Introduction
Na,K-ATPase (NKA) is a membrane protein that is essential for the survival of the organism. This enzyme is expressed in all the cells of the human body, having many functions including the maintenance of osmotic balance, cell volume, pH and membrane potential. This occurs by the hydrolysis of an adenosine triphosphate (ATP) molecule leading to the export of three sodium ions and the import of two potassium ions into the cell, which is fundamental for neuronal excitability and cell maintenance [
1],[
2].
NKA is constituted of three subunits: α, β and γ [
3], with each subunit having a number of isoforms that provide functional versatility across different cell types, in turn highlighting the different roles and responses produced by NKA activation across cell types [
4]-[
8]. However, the γ (gamma) subunit, is not present in all the cells, with the other subunits being required for NKA to be functional [
9].
In the adult brain, α
1 is expressed in all cells, with α
2 being expressed primarily in astrocytes and α
3 in neurons [
10],[
11]. Mutations in the α
2- and α
3-isoform genes are involved in neurological disorders, such as familial hemiplegic migraine type-2 [
12], rapid-onset dystonia [
13], alternating hemiplegia of childhood [
14] and cerebellar ataxia, areflexia, pes cavus, optic atrophy and sensorineural hearing loss (CAPOS) [
15], with genetic variations in NKA also associating with bipolar disorder, suggesting a role for this enzyme in the etiology of this disease [
16]. The NKA α-isoform plays a critical role in the modulation of learning and memory, in turn regulating susceptibility to Alzheimer’s disease [
17]. Several works show NKA to operate as a receptor and not only as a pump, with a number of intracellular pathway activations driving its effects [
18],[
19].
Ouabain (OUA) is synthesized by the adrenal gland and hypothalamus [
20],[
21] and is likely to have important physiological roles in both the central and peripheral nervous systems [
22],[
23]. OUA binds to NKA in hippocampal astrocytes, activating inositol trisphosphate receptor (InsP3R), which generates calcium oscillations, thereby activating NF-κB [
23]. Xie and Askari [
24] also showed OUA to act as a signal transducer, by binding to NKA and thereby activating the Ras-Raf-MAPK signaling cascade by the epidermal growth factor receptor (EGFR).
OUA has a dual role, given its dose-dependent response curve effects. A high concentration of OUA can cause cell death, driving neuronal necrosis via NKA inhibition, leading to potassium ion depletion and thereby increasing intracellular sodium and calcium ions [
25]. Conversely, low concentrations of OUA (0.01 nM) are protective against kainic acid-induced lesions in the rat striatum, where it reduces apoptosis by increasing Bcl-2 [
26]. Similarly, OUA affords protection in rat kidney primary cultures against Shiga toxin [
27]. As such, OUA can afford protection both peripherally and centrally.
NF-κB is a nuclear transcription factor, which is commonly induced following danger or inflammatory signaling, including by lipopolysaccharide (LPS) [
28]. NF-κB comprises homo- and heterodimers via the combination of the subunits p65 (RELA), p50, p52, c-REL and REL of the REL/NF-κB family of proteins [
28]. Different dimer combinations can activate or block distinct gene transcriptions, exemplified by the inhibitory homodimers p50/p50 and p52/p52 [
29]. This transcription factor is evolutionarily conserved, driving a wide range of effects that depend on the specific activating stimulus, particular cell type and the cellular phenomenon that it regulates.
When it is not stimulated, NF-κB resides in the cytoplasm in association with the inhibitory protein, IκB (IKB) [
30]. When IKB is phosphorylated by IKK (IκB kinase), IKB is degraded by proteasome 26S [
31], freeing NF-κB, which can then translocate to the nucleus and bind to the regulatory sequence close to the promotor region, thereby regulating the expression of target genes such as, the pro-apoptotic
Bax, anti-apoptotic
Bcl2, inducible nitric oxide synthase (iNOS), several cytokines, manganese-superoxide dismutase (MnSOD) and brain-derived neurotrophic factor (BDNF) [
29]. BDNF is an important trophic protein, including in the central nervous system (CNS), where it plays important roles in brain development and plasticity, with its malfunction being involved in many CNS diseases [
32]. In the CNS, NF-κB plays a dual role in neurodegenerative diseases, enhancing survival in neurons, whilst driving pathological glial inflammatory processes [
33].
LPS is a bacterial Gram-negative membrane element which is released in a free form or in aggregates. LPS is classically utilized as a model of inflammation and sepsis, with effects via toll-like receptor 4 (TLR4) [
34],[
35]. Peripheral LPS administration induces NF-κB activation in different brain areas [
36], as well as
de novo synthesis of
Iκb mRNA (an NF-κB activation index), in the brain parenchyma [
37]. Peripheral LPS can, therefore, activate pro-inflammatory CNS genes [
38]. The present work aims to evaluate the alterations induced by a low dose of OUA in the rat hippocampus, in an inflammation model induced by intraperitoneal (ip) LPS injection.
Methods
Animal and tissue preparation
Three-month old male Wistar rats (Biomedical Sciences Institute, University of São Paulo) were kept under 12 hour light/dark cycle (lights on at 7:00 am) and allowed free access to food and water. Animals were treated with OUA (1.8 μg/kg, ip) or saline 20 minutes before the injection LPS (200 μg/kg, ip) or saline and euthanized 2 hours after the administration (between 9:00 and 11:00 am) following procedures approved by the Biomedical College of Animal Experimentation (COBEA). All procedures were also approved by the Ethical Committee for Animal Research (CEEA) of the Biomedical Sciences Institute of the University of São Paulo. The brain was immediately removed and immersed in cold PBS. Each hippocampus was rapidly dissected, quickly immersed in liquid nitrogen, and stored at −80°C for later use.
Hemodynamic parameters
Male Wistar rats (n = 4) were anesthetized with a ketamine, xylazine and acepromazine mixture (64.9, 3.2 and 0.78 mg/kg). The left femoral artery was cannulated with a polyethylene catheter (PE-10 connected to PE-50 filled with heparinized saline, (BD,New Jersey, NY, USA) that was exteriorized in the mid-scapular region. After 24 hours, arterial pressure and heart rate were measured in conscious animals by a pressure transducer (model DT-100, Utah Medical Products, Midvale, UT, USA) and recorded using an interface and software for computer data acquisition (Power Lab 4/25, AD Instruments, Sidney, Australia). Heart rate was determined from the intra-beat intervals. The effects of OUA (1.8 μg/kg, ip) on the arterial blood pressure and heart rate, was evaluated before and 1 hour after OUA administration in conscious animals. Results are expressed as mean ± SE.
Chemicals and kits
Routine reagents, OUA and LPS from Escherichia coli O111:B4 were purchased from Sigma Chemicals (St. Louis, MO, USA); Bio-Rad protein assay kit was purchased from Bio-Rad (Hercules, CA, USA). Corticosterone, TNF-α and BDNF immunoassay kits were purchased from Enzo Life Sciences, Inc. (Farmingdale, NY, USA), eBioscience (San Diego, CA, USA) and Promega (Fitchburg, WI, USA), respectively. The kits were utilized according to manufacturer instructions. All solutions were prepared immediately before use.
Semiquantitative RT-PCR determination of inducible nitric oxide synthase (iNos), Il-1β, Bax and Bcl2mRNA levels
The effect of OUA on LPS-modulated gene expression in the hippocampus of rats was measured. Total RNA was isolated with Trizol reagent (Invitrogen, Carlsbad, CA, USA) from the hippocampus according to the manufacturer's instructions. Semiquantitative reverse transcription-PCR (RT-PCR) amplification was performed using the ThermoScript RT kit (Invitrogen, Carlsbad, CA, USA) according to the manufacturer's instructions. The primer sequences were: iNos (GenBank access number 012611.3, 651 bp) 5′-GTGCTAATGCGGAAGGTCATA-3′ (sense) and 5′CCAAATGTGCTTGTCACCACA-3′ (antisense); Bax (GenBank access number 017059.1, 260 bp), 5′-TGAACTGGACAACAACATGGAGC-3′ (sense) and 5′-GGTCTTGGATCCAGACAAACAGC-3′ (antisense); Bcl2 (GenBank access number 016993.1, 271 bp), 5-′GGAGGATTGTGGCCTTCTTTGAG-3′ (sense) and 5′-TATGCACCCAGAGTGATGCAGGC-3′(antisense); Il-1β (GenBank access number 031512.2, 1,339 bp), 5′-ATGCTCAGCAGTCAAGTGCC-3′ (sense) and 5′-AGCCTT CCTTCGTGTAACCC-3′ (antisense).
The PCR conditions consisted of 5 minutes at 94°C, 33 cycles of 94°C for 45 seconds, 63 °C for 45 seconds, and 72°C for 1 minute and 30 seconds and a final extension at 72°C for 10 minutes. Glyceraldehyde-3-phosphate dehydrogenase (Gapdh; GenBank access number 017008.3, 264 bp) was also amplified as an internal PCR control using the following primers: 5′-CGGGAAGCTTGTGATCAATGG-3′ (sense) and 5′-GGCAGTGATGCCATGGACTG-3′ (antisense). In this case, the temperature cycling conditions were as follows: 5 minutes at 94°C, 20 cycles of 94°C for 45 seconds, 63°C for 45 seconds, and 72°C for 1 minute and 30 seconds and a final extension at 72°C for 10 minutes. Gel electrophoresis of the PCR product was performed using an ethidium bromide-containing agarose gel (2%), and resulting bands were visualized under UV light.
The photographs were captured by photo documentation system DP-001-FDC (VilberLourmat, Torcy, France), and the optical density of the bands was determined using NIH ImageJ software (
http://rsb.info.nih.gov/ij). Results were expressed in relation to the intensity of
Gapdh mRNA levels.
Nuclear extract of each hippocampus was prepared as previously described [
39]. Briefly, hippocampal structures were homogenized using a Dounce homogenizer in cold PBS supplemented with 0.5 mM dithiothreitol (DTT), 0.5 mM phenylmethylsulfonide fluoride (PMSF), 2 μg/ml leupeptin, 2 μg/ml antipain, and 3 mM sodium orthovanadate and centrifuged at 4°C for 30 seconds at 12,000 g. Supernatant was discarded and pellet was resuspended in lysis buffer (10 mM HEPES, pH 7.9, 1.5 mM MgCl
2, 10 mM KCl, 0.1 mM ethylenediaminetetraacetic acid (EDTA), 0.5 mM DTT, 0.5 mM PMSF, 2 μg/ml leupeptin, 2 μg/ml antipain, and 3 mM sodium orthovanadate) and incubated on ice for 10 minutes. After addition of NP-40 (10%), samples were vigorously mixed and centrifuged for 30 seconds at 12,000 g. The supernatant was reserved for Western blotting and enzymatic assays (cytosolic fraction), and the pellet was resuspended in lysis buffer (10 mM HEPES, pH 7.9, 1.5 mM MgCl
2, 10 mM KCl, 0.1 mM EDTA, 0.5 mM DTT, 0.5 mM PMSF, 2 μg/ml leupeptin, 2 μg/ml antipain, and 3 mM sodium orthovanadate) and incubated on ice for 10 minutes. After addition of NP-40 (10%), samples were vigorously mixed and centrifuged for 30 seconds at 12,000 g. Supernatant was discarded, and the pellet was resuspended in extraction buffer (20 mM HEPES, pH 7.9, 25% glycerol, 1.5 mM MgCl
2, 300 mM NaCl, 0.25 mM EDTA, 0.5 mM DTT, 0.5 mM PMSF, 2 lg/ml leupeptin, 2 lg/ml antipain, and 3 mM sodium orthovanadate), incubated for 20 minutes on ice, and centrifuged for 20 minutes at 12,000 g at 4°C. The resulting supernatants containing nuclear proteins were stored at −80°C and used to test the expression of RELA. Protein concentration was determined using the Bio-Rad protein reagent (Hercules, CA, USA).
Western blotting
Electrophoresis was performed using 10% polyacrylamide gel and the Bio-Rad mini-Protean III apparatus (Bio-Rad, Hercules, CA, USA). In brief, the proteins present in the hippocampal cytosolic and nuclear fractions were size-separated in 10% SDS-PAGE (90 V). The proteins were blotted onto a nitrocellulose membrane (Bio-Rad, Hercules, CA, USA) and incubated with the specific antibody RELA (p65) (sc-0372; Santa Cruz Biotechnology, Santa Cruz, CA, USA) and IKB (sc-0371; Santa Cruz Biotechnology, Santa Cruz, CA, USA). The Ponceau method to immunoblot was used to ensure equal protein loading [
40]. Proteins recognized by antibodies were revealed by an electrochemiluminescence (ECL) technique, following the manufacturer's instructions (Amersham Biosciences, Amersham, UK). To standardize and quantify the immunoblots, we used the photo documentation system DP-001-FDC (VilberLourmat, Torcy, France) and NIH ImageJ software (
http://rsb.info.nih.gov/ij). Several exposure times were analyzed to ensure the linearity of the band intensities. β-ACTIN antibody (sc-1616; Santa Cruz Biotechnology, Santa Cruz, CA, USA) was used as an internal experimental control, with results expressed in relation to β-ACTIN intensity.
Measurement of Na, K-ATPase activity
The NKA activity was determined by assaying Pi released from ATP hydrolysis. This inorganic compound forms a complex with molybdate which can be read spectrophotometrically at 700 nm [
41]. For this colorimetric ATP assay, hippocampus supernatant (S1) was centrifuged (12,000 g for 15 minutes at 4°C). The particulate fraction was resuspended in a buffer containing: 0.32 M sucrose, 20 mM HEPES, 1 mM EDTA, 1 mM DTT, and 1 mM PMSF, pH 7.4.
Protein content was determined in particulate samples by colorimetric assay (Bio-Rad, Hercules, CA, USA) [
42]. NKA activity was tested by adding 10 μg of the particulate fraction (in 40 μl of buffer) to 360 μl of buffer containing: 3 mM ATP, 120 mM NaCl, 2 mM KCl, 3 mM MgCl
2, and 30 mM histidine (pH 7.2), with or without OUA (3 μM or 3 mM). After 20 minutes of incubation at 37°C, NKA activity was measured. The reaction was terminated by the addition of a quenching solution (0.6 ml) containing 1 N H
2SO
4 and 0.5% ammonium molybdate. Formation of a phosphomolybdate complex was determined spectrophotometrically at 700 nm [
43].
The total ATPase, Mg-ATPase, NKA α1- and α2/3-isoform activities were linearly related up to 20 minutes. In rodents, the NKA α1-isoform is 1,000 times less sensitive to the cardiac glycoside than the NKA α2/3isoform measured from the difference between OUA-untreated and OUA-treated samples.
The high-affinity α2/3-isoform fraction was calculated by subtracting the activity obtained with 3 μM OUA from total-ATPase activity. To determine the low-affinity fraction (α1 subunit-associated NKA activity), the values obtained in the presence of 3 μM OUA were subtracted from those obtained in the presence of 3 mM OUA. The NKA activity was expressed as nmol/mg protein x minutes.
Immunofluorescence in the hippocampus
The brain was fixed with paraformaldehyde and kept in 30% sucrose for 48 hours. Hippocampal coronal sections (30 μm) were cut in the microtome and the tissues collected were kept in 0.1 M PBS. The sections were incubated with 2% normal donkey serum for 2 hours. For immunofluorescence reactions, the sections were incubated overnight with primary antibody (glial fibrillary acidic protein (GFAP), Sigma-Aldrich, St. Louis, MO, USA) and 4',6-diamidino-2-phenylindole; DAPI), followed by 2-hours incubation with secondary antibody (Alexa fluor 488 donkey anti-rabbit for GFAP). Six slices were placed in each slide and mounted with a coverslip. The sections were examined by fluorescence microscopy (Nikon Eclipse 80i with DXM 1200C digital camera; Nikon, Tokyo, Japan).
Statistical analysis
Results are expressed as mean ± SEM of the indicated number of experiments. Statistical comparisons for OUA-induced changes in mRNA levels, protein expression, ELISA kits and NKA activities were performed by one-way analysis of variance (ANOVA), followed by the Newman-Keuls post-test. All analyses were performed using a Prism 6 software package (GraphPad Software, San Diego, CA, USA). P-values < 0.05 were considered to reflect a statistically significant difference.
Discussion
Neuroinflammation can be associated with neurological insults and neurodegenerative disorders. Neuroinflammation is characterized by increased pro-inflammatory cytokines, such as TNF-α and the expression on endothelial cells of adhesion molecules that increase leukocyte infiltration over the blood–brain barrier (BBB). Concurrently, astrocytes and microglia are activated [
43].
LPS is an inflammation model that can activate NF-κB, partly mediated by glutamate acting at N-methyl-D-aspartate (NMDA) receptors, in turn increasing calcium-dependent activation of NOS and reactive oxygen species generation; the latter contributing to membrane peroxidation [
36]. NF-κB activation induces the expression of many inflammatory cytokines and inflammatory factors that drive the innate immune response [
29],[
44].
However, it is unpredictable as to whether circulating high concentrations of LPS increase BBB permeability, leading to the entry of LPS and other molecules into the brain parenchyma [
36],[
37]. In the early stages of LPS infection, central areas not protected by the BBB are likely to contribute to the inflammatory process, including the actions of LPS at TLR4 in the pineal gland, which inhibits pineal melatonin production, in turn contributing to increased BBB permeability and immune system responsivity (reviewed in [
45]).
TLR4 is also constitutively expressed in the leptomeninges, choroid plexus, subfornical organ, organum vasculosum of the lamina terminalis, median eminence, and area postrema. LPS effects in these non-BBB protected areas are likely to influence the inflammatory response in BBB protected areas, such as the hippocampus [
46]. As such, LPS inflammatory effects may not be dependent on increased BBB permeability. The activation of inflammatory cytokines by LPS in this study confirms the results of previous studies from our laboratory, which showed that most of the transcriptional activity regulated by LPS administration is mediated by the p50/p65 dimer of NF-κB [
36],[
38]. LPS intraperitoneally causes astrocyte activation in the dentate gyrus in aged rats, with this effect can be prolonged for many days [
47]. Inflammation in the dentate gyrus can block neurogenesis in adult rats, which can be restored by an anti-inflammatory drug [
48].
It is known that OUA can produce negative effects in a dose-dependent manner, but many studies have shown OUA to afford protection centrally and peripherally. In a serum deprivation model in rat embryonic kidney cell cultures, OUA prevents cell death by the activation of NF-κB [
49]. It has also been shown that OUA can protect proximal tubular cells against Shiga toxin by activating the anti-apoptotic Bcl-xL [
27].
Although OUA circulates in blood plasma of resting humans in the subnanomolar-to-nanomolar concentration range, non-inhibitory subnanomolar concentration of OUA might be linked to activation of a signal transducer pathway in rats since the Km for OUA inhibition of NKA is 10 to 100 μM for isolated rat vascular smooth muscle, whilst in humans it is 10 to 100 nM [
50],[
51].
Thus, the OUA concentration (1.8 μg/kg, ip) used in the present study is likely linked to activation of the NKA signaling cascade, since in this study we used an OUA concentration that had no significant impact on blood pressure and it did not inhibit hippocampal NKA. As such, the results here are not dependent on NKA inhibition, but are dependent on changes in NKA-related signaling. Our data that showed ip LPS administration increased the mRNA levels of iNos and Il-1β, as well as the Bax/Bcl2 ratio, whereas OUA alone had no impact on the mRNA levels of these factors. However, we observed a protective effect of OUA, given its decrease in the mRNA levels of iNos and Il-1β, as well as a decrease in the Bax/Bcl2 ratio induced by LPS in the hippocampus.
This protection is likely to be afforded by OUA blocking LPS-induced nuclear translocation of NF-κB via the RELA (p65) subunit and by decreasing the degradation of cytosolic IKB, thereby maintaining IKB linked to NF-κB in the cytosol. The major OUA protective effect occurred in the adult neurogenesis-associated dentate gyrus [
52].
Previous studies from our laboratory have reported that OUA can increase cytokine levels. Such variability in OUA effects may be due to a number of factors, including testing times and type of administration, as well as different tissue and cell models. In fact, we detected changes in cytokines gene expression 1 hour after injecting OUA directly in to the CA1 region of the hippocampus at a concentration of 10 nM [
53], as well as in
in vitro studies (OUA = 10 μM) in cerebellar primary culture cells [
54].
TLR4 decreases neurogenesis and neuronal differentiation, with consequences for neuronal plasticity and memory [
55]. BDNF increases neurogenesis, improves memory acquisition and has anti-apoptotic and anti-inflammatory effects, as well as protecting against hypoxia/ischemia-induced brain injury [
56]. OUA pretreatment prevented the decrease in BDNF by LPS, although OUA alone also decreased BDNF. In fact, we cannot rule out that BDNF can also be modulated by other transcription factors that might be activated by OUA. OUA has both toxic [
57],[
58] and protective actions against damage to cells [
59],[
60], including neurons [
26]. In the present study, OUA pretreatment reverted LPS-induced decreases in BDNF levels, suggesting a specific action of this compound against the inflammatory signaling response. OUA pretreatment also provided protection against LPS in the rat hippocampus by decreasing the LPS induction of the pro-inflammatory cytokine, TNF-α. OUA alone increased TNF-α, as we found previously [
53],[
54]. This is surprising as another study showed OUA to block the activation of the TNF/NF-κB pathway by interfering with the interaction between TNF receptor 1 and TRADD in HeLa cell cultures [
61]. Further work should clarify the temporal regulation of TNF-α and/or BDNF by OUA and also its perhaps differential effects in different cell types. In the periphery, our data showed that LPS, but not OUA, increased serum levels of corticosterone and TNF-α, with OUA pretreatment unable to block these changes. This could suggest that the OUA concentration used in the present study may be too low to reverse LPS peripheral activation, although it was high enough to protect against LPS effects in the hippocampus. This would imply that OUA protection could be mediated by its direct action in the brain. Alternatively, the peripheral effect of LPS may be stronger, with the OUA concentration used in the current study unable to reverse the peripheral effects of LPS.
In the peripheral system, mice treated with zymosan and carrageenan leads to paw edema, with OUA decreasing the inflammatory response in these models, suggesting that OUA has peripheral anti-inflammatory effects [
62]. However, the OUA concentrations used were higher than in this current study, with the anti-inflammatory effects being mediated by different intracellular pathways, involving the inhibition of prostaglandin E2, bradykinin and mastocyte degranulation [
62]. However, it should be noted that other mechanisms may be involved in the anti-inflammatory effects of steroid glycosides, including decreasing IL-6 [
63] and inhibition of genes activated by TNF-α [
64].
Recent studies have shown that low doses of OUA have anti-inflammatory properties in LPS-treated reactive astrocytes, by reducing IL-1β release. OUA also prevented the LPS-induced downregulation of NKA and restored the actin filaments in reactive astrocytes [
65]. This is in contrast to the effects of OUA in LPS-treated microglia, where this compound had no effect on levels of microglial reactivity [
66]. This could suggest that some of the differential effects of OUA on central processing are determined by the relative levels of microglial and astrocyte activation, including at different time points in the inflammatory process.
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Competing interests
The authors declare that they have no competing interests.
Authors’ contributions
PFK, EMK and CS participated in the research design, data analysis and wrote or contributed to the writing of the manuscript. All authors read and approved the final version of the manuscript. PFK performed the experiments. LMY participated in the data analysis and contributed to writing the manuscript. ARV, AMMO and LSL participated in the writing of the manuscript and performed experiments. APDC and LVR participated in the research design, data analysis and wrote the manuscript section dealing with blood pressure.