanol-activated polyvinylidene difluoride (PVDF, Bio-Rad Laboratories, Hercules, CA, USA) membrane by wet transfer (100 V, 90 min). The PVDF membrane was blocked at room temperature for 1 h using 5% (
w/
v) bovine serum albumin (BSA) in 0.1% Tris-buffered saline-Tween 20 solution (TBST). Subsequently, the membrane was incubated with appropriate dilutions of primary antibodies targeting NK1R, Nrf2, Gpx4, and GAPDH (
Table 1) overnight at 4 °C with gentle agitation. The membrane was washed with TBST and then incubated with HRP-conjugated secondary antibodies (1:5000) at room temperature for 1 h the following day. After washing with TBST, the membrane was detected with ECL Western blotting substrate solution (Thermo Fisher Scientific, Waltham, MA, USA), followed by visualizing the bands on a UVITec Alliance Q9 Advanced machine (Uvitec Cambridge Ltd., Cambridge, UK). Bands were semi-quantitated by the ImageJ software version 1.54d and compared for relative intensities. Results were expressed as fold increases over the control.
2.8. Immunohistochemistry Staining
Formalin-fixed lung tissues were processed using a tissue processor (Leica Biosystems, Wetzlar, Germany) and embedded in paraffin wax using an embedding station (Leica Biosystems, Wetzlar, Germany). Prior to staining, 4 µm tissue sections were prepared using a microtome (Leica Biosystems, Wetzlar, Germany), followed by mounting onto adhesive microscope slides (Trajan Scientific and Medical, Ringwood, Australia). Tissue sections were further deparaffinized and rehydrated. These pre-processed tissue sections underwent an antigen retrieval process completed in a pressure cooker (100 °C, 4 min) with Tris-EDTA buffer (pH 9.0), followed by cooling down to room temperature in the buffer (~two hours). These sections were then permeabilizated by PBS with 0.25% Triton (
w/
v) for 15 min at 4 °C. After washing with PBST, tissue sections were blocked with 5% BSA in the permeabilization buffer for 1 h at room temperature, followed by incubation with appropriate dilutions of primary antibodies targeting to Nrf2 and Gpx4 overnight in a humidified chamber (4 °C), as described in
Table 1. After 3 washes with PBST, lung sections were incubated with 3% H
2O
2 for 15 min to inactivate tissue endogenous peroxidases (room temperature). Subsequently, lung sections were incubated with an appropriate dilution of HRP-conjugated secondary antibody (
Table 1) for 1 h (room temperature). After washing, these sections were incubated with DAB solution for 3 min (Nrf2) or 5 min (Gpx4) in the dark (room temperature). Slides were dehydrated, permanently mounted, and observed under a light microscope. The expressions of Nrf2 and Gpx4 were quantitated using ImageJ software version 1.54d (IHC profiler plugin).
2.9. Measurement of Iron, Malondialdehyde (MDA), and GSH in Tissues
The concentrations of iron (Universal Biologicals Ltd., Cambridge, UK), MDA (BQC Redox Technologies, Asturias, Spain), and GSH (Cayman Chemical, Ann Arbor, MI, USA) were measured in the liver and lung directly according to the instructions of the corresponding assay kits. The concentrations of these mediators in tissues were corrected for the total protein content of the tissues. The results were presented as fold increases over the control.
2.10. Histological Analysis
Pre-processed tissue slides were stained with haematoxylin and eosin and the tissue structure was observed under a light microscope (Leica Biosystems, Wetzlar, Germany). The severity of acute liver injury was measured according to the “Hepatic Injury Severity Scoring”, as described previously [
34]. The severity of sepsis-associated acute lung injury was evaluated according to a previously reported semiquantitative scoring system [
35].
2.11. Statistical Analysis
Data are presented as mean ± SD. GraphPad Prism Software version 9.2.0 (GraphPad Software Incorporated, San Diego, CA, USA) was used to perform all the statistical analyses in this study. All data were analysed for normal distribution by the Shapiro–Wilk test. One-way or Two-way Analysis of Variance (ANOVA) with post hoc Tukey’s multiple comparisons test was performed with the normal distribution data to compare multiple groups. Statistical significance was set as p-value < 0.05.
4. Discussion
The pathogenesis of dysregulated acute inflammatory reaction in sepsis involves many mechanisms [
3,
36]. As an immune-derived cell death, ferroptosis is also closely associated with the dysregulation of host acute inflammatory responses under various pathological conditions [
12,
24,
25]. Moreover, dysregulated ferroptosis has been linked to the physiopathological mechanism of dysregulated acute inflammatory response in sepsis and related organ injury [
14,
15,
16]. This study demonstrated that CLP surgery significantly activated SP-NK1R signalling in the liver and lungs, leading to increased ferroptosis in these tissues in mice. In contrast, suppressing the increased SP-NK1R signalling attenuated these alterations in mice. This protection effect was accompanied by an attenuated acute inflammatory response (pro-inflammatory cytokines and chemokines) and injury (architectural destructions) in the liver and lungs and clinical signs (hypothermia, piloerection, and shivering) in mice and improved the physical conditions of mice (sepsis severity scores). This study also demonstrated that the CLP surgery inactivated Nrf2-Gpx4/GSH signalling, thereby promoting ferroptosis in the liver and lungs in mice, which was associated with the detrimental impact of the SP-NK1R axis in sepsis.
Ferroptosis is a recently recognized programmed cell death resulting from the increased accumulation of intracellular iron-mediated dysregulation of lipid peroxidation [
10]. Many studies have illustrated that aberrant ferroptosis contributes to organ impairment caused by sepsis, whereas inhibiting ferroptosis attenuates sepsis-related organ injury [
14,
15,
16]. Intracellular iron overload and increased lipid peroxidation are two well-recognized markers of ferroptosis [
10,
37]. In line with previous investigations, this study also observed a significant elevation in the concentration of iron in the liver and lungs in mice following CLP-surgery-induced sepsis [
38,
39]. MDA is a crucial final product of the process of lipid peroxidation; thus, MDA concentration is a frequently used index of lipid peroxidation [
40]. Consistent with previous investigations, we found that the concentration of MDA in the liver and lungs in mice with CLP-surgery-induced sepsis was also increased [
38,
39]. These alterations show that the dysregulation of intracellular iron accumulation and lipid peroxidation in the liver and lungs in mice arises following CLP-surgery-induced sepsis, indicating that ferroptosis was increased in these tissues in mice with sepsis. Given the roles of the SP-NK1R axis in promoting acute inflammatory response [
5,
41,
42] and COX-2 expression [
27,
28,
29] in inflammation-related pathological circumstances, it is worth probing into the impact of this axis on the profile of ferroptosis in sepsis. Notably, this study showed that these increases in the concentration of iron and MDA in the liver and lungs in mice following CLP-surgery-induced sepsis were reduced by either the deletion of the
Tac1 gene, the pharmacological blockage of NK1R, or the combination of these two methods. These results collectively suggest that increased SP-NK1R signalling contributes to ferroptosis in the liver and lungs in mice following CLP-surgery-induced sepsis. Notably, SP-NK1R signalling has a similar impact on the acute inflammatory response and injury in the liver and lungs in mice following CLP-surgery-induced sepsis, indicating that elevated ferroptosis is associated with acute liver and lung injury in sepsis.
The discovery of the role of the SP-NK1R axis in ferroptosis in the liver and lungs in mice with CLP-surgery-induced sepsis and the potential association between ferroptosis and acute liver and lung injury in sepsis prompted us to investigate the underlying mechanisms by which the SP-NK1R axis participates in CLP-surgery-induced ferroptosis. Ferroptosis is a step-wise cell death process involving the dysregulated activation of various signalling cascades [
43]. Gpx4 is crucial to the maintenance of lipid homeostasis, suggesting that Gpx4 is involved in ferroptosis [
18,
43]. Gpx4 is a crucial enzyme in converting toxic lipid hydroperoxide to nontoxic lipid alcohol [
18,
43]. Thus, Gpx4 has been widely recognized as a cornerstone of lipid antiperoxidative defence and a gatekeeper of ferroptosis [
18,
43]. This study showed a significant decrease in the expression of Gpx4 in the liver and lungs in mice following CLP-induced sepsis, which agrees with previous research [
38,
39]. The antioxidant GSH is an essential reducing substrate for Gpx4, and it is also crucial to maintaining the activity of Gpx4. Thus, GSH is also treated as a critical regulator of ferroptosis [
18,
43]. In line with previous studies, we found that the concentration of GSH in the liver and lungs was significantly downregulated in mice with CLP-surgery-induced sepsis [
38,
39]. Notably, this study also demonstrated that these decreases in the expression of Gpx4 and GSH in the liver and lungs in mice with CLP-surgery-induced sepsis were reversed by suppressing SP-NK1R signalling. Compelling evidence has pointed to the involvement of transcription factors in ferroptosis [
20,
43]. It was reported that Nrf2 regulates the expression of several genes involved in iron metabolism; thus, Nrf2 plays a crucial role in maintaining iron homeostasis. Moreover, multiple genes involved in detoxification or antioxidant responses, including Gpx4, and genes that regulate GSH metabolism, are the target genes of Nrf2; therefore, Nrf2 also plays a central role in suppressing lipid peroxidation. The role of Nrf2 in maintaining the homeostasis of iron and lipid makes it a well-recognized inhibitor of ferroptosis [
19,
20]. In line with previous investigations, the expression of Nrf2 in the liver and lungs was significantly decreased in mice with CLP-surgery-induced sepsis [
38,
39]. In contrast, the disruption of the SP-NK1R axis reversed the decreases in the expression of Nrf2 in these tissues in mice following CLP-surgery-induced sepsis. These results collectively indicate that increased SP-NK1R signalling inactivates the Nrf2-Gpx4/GSH cascade, thereby promoting ferroptosis in CLP-surgery-induced sepsis.
We also found that NK1R antagonist treatment did not cause any further effect on the profile of ferroptosis as well as acute inflammatory response and injury in the liver and lungs in Tac1−/− mice with CLP-surgery-induced sepsis. Moreover, if the NK1R antagonist was utilized to block the actions of NK1R, the deletion of the Tac1 gene did not cause any further effect on the profile of ferroptosis as well as acute inflammatory response and injury in the liver and lungs in mice with CLP-surgery-induced sepsis. These results suggest that SP contributes to ferroptosis and acute inflammatory responses and injury in the liver and lungs in sepsis via priming NK1R.
This study has some limitations. Firstly, this study was limited to only one time point (8 h after the CLP surgery) and represented alterations emerging at that point only. Another limitation of this study is that the impacts of the SP-NK1R axis on sepsis-associated acute inflammatory response and ferroptosis were only investigated in mice. It would be helpful to investigate the role of this axis in organ impairment and ferroptosis in patients with sepsis, as many differences exist in the pathophysiology of sepsis between mice and humans.