Brain Histology and Immunohistochemistry After Resuscitation From Hemorrhagic Shock in Swine With Pre-Existing Atherosclerosis and Sodium Thiosulfate (Na2S2O3) Treatment.

Background: The hydrogen sulfide (H2S) and the oxytocin/oxytocin receptor (OT/OTR) systems interact in the central nervous and cardiovascular system. As a consequence of osmotic balance stress, H2S stimulates OT release from the paraventricular nuclei (PVN) in the hypothalamic regulation of blood volume and pressure. Hemorrhagic shock (HS) represents one of the most pronounced acute changes in blood volume, which, moreover, may cause at least transient brain tissue hypoxia. Atherosclerosis is associated with reduced vascular expression of the main endogenous H2S producing enzyme cystathionine-γ-lyase (CSE), and, hence, exogenous H2S administration could be beneficial in these patients, in particular after HS. However, so far cerebral effects of systemic H2S administration are poorly understood. Having previously shown lung-protective effects of therapeutic Na2S2O3 administration in a clinically relevant, long-term, porcine model of HS and resuscitation we evaluated if these protective effects were extended to the brain.
Methods: In this study, available unanalyzed paraffin embedded brain sections (Na2S2O3 N = 8 or vehicle N = 5) of our recently published HS study were analyzed via neuro-histopathology and immunohistochemistry for the endogenous H2S producing enzymes, OT, OTR, and markers for brain injury and oxidative stress (glial fibrillary acidic protein (GFAP) and nitrotyrosine).
Results: Neuro-histopathological analysis revealed uninjured brain tissue with minor white matter edema. Protein quantification in the hypothalamic PVN showed no significant inter-group differences between vehicle or Na2S2O3 treatment. Conclusions: The endogenous H2S enzymes, OT/OTR co-localized in magnocellular neurons in the hypothalamus, which may reflect their interaction in response to HS-induced hypovolemia. The preserved blood brain barrier (BBB) may have resulted in impermeability for Na2S2O3 and no inter-group differences in the PVN. Nonetheless, our results do not preclude that Na2S2O3 could have a therapeutic benefit in the brain in an injury that disrupts the BBB, e.g., traumatic brain injury (TBI) or acute subdural hematoma (ASDH).

Introduction

Recently, we described lung-protective effects of therapeutic sodium thiosulfate (Na2S2O3) administration in a clinically relevant, long-term, porcine model of hemorrhagic shock (HS) and resuscitation in swine with pre-existing atherosclerosis (1). The lung-protective effects comprised amelioration of shock-induced impairment of lung mechanics and gas exchange, and coincided with a significantly higher glucocorticoid receptor (GR) expression in the lung tissue of treated animals (1). It is not yet understood, to what extent relevant effects of systemic Na2S2O3 administration reach the brain (2–4). However, exogenous hydrogen sulfide (H2S) administration was shown to stimulate H2S availability by upregulation of its endogenous enzymes cystathionine-γ-lyase (CSE) and cystathionine-β-synthase (CBS) (5, 6) as an adaptive stress response (7). In a previous study, we reported a significant reduction of CSE in the media of the coronary arteries in atherosclerotic pigs, which was further aggravated in circulatory shock (8). A reduction of CSE is implicated in barrier dysfunction in the kidney (9, 10) and reduced vascular H2S availability (6). Therefore, Na2S2O3 administration after HS may be beneficial for atherosclerotic patients since the lack of vascular H2S production might be compensated by the exogenous administration. Moreover, H2S and the oxytocin (OT)/ oxytocin receptor (OTR) systems interact in trauma in the heart and the brain (11–15) and are both reported to have anti-oxidative, and vasculo-protective effects (15). Hence, activation of either system could be beneficial in HS, since severe hypovolemia can induce at least transitory cerebral tissue hypoxia events (16–19), redox imbalance (20), barrier dysfunction (18, 21) and, upon resuscitation, ischemia/reperfusion (I/R) injury (22).

Interestingly, HS has been shown to induce OT release (23), and OTR upregulation was associated with protection against ischemic injury around the cerebral vasculature and was co-localized with glial fibrillary acidic protein (GFAP), an established marker of reactive astroglial cells, which are reported to be increased in regions of ischemic injury. Moreover, H2S can stimulate hypothalamic release of OT in response to fluid deprivation in rats and osmotic challenge in uninjured rat hypothalamic explants, respectively (23, 24). Central to these observations is the paraventricular nucleus (PVN) (25) of the hypothalamus, the PVN is highly vascularized, protected by the BBB and adjacent to the third ventricle, (not to be confused with periventricular nucleus which lies below the third ventricle and does not have an effective BBB), as part of the hypothalamic-pituitary-adrenal axis (26), important interface in the regulation of fluid homeostasis (27) and site for cardiorespiratory output, blood pressure and heart rate regulation during hypoxia (23, 28). Thiosulfate can release H2S under hypoxic conditions, thus we investigated Na2S2O3 as a H2S donor during resuscitated HS, since it is a clinically approved drug with a good safety profile and antioxidant properties (29–31).

Thiosulfate is proposed to be “a circulating ‘carrier’ molecule of beneficial effects of H2S” (4, 30). Furthermore, Na2S2O3 elicited neuroprotective effects in a rodent global cerebral ischemia model (4) and its therapeutic efficacy has been shown in other in vivo models of organ failure and cardiovascular dysfunction (31, 32). We therefore investigated the effects of Na2S2O3 on the brain, and how the H2S and OT/OTR systems in swine with pre-existing atherosclerosis are regulated after HS and resuscitation. The hypothalamic PVN was investigated, since H2S and OT are known to interact in the hypothalamic regulation of fluid homeostasis and HS represents the most drastic shift in blood volume after trauma. The data presented are a post hoc analysis of material available from the above-mentioned previous study (1).

Materials and Methods

The present study is a post-hoc analysis of post mortem brain tissue sections obtained from the previous study of Datzmann et al. (1). Experiments were conducted after approval by the Federal Authorities for Animal Research (Regierungspräsidium Tübingen; Reg.-Nr. 1341, date of approval May 2, 2017), and the local University of Ulm Animal Care Committee, in adherence to the National Institute of Health Guidelines on the Use of Laboratory Animals and the European Union “Directive 2010/63/EU on the protection of animals used for scientific purposes.” Anesthesia, surgical instrumentation, as well as the protocol of hemorrhage and resuscitation have been described in detail previously (1). Briefly, induction of HS was performed by passive blood withdrawal of 30% of the calculated total blood volume. Hemorrhage was titrated to a targeted mean arterial pressure of 40 ± 5 mmHg for 3 h. Resuscitation of the animals included shed blood re-transfusion, fluid administration (balanced electrolyte solutions), vasopressor support (norepinephrine) based on need to restore mean arterial pressure to baseline values, and lung-protective mechanical ventilation. Sodium thiosulfate (Na2S2O3) (Dr. Franz Köhler Chemie GmbH, Bensheim, Germany, 25%, diluted in 500 mL NaCl 0.9%; infusion rate 0.1 g·kg−1·h−1) (N = 8) or the vehicle solution (2 mL·kg−1·h−1) (N = 5) was administered during the first 24 h of re-transfusion. After 72 h of intensive care treatment or premature termination of the experiment due to pre-defined termination criteria (acute respiratory distress syndrome, refractory hypotension), pigs were sacrificed under further deepened anesthesia, by injection of potassium chloride, and the brain was immediately removed (1).

Experimental Protocol

Available porcine brain tissue sections from a recently published HS study (1) were analyzed in this study. Brain sections from seven female and six castrated male “Familial Hypercholesterolemia Bretoncelles Meishan” (FBM) pigs with median (interquartile range) body weight of 58 (49, 66) kg and age of 24 (23, 28) months, were investigated. These FBM pigs are a model for “human-like coronary atherosclerosis” (8, 33, 34). Group assignment was performed randomly, irrespective of sex.

Neuro-Histophathology and Immunohistochemistry

All brains were identically fixed in 4% formalin for 6days, dissected into 4 mm thick consecutive coronal sections: frontal to occipital. If the macroscopic section was too large to fit as a whole into the embedding cassette (26 x 31 x 4 mm) they were laid flat and further dissected in up to five pieces in a manner which allows for reconstruction of the entire section. For the purpose of this study the macroscopic section, which included the hypothalamus was selected for analysis. The tissue was then dehydrated and embedded in paraffin blocks. 3–5 μm sections, were deparaffinized in xylene, and rehydrated in a graded series of ethanol and deionized water. Hematoxylin and eosin (HE) staining was performed for general neuro-histophathological evaluation, an experienced neuro-histopathologist (AS) focused on determining if hypoxic events led to brain tissue injury in cortico-subcortical brain regions. Criteria to evaluate brain tissue injury included: morphology of nerve and glia cells, white matter and perivascular edema formation, necrosis of parenchyma and appearance of eosinophilic cells. Due to minor injury, descriptive evaluation was performed without quantification.

Immunohistochemical (IHC) analysis with a colorimetric detection system, as method of choice, allowed for visualizing tissue architecture, cellular morphology and cytoplasmic or nuclear protein localization, in the general landscape of the brain. Important here, by not homogenizing the tissue spatial expression patterns remain intact, and it is possible to distinguish e.g,. between vasculature (containing blood) and brain parenchyma, which is a known confounding factor in techniques requiring tissue homogenates.

IHC was performed as previously described (15). Briefly, after deparaffinizing, heat-induced antigen retrieval in citrate buffer (pH 6) was performed, followed by blocking with normal goat serum (10%) before incubating with the following primary antibodies: endogenous H2S producing enzymes anti-cystathionine-γ-lyase (CSE) (Protein Tech, 12217-1-AP, RRID:AB_2087497) and anti-cystathionine-β-synthase (CBS) (Protein Tech, 14787-1-AP, RRID:AB_2070970), anti-OT (Millipore, AB911, RRID:AB_2157629), anti-OTR (Protein Tech, 23045-1-AP, RRID:AB_2827425), which were verified in porcine cerebral tissue previously by Denoix et al. (22), anti-GFAP (Abcam, ab7260, RRID:AB_305808) as a marker of cerebral injury, anti-pig Albumin (Abcam, ab79960, RRID:AB_1658916) as a marker of barrier dysfunction and anti-nitrotyrosine (Merck Millipore, ab5411, RRID:AB_177459), as a marker of oxidative and nitrosative stress, since NO can react with superoxide to peroxynitrite, leading to nitrotyrosine formation due to nitration of protein tyrosine residues (13). All primary antibodies were titrated to their optimal dilution according to the manufacturer recommendations (see Table 1). Negative controls were performed concurrently (15) by incubation with diluent instead of primary antibody in order to control for specificity of the secondary system, or, whenever available, we performed pre-incubation of the primary antibody with the respective immunogen peptide and incubated the brain tissue with the pre-absorbed primary antibody instead of normal primary antibody (15). Additionally, NCBI BLAST searches were performed in order to compare immunogen sequences of the used antibodies to the sus scrofa database (courtesy of the U.S. National Library of Medicine) (Table 1) to further confirm the specificity of the used primary antibodies.

Table 1

Primary antibodies (anti-human) to sus scrofa Protein BLAST search.

Primary antibody (source, catalog No., RRID)	Host species	Query cover	Homology	Immunogen sequence	Concentration used for IHC
anti-CSE (Protein Tech, 12217-1-AP, AB_2087497)	Rabbit Polyclonal	100 %	87.05 %	Gamma cystathionase fusion protein Ag2872	1:200
anti-CBS (Protein Tech, 14787-1-AP, AB_2070970)	Rabbit Polyclonal	100 %	90.46 %	CBS fusion protein Ag6437	1:100
anti-OT (Millipore, AB911, AB_2157629)	Rabbit Polyclonal	100 %	100 %	CYIQNCPLG (Synthetic oxytocin (Sigma) conjugated to thyroglobulin)	1:500
anti-OTR (Protein Tech, 23045-1-AP, AB_2827425)	Rabbit Polyclonal	92 %	83.05 %	Oxytocin Receptor fusion protein Ag19074	1:100
anti-GFAP (Abcam, ab7260, AB_305808)	Rabbit Polyclonal	100 %	92.13 %	full length GFAP sequence UniProt ID: 14136	1:2500

Primary antibodies were detected via the Dako REAL detection system based on alkaline phosphatase conjugated secondary antibodies (anti-mouse; anti-rabbit) and visualized with a Fast Red-type chromogen followed by counterstaining with Mayer's hematoxylin (9, 10). A Zeiss Axio Imager A1 microscope with a 10X objective was used for visualizing the slides. Multiple 800,000-μm2 sections were used for quantification of % positive area using the Zen Image Analysis Software (Zeiss). Data are presented as % positive area.

Statistical Analysis

Graph Pad Prism Version 8 was used for statistical analysis. Normal distribution was excluded with the Kolmogorov–Smirnov test and inter-group differences were analyzed with the Mann-Whitney rank sum test. The data are presented as median (quartiles) with interquartile ranges.

Results

Minor Neuro-Histopathological Damage

The histopathological findings were minimal with signs of discrete swelling and minor perivascular edema in cortico-subcortical brain regions (in the same macroscopic sectional plane as the PVN, see Figure 1), otherwise the brain tissue looked histologically uninjured, presenting with normal appearing singular heterotopic ganglion cells, and intact parenchyma. There were no indications of blood brain barrier disruption.

Figure 1

Neuro-histopathological evaluation. Exemplary pictures of HE staining in cortico-subcortical brain tissue with signs of minor perivascular edema in sections from the same macroscopic sectional plane as the PVN at 10X (A) and 20X (B). Black arrows point to intact parenchyma, black arrowheads depict nerve cells, open arrowheads point to minor perivascular edema. HE, Hematoxylin and eosin; PVN, paraventricular nucleus.

Lack of Effect of Na2S2O3 on CSE, CBS, OT, OTR, GFAP and Nitrotyrosine in the PVN

None of the proteins of interest showed any significant inter-group difference in the porcine hypothalamic PVN (Figures 2–4). The endogenous H2S producing enzymes CSE, CBS, and OT and its receptor were present in the porcine hypothalamic PVN (Figures 2, 3). CSE, CBS, OT and the OTR were found to be present in the magnocellular neurons of the PVN in consecutive sections of the porcine hypothalamus (35). GFAP was also present in the PVN of both groups (see Figure 4) but, again, did not show a significant inter-group difference. Nitrotyrosine showed negligible to no expression in the analyzed tissue specimens (vehicle: n = 5, 0.00[0.00; 0.00] %; Na2S2O3: n = 8, 0.01[0.00; 0.03] %). No Albumin extravasation could be detected (data not shown).

Figure 2

H2S producing enzymes in the porcine PVN. Quantification of the immunohistochemical stainings as positive percentage area in the PVN for CSE (vehicle: n = 4; Na2S2O3: n = 6) and CBS (vehicle: n = 5; Na2S2O3: n = 7). Boxes represent the interquartile ranges with the median (black line), whiskers represent minimum and maximum values. Exemplary immunohistochemical pictures of CSE and CBS in the PVN of vehicle and Na2S2O3 treated animals (10X). Higher magnification pictures of CSE and CBS originate from the black box in the respective 10X picture. PVN, paraventricular nucleus; CSE, cystathionine-γ-lyase; CBS, cystathionine-β-synthase; Na2S2O3, sodium thiosulfate.

Figure 4

GFAP in the porcine PVN. Quantification of the immunohistochemical stainings as positive percentage area in the PVN for GFAP (vehicle: n = 5; Na2S2O3: n = 8). Boxes represent the interquartile ranges with the median (black line), whiskers represent minimum and maximum values. Exemplary immunohistochemical pictures of GFAP in the PVN of vehicle and Na2S2O3 treated animals (10X). PVN, paraventricular nucleus; GFAP, glial fibrillary acidic protein; Na2S2O3, sodium thiosulfate.

Figure 3

OTR and OT in the porcine PVN. Quantification of the immunohistochemical stainings as positive percentage area in the PVN for the OTR (vehicle: n = 5; Na2S2O3: n = 7) and OT (vehicle: n = 5; Na2S2O3: n = 7). Boxes represent the interquartile ranges with the median (black line), whiskers represent minimum and maximum values. Exemplary immunohistochemical pictures of the OTR and OT in the PVN of vehicle and Na2S2O3 treated animals (10X). Higher magnification pictures of the OTR and OT originate from the black box in the respective 10X picture. OT, oxytocin; OTR, oxytocin receptor; Na2S2O3, sodium thiosulfate.

Discussion

The aim of this study was to investigate the protein levels of CSE, CBS, OT, and OTR in the PVN after HS-and resuscitation in a clinically relevant, long-term porcine model, since HS represents one of the most pronounced acute fluid shifts in blood volume. Given the fact that the H2S and OT systems interact in trauma (11–15) and in hypothalamic regulation of fluid homeostasis (23–28), we hypothesized that Na2S2O3 would lead to changes in the expression of theses markers. The results in this porcine model of HS-and resuscitation, showed mostly uninjured brain tissue with minor perivascular edema in cortico-subcortical brain regions. Immunohistochemical data revealed that (i) the proteins of interest CSE, CBS, OT and OTR were all localized in the porcine PVN after HS, but in contrast to our underlying hypothesis, (ii) there were no significant differences in protein levels of CSE, CBS, OT, OTR, GFAP nor nitrotyrosine in the PVN of either group after HS.

Previously, we showed in atherosclerotic swine that CSE, CBS, OT and the OTR were found to be present in magnocellular neurons in consecutive sections of the porcine hypothalamus after HS, which may be indicative of their hypothalamic interaction in response to HS-induced hypovolemia (35). In rodents, there is evidence that Na2S2O3 can reach the brain 90 min after intraperitoneal administration, as demonstrated by elevated Na2S2O3 levels in plasma and brain tissue, mediating protective effects after neuronal I/R injury in un-resuscitated, young and otherwise healthy male mice (4). In our model of HS, we did not see the same results as in the previously mentioned I/R injury rodent model, which may be due to the fact that our large animal model included a pre-existing comorbidity and was resuscitated in an ICU, thus mimicking the human situation unlike the rodent model (4). In fact, the pig is a very relevant translational model: structurally very similar to the human brain, the presence of gyri and sulci (gyrencephalic brain), white matter to gray matter proportion and tentorium cerebelli, unlike in the rodent brain, is reflective of the human pathophysiology (36). Administration of Na2S2O3 after brain injury in rodents stimulated H2S availability by upregulation of CBS (5). In contrast, in this pig study, CSE, CBS and OT/OTR expression levels did not show any inter-group difference. Although the systemic blood sulfide levels were significantly higher in animals at 24 h of Na2S2O3 administration compared to vehicle treated swine (1). Clearly, Na2S2O3 administration had lung-protective effects and induced higher pulmonary GR expression, whereas the other visceral organs and blood cells were not affected (1). Organ specific pathophysiology has been shown in other models of circulatory shock, which led to the concept of compartmentalization, suggesting that there are differences in response patterns between single organs and systemic factors, as proposed by Cavallion et al. (37). The compartmentalization in the brain may be due in part to the blood brain barrier (BBB). The lack of effect of Na2S2O3 on the evaluated parameters in the brain in our pig model may suggest its inability to cross the BBB, which is, in contrast to the aforementioned results in rodents, but would be, however, consistent with findings in humans that show that Na2S2O3 does not cross the intact BBB (3, 38). In comparison to our applied dose of Na2S2O3 (0.1 g·kg−1·h−1), even more than 5-fold higher doses of Na2S2O3 did not cross the intact BBB in humans (3, 38). The lack of resuscitation in the reported rodent studies might have facilitated the breakdown of the BBB and thus allowed for Na2S2O3 to cross the dysfunctional barrier and promote neuroprotective effects. These results, however, would not translate to the human clinical situation, which would always entail resuscitation to defined neuro-intensive care endpoints. The clinical scenario was closely replicated in the present large animal study, suggesting that the results presented here are very relevant observation for translational medicine. Based on previous data from rodent experiments, which show that exogenous H2S administration can induce neuroprotective effects and the hypothalamic OT system and endogenous H2S producing enzymes in response to fluid shifts (5, 23, 24, 27), we specifically looked for CSE, CBS, OT and OTR in the PVN with other markers, relevant to hypoxia, fluid shifts and injury (GFAP, Albumin and nitrotyrosine) after resuscitated HS with and without systemic Na2S2O3 administration and could not find significant effects. Our negative findings, though disappointing, assume significance in the light of the many successful unresuscitated rodent pre-clinical trials that ultimately failed to translate to the clinic in neurotrauma research (15, 36).

It remains to be elucidated whether the Na2S2O3-mediated neuroprotective effects (observed in vitro and in in vivo experiments in young and otherwise healthy male mice) as well as the stimulating effect of H2S on OT release within the hypothalamus during osmotic balance stress (observed in healthy, fluid deprived rats or uninjured, brain explants osmotically challenged), are translatable into large animals or humans (4, 23, 24). Long-term studies in large animals, which focus on the brain after HS, are scarce and report impaired cerebral microcirculation and perfusion pressure, increase in cerebrovascular resistance, altered energy metabolism and BBB dysfunction due to damaged astroglial cells immediately after blood loss (18, 39). GFAP expression is reported to increase in ischemic events, but there was no difference in GFAP expression between vehicle and Na2S2O3 treated animals after HS in the current study. To the best of our knowledge, reports on HS-induced histopathological changes or protein expression variations after profound tissue hypoxia in adult porcine brain tissue are lacking. Most large animal studies, either perform a combination of HS and acute brain injury or cardiac arrest, which indicates a “no-flow” instead of a “low-flow” state and are therefore not comparable to our results (40, 41). Large animal studies that specifically investigate cerebral effects of HS often lack post HS intensive care (42). Although it has been shown for both pigs and rodents that implementation of resuscitative measures effectively preserves the BBB (43), which was also the case in our study, as indicated by the lack of albumin extravasation. The existing literature about HS alone without brain injury does not seem to result in major morphological damage (42), which is in agreement with our findings. Histopathological examination of brain sections in this study revealed generally uninjured brain tissue morphology with only minor perivascular edema in cortico-subcortical brain regions.

Hypoxia-induced cellular injury can start immediately with hemodynamic decompensation (18, 20) and may cause damage that is first visible on protein level. We recently characterized the gyrencephalic porcine brain after acute subdural hematoma with concomitant pressure-induced brain injury and BBB disruption (15). CBS, OT and the OTR were more localized at the injury site, whereas CSE was constitutively expressed in the uninjured brain tissue and reduced at the injury site (15). In the present study we now quantified protein levels in the PVN after a massive drop in blood volume, which revealed that OT and the OTR are present in the porcine PVN, and that CBS is generally expressed in higher quantity than CSE.

Limitations of the Study

The present study was a post-hoc analysis of brain tissue from a previous experiment. The brain was not a target organ to be investigated in the original study. Thus, no brain monitoring was performed and we cannot comment on how the cerebral perfusion pressure and/or cerebral blood flow have been affected by the hemorrhagic shock. It may well-be, that cerebral autoregulation prevented any effect of the lower MAP on cerebral perfusion.

Conclusion

We found neither neuro-histopathological differences, nor differences in the pattern or levels of CSE, CBS, OT, OTR, GFAP nor nitrotyrosine in the porcine PVN between Na2S2O3 and vehicle administration after HS-and resuscitation. These findings are in contrast to the findings in unresuscitated rodents and may be indicative of the reason the neurotrauma pre-clinical trials in rodents have failed to translate to the clinic. The presence of CSE, CBS, OTR and OT in magnocellular neurons of the porcine hypothalamus may reflect their interaction in response to HS-induced hypovolemia (35). The lack of inter-group differences in the PVN may be attributed to the organ-specific compartmentalization due to preserved impermeability of the intact BBB for Na2S2O3 as observed in humans. Nonetheless, our results do not preclude that Na2S2O3 could have a therapeutic benefit in the brain in an injury that disrupts the BBB, e.g., traumatic brain injury (TBI), acute subdural hematoma (ASDH), asphyxiation or “no flow” scenarios such as cardiopulmonary resuscitation.

Data Availability Statement

The raw data supporting the conclusions of this article will be made available by the authors, without undue reservation.

Ethics Statement

The animal study was reviewed and approved by Regierungspräsidium Tübingen; Reg.-Nr. 1341, date of approval May 2, 2017.

Author Contributions

ND performed the immunohistochemistry, data analysis and interpretation, and drafting of the manuscript. AH performed animal experiments and removal of the brain during the necropsy. AS performed the neuro-histopathological evaluation with ND and helped with data interpretation, critical comments, and expert feedback on the manuscript. CS, CW, HG, and TK contributed critical comments and expert feedback on the manuscript. OM and TM contributed to the experimental design, supervising immunohistochemistry, data interpretation, and writing of the manuscript. PR contributed to the study design and edited and approved the final version of the manuscript. All authors read and approved the final version of the manuscript.

Funding

This research was funded by the Deutsche Forschungsgemeinschaft (DFG), grant number Project-ID 251293561 – Collaborative Research Center (CRC) 1149, the German Ministry of Defense, and an unrestricted research grant from the Dr. Franz Köhler Chemie GmbH, Bensheim, Germany. The funder was not involved in the study design, collection, analysis, interpretation of data, the writing of this article, or the decision to submit it for publication. All authors declare no other competing interests.

Conflict of Interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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