Dexmedetomidine is neuroprotective in an in vitro model for traumatic brain injury
© Schoeler et al; licensee BioMed Central Ltd. 2012
Received: 25 October 2011
Accepted: 11 April 2012
Published: 11 April 2012
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© Schoeler et al; licensee BioMed Central Ltd. 2012
Received: 25 October 2011
Accepted: 11 April 2012
Published: 11 April 2012
The α2-adrenoreceptor agonist dexmedetomidine is known to provide neuroprotection under ischemic conditions. In this study we investigated whether dexmedetomidine has a protective effect in an in vitro model for traumatic brain injury.
Organotypic hippocampal slice cultures were subjected to a focal mechanical trauma and then exposed to varying concentrations of dexmedetomidine. After 72 h cell injury was assessed using propidium iodide. In addition, the effects of delayed dexmedetomidine application, of hypothermia and canonical signalling pathway inhibitors were examined.
Dexmedetomidine showed a protective effect on traumatically injured hippocampal cells with a maximum effect at a dosage of 1 μM. This effect was partially reversed by the simultaneous administration of the ERK inhibitor PD98059.
In this TBI model dexmedetomidine had a significant neuroprotective effect. Our results indicate that activation of ERK might be involved in mediating this effect.
In the United States an estimated 1.1 million patients are treated for traumatic brain injury (TBI) annually . Of these, 124.000 patients suffer from long-term disabilities and 50.000 die, which makes TBI a major cause of premature death [1, 2]. In addition, long term medical care and loss of income create a considerable social and economical burden, which remains an unsolved public health problem . Regrettably, to date there exists no clinically established therapy targeting the mechanisms involved in TBI and treatment remains limited to symptomatic approaches.
Dexmedetomidine is a highly selective α2-adrenoreceptor agonist with sedative, analgesic and sympatholytic properties. It was developed and investigated during the 1980s and 1990s and was initially used to achieve sedation and analgesia in veterinary medicine. In 1999 it was approved for use in humans by the US Food and Drug Administration for short-term sedation (< 24 h) of patients in intensive care units and non-intubated patients prior to and during surgical procedures. Recently, dexmedetomidine was approved in Europe for sedation of adult intensive care unit patients requiring a sedation level not deeper than arousal in response to verbal stimulation.
Besides dexmedetomidine's well-proven sedative effects an increasing body of both in vitro and in vivo evidence indicates that dexmedetomidine also exerts a cell-protective effect on nervous tissue under ischemic conditions [4–7]. There is recent evidence suggesting that this effect is mediated not only by dexmedetomidine's α2-agonistic properties, but also by the binding to imidazoline I1-recepors . The signal transduction cascade linked to these receptors comprises extracellular signal-regulated protein kinase 1 and 2 (ERK 1&2) and is known to be an important regulator for cell survival and mediator of neuroprotective effects of various agents [9–11]. Nevertheless it has yet to be determined whether dexmedetomidine also promotes survival of nervous tissue that has suffered traumatic injury.
In this study we tested the hypothesis that dexmedetomidine has a protective effect on traumatically injured brain tissue as well. We used organotypic hippocampal brain-slice cultures subjected to a focal mechanical trauma as an in vitro model of TBI to analyse a potential neuroprotective effect of dexmedetomidine in TBI.
All experiments in the course of this study were approved by the animal protection representative at the Institute of Animal Research at RWTH Aachen University Hospital, according to the German animal protection law §4, Section 3. Unless otherwise stated all chemicals were obtained from PAA Laboratories GmbH (Pasching, Austria).
The organotypic hippocampal slice cultures were prepared from brains of 5-7 day old C57/BL6 mice pups using a well-established technique [12–14]. After decapitation of the pups the brains were quickly extracted from the sculls and placed into ice cold preparation medium comprising Gey's balanced salt solution (Sigma Aldrich, Steinheim, Germany), 5 mg/ml D-(+)-glucose (Roth, Karlsruhe, Germany) and 0.1% antibiotic/antimycotic solution (containing penicillin G 10,000 U/ml, streptomycin sulphate 10 mg/ml and amphotericin B 25 μg/ml).
The hippocampi were then dissected from the brains under stereomicroscopic vision, cut into 400 μm thick slices and dispersed onto the semi-permeable membrane of MilliCell tissue culture inserts (MilliCell-CM, Millipore Corporation, Billerica, MA, USA). These inserts were placed inside 35 mm tissue culture plates (Sarstedt, Newton, MA, USA) and 1 ml of growth medium (50% Eagle minimal essential medium with Earle's salts, 25% Hank's balanced salt solution (Sigma-Aldrich, Steinheim, Germany), 25% heat inactivated horse serum, 2 mM L-glutamine, 5 mg/ml D-glucose, 1% antibiotic/antimycotic solution and 50 mM HEPES (hydroxyethyl-piperazine-ethanesulfonic acid) buffer solution (Sigma-Aldrich, Munich, Germany), titrated to pH 7.2) was instilled under the membranes to ensure optimal nutrition of the slices. The slices were then incubated for 14 days at 37°C and a moist atmosphere of 95% air and 5% CO2. The growth medium was replaced 24 h after preparation and on every third day thereafter.
On the day of the experiment growth medium was exchanged for experimental medium containing 4.5 μM propidium Iodide. Experimental medium differed from growth medium only in the substitution of horse serum for more Eagle minimal essential medium assuring a standardized experimental environment for all slices. The slices were then incubated for 30 min at 37°C with a moist atmosphere of 95% air and 5% CO2 before capturing baseline fluorescence images. Slices were then traumatized using a specially designed apparatus that ensured an equal and reproducible trauma during the course of the experiments [15, 16]. For this purpose a metal stylus was lifted 7 mm above the slice with the aid of an electromagnet. When power to the magnet was switched off the stylus fell onto the slices producing a mechanical trauma of 5.26 μJ onto the hippocampus's CA1 region. The stylus was retrieved immediately after the impact and experimental medium was exchanged for new experimental medium in those plates belonging to the positive control group. In the experimental groups dexmedetomidine (Precedex® 100 μg/ml Dexmedetomidine, Orion Pharma, Espoo, Finland) was added to this experimental medium in various concentrations (100 μM, 10 μM, 5 μM, 1 μM, 0.1 μM, 0.01 μM). Concentrations were prepared based upon a molar weight of 236.7 g/mol for dexmedetomidine-HCl as a basis. For the negative control group (non-traumatized slices), data from a previous, methodically identical study was used .
To further investigate the protective properties of dexmedetomidine, a series of other experiments was performed using a 1 μM concentration which in the dose-finding study had been proven to be the most effective dose. To assess possible neuroprotective effects in a delayed application, experiments were repeated for 1 μM dexmedetomidine, exchanging experimental medium at 2 and 3 h after the trauma, respectively. In order to verify the hypothesis that dexmedetomidine's neuroprotective properties involve activation of ERK the mitogen-activated/extracellular signal-regulated protein kinase kinase 1 (MEK1) -inhibitor PD98059 (Cell Signaling Technology, Danvers, MA, USA) was added in a 5 μM concentration to the experimental medium containing 1 μM dexmedetomidine.
All slices were incubated for 72 h at 37°C and a moist atmosphere of 95% air and 5% CO2 after trauma.
In order to compare the effects of dexmedetomidine on cell survival with those of hypothermia, a positive control group of slices was incubated at 32° and a moist atmosphere of 95% air and 5% CO2 for 72 h after trauma. An experimental group exposed to 1 μM of Dexmedetomidine was also incubated at 32°C for 72 h after trauma to study a possible synergistic effect of dexmedetomidine and hypothermia.
After the incubation period final fluorescence images were taken.
To quantify cell death propidium iodide was present in the media throughout all experiments. Propidium iodide is a widely used dyeing agent able to bind to nuclear DNA in a non-specific manner. Upon binding it becomes highly fluorescent with a peak emission in the spectrum of visible red light. Its properties render it incapable of penetrating intact phospholipids bilayers such as the cell membrane and the nuclear membrane. However, if the integrity of the cellular membranes is disrupted as in apoptotic or necrotic processes, propidium iodide can diffuse into the nucleus and stain the DNA.
Baseline and final fluorescence images were taken using an upright fluorescence microscope (Zeiss Axioplan, Carl Zeiss MicroImaging GmbH, Jena, Germany) equipped with a rhodamine filter and a low-power x4 objective lens (Zeiss Achroplan 4x/0.10, Carl Zeiss MicroImaging GmbH, Jena, Germany) and captured with a digital camera (SPOT Pursuit 4 MP Slider, Diagnostic Instruments Inc, Sterling Heights, MI, USA) and applicable software.
To eliminate any influence of the mercury lamp's fluctuating intensity, the exposure time was adapted before each imaging session using a standard fluorescence slice (Fluor-Ref, Omega Optical, Brattleboro, VT, USA) as reference.
Mean ± SEM (standard error of the mean) was calculated for each group using SPSS 19 (IBM® SPSS® Statistics, IBM Corporation, Somers, NY, USA). The fluorescence value of the positive control group was set to unity (1 ± 0.037) and served as a reference to put the observed effect of dexmedetomidine on cell survival into perspective. Values of all other groups were normalized to the positive-control group. Statistical relevance of the results was assessed performing an analysis of variance (ANOVA). P ≤ 0.05 was considered statistically significant.
The aim of this study was to investigate the effects of the α2-adrenoreceptor agonist dexmedetomidine on cell survival in an established in vitro model for TBI. Using organotypic hippocampal slice cultures subjected to a focal mechanical trauma we found that dexmedetomidine had a dose-dependent protective effect on hippocampal cells. The dose-effect curve was U-shaped, with a concentration of 1 μM showing the strongest effect. Moreover, we observed neuroprotection by dexmedetomidine even when applied with a delay after the onset of the traumatic injury. Apparently, the neuroprotective effects of dexmedetomidine are mediated - at least in part - by ERK as they were abolished by the co-administration of PD98059. Interestingly, the co-application of hypothermia and dexmedetomidine did not exert synergistic effects.
We treated experimental groups with varying concentrations of dexmedetomidine after trauma. Results show that a concentration of 1 μM dexmedetomidine was most effective at reducing trauma intensity. This finding is consistent with data from a recent study using hippocampal slice culture subjected to oxygen and glucose deprivation . Further dilution as well as a higher concentration of dexmedetomidine provided lower protection until finally, at 100 μM and 0.01 μM, no difference compared to the positive control group was observed. Comparable observations have been made in other studies investigating dexmedetomidine's protective properties [5, 18].
Dexmedetomidine's neuroprotective properties have largely been attributed to its agonist actions at α2-adrenoreceptors [19, 20]. Although recent investigations point out that its interaction with imidazoline I1 receptors and the activation of ERK might also play a role [5, 8, 21] we did not explicitly analyze imidazoline I1 receptors. However, the results of our experiments indicate that activation of ERK is an important factor in the protection of traumatized nervous tissue by dexmedetomidine. ERK is a key enzyme in cell metabolism activated by many different types of tissue injury and has been attributed a "survival"- function. The inhibition of a survival signals itself can cause cells to undergo apoptosis; therefore application of PD98059, inhibitor of ERK's direct activator MEK1, might as well have had a negative effect on cellular survival that superposed with the positive effect of dexmedetomidine without specifically counteracting dexmedetomidine. To rule out this possibility western blots could have been performed. Comparison of levels of activated ERK for the positive control group, the 1 μM dexmedetomidine group and the 1 μM dexmedetomidine + PD98059 group could have backed up our hypothesis. This has recently been performed in a similarly designed study investigating dexmedetomidine's neuroprotective properties using organotypic hippocampal slice cultures subjected to oxygen and glucose deprivation. Results of this study showed that dexmedetomidine's and PD98059's effects do not simply superpose but that both act as two opponents on the same cascade . We therefore decided not to perform these tests and interpreted our finding as a sufficient hint towards an involvement of ERK in the mediation of the brain protective properties of dexmedetomidine in TBI.
Many experimental studies have revealed neuroprotective properties of hypothermia [13, 16, 22, 23] and the advantages of hypothermia in certain clinical circumstances have been demonstrated . To put our findings into context we subjected a group of slices to mild hypothermia of 32°C from trauma until final imaging. As expected, hypothermia alone did prove to be strongly protective, but 1 μM dexmedetomidine was even more effective at reducing trauma intensity. Interestingly, as described before in in vivo models of incomplete cerebral ischemia, a combination of hypothermia and 1 μM dexmedetomidine did not result in synergistic effects .
In a clinical setting, unpredictability is in the nature of TBI and application of any specific therapy will inevitably be delayed. Therefore we investigated the effect of dexmedetomidine when applied 2 or 3 h after trauma. In our model dexmedetomidine proved to be even more efficient when application was delayed by 2 h. However, by delaying application for 3 h no appreciable difference could be observed any more compared to immediate application.
We acknowledge that our results should be interpreted within the context of several limitations.
Propidium iodide labels the DNA of any disrupted cell and we were therefore not able to distinguish between necrosis and apoptosis. However, we aimed to quantify the total amount of cell death and it is agreed that propidium iodide uptake correlates well with the number of damaged cells [15, 25].
We opted for organotypic slice cultures because this model allows easy access to in vitro manipulation of nervous tissue and yet mimics closely the in vivo state of the tissue with respect to morphological and functional characteristics [26, 27]. Concerning the extrapolation to an in vivo situation, results from organotypic slice cultures have been demonstrated to be a satisfying compromise between dissociated cell culture and in vivo models using whole animals [28, 29]. We admit, however, that extrapolation of our results to the in vivo situation is complex. In a living organism, the development and the outcome from TBI is significantly affected by a plethora of different variables that can only partly, if at all, be taken into consideration in an in vitro model (e.g. cerebral perfusion pressure, edema of surrounding tissue, focal or global cerebral ischemia). Such conditions may be affected by dexmedetomidine independently from its direct effects on neuronal survival. Despite these disadvantages we believe that our model is appropriate as it focuses on the mechanical component of the injury and allows the analysis of the intrinsic neuroprotective properties of a drug independently from its possible interactions with confounding variables that can only poorly be controlled in an in vivo setting.
We have found that dexmedetomidine has a protective effect on hippocampal slice cultures subjected to a focal mechanical trauma. The maximum effect was observed at 1 μM, with the observed trauma reduction being significantly more pronounced than observed in slices treated with hypothermia. Trauma intensity did not further decline when applying dexmedetomidine and hypothermia simultaneously. Also, dexmedetomidine's effect was partially reversed by simultaneous application of MEK1 Inhibitor PD98059 indicating the involvement of the ERK-signalling cascade.
Dexmedetomidine exerts a neuroprotective effect when administered after TBI in this model of organotypic hippocampal slice cultures
The protective effect of dexmedetomidine is significantly stronger than the effect of mild hypothermia at 32°C
Dexmedetomidine has a protective effect even if application after TBI is delayed by 2 and 3 h, respectively
Activation of ERK might be involved in mediating Dexmedetomidine's protective effect
Traumatic brain injury
Extracellular signal-regulated protein kinase
Mitogen-activated/extracellular signal-regulated protein kinase kinase
Standard error of the mean
Analysis of variance.
We would like to thank Rosemarie Blaumeiser-Debarry and Jenny Hoffmann for their help with data acquisition as well as the Departments of Neuropathology, Pathology and Animal Research teams at the University Hospital Aachen for expert laboratory advice and assistance. Finally we would like to thank Monroe Coburn for editorial suggestions.