The PGE2 EP2 receptor and its selective activation are beneficial against ischemic stroke
- Muzamil Ahmad†1,
- Sofiyan Saleem†1,
- Zahoor Shah1,
- Takayuki Maruyama2,
- Shuh Narumiya3 and
- Sylvain Doré1, 4Email author
© Ahmad et al; licensee BioMed Central Ltd. 2010
Received: 15 March 2010
Accepted: 8 July 2010
Published: 8 July 2010
The prostaglandin E2 EP2 receptor has been shown to be important in dictating outcomes in various neuroinflammatory disorders. Here, we investigated the importance of the EP2 receptor in short- and long-term ischemic outcomes by subjecting wildtype (WT) and EP2 knockout (EP2-/-) mice to two distinct and complementary stroke models [transient and permanent middle cerebral artery occlusion (tMCAO and pMCAO)] and by using the EP2 receptor agonist ONO-AE1-259-01.
First, WT and EP2-/- mice were subjected to 90-min tMCAO with a monofilament followed by 4-day reperfusion. Second, WT mice were infused intracerebroventricularly with vehicle or ONO-AE1-259-01 45-50 min before being subjected to tMCAO. Finally, WT and EP2-/- mice were subjected to pMCAO and allowed to survive for an extended period of 7 days.
Infarct volumes in EP2-/- mice were 55.0 ± 9.1% larger after tMCAO and 33.3 ± 8.6% larger after pMCAO than those in WT mice. Neurobehavioral deficits also were significantly greater in the EP2-/- mice. These results suggest that EP2 is beneficial and that activation is sustained for days after the stroke. We also found that pharmacologic activation of EP2 with 1.0- and 2.0-nmol doses of ONO-AE1-259-01 was sufficient to significantly reduce the infarct volume in WT mice compared with that in vehicle-treated controls (20.1 ± 3.9% vs. 37.1 ± 4.6%). This reduction correlated with improved neurologic scores. No significant effect on physiologic parameters was observed.
Together, our results reveal that pharmacologic stimulation of the EP2 receptor has an important beneficial role in cerebral ischemia and might be considered as an adjunct therapy for ischemic stroke.
Prostaglandin E2 (PGE2), formed from arachidonic acid by the action of cyclooxygenases and PGE2 synthases, was previously considered to be a pro-inflammatory prostaglandin, but it may have a much more complex role. PGE2 executes its functions by binding mainly to four membrane-bound G-protein-coupled receptors known as E-prostanoid (EP) 1, 2, 3, and 4. These EP receptors have varied effects on cyclic adenosine monophosphate (cAMP) production, phosphoinositol turnover, and intracellular calcium level regulation . The EP1 receptor increases levels of intracellular calcium . The EP3 receptor, which has several isoforms and consequently couples to several different G-proteins, elicits varied signaling pathways that lead to changes in cAMP levels, calcium mobilization, and activation of phospholipase C . The EP2 and EP4 receptors, which increase the intracellular levels of cAMP, work via a G-protein-coupled mechanism that stimulates adenylyl cyclase [4–6].
In mice, the EP2 receptor has been reported to be highly expressed in cerebral cortex, striatum, and hippocampus [7, 8]. Genetic knockout of this receptor significantly increases lesion volume at the 24-h time point in mice subjected to ischemic paradigms, with no apparent change in behavior [9, 10]. It is important to understand the etiopathology of stroke damage and especially its inflammatory cascade over time. Therefore, our goal was to determine whether the anatomical protective effects of EP2 activation are sustained over time (and are not only transient or delayed) and whether such changes correlate with neurologic improvements.
Furthermore, even though previous studies that used EP2 knockout (EP2-/-) mice reported that the presence of EP2 is beneficial in ischemic stroke in vivo, none has demonstrated that EP2 stimulation indeed limits infarct damage. To test this paradigm, we investigated whether the highly selective EP2 agonist ONO-AE1-259-01 could reduce ischemic brain damage in C57BL/6 WT mice. ONO-AE1-259-01 has no detectable affinity to any other prostaglandin receptor  and binds with higher affinity to the EP2 receptor (Ki = 3 nM) than does PGE1, 16,16-dimethyl-PGE2, 11-deoxy-PGE1, butaprost, or AH-6809 (Ki = 10, 17, 45, 110, and 350 nM, respectively) [5, 6, 12].
Materials and methods
Animals and Treatments
These studies were carried out in male C57BL/6 mice (25 to 30 g) purchased from Charles River Laboratories, Inc (Wilmington, MA). The EP2-/- mouse colony was maintained in the Johns Hopkins animal facility. Animal protocols for these studies were approved by the Johns Hopkins University Animal Care and Use Committee. The animals were allowed free access to water and food before and after surgery. ONO-AE1-259-01 [(16S)-9-deoxy-9beta-chloro-15-deoxy-16-hydroxy-17,17-trimethylene-19,20-didehydro-PGE2 sodium salt] was provided by Ono Pharmaceutical Co. Ltd.
Cerebral Vessel Diameter and Anatomy
To determine the large cerebral vessel gross anatomy in WT and EP2-/- mice, three naïve mice of each genotype were anesthetized deeply and perfused via the heart left ventricle with 5 mL of ice-cold saline followed by 1 mL of black latex paint. Then the mice were decapitated and their brains removed with the circle of Willis intact. The brains were placed in 10% formalin for 24 h before examination with MetaVue software (Meta Imaging Series Software, Downingtown, PA).
Experimental Design and Drug Injection
In this study, three sets of experiments were performed. In the first experiment, WT (n = 9) and EP2-/- (n = 14) mice were subjected to 90 min of transient middle cerebral artery occlusion (tMCAO) and 96 h of reperfusion. In the second experiment, WT mice (n = 9/group) were given intracerebroventricular injections of ONO-AE1-259-01 (0.5, 1.0, 2.0 nmol) or vehicle (water) 45-50 min before tMCAO. Briefly, mice were anesthetized and mounted on a stereotaxic frame, the skull was exposed under aseptic conditions, and a hole was drilled according to the coordinates: anteroposterior, 0.5 mm; lateral, 1.0 mm from the bregma; and ventral, 2.5 mm relative to the dura. ONO-AE1-259-01 or vehicle was injected in a volume of 0.2 μL into the right lateral ventricle; the needle was left in place for 10 min before being slowly retracted. Finally, the hole was blocked, and the skin overlying the skull was sutured. Mice were then prepared for tMCAO surgery as described below. Physiologic studies were carried out in a separate cohort of correspondingly treated EP2-/- and ONO-AE1-259-01-treated mice. In the third experiment, WT (n = 8) and EP2-/- (n = 7) mice were subjected to distal permanent middle cerebral artery occlusion (pMCAO).
Transient Focal Cerebral Ischemia (tMCAO) and Reperfusion
Transient focal cerebral ischemia was induced by occlusion of the middle cerebral artery (MCA) with an intraluminal filament, as described previously . Each mouse was maintained with continuous-flow 1.0-1.5% halothane (after induction with 3.0% halothane) in oxygen-enriched air via a nose cone. The core body temperature (rectal) was maintained at 37.0 ± 0.5°C by a heating pad. No differences in rectal temperature between genotypes were noted before, during, or immediately after ischemia. Relative cerebral blood flow (CBF) was measured by laser-Doppler flowmetry (Moor Instruments, Devon, England) with a flexible fiberoptic probe affixed to the skull over the parietal cortex supplied by the MCA (2 mm posterior and 6 mm lateral to the bregma). Under aseptic conditions, the neck and carotid bifurcation were dissected, and the common carotid artery was temporarily ligated. A 7-0 Ethilon nylon monofilament (Ethicon, Inc., Somerville, NJ) coated with flexible silicone (Cutter Sil light universal hardener, Heraeus Kulzer GmbH, Hanau, Germany) was inserted to occlude the MCA. The filament was advanced through an incision in the external carotid artery stump, through the internal carotid artery to the origin of the MCA; successful occlusion was documented by a decrease in laser-Doppler signal of at least 80%. The filament was left in position for 90 min. During occlusion, the neck was closed with sutures, anesthesia was discontinued, and the animals were transferred to a temperature-controlled chamber to maintain the body temperature at 37.0 ± 0.5°C. At 90 min of occlusion, the mouse was briefly re-anesthetized with halothane, and reperfusion was achieved by slowly withdrawing the filament. After its neck was sutured, the mouse was again placed in the temperature-controlled chamber for 2 h and then returned to its home cage for 4 days. The 4-day time point was selected because it allows maximal survival following the tMCAO.
Permanent Distal Middle Cerebral Artery Occlusion (pMCAO)
Permanent MCAO studies were carried out by the method of Majid et al. [14, 15] with minor modifications. This permanent distal ischemic protocol was selected because it is highly reproducible and it affects mainly the cortical region, whereas the transient ischemic model causes striatal damage that then extends to the cortical region. The permanent model also allows the study of more distal time points (as described below). Briefly, mice were anesthetized with halothane, and a 1.0-cm vertical skin incision was made between the right eye and ear. The temporal muscle was moved aside to expose the temporal bone. Under a surgical microscope, a 2.0-mm burr hole was drilled over the MCA, transparently visible through the temporal bone. The distal part of the MCA was occluded with a bipolar coagulator, and complete interruption of blood flow at the occlusion site was confirmed by severance of the occlusion site of the MCA. Core body temperature was maintained between 36.5 and 37.5°C during and after the procedure. Animals not circling toward the paretic side after the onset of ischemia and those that developed subarachnoid hemorrhage were eliminated from the study. The successful occlusion was confirmed by placing the laser-Doppler probe above the temporal ridge to establish that blood flow into the region was stopped. At 7 days, mice were euthanized and the brains sectioned. The 7-day time point was selected rather than the 24-h time point because it allows time for extended permanent ischemic damage and can be achieved with 100% survival.
Assessment of Neurologic Function and Physiologic Parameters
Mice subjected to tMCAO were evaluated for neurologic deficit via a 5-point scale after 96 h of reperfusion. The scores were recorded as: 0, no deficit; 1, forelimb weakness and torso turning to the ipsilateral side when held by the tail; 2, circling to the affected side; 3, unable to bear weight on the affected side; and 4, no spontaneous locomotor activity, according to the protocol used in our previous studies [13, 15–17, 19]. In a separate cohort, physiologic parameters were measured before occlusion, during occlusion, and during reperfusion. A catheter was inserted into the femoral artery and attached to an automated blood pressure monitor to measure mean arterial blood pressure (MABP). At regular intervals, blood samples were collected through the catheter for analysis of pH, PaO2, and PaCO2.
Mice subjected to pMCAO were tested for neurologic deficits 7 days after occlusion by an experimenter blinded to the mouse genotype according to a 28-point scoring system [15, 20]. Since the pMCAO lesion is distinct from that which occurs with the tMCAO model, we have optimized a neurobehavioral test that enables us to look for subtle and reproducible differences between groups. The tests included assessments of body symmetry, gait, climbing, circling behavior, front limb symmetry, compulsory circling, and whisker response. Each test was graded from 0 to 4, establishing a maximum deficit score of 28. Immediately after the testing, the mice were sacrificed for infarct volume analysis.
Quantification of Infarct Volumes
After tMCAO and pMCAO, mice were deeply anesthetized, and brains were harvested and cooled in a deep freezer. Five coronal sections of 2-mm thickness were cut and then incubated in 2% 2,3,5-triphenyl-tetrazolium chloride (TTC) in saline for 20 min at 37°C. The area of infarct, which remains white, was measured on the rostral and caudal surfaces of all five slices and numerically integrated across the thickness of the slice to obtain an estimate of infarct volume (SigmaScan Pro, SPSS Inc. Port Richmond, CA). Infarct volume was converted by multiplying the measured infarct volume by the ratio of the contralateral structure to the ipsilateral structure .
Data, expressed as mean ± SEM, were analyzed by ANOVA and when appropriate, Newman-Keuls multiple range test. Statistical significance was set at P < 0.05.
Comparison of Cerebrovascular Anatomy in WT and EP2-/- Mice
Effect of EP2 Receptor Genetic Deletion on Monitored Physiologic Parameters of Mice Subjected to tMCAO
Physiologic Parameters in WT and EP2-/- Mice
EP2 -/- Mice
1 h MCAO
1 h Reperfusion
1 h MCAO
1 h Reperfusion
7.37 ± 0.02
7.34 ± 0.02
7.35 ± 0.01
7.32 ± 0.01
7.33 ± 0.01
7.33 ± 0.01
38.2 ± 1.4
40.0 ± 1.5
38.7 ± 1.5
42.5 ± 1.3
41.2 ± 2.2
41.4 ± 1.0
113 ± 6
131 ± 3
121 ± 9
127 ± 3
124 ± 5
120 ± 4
Effect of EP2 Receptor Genetic Deletion on Neurologic Scores and Infarct Volume after tMCAO
Effect of the EP2-selective Agonist ONO-AE1-259-01 on Physiologic Parameters of Mice Subjected to tMCAO
Effect of ONO-AE1-259-01 on Physiologic Parameters
7.31 ± 0.02
7.28 ± 0.47
7.30 ± 0.46
7.25 ± 0.23
43.2 ± 1.8
44.4 ± 2.0
45.2 ± 1.6
43.0 ± 1.3
133 ± 5
139 ± 5
130 ± 8
134 ± 9
78.6 ± 3.9
75.6 ± 1.7
77.4 ± 2.8
72.8 ± 2.5
7.28 ± 0.02
7.29 ± 0.64
7.26 ± 0.03
7.33 ± 0.02
44.0 ± 1.8
43.2 ± 1.5
45.6 ± 2.6
43.16 ± 1.6
129 ± 5
133 ± 4
124 ± 6
133 ± 5
74.4 ± 1.7
76.6 ± 2.5
74.4 ± 1.8
74.8 ± 1.7
7.26 ± 0.03
7.28 ± 0.05
7.29 ± 0.40
7.28 ± 0.25
43.0 ± 1.8
45.8 ± 1.4
47.2 ± 1.3
44.8 ± 2.7
135 ± 9
129 ± 6
126 ± 7
138 ± 9
74.6 ± 1.3
73.8 ± 1.7
76.0 ± 1.6
74.0 ± 1.6
ONO-AE1-259-01 Attenuates Neurologic Dysfunction and Infarct Volume in Mice Subjected to tMCAO
Effect of EP2 Receptor Genetic Deletion on Neurologic Deficits and Infarct Volume in Mice Subjected to pMCAO
This study was designed to further ascertain the unique neuroprotective properties of the PGE2 EP2 receptor in ischemic stroke. Using EP2-/- mice, we showed that the EP2 receptor is protective in cortical and striatal brain regions affected by tMCAO and in the cortex after pMCAO but that its deletion does not affect the gross cerebrovascular anatomy or the physiologic parameters of blood pH, PaO2, PaCO2, or MABP. We also demonstrated that this protective action of EP2 receptors is not simply transient or acute, as previously suggested, but lasts for days. Furthermore, pretreatment of mice with 1.0- and 2.0-nmol doses of the highly selective EP2 receptor agonist ONO-AE1-259-01 significantly reduced the infarct volume induced by transient ischemia, again without affecting the physiologic parameters monitored. These results clearly demonstrate that pharmacologic stimulation of the EP2 receptors in the brain attenuates brain damage caused by cerebral ischemia and support the hypothesis that EP2 receptor stimulation is important throughout an extended duration of the pathophysiologic response to brain ischemic damage. Measurements of relative CBF showed that tMCAO caused a reduction in cortical perfusion throughout the ischemic period that was similar in the EP2-/- and drug-treated mice to that in their corresponding controls, suggesting that neither genetic deletion nor pharmacologic activation of the EP2 receptor affected the severity of the ischemic insult. Thus, our findings indicate a protective role for EP2 by mechanisms that are likely other than those involving cerebrovascular effects. Moreover, no significant differences were observed in body temperature or MABP.
EP2-/- mice that underwent tMCAO or pMCAO had greater neurologic disability and infarct size than did WT mice. Although compensatory pathways might occur in the knockout animals, we show here that WT mice that received the two higher doses of the EP2 agonist ONO-AE1-259-01 before tMCAO had significantly less severe neurologic deficits and less infarct damage, supporting observations that EP2 receptors are beneficial in excitotoxicity  and in ischemic stroke .
Previous reports have shown that the EP2 receptor elicits neuroprotective effects under conditions of excitotoxicity and oxygen-glucose deprivation by increasing intracellular levels of cAMP and activating PKA signaling [9, 10]. We have also previously reported that pharmacologic activation of EP2 receptors leads to neuroprotection via the cAMP-PKA pathway . Moreover, the pharmacologic stimulation of EP4/EP3 receptors affords protection by increasing intracellular levels of cAMP and through activation of the ERK pathway . These cAMP cascades can provide protection for example by: (1) reducing the release of endoplasmic Ca2+ through the inositol triphosphate receptor , (2) inhibiting the expression of adhesion molecules , (3) suppressing the activity of neuronal nitric oxide synthase , (4) stimulating cAMP response element binding (CREB) , and (5) stimulating the high-affinity glutamate transporter . Interestingly, ONO-AE1-259-01 has been suggested to elevate cAMP and inhibit expression of inflammatory molecules such as ICAM-1 and B7.2 (CD86) [28, 29], and such inflammatory molecules affect stroke outcomes [30, 31]. The exact cascade in vivo is likely to be much more elaborate than what we can begin to address in isolated neuronal cultures, especially considering the complexity of the different cells and interactions between them and their environment (blood flow, oxygenation, inflammation, etc) over time. The signaling pathways of these molecules and kinases are continually expanding (kinome-phosphorylome projects ), with many branches that link to other pathways. Therefore, the complete cascade of events that takes place within any given cell based on its location with respect to the infarct is likely to differ substantially. Indeed, it is highly probable that the neuroprotection provided by EP2 stimulation results from a combination of pathways rather than a single one. For these reasons, we have first focused here on demonstrating that in the brain, stimulating the EP2 receptors leads to anatomical and behavioral protection. To build on our work with the tMCAO model, we are now endeavoring to confirm that the EP2-selective agonist is also protective in the pMCAO model and to address potential targets/biosystems that could begin to explain some of the steps leading to neuroprotection.
Two previous studies have indicated that activation of the PGE2 EP2 receptor can protect against excitotoxic and anoxic injury [9, 10]. In one of those studies, the tMCAO was followed by only 22.5 h of reperfusion, and no behavioral outcomes were reported. It is important to document that such ischemic-reperfusion-related change in the knockout animal is not transient or delayed, and that it is indeed maintained at later time points. When a brief ischemic event is followed by reperfusion, a second phase of injury occurs (potentially mediated by a surge in inflammatory markers). What's more, over time, endogenous repair pathways can be activated. Although it is more challenging to keep a mouse alive for 96 h after transient ischemia, we selected this extended reperfusion time because it enables us to document that the protective role of EP2 is sustained during the entire period. In the other study, Liu et al. first tested the stroke outcomes (without behavioral outcomes) in mice subjected to pMCAO after only 24 h of survival  and then a subsequent study suggested that misoprostol (which is a poorly selective mouse EP2 receptor agonist) has a protective effect against MCAO injury . For reasons similar to those described above, it is important to determine the potential contributions of EP2 to neurobehavioral and ischemic outcomes at later time points; that is why in our study we selected 7 days. Both of these previous studies led to the suggestion that activation of the PGE2 EP2 receptor can protect against ischemic injury, although no data were provided to support this hypothesis. To make such a conclusion, one needs to test whether selectively targeting EP2 would result in neuroprotection. Furthermore, it has been suggested that compensatory mechanisms can occur in knockout animals. Therefore, we chose to directly activate the EP2 receptor with a selective agonist to complement the findings in knockout mice.
Based on these novel observations, we can conclude that pharmacologic stimulation of the EP2 receptor with a selective pharmacologic agent could potentially be used therapeutically in translational medicine (most likely in combination with other standard treatments) to limit brain damage following ischemic stroke.
This study was supported by NIH grants (NS046400, AG022971). We thank Claire Levine for assistance in the preparation of the manuscript and all Doré lab team members for their active participation.
- Doré S: GPCR antagonists as an alternative to COX-2 inhibitors: a case for the PGE 2 EP1 receptor. Trends Pharmacol Sci 2006, 27: 458–460. 10.1016/j.tips.2006.07.001PubMedView ArticleGoogle Scholar
- Kawano T, Anrather J, Zhou P, Park L, Wang G, Frys KA, Kunz A, Cho S, Orio M, Iadecola C: Prostaglandin E 2 EP1 receptors: downstream effectors of COX-2 neurotoxicity. Nat Med 2006, 12: 225–229. 10.1038/nm1362PubMedView ArticleGoogle Scholar
- Namba T, Sugimoto Y, Negishi M, Irie A, Ushikubi F, Kakizuka A, Ito S, Ichikawa A, Narumiya S: Alternative splicing of C-terminal tail of prostaglandin E receptor subtype EP3 determines G-protein specificity. Nature 1993, 365: 166–170. 10.1038/365166a0PubMedView ArticleGoogle Scholar
- Hata AN, Breyer RM: Pharmacology and signaling of prostaglandin receptors: multiple roles in inflammation and immune modulation. Pharmacol Ther 2004, 103: 147–166. 10.1016/j.pharmthera.2004.06.003PubMedView ArticleGoogle Scholar
- Narumiya S, FitzGerald GA: Genetic and pharmacological analysis of prostanoid receptor function. J Clin Invest 2001, 108: 25–30.PubMed CentralPubMedView ArticleGoogle Scholar
- Narumiya S, Sugimoto Y, Ushikubi F: Prostanoid receptors: structures, properties, and functions. Physiol Rev 1999, 79: 1193–1226.PubMedGoogle Scholar
- Zhang J, Rivest S: Distribution, regulation and colocalization of the genes encoding the EP2- and EP4-PGE2 receptors in the rat brain and neuronal responses to systemic inflammation. Eur J Neurosci 1999, 11: 2651–2668. 10.1046/j.1460-9568.1999.00682.xPubMedView ArticleGoogle Scholar
- Ahmad AS, Zhuang H, Echeverria V, Doré S: Stimulation of prostaglandin EP2 receptors prevents NMDA-induced excitotoxicity. J Neurotrauma 2006, 23: 1895–1903. 10.1089/neu.2006.23.1895PubMedView ArticleGoogle Scholar
- McCullough L, Wu L, Haughey N, Liang X, Hand T, Wang Q, Breyer RM, Andreasson K: Neuroprotective function of the PGE 2 EP2 receptor in cerebral ischemia. J Neurosci 2004, 24: 257–268. 10.1523/JNEUROSCI.4485-03.2004PubMedView ArticleGoogle Scholar
- Liu D, Wu L, Breyer R, Mattson MP, Andreasson K: Neuroprotection by the PGE 2 EP2 receptor in permanent focal cerebral ischemia. Ann Neurol 2005, 57: 758–761. 10.1002/ana.20461PubMedView ArticleGoogle Scholar
- Kitagawa K, Hayasaka S, Watanabe K, Nagaki Y: Aqueous flare elevation induced by transcorneal application of highly selective agonists for prostaglandin E2 receptor subtypes in pigmented rabbits: effect of tetramethylpyrazine. Prostaglandins Other Lipid Mediat 2001, 65: 189–198. 10.1016/S0090-6980(01)00137-XPubMedView ArticleGoogle Scholar
- Kiriyama M, Ushikubi F, Kobayashi T, Hirata M, Sugimoto Y, Narumiya S: Ligand binding specificities of the eight types and subtypes of the mouse prostanoid receptors expressed in Chinese hamster ovary cells. Br J Pharmacol 1997, 122: 217–224. 10.1038/sj.bjp.0701367PubMed CentralPubMedView ArticleGoogle Scholar
- Ahmad M, Saleem S, Zhuang H, Ahmad AS, Echeverria V, Sapirstein A, Doré S: 1-HydroxyPGE 1 reduces infarction volume in mouse transient cerebral ischemia. Eur J Neurosci 2006, 23: 35–42. 10.1111/j.1460-9568.2005.04540.xPubMedView ArticleGoogle Scholar
- Majid A, He YY, Gidday JM, Kaplan SS, Gonzales ER, Park TS, Fenstermacher JD, Wei L, Choi DW, Hsu CY: Differences in vulnerability to permanent focal cerebral ischemia among 3 common mouse strains. Stroke 2000, 31: 2707–2714.PubMedView ArticleGoogle Scholar
- Saleem S, Shah ZA, Urade Y, Doré S: Lipocalin-prostaglandin D synthase is a critical beneficial factor in transient and permanent focal cerebral ischemia. Neuroscience 2009, 160: 248–254. 10.1016/j.neuroscience.2009.02.039PubMed CentralPubMedView ArticleGoogle Scholar
- Zeynalov E, Doré S: Low doses of carbon monoxide protect against experimental focal brain ischemia. Neurotox Res 2009, 15: 133–137. 10.1007/s12640-009-9014-4PubMed CentralPubMedView ArticleGoogle Scholar
- Saleem S, Kim YT, Maruyama T, Narumiya S, Doré S: Reduced acute brain injury in PGE 2 EP3 receptor-deficient mice after cerebral ischemia. J Neuroimmunol 2009, 208: 87–93. 10.1016/j.jneuroim.2009.01.015PubMed CentralPubMedView ArticleGoogle Scholar
- Ahmad M, Ahmad AS, Zhuang H, Maruyama T, Narumiya S, Doré S: Stimulation of prostaglandin E 2 -EP3 receptors exacerbates stroke and excitotoxic injury. J Neuroimmunol 2007, 184: 172–179. 10.1016/j.jneuroim.2006.12.012PubMed CentralPubMedView ArticleGoogle Scholar
- Ahmad AS, Saleem S, Ahmad M, Doré S: Prostaglandin EP1 receptor contributes to excitotoxicity and focal ischemic brain damage. Toxicol Sci 2006, 89: 265–270. 10.1093/toxsci/kfj022PubMedView ArticleGoogle Scholar
- Wang J, Zhuang H, Doré S: Heme oxygenase 2 is neuroprotective against intracerebral hemorrhage. Neurobiol Dis 2006, 22: 473–476. 10.1016/j.nbd.2005.12.009PubMedView ArticleGoogle Scholar
- Doré S, Otsuka T, Mito T, Sugo N, Hand T, Wu L, Hurn PD, Traystman RJ, Andreasson K: Neuronal overexpression of cyclooxygenase-2 increases cerebral infarction. Ann Neurol 2003, 54: 155–162. 10.1002/ana.10612PubMedView ArticleGoogle Scholar
- Echeverria V, Clerman A, Doré S: Stimulation of PGE 2 receptors EP2 and EP4 protects cultured neurons against oxidative stress and cell death following b-amyloid exposure. Eur J Neurosci 2005, 22: 2199–2206. 10.1111/j.1460-9568.2005.04427.xPubMedView ArticleGoogle Scholar
- Hartikka J, Staufenbiel M, Lubbert H: Cyclic AMP, but not basic FGF, increases the in vitro survival of mesencephalic dopaminergic neurons and protects them from MPP(+)-induced degeneration. J Neurosci Res 1992, 32: 190–201. 10.1002/jnr.490320208PubMedView ArticleGoogle Scholar
- Ballestas ME, Benveniste EN: Elevation of cyclic AMP levels in astrocytes antagonizes cytokine-induced adhesion molecule expression. J Neurochem 1997, 69: 1438–1448.PubMedView ArticleGoogle Scholar
- Dinerman JL, Steiner JP, Dawson TM, Dawson V, Snyder SH: Cyclic nucleotide dependent phosphorylation of neuronal nitric oxide synthase inhibits catalytic activity. Neuropharmacology 1994, 33: 1245–1251. 10.1016/0028-3908(94)90023-XPubMedView ArticleGoogle Scholar
- Berridge MJ: Neuronal calcium signaling. Neuron 1998, 21: 13–26. 10.1016/S0896-6273(00)80510-3PubMedView ArticleGoogle Scholar
- Pisano P, Samuel D, Nieoullon A, Kerkerian-Le Goff L: Activation of the adenylate cyclase-dependent protein kinase pathway increases high affinity glutamate uptake into rat striatal synaptosomes. Neuropharmacology 1996, 35: 541–547. 10.1016/0028-3908(96)84624-7PubMedView ArticleGoogle Scholar
- Akagi R, Takahashi T, Sassa S: Fundamental role of heme oxygenase in the protection against ischemic acute renal failure. Jpn J Pharmacol 2002, 88: 127–132. 10.1254/jjp.88.127PubMedView ArticleGoogle Scholar
- Takahashi HK, Iwagaki H, Yoshino T, Mori S, Morichika T, Itoh H, Yokoyama M, Kubo S, Kondo E, Akagi T, Tanaka N, Nishibori M: Prostaglandin E 2 inhibits IL-18-induced ICAM-1 and B7.2 expression through EP2/EP4 receptors in human peripheral blood mononuclear cells. J Immunol 2002, 168: 4446–4454.PubMedView ArticleGoogle Scholar
- Andaluz N, Zuccarello M, Wagner KR: Experimental animal models of intracerebral hemorrhage. Neurosurg Clin N Am 2002, 13: 385–393. 10.1016/S1042-3680(02)00006-2PubMedView ArticleGoogle Scholar
- del Zoppo G, Ginis I, Hallenbeck JM, Iadecola C, Wang X, Feuerstein GZ: Inflammation and stroke: putative role for cytokines, adhesion molecules and iNOS in brain response to ischemia. Brain Pathol 2000, 10: 95–112.PubMedView ArticleGoogle Scholar
- Sopko R, Andrews BJ: Linking the kinome and phosphorylome--a comprehensive review of approaches to find kinase targets. Mol Biosyst 2008, 4: 920–933. 10.1039/b801724gPubMedView ArticleGoogle Scholar
- Li J, Liang X, Wang Q, Breyer RM, McCullough L, Andreasson K: Misoprostol, an anti-ulcer agent and PGE2 receptor agonist, protects against cerebral ischemia. Neurosci Lett 2008, 438: 210–215. 10.1016/j.neulet.2008.04.054PubMed CentralPubMedView ArticleGoogle Scholar
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.