1. Introduction
Insulin resistance is a key link between obesity and type 2 diabetes. These disorders are related to a wide array of other pathophysiologic sequelae including dyslipidemia, hyperglycemia, hyperinsulinemia, hypertension, atherosclerosis and cardiovascular disease [
1,
2,
3]. Altered lipid metabolism has the greatest effect on disturbance of insulin signaling in skeletal muscles which are responsible for 70–80% of the whole body insulin-stimulated glucose uptake, making them the most important site of insulin resistance [
4].
Over the years, numerous hypotheses have been suggested to explain the mechanism by which increased lipid availability induces muscle insulin resistance [
5,
6,
7,
8]. Nowadays, fatty-acid-induced insulin resistance is most often attributed to intramuscular lipid accumulation. This view is strengthened by the fact that insulin resistance develops with the accumulation of fatty acid metabolites, especially long-chain fatty acyl-CoA (LCACoA), diacylglycerol (DAG) and ceramide (Cer), even in the absence of elevated levels of free fatty acids (FFA) in the plasma [
9].
Ceramides belong to a group of lipid-derived molecules that consist of a sphingosine (SPH) base linked to a fatty acid moiety. They constitute structural elements of the membrane lipid bilayer and play a role as substantial signaling molecules that are implicated in a large number of cellular and physiological processes [
10]. These lipid intermediates are accumulated in cells via two major routes: hydrolysis of the membrane phospholipid sphingomyelin, which is coordinated by the enzyme sphingomyelinase, or through de novo synthesis from long-chain acyl-CoA(LCA-CoAs), which involves a multi-step biosynthetic pathway [
11]. The first rate-limiting step of de novo synthesis of ceramide is the condensation of acyl-CoA––usually palmitoyl-CoA––with serine, which is catalyzed by the enzyme serine palmitoyltransferase (SPT) [
12], to form 3-ketosphinganine that is rapidly reduced to sphinganine (SPA) by the enzyme 3-ketosphinganine reductase. Next, SPA is acylated to form dihydroceramide by the action of dihydroceramide synthase. The last step of ceramide synthesis is the conversion of dihydroceramide to ceramide by insertion of a 4,5-trans-double bond into dihydroceramide. This reaction is catalyzed by the enzyme dihydroceramide desaturase [
13].
As mentioned above, ceramides play important roles in cell biology, but their accumulation induces the development of metabolic dysfunction and insulin resistance in rodents and humans [
14,
15]. The connection between ceramide accumulation and insulin resistance is associated with protein kinase B (PKB/Akt) inhibition. PKB/Akt is a protein in the insulin pathway that directly participates in the translocation of GLUT4 to the plasma membrane, thus facilitating glucose uptake [
16]. It has been demonstrated that ceramides are directly responsible for the activation of protein phosphatase 2A (PP2A) that triggers PKB/Akt dephosphorylation. Thus, ceramide inhibits the insulin pathway at this stage [
17,
18,
19]. The second route by which ceramides are known to promote insulin resistance involves disruption of translocation GLUT4 to the membrane and reduced phosphorylation of PKB/Akt by a process dependent on the activation of atypical protein kinase C (aPKC)
λ/
ζ isoforms [
20]. aPKCs, isoforms
λ/
ζ serve as actual molecular switches to activate GLUT4 translocation or glucose transport responses under the influence of insulin and certain other relevant stimuli in skeletal muscles and adipocytes [
21].
Research results published to date have supported the hypothesis that ectopic lipid accumulation plays a fundamental role in the development of insulin resistance. However, there is an ongoing debate as to which group of lipid mediators plays the most important role here. Numerous published studies have confirmed the significant effect of intramuscular accumulation of ceramides. Studies with the SPT inhibitor myriocin or utilizing a
SPT knockout in mice have shown that decreased ceramide levels protect against high-fat diet-induced insulin resistance [
22]. However, the knockout animals or the use of inhibitors, reflect systemic changes that may result from altered metabolism in tissues other than muscle. The decrease in the level of ceramide in adipose tissue obtained in
SPT knockout mice or by the use of myriocin, may alter the production and/or secretion of adipocytokines, which significantly affect skeletal muscle insulin sensitivity [
23].
The aim of this study was to elucidate the role of ceramide accumulation in inducing muscle insulin resistance. To achieve this goal, the gene encoding SPT was locally silenced in the gastrocnemius muscle of HFD-fed animals.
2. Materials and Methods
2.1. Animals and Diets
The experiments were approved by the Local Ethics Committee for Animal Experiments (Olsztyn, Poland, approval number 43/2016). The study was performed using male C57BL/6 mice brought from the Jackson Laboratory (Bar Harbor, ME, USA). The animals were randomly divided into two groups, placed in standard conditions in a 12-h day/night cycle and provided with ad libitum access to food and water for 8 weeks, except when defined by the experimental protocol. The first group (n = 8), as the control, was fed a standard rodent diet containing 70% carbohydrates, 10% fat and 20% protein (% energy) (D12450J, Research Diets INC, New Brunswick, NJ, USA). The second group (n = 8) was fed a high-fat diet composed of 20% carbohydrates, 60% fat and 20% protein (% energy) (D12492, Research Diets INC, New Brunswick, NJ, USA).
2.2. Plasmid Preparation
Plasmids used in the experiment were obtained from bacterial stocks purchased from Dharmacon (currently: Horizon Discovery, Cambridge, UK). All plasmids produced by the bacteria encoded turbo green fluorescent protein (TurboGFP) gene as an exogenous expression control and shRNA targeted towards Sptlc2, a subunit of SPT––the enzyme responsible for de novo ceramide synthesis, or shRNA scrambled sequences. Bacterial cultures were prepared according to the manufacturer’s guidelines. Plasmids were isolated with the GeneJET Plasmid Maxiprep Kit (Thermo Scientific, Waltham, MA, USA), suspended in 150 mM PBS (pH = 7.2) and stored at −80 °C.
2.3. Plasmid Injection and Muscle Electroporation
Gene silencing was performed two weeks after starting the allocated diets. In animals of all groups, the gastrocnemius muscle areas were shaved. Two hours prior to plasmid administration, 30 µL of hyaluronidase (0.4 U/µL hyaluronidase in sterile Tyrode) was injected in two equal doses from two sides of the muscle. The solution of 40 µg plasmid with a concentration of 2 µg/µL was slowly injected into the gastrocnemius muscle using a 27-gauge needle. Gastrocnemius muscles of both the hindlimbs in animals from the first group were treated with scrambled shRNA plasmid (control LFD). One hindlimb gastrocnemius muscle in mice from the fat-fed group was treated with shRNA plasmid mixture encoding three different sequences targeted towards
Sptlc2 (HFD
Sptlc2-shRNA). The opposite hindlimb gastrocnemius muscle was treated with scrambled shRNA plasmids (HFD
+scrshRNA) which activated shRNA-related mechanisms but preserved
Sptlc2 expression. After shRNA plasmid administration, the gastrocnemius muscles were electroporated with the use of a pair of stainless-steel electrode plates (1 cm
2 area) and BTX ECM 830 Electroporation Generator (Holliston, MA, USA). During the electroporation procedure, eight electric pulses were applied at 200 ms intervals (175 volts/cm) [
24]. Prior to all procedures, i.e., shaving, hyaluronidase/shRNA plasmid administration and electroporation, the animals were anesthetized in an induction chamber with ~2% isoflurane in oxygen with UNO BV rodent anesthesia system (UNO, Zevenaar, the Netherlands). GFP reporter gene expression in both legs was monitored transcutaneously once a week using a UV flashlight. The in-vivo GFP fluorescence at the time of euthanasia and after skeletal muscle excision was visualized with a stereomicroscope equipped with a Nightsea SFA-RB-GO add-on and DeltaPix Invenio 5SIII CMOS camera (
Figure 1).
2.4. Insulin and Glucose Tolerance Tests
Six weeks after the commencement of the experimental diet in the animals, an oral glucose tolerance test (OGTT) was performed, followed by an insulin tolerance test (IPTT) one week later. For both procedures, the mice had been fasted for 6 h, and then baseline blood glucose concentrations measured from the tail vein by using glucometer AccuChek Aviva (Roche, Mannheim, Germany). Next, animals received glucose (in a dose of 2 g/kg) orally (OGTT) and insulin (dose of 0.75 U/kg) intraperitoneally (IPTG). Subsequent measurements of the glucose level were made at pre-determined intervals over 2–3 h (OGTT—15′, 30′, 45′, 60′, 90′, 120; IPTT—15′, 30′, 45′, 60′, 90′, 120; 180′). During OGTT at 15 and 60 min, blood was also collected for an insulin concentration assay with an ELISA insulin assay kit (Rat/Mouse Insulin Millipore, Merck KGaA, Darmstadt, Germany). The area under the glucose concentration curve was measured according to the trapezoidal rule.
2.5. HOMA-IR (Homeostatic Model Assessment for Insulin Resistance)
The HOMA-IR index value was calculated according to the formula [
25]:
2.6. Lipid Extraction and Analysis
2.6.1. Sphingolipids
The content of sphingolipids was measured using a modified method according to Blachnio-Zabielska et al. [
26]. The chromatographic lipid separation was conducted using an ultra-high performance liquid chromatography (Shimadzu Nexera X2 UHPLC, Shimadzu Corporation, Kyoto, Japan) in binary gradient with 1 mM ammonium formate and 0.1% formic acid in water (solvent A), and 2 mM ammonium formate and 0.1% formic acid in methanol (solvent B) at the flow rate of 0.4 mL/min. The analytical column was a reverse-phase Zorbax SB-C8 column 2.1 × 150 mm, 1.8 µm (Agilent Technologies, Santa Clara, CA, USA). The analysis was performed by means of a Sciex QTRAP 6500+ triple quadrupole mass spectrometer (AB Sciex Germany GmbH, Darmstadt, Germany) using a positive ion electrospray ionization (ESI) source (except for S1P, which was analyzed in the negative mode) with multiple reaction monitoring (MRM) against standard curves constructed for each compound. Sphingolipids were extracted from ~20 mg of pulverized skeletal muscle. Tissue samples were homogenized in 250 mM sucrose, 25 mM KCl, 50 mM Tris and 0.5 mM EDTA, pH 7.4. An internal standard solution was added to the homogenates (SPH-d7, SPA-d7, S1P-d7, C15:0-d7-Cer, C16:0-d7-Cer, C18:1-d7-Cer, C18:0-d7-Cer, 17C/20:0-Cer, C24:1-d7-Cer and C24-d7-Cer, Avanti Polar Lipids, Alabaster, AL, USA) and extraction mixture (isopropanol:water:ethyl acetate, 30:10:60;
v/
v/
v). All samples were vortexed, sonicated and centrifuged. The extraction process was repeated.
The obtained supernatant was transferred to new vials and evaporated under a stream of nitrogen, and the dried samples were dissolved in solvent B.
2.6.2. Diacylglycerols
The level of DAG was measured according to Blachnio-Zabielska et al. [
27] by means of a triple quadrupole mass spectrometer (Sciex QTRAP 6500+ AB Sciex Germany GmbH, Darmstadt, Germany) and a positive ion electrospray ionization (ESI) source with multiple reaction monitoring (MRM) against the concentration standard curves prepared for each compound. Briefly, skeletal muscles were pulverized and homogenized, and internal standard mix (Deuterated DAG Mixture I and Mixture II, Avanti Polar Lipids, Alabaster, AL, USA) was added before the diacylglycerol extraction. The following DAG were quantified: C18:1/18:2, C16:0/18:2, C16:0/16:0, C16:0/18:1, C18:0/20:0, C18:0/18:1, C18:1/18:1, C18:0/18:2 and C16:0/18:0.
2.6.3. Plasma FFA
Plasma FFA concentration was measured according to Persson et al. [
28] by ultra-high performance liquid chromatography mass spectrometry (UHPLC/MS) against a six-point standard curve. Fatty acids were separated using a reverse-phase Zorbax SB-C18 column 2.1 × 150 mm, 1.8 μm (Agilent Technologies, Santa Clara, CA, USA) by means of a two-buffer system (buffer A: 80% acetonitrile and 0.5 mM ammonium acetate; buffer B: 99% acetonitrile and 1% 0.5 mM ammoniumacetate). An internal standard containing appropriate concentrations of C14:0-d27, C15:0, C16:0-d31, C17:0, C18:1-d9 and C18:0-d35 (Avanti Polar Lipids, Alabaster, AL, USA) was added to the plasma samples and then extractions were performed with freshly prepared Dole solution (isopropanol: heptane:1 M H
2SO
4, 40:10:1;
v/
v/
v). The extracts were evaporated under a nitrogen stream and resuspended in buffer A for the LC/MS analysis.
2.6.4. Triacylglycerols
The TAG content was measured by means of High Sensitivity Triglyceride Fluorometric Assay Kit (MAK264-1KT, Merck KGaA, Darmstadt, Germany) pursuant to the attached protocol.
2.6.5. Malonyl-CoA and Long-Chain Acyl-CoA
Malonyl-CoA and LCA-CoA were extracted according to Minkler et al. [
29] and their concentrations were measured according to Blachnio-Zabielska et al. [
30]. Before extraction, the internal standard: C15:0-CoA, 16:0(d4)CoA, C17-CoA, C19:0-CoA, C21:0-CoA, C23:0-CoA and 24:0-(d4)-CoA (Avanti Polar Lipids, Alabaster, AL, USA) was added to all samples. The molecules were separated on a reversed-phase Agilent ZORBAX Extend-C18 column, 2.1 × 150 mm, using a binary gradient with ammonium hydroxide (NH
4OH) in water and NH
4OH in ACN. The concentration of LCA-CoA was quantified using multiple reaction monitoring (MRM) on a triple quadrupole mass spectrometer (Sciex QTRAP 6500+, AB Sciex Germany GmbH, Darmstadt, Germany) in positive electrospray ionization (ESI) mode against the concentration standard curves prepared for each compound (C14:0-CoA, C16:0-CoA, C16:1-CoA, C18:2-CoA, C18:1-CoA, C18:0-CoA, C20:0-CoA, C22:0-CoA, C24:1-CoA and C24:0-CoA, Avanti Polar Lipids, Alabaster, AL, USA).
2.6.6. Acyl-Carnitines
Muscle acyl-carnitine content was measured based on a modified method of Giesbertz [
31]. Pulverized gastrocnemius samples were homogenized and internal standard (C17-carnitine) was added. Next, the samples were extracted with the use of ice-cold methanol, centrifuged (10,000×
g/4 °C/10 min), and the supernatants were dried under nitrogen in fresh tubes. After that, dried acyl-carnitine samples were derivatized to form butyl esters. In this step, the samples were shaken for 20 min at 60 °C in 100 µL n-butanol containing 5%
v/
v acetyl chloride. Then the samples were evaporated again, reconstituted in 100 µL methanol/water and transferred to glass vials for UHPLC/MS/MS analyses. Acyl-carnitines were quantified on a Sciex QTRAP 6500+ triple quadrupole mass spectrometer (AB Sciex Germany GmbH, Darmstadt, Germany) using positive ion electrospray ionization (ESI) with multiple reaction monitoring (MRM) against standard curves constructed for each compound. The chromatographic separation was performed with ultra-performance liquid chromatography (Shimadzu Nexera-X2 UHPLC). The analytical column was a reversed-phase Zorbax SB-C18 column 2.1 × 150 mm, 1.8 µm (Agilent Technologies, Santa Clara, CA, USA).
2.7. Western Blot Analysis
Gastrocnemius samples were homogenized in RIPA buffer (Merck KGaA, Darmstadt, Germany) with 0.5 mM tris(2-carboxyethyl)phosphine (TCEP, reducing agent, Merck KGaA, Darmstadt, Germany) containing protease and phosphatase inhibitors. Protein content in the homogenates was measured with the Pierce 660 nm protein assay kit (Thermo Fisher Scientific, Waltham, MA, USA). Bovine serum albumin (fatty acid-free) was used as a standard. Before protein separation by SDS-PAGE (AnykD Criterion TGX gels and Criterion Cell electrophoresis cell, BioRad, Hercules, CA, USA) and transferring it to PVDF membrane (BioRad Trans Blot SD semidry transfer cell with discontinuous buffer system: Tris/CAPS/15% methanol for anode and Tris/CAPS 0.1% SDS for cathode), the samples were denatured in Laemmli buffer. Finally, the membrane with the transferred proteins was incubated with the appropriate rabbit primary antibody. The following target proteins were quantified using rabbit primary antibodies: glucose transporter 4 (GLUT4) (Abcam, Cambridge, MA, USA), CD36 (Novus Biologicals, Centennial, CO, USA), FATP1 (Novus Biologicals, Centennial, CO, USA), FABPpm, creatinine O-palmitoyltransferase 1 (CPT1) (Abcam, Cambridge, MA, USA), Sptlc2, (Abcam, Cambridge, MA, USA), Akt, pAktSer473, IRS1, pIRS1 (Tyr632), pIRS1 (Ser1101) (Cell Signalling Technology, Danvers, MA, USA) and glyceraldehyde 3-phosphate dehydrogenase (GAPDH) (Abcam, Cambridge, MA, USA). Binding of the primary antibody was detected after incubation with HRP-conjugated secondary antibody, Clarity™ Western ECL chemiluminescent substrate (Bio-Rad), and visualized using the Bio-Rad ChemiDoc XRS+ imaging system. Band intensities were quantified with the Image Lab 6.1. (Bio-Rad Software). Values were normalized to GAPDH referent protein expression measured from parallel runs and expressed as fold changes over control group values. All chemical substances as well as the equipment used for immunoblotting were purchased from Bio-Rad.
2.8. RT-PCR
Total RNA was isolated from gastrocnemius muscles using the mirVana Isolation Kit (ThermoScientific, Waltham, MA, USA) according to the manufacturer’s protocol. The RNA was reverse-transcribed into cDNA using the Transcriptor First Strand cDNA Synthesis Kit (Roche, Mannheim, Germany). Real-time PCR was performed with RealTime Ready Custom Assays for Sptlc2 and Gapdh as referent genes using a LightCycler480 system (Roche, Mannheim, Germany). The results were normalized to Gapdh expression measured in each sample.
2.9. Statistical Analysis
Results were expressed as medians and interquartile ranges (25th–75th percentiles, IQR). The significance of change was estimated with the Mann–Whitney U non-parametric test. Normality of the data was not assumed. The significance threshold was set at p < 0.05. Statistical analysis was performed using Prism 9.3.1. (GraphPad Software).
4. Discussion
Numerous studies suggest that exposing the muscle tissue to saturated free fatty acids triggers the accumulation of ceramide that has been shown to inhibit the early steps of insulin signaling [
33,
34,
35]. The goal of this research was to determine the extent to which biologically active lipid ceramide, leads to the development of disorders associated with skeletal muscle insulin resistance, under the conditions of increased supply of fatty acids.
To achieve the intended goal, the expression of gene encoding serine palmitoyltransferase (Sptlc2), a key enzyme involved in de novo ceramide synthesis, was locally silenced in the gastrocnemius muscle of HFD-fed mice by electroporation-mediated, shRNA plasmid-based transfection. To isolate the effects of Sptlc2 silencing, one mouse hindlimb was silenced with shRNA plasmids (HFDSptlc2-shRNA muscle), while the muscle of the other limb was transfected with scrambled shRNA plasmids (HFD+scrshRNA muscle).
As expected, increasing dietary fat intake triggered insulin resistance at both the systemic and muscular level. Decreased insulin sensitivity was manifested by increased fasting glucose and insulin levels, impaired glucose tolerance, decreased insulin sensitivity, and increased HOMA-IR. The same effects of consuming a high-fat diet have also been reported in other studies [
23,
36,
37,
38,
39,
40,
41]. In addition, it has also been confirmed that the HFD diet leads to an increase in total free fatty acids in plasma. Increased plasma FFA levels associated with the consumption of a high-fat diet have also been observed in other human and rodent studies [
42,
43,
44,
45].
In the studies conducted here, we also found that the elevated plasma FFA concentration was accompanied by an increase in the level of the proteins CD36, FATP1 and FABPpm involved in the transport of fatty acids in skeletal muscles. The same results were obtained by Yun et al. [
46] and other researchers [
47,
48,
49]. They confirmed the effect of a HFD on an increase of fatty acid transporter expression. In our study, silencing of
Sptlc2 gene resulted in a significant decrease in the content of CD36 and FATP1 in high-fat diet-fed animals. The levels of these transporters were even lower than in the control LFD group. The decreased level of CD36 may lead to lower availability of FFA used for de novo lipid synthesis. FATP1 is acyl-CoA synthetase highly expressed in skeletal muscles, and it modulates fatty acid uptake as well as metabolism by converting fatty acids into fatty acyl-CoA [
50]. In studies using FATP1-knockout mice, it has been shown that in the absence of this transporter, insulin-stimulated fatty acids uptake in skeletal muscle is significantly reduced [
51]. In addition, FATP1 deletion was shown to protect mice from fat-induced insulin resistance and muscle lipid accumulation [
51,
52].
In our research, the level of FABPpm significantly increased in the HFD
+scrshRNA muscles and
Sptlc2 silencing resulted in an even greater, statistically significant increase compared with both control LFD and HFD
+scrshRNA muscles. Talanian et al. imply that the higher content of FABPpm in skeletal muscle results not so much in increased fatty acid influx but more enhanced their oxidation [
53]. Additionally, an increase in levels of this protein during endurance training suggests that FABPpm expression in skeletal muscle may determine oxidative capacity [
54].
Our research was based on
SPT silencing in high-fat diet-fed animals. This enzyme is involved in the first steps of sphingolipid biosynthesis—condensation of serine and palmitoyl-CoA. The level of SPT activity may differ depending on the types of tissues and cells [
55,
56,
57] or developmental stage of tissues [
58]. Furthermore, the enzyme activity is affected by diet [
59,
60]. During our study we proved that the contents of mRNA for
Sptlc2 subunits and Sptlc2 protein were significantly increased in HFD
+scrshRNA muscles.
Sptlc2 silencing was clearly observed at both the mRNA and protein levels. The content of Sptlc2 protein dropped to values lower than those observed in the control LFD group. SPT is suggested to be a pivotal enzyme for the regulation of sphingolipid levels in cells. Regulation of sphingolipid synthesis at the SPT stage prevents the harmful accumulation of both intermediates (sphingolipid bases) and ceramide, whereas inhibiting sphingolipid synthesis at a later stage may result in the accumulation of intermediates, including sphinganine. [
12]. In our research,
SPT silencing led to the reduction of the content of ceramide intermediates, including sphinganine as well as sphingolipids which are products of ceramide catabolism, sphingosine and sphingosine-1-phosphate (S1P). A decrease in the amount of sphinganine and sphingosine was also observed in a study on cardiomyocyte-specific Sptlc2-deficient mice [
61]. The use of myriocin as an SPT inhibitor also decreased the level of these compounds [
62,
63]. Of particular importance is the reduced content of sphingosine, which inhibits PKC and thus affects the glucose metabolism in skeletal muscle cells [
64,
65,
66]. Elevated S1P levels in our research in the HFD
+scrshRNA group could be recognized as one of the important features of obesity [
67,
68]. It has been demonstrated, that saturated fatty acids induce an increase in S1P concentration [
69]. In our study, we noted an increased level of S1P in HFD
+scrshRNA muscles and a decrease in the content of this compound in HFD
Sptlc2-shRNA muscles, which was most likely related to a decrease in SPH levels [
70].
Regarding ceramide, the observed differences in the amount of this lipid were significant in all the three examined muscles. High-fat diet consumption contributed to an over-70% increase in ceramide content in the gastrocnemius muscle. By
Sptlc2 silencing, the impact of HFD was eliminated and the ceramide level was similar to those observed in LFD-fed animals. Moreover, in other studies, SPT inhibition had a significant effect on reducing ceramide accumulation. Studies on L6 cell lines have shown that inhibition of
SPT expression in myocytes with a specific shRNA or cells incubated with myriocin, an SPT inhibitor, leads to a reduction of ceramide accumulation, which positively affects the activity of the insulin pathway [
62,
71]. Moreover, in mice with cardiomyocyte-specific deficiency of Sptlc2, an approximately 35% reduction in de novo ceramide synthesis was observed [
61]. The results of studies conducted in animals fed HFD and treated with myriocin, also showed a decrease in muscle ceramide levels compared with animals fed HFD without administration of this inhibitor, which was associated with an improvement in insulin sensitivity despite the observed elevated muscle DAG levels in these animals [
63]. In our present research, although in the HFD
Sptlc2-shRNA muscle we observed a significant decrease of ceramide level, it did not affect the other total lipid content. In both muscles, HFD
+scrshRNA and HFD
Sptlc2-shRNA, we obtained similar, increased levels of total DAG, TAG, LCA-CoA and LCA-carnitine compared to the levels of these compounds in the muscles of LFD-fed animals. According to some studies which confirmed that it is impossible to utilize palmitoyl-CoA for ceramide synthesis via the SPT pathway, palmitate may be channeled into other pathways, such as those responsible for DAG synthesis [
62,
71]. In our study,
Sptlc2 gene silencing was local, which might be the reason for not obtaining similar results. However, interesting changes occurred in the content of DAG C16:0/16:0. Silencing of
Sptlc2 in the gastrocnemius muscle significantly increased the concentration of this lipid in high-fat diet-fed mice. Similar results were obtained by Ruangsiriluk et al. [
72]. Although the total level of each lipid class was not altered, there were considerable changes at the subspecies level. These authors showed that the most frequently changed lipids in cells with inhibited ceramide synthesis were those containing palmitate. The lack of changes in total lipid content other than ceramides in the silenced muscles may also be associated with an increased rate of fatty acid oxidation. In our research, in the HFD
Sptlc2-shRNA muscles we observed increased levels of CPT1B1, which controls the entry of long-chain acyl CoA into mitochondria and thus facilitates the oxidation of fatty acids [
73]. Bruce et al. showed that 20% upregulation of CPT1B in the muscles of rats fed HFD may decrease the triacylglycerol content and membrane-to-cytosolic ratio of diacylglycerol [
72]. These authors also found that overexpression of CPT1 reduced IRS1 serine phosphorylation. In addition, numerous studies have shown that changes in the influx of fatty acids into the mitochondria are crucial in generating muscle insulin resistance [
73,
74,
75,
76].
Our results confirmed that HFD is the cause of disturbances related to the inulin signaling pathway and, consequently, to glucose metabolism. Under physiological conditions, the tyrosine kinase activity of insulin receptors is stimulated in response to insulin, leading to autophosphorylation and subsequent phosphorylation of tyrosine residues of insulin receptor substrate (IRS) [
77].
In the work presented here, we observed inhibition of tyrosine phosphorylation (Tyr632) and upregulation of IRS1 serine phosphorylation (Ser1101) in HFD+scrshRNA muscles. Inhibition of de novo ceramide synthesis has a positive effect on muscle sensitivity to insulin. In HFDSptlc2-shRNA muscles, the degree of phosphorylation of IRS tyrosine residues increased and that of serine residues decreased, which indicates an inhibition of the insulin pathway. Unfortunately, the mechanisms by which ceramide affected this protein remain unknown. Higher phosphorylation of tyrosine residues in IRS due to SPT silencing could have had an impact on PI3K, the next protein of the insulin signaling pathway. We found a significant decrease in the content of this protein in the HFD+scrshRNA muscles. In HFDSptlc2-shRNA muscles the content of PI3K rose to a level much higher than that observed in the control LFD mice. This confirms that silencing the Sptlc2 gene and decreasing ceramide production enhances the action of the insulin pathway also at this stage.
A key enzyme in the insulin pathway inhibited by ceramide is PKB/Akt. Experimental studies revealed that ceramides might weaken insulin activity through maintaining PKB/Akt in an inactive dephosphorylated state in two ways: firstly, by activation of atypical PKC isoforms (
ζ/
λ), which favors their combination with PKB/Akt and prevents the activation of PKB/Akt in response to insulin [
78,
79,
80]; and secondly, ceramides indirectly suppress the PKB/Akt activity by stimulation of serine/threonine phosphatase PP2A [
64]. In our research, we demonstrated that significant dephosphorylation of serine 473 in PKB/Akt occurs in high-fat diet-fed animals. The reduced ceramide content achieved by
SPT gene silencing returned the degree of serine 473 phosphorylation to the control level, which is necessary for proper functioning of the insulin pathway. Other studies [
62,
63,
71] also confirmed that ceramide synthesis inhibition by blocking SPT action increases the phosphorylation of PKB/Akt.
The stimulatory effect of insulin on IRS, PI3K and PKB/Akt is crucial for the subsequent translocation of GLUT4 to the plasma membrane. The observed growth in the quantity or phosphorylation level of these proteins in HFDSptlc2-shRNA muscles is reflected in the increase of GLUT4 content. All the changes observed in our study, resulting from the silencing of SPT expression, lead to the improvement of the insulin pathway.