- Open Access
Ceftriaxone attenuates hypoxic-ischemic brain injury in neonatal rats
Journal of Biomedical Science volume 18, Article number: 69 (2011)
Perinatal brain injury is the leading cause of subsequent neurological disability in both term and preterm baby. Glutamate excitotoxicity is one of the major factors involved in perinatal hypoxic-ischemic encephalopathy (HIE). Glutamate transporter GLT1, expressed mainly in mature astrocytes, is the major glutamate transporter in the brain. HIE induced excessive glutamate release which is not reuptaked by immature astrocytes may induce neuronal damage. Compounds, such as ceftriaxone, that enhance the expression of GLT1 may exert neuroprotective effect in HIE.
We used a neonatal rat model of HIE by unilateral ligation of carotid artery and subsequent exposure to 8% oxygen for 2 hrs on postnatal day 7 (P7) rats. Neonatal rats were administered three dosages of an antibiotic, ceftriaxone, 48 hrs prior to experimental HIE. Neurobehavioral tests of treated rats were assessed. Brain sections from P14 rats were examined with Nissl and immunohistochemical stain, and TUNEL assay. GLT1 protein expression was evaluated by Western blot and immunohistochemistry.
Pre-treatment with 200 mg/kg ceftriaxone significantly reduced the brain injury scores and apoptotic cells in the hippocampus, restored myelination in the external capsule of P14 rats, and improved the hypoxia-ischemia induced learning and memory deficit of P23-24 rats. GLT1 expression was observed in the cortical neurons of ceftriaxone treated rats.
These results suggest that pre-treatment of infants at risk for HIE with ceftriaxone may reduce subsequent brain injury.
Perinatal hypoxia and ischemia cause serious complications . Preterm and sick infants are at high risk for brain injury and neurodevelopmental problems . The hypoxia and ischemia induced brain injury in neonates is defined as hypoxic-ischemic encephalopathy (HIE) which is the leading cause of neurological sequelae in premature infants. The pathophysiology of HIE includes energy failure, intracellular calcium accumulation, glutamate and nitric oxide neurotoxicity, lipid peroxidation, free radical formation, and inflammation [3, 4]. As the survival rate of premature infants increased since 1990s, increased risk of significant neurodevelopmental impairment was also noted . Intervention strategies to HIE include hypothermia and erythropoietin therapy, which reduce neurological damage in animal models of HIE . In recent human studies, therapeutic hypothermia demonstrated a significant reduction of the risk of death and neurological impairment at 18 months of age . But, there was no significant difference in the severe neurodevelopmental delay in the survivors. Further studies are warranted to improve the neurological sequelae after HIE damage.
Five subtypes of glutamate transporter (excitatory amino acid transporters; EAAT 1-5) have been characterized in human. In other mammalian species, GLAST, GLT1, and EAAC1 have been found to correspond to human EAAT1, 2, and 3, respectively . The glutamate transporters are responsible for the rapid removal of glutamate from the extracellular space . GLT1 (or EAAT2), expressed mainly in the glial cells, plays a principal role in removing the excessive glutamate from the extracellular space [9, 10]. Some pathological conditions have been associated with alteration in EAAT2 expression, such as amyotrophic lateral sclerosis , Alzheimer's disease , and Huntington disease . Interventions targeting on the glutamate transporter have been conducted [14, 15]. Several antibiotics were found to upregulate significantly GLT1 expression. Ceftriaxone, a third generation cephalosporin, was one of the antibiotics found to exert neuroprotection by increasing GLT1 expression in an animal model of amyotrophic lateral sclerosis . Ceftriaxone also exhibited beneficial effects in in vitro and in vivo model of stroke [16, 17]. However, there is no report investigating the effects of ceftriaxone in neonatal HIE.
In this study, we used a rodent model of neonatal HIE with unilateral carotid artery ligation and subsequent exposure to 8% oxygen for 2 hrs on postnatal day 7 rats (the day of birth was designated as P0). The P7 neonatal rat is comparable to the 34 weeks old human fetus . Different dosages of ceftriaxone were used in these rat pups to clarify if ceftriaxone treatment could offer neuroprotection against the hypoxic-ischemic brain injury. Our results indicate that pretreatment with ceftriaxone in neonatal rats can reverse hypoxic-ischemic induced morphological and functional alterations.
This study was approved by the Institutional Animal Care and Use Committee of Tzu Chi University. Pregnant Sprague-Dawley (SD) rats were housed in individual cages with 12 hrs light/dark cycle at 22 ± 2°C with free access to food and water. After normal delivery, the size of the litter was adjusted to 10 male rat pups to eliminate the gender difference of neonatal HIE .
Neonatal rat model of hypoxic-ischemic encephalopathy and treatment design
The neonatal rat model of HIE as described previously  was followed with minor modifications. Briefly, a less than 1 cm longitudinal midline incision of the neck was performed under ether anesthesia on P7 rats. The left carotid artery was exposed and permanently ligated with 4-0 surgical silk. The surgery lasted less than 5 min. Animals with excessive bleeding were excluded. The rat pups were returned to home cage with their dam for 1 hr followed by exposure to hypoxia (92% N2 + 8% O2) for 2 hrs by placing them in an airtight chamber partially submersed in a 37°C water bath. At the end of 2 hrs hypoxia, the pups were returned to their dam again for recovery.
Ceftriaxone (Sigma Chemical Co, St. Louis, MO) was dissolved in sterile water and dosage of 50, 100 or 200 mg/kg was given intraperitoneally to three different groups of randomly assigned rats. Rats were pre-treated daily with ceftriaxone for 2 days followed by a third dose given 1 hr before ligation and hypoxia. These animals were assigned to the drug treatment group. Animals in the control or normal group were treated with the same volume of saline. Similar to previous report , the control animals received sham operation that consisted of left carotid artery exposure without ligation and then exposed to hypoxia for 2 hrs.
Brain tissue preparation
Rats were administered intraperitoneally an overdose of 10% chloral hydrate on P14, and perfused transcardially with 20 ml ice-cold saline followed by 20 ml 4% paraformaldehyde in 0.1 M phosphate buffer (pH 7.4). Brains were removed and fixed in 4% paraformaldehyde in 0.1 M phosphate buffer overnight at 4°, transferred sequentially to 15% sucrose and then 30% sucrose in 0.1 M phosphate buffer until the brains sank for cryoprotection. Brains were then embedded in O.C.T (Sakura, Torrance, CA) and stored at -80°C for immunohistochemistry and immunofluorescence studies. The brains were sectioned coronally into 10 μm slices with a cryostat (Leica CM3050, Leica Instruments, Nussloch, Germany) at -20°C to -22°C. Brain sections were mounted onto superfrost plus slides (Menzel Gläser, Braunschweig, Germany) and stored at -20°C until use.
Nissl stain and brain injury score
Coronal brain sections corresponding to plate 18 and 31 according to the rat brain atlas  were examined. The selected brain sections were stained with 0.5% cresyl violet acetate (Sigma, #C1791). We used a standard histological scoring system for evaluating the rodent model of HIE . Brain sections were scored according to: 0 = no detectable lesion, 1 = small focal area of neuronal cell loss, 2 = columnar damage in the cortex involving the layers II-IV or moderate neuronal cell loss, and 3 = cystic infarction and gliosis. Eight brain regions (hippocampus: CA1, CA2, CA3, dentate gyrus; anterior and middle regions of cortex; striatum and thalamus) were evaluated, scored, and the scores summed to yield the final scores, ranging from 0 to 24 for each animal.
Conventional procedures were followed with some modifications. Briefly, brain sections were rehydrated with decreasing ethanol concentrations (100%, 95%, 75%, 50%) for 5 min each and washed with phosphate-buffered saline (PBS). Background staining was blocked using protein block (NovoLink™ Polymer Detection System, Novocastra, Newcastle Upon Tyne, UK). After washing with PBS, sections were incubated with primary antibodies with the following dilution ratio: anti-MBP (1:200, sc-13914, Santa Cruz Biotechnology Inc., Santa Cruz, CA), and anti-EAAT 2 (1:100, #3838s, Cell Signaling Technology, Danvers, MA). Sections were treated for 2 hrs at room temperature with horseradish peroxidase-conjugated secondary antibodies (1:1000, sc-2352, Santa Cruz) for MBP (myelin basic protein), or incubated with NovoLink™ Polymer for 30 min for EAAT2. Substrate 3, 3'-diaminobenzidine (DAB, Dako, Denmark) was added for less than 5 min. Slides were examined with a computer-assisted Olympus BX51 microscope and images were taken with an Olympus DP72 microscope digital camera.
Cliff avoidance test
Cliff avoidance test was performed on P14 rats for assessing the integrity of exteroceptive input and locomotor output . Rats were placed in the edge of a platform (30 cm × 30 cm × 30 cm) with forepaws and chest extending over the edge. The latency of the rats to turn away or withdraw from the edge was recorded. If the pups fell from the platform or did not response within 60 seconds, the latency was recorded as 60 seconds.
Negative geotaxis test
Negative geotaxis test examines the sensorimotor function of neonatal rats . The P14 rat pups were placed on a 30-degree inclined plate with rough surface. Their heads were facing downward. The latency to turned 180 degree to an upward direction was recorded. The maximum duration of recording was 90 seconds.
Rotarod performance test
The rotarod test was used for evaluating the motor and coordination performance in animals . The test was performed on P21 rats with the rolling rate of 5 rpm. Rats were placed on the rod and observed for 3 min. The duration of rats holding on the rod without falling down was recorded as the day one trial. On the following day P22, rats were placed on the rod again with the rolling rate of 5 rpm. The duration of holding on the rod was recorded.
Step-down passive avoidance test
Step-down passive avoidance test was used to measure the learning and memories in animals . Rats were place in a 30 cm × 30 cm × 30 cm black acrylic chamber. The floor was made of paralleled 2 mm in diameter and 1 cm apart from each other stainless steel rods. The floor of steel rods was connected to an electric shock generator. At the center of the floor, an acrylic board (15 cm × 15 cm × 2.5 cm) was placed and served as a safe platform on the floor. In session one, each animal (P23) was placed initially on the safe acrylic board. When rats stepped down to the metal rods, they received an electrical foot shock (1sec, 0.5 mA). Rats stepped down and up on the safe board, and the latency of stepping down till the rats stayed on the board for 2 min were recorded. Session two (P24) was conducted one day later. Rats were placed on the safe board and the latency of each animal stayed on the safe board before starting to step down to the metal rods was recorded as retention time. If the animal stayed on the safe board without stepping down to the metal rods, the latency is recorded as 2 min. Following the latency of staying on safe board, the duration of stepping down till the animal again stayed on the board for 2 min was recorded. If the animal stayed still on the safe board after placing on the safe board for more than 5 min, the duration of stepping down was recorded as zero.
Conventional methodologies were used. Particulate fractions from P7 brain homogenates were solubilized with protein extraction solution (PRO-PREP™ protein extraction solution, iNtRON Biotechnology Inc., Seoul, Korea). After 30 min incubation, the sample was centrifuged at 13,000 rpm (Allegra™ 21R centrifuge, Beckman Coulter, Palo Alto, CA) at 4°C for 10 min. The supernatant consisted of the solubilized membrane portion of tissue.
Primary antibody, anti-EAAT2 (1:1000, #3838s, Cell Signaling Technology Inc., Danvers, MA), was used. Expression of α-tubulin (1:2000, sc-8035, Santa Cruz) was used as internal standard. Immunocomplexes were observed with enhanced chemiluminescent detection.
P14 post HIE rat brain tissue was evaluated with in situ apoptosis detection kit (NeuroTACS™ II; R&D Systems, Minneapolis, MN) as recommended by the manufacturer. Brain sections corresponding to plates 31 of the rat brain atlas  were chosen for evaluating the hippocampal neuronal apoptosis. Hippocampus (CA1, CA2 and CA3) ipsilateral to carotid artery ligation was examined and the number of apoptotic cells was calculated under 200X light microscope. TUNEL positive cells were counted in 3 separate fields of CA1, CA2 and CA3 areas and summated for each animal.
Image analysis and statistical analysis
Image J of NIH was used for densitometric analysis of Western blots and MBP expression density in the external capsule between ipsi- and contra-lateral sides to the carotid ligation. All data were expressed as mean ± standard error of mean (SEM). Statistical comparison between groups was carried out using one way ANOVA or Student's t test. A p value of less than 0.05 was considered statistically significant.
Ceftriaxone protected against hypoxic-ischemic brain injury in neonatal rats
Figure 1 shows the Nissl staining of coronal brain sections from P14 rat after left carotid artery ligation and subsequent exposure to 8% oxygen for 2 hrs on P7. Panels A to D show representative brain injury score increasing from 0 to 3. Brain injury score was significantly and dose-dependently attenuated by pre-treatment with 3 different dosages of ceftriaxone 48 hrs prior to hypoxia-ischemia challenge (Figure 1E). Ceftriaxone at 200 mg/kg almost completely reversed the hypoxia-ischemia induced brain damage.
Ceftriaxone attenuated hypoxic-ischemic white matter injury in neonatal rats
White matter damage was also observed in this rodent model of hypoxic-ischemic brain injury. The white matter injuries included delayed pre-oliogodendrocytes maturation, loss of MBP, white matter cell death, and gliosis . Figure 2 shows the result of MBP immunostaining from P14 rat brain. The inset in panel A shows the Nissl stain of external capsule region examined for MBP staining following ipsilateral ligation, and the enlarged photographs of MBP staining were shown from panel B to F. Large extent of MBP loss was observed in the P14 rat brain ipsilateral to the carotid ligation (panel C). Pre-treatment with ceftriaxone attenuated the MBP loss of P14 rats in a dose-dependent manner (panel D-F) with the highest ceftriaxone dose (200 mg/kg) almost completely rescued the white matter injury (panel F vs. panel B). The relative density of MBP in the ischemic-hypoxic side was calculated as the ratio of the MBP staining level in the ipsilateral side divided by that of the contralateral side of the same tissue section. Figure 2G shows quantitatively that pre-treatment with ceftriaxone significantly attenuated the MBP loss in P14 rats.
Ceftriaxone reduced hypoxic-ischemic cell damage in the hippocampus
TUNEL assay was performed in coronal brain slices of P14 rats. Hippocampal cell loss was noted after HIE (Figure 3B). The HIE induced hippocampal cell damage included both necrosis and apoptotic cell damage . TUNEL assay was evaluated under 200X light microscope in 3 fields each of hippocampal CA1, CA2 and CA3 area, which were summed for each animal. Figure 3C demonstrates that pre-treatment with ceftriaxone reduced the TUNEL positive cells in hippocampal area in a dose-dependent manner with statistical significance found for 100 and 200 mg/kg dosages.
Ceftriaxone improved learning and memory performance in rats exposed to HIE
Based on the above morphological observations that pre-treatment with 3 dosages of ceftriaxone reversed the brain damage caused by ischemic-hypoxic insult, this treatment protocol was followed to evaluate its effects on several behavioral tests reflecting motor, learning, and memory functions. Figure 4 shows that ceftriaxone was without effect on cliff avoidance on P14 (Figure 4A), negative geotaxis on P14 (Figure 4B), rotarod test on P21 and P22 (Figure 4C and 4D) or the first session of step-down passive avoidance on P23 rats (Figure 4E). However, in session two trial of step-down passive avoidance (P24 rats), pre-treatment with ceftriaxone significantly reduced the duration of foot shock (Figure 4G).
Ceftriaxone did not alter GLT1 protein expression in rat brain homogenate
After pre-treatment with different dosages (50, 100 or 200 mg/kg) of ceftriaxone or saline, the membrane portion of P7 rat brain lysate was used for measuring the expression of GLT1 protein. A representative immunoblotting is demonstrated in Figure 5A. The expression of GLT1 was not altered by pre-treatment with ceftriaxone (Figure 5B).
Ceftriaxone induced the expression of GLT1 in the cortical neurons of neonatal rat brain
We further examined if there was regional difference in the expression of GLT1 protein that could explain at least partly the neuroprotection mediated by ceftriaxone administration. Pre-treatment with 3 dosages of 200 mg/kg ceftriaxone was followed since it significantly reduced the histological and behavioral deficits. Immunohistochemial study with anti-EAAT2 antibody was carried out in brain slides to reveal the regional difference of GLT1 expression between ceftriaxone treated and saline group. Figure 6 demonstrates immunohistochemical staining of GLT1 in saline and ceftriaxone treatment groups. Each panel showed different regions of brain section (A,E: corpus callosum; B,F: cerebral cortex; C,G: hippocampus and D,H: striatum). Figure 6B shows that cerebral cortex from control P7 brain expressed little GLT1 protein. Figure 6F demonstrates that ceftriaxone pre-treatment, however, induced GLT1 protein expression in this area. After counterstained with Nissl stain, the GLT1 protein was found to be expressed in cortical neuronal cells (Figure 7B arrow). Image J was used to analyze the percentage of EAAT2 (GLT1) immunoreactive area of P7 rat cortex under 400X light microscope in saline and ceftriaxone pre-treated groups. Ceftriaxone pre-treatment significantly induced GLT1 protein expression in cortical neuron (Figure 7, P = 0.031).
In this study, we showed that neonatal ischemic-hypoxic brain damage can be attenuated by pre-treatment with ceftriaxone. Our data are consistent with similar approaches reported in the literature . However, the present study is the first to investigate the utility of ceftriaxone in a neonatal rat model of ischemic-hypoxic brain damage. Since ceftriaxone is a FDA approved drug and exhibits relatively few adverse effects, the potential clinical benefit of ceftriaxone and related antibiotics in human neonatal HIE warrants further investigation.
For the pathophysiology of neonatal HIE, glutamate neurotoxicity remains an important issue in subsequent calcium influx, free radical formation, necrosis, and apoptosis . During brain development, glutamate plays an important role in oligodendrocyte maturation and myelination, but can lead to detrimental consequences from excessive release after HIE [29, 30]. The blockade of glutamate receptor by antagonists improved white matter injury [25, 31, 32]. Experimental drugs that block NMDA-type glutamate receptor could protect the brain from severe hypoxic-ischemic insults if given before or shortly after the insult, but were ineffective if administration was delayed for more than several hrs [33–36]. These data suggest that downstream events quickly become self-sustaining after neonatal HIE .
An alternative approach to reduce glutamate neurotoxicity is to augment the glutamate reuptake. GLT1 glutamate transporter plays a major role in the reuptake of extracellular glutamate and is expressed mainly in mature astrocytes although minor expression has been found in neurons, microglias, and oligodendrocytes. But, astrocytes in immature human or rat brain do not express EAAT2 or GLT1 [37–40]. GLT1 expression is very low in the early postnatal period and reaches adult levels in hippocampus at 3-4 weeks old in rat brain tissue and hippocampus [16, 40, 41]. The roles of GLT1 in immature brain remained unclear. In human premature infant, expression of EAAT2 was observed in pre-oligodendrocytes which might be the cause of white matter vulnerability to HIE injury. Upregulation of EAAT2 (or GLT1) was observed in reactive astrocytes and macrophages in the area of periventricular leukomalacia (PVL) [38, 39]. In a rat model of neonatal HIE, altered expression of glutamate transporter and decreased GLT1 expression were observed in the area of ischemic core . Prolonged hypoxia reduced GLT1 expression in astrocytes resulting in the accumulation of extracellular glutamate . Furthermore, functional reversal of glutamate transporter in glial cells occurred during hypoxia and ischemia also contributed to the excessive extracellular glutamate toxicity . In this study, we used a FDA approved beta-lactam antibiotic, ceftriaxone. It has been found that a 5-7 days course of ceftriaxone increased GLT1 protein expression in organotypic spinal cord slice cultures, neuronal culture under glucose-oxygen deprivation, human fetal astrocytes culture, and in the rat brain . These results have been confirmed in hippocampal slice culture and in rat brains [27, 45]. In contrast, upregulation of GLT1 expression by ceftriaxone treatment was not observed in a rat stroke model, in organotypic hippocampal slices or in a mouse model of multiple sclerosis [16, 17, 46]. Ceftriaxone may offer neuroprotection via other mechanisms, such as increased GLT1 transporter activity, stimulation of neurotrophin release or reduction of T cell activation by modulation of cellular antigen-presentation [17, 46].
In our studies, GLT1 protein expression in the whole brain lysate of P7 rat did not change after ceftriaxone treatment. But, immunohistochemical study showed that pre-treatment with ceftriaxone induced GLT1 protein expression in cerebral cortex of P7 rat. GLT1 expressed in neurons of the brain is observed during early stages of development and is present during axonal growth, which disappears on maturation . The role of GLT1 in immature neuron remains to be investigated. In mature rat brain, neuronal expression of GLT1 protein and mRNA had also been found and might play a role in the pathophysiology of excitotoxicity [48–50]. But, in our study, pretreatment with ceftriaxone increased expression of GLT1 in the cerebral cortical neuron of P7 rat. Neuronal expression of GLT1 protein was confirmed after counterstained with Nissl stain. The presence of GLT1 in neurons might enhance glutamate uptake after hypoxic-ischemic injury. However, other mechanisms, such as enhanced GLT activity and/or anti-inflammatory effect of ceftriaxone, cannot be excluded.
Several behavioral paradigms mimic the childhood behavior in human were examined in the young rat. No difference was detected in the primitive reflexes (cliff avoidance and negative geotaxis test) and motor function test among treatment, vehicle, and sham groups. On the other hand, significant improvement in step-down passive avoidance test was found after ceftriaxone treatment. The difference of behavior between HIE group and normal control group included long-lasting sensorimotor and locomotor deficits . But, unlike human, rats exposed to HIE injury did not exhibit gross motor function deficit in some studies although some permanent deficit has also been observed . This may be due to a higher degree of plasticity of neonatal rat brain compared with that of human brain. Step-down passive avoidance reflects learning and memory function. In our studies, ceftriaxone rescued hippocampal cells from apoptosis which may contribute to improved step-down passive avoidance results.
Pre-treatment with agents prior to the appearance of pathological changes remains debatable in clinical application. But, in premature baby, pre-treatment may be acceptable because pregnant mother usually receives tocolysis for prevention of preterm birth. In addition, ceftriaxone exhibits antibiotic effect which could eliminate the pathogens if maternal chorioamnionitis is diagnosed  since ceftriaxone effectively crosses the placenta .
In conclusion, pre-treatment with ceftriaxone for 48 hrs prior to hypoxic-ischemic brain injury in neonatal rats reduced brain injury score, improved myelination, decreased hippocampal apoptotic cell death, and restored learning and memory deficit. Induction of GLT1 protein expression in cerebral cortex after ceftriaxone pre-treatment was observed in P7 rats, which might partially explain the neuroprotective effect of ceftriaxone. Ceftriaxone may be an effective therapeutic agent for the treatment of neonatal HIE.
van Bel F, Groenendaal F: Long-term pharmacologic neuroprotection after birth asphyxia: where do we stand?. Neonatology. 2008, 94: 203-210. 10.1159/000143723.
van Handel M, Swaab H, de Vries LS, Jongmans MJ: Long-term cognitive and behavioral consequences of neonatal encephalopathy following perinatal asphyxia: a review. Eur J Pediatr. 2007, 166: 645-654. 10.1007/s00431-007-0437-8.
Perlman JM: Intervention strategies for neonatal hypoxic-ischemic cerebral injury. Clin Ther. 2006, 28: 1353-1365. 10.1016/j.clinthera.2006.09.005.
Vannucci RC, Connor JR, Mauger DT, Palmer C, Smith MB, Towfighi J, Vannucci SJ: Rat model of perinatal hypoxic-ischemic brain damage. J Neurosci Res. 1999, 55: 158-163. 10.1002/(SICI)1097-4547(19990115)55:2<158::AID-JNR3>3.0.CO;2-1.
Wilson-Costello D, Friedman H, Minich N, Fanaroff AA, Hack M: Improved survival rates with increased neurodevelopmental disability for extremely low birth weight infants in the 1990s. Pediatrics. 2005, 115: 997-1003. 10.1542/peds.2004-0221.
Edwards AD, Brocklehurst P, Gunn AJ, Halliday H, Juszczak E, Levene M, Strohm B, Thoresen M, Whitelaw A, Azzopardi D: Neurological outcomes at 18 months of age after moderate hypothermia for perinatal hypoxic ischaemic encephalopathy: synthesis and meta-analysis of trial data. BMJ. 2010, 340: c363-369. 10.1136/bmj.c363.
Arriza JL, Fairman WA, Wadiche JI, Murdoch GH, Kavanaugh MP, Amara SG: Functional comparisons of three glutamate transporter subtypes cloned from human motor cortex. J Neurosci. 1994, 14: 5559-5569.
Shigeri Y, Seal RP, Shimamoto K: Molecular pharmacology of glutamate transporters, EAATs and VGLUTs. Brain Res Brain Res Rev. 2004, 45: 250-265.
Rao VL, Dogan A, Todd KG, Bowen KK, Kim BT, Rothstein JD, Dempsey RJ: Antisense knockdown of the glial glutamate transporter GLT-1, but not the neuronal glutamate transporter EAAC1, exacerbates transient focal cerebral ischemia-induced neuronal damage in rat brain. J Neurosci. 2001, 1: 1876-1883.
Rothstein JD, Dykes-Hoberg M, Pardo CA, Bristol LA, Jin L, Kuncl RW, Kanai Y, Hediger MA, Wang Y, Schielke JP, Welty DF: Knockout of glutamate transporters reveals a major role for astroglial transport in excitotoxicity and clearance of glutamate. Neuron. 1996, 16: 675-686. 10.1016/S0896-6273(00)80086-0.
Rothstein JD, Van Kammen M, Levey AI, Martin LJ, Kuncl RW: Selective loss of glial glutamate transporter GLT-1 in amyotrophic lateral sclerosis. Ann Neurol. 1995, 38: 73-84. 10.1002/ana.410380114.
Li S, Mallory M, Alford M, Tanaka S, Masliah E: Glutamate transporter alterations in Alzheimer disease are possibly associated with abnormal APP expression. J Neuropathol Exp Neurol. 1997, 56: 901-911. 10.1097/00005072-199708000-00008.
Arzberger T, Krampfl K, Leimgruber S, Weindl A: Changes of NMDA receptor subunit (NR1, NR2B) and glutamate transporter (GLT1) mRNA expression in Huntington's disease--an in situ hybridization study. J Neuropathol Exp Neurol. 1997, 56: 440-454. 10.1097/00005072-199704000-00013.
Rothstein JD, Patel S, Regan MR, Haenggeli C, Huang YH, Bergles DE, Jin L, Dykes Hoberg M, Vidensky S, Chung DS, Toan SV, Bruijn LI, Su ZZ, Gupta P, Fisher PB: Beta-lactam antibiotics offer neuroprotection by increasing glutamate transporter expression. Nature. 2005, 433: 73-77. 10.1038/nature03180.
Sheldon AL, Robinson MB: The role of glutamate transporters in neurodegenerative diseases and potential opportunities for intervention. Neurochem Int. 2007, 51: 333-355. 10.1016/j.neuint.2007.03.012.
Lipski J, Wan CK, Bai JZ, Pi R, Li D, Donnelly D: Neuroprotective potential of ceftriaxone in in vitro models of stroke. Neuroscience. 2007, 146: 617-629. 10.1016/j.neuroscience.2007.02.003.
Thone-Reineke C, Neumann C, Namsolleck P, Schmerbach K, Krikov M, Schefe JH, Lucht K, Hortnagl H, Godes M, Muller S, Rumschussel K, Funke-Kaiser H, Villringer A, Steckelings UM, Unger T: The beta-lactam antibiotic, ceftriaxone, dramatically improves survival, increases glutamate uptake and induces neurotrophins in stroke. J Hypertens. 2008, 26: 2426-2435. 10.1097/HJH.0b013e328313e403.
Hagberg H, Bona E, Gilland E, Puka-Sundvall M: Hypoxia-ischaemia model in the 7-day-old rat: possibilities and shortcomings. Acta Paediatr. 1997, 422 (Suppl): 85-88.
Nunez J, Yang Z, Jiang Y, Grandys T, Mark I, Levison SW: 17beta-estradiol protects the neonatal brain from hypoxia-ischemia. Exp Neurol. 2007, 208: 269-276. 10.1016/j.expneurol.2007.08.020.
Rice JE, Vannucci RC, Brierley JB: The influence of immaturity on hypoxic-ischemic brain damage in the rat. Ann Neurol. 1981, 9: 131-141. 10.1002/ana.410090206.
George Paxinos CW: The rat brain in stereotaxis of coordinates. 1986, Orlando, Florida, Academic press
Sheldon RA, Sedik C, Ferriero DM: Strain-related brain injury in neonatal mice subjected to hypoxia-ischemia. Brain Res. 1998, 810: 114-122. 10.1016/S0006-8993(98)00892-0.
Fan LW, Lin S, Pang Y, Lei M, Zhang F, Rhodes PG, Cai Z: Hypoxia-ischemia induced neurological dysfunction and brain injury in the neonatal rat. Behav Brain Res. 2005, 165: 80-90. 10.1016/j.bbr.2005.06.033.
Lubics A, Reglodi D, Tamas A, Kiss P, Szalai M, Szalontay L, Lengvari I: Neurological reflexes and early motor behavior in rats subjected to neonatal hypoxic-ischemic injury. Behav Brain Res. 2005, 157: 157-165. 10.1016/j.bbr.2004.06.019.
Follett PL, Deng W, Dai W, Talos DM, Massillon LJ, Rosenberg PA, Volpe JJ, Jensen FE: Glutamate receptor-mediated oligodendrocyte toxicity in periventricular leukomalacia: a protective role for topiramate. J Neurosci. 2004, 24: 4412-4420. 10.1523/JNEUROSCI.0477-04.2004.
Scott RJ, Hegyi L: Cell death in perinatal hypoxic-ischaemic brain injury. Neuropathol Appl Neurobiol. 1997, 23: 307-314. 10.1111/j.1365-2990.1997.tb01300.x.
Chu K, Lee ST, Sinn DI, Ko SY, Kim EH, Kim JM, Kim SJ, Park DK, Jung KH, Song EC, Lee SK, Kim M, Roh JK: Pharmacological induction of ischemic tolerance by glutamate transporter-1 (EAAT2) upregulation. Stroke. 2007, 38: 177-182.
Johnston MV, Trescher WH, Ishida A, Nakajima W: Neurobiology of hypoxic-ischemic injury in the developing brain. Pediatr Res. 2001, 49: 735-741. 10.1203/00006450-200106000-00003.
Micu I, Jiang Q, Coderre E, Ridsdale A, Zhang L, Woulfe J, Yin X, Trapp BD, McRory JE, Rehak R, Zamponi GW, Wang W, Stys PK: NMDA receptors mediate calcium accumulation in myelin during chemical ischaemia. Nature. 2006, 439: 988-992.
Yuan X, Eisen AM, McBain CJ, Gallo V: A role for glutamate and its receptors in the regulation of oligodendrocyte development in cerebellar tissue slices. Development. 1998, 25: 2901-2914.
Follett PL, Rosenberg PA, Volpe JJ, Jensen FE: NBQX attenuates excitotoxic injury in developing white matter. J Neurosci. 2000, 20: 9235-9241.
Manning SM, Talos DM, Zhou C, Selip DB, Park HK, Park CJ, Volpe JJ, Jensen FE: NMDA receptor blockade with memantine attenuates white matter injury in a rat model of periventricular leukomalacia. J Neurosci. 2008, 28: 6670-6678. 10.1523/JNEUROSCI.1702-08.2008.
Andine P, Lehmann A, Ellren K, Wennberg E, Kjellmer I, Nielsen T, Hagberg H: The excitatory amino acid antagonist kynurenic acid administered after hypoxic-ischemia in neonatal rats offers neuroprotection. Neurosci Lett. 1988, 90: 208-212. 10.1016/0304-3940(88)90813-0.
Ford LM, Sanberg PR, Norman AB, Fogelson MH: MK-801 prevents hippocampal neurodegeneration in neonatal hypoxic-ischemic rats. Arch Neurol. 1989, 46: 1090-1096.
Hagberg H, Gilland E, Diemer NH, Andine P: Hypoxia-ischemia in the neonatal rat brain: histopathology after post-treatment with NMDA and non-NMDA receptor antagonists. Biol Neonate. 1994, 66: 205-213. 10.1159/000244109.
McDonald JW, Silverstein FS, Johnston MV: MK-801 protects the neonatal brain from hypoxic-ischemic damage. Eur J Pharmacol. 1987, 140: 359-361. 10.1016/0014-2999(87)90295-0.
Bar-Peled O, Ben-Hur H, Biegon A, Groner Y, Dewhurst S, Furuta A, Rothstein JD: Distribution of glutamate transporter subtypes during human brain development. J Neurochem. 1997, 69: 2571-2580.
Desilva TM, Billiards SS, Borenstein NS, Trachtenberg FL, Volpe JJ, Kinney HC, Rosenberg PA: Glutamate transporter EAAT2 expression is up-regulated in reactive astrocytes in human periventricular leukomalacia. J Comp Neurol. 2008, 508: 238-248. 10.1002/cne.21667.
Desilva TM, Kinney HC, Borenstein NS, Trachtenberg FL, Irwin N, Volpe JJ, Rosenberg PA: The glutamate transporter EAAT2 is transiently expressed in developing human cerebral white matter. J Comp Neurol. 2007, 501: 879-890. 10.1002/cne.21289.
Furuta A, Rothstein JD, Martin LJ: Glutamate transporter protein subtypes are expressed differentially during rat CNS development. J Neurosci. 1997, 17: 8363-8375.
Kugler P, Schleyer V: Developmental expression of glutamate transporters and glutamate dehydrogenase in astrocytes of the postnatal rat hippocampus. Hippocampus. 2004, 14: 975-985. 10.1002/hipo.20015.
Fukamachi S, Furuta A, Ikeda T, Ikenoue T, Kaneoka T, Rothstein JD, Iwaki T: Altered expressions of glutamate transporter subtypes in rat model of neonatal cerebral hypoxia-ischemia. Brain Res Dev Brain Res. 2001, 132: 131-139.
Dallas M, Boycott HE, Atkinson L, Miller A, Boyle JP, Pearson HA, Peers C: Hypoxia suppresses glutamate transport in astrocytes. J Neurosci. 2007, 27: 3946-3955. 10.1523/JNEUROSCI.5030-06.2007.
Nicholls D, Attwell D: The release and uptake of excitatory amino acids. Trends Pharmacol Sci. 1990, 11: 462-468. 10.1016/0165-6147(90)90129-V.
Ouyang YB, Voloboueva LA, Xu LJ, Giffard RG: Selective dysfunction of hippocampal CA1 astrocytes contributes to delayed neuronal damage after transient forebrain ischemia. J Neurosci. 2007, 27: 4253-4260. 10.1523/JNEUROSCI.0211-07.2007.
Melzer N, Meuth SG, Torres-Salazar D, Bittner S, Zozulya AL, Weidenfeller C, Kotsiari A, Stangel M, Fahlke C, Wiendl H: A beta-lactam antibiotic dampens excitotoxic inflammatory CNS damage in a mouse model of multiple sclerosis. PLoS One. 2008, 3: e3149-3160. 10.1371/journal.pone.0003149.
Danbolt NC: Glutamate uptake. Prog Neurobiol. 2001, 65: 1-105. 10.1016/S0301-0082(00)00067-8.
Chen W, Aoki C, Mahadomrongkul V, Gruber CE, Wang GJ, Blitzblau R, Irwin N, Rosenberg PA: Expression of a variant form of the glutamate transporter GLT1 in neuronal cultures and in neurons and astrocytes in the rat brain. J Neurosci. 2002, 22: 2142-2152.
Furness DN, Dehnes Y, Akhtar AQ, Rossi DJ, Hamann M, Grutle NJ, Gundersen V, Holmseth S, Lehre KP, Ullensvang K, Wojewodzic M, Zhou Y, Attwell D, Danbolt NC: A quantitative assessment of glutamate uptake into hippocampal synaptic terminals and astrocytes: new insights into a neuronal role for excitatory amino acid transporter 2 (EAAT2). Neuroscience. 2008, 157: 80-94. 10.1016/j.neuroscience.2008.08.043.
Holmseth S, Scott HA, Real K, Lehre KP, Leergaard TB, Bjaalie JG, Danbolt NC: The concentrations and distributions of three C-terminal variants of the GLT1 (EAAT2; slc1a2) glutamate transporter protein in rat brain tissue suggest differential regulation. Neuroscience. 2009, 162: 1055-1071. 10.1016/j.neuroscience.2009.03.048.
Jansen EM, Low WC: Long-term effects of neonatal ischemic-hypoxic brain injury on sensorimotor and locomotor tasks in rats. Behav Brain Res. 1996, 78: 189-194. 10.1016/0166-4328(95)00248-0.
Duff P: Antibiotic selection in obstetric patients. Infect Dis Clin North Am. 1997, 11: 1-12. 10.1016/S0891-5520(05)70338-X.
Bourget P, Quinquis V, Fernandez H, Frydman R: Clinical pharmacokinetics of ceftriaxone during the third trimester of pregnancy and study of its transplacental passage in two patients. Pathol Biol (Paris). 1993, 41: 242-248.
This study was partially supported by a grant (TCRD98-21) from Buddhist Tzu Chi General Hospital, Hualien, Taiwan.
The authors declare that they have no competing interests.
PCL and YTH carried out animal study, participated in the immunohistochemistry, performed the statistical analysis, and drafted the manuscript. CCW carried out the West blot. PJW and THC conceived the study, participated in its design and coordination, and helped to draft the manuscript. All authors read and approved the final manuscript.
Authors’ original submitted files for images
Below are the links to the authors’ original submitted files for images.
Rights and permissions
Open Access This article is published under license to BioMed Central Ltd. This is an Open Access article is distributed under the terms of the Creative Commons Attribution License ( https://creativecommons.org/licenses/by/2.0 ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
About this article
Cite this article
Lai, P.C., Huang, Y.T., Wu, C.C. et al. Ceftriaxone attenuates hypoxic-ischemic brain injury in neonatal rats. J Biomed Sci 18, 69 (2011). https://doi.org/10.1186/1423-0127-18-69
- β-lactam antibiotics
- hypoxic-ischemic injury
- neonatal rat