Translational Block in Stroke: A Constructive and “Out-of-the-Box” Reappraisal

Abstract

Why can we still not translate preclinical research to clinical treatments for acute strokes? Despite > 1000 successful preclinical studies, drugs, and concepts for acute stroke, only two have reached clinical translation. This is the translational block. Yet, we continue to routinely model strokes using almost the same concepts we have used for over 30 years. Methodological improvements and criteria from the last decade have shed some light but have not solved the problem. In this conceptual analysis, we review the current status and reappraise it by thinking “out-of-the-box” and over the edges. As such, we query why other scientific fields have also faced the same translational failures, to find common denominators. In parallel, we query how migraine, multiple sclerosis, and hypothermia in hypoxic encephalopathy have achieved significant translation successes. Should we view ischemic stroke as a “chronic, relapsing, vascular” disease, then secondary prevention strategies are also a successful translation. Finally, based on the lessons learned, we propose how stroke should be modeled, and how preclinical and clinical scientists, editors, grant reviewers, and industry should reconsider their routine way of conducting research. Translational success for stroke treatments may eventually require a bold change with solutions that are outside of the box.

Introduction – The Problem of Translational Failure in Stroke

Stroke remains the third leading cause of death in industrialized countries (Dirnagl et al., 1999). The literature is saturated by >1000 effective preclinical studies in acute stroke research (O’Collins et al., 2006), yet almost none are successfully transferred to the acute clinical routine. This is the well-known translational failure or block in stroke research (Endres et al., 2008).

The “basket” of stroke translational failure so far includes neuroprotective agents (O’Collins et al., 2006), stem cells (Borlongan, 2019), or even novel immunological treatments (Elkins et al., 2017), despite rigorous or/and large preclinical effect sizes. Yet we keep on modeling acute stroke and experimenting using, in most cases, the same concepts based on widely cited models. Is this the right way to continue and progress or do we simply need to critically reassess how we model ischaemic stroke?

The fact is that many pathophysiological principles of stroke were actually discovered in translation (Dirnagl and Endres, 2014). Failed clinical trials for acute stroke were probably based on rather weak preclinical evidence or inappropriate models (Drieu et al., 2020). If we consider stroke a “chronic, relapsing” disease, with multiple repeating small or large ischemic insults, then secondary prevention counts for several successes (Kernan et al., 2014). On the other hand, the differences between preclinical rodent modeling and clinical routine practice in human acute stroke are significant (Corbett et al., 2015). Nevertheless, preclinical research has several translational success stories, such as the case of experimental autoimmune encephalomyelitis (EAE) – multiple sclerosis (MS), migraine, and hypothermia in hypoxic-ischaemic encephalopathy (HIE). In addition, existing recommendation papers and consortiums [e.g., ARRIVE (Kilkenny et al., 2010), STAIR (Corbett et al., 2017), STEPS (Savitz et al., 2011)] have repeatedly proposed pathways to success. However, either few groups worldwide are implementing these guidelines or we are still missing some of the factors that are involved in failure.

Hence, we provide here a critical, interdisciplinary, and revisionary overview of stroke translational failure, taking into consideration lessons from “success stories” and “failed concepts” in neuro-research. We argue that translational failure is also the rule in ischaemia of other organs, such as myocardial infarction. Collectively, we believe that translational failure probably lies in fundamental components and “false” choices in the laboratory and clinical research. If we want to succeed, we need to improve not only the current technical hurdles in contemporary neurosciences, but also the way we put our question into perspective (Kola and Landis, 2004; Duda et al., 2014; Garner, 2014; Alteri and Guizzaro, 2018).

“We can’t solve problems by using the same kind of thinking we used when we created them.”

Albert Einstein (1879–1955)

Translational Roadblock in Brain Ischaemia: Summarizing the Current Status, Understanding the Problem

The translational block in acute stroke has two key aspects. One is the inability of effective preclinical treatments to successfully reach clinical practice in humans. The other is the failure of clinical advances and routine therapeutic applications in Stroke Units to reach and change the way stroke is modeled in preclinical research routine. To put it differently, the blockage lies in missing or ineffective cross-talk between the preclinical side of stroke (which works with cell cultures, cells slides, rodents, and on rare occasions primates, and is usually guided by mechanism-based data for discoveries; Box 1, the typical rodent stroke “patient”), and the clinical side of stroke (which treats patients, designs and runs clinical trials and is guided by clinical and evidence-based data for decisions; Box 1, the typical human stroke patient). In pragmatic terms (Box 1), the typical stroke clinician is rarely a translational scientist and does not incorporate non-”translational” preclinical concepts into clinical routine and decision-making processes for patients. Similarly, the typical neurobiologist is rarely familiar with the clinical reality and clinical needs of stroke and rarely translates clinical advances into experimental routine (Yarborough and Dirnagl, 2017).

Preclinically, in vivo modeling of ischaemic stroke is mainly conducted in rodents (mice and rats) via three main experimental approaches (intraluminal, extraluminal, and chemical), summarized in detail in Table 1 (pros/cons, technical pitfalls, and translational significance) and extensively reviewed elsewhere (Carmichael, 2005; Howells et al., 2010; Fluri et al., 2015). Among all rodent models, the filament – or thrombus – MCAo (fMCAo or thMCAo) model and – under certain conditions – the photothrombotic model fulfill the prerequisite for “closed sterile head injury” and are probably closer to human ischaemic stroke. Additionally, the fMCAo and thMCAo are also the only ones that model recent recanalization advances in stroke. Stroke modeling in large animals (Table 2), such as non-human primates, ovine, porcine, and canine – though rarely used, in only a few selected laboratories in the world due to significant practical and ethical restrictions – possesses significant advantages as a “second species” in the translation pipeline for stroke therapies (extensively reviewed in Cai and Wang, 2016; Sorby-Adams et al., 2018; Kaiser and West, 2020). Others have also provided evidence that the rabbit small clot embolic stroke model (RSCEM) may correlate better with human brain time-windows, and probably should be used before decisions are made to authorize the clinical transfer of any novel treatment (Lapchak, 2010). In vitro cultures or brain slices from rodents as models of hypoxia are useful only as “add-on” methods to study isolated molecular pathways and genetic expression on cell substrates, considering all the limitations of such extra-corporal methods that lack the physiological cross-talk between the brain and the body (Honegger, 2001; Lo, 2014; Sunwoldt et al., 2017). Eventually, the selection of an appropriate model and type of study (screening, discovery, mechanistic, proof-of-concept or effectiveness of new treatment) (Gannon, 2014) may determine the result of translational research (Kola and Landis, 2004; Shanks et al., 2009; Howells et al., 2010; Dalgaard, 2015). A discovery or mechanistic preclinical study on cells or small rodents, studied for 24 h post-infarct, should not per se “claim” translational effectiveness in a human stroke patient (Gannon, 2014).

Clinically, the field of stroke trials also faces pitfalls, which are also found in other diseases (Lowenstein and Castro, 2009). Systematic errors and bias, such as recruitment of patients according to their ability to consent (Lowenstein and Castro, 2009), recruitment of “ideal” patients with less severe symptoms (Hotter et al., 2017), false-positive Phase II studies due to inappropriate time window of treatment or inappropriate outcome measures, studies that may not translationally consider significant preclinical neuropathological mechanisms, and improperly designed extensive Phase III studies with negative results (Dirnagl and Endres, 2014), are just some of these. Results based on oversimplified but easy to complete clinical scales, such as the modified Rankin Scale (mRS) (Harrison et al., 2013), may be too rough to measure subtle or localized improvements per system. Still, even in the best-designed studies (to name some examples, the NXY-059 SAINT-I and -II studies, Natalizumab ACTION-1 and -2 studies, ESCAPE-NA1 study) (Lees et al., 2006; Shuaib et al., 2007; Elkins et al., 2017; Elkind et al., 2020; Hill et al., 2020), the drug under study is either administered > 1.5 h after stroke onset, or it is exposed to interactions with the other standard medical/drug interventions (e.g., alteplase, aspirin, antihypertensives).

The wide heterogeneity of types of clinical stroke, in terms of size, location, time-windows, degrees of reperfusion or collaterals, comorbidities, and the presence or not of salvageable penumbra, may eventually be the main reason for translational failure (Howells et al., 2010). Regarding the effective time window, it is known that while rodent “patients” receive complete recanalization at exactly 45–60 min (e.g., for mice) plus treatment at the beginning of or early during ischaemia, patients have to call an ambulance at home (usually with at least a 30–45 min delay), need to go through diagnostics to exclude bleeding, and, if eligible, could potentially receive reperfusion treatment at minimum 80–90 min after ischaemia onset, thrombectomy at 3–6 hours, and finally their vessels may eventually open a few hours after stroke onset (Tsivgoulis and Alexandrov, 2014). At this time-point, the ischaemic core may already be largely established (Saver, 2006; Vilela and Rowley, 2017). As such, a clinical study of a preclinical treatment may not even be close to what rodents receive in the laboratory (Box 1), meaning that patients may fall outside of the effective time window for the treatment (Moskowitz et al., 2010). In addition to the above, stroke patients typically receive a standard and most effective “best medical treatment” in Stroke Units (Stroke Unit Trialists’ Collaboration, 2013; Powers et al., 2019), an equivalent of which (Lourbopoulos et al., 2017) is usually absent from most preclinical settings or even the recent IMPROVE guidelines for conducting rodent preclinical stroke (Percie du Sert et al., 2017). This “best medical treatment” is the obligatory control group in all clinical trials and thus a pre-existing “bias” for every tested novel drug. Eventually, admitted patients also have comorbidities and receive aspirin, beta-blockers, statins, angiotensin receptor-II (AT), or angiotensin-converting enzyme (ACE)-blockers as standard therapy, all of which have significant effects on brain and body pathophysiology per se (Powers et al., 2019). For several common, practical reasons (cost, difficulty in reliably and reproducibly modeling, difficulty in getting appropriate resources for these experiments), such comorbidities have not commonly been widely included in preclinical rodent modeling (Garner, 2014; Dirnagl, 2016; Modo et al., 2018). As a result, rodent studies probably test their novel treatments against translationally inappropriate control groups and neglect the effects of drug-drug interactions, polypharmacy, and comorbidities on the organism under test. These in themselves create a discrepancy between “standards” in preclinical and clinical studies, responsible for translation discordances.

Taking the problem to the level of organisms, it is fact that humans and rodents do have many similarities and hundreds of conserved molecular/genetic pathways in common as mammals (for an extensive review see Dirnagl and Endres, 2014), but there are also differences that may provoke the translational roadblock (Mestas and Hughes, 2004; Mergenthaler and Meisel, 2012; Jackson et al., 2017). For example, dissimilarities in pharmacodynamic or pharmacokinetic responses and drug bioavailability may be a result of differences in molecular pathways between species (Mestas and Hughes, 2004; Schulte-Herbruggen et al., 2006; Greek and Shanks, 2011; Bolker, 2017; Stortz et al., 2017; Zeiss and Johnson, 2017; Leenaars et al., 2019). Although the identical genetic background and capacity for genetic manipulations in mice have apparent huge advantages, these have to be carefully considered when it comes to translation because humans are genetically and environmentally highly variable (Lowenstein and Castro, 2009; Garner, 2014; Steffen et al., 2016; Vina and Sanz-Ros, 2018). Moreover, at the phenotypic level, we also need to consider the differences in the size and complexity of rodent and human brains (Herculano-Houzel, 2009). Apart from the clear difference in size [approximately 5 cm³ for a mouse (Badea et al., 2007) compared to 1320–1510 cm³ for the human brain] the mouse brain is composed of approximately 90% gray matter compared to approximately 50% of the human brain (740–820 cm³ gray, 360–420 cm³ white matter, and 230–270 cm³ CSF; Luders et al., 2002) and exhibits an increased glucose and oxygen metabolism (Dirnagl et al., 1999; Sorby-Adams et al., 2018; Gennaro et al., 2019). As such, a human stroke occupies different proportions of gray/white matter, with significantly different glucose/oxygen local metabolism and different vulnerability (Wang et al., 2016). At the histological level, humans and rodents – despite their stated similarities – also have anatomical, functional, morphological, and genetical differences in their astrocytes (Oberheim et al., 2009) and neurons (Kalmbach et al., 2018; Hodge et al., 2019), and to a lesser extent in oligodendrocytes/myelin (Ishii et al., 2009) and microglia (Gosselin et al., 2017). These can probably make a difference in terms of survival times and response of cells in ischaemia, different responses of the remaining network in the injured brain, and differences in plasticity and recovery mechanisms (Caleo, 2015; La Rosa and Bonfanti, 2018). Additionally, they result in a different structure and functionality of neuronal networks between the two species [e.g., the specialized corticospinal tract of quadruped rodents (Corbett et al., 2017) or the networks of higher cognitive functions in humans (Vina and Sanz-Ros, 2018)], that render translation of behavioral/neurological outcomes in stroke ever more complex. In fact, non-human primates and larger animals are closer than rodents to humans in many aspects, but are not widely available due to significant costs and ethical and practical concerns in handling and housing them (Dutta and Sengupta, 2016; Yarborough et al., 2018; Kaiser and West, 2020). Evidently, these lead to the inability to measure and translate key behavioral/neurological outcomes between humans and rodents, and on the other hand create an oversimplification of outcomes in most laboratories (e.g., using the oversimplified four-level Bederson’s neurological scale to report the neurological deficits of an infarct; Lourbopoulos et al., 2008; Balkaya et al., 2013). The latter masks relevant neuroanatomical outcome data and hinders translation (Garner, 2014; Bolker, 2017).

Finally, we believe that the age of the preclinical animals is fundamental for translation. Laboratory animals (rodents) used in preclinical studies are young (usually 8–12 weeks old), raised under strictly controlled laboratory conditions (Dirnagl et al., 1999) in a specific pathogen-free environment (Rosshart et al., 2017), and on a diet optimized for high fertility and overall health (Dirnagl, 2016). It can be argued that an 8–12 weeks old mouse corresponds to an approximately 7–11-year-old human (Jackson et al., 2017). A human trial on stroke is never performed in “7–11-year-old males with identical educational levels, identical socioeconomic statuses, identical jobs, identical – almost sterile – houses with identical (locked) thermostats, identical wives, identical diets, identical exercise regimes, in the same small town, who all incidentally had the same grandfather” (Richter et al., 2009). Age alone is a risk factor for stroke (Donnan et al., 2008) and determines the function of lesion/recovery mechanisms (Wyss-Coray, 2016), both clinically (Bindawas et al., 2017) and preclinically (Popa-Wagner et al., 2007; Li et al., 2011; Rosenzweig and Carmichael, 2013). Large clinical registries indicate that on the rare occasions that stroke does occur in children up to age 18, stroke recovery is better than in adults (deVeber et al., 2017). As such, to properly model stroke before proceeding to clinical studies, we would ideally need at least middle-aged rodents (i.e., above 14 months old, corresponding to an at least 48-year-old human) and these would have to be raised and studied in a “proper,” “humanized” environment to account for at least a rich microbiome (Rosshart et al., 2017; Hamilton and Griffith, 2019) and environment (Mering and Jolkkonen, 2015; de Boer et al., 2020).

Known Methodological Pitfalls in Preclinical/Clinical Research in Stroke. Is this Alone the Reason for Translational Failure?

The translational roadblock in stroke is overwhelming and costly (Howells et al., 2012; London and Kimmelman, 2015). Apart from the evident aforementioned modeling, clinical/preclinical and species differences, a part of the problem lies in “how stroke research topics have been chosen and how studies have been designed, conducted, analyzed, regulated, managed, disseminated, or reported,” as recently reviewed (Berge et al., 2017). Consensus papers and consortiums [e.g., ARRIVE (Kilkenny et al., 2010), STAIR (Corbett et al., 2017), STEPS (Savitz et al., 2011), and RIGOR (Lapchak et al., 2013)] have already addressed the problem extensively. However, despite a partial improvement in stroke preclinical methodology (Bahor et al., 2017), these guidelines have only had a limited impact on the way stroke preclinical research is conducted. True compliance with guidelines such as the ARRIVE criteria remains low (Hair et al., 2019). Similarly, the applied STAIR criteria (reported from 2004 to 2011) failed to produce any benefits from subsequent clinical trials that relied on these (Lapchak et al., 2013) and appear to have had no effect on anesthetic and monitoring techniques during experimental stroke in rodents (Thomas et al., 2017).

The main current methodological pitfalls in stroke research are summarized in Table 3. Large animal stroke models have the same shortcomings as rodent ones (Kringe et al., 2020). Small studies consistently give more positive results than larger ones. Study quality is inversely related to effect size (Button et al., 2013). This, combined with rather high variance (SDs typically similar to effect size), results in low statistical power and positive predictive value (Dirnagl and Endres, 2014). In parallel, exploratory studies (usually small ones that are suitable for discovering/developing new pathophysiological theories) cannot compensate for confirmatory ones (required to be powered to investigate efficient treatments with translational significance and probability) (Kimmelman et al., 2014; Huang et al., 2020). As the field is biased toward exploratory investigation (Dirnagl, 2016), the probability of false-positive results from small and inappropriately designed studies increases (Button et al., 2013). Such studies bear low external validity, i.e., there is a small chance that their results can be applied (generalized) to other situations, groups, or events (Dirnagl, 2016; du Sert et al., 2017; Patino and Ferreira, 2018), implying low translationality. Eventually, as the typical stroke patients differ substantially from their rodent “representatives” (as discussed in detail above) (Dirnagl et al., 1999; Dirnagl, 2016; Corbett et al., 2017), a preclinical study with additionally low external validity will most probably fail to translate its result in humans (Patino and Ferreira, 2018).

In addition, the stroke research field is characterized by publication bias (Dirnagl, 2016) or publishing under pressure (Dirnagl and Endres, 2014; Norris et al., 2018). On the one hand, and most importantly, this means that many negative experimental stroke studies are not published (Dirnagl and Endres, 2014), so that data from as many as one in seven experiments remain unpublished (Sena et al., 2010b). On the other hand, this also means there is a preference to publish based on research directions, authors’ nationalities, or institutes’ professional ranks (Liu, 2009). Publication bias – especially the “concealing” of negative studies – has been estimated to lead to an approximately 30% overestimation of published effect sizes (Dirnagl and Endres, 2014). As a study on an “innovative idea” is easier to publish than a “verification/validation study of data,” most groups focus on such “innovative idea” studies. These produce high-impact factor publications or technologies, attract further funding and increase reputation, all the while avoiding the time- and money-consuming challenge of validating existing findings. This bias is partly attributed to a highly competitive way of doing science that sometimes runs like a “business,” where success equals more and more publications (Button et al., 2013). Stroke researchers usually seek large and acute effect sizes (”quick and large”), that make for impressive publications but are far from translational reality (Ioannidis, 2005; Sena et al., 2010b; Button et al., 2013). Eventually, these positive results lead to an overestimation of the treatment’s effectiveness in meta-analyses (Liu, 2009; Martic-Kehl et al., 2012; Dirnagl and Endres, 2014; Dirnagl, 2016; Alteri and Guizzaro, 2018), which misleads science and leads to translational failure. A classic example of this is the case of NXY-059, which had positive preclinical studies and meta-analysis but the expensive and large clinical translational program (SAINT-1 and -2 trials) was a complete failure (Bath et al., 2009).

Similar methodological pitfalls also exist in other fields of science, such as multiple sclerosis and cardiovascular research (see sections below). In the former, they seem not to affect the field, in the latter they are similarly considered a hurdle, as discussed in detail in the sections to follow. So, are methodological pitfalls alone responsible for translational failure?

What Do We Learn From the Application of Therapeutic Hypothermia in Stroke? (Comparing a Positive and a Negative Translational Story)

Methodological problems alone probably do not suffice to create translational block, because they also exist in research fields that translate successfully. Here, we compare the example of therapeutic hypothermia (TH), studied clinically in both acute ischaemic stroke (AIS) and hypoxic brain injury after cardiopulmonary arrest. Hypothermia failed translationally in ischaemic stroke (negative story) (Kuczynski et al., 2020) but succeeded in brain hypoxia after cardiopulmonary resuscitation (positive story).

Therapeutic hypothermia has not reached bedside translation in the case of large territorial AIS (Kuczynski et al., 2020). Numerous positive preclinical studies (rats and mice) report (neuro)protection via post-ischaemic moderate hypothermia (Baron, 2018; Wu et al., 2020): it decreases brain metabolism and inhibits deleterious effects of ischaemia, including excessive neuroinflammation, cytokine release, blood-brain-barrier disruption, apoptosis, and free radical production, activated matrix metalloproteinases, ion channel change, and excitotoxicity (for extended reviews see Truettner et al., 2005; Liu et al., 2016; Wu et al., 2020). Therefore, TH preserves cell and tissue integrity during and after AIS in rodents. However, the available clinical evidence shows rather neutral brain effects and negative systemic complications in humans (Schneider et al., 2017; Wu et al., 2020). Global hypothermia induces multiple and severe systemic side effects, such as shivering, cardiac arrhythmias, vasoconstriction, pneumonia, kidney dysfunction, diffuse coagulopathy, and electrolyte imbalances (Huber et al., 2019; Kuczynski et al., 2020). Moreover, the neuroprotective effects of TH are largely time-sensitive (early hypothermia is protective, late is deleterious) (Kawamura et al., 2005; Huber et al., 2019) and depend on magnitude (mild or strong), duration of application, site of application (local on brain versus systemic application), and inherent characteristics of the organism (age and comorbidities, rodent vs. human differences) (Wu et al., 2020). Importantly, large AIS actually induces systemic hypothermia (with complications) in humans (Kvistad et al., 2012) and mice (Lourbopoulos et al., 2017). As such, the current AHA/ASA guidelines advise against systemic hypothermia in human AIS (Powers et al., 2019).

In contrast to AIS, TH is successfully used as neuroprotection after cardiac arrest and cardiopulmonary resuscitation (CPR) in adults or in neonatal hypoxic-ischaemic encephalopathy (HIE) in humans (Tagin et al., 2012; Uchino et al., 2016; Yildiz et al., 2017). The mechanisms of TH-neuroprotection are practically the same as AIS. Brain hypoxia results in abrupt energy depletion and eventually neuronal cell death, as in AIS; TH reduces brain metabolism, the toxic cascades and eventually brain damage in animal preclinical studies (Thoresen et al., 1996a,b; Ma et al., 2012; Patel et al., 2015; Shah et al., 2017; Doman et al., 2018). The prerequisites for the successful application of TH in HIE have already been defined preclinically in rodents: rapid and early onset of cooling after the hypoxic-ischaemic event (Thoresen et al., 1996b; Doman et al., 2018), prolonged duration, for several hours (3–12 h) (Thoresen et al., 1996b), reduction in rectal temperature by 4–6°C (Thoresen et al., 1996b), efficacy with both selective head cooling or whole-body hypothermia (Ma et al., 2012; Tagin et al., 2012). Here, clinical translation proved successful: TH reduces morbidity/mortality and neurological deficits in full-term infants with neonatal HIE (Jacobs et al., 2011; Tagin et al., 2012; Douglas-Escobar and Weiss, 2015; Silveira and Procianoy, 2015a,b; Purkayastha et al., 2016; Chiang et al., 2017; Giesinger et al., 2017; Rao et al., 2017; Yildiz et al., 2017; Carreras et al., 2018) as well in adults with HIE after cardiopulmonary arrest (Hypothermia after Cardiac Arrest Study Group, 2002). TH for HIE is strongly indicated – according to the latest guidelines – for adults (Panchal et al., 2020) and full-term infants (Aziz et al., 2020).

So why are the effects of TH in AIS and HIE different? In principle, both AIS and HIE receive similar clinical protocols of TH and the underlying neuroprotective mechanisms of TH are basically the same. Thus, failure or success may depend on differences between the underlying pathogenesis of hypoxia-ischaemia in AIS and HIE (Saver, 2006; Donnan et al., 2008; Douglas-Escobar and Weiss, 2015; Yildiz et al., 2017). First, the subjects in neonatal preclinical and clinical studies on HIE are very similar (same age, without comorbidities and similar – optimum – brain recovery and regeneration capacities for both species); they have high external validity, and translation succeeds. In adult HIE the age/comorbidities of rodents and humans may differ: rodent subjects in the successful preclinical studies are usually young and healthy; the effects of TH in older humans (>65 years old) are still positive but weaker (Ahn et al., 2018). Still, translation succeeds, but only under specific conditions. In AIS, age, comorbidities, and the regeneration capacity of the brain differ substantially between humans and rodents (low external validity); here, translation fails. Second, AIS and HIE probably differ in terms of the frequency and susceptibility of cortical spreading depressions (CSDs) that are triggered by and cause tissue hypoxia (Dreier, 2011; Dreier and Reiffurth, 2015). Although CSDs are established in the post-ischaemic period of AIS in animals and humans (Dreier and Reiffurth, 2015), CSD appears to be absent during the post-resuscitation period of HIE (Hansen et al., 2017), although more studies are needed. An absent CSD in HIE would imply more salvageable tissue compared to AIS. Finally, the duration of ischaemic/hypoxic injury and time of TH application determines its effect. As “time is brain” (Saver, 2006), it determines the extent of salvageable tissue and affected neuronal types (Sims, 1992; Katchanov et al., 2003) and thus their potential to be rescued. Additionally, intra-ischaemically administered TH is more effective compared to post-ischaemic cooling (Krieger and Yenari, 2004). In vitro models show a linear time-dependent progression of neuronal death in hypoxia (le Feber et al., 2016); thus, short ischaemia/hypoxia equals reversible damage. In transient ischaemic attacks (TIA), initial lesions are reversible due to the short duration of ischaemia. In large territorial AIS, the long duration of focal ischaemia (>1 h) “produces” irreversible necrotic injuries (infarct core), some tissue-at-risk, and initiates secondary toxic cascades (e.g., release of DAMPs, cortical spreading depressions and aseptic inflammation) that aggravate damage (Moskowitz et al., 2010; Iadecola et al., 2020); here, TH fails. In the case of HIE, brief hypoxia (several minutes) with restoration of circulation causes diffuse “tissue-at-risk” with no necrotic core; it resembles TIA. Its reversible injury depends strictly on the duration of the insult (Douglas-Escobar and Weiss, 2015; Uchino et al., 2016; Elmer and Callaway, 2017; Sekhon et al., 2017). When HIE is relatively short, TH can improve cerebral metabolism and act protectively by decreasing free radical production, inflammation, excitotoxicity, and intracranial pressure (Darwazeh and Yan, 2013). As such, TH is clinically highly effective in both adults (Hypothermia after Cardiac Arrest Study Group, 2002; Geocadin et al., 2006) and newborns (Jacobs et al., 2013) after a relatively fast “return-of-spontaneous-circulation” (ROSC). On the other hand, prolonged cardiac arrest (≥40 min) aggravates neuronal injury to an irreversible injury with a worse prognosis (Welbourn and Efstathiou, 2018). Indeed, an indirect comparison of two study cohorts treated with TH after cardiac arrest shows there were good neurological outcomes in 18% of patients with 40 min CPR versus 55% of patients with 22 min CPR, confirming the time-sensitive protective effect of TH (Hypothermia after Cardiac Arrest Study Group, 2002; Ahn et al., 2018).

As such, differences in the ages of subjects, the presence of secondary cascades such as CSD and duration of hypoxia/ischaemia in AIS/HIE determine the success or failure for translation of hypothermia. Methodological problems in preclinical studies seem to play only a minor role.

Same Problem in a Different Organ: Translational Roadblock in Heart Ischaemia

The translational block is not a “privilege” of neurology alone but also exists in other scientific fields with analogies that are worth considering (Box 2).

In the case of heart ischaemia, the fact is that despite timely reperfusion, morbidity and mortality following ST-elevation myocardial infarction (STEMI) remain substantial (Fokkema et al., 2013; Pedersen et al., 2014; Ibanez et al., 2018). Despite applied reperfusion techniques and optimal pharmacotherapy, almost half of all patients will develop structural and functional heart failure (van der Bijl et al., 2020), while nearly 30% of patients will additionally develop clinical signs and symptoms of heart failure within 1 year (Velagaleti et al., 2008; Ambrosy et al., 2014) (Box 2: the typical human patient with “heart attack”). Here, cardioprotection in patients with acute myocardial infarction parallels neuroprotection in ischaemic stroke. It aims to reduce myocardial injury, the attenuation of heart failure development, and to improve survival and quality of life. However, the translation of thousands of preclinical studies on mechanical and pharmacological cardioprotective interventions in these patients has been particularly disappointing over the last 30 years (Heusch, 2013, 2017). Different cardioprotective strategies, such as coronary postconditioning, hypothermia, GP IIb/IIIa inhibitors, drugs targeting nitric oxide pathways, cyclosporine, adenosine, erythropoietin, glucose modulators, and others, have shown successful preclinical results but all failed in clinical trials to improve patient outcomes (Ludman et al., 2011; Heusch, 2019). Typical examples of translational failure are large and expensive Phase III clinical trials with thousands of STEMI patients, where the primary intervention (e.g., remote ischaemic conditioning) cannot reduce either infarct size or cardiac mortality and hospitalization for heart failure (Hausenloy et al., 2019).

As such, the translation of cardioprotection from bench to bedside remains a significant challenge. Regarding cardiology, the differences between the human patient with acute myocardial infarction (AMI) and the corresponding animal models are at the core of this problem (Box 2: the typical rodent “patient” with “heart attack”). The experimental studies are mostly performed in young and otherwise healthy animals without comorbidities and cardiovascular risk factors that cause endothelial dysfunction. On the other hand, humans with AMI usually have several comorbidities (diabetes, hypothyroidism, hypertension) and risk factors (smoking, hypercholesterolemia) that interfere with cardioprotective interventions (Ferdinandy et al., 2014). Smoking is related to reduced efficacy of remote ischaemic conditioning to improve infarct size (Sloth et al., 2015). In diabetes and hypothyroidism, hearts are found to be resistant to the protective effect of ischaemic conditioning (Pantos et al., 2004; Kleinbongard et al., 2019). Furthermore, cardioprotective strategies may become redundant due to several routine medications that are used in patients with AMI and may reduce myocardial injury per se (Heusch and Gersh, 2017). These medications include β-blockers, statins, nitrates, antiplatelets, and opioids (Pugsley, 2002; Ferdinandy et al., 2014). A retrospective analysis showed that antiplatelets (P2Y₁₂ antagonists) may abrogate the effect of ischaemic postconditioning on infarct size reduction (Roubille et al., 2012). On the other hand, medications such as insulin or anti-diabetic drugs and ACE inhibitors may also induce cardioprotection. The effect of sex is often neglected in experimental studies. Most studies are performed in male animals, while female patients with AMI may have a worse prognosis (Cenko et al., 2018).

Apart from the above problems, a crucial issue is the definition of the proper inclusion-exclusion criteria in clinical trials to include patients with AMI that may benefit from cardioprotective intervention. The existence of salvageable myocardium (in correlation to penumbra in the brain) is important and has to do mostly with cases reperfused 1–6 h after the onset of symptoms (Gersh et al., 2005; Heusch and Gersh, 2017). A small myocardium infarct usually leads to a low risk for heart failure. If reperfusion is very early, then myocardial injury will be negligible and cardioprotection is redundant. If reperfusion is late, little salvageable myocardium will remain (Gersh et al., 2005; Heusch and Gersh, 2017). “Time is heart” in the same way that “time is brain.” Factors such as the presence of pre-infarction angina (it functions like ischaemic preconditioning and results in minimal infarcts; Kleinbongard et al., 2019) or the presence of myocardial injury that occurs during the first few minutes of reperfusion (Rossello and Yellon, 2016) may also change the final outcome and have to be addressed in study designs (Bøtker et al., 2010). On top of that, the selection of the proper dose and timing of administration of cardioprotective interventions may be crucial for successful translation. Unfortunately, in most cases, adequate Phase II pharmacokinetic trials that aim to define the effective time and dose are missing. On the other hand, experimental studies rarely determine effective drug concentrations or routes in blood or serum. For example, adenosine reduces myocardial infarction after reperfusion only when a high dose and prolonged intracoronary infusion of the drug is used (Yetgin et al., 2015).

Infarct size reduction has been the focus of nearly all experimental studies on cardioprotection. However, clinical reality based on recent trials indicates that this focus may have been too narrow (Heusch, 2019). There is no doubt that infarct size is a determinant of patients‘ prognosis (Stone et al., 2016) but other important factors may independently determine the prognosis of patients with reperfused STEMI. In contrast to infarct size, the long-term effects of cardioprotective interventions on myocardial function, repair, remodeling, and mortality have not been thoroughly investigated in preclinical studies (Heusch, 2017). The recent examples of cyclosporine and remote ischaemic conditioning are indicative. In several preclinical and small clinical studies, both interventions proved efficient in reducing infarct size but the large Phase III clinical trials were completely neutral regarding mortality, heart failure hospitalisations, and cardiac remodeling at 1 year (Cung et al., 2015; Hausenloy et al., 2019). Furthermore, besides infarct size, other important factors of myocardial injury, such as microvascular obstruction (MVO) have been neglected in experimental studies. Clinical data show that any evidence of MVO in patients with reperfused AMI is associated with poorer prognostic outcomes, more adverse remodeling, and lower ventricular function on follow-up (Borlotti et al., 2019; Mangion et al., 2019) and with more cardiovascular events, notably higher mortality on follow-up (van Kranenburg et al., 2014; Reinstadler et al., 2018; Galea et al., 2019). Indeed, only MVO but not infarct size predicted cardiac mortality after 2 years of follow-up (van Kranenburg et al., 2014). Eventually, reassessment of the primary end-points that we set in experimental studies seems necessary to produce data with more translational value in cardiology.

Looking at the Bright Side of Translation: The Successful Examples of Multiple Sclerosis and Migraine

On the other hand, translation does work in some fields of neuroscience. In our opinion, the best examples of this are Experimental Autoimmune Encephalomyelitis (EAE) and Multiple Sclerosis (MS) (t Hart et al., 2018) along with the development of CGRP-targeted drugs for migraine (Wattiez et al., 2019). Despite existing failures (Rolfes et al., 2020), EAE led to the development of multiple drugs for MS that control its inflammatory component, such as INF-β, fingolimod, fumarate, mitoxantrone, cladribine, teriflunomide, glatiramer acetate, siponimod, and antibodies such as ocrelizumab, natalizumab, rituximab, and alemtuzumab (Grzegorski and Losy, 2019; Yamout et al., 2020). Migraine preclinical research resulted in targeted CGRP-antagonists and antibodies for migraine (Edvinsson et al., 2018; Charles and Pozo-Rosich, 2019). Hence, what are the keys to these successes?

EAE and MS share many common features (Box 3: typical human and rodent “patients”). EAE is a collection of models, each of which reproduces different clinical, neuropathological, and immunological features of MS (but none alone reproduce complete human MS disease, for an extensive review see Gold et al., 2006; Lassmann and Bradl, 2017; Hochstrasser et al., 2018; Titus et al., 2020). Here the correct choice of model is decisive for each scientific question posed. The immune system in rodents and humans is both similar (structural) and different (molecular) (Mestas and Hughes, 2004). The two diseases share several immunological and pathological pathways and mechanisms (immune-mediated demyelination and axonal injury) that serve well for pathomechanistic understanding and drug discoveries (for extensive and detailed reviews please see Steinman and Zamvil, 2005; Gold et al., 2006; Lassmann and Bradl, 2017; Bjelobaba et al., 2018; Glatigny and Bettelli, 2018). Such corresponding common features can also be found in the field of stroke (pathomechanisms, structure, pathways, clinic). Furthermore, studies on EAE face the same severe methodological and bias problems as stroke studies. Publication bias, insufficient sample sizes, and statistics, lack of blinding and randomisation procedures, lack of multicenter studies, lack of validation studies, etc. are widespread in the EAE field (Vesterinen et al., 2010) but these pitfalls do not block translation. However, EAE and MS have some striking similarities that do not exist in the field of ischaemic stroke. Both involve subjects of a similar age without comorbidities (young mice and patients) (Box 3), both have a decisive peripheral inflammatory component that is easy to reach via bloodstream medications, both have an extended “incubation” period for interventions before disease onset in the CNS that equals to a wide therapeutic window and the aim for both EAE and MS is to develop prophylactic treatment to prevent a relapse (or immune activation) rather than the correction of an already established lesion. Practically, such successfully “translated” MS drugs target and reach mainly the peripheral inflammatory component of the disease (Meuth et al., 2010). In that sense, the prevention of stroke is also successful through secondary prevention medications (statins, antiplatelets, antihypertensives, anticoagulation) (Hankey, 2017). When all the above parameters are considered collectively and critically, the translational block seems to arise when we try to restore/treat cellular degeneration. In other words, it seems easier to succeed translationally when treating a disease target outside of the blood-brain-barrier, in a preventive manner, with an extended therapeutic time window and in young subjects without comorbidities.

The second example is migraine, a disease that enjoys a rapidly advancing understanding of its pathophysiology (for extensive reviews please see Russell et al., 2014; Charles, 2018; Hay et al., 2018; Wattiez et al., 2019). Such knowledge comes in large from preclinical research on small animal models of migraine-related pain, as reviewed in detail (Harriott et al., 2019). Initially, research on serotonin mechanisms in migraine led to the successful and large class of triptans (Goadsby, 2005), as well as the brand new class of selective 5-HT1F agonists (Lasmiditan) (Clemow et al., 2020). In parallel, the calcitonin gene-related peptide (CGRP) pathway (Hay et al., 2018) has been studied extensively, its contribution is well characterized during pain, as CGRP is – uniquely – released during migraine (Edvinsson, 2017), its release into the cranial venous outflow during migraine attacks is proven and intravenous CGRP can induce migraine-like symptoms in migraine patients (Edvinsson, 2017) (direct cause-effect connection). As such, the related CGRP-targeted therapies tested for its treatment to date have consistently produced positive results (Edvinsson, 2017; Schuster and Rapoport, 2017): CGRP-receptor antagonists (gepants) and antibodies (erenumab, galcanezumab, fremanezumab, and eptinezumab) currently being developed are well tolerated and constitute a useful therapeutic tool (Steiner et al., 2013; Edvinsson, 2015; Schuster and Rapoport, 2016; May, 2017; Edvinsson et al., 2018; Charles and Pozo-Rosich, 2019). In addition, studies on new migraine-associated genes, visualization of early activated brain regions just before a migraine attack (e.g., hypothalamic and brainstem activation in collaboration with cortical spreading depolarisation), and the role for neuropeptides on pain (e.g., Pituitary adenylate cyclase-activating polypeptide, PACAP) (Rubio-Beltran et al., 2018) pave the path for new prophylactic options for migraine (Pascual, 2015; Charles, 2018; Harriott et al., 2019). It seems that the field of migraine research is characterized by clearly defined molecular pathways with a crystal-clear cause-effect connection, the age of preclinical and clinical subjects is similar, comorbidities are absent, the targeted pathway is not “behind” the blood-brain barrier (Miller et al., 2016), the primary clinical target is functional (symptom control of viable tissue) rather than anatomical (no evident tissue lesion) and treatment is prophylactic. Most of these features are common denominators in the aforementioned successful MS-EAE paradigm as well.

Seeking “Out-Of-The-Box” Solutions for the Current Common Stroke Practice and Translation Pipeline

Based on the above argumentation, the translationability of our acute therapeutic strategies could be assumed to correlate linearly with the capacity of our models to mimic human acute ischemic physiology: in other words, the more reliably we mimic the human body at the bench the more efficient our drugs will be at the bedside.

In our opinion, the first step should be preclinical testing of drugs on human tissue, after initial screening in rodents and before the transfer of potent drugs to clinical studies. Rodent cells cannot always mimic one-to-one the effects of drugs on human cells, reflecting cellular differences between species. One striking example of this is the neuroprotectant NXY-059, which was a success in rat models but a complete failure in clinical settings, and was recently shown to offer no protection when tested on stem cell-derived human neurons (Antonic et al., 2018). To this end, tissue engineering and stem cell technologies could provide the next-generation human tissue substrate for drug testing. Stem cell-derived 3D engineered tissues or organoids can efficiently mimic key features of the original organ and have been used successfully to model certain facets of human organogenesis and disease, personalized drug testing, and discovery studies. (reviewed in Li and Izpisua Belmonte, 2019; Xinaris, 2019; Steimberg et al., 2020). Human organoids enable the study of human developmental processes and pathogenetic pathways in multilayer and multicellular complexes, especially when the pathways involve interactions between different cell types of the organ. For instance, brain human organoids have been used to examine cell division orientation in human radial glial cells (Lancaster et al., 2013) and human cortical progenitor expansion (Otani et al., 2016) – both processes significantly different in humans compared to other species and especially rodents (Lancaster et al., 2013; Otani et al., 2016). Nevertheless, organoids still have crucial insufficiencies compared to the original human organs, such as a lack of vasculature and immune cells [for a detailed review of organoids’ limitations Ref (Xinaris, 2019)]. This means that they are limited in terms of how much they can grow without cell death and how they are influenced by circulating molecules, mechanical stress, and neural inputs. Lab-grown organoids also exhibit significant anatomic inadequacies due to the absence of normal directional cues (both biochemical and mechanical) that drive the correct organization of cells within tissues and organs (Bhaduri et al., 2020). Yet, despite these aforementioned precautions, the preclinical testing of candidate drugs on human organoids could most probably avoid failures of expensive clinical trials due to species’ cellular differences. Here, studies of “reverse translation,” i.e., testing failed drugs from humans back to rodents to compare responses under the insights provided by their relevant trials, would reveal patterns of translational success/failure and would improve our future strategy in drug development in stroke.

Maybe we should simply find what rodent model best mimics translation, or we could also “humanize” our rodent preclinical models, at least before bringing the candidate drugs to the clinic phase. Rats may eventually not be the optimal rodent species for drug translation in stroke; mice may be more “translational.” Comparative data from preclinical and clinical studies for the Natalizumab, NXY-059, Magnesium, and especially mesenchymal stem cells treatment in stroke imply that mice either reflect the negative human results or the effect size better than rats (Shuaib et al., 2007; Bath et al., 2009; Vu et al., 2014; Llovera et al., 2015; Saver et al., 2015; Elkind et al., 2020). Recent studies indicate that preclinical inbred and SPF rodents fail to recapitulate a normal “dirty” human environment due to their poor and altered microbiome, mycobiome, and virome. The restoration of the organism’s wild environment results in mice and rats (”wildlings”) that can phenocopy human immune responses due to their “wild” immune system trained by the normal environment (Beura et al., 2016; Rosshart et al., 2017, 2019; Hamilton and Griffith, 2019; de Boer et al., 2020). Such “wildings” affect the immune landscape of multiple organs, bring them closer to human status and are also more resistant to diseases compared to inbred laboratory ones (Rosshart et al., 2017). As the immune post-stroke local and systemic reactions largely dictate and shape neuroplasticity and regeneration after stroke (Iadecola et al., 2020), such a “wild” immune system could provide a “human” background for preclinical stroke rodent studies. Furthermore, mice can be “humanized” after being engrafted with human myeloid, lymphoid cell lineages, and tissues (Rongvaux et al., 2014; Bryce et al., 2016; Ito et al., 2018) or via the introduction of human genes that do not exist in mice (“humanized” knock in-mouse models) (Casas et al., 2019). Studies from other research fields indicate that such mouse strains could be biologically closer to humans with higher translational validity, proven so far in cancer immunotherapy, regenerative medicine, allergy and graft-versus-host disease (Ito et al., 2018). Given that the immune system is key to degeneration and regeneration processes after ischaemic stroke, the aforementioned “humanized” strains could bridge the gap between preclinical models and stroke patients.

However, preclinical and clinical fields can be also bridged through computational approaches, such as Machine Learning (ML) and Neural Networks (NN) or study design web-platforms such as the Experimental Design Assistant (EDA) and study-reporting databases. Here, computational science can dig through the vast web-information or “omics” data provided nowadays and reveal similarities or resolve discrepancies between species that result in successful or failed translation (Brubaker et al., 2019). The challenge is to simply predict human biology from non-human species. In the Found In Translation project¹, a ML model applied on gene expression datasets from mouse models of 28 different human diseases achieved an improvement in predictions for human phenotype by 20–50%, compared to simple and direct cross-species extrapolation (Normand et al., 2018). According to the authors, this approach highlights signals that may otherwise be missed and – most importantly – reduces false leads, and thus could enhance translational output for stroke at no additional costs (Normand et al., 2018). Alternative approaches used microarray datasets (from trauma, burn, sepsis) to train a neural network in order to identify true human biological associations after interpreting mouse experiments (Brubaker et al., 2019) or used data from human genome-wide disease studies combined with in silico network models of tissue- and cell-specific function in model organisms to spot candidate molecules that are functionally conserved between rodent-human species (Yao et al., 2018). Interestingly, all achieved truer human biological associations, while mouse experiments alone (i.e., “traditional translation”) failed to capture a large portion of human in vivo biology (Brubaker et al., 2019). Additionally, recently developed preclinical study design assistants, such as the Experimental Design Assistant can help researchers improve the design of animal experiments (du Sert et al., 2017). We believe that such platforms can significantly facilitate preclinical stroke study quality. They should be used widely, and the produced flow-diagrams of each study should be included as figures in manuscripts. Moreover, the preclinical stroke studies should be registered for transparency on websites such as https://www.preclinicaltrials.eu/ or https://www.animalstudyregistry.org, as is routinely done for clinical trials (FDA-based website²). Such registries enhance proper study design, validity, and the reproducibility of experiments/data while simultaneously securing intellectual property.

Finally, we strongly suggest that the drug discovery pipeline in stroke should include at least one validation study of the results in aged animals, optimally in a multicenter design and under co-administration of alteplase. The importance of aging in the biology of the organism is extensively discussed above. STAIR criteria highlight this (Fisher et al., 2009). Data from research fields other than stroke strongly imply that differences in age may be the key to things being lost translation in stroke. To name a few examples, old microglia respond weakly compared to young ones (Daria et al., 2017), aging alters cerebral arteries’ neurovascular coupling in mice (Balbi et al., 2015), aging alters cortex energy and the redox metabolism of the brain (Bayliak et al., 2021), aging changes the response to bacterial endophthalmitis, aging alters the immunological response to stroke (Ritzel et al., 2018), heart systolic function is decreased in older rats (Raya et al., 1997). As aged animals and multicenter preclinical trials can be costly (Llovera et al., 2015), we suggest running one multicenter trial in aged rodents as the “decision-maker” before proceeding to the (more expensive) Phase II clinical stroke studies. As such, in case of negative results, a failed transfer to the clinical setup can be avoided. A typical example of this concept is the negative anti-CD49d preclinical multicenter study in fMCAo in mice (Llovera et al., 2015) that was recently “replicated” with similar negative results in two large Phase II clinical trials (ACTION-1 and -2) (Elkins et al., 2017; Elkind et al., 2020). Eventually, preclinical stroke research should test novel compounds for interactions with alteplase before going to the clinic. In addition to its beneficial thrombolytic action, Alteplase has neurotoxic side effects (Kaur et al., 2004; Dong et al., 2016) and may mask positive results in stroke clinical trials when thrombolysis is used as the standard reperfusion option in treatment-placebo arms (Hankey, 2020). This suggestion is based on the recent ESCAPE-NA1 trial that studied the neuroprotectant nerinetide in human ischaemia-reperfusion that occurs with rapid endovascular thrombectomy (Hill et al., 2020). The ESCAPE-NA1 trial was optimally translationally designed based on a preclinical development program following STAIR criteria and studies on rodents and non-human primates (Hankey, 2020; Hill et al., 2020). Subgroup analysis indicated that patients under only mechanical thrombectomy but not alteplase-thromboysis benefit from nerinetide, supporting a “toxic” masking effect of alteplase in this group.

Conclusion: Opinion Statement and Suggested Path for Translation

In conclusion, translation seems to work mainly at the mechanistic/discovery level. For example, the mechanisms of excitotoxicity, periinfarct depolarisations, inflammation, glymphatic system, and programmed cell death have been discovered in rodents and have also been verified in humans (Dirnagl et al., 1999; Moskowitz et al., 2010; Gennaro et al., 2019; Mestre et al., 2020). On the other side, if we consider stroke as a “chronic” vascular disease with “relapses” of small or large ischemic insults, then its secondary prevention is also a translational success (Kernan et al., 2014), as applies for the case of relapse-prevention in MS as well. Under this assumption, translational failure is a problem only of the acute/subacute phase of stroke, or, named otherwise, a problem of neuroprotective and/or neuroregenerative efforts. Eventually, to overcome this blockage for acute/subacute treatments we believe we need to bridge concepts and practices from both pre- and clinical sides of stroke research (Figure 1) and introduce concepts that arise from research fields other than brain stroke as well.

FIGURE 1

Collectively, we believe that methodological and statistical pitfalls alone do not block acute translation. It remains disappointing that despite the ARRIVE (Kilkenny et al., 2010), STAIR (Corbett et al., 2017), and STEPS(Savitz et al., 2011) guidelines for in vivo experimentation, very few preclinical manuscripts have achieved full compliance with these. Similar suggestions have come from other fields, such as the field of preclinical cardioprotective therapies (Jones et al., 2015; Lindsey et al., 2018). We should not neglect the fact that the only translated and clinically applied treatment to human stroke is the recanalization of the occluded vessel per se (thrombectomy or thrombolysis) (Powers et al., 2019), when we model thrombectomy preclinically in the fMCAo model (Carmichael, 2005). And this is repeated over decades, despite methodological and statistical pitfalls.

Therefore, in addition to existing suggested guidelines (Kilkenny et al., 2010; Savitz et al., 2011; Mergenthaler and Meisel, 2012; Corbett et al., 2017), we believe that we need to think about acute stroke research differently, as summarized in Figures 1, 2. We need preclinical research conditions that mimic the acute clinical ones: a “stroke unit” and “best medical treatment” support for rodents with aspirin, statin, alteplase, treatment of infections, fluids, nutritional support (even if this means negative preclinical results) (Lourbopoulos et al., 2017), and standard translational “rehabilitation approaches” for rodents, such as enriched environments (Garner, 2014; Winek et al., 2016; Bolker, 2017). We need to bring our rodent “patients” closer to the “reality” of human patients: middle-aged to elderly patients, with vascular comorbidities (worn-out vessels, “multi-hits” concept of a chronic pathophysiology) and western-diet, an intravascular (embolic or thrombotic) model of stroke, at least some degree of reperfusion, with an intact skull. We need to incorporate computational aids to design and analyze our data, run multicenter preclinical trials before going clinical, and run “reverse translational studies” (i.e., testing concepts from humans back to animals for translational validity). These are needed along with the high methodological quality of preclinical research that should be guaranteed and accessed via a preclinical trials registry and structured review process by the journals. For this, journals and reviewers hold the key to implementation. Success will come only when we bridge current standards between bench and bedside, conduct quality research and think boldly “out-of-the-box” of the current routine.

FIGURE 2

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