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Int. J. Mol. Sci. 2014, 15(1), 1402-1417; doi:10.3390/ijms15011402
Published: 20 January 2014
Abstract: Phenoxybenzamine (PBZ) is an FDA approved α-1 adrenergic receptor antagonist that is currently used to treat symptoms of pheochromocytoma. However, it has not been studied as a neuroprotective agent for traumatic brain injury (TBI). While screening neuroprotective candidates, we found that phenoxybenzamine reduced neuronal death in rat hippocampal slice cultures following exposure to oxygen glucose deprivation (OGD). Using this system, we found that phenoxybenzamine reduced neuronal death over a broad dose range (0.1 μM–1 mM) and provided efficacy when delivered up to 16 h post-OGD. We further tested phenoxybenzamine in the rat lateral fluid percussion model of TBI. When administered 8 h after TBI, phenoxybenzamine improved neurological severity scoring and foot fault assessments. At 25 days post injury, phenoxybenzamine treated TBI animals also showed a significant improvement in both learning and memory compared to saline treated controls. We further examined gene expression changes within the cortex following TBI. At 32 h post-TBI phenoxybenzamine treated animals had significantly lower expression of pro-inflammatory signaling proteins CCL2, IL1β, and MyD88, suggesting that phenoxybenzamine may exert a neuroprotective effect by reducing neuroinflammation after TBI. These data suggest that phenonxybenzamine may have application in the treatment of TBI.
Traumatic brain injury (TBI) is a national health concern that affects over 1.7 million individuals each year in the United States [1–3]. Of further concern is the lack of effective treatments to reduce the primary or secondary phase of neuropathology induced by TBI. The development of novel neuroprotective agents has proven difficult as TBI represents a heterologous injury [4–9]. In an effort to discover new treatments for TBI, we have used a rat organotypic, hippocampal slice culture model of oxygen glucose deprivation (OGD) as an initial screen to identify potential neuroprotective candidate compounds . While it is clear there are differences between stroke and TBI, there are similarities in the mechanisms that lead to neuropathology. Both injuries induce the development of inflammation, reactive oxygen species (ROS), reactive nitrogen species (RNS), excitotoxicity, calcium dysregulation, and apoptosis [5,8–12]. TBI also results in sheared blood vessels leading to impaired blood flow and ischemia [11–13]. Thus, utilizing an in vitro model of OGD to screen for potential neuroprotective compounds represents an efficient method to identify potential neuroprotective compounds. We previously used this approach to identify low dose methamphetamine as a potential neuroprotective candidate, which was highly effective when tested in the rat lateral fluid percussion (LFP) injury model of severe TBI .
Using the rat hippocampal slice culture model, we have recently made the novel observation that phenoxybenzamine exerts a profound neuroprotective effect following OGD. Currently, phenoxybenzamine is an FDA approved treatment for humans and animals to reduce hypertension and excessive sweating associated with adrenal tumors (pheochromocytoma) [14–16]. Pharmacologically, phenoxybenzamine (Dibenzyline; Wellspring Pharmaceuticals) is a halo-alkylamine that blocks both α-1 and α-2 adrenergic receptors, but has a higher affinity for the α-1 receptor [16,17]. Following i.v. administration, receptor antagonism achieves a peak effect at approximately 1 h . However, phenoxybenzamine exerts a long-term effect in the brain with a half-life of approximately 24 hours. As an antagonist, phenoxybenzamine forms an irreversible covalent bond with α-adrenergic receptors, thus the effect of the drug lasts longer than its metabolic half-life . This observation is supported by studies showing the reversal of the effect of phenoxybenzamine is dependent on the synthesis of new receptors and not metabolism of the drug. Hamilton et al. demonstrated that only 50% of α-1 receptors had recovered eight days after a single administration of phenoxybenzamine . Based on prior FDA approval of phenoxybenzamine, its stability and ease of administration, relatively long effect, and the absence of harmful side effects; we elected to further investigate phenoxybenzamine as a potential neuroprotective agent in the treatment of TBI.
As a proof-of-concept study, we utilized the rat LFP injury model to test the neuroprotective potential of phenoxybenzamine . Importantly, we chose the clinically relevant time point of 8 h after injury to test the potential neuroprotective effect. The administration of a single, i.v., bolus dose of 1.0 mg/kg at 8 h after injury resulted in significant, long-term behavioral and cognitive improvements. To investigate the possible mechanisms of phenoxybenzamine-mediated neuroprotection we performed a gene array analysis and identified relevant gene targets that were altered as a result of phenoxybenzamine treatment and then confirmed the changes in gene expression by quantitative real-time PCR.
2. Results and Discussion
2.1. Phenoxybenzamine Prevents Hippocampal Cell Death after Oxygen Glucose Deprivation
Our preliminary studies in the rat hippocampal slice culture (RHSC)-OGD model identified phenoxybenzamine as a potential neuroprotective candidate compound. We further tested phenoxybenzamine in the RHSC-OGD model by conducting a dose response study. Phenoxybenzamine preserved primary neurons within the CA1, CA3 and dentate gyrus and produced a robust neuroprotective effect over a broad dose range (0.1 μM–1 mM final media concentration) (Figure 1a). Neuroprotective compounds must be effective when administered at a clinically relevant time point, which in the case of stroke or traumatic brain injury can be hours after injury. Therefore, we examined the potential therapeutic window of phenoxybenzamine in the RHSC-OGD model. A middle dose (100 μM) was selected and added to the cultures at 2, 4, 8, or 16 h post-OGD. We found that phenoxybenzamine prevented neuronal death from OGD in all regions of the hippocampus when delivered at 2, 4, and 8 h post-OGD. When delivered at 16 h post-OGD, phenoxybenzamine prevented neuronal death only in the CA1 region of the hippocampus (Figure 2a). Taken together, these data demonstrated a neuroprotective role for phenoxybenzamine under OGD conditions.
2.2. Phenoxybenzamine Prevents Neurological Dysfunction that Occurs as a Result of Severe TBI
To test the effect of phenoxybenzamine in TBI, we utilized the rat lateral fluid percussion (LFP) injury model. The LFP model is one of the most widely used models of closed head injury and reproduces many of the conditions observed in humans following TBI . In this model, a fluid pulse delivered to the intact dura produces a rotational torque and coup/contre coup typically observed with closed head injury [20,21]. In choosing our test dose, we extrapolated a relevant rat dose based on current FDA approved levels. In humans, phenoxybenzamine can be administered daily at doses up to 120 mg total [14,16,17,22]. Based on an average human weight of 70 kg, this represents 1.7 mg/kg. Therefore, we selected a slightly lower, single, i.v. dose of 1 mg/kg. This dose was then administered at the clinically relevant time point of 8 h after severe TBI. Therapeutic effectiveness was determined based on behavioral and cognitive outcomes.
Neurological severity score (NSS) and foot fault assessments were used to test the hypothesis that phenoxybenzamine treatment could improve behavioral outcomes. Animals were assessed 24 h after injury and on 7, 14, 21, and 30 days post-TBI. We found no significant differences in NSS or foot fault scoring between the saline treated controls and phenoxybenzamine treated animals at 24 h or 7 days after the TBI. These data confirm that all animals in both treatment groups experienced injuries of similar severity. However, phenoxybenzamine treated animals showed significant improvements in NSS and foot fault scoring on days 14, 21, and 30 (Figure 3a,b). It is worth noting that phenoxybenzamine treated rats had foot fault values that were not significantly different from uninjured control rats on days 21 and 30 of testing.
2.3. Phenoxybenzamine Reduces Cognitive Impairment Associated with Severe TBI
The Morris water maze (MWM) was used to assess cognitive function of rats beginning 25 days after injury. A single, i.v., administration of phenoxybenzamine at 8 h after TBI resulted in significant learning improvement on days 2–5 of the training phase (Figure 4a). Phenoxybenzamine treated animals were not significantly different from the un-injured, sham operated control animals on any of the training days. After the learning phase was completed, a probe trial was conducted to assess spatial memory function. During the probe trial the phenoxybenzamine treated animals displayed significantly greater spatial memory capacity compared to the saline treated controls (Figure 3b). The phenoxybenzamine treated TBI animals spent approximately 28% of available time searching the target quadrant for the removed escape platform. In contrast, saline treated controls spent approximately 10% of available time searching the target quadrant. As in the training phase, the phenoxybenzamine treated TBI injured animals did not differ from un-injured sham controls, which spent approximately 25% of their time searching the target quadrant (Figure 4b).
2.4. Phenoxybenzamine Reduces the Expression of Pro-Inflammatory Genes
In an effort to elucidate the possible mechanisms involved in phenoxybenzamine-mediated neuroprotection, we performed a gene array analysis of cortical tissue taken from animals at 32 h after the injury (8 h delay to treatment + 24 h after treatment). This time point was chosen in an effort to detect possible gene changes that would affect the development of secondary damage. The gene array screened for expression change in 24,0000 genes. From this initial screen, we identified a subset of 12 genes that appeared to exhibit significant changes and were potentially relevant to mechanisms of neuroprotection (Table 1). We further examined this subset of genes by quantitative rtPCR. Importantly, we detected a significant increase in the expression of the pro-inflammatory signaling proteins CCL2 (11 fold, p = 0.004), IL1β (4.6 fold, p = 0.005) and MyD88 (3 fold, p = 0.0001) following severe TBI (Table 1). In contrast, rats treated with phenoxybenzamine after severe TBI showed no significant increase in the expression of these proinflammatory genes. These data suggest that phenoxybenzamine may mediate neuroprotection by modulating the neuroinflammatory response. TBI also induced significant changes in cellular retinol binding protein 2 (Rbp2) and corticotrophin releasing hormone (CRH). However, similar changes to the expression of these genes were seen in both saline and methamphetamine treated groups. Finally, TBI induced a slight but statistically significant increase in the expression of the calcium permeable AMPA receptor (GRIA4). In contrast, methamphetamine treatment resulted in no significant increase in GRIA4 expression.
We have demonstrated that a single i.v. administration of 1.0 mg/kg of phenoxybenzamine, delivered 8 h after TBI, significantly reduced both behavioral and cognitive impairment. This represents a novel finding as there are no previous studies indicating that phenoxybenzamine exerts any type neuroprotective effects. Currently, phenoxybenzamine is used to treat hypertension and excessive sweating associated with adrenal tumors (pheochromocytoma). Interestingly, phenoxybenzamine does not appear to decrease global cerebral blood flow . It does, however, appear to re-distribute flow among certain regions of the brain . Buchweitz and Weiss  performed studies in which they found phenoxybenzamine reduced blood flow in certain cortical regions and the hippocampus, but increased blood flow in the pons and substantia nigra. Mechanistically, phenoxybenzamine acts as a potent α-1 adrenergic antagonist (with secondary α-2 antagonism) and thus blocks the effects of epinephrine and norepinephrine [16,24]. There is evidence that suggests blocking the effects of epinephrine and norepinephrine may provide significant benefits to TBI patients. Severe TBI increases the activity of the sympathetic nervous system resulting in the excessive release of epinephrine and norepinephrine . Previous research indicates a direct correlation between the severity of TBI, plasma epinephrine and norepinephrine levels, and recovery rates . Patients remaining in a persistent coma have epinephrine and norepinephrine plasma levels several-fold higher than controls. Furthermore, these catecholamine levels remain elevated for the duration of the comatose state. Conversely, TBI patients with initial catecholamine levels that are mildly elevated have been found to consistently improve to a Glasgow Comma Scale (GCS) value greater than 11 at one week post-TBI. In patients with multisystem trauma and TBI, plasma norepinephrine levels at 48 h post injury were predictive of the GCS at one week [26,27]. Plasma norepinephrine also correlated with patient survival, the number of ventilator days, and the length of hospital stay [24,26,27].
In terms of cognitive function, the increased presence of norepinephrine in TBI has been associated with poor neuropsychological outcome. Kobori et al. , found that the administration of the α-1 antagonist Prazosin, at 14 days after a TBI, significantly improved working memory in rats . Kobori et al.  went on to elucidate a proposed mechanism that linked the impaired working memory with TBI mediated increase in the presence of α-1 in the medial pre-frontal cortex. The increased α-1 was linked to a CREB mediated increase in α-1 receptor gene transcription through binding of phospho-CREB to CRE sites on the α-1A receptor suggesting a positive feedback effect.
Based on these studies, the neuroprotective effect of phenoxybenzamine may be a direct result of the α-1 and α-2 antagonism that blocks the secondary effects of norepinephrine signaling in the brain. The alpha 1 adrenergic receptor is coupled to a heterotrimeric G protein, Gq, which activates phospholipase C (PLC) . PLC produces an increase in IP3 and calcium, which, in turn, activates protein kinase C (PKC) [30,31]. Previous studies in TBI have demonstrated that PKC is rapidly elevated as a result of the injury . Another potential mechanism of neuroprotection associated with phenoxybenamine may be a reduction in calmodulin(CaM)/CaMKII activity. Phenoxybenzamine is also a potent inhibitor of CaM/CaMKII activity . Under basal conditions CaMKII is a major mediator of glutamate signaling, however, under acute injury conditions, CaM/CaMKII interacts with the NR2B subunit of NMDA receptors leading to excitotoxic death . There is evidence that CaM/CaMKII increases the trafficking of AMPA receptors to the cell surface leading to greater excitotoxic death during acute injury . Supporting a neurodestructive role for CaMKII, Zhang et al.  found that TBI increased the expression of CaMKIIδ. Pre-treating rats with a CaMKIIδ inhibitor before TBI resulted in a significant decrease in lesion volume and a significant increase in neuromotor function . Zhang et al.  went on to elucidate a mechanism in which CaMKIIδ actively promotes apoptosis in neurons by increasing the pro-apoptotic protein BAX and subsequent caspase 3 activation .
From gene array studies we found that phenoxybenzamine appears to block critical gene changes that occur after TBI. Genes involved in inflammation such as CCl2, IL-1β, and MyD88 were all significantly elevated in TBI animals, but phenoxybenzamine treated animals did not differ from uninjured control rats. This is a crucial finding because inflammation contributes to the formation of edema, a loss of neurons, and negatively affects patient recovery. A key component of brain inflammation is the recruitment of neutrophils and monocytes, which are toxic to neurons [34–38]. Recruitment of monocytes into the brain is primarily controlled by monocyte chemotactic protein 1 (MCP-1) also known as CCL2, which is expressed by astrocytes, macrophages, and reactive microglia [36,39]. After TBI, CCL2 actively recruits monocytes to areas of brain damage leading to inflammation, edema and neuronal damage . Rhodes et al. , found a rapid increase in CCL2 in human spinal fluid following severe TBI. Furthermore, CCL2 levels remained significantly elevated for up to 10 days post-injury . Semple et al.  reported that elevated levels of CCL2 were detected in the serum of patients who died after TBI.
Epithelial cells actively synthesize CCL2 in response to the proinflammatory cytokine, interleukin-1β (IL-1β) [41,42]. From our gene array analysis, we found that saline treated animals had a significant increase in IL-1β after TBI whereas phenoxybenzamine treated animals showed no significant increase. In terms of TBI, IL-1β is the primary activator of microglia and is directly responsible for inducing inflammation [6,8,43]. IL-1β further contributes to immunoexcitoxicty by enhancing the sensitivity of NMDA receptors and tumor necrosis factor alpha (TNF-α) leading to increased brain inflammation and excitotoxicity [8,44–46].
Phenoxybenzamine may further reduce post-traumatic inflammation by reducing expression of myeloid differentiation primary response protein 88 (Myd88). Myd88 is a key adaptor protein involved in Toll-like receptor and pro-inflammatory cytokine signal transduction [47,48]. In saline treated TBI animals, Myd88 was significantly up-regulated over uninjured controls. However, MyD88 expression levels were equivalent to uninjured controls in phenoxybenzamine treated rats after TBI. Mechanistically, Myd88 is a key adaptor protein for Toll-like receptors, cytokines, and nuclear factor kappaB (NF-κB) [47,48]. Previous research suggests activation of Toll-like receptors results in the recruitment of Myd88 and the subsequent activation of NF-κB, which in turn, induces the rapid expression of pro-inflammatory molecules including tumor necrosis factor a (TNF-α), IL-1β, interleukin-6 (IL-6), and intracellular adhesion molecule-1 (ICAM-1) leading to a pro-inflammatory response [47–50]. These data strongly suggest that phenoxybenzamine is a valid candidate for further investigation as a potential neuroprotective agent and treatment for TBI.
3. Experimental Section
3.1. Rat Organotypic Hippocampal Slice Cultures
All experimental animal procedures were approved by the University of Montana Institutional Animal Care and Use Committee in accordance with National Institutes of Health guide for the care and use of Laboratory animals (NIH Publications No. 8023). Hippocampal slice cultures were prepared from the brains of 7-day-old Sprague-Dawley rat pups as previously described . After 7 days in culture, slices were exposed to oxygen-glucose deprivation. A glucose free balanced salt solution (BSS) composed of 120 mM NaCl (EMD Science, Gibbstown, NJ, USA), 5 mM KCl (Sigma Aldrich, St. Louis, MO, USA), 1.25 mM NaH2PO4 (EMD Science, Gibbstown, NJ, USA), 2 mM MgSO4 (Sigma Aldrich, St. Louis, MO, USA), 2 mM CaCl2 (Sigma Aldrich, St. Louis, MO, USA), 25 mM NaHCO3 (Sigma Aldrich, St. Louis, MO, USA), 20 mM HEPES (EMD Science, Gibbstown, NJ, USA), 25 mM sucrose (Sigma Aldrich, St. Louis, MO, USA); pH 7.3 was bubbled for 1 h with 5% CO2/95% N2 at 10 L/h. Slices were washed 6 times in deoxygenated SBSS to remove residual glucose, transferred into deoxygenated SBSS and placed in a 37 °C chamber with a ProOx 110 oxygen feedback sensor (BioSpherix, Lacona, NY, USA) that maintained gas levels at 0.1% O2, 5% CO2, 94.4% Nitrogen for 60 min. After OGD, the slices were immediately transferred back into pre-warmed Neurobasal media containing B27 without anti-oxidants (Life technologies Carlsbad, CA, USA) under normal oxygen conditions. Slices treated with phenoxybenzamine (Sigma Aldrich, St. Louis, MO, USA) in the dose-response study were placed in pre-warmed Neurobasal media containing 0.1 μM–1 mM phenoxybenzamine immediately after OGD. For the time course studies, 100 μM phenoxybenzamine was added to Neurobasal media at 2, 4, 8, or 16 h after OGD. Neuronal damage was determined by staining slices with propidium iodide (PI) (Molecular Probes, Eugene, OR, USA) and quantifying the relative fluorescence intensity (excitation 540/emission 630) using ImagePro Plus software (Media Cybernetics, Silver Springs, MD, USA). PI was added to the media at a concentration of 2 μM , 4 h prior to OGD. Images were taken of the hippocampal slices prior to OGD to establish baseline fluorescence. After OGD, slices were placed in normal media containing 2 μM PI and imaged again at 24 h post-OGD using fluorescence optics with an Olympus IMT-2 microscope and a Hamamatsu camera. The total fluorescent intensity in each slice was determined using ImagePro Plus software (Media Cybernetics, Silver Springs, MD, USA) and all values were expressed as an integrated optical density (IOD) which calculates the area multiplied by the pixel number and intensity to give a total fluorescent staining intensity that measures the amount of cell death.
3.2. TBI Procedure
Male Wistar rats (350–500 g) were obtained from Charles River Laboratories (Wilmington, MA, USA) and housed with a 12-h light/dark cycle and ad libitum access to food and water. Severe TBI was induced using the LFP procedure as previously described . Briefly, a 5 mm craniotomy was made over the right hemisphere equidistant between the lambda and the bregma. Animals were given a fluid pulse to the brain at 1.9–2.3 ATM of pressure with a 20 ms duration using an FP 302 LFP machine (AmScien Instruments, Richmond, VA, USA). All animals experienced apnea and were manually ventilated on 0.5 liters O2/min until normal breathing occurred. Throughout the procedure and for 3 h post-injury, body temperature, heart rate, and spO2 levels were monitored and recorded. Animals had an average righting time of 24 min and an average mortality rate of 25% was observed. Mild to moderate TBI injuries (NSS < 9) that were excluded from the study was 14%. At 8 h post-TBI, phenoxybenzamine hydrochloride (Sigma Aldrich, St. Louis, MO, USA) at 1 mg/kg dissolved into 200 μL of sterile saline was injected into the tail vein of randomly selected rats using a 25-gauge needle. Saline treated animals underwent the same tail vein injection procedure but received 200 μL of saline. Sham operated animals received a craniotomy but did not receive a TBI. Post surgery, the animals were monitored twice daily for one week. Each day of the first week following TBI, all animals were given 10 mL pre-warmed supplemental saline given subcutaneously, and 100 g of AD Veterinary diet (to stimulate eating and minimize weight loss). All animals were weighed once daily for two weeks post TBI.
3.3. Neurological Severity Scoring
Neurological severity scoring (NSS) and foot fault assessments were performed as previously described [10,18]. Assessements were conducted on days 1, 7, 14, 21, and 30 by a blinded observer. Scores ranged from 0–16 with 16 indicating maximal impairment. Scoring criteria for a severe TBI was an NSS in the range of 10–16. Animals scoring an NSS of 9 or less on day 1 post injury were identified as having a moderate/mild injury and were excluded. Animals that scored 10 or greater on their NSS were randomly distributed into saline or phenoxybenzamine treated groups. For this study 13 animals were placed in the saline group with a mean day 1 NSS of 12.7 and nine animals were placed in the phenoxybenzamine group with a mean day 1 NSS of 12.0.
3.4. Foot Faults Assessments
Foot fault assessments were conducted as previously described [10,18]. Briefly, rats were set on an elevated grid. With each weight-bearing step, the paw may fall or slip off the wire grid. Each time the left forelimb (affected by damage to the right hemisphere) missed a placement on the wire rack it was recorded as a foot fault. The total number of steps that the rat used to cross the grid was counted, and the total numbers of foot faults for the left forelimb was recorded. The total number of left forelimb misses out of 100 forelimb steps was reported.
3.5. Assessment of Cognitive Function
The Morris water maze (MWM) was used to assess the impact of phenoxybenzamine on cognitive function (learning and memory) following TBI. The assessment procedure was performed as previously published . Pre-acclimation began on day 24 post-TBI. The training phase began on day 25 post-injury, and the probe trial was conducted on day 30 post-injury. The water temperature was maintained at a constant 19 degrees Celsius with the clear plexiglas escape platform 2 cm below the water level. All data was recorded and analyzed using Anymaze software connected to a Logitech camera. All data sets were analyzed by a blinded researcher. There were no significant differences in swim speeds between any of the animals tested.
3.6. RNA Isolation/Qrt-PCR
Three biological replicates were used for each experimental group and each replicate was run in triplicate. Total RNA was isolated from the rat ipsilateral cortex utilizing Trizol LS (Life technologies Carlsbad, CA, USA) according to the manufacturer’s protocol. To remove any contaminating chemicals that could affect downstream analysis, RNA was further purified using the RNeasy MinElute Cleanup Kit (Qiagen, Valencia, CA, USA) according to the manufacturer’s protocol. RNA was quantified using a Nano Drop spectrophotometer (Cole-Parmer, Vernon Hills, IL, USA. RNA was considered acceptable if the 260/280 and 260/230 ratios were 2.0 or greater. A 1 μg aliquot of total RNA was reverse transcribed to cDNA using Qiagen’s RT2 First Strand Kit (Qiagen, Valencia, CA, USA). One half of the cDNA reaction was mixed with 675 μL of Qiagen’s 2X RT SYBR Green Mastermix and 624 μL H2O. This was then added to a custom array panel (SA Biosciences, Valencia, CA, USA) and cycled according to the manufacturer’s suggested qPCR protocol on a iQ5 thermocycler (Bio-Rad, Hercules, CA, USA). Values were normalized for GAPDH. For data analysis, the ΔΔCt method was used with the aid of the manufacturer’s online software suite RT2 Profiler PCR Array Data Analysis version 3.5 (SA Biosciences, Valencia, CA, USA). Fold-changes were calculated and results compared to normal controls. Please note: (2−ΔΔCt) is the normalized gene expression (2−ΔCt) in the test sample divided the normalized gene expression (2−ΔCt) in the Control Sample. Fold-Regulation represents fold-change results in a biologically meaningful way. Fold-change values greater than one indicate a positive- or an up-regulation, and the fold-regulation is equal to the fold-change. Controls for this experiment underwent the trephination surgery but did not receive a TBI.
3.7. Statistical Analysis
All data was analyzed using Prizm software (GraphPad, La Jolla, CA, USA). To determine Gaussian (normal) distribution a Kolmogorof-Smirnov test was performed on all data sets. Analysis on data sets with more than two groups was done using one-way ANOVA with Tukey’s post-hoc to determine statistical significance between groups. A p < 0.05 or less was considered significant.
Clinically, phenoxybenzamine is FDA approved and currently used to treat hypertension and sweating associated with pheochromocytoma, a condition in which the adrenal glands secrete high levels of noradrenaline and adrenaline. As a therapeutic, the side effects of phenoxybenzamine are minimal: stuffy nose, mild drowsiness, blurred vision, and upset stomach. As a treatment for TBI it possesses several advantages. It can be delivered intravenously, it efficiently crosses the blood brain barrier, it produces mild side effects, and it significantly reduces neurological and cognitive dysfunction when delivered 8 h after a severe TBI. Taken together, it is our opinion that phenoxybenzamine warrants further investigation as a potential neuroprotective agent for TBI.
This work was supported through the University of Montana Drug Discovery Program.
Conflicts of Interest
The authors declare no conflict of interest.
- Faul, M.; Xu, L.; Wald, M.; Coronado, V. Traumatic Brain Injury in the United States: Emergency Department Visits, Hospitalizations and Deaths 2002–2006; CDC: Atlanta, GA, USA, 2006.
- Dempsey, K.E.; Dorlac, W.C.; Martin, K.; Fang, R.; Fox, C.; Bennett, B.; Williams, K.; Flaherty, S. Landstuhl Regional Medical Center: Traumatic brain injury screening program. J. Trauma Nurs 2009, 16, 6–7.
- Dean, P.J.; O’Neill, D.; Sterr, A. Post-concussion syndrome: Prevalence after mild traumatic brain injury in comparison with a sample without head injury. Brain Inj 2011, 26, 14–26.
- Barth, J.T.; Diamond, R.; Errico, A. Mild head injury and post concussion syndrome: Does anyone really suffer? Clin. Electroencephalogr 1996, 27, 183–186.
- Beauchamp, K.; Mutlak, H.; Smith, W.R.; Shohami, E.; Stahel, P.F. Pharmacology of traumatic brain injury: Where is the “golden bullet”? Mol. Med 2008, 14, 731–740.
- Blaylock, R.L.; Maroon, J. Immunoexcitotoxicity as a central mechanism in chronic traumatic encephalopathy-A unifying hypothesis. Surg. Neurol. Int 2011, 2, 107.
- Roozenbeek, B.; Maas, A.I.; Menon, D.K. Changing patterns in the epidemiology of traumatic brain injury. Nat. Rev. Neurol 2013, 9, 231–236.
- Arand, M.; Melzner, H.; Kinzl, L.; Bruckner, U.B.; Gebhard, F. Early inflammatory mediator response following isolated traumatic brain injury and other major trauma in humans. Langenbecks Arch. Surg 2001, 386, 241–248.
- Baugh, C.M.; Stamm, J.M.; Riley, D.O.; Gavett, B.E.; Shenton, M.E.; Lin, A.; Nowinski, C.J.; Cantu, R.C.; McKee, A.C.; Stern, R.A. Chronic traumatic encephalopathy: Neurodegeneration following repetitive concussive and subconcussive brain trauma. Brain Imaging Behav 2012, 6, 244–254.
- Rau, T.F.; Kothiwal, A.; Zhang, L.; Ulatowski, S.; Brooks, D.M.; Cardozo-Pelaez, F.; Chopp, M.; Poulsen, D.J. Low dose methamphetamine mediates neuroprotection through a PI3K-AKT pathway. Neuropharmacology 2011, 61, 677–686.
- Bullock, R.Z.A.; Woodward, J.J.; Myseros, J.; Choi, S.C.; Ward, J.D.; Marmarou, A.; Young, H.F. Factors affecting excitatory amino acid release following severe human head injury. J. Neurosurg 1998, 89, 507–518.
- Chan, P.H. Mitochondria and neuronal death/survival signaling pathways in cerebral ischemia. Neurochem. Res 2004, 29, 1943–1949.
- Faden, A.I. Neuroprotection and traumatic brain injury: Theoretical option or realistic proposition. Curr. Opin. Neurol 2002, 15, 707–712.
- Stokes, G.S.; Marwood, J.F. Review of the use of alpha-adrenoceptor antagonists in hypertension. Methods Find Exp. Clin. Pharmacol 1984, 6, 197–204.
- Strosberg, A.D. Structure, function, and regulation of adrenergic receptors. Protein. Sci 1993, 2, 1198–1209.
- Te, A.E. A modern rationale for the use of phenoxybenzamine in urinary tract disorders and other conditions. Clin. Ther 2002, 24, 851–861. discussion 837.
- Hamilton, C.A.; Dalrymple, H.W.; Reid, J.L.; Sumner, D.J. The recovery of alpha-adrenoceptor function and binding sites after phenoxybenzamine. An index of receptor turnover? Naunyn. Schmiedebergs Arch. Pharmacol 1984, 325, 34–41.
- Rau, T.F.; Kothiwal, A.S.; Rova, A.R.; Brooks, D.M.; Poulsen, D.J. Treatment with low-dose methamphetamine improves behavioral and cognitive function after severe traumatic brain injury. J. Trauma Acute. Care Surg 2012, 73, S165–S172.
- Antunes, M.; Biala, G. The novel object recognition memory: Neurobiology, test procedure, and its modifications. Cogn. Process 2012, 13, 93–110.
- Xiong, Y.; Mahmood, A.; Chopp, M. Animal models of traumatic brain injury. Nat. Rev. Neurosci 2012, 14, 128–142.
- Shultz, S.R.; Bao, F.; Omana, V.; Chiu, C.; Brown, A.; Cain, D.P. Repeated mild lateral fluid percussion brain injury in the rat causes cumulative long-term behavioral impairments, neuroinflammation, and cortical loss in an animal model of repeated concussion. J. Neurotrauma 2012, 29, 281–294.
- Caine, M.; Perlberg, S.; Meretyk, S. A placebo-controlled double-blind study of the effect of phenoxybenzamine in benign prostatic obstruction. Br. J. Urol 1978, 50, 551–554.
- Buchweitz, E.; Weiss, H.R. Effects of phenoxybenzamine or N-methyl chlorpromazine on regional cerebral blood flow: Comparison of central and peripheral alpha adrenergic receptor antagonism. J. Pharmacol. Exp. Ther 1982, 223, 322–326.
- Hamill, R.W.; Woolf, P.D.; McDonald, J.V.; Lee, L.A.; Kelly, M. Catecholamines predict outcome in traumatic brain injury. Ann. Neurol 1987, 21, 438–443.
- Tran, T.Y.; Dunne, I.E.; German, J.W. Beta blockers exposure and traumatic brain injury: A literature review. Neurosurg. Focus 2008, 25, E8.
- Woolf, P.D.; Hamill, R.W.; Lee, L.A.; Cox, C.; McDonald, J.V. The predictive value of catecholamines in assessing outcome in traumatic brain injury. J. Neurosurg 1987, 66, 875–882.
- Woolf, P.D.; Hamill, R.W.; Lee, L.A.; McDonald, J.V. Free and total catecholamines in critical illness. Am. J. Physiol 1988, 254, E287–E291.
- Kobori, N.; Hu, B.; Dash, P.K. Altered adrenergic receptor signaling following traumatic brain injury contributes to working memory dysfunction. Neuroscience 2011, 172, 293–302.
- Cimino, M.; Weiss, B. Characteristics of the binding of phenoxybenzamine to calmodulin. Biochem. Pharmacol 1988, 37, 2739–2745.
- Yang, K.; Taft, W.C.; Dixon, C.E.; Todaro, C.A.; Yu, R.K.; Hayes, R.L. Alterations of protein kinase C in rat hippocampus following traumatic brain injury. J. Neurotrauma 1993, 10, 287–295.
- Tomycz, N.D.; Friedlander, R.M. α-1 Adrenergic receptor signaling linked to memory dysfunction following brain trauma. Neurosurgery 2011, 68, N16–N18.
- Vest, R.S.; O’Leary, H.; Coultrap, S.J.; Kindy, M.S.; Bayer, K.U. Effective post-insult neuroprotection by a novel Ca(2+)/calmodulin-dependent protein kinase II (CaMKII) inhibitor. J. Biol. Chem 2010, 285, 20675–20682.
- Zhang, M.; Shan, H.; Gu, Z.; Wang, D.; Wang, T.; Wang, Z.; Tao, L. Increased expression of calcium/calmodulin-dependent protein kinase type II subunit delta after rat traumatic brain injury. J. Mol. Neurosci 2012, 46, 631–643.
- Semple, B.D.; Frugier, T.; Morganti-Kossmann, M.C. Role of CCL2 (MCP-1) in traumatic brain injury (TBI): Evidence from severe TBI patients and CCL2−/− mice. J. Cereb. Blood Flow Metab 2010, 30, 769–782.
- Semple, B.D.; Frugier, T.; Morganti-Kossmann, M.C. CCL2 modulates cytokine production in cultured mouse astrocytes. J. Neuroinflammation 2010, 7, 67.
- Semple, B.D.; Kossmann, T.; Morganti-Kossmann, M.C. Role of chemokines in CNS health and pathology: A focus on the CCL2/CCR2 and CXCL8/CXCR2 networks. J. Cereb. Blood Flow Metab 2010, 30, 459–473.
- Sozzani, S.; Rieppi, M.; Locati, M.; Zhou, D.; Bussolino, F.; Proost, P.; van Damme, J.; Mantovani, A. Synergism between platelet activating factor and C–C chemokines for arachidonate release in human monocytes. Biochem. Biophys. Res. Commun 1994, 199, 761–766.
- Sozzani, S.; Zhou, D.; Locati, M.; Rieppi, M.; Proost, P.; Magazin, M.; Vita, N.; van Damme, J.; Mantovani, A. Receptors and transduction pathways for monocyte chemotactic protein-2 and monocyte chemotactic protein-3. Similarities and differences with MCP-1. J. Immunol 1994, 152, 3615–3622.
- Ziebell, J.M.; Morganti-Kossmann, M.C. Involvement of pro- and anti-inflammatory cytokines and chemokines in the pathophysiology of traumatic brain injury. Neurotherapeutics 2010, 7, 22–30.
- Rhodes, J.K.; Sharkey, J.; Andrews, P.J. The temporal expression, cellular localization, and inhibition of the chemokines MIP-2 and MCP-1 after traumatic brain injury in the rat. J. Neurotrauma 2009, 26, 507–525.
- Prodjosudjadi, W.; Gerritsma, J.S.; Klar-Mohamad, N.; Gerritsen, A.F.; Brujin, J.A.; Daha, M.R.; van Es, L.A. Production and cytokine-mediated regulation of monocyte chemoattractant protein-1 by human proximal tubular epithelial cells. Kidney. Int 1995, 48, 1477–1486.
- Prodjosudjadi, W.; Gerritsma, J.S.; van Es, L.A.; Daha, M.R.; Bruijn, J.A. Monocyte chemoattractant protein-1 in normal and diseased human kidneys: An immunohistochemical analysis. Clin. Nephrol 1995, 44, 148–155.
- Block, M.L.; Zecca, L.; Hong, J.S. Microglia-mediated neurotoxicity: Uncovering the molecular mechanisms. Nat. Rev. Neurosci 2007, 8, 57–69.
- Monje, M.L.; Toda, H.; Palmer, T.D. Inflammatory blockade restores adult hippocampal neurogenesis. Science 2003, 302, 1760–1765.
- Lloyd, E.; Somera-Molina, K.; van Eldik, L.J.; Watterson, D.M.; Wainwright, M.S. Suppression of acute proinflammatory cytokine and chemokine upregulation by post-injury administration of a novel small molecule improves long-term neurologic outcome in a mouse model of traumatic brain injury. J. Neuroinflammation 2008, 5, 28.
- Brown, G.C.; Neher, J.J. Inflammatory neurodegeneration and mechanisms of microglial killing of neurons. Mol. Neurobiol 2010, 41, 242–247.
- Li, B.; Mahmood, A.; Lu, D.; Wu, H.; Xiong, Y.; Qu, C.; Chopp, M. Simvastatin attenuates microglial cells and astrocyte activation and decreases interleukin-1beta level after traumatic brain injury. Neurosurgery 2009, 65, 179–185. Discussion 185–186.
- Li, G.Z.; Zhang, Y.; Zhao, J.B.; Wu, G.J.; Su, X.F.; Hang, C.H. Expression of myeloid differentiation primary response protein 88 (Myd88) in the cerebral cortex after experimental traumatic brain injury in rats. Brain Res 2011, 1396, 96–104.
- Ling, H.P.; Li, W.; Zhou, M.L.; Tang, Y.; Chen, Z.R.; Hang, C.H. Expression of intestinal myeloid differentiation primary response protein 88 (Myd88) following experimental traumatic brain injury in a mouse model. J. Surg. Res 2013, 179, e227–e234.
- Janssens, S.; Beyaert, R. A universal role for MyD88 in TLR/IL-1R-mediated signaling. Trends Biochem. Sci 2002, 27, 474–482.
- Selkirk, J.V.; Stiefel, T.H.; Stone, I.M.; Naeve, G.S.; Foster, A.C.; Poulsen, D.J. Over-expression of the human EAAT2 glutamate transporter within neurons of mouse organotypic hippocampal slice cultures leads to increased vulnerability of CA1 pyramidal cells. Eur. J. Neurosci 2005, 21, 2291–2205.
- Noraberg, J.; Kristensen, B.W.; Zimmer, J. Markers for neuronal degeneration in organotypic slice cultures. Brain Res. Brain Res. Protoc 1999, 3, 278–290.
|Table 1. Gene Expression Analysis.|
|Fold Change||p-value||Fold Change||p-value|
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