Traumatic brain injury (TBI) in its various forms has emerged as a major problem for modern society. Acute TBI can transform into a chronic condition and be a risk factor for neurodegenerative diseases such as Alzheimer’s and Parkinson’s diseases, probably through induction of oxidative stress and neuroinflammation. Here, we examined the ability of the antioxidant molecular hydrogen given in drinking water (molecular hydrogen water; mHW) to alter the acute changes induced by controlled cortical impact (CCI), a commonly used experimental model of TBI. We found that mHW reversed CCI-induced edema by about half, completely blocked pathological tau expression, accentuated an early increase seen in several cytokines but attenuated that increase by day 7, reversed changes seen in the protein levels of aquaporin-4, HIF-1, MMP-2, and MMP-9, but not for amyloid beta peptide 1–40 or 1–42. Treatment with mHW also reversed the increase seen 4 h after CCI in gene expression related to oxidation/carbohydrate metabolism, cytokine release, leukocyte or cell migration, cytokine transport, ATP and nucleotide binding. Finally, we found that mHW preserved or increased ATP levels and propose a new mechanism for mHW, that of ATP production through the Jagendorf reaction. These results show that molecular hydrogen given in drinking water reverses many of the sequelae of CCI and suggests that it could be an easily administered, highly effective treatment for TBI.
Traumatic brain injury (TBI) has emerged as a signature injury of the early 21st century. In addition to blast injuries in theaters of war, TBI in the civilian population takes many forms with falls recently supplanting automobile accidents as the most common cause of TBI . Injuries that penetrate the skull are more rare but a very serious form of TBI . Although TBI arises from a variety of injuries, the clincial endpoints that result and the mechanisms that drive the CNS towards those endpoints are thought to be shared not only among TBI’s, but also by a host of neurodegenerative diseases . These endpoints and mechanisms include brain edema, tauopathy, blood-brain barrier (BBB) disruption and dysfunction, and neuroinflammation . Once set in motion, these processes often become self-reinforcing unless the cycle can be disrupted. Thus, preventative and interventive therapeutics are needed to treat TBI as early as possible.
Ideally, these treatments could be given immediately, even at the time of injury. This would require the therapeutic to have low toxicity and to be easily administered. One such potential therapeutic is molecular hydrogen. First introduced by Ohsawa et al in 2007, molecular hydrogen acts at least in part as an anti-oxidant, combining with hydroxyl ions that are produced by CNS injuries, although other mechanisms may also exist. As a low molecular weight (2 Da), uncharged molecule, molecular hydrogen has the ability to penetrate biological membranes. The membranes penetrated would include those that form the BBB; thus, molecular hydrogen should have unrestricted access to the CNS, a characteristic shared with few potential therapeutics. This high membrane penetrability explains why molecular hydrogen has therapeutic effects when given by a variety of routes. Here, we investigated the effects of molecular hydrogen given in drinking water (mHW), a method of delivery that should be readily translatable to clinical situations, on the brain edema, tau pathology, neuroinflammation, and gene expression induced by controlled cortical impact (CCI), an animal model of TBI.
The CCI model of TBI we used here is one of the gold standard models and delivers a controlled, reproducible, and quantified amount of mechanical force to the brain. According to the classification of Cernak , it is a dynamic, direct impact, penetrating injury model that results in direct contusion of brain tissue. It reproduces many of the characteristics of TBI seen in patients, including brain edema, alterations in cerebral blood flow, and metabolic changes and is widely used both in the investigations of mechanisms of TBI as well as for drug development .
Materials and Methods
A stereotactic impactor (Leica Microsystems, Inc) was used to induce CCI in 8 week old C57BL/6 male mice (Harlan Sprague Dawley). All studies were conducted under protocols approved by the local animal care and use committee at the Veterans Affairs Puget Sound Institutional Animal Care and Use Committee, an AAALAC approved facility, and all studies adhered to the NIH Guide for the Care and use of Laboratory Animals. Anesthesia was induced with isoflurane (2–4% at 0.5 l/min) and maintained by administration with a nose cone. The head was shaved, the skin overlying the skull infiltrated with a lidocaine/bupivicaine mixture, and the mouse mounted in a stereotaxic apparatus that is part of a Lighthall stroke-contained pneumatic compression device. Using sterile technique, the skull was exposed through a midline incision and skin and muscle retracted. A 4 mm diameter opening was made in the skull 3 mm lateral and 2 mm caudal of the bregma, thereby exposing the right parietotemporal cortex. The bone was removed and the dura cut to expose the cortex. The cortex was compressed by using the impactor device to deliver a 3 mm diameter flat tip weight at a velocity of 5.82 m/s to a depth of 1.2 mm for a duration of 47 ms at a driving pressure of 73 psi. The injured area was covered with a 4 mm diameter artificial dura (GORE Peclude, WL Gore & Associates, Newark, NY) and a 5 mm diameter artificial bone plate made from dental cement (GC Fuji I, GC Corporation, Tokyo, Japan), the skin placed back into position and cemented, the isoflurane discontinued, and the mouse placed in an incubator at 37°C until regaining consciousness (return of righting reflex and mobility). Sham mice went through the entire procedure except for delivery of impact.
Production and Administration of mHW
The mHW was prepared by dissolving molecular hydrogen (H2) in water under high pressure (1.6–1.8 ppm) to a supersaturated level using a hydrogen-water producing apparatus (Arega Co, Aich Japan). The saturated mHW was kept in an aluminum bag until use and freshly prepared each week and only water with a minimum hydrogen content of 1.6 mM was used. Mice were placed on mHW as their sole source of drinking water from 24 h before CCI/sham surgery until study. The mHW drinking water was given in glass water bottles having a stainless steel ball bearing; the ball bearing prevents degassing of the molecular hydrogen. We found that drinking, feeding, and grooming patterns did not differ between CCI and sham mice and that neither onset of drinking nor amount of water drank in 24 h was altered by CCI (data not shown).
Brains were harvested 24 h after sham surgery or 24 h, 3 days (72 h) or 7 days after CCI (n = 4–5/group). The hemi-cortex ipsilateral to CCI or sham surgery was weighed (wet weight), put in metal canisters that were placed on a heating plate at 125°C for 24 h, reweighed (dry weight), and the percent of water determined by the equation:
Additionally, the Edema Index of Keep et al was applied to the 24 h time point using the equation:
Mice were examined by immunohistochemistry and the images presented are representative of each group. To prepare tissue for analysis, mice were anesthetized and fixed by transcardial perfusion with 4% paraformaldehyde. Brains were removed, paraffin embedded, and coronal sections were cut at 10 µm thickness and stored at 4°C until use. Sections were immunostained with AT8 (1∶250), Alz50 (1∶25), GFAP (1∶400), and IBA1 (1∶1000). Sections were deparaffinized and rehydrated through alcohols, and an antigen retrieval step consisting of heat pretreatment by microwave or autoclave in DakoCytomation Target Retrieval Solution (Vector, Burlingame, CA) was used. Sections were treated for endogenous peroxidases with 3% hydrogen peroxide in PBS (pH 7.4), blocked in 5% non-fat milk in PBS, incubated with primary antibody overnight at 4°C followed by biotinylated secondary antibody for 45 minutes at room temperature. Finally, sections were incubated in an avidin-biotin complex (Vector’s Vectastain Elite ABC kit, Burlingame, CA) and the reaction product was visualized with 0.05% diaminobenzidine (DAB)/0.01% hydrogen peroxide in PBS. Negative controls with secondary antibody alone did not immunostain tissue sections (data not shown). Photomicrographs were taken with a digital camera and imported into Adobe Photoshop for mounting. To optimize visualization of staining, photomicrographs were modified, when necessary, by adjusting brightness and contrast.
Mice were divided into 3 groups of 6 each. Group 1 underwent sham surgery, group 2 underwent CCI, and group 3 underwent CCI but was started on mHW 24 h prior to CCI. All mice were sacrficed 4 h after CCI/sham surgery, and the hemicortex ipsilateral to surgery collected. The RNA was extracted from two pooled hemicortices using the MN nucleopsin II kit (Macherey-Nagel Inc, Bethlehem, PA). mRNA-seq libraries were constructed using the ScriptMiner kit (Epicentre, Madison, SI) and sequenced with TruSeq v3 chemistry on a HiSeq 2500 (Illumina, San Diego, Ca). Data was analyzed with GeneSifters software filtering tools (Geospiza, Seattle, WA).
The hemibrain ipsilateral to CCI/sham surgery was homogenized in 1 ml of extraction buffer (0.01 M phosphate buffered saline (PBS; 2.7 mM potassium chloride, 0.137 M sodium chloride, pH 7.4) 2.7 mM, 1 mM EDTA, 1 mM PMSF, Protease Inhibitor cocktail) using a mini beadbeater set at 4800 RPM for 30 sec to produce the PBS homogenate. Triton X-100 was added to the PBS homogenate to a final concentration of 0.1%, and vortexed vigorously. The homogenate was then centrifuged at 20,000 g for 10 min at 4°C. The resulting supernatant was used to measure brain cytokines and amyloid beta peptide (Aβ). Triton X-100 was added to a third portion of PBS homogenate to a final concentration of 1%, vortexed vigorously, and centrifuged at 20,000 g for 10 min at 4°C. The protein level of the resulting supernatant was measured (BCA, Pierce, Rockford, IL) and adjusted to 4 mg/ml with extraction buffer containing 1% Triton X-100 and frozen at −80°C as the 1% Triton X-100 extraction. Aliquots of this extraction were frozen and used for all Westerns and dot blots except for pan-tau immunoblotting.
For total tau detection, mouse brains were dissected from euthanized animals and rapidly snap frozen in liquid nitrogen prior to extraction. Mouse brain hemispheres were homogenized in high salt re-assembly buffer (RAB-High Salt [0.1 M MES, 1 mM EGTA, 0.5 mM MgSO¬4, 0.75 M NaCl, 0.02 M NaF, 0.5 mM PMSF, 0.1% protease inhibitor cocktail, pH 7.0]). For semi-quantitative immunoblotting, we detected mouse and human tau using the pan-tau antibody 17025 (provided as a generous gift of Virginia Lee, see for details) at a dilution of 1∶3000 as described previously and anti-actin antibody at 1∶1000 (DSHB). Rabbit polyclonal 17025 is a pan-tau antibody recognizing total mouse and human tau raised against full length recombinant tau.
Serum and Brain Cytokine Measurements
At 4 h, 24 h, and 7 days after CCI or sham surgery, mice were anesthetized with urethane, the carotid artery exposed, severed, and blood collected from it, and the hemibrain ipsilateral to CCI/sham surgery was obtained and processed as above; the 0.1% Triton X-100 extract was used to measure brain cytokines. The arterial blood was centrifuged at 4500 g for 10 min at 4°C and cytokine levels measured on the resulting serum. Brain cytokine levels were measured at the 4 h, 24 h, and 7 day time points and serum cytokines on the 24 h and 7 day time points. The multi-plex kit for murine cytokines from BioRad was used and measures 23 cytokines: IL-1α, IL-1β, IL-2, IL-3, IL-4, IL-5, IL-6, IL-9, IL-10, IL-12(p40), IL-12(p70), IL-13, IL-17, Eotaxin (CCL11), G-CSF, GM-CSF, IFN-γ, KC (CXCL1), MCP-1 (CCL2), MIP-1α (CCL3), MIP-1β (CCL4), RANTES (CCL5), and TNF-α. Brain levels were reported relative to the protein content of the brain sample and are reported as pg/mg.
Dot blots for Cyclophilin A and Amyloid Precursor Protein (APP)
Brains extracted in 1% Triton X-100 were analyzed for APP and Cyclophilin A expression by dot blot as described previously . Briefly, 2 ug of protein in a volume of 250 ul PBS was loaded in duplicate wells of a Bio-dot microfiltration apparatus (Biorad). To normalize for antibody sensitivity, a standard curve was also prepared using one of the control samples with protein amounts per well ranging from 0.125 to 4 ug in a volume of 250 ul PBS and loaded in duplicate. Samples and standards were bound to a nitrocellulose membrane by vacuum, the membrane was washed, blocked in 5% milk, and incubated overnight with APP antibody (Epitomics, 1 µg/ml) or CypA antibody (Epitomics, 1 µg/ml) in blocking buffer. The membrane was then washed in PBS, and anti-rabbit secondary (Santa Cruz) prepared 1∶5000 in 5% milk and incubated with the membranes for 1 hour at room temperature. After washing, signal was visualized with West Pico chemiluminescent substrate. Images were captured using an ImageQuant LAS4000, and IQTL software used to quantify spot intensities. A standard curve was generated using spot intensities of the standards with Graphpad Prism software, and the spot intensity of each sample was normalized to the standard curve prior to statistical analysis.
Sandwich ELISA kits which detect rodent Aβ40 or Aβ42 (Wako) were used to quantify Aβ levels. 0.1% Triton X-100 extracts were diluted 1∶1 in standard diluent provided in the kit, and subsequently assayed according to kit instructions. We have found that these kits specifically detect rodent Aβ40 and Aβ42 as evidenced by absence of signal for both analytes in APP knockout brains processed and assayed identically. Furthermore, this kit has been used by other groups to quantify changes in rodent Aβ in aging and blast injury . In the latter study, it was reported that the majority of rodent Aβ detected by this assay is found in the Triton-X fraction .
Brain Homogenates for Aquaporin-4 (AQP-4), Hypoxia-inducible factor-1 alpha (HIF-1), Matrix Metalloproteinase (MMP)-2 & -9
The hemibrain ipsilateral to CCI/sham surgery was homogenized and extracted in Tris-EDTA extraction buffer (20 mM TRIS, 150 mM NaCl, 2 mM EDTA, 2% Triton X-100) with protease inhibitors. The brain extracts were run on a 4–12% Bis-Tris gels and transferred onto nitrocellulose membranes (Invitrogen, USA). The membranes were probed with a AQP-4 (Abcam, USA), HIF-1α (Novus Biologicals, USA), MMP-2 (R&D systems, USA) and MMP-9 (R&D systems, USA) primary antibodies, followed by horseradish peroxidase-conjugated secondary antibodies (Santa Cruz, USA). To verify uniformity of protein loading membranes were stripped and reprobed with GAPDH or β-actin antibody (Cell Signaling Technology, USA). The enhanced chemiluminescence western blot was digitalized with a LAS4000 CCD imaging system (GE Healthcare, USA) and analyzed by ImageQuant TL software.
Brain-to-blood Efflux of Aβ and CSF Reabsorption
Brain-to-blood efflux of radioactively labeled Aβ and albumin were measured as previously described . Murine Aβ1–40 was radioactively labeled with 125I and human serum albumin with 131I by the chloramine-T method and purified on columns of Sephadex G-10. Mice received an injection of 25,000 cpm of I-Aβ and 25,000 cpm of I-Albumin into the lateral ventricle of the brain contralateral to CCI and 10 min later the brain was harvested. Mice that had been dead between 10–30 min were used to estimate the amount of radioactive ligand available for transport. The amount of radioactive ligand transported was calculated as the difference between the 10 min value in alive mice and the 10 min value in dead mice.
Effects of mHW on Cellular Respiration and ATP Production
Conditionally immortalized mouse cerebral pericyte cells (ImBPC) established as previously described were cultured in growth medium, which consisted of 5.5 mM glucose Dulbecco minimal essential media (DMEM) (Sigma-Aldrich, St. Louis, MO) supplemented with 10% fetal bovine serum (FBS), non-essential amino acids (NEAA), interferon-γ (44 U/ml; R&D Systems, Minneapolis, MN), penicillin (100 U/mL), and streptomycin (0.1 mg/mL). All cultures were maintained at 33°C under 5% CO2. For pretreated cell experiments, media was freshly prepared using mHW (1.6 mM) or deionized water with Dulbecco minimal essential media powder (DMEM) (Sigma-Aldrich, St. Louis, MO) supplemented with 10% fetal bovine serum (FBS), non-essential amino acids (NEAA), interferon-γ (44 U/ml; R&D Systems, Minneapolis, MN), penicillin (100 U/mL) and streptomycin (0.1 mg/mL). Cells for Seahorse analyzer experiments were harvested using 1× Trypsin containing EDTA (Sigma-Aldrich, St. Louis, MO) and plated into 24-well culture plates at a density of 5×104 cells/well. An n = 10 was used in each experiment and each experiment was completed at least three times. Cells for ATP assay were harvested and plated into 96-well culture plates at a density of 5×103 cells/well. An n = 8 was used in each experiment and each experiment was completed three times.
A Seahorse Bioscience XF24 Extracellular Flux Analyzer (Seahorse Bioscience, North Billerica, MA) was used to measure the rate of oxidative metabolism of glucose (respiration). Under typical in vitro cell culture conditions, the rate of oxygen consumption (OCR) is an indicator of mitochondrial respiration and the extracellular acidification rate (ECAR) is predominantly a measure of lactic acid formed during glycolytic energy metabolism. ImBPC were seeded into a specialized Seahorse microplate (V7; 0.32 cm2 growth area) at 5×104 cells per well in 100 µl of growth medium and incubated at 33°C in 5% CO2 for 2 h. An additional 150 µl of medium was added after the cells had adhered. On the following day, assays were initiated by replacing the media with XF-DMEM (supplemented with 5 mM glucose and 1 mM sodium pyruvate at pH 7.4) nonbuffered media and incubating at 37°C for 60 min to allow the temperature and pH to reach equilibrium. The microplate was then placed into the XF24 instrument to measure OCR and ECAR. Basal measurements of OCR and ECAR were established, and inhibitors of mitochondrial respiration were injected sequentially as indicated to determine mitochondrial function and glycolysis. The inhibitors were used at the following concentrations: oligomycin- 3 µM; carbonyl cyanide 4-(trifluoromethoxy)phenylhydrazone (FCCP)- 3 µM; rotenone- 3 µM; and antimycin A- 1.5 µM. ATP production is measured as (basal respiration – oligomycin respiration). Proton leak is measured as (oligomycin respiration – rotenone/Antimycin A respiration). Maximal respiration is the respiration measured after FCCP treatment. Reserve capacity is measured as (FCCP respiration – basal respiration). Non-mitochondrial respiration is the respiration that occurs after rotenone/Antimycin A treatment.
ATP levels in ImBPC were measured using an ATPlite detection assay (Perkin Elmer; Waltham, MA) according to manufacturer’s protocol. Briefly, cells were lysed at various time points in mammalian cell lysis solution followed by incubation in substrate solution. After 10 min for dark adaption, luminescence was measured using the Victor3 multi label plate reader (Perkin-Elmer; Waltham, MA).
Results are reported at the mean +/− the standard error of the mean. Two means were compared by two-tailed t-test. More than two means were compared by analysis of variance (ANOVA) followed by Newman-Keuls post-test. Studies done using the XF24 Seahorse Analyzer were analyzed using AUC ANOVA software provide by Seahorse Bioscience.
Figure 1 shows the results of CCI and treatment with mHW on the percent of water content in the ipsilateral hemi-brain. A two way ANOVA showed statistical significance for day [F(3,30) = 30.4, p<<0.001], treatment [F(1,30) = 11.2, p<0.01], and interaction [F(1,30) = 5.9, p<0.01] for % water. Tukey‘s post-test showed that % water was significantly increased 24 h after CCI (p<0.001), but was inhibited to a statistically significant degree by mHW (p<0.001). Analysis of the 24 h data using the Keep method showed significant edema that was reversed by mHW (inset).
Immunohistochemistry & Immunoblotting
Staining of phosphorylated tau with both AT8 and Alz 50 were greatly increased in the cortex of CCI mice (Figures 2 & 3) with extension into the hippocampal CA3 region (Figure 2). Total tau as detected with the pan-tau antibody 17026 was not altered 12, 18, 24, or 48 h after CCI (data not shown). Treatment with mHW abolished these increases in tau (Figures 2 & 3). CCI did not produce a remarkable increase in GFAP staining, but CCI mice treated with mHW had less GFAP staining that either sham or CCI mice (Figure 4). CCI increased Iba1 immunostaining; mHW decreased Iba1 immunostaining to levels lower than those seen in sham mice. (Figure 5).
Serum and Brain Cytokine Measurements
For serum, only granulocyte-colony stimulating factor (G-CSF) was significantly affected by CCI in comparison to sham surgery and only at 24 h (Figure 6); mHW had no effect.
Because of an apparrent effect of sham surgery on brain cytokine levels at 4 h, separate ANOVAs were conducted for the 4 h, 24 h, and 7 day results. Three cytokines were not detectable in the brain sample (IL-9, eotaxin, INF-gamma). Table 1 shows the effects of CCI and mHW on brain levels of the other 20 cytokines. Six of the detected cytokines were not affected by CCI (IL-2, IL-5, IL-10, IL-13, IL-17, TNF). Of the remaining 14 cytokines, all had elevated brain levels at one or more time points after CCI. Eight were elevated at all time points (IL-1α, IL-4, IL-6, IL-12p40, G-CSF, MCP-1, MIP-1α, RANTES), four at 4 h and 24 h but not at 7 days (IL-1β, IL-12p70, KC, MIP-1β), 1 at 4 h only (GM-CSF) and one at 24 h and 7 days but not at 4 h (IL-3). Seven cytokines had CCI+mHW levels at one or more time points that differed significantly from CCI levels (Table 1 & Figure 7). Except for the IL-1α 7 day value, the CCI+mHW values were higher than those for CCI alone. These increases were statistically significant at 4 h and 24 h for IL-1α and MIP-1α and at 4 h for IL-1β, G-CSF, KC, and MIP1α (Figure 7). For many cytokines, the CCI value tended to be higher at 7 days than the CCI+mHW value, but only reached statistical significance for IL-1α. TNF levels were lower in CCI+mHW than in sham mice 4 h after CCI and IL-13 levels were higher in CCI+mHW than in sham mice 24 h after CCI.
|4 h Post CCI||24 h Post CCI||7 Days Post CCI|
|Sham (n = 6)||CCI (n = 5–6)||CCI+mHW (n = 5)||Sham (n = 7)||CCI (n = 7)||CCI+mHW (n = 7)||Sham (n = 4)||CCI (n = 6)||CCI+mHW (n = 4)|
After CCI, 246 genes had increased expression by 2 fold or more and 38 genes had expression that was decreased by 50% or more. mHW reduced by 50% or more 236 genes whose expression was increased by 2 fold or more by CCI. We used GeneSifter to analyze which categories of Biological Processes (Table 2), Cellular Components (Table 3), and Molecular Functions (Table 4) were most affected, restricting categories to those containing a minimum of 6 genes and having at least 3 genes altered. Z-score was used as a further filter with an absolute value of ≥3.5 for Biological Processes and ≥2.0 for Cellular Components and Molecular Functions. Of 15 significant categories for Biological Processes, all Z-scores indicated positive enrichment and recurring categories related to cytokine release (3 categories), oxidation/carbohydrate metabolism (4 categories), and leukocyte or cell migration/chemotaxis (3 categories). 8 categories involved transport/secretion with most overlapping with an above category (e.g., cytokine transport). These findings suggest that mHW is very effective at reversing CCI-activation of genes related to oxidation, carbohydrate metabolism, and neuroinflammation. Molecular Functions that were positively enriched included enzymatic genes, receptor genes, and transporter, channel, and transmembrane transporter genes. Molecular Functions was negatively enriched in genes relating to ATP and nucleotide binding. Cellular Components was positively enriched in those genes related to the extracellular and cell membrane environment and negatively enriched in those related to the intracellular, nuclear, and cytoplasmic environments.
|Biological ProcessesPositive Z-score||# Affected Genes||# in Gene Set||Z-Score|
|Positive regulation of cytokine transport||3||33||5.21|
|Positive regulation of hormone secretion||4||61||4.91|
|Positive Regulation of Secretion||7||170||4.72|
|Regulation of Oxidoreductase Activity||3||41||4.56|
|Regulation of Cytokine Secretion||3||45||4.30|
|Positive Regulation of Protein Secretion||3||53||3.86|
|Regulation of Secretion||9||9||3.86|
|Secretion by Cell||11||469||3.63|
|Cellular ComponentPositive Z-score||# Affected Genes||# in Gene Set||Z-Score|
|Intracellular Membrane-bounded Organelle||45||7982||−3.60|
|Intracellular Organelle Part||16||3899||−3.36|
|Intracellular non-membrane-bounded Organelle||6||2328||−3.33|
|Molecular FunctionPositive Z-score||# Affected Genes||# in Gene Set||Z-Score|
|Methyl Indole-3-acetate Esterase Activity||3||7||12.01|
|Methyl Jasmonate Esterase Activity||3||7||12.01|
|Methyl Salicylate Esterase Activity||3||7||12.01|
|Neuropeptide Receptor Binding||3||21||6.65|
|Serine Hydrolase Activity||7||203||4.00|
|G-protein-coupled Receptor Binding||6||183||3.55|
|Serine-type Peptidase Activity||6||200||3.28|
|Serine-type Endopeptidase Activity||5||155||3.19|
|Sodium Ion Transmembrane Transporter Activity||3||80||2.80|
|Transferace Activity, Transferring Acyl Groups Other Than Amino-acyl Groups||5||193||2.61|
|Transmembrane Transporter Activity||14||835||2.59|
|Passive Transmembrane Transporter Activity||8||389||2.57|
|Transferase Activity, Transferring Acyl Groups||5||198||2.54|
|Monovalent Inorganic Cation Transmembrane Transporter Activity||4||149||2.41|
|Ion Transmembrane Transporter Activity||11||654||2.30|
|Substrate-specific Transmembrane Transporter Activity||12||754||2.20|
|Substrate-specific Channel Activity||7||376||2.11|
|Substrate-specific Transporter Activity||13||863||2.09|
|Adenyl Nucleotide Binding||4||1446||−2.49|
|Adenyl Ribonucleotide Binding||4||1439||−2.48|
|Nucleic Acid Binding||12||2510||−2.22|
|Purine Ribonucleoside Triphosphate Binding||7||1718||−2.13|
AQP-4, HIF-1, and MMP-2 &- 9 Measures
AQP-4 was suppressed 24 h after CCI but had recovered to baseline by 3 days (Figure 8, upper left panel). Treatment with mHW induced a statistically significant increase in comparison to CCI at 24 h and 3 days. HIF-1 was significantly increased by CCI at all time points, peaking at 24 h; treatment with mHW suppressed this increase to a statistically significant degree at day 3 and 7, although HIF-1 was still elevated in comparison to sham treated mice (Figure 8, upper right panel). MMP-9 showed a biphasic increase, being elevated at 24 h and 7 days but not at 3 days; mHW reversed these increases (Figure 8, lower left panel). MMP-2 decreased 24 h after CCI; mHW induced a statistically signifcant increase in MMP-2 at all time points in comparison both to the sham and to the time-matched CCI groups (Figure 8, lower right panel).
Measures of Cyclophilin A, APP, and Aβ
CCI reduced CypA levels 7 days but not 24 h after CCI; mHW further reduced CypA at 7 days after CCI (Figure 9, lower left panel). Protein levels of APP were decreased by CCI at 7 days, but not at 24 h (Figure 9, upper left panel). The CCI+mHW group did not differ from the CCI group at either time point, but was lower than sham mice at both 24 h and 7 days. Aβ1–40 was not affected at 24 h but was increased at 7 days in both the CCI and CCI+mHW groups (Figure 9, upper right panel). Aβ1–42 was decreased 24 h after CCI and CCI+mHW but was not altered by 7 days; there were no differences at either time for CCI vs CCI+mHW (Figure 9, lower right panel). The Aβ1–42/Aβ1–40 ratios were lower at both 24 h and 7 days for both CCI and CCI+mHW groups, but showed no differences between CCI vs CCI+mHW (data not shown).
CSF Reabsorption and Brain-to-blood Efflux of Aβ
Neither CSF reabsorption as measured by I-Albumin efflux nor Aβ efflux was affected 24 h, 3 days, or 7 days after CCI (data not shown).
Effects on Cellular Respiration
To assess mitochondrial function that occurs in response to mHW, a Seahorse analyzer assay was performed by exposing the mHW-pretreated ImBPC to oligomycin, FCCP (carbonyl cyanide p-trifluoromethoxyphenylhydrazone) and rotenone/antimycin A in succession and measuring OCR (Figure 10A) and ECR (Figure 10C). The results showed that molecular hydrogen increased basal respiration, reserve capacity, and non-mitochondrial respiration, but not maximal respiration, proton leak, or the oxygen-dependent production of ATP (Figure 10B). The direct measure of ATP showed increased levels after 24 h of exposure to mHW, but not after a 10 min or 6 h exposure.
In other ImBPCs (Figure 11), the ETC was shut off before exposure to molecular hydrogen. OCR and ECAR were unaffected by molecular hydrogen (Fig. 1 A–C) as measured for up to 6 h. However, molecular hydrogen was associated with an increase in ATP levels after 6 h of exposure (Figure 11D).
TBI results in long-term injuries to the CNS that involve immediate effects, such as brain edema, and more sustained effects, such as neuroinflammation. Here, we found that many of the immediate and sustained effects were modulated by treating mice with mHW.
Edema is a significant clinical end point in the pathophysiology of TBI. It occurs because of ongoing events, including BBB disruption, and it leads to further damage to the brain from multiple mechanisms that can include pressure, electrolyte disturbances, and the toxins from BBB leakage. Edema peaked at our 24 h point with the arithmetic increase seen at the third day (72 h after CCI) not being statistically significant. mHW decreased CCI-induced edema by about half at 24 h. Edema was also reduced as measured by the Keep method. As the Keep method uses dry weight as the denominator, it is much less influenced by either edema or tissue loss than the traditional method that uses wet weight in the denominator. The results showed that water content increased from being 4-fold greater than dry weight to 6.5-fold greater with CCI and that mHW preserved the ratio at 4.7-fold.
TBI, stroke, and hypoxia alter the expressions and functions of AQP-4, HIF-1, and the MMP’s; these in turn affect edema formation, BBB disruption, and alterations in brain interstitial fluid circulations . Cyclophilin A is associated with BBB disruption, especially in humans or transgenic rodents that are APOE4 positive, through its effects on MMP-9 CCI induced changes at 24 h in AQP-4, HIF-1, and both MMP-2 and -9. Changes were still present in comparison to shams at day 7 for HIF-1 and MMP-9. In contrast, the effect of CCI on Cyclophilin A was delayed, occurring at day 7 but without effect 24 h after CCI. We found that mHW counteracted the CCI-induced perturbance of each of these factors. These effects of mHW countering the CCI-induced alterations for AQP-4, HIF-1, the MMP’s, and Cyclophilin A provide mechanisms by which mHW can protect against edema and BBB disruption.
Alterations in AQP-4, which others have also found is down regulated in TBI, has been associated with alterations in clearance of Aβ through its effects on the circulation of interstitial fluid in the brain. We, however, found that neither the brain-to-blood clearance of Aβ nor the reabsorption of cerebrospinal fluid back into the circulation was altered by CCI at the time points examined here. Although CCI did affect protein levels of APP and the Aβ’s, mHW did not alter the effects of CCI.
Treatment with mHW totally blocked the pathological phosphorylated tau changes induced by CCI. In contrast, total tau was not altered at 12, 18, 24 or 48 h after CCI. TBI causes early transient accumulation of abnormally phosphorylated tau and repeated injury can result in chronic traumatic encephalopathy which is classified as a tauopathy characterized by tau hyperphosphorylation, and accumulation of conformationally altered or aggregated pathological tau. Pathological tau changes are also a hallmark of Alzheimer’s disease, ultimately resulting in neurofibrillary tangles, and is one of the findings that suggests TBI and Alzheimer’s disease may share pathophysiological mechanisms. Here, we found elevations of phosphorylated tau after CCI in both hippocampal and cortical regions as detected by AT8 and Alz50, but not in total tau. The AT8 antibody detects tau that is phosphorylated at Ser202 and Thr205, a phosphorylation pattern typical of the immature neurofibrillary tangles of Alzheimer’s disease. Alz50 also recognizes a pre-tangle phosphorylation pattern similar to one found in Alzheimer’s. Treatment with mHW totally blocked the detection of these CCI-induced forms of phosphorylated tau.
Neuroinflammation is thought to be a significant driver of the long-term pathology resulting from TBI. Specific agents of inflammation, particularly cytokines, likely play roles in both disease progression and recovery. Neuroinflammation is an early event in CCI as seen here by elevations in cytokines and cytokine-related genes. CCI-induced peripheral inflammation as assessed by serum cytokines was, with the exception of an early rise in serum G-CSF, unremarkable. The inflammatory drivers, then, are likely centered in the CNS rather than as peripheral-to-brain events. This is not surprising considering the CCI model of TBI inflicts significant damage directly to the CNS, although it is surprising given that neuroinflammation can influence the peripheral immune system. Immunohistochemical staining suggested that microglia, but not astrocytes, were activated by CCI. Staining showed that microglia were activated in both the cortex and hippocampus. The effect of mHW was profound on CCI-induced microglial activation and seemed to have reduced levels of activation lower than those seen in sham mice, especially in cortex. Of the 14 cytokines whose levels were increased by CCI, 7 of them had levels that were significantly affected by mHW at one or more time points. However, mHW mostly induced a further increase in brain cytokine levels, elevating them even higher than did CCI alone. This disconnect between the effect of mHW on microglial activation as detected by Iba1 staining and on brain cytokine levels suggests that another cell type is responsible for cytokine production. Both brain endothelial cells and pericytes are known to secrete cytokines constitutively and in response to neuroimmune stimuli . Additionally, the transport rate of cytokines across the BBB could be increased as shown to occur in other types of CNS injury or CCI could increase immune cell trafficking into the CNS and their contribution to the pool of CNS cytokines . The results further suggest, given the therapeutic effects of mHW, that the 7 cytokines which had further elevations with mHW treatment may play a therapeutic role in recovery from TBI rather than a pathological role in progression. Some cytokines, such as TNF, are notorious for being either beneficial or deleterious depending on concentration and context and TBI is one such condition in which cytokines play both of these roles .
Despite the paradoxic effect on brain cytokine protein levels, the effects of mHW was to reverse CCI-induced increases in the expression of genes related to cytokines. Treatment with mHW affected genes whose proteins were active at the cell surface and tended to not affect CCI-induced activated genes that affected intracellular, nuclear, or ATP and nucleotide processes. The surface genes affected were those that tended to relate to cytokine release and secretion, oxidation and carbohydrate metabolism, leukocyte trafficking, and receptors, channels, and transporters.
Recent work has shown that brain pericytes are critical to protecting the BBB and the neurovascular unit from oxidative stress, but are themselves very sensitive to oxidative stress, especially as induced by mitochondrial respiration . The work summarized in Table 2 shows that mHW reverses the CCI-induced altered gene expression related to oxidation and carbohydrate metabolism and, as such, brain pericytes are the logical cell type to examine when assessing the protective effects of a CNS anti-oxidant. Assessment of cellular respiration showed that exposure of brain pericytes to molecular hydrogen for 24 h increased basal respiration, reserve capacity, and non-mitochondrial respiration, where “non-mitochondrial respiration” is defined as oxygen use that occurs despite shutdown of the electron transport chain (Figure 10). In cells not exposed to the metabolic stressors (Figure 10D), ATP production as assessed by oxygen consumption was not increased but direct measurement of ATP showed that it was, again indicating ATP production independent of oxygen use. In pericytes in which the electron transport chain was inactivated (Figure 11), molecular hydrogen was without effect on oxygen consumption or ECAR, but ATP levels were found to be elevated. Thus, the work in figures 10 and and1111 provide evidence that molecular hydrogen can support ATP production independent of the electron transport chain. We propose that these findings can all be explained by the Jagendorf reaction, defined as ATP production that results from an inequality of hydrogen ion electrochemical activity that has been produced independently of the electron transport chain . Under normal circumstances, the electron transport chain establishes the proton gradient and the gradient results in ATP production. Jagendorf, however, showed that the electron transport chain could be bypassed and ATP produced independently of it by establishing the hydrogen gradient with an acid environment. We propose that molecular hydrogen may also be producing a hydrogen gradient, thus promoting mitochondrial ATP production independent of electron transport chain activity. Thus, molecular hydrogen may be working in part by overcoming the deficit in ATP that cells undergoing TBI, and so having mitochondrial damage , experience.
Overall, these studies provide proof of principle that mHW can potently reverse, block, or attenuate many of the effects of CCI. These include effects on edema formation, tau pathology, regulators of fluid and BBB functions, neuroinflammation, and gene expression. These studies were limited in that they did not evaluate mHW treatment without a pretreatment phase, but suggest that mHW could be an important, nontoxic treatment for acute TBI. Because of its nontoxicity and ease of administration, mHW could be readily adapted for clinical, emergency, and even first responder use.
This article is reprinted from https://www.ncbi.nlm.nih.gov/pubmed , original article please see https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4176020/