A1 adenosine receptor attenuates intracerebral hemorrhage-induced secondary brain injury in rats by activating the P38-MAPKAP2-Hsp27 pathway

Zhai, Weiwei; Chen, Dongdong; Shen, Haitao; Chen, Zhouqing; Li, Haiying; Yu, Zhengquan; Chen, Gang

doi:10.1186/s13041-016-0247-x

Research
Open Access
Published: 14 June 2016

A1 adenosine receptor attenuates intracerebral hemorrhage-induced secondary brain injury in rats by activating the P38-MAPKAP2-Hsp27 pathway

Weiwei Zhai¹,
Dongdong Chen¹,
Haitao Shen¹,
Zhouqing Chen¹,
Haiying Li¹,
Zhengquan Yu¹ &
Gang Chen¹

Molecular Brain volume 9, Article number: 66 (2016) Cite this article

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Abstract

Background

This study was designed to determine the role of the A1 adenosine receptors in intracerebral hemorrhage (ICH)-induced secondary brain injury and the underlying mechanisms.

Methods

A collagenase-induced ICH model was established in Sprague–Dawley rats, and cultured primary rat cortical neurons were exposed to oxyhemoglobin at a concentration of 10 μM to mimic ICH in vitro. The A1 adenosine receptor agonist N(6)-cyclohexyladenosine and antagonist 8-phenyl-1,3-dipropylxanthine were used to study the role of A1 adenosine receptor in ICH-induced secondary brain injury, and antagonists of P38 and Hsp27 were used to study the underlying mechanisms of A1 adenosine receptor actions.

Results

The protein level of A1 adenosine receptor was significantly increased by ICH, while there was no significant change in protein levels of the other 3 adenosine receptors. In addition, the A1 adenosine receptor expression could be increased by N(6)-cyclohexyladenosine and decreased by 8-phenyl-1,3-dipropylxanthine under ICH conditions. Activation of the A1 adenosine receptor attenuated neuronal apoptosis in the subcortex, which was associated with increased phosphorylation of P38, MAPK, MAPKAP2, and Hsp27. Inhibition of the A1 adenosine receptor resulted in opposite effects. Finally, the neuroprotective effect of the A1 adenosine receptor agonist N(6)-cyclohexyladenosine was inhibited by antagonists of P38 and Hsp27.

Conclusions

This study demonstrates that activation of the A1 adenosine receptor by N(6)-cyclohexyladenosine could prevent ICH-induced secondary brain injury via the P38-MAPKAP2-Hsp27 pathway.

Background

Intracerebral hemorrhage (ICH) is a frequent cause of mortality (estimated mortality rate ~ 50 %) and morbidity (accounts for ~ 10–15 % of all strokes) during the perioperative period and may cause patient paralysis or even death [1, 2]. Progression of the pathophysiology of ICH is still not very well understood [3, 4]. However, there is a general consensus that hemorrhage in the brain [5] leads to tissue disruption and displacement [6]. A series of secondary pathophysiological processes, which are referred to as secondary brain injury (SBI) [7], includes ischemia of brain tissue surrounding the hematoma, development of brain edema [8, 9], activation of apoptotic programs [10, 11], and toxic effects of the hematoma [12–14]. Finding treatments that relieve the pathophysiology of ICH has challenged neurosurgeons for many years.

As a potent biological mediator, adenosine has been reported to be extensively released during hemorrhage and eliminated quickly from plasma by the uptake mechanism and adenosine deaminase [15]. And both the uptake and the deamination are effective in removing extracellular adenosine and regulate the activation balance of adenosine receptors [16]. All the four adenosine receptor subtypes, including A1, A2a, A2b and A3, can be stimulated by extracellular adenosine when its concentration reaches the micromolar range [17]. It has been reported that adenosine deaminase activity in the poor-grade subarachnoid hemorrhage (SAH) patients was higher than that in the good-grade SAH patients [18]. In recent years, evidence has shown that the adenosine receptors, particularly A2a adenosine receptor (A2aAR), are of critical importance in hemorrhagic stroke [19]. A2aAR has been shown to be involved in the beneficial effect of 17beta-estradiol in attenuating SAH-induced apoptosis and vasospasm [20]. And A2aAR agonism is effective in preventing SAH-induced vasospasm. However, global inactivation of A2aAR could confer protection against the early ischemic vascular injury after SAH, suggesting that early inhibition of A2aAR after SAH might reduce cerebral injury. As shown above, the previous studies are mainly focused on the role of A2aAR in SAH-induced brain injury, which is controversial and may be selectively manipulated by targeting different cellular elements [19]. Besides, the positive roles of A1AR in SAH-induced vasospasm [21] and A2aAR in ICH-induced proinflammatory events and cell death have been reported. However, the effects of the four adenosine receptor subtypes on ICH-induced SBI still remain elusive and must be clarified.

Mitogen-activated protein kinase (MAPK) family, including extracellular signal-regulated kinase (ERK), p38, and Jun N-terminal Kinase (JNK), widely mediates inflammation, cell proliferation, and apoptosis. As the activation of MAPK pathways by A1 [22, 23], A2a [22, 24, 25] and A2b [22, 26] and A3 [22] adenosine receptors has been demonstrated, the involvement of this intracellular phosphorylative cascade in adenosine receptor regulation has attracted more and more attention. A1AR mediated p38 MAPK activation plays a crucial role in the presynaptic inhibitory effect of adenosine on CA3–CA1 synaptic transmission [27]. A1AR-mediated p38 MAPK and JNK activation is a crucial step in regulating AMPAR trafficking during prolonged hypoxia [28]. Human adenosine A1, A2A, A2B, and A3 receptors expressed in Chinese hamster ovary cells all mediate the phosphorylation of ERK [23]. Elucidating the signaling pathway involved in the action of adenosine receptors will facilitate the understanding of death or survival mechanisms in ICH and the development of targeting drugs.

In addition, it has been pointed out that differences in the efficacy of adenosine receptors may be caused by differences in expression. Overexpressions of adenosine receptors can lead to signal transductions that do not occur in cells with the receptors expressed at a normal level [29]. In the present study, we tested the time course of the expression of the four adenosine receptor subtypes and evaluated the effects of ICH on these parameters. We hypothesized that pharmacological agonists selective for adenosine receptors would provide neuroprotection following ICH. Our results demonstrated that, among the four adenosine receptor subtypes, only the protein level of A1AR was significantly increased in rat brain after ICH and oxyHb-treated neurons, while the other three receptors have no significant changes. 48 h after ICH, activation of A1AR by R-PIA could prevent ICH-induced SBI via the p38-MAPKAP2-Hsp27 pathway.

Results

Time course

We first performed a time course experiment (Fig. 1). After establishment of the ICH model, rats were killed at the following time points after induction of ICH: 0 h, 6 h, 12 h, 24 h, 48 h, 72 h, and 1 week. In western blot analysis, compared with the other adenosine receptors, A1AR levels varied the most (Fig. 1a and b). In contrast to the group subjected to ICH, the sham group expressed a low level of A1AR. After induction of ICH, the level of A1AR increased with time, peaking at 48 h, and then decreased. Consistant with the in vivo data, western blot assay showed that the protein level of A1AR in cultured primary neurons was significantly increased after oxyHb-incubated for 48 h (Fig. 1c and d). Double immunofluorescence assay further verified the ICH-induced increase in the protein level of A1AR in neurons (Fig. 1e). In addition, Jeong et al. reported that astrogliosis participated in neuronal recovery in ATP-injected brain [30]. To pursue the potential role of astrogliosis in A1AR action in this ICH model, we also tested the protein level of A1AR in astrogliosis by double immunofluorescence. And the results showed that there was no significant change in the protein level of A1AR in astrogliosis between sham group and ICH group (Fig. 1f). Finally, double immunofluorescence also showed that oxyHb treatment could increase the protein level of A1AR in cultured neurons (Fig. 1g). So, we focused on A1AR in neurons in the following study.

A1AR activation suppressed caspase-3 activation and albumin extravasation

We conducted further studies using the A1AR agonist, N(6)-cyclohexyladenosine (R-PIA), and the A1AR antagonist, 8-phenyl-1,3-dipropylxanthine (8-PT). Both agonist and antagonist were administered 30 min before induction of ICH. Rats were randomly divided into 4 groups: sham group, ICH group, ICH + R-PIA group, and ICH + 8-PT group. We performed western blot analysis at 48 h after ICH onsets and detected changes in the protein levels of active caspase-3 and albumin (Fig. 2a and b). Protein levels of active caspase-3 and albumin showed significant increases in the ICH group compared with the sham group. Treatment with the agonist R-PIA suppressed the ICH-induced increase in levels of caspase-3 and albumin (p < 0.05). In contrast, treatment with the A1AR antagonist, 8-PT, enhanced ICH-induced upregulation of caspase-3 and albumin protein levels (p < 0.05).

A1AR decreased neuronal death and degeneration and relieved brain edema

We evaluated neuronal death and degeneration using terminal deoxynucleotidyl transferase-mediated dUTP nick end labeling (TUNEL) and Fluoro-Jade B (FJB), respectively. Rats subjected to ICH or ICH + DMSO demonstrated histological evidence of neuronal death compared with the sham group (Fig. 2c and d), while there was no obvious differences observed between the ICH and ICH + DMSO groups. The group pretreated with R-PIA before ICH injury demonstrated a significant decrease in cell death ratio in the rat brain sample. In contrast, pretreatment with the A1AR receptor antagonist 8-PT before ICH injury led to an increase in the number of TUNEL-positive cells.

In addition, in ICH group, the number of FJB-positive cells clearly increased compared with the sham group. And the number of FJB-positive cells decreased significantly in the ICH + R-PIA group and increased significantly in the ICH + 8-PT group (Fig. 3a and b) (p < 0.05).

Brain water content was also examined at 48 h after ICH and showed a significantly higher brain water content in brain samples of ICH group compared with those in the sham group (Fig. 3c) (p < 0.05). And the mean value of brain water content was decreased after administration of the A1AR agonist R-PIA (p < 0.05). In contrast, after administration of the A1AR antagonist 8-PT, brain water content increased significantly. In addition, we performed TUNEL studies in vitro (Fig. 3d and e) and results were similar to those from in vivo experiments.

As described above, these results suggested that pharmacological activation targeting A1AR provided effective inhibition of brain injury that occur following ICH.

A1AR increased phosphorylation levels of P38, MAPKAP2, and Hsp27

To investigate the underlying mechanism by which A1AR prevent ICH-induced SBI and whether MAPK family participates in the process, the activation of ERK, p38 and JNK was tested by western blot analysis. Compared with sham group, the phosphorylation levels of ERK, p38 and JNK all were increased at 48 h after ICH onsets, suggesting ICH may induce the activation of ERK, p38 and JNK. In addition, R-PIA caused a statistically significant increase in phospho- p38, however, did not modify the phosphorylation of both ERK and JNK. These results showed that protection attained 48 h after ICH, by administration of A1AR agonists, involves increased activation of p38 MAPK (Fig. 4a-c).

Lee et al. have suggested that A1AR could exert a protective effect in transient renal ischemia through activation of the P38-MAPKAP2-Hsp27 pathway [31]. In this study, compared with the sham group, remarkable increases in the phosphorylation levels of MAPKAP2 and Hsp27 were observed in the ICH group (p < 0.05), which were further increased by R-PIA treatment and reversed by 8-PT(p < 0.05) (Fig. 4b and c). Similar results were also obtained in vitro (Fig. 4d and e).

Blocking P38 or Hsp27 inhibited the neuroprotective effect of A1AR

We further investigated the role of P38/MAPKAP2/Hsp27 in A1AR’s action using antagonists of p38 (SB203580) and Hsp27 (KNK437) (Fig. 4e and f). Following pretreatment with R-PIA before ICH, the phosphorylation levels of P38, MAPKAP2, and Hsp27 increased significantly compared with the ICH group (p < 0.05). After blocking Hsp27, the phosphorylation level of Hsp27 showed a significant decrease compared with the R-PIA group, while the phosphorylation levels of p38 and MAPKAP2 showed little change. After blocking p38, the phosphorylation levels of P38, MAPKAP2, and Hsp27 were all clearly decreased compared with the R-PIA group (p < 0.05) (Fig. 4f and g). In addition, in the presence of any of these antagonists, R-PIA -induced A1AR activation could not effectively suppress neuronal death and degeneration induced by ICH (Fig. 5a-d). Thus, we speculated that A1AR exhibited a neuroprotective function, which might act through the P38-MAPKAP2-Hsp27 pathway.

Finally, we used Evans blue (EB) to assess permeability of the blood–brain barrier (BBB). The content of EB exuded from blood vessels in different groups is shown in Fig. 5e and f. Compared with the sham group, EB content in the brain increased significantly in the ICH group (p < 0.05), which was significantly suppressed by R-PIA treatment and aggravated by 8-PT treatment (p < 0.05). And both SB203580 and KNK437 could abolish the protective effects of R-PIA on ICH-induced BBB dysfunction.

Discussion and Conclusions

Although the A2AR has been the subject of most previous studies (see Introduction), our results show that the protein level of A1AR, but not A2A, A2B, or A3, was significantly increased after ICH. In addition, we have demonstrated that the A1AR agonist R-PIA could reduce ICH-induced SBI via modifying the activation of p38, but not ERK1/2 and JNK. Base on these results, we hypothesized here that adenosine is extensively generated from ATP released by ruptured red cell during ICH and quickly activates its receptor, A1AR at least partially, in neuron cells, and then elevated the activity of P38-MAPKAP2-Hsp27 pathway, which exerts neuroprotective effect and suppresses ICH-induced EBI (Fig. 5g).

As firstly put forward by Drury in 1929, the concept of purines as extracellular signaling molecules was approved. Extracellular purines (ATP, ADP, and adenosine) have been proved to be involved in diverse biological functions, including neurotransmission, smooth muscle contraction, exocrine and endocrine secretion, inflammation, the immune response, and platelet aggregation, via cell-surface receptors termed purine receptors. As early as minutes after ICH, extravasated blood components and damage-associated moleculars, such as ATP released from damaged and necrotic tissue, impose a pro-oxidative, strong cytotoxic, and proinflammatory insult toward adjacent viable brain cells [32]. And it has been reported that, both in the ATP-injected substantia nigra and cortex, ATP rapidly induced death of the neurons and astrocytes in the injection core area within 3 h [30, 33]. Given the above evidence, the cytotoxic effects of ATP tend to occur at the early stage of ICH-induced brain injury, which may be related to the narrow therapeutic window for the acute phase of ICH. Fortunately, the released ATP can be hydrolyzed extracellularly by a variety of cell surface-located enzymes referred to as ectonucleotidases. Extracellular ATP and ADP can be step by step hydrolyzed to adenosine by ectonucleotide pyrophosphatase/phosphodiesterases (E-NPPs), ectonucleoside triphosphate diphophohydrolases (E-NTPDases), and alkaline phosphatases (APs), while extracellular AMP is substrate of ecto-5′-nucleotidase (eN) and APs [34]. As the final product of hydrolysis cascade, adenosine and its receptors attracted more and more attention. In this study, we focused on the role of adenosine receptors in ICH-induced SBI and the underlying mechanisms.

There are 4 adenosine receptor subtypes: A1AR, A2aAR, A2bAR, and A3AR [35, 36]. Numerous authors indiscriminately select A2aAR, and Lin et al. have shown that an A2aAR agonist is effective in preventing vasospasm in subarachnoid hemorrhage conditions by inhibiting eNOS expression in brain vessels and inducing iNOS expression [37, 38]. However, in our time course experiment, A2aAR did not increase as much as A1AR after ICH. Thus, we selected A1AR for further study. In addition, as shown in Fig. 2a and b, the protein level of A1AR was increased to some extent under ICH, which is enhanced by its agonists R-PIA and inhibited by its antagonists 8-PT. Accordingly, R-PIA treatment alleviated ICH-induced SBI, which was aggravated by 8-PT treatment. The results are consistent with the previous report about the correlation between the efficacy and the expression of adenosine receptors [29] and suggest that ICH-induced A1AR activation maybe a self-help measure in neurons.

Many authors have suggested that A1AR activation has a beneficial effect [39–41]. Lee et al. indicated that endogenous A1AR activation produced cytoprotective effects in the renal proximal tubule, and Kim found that endogenous A1AR activation prevented murine liver ischemia reperfusion injury from worsening. However, others also have suggested that blocking A1AR exerted protection [42, 43]. In this study, we used R-PIA, a specific A1AR receptor agonist, to evaluate the role of A1AR in neuronal function under ICH conditions. At 48 h, the numbers of apoptotic or necrotic cells were clearly reduced in ICH groups pretreated with R-PIA (Fig. 2 and 3). A positive effect of 8-PT on apoptosis and necrosis was observed.

Lee demonstrated that endogenous A1AR activation produced cytoprotective effects by modulating the P38-MAPKAP2-Hsp27 pathway in renal cells [31]. However, no one has reported such effects in ICH conditions. In our experiment, inhibition of P38 suppressed the upregulation of phosphorylation of P38, MAPKAP2, and Hsp27, while the antagonist of Hsp27 (KNK437) clearly inhibited upregulation of Hsp27 phosphorylation. And both the two antagonists could almost completely abolish R-PIA- mediated neuroprotective effect (Fig. 5). Thus, these data suggest a crucial role for the P38-MAPKAP2-Hsp27 pathway in ICH conditions. In support of this concept, Carroll and Yellon have presented preliminary results from a cardiac myoblast cell line showing that pretreatment with P38 MAPK inhibitor SB203580 completely abolished delayed protection after ischemic- or adenosine-induced preconditioning [44].

Hsp27, a member of the heat shock protein family, is a molecular protein with diverse cytoprotective effects. Van Why et al. [45] have demonstrated that Hsp27, together with the actin cytoskeleton, restricts injury in vitro. The preservation of cytoskeletal actin contributes to architectural integrity of the cytoskeleton, at least in part. Phosphorylation of Hsp27 maintains the integrity of cells and enhances their ability to resist breaking down after ATP depletion [46]. In addition, Hsp27, acting as a molecular chaperone, prevents unfolded proteins from irreversible aggregation, reduces oxidative stress-mediated injury, and counteracts apoptosis by interacting with caspases [47, 48]. We propose that induction and increased phosphorylation of Hsp27 may provide protection against necrosis as well as apoptosis in neurons. In this study, we showed that activating A1AR with agonist R-PIA increased the phosphorylation level of Hsp27.

Finally, our experiments had limitations. The animals were intraperitoneally injected with A1AR agonist R-PIA and A1AR antagonist 8-PT. When these drugs crossed the BBB and finally reached the brain, their biological activity was limited. In addition, although there was no significant cardiovascular complications of R-PIA and 3-PT (see Methods), further pharmacological and toxicology experiment is still urgently needed to eliminate other potential side effects of them. In our experiment, we used healthy Sprague–Dawley (SD) rats to mimic the progression of ICH; however, in the clinic, we often see older patients. Finally, in vitro, we only treated neurons with oxyhemoglobin (OxyHb), and it remains to be determined if it is appropriate for activation of A1AR.

In conclusion, the present study demonstrated that, following ICH, the release of hematoma components, such as adenosine, may induce an increase in the protein level of A1AR, which maybe a self-help measure in neurons. A1AR agonist R-PIA could significantly increase the protein level of A1AR and alleviate ICH-induced SBI via P38-MAPKAP2-Hsp27 pathway, while A1AR antagonist 8-PT exerts opposite effects. We thus propose A1AR as a critical endogenous physiological regulator in neurons and suggest it may be potential therapeutic target in the treatment of ICH.

Methods

Study design and experimental groups

Drug administration was shown in Fig. 6a-c. Briefly, R-PIA, prepared in normal saline containing 20 % DMSO at a concentration of 5 μg/ml, was injected intraperitoneally at a dose range of μg/kg body weight. 8-PT was prepared in normal saline containing 10 % DMSO at a concentration of 0.2 mg/ml and injected intraperitoneally at a dose of 3 mg/kg body weight. KNK was prepared in DMSO at a concentration of 2.5 μg/μl and injected intracerebroventricularly at a dose of 16.7 μg/kg body weight [49]. 5 μl SB203580 in normal saline containing 0.1 % DMSO at a concentration of 1 mM were given via intracerebroventricular injection [50]. All the drugs were administered 30 min before induction of ICH. To pursue the potential toxic side effects of all the four drugs, we have treated normal rats with them at the same dosage of that used in this study in preliminary experiments. No rat died in all the groups. Blood pressure and heart rate were measured via the cannulated right femoral artery. There were no significant differences in blood pressure and heart rate among vehicle group, R-PIA group, 8-PT group, KNK group, and SB203580 group (Data not shown).

Antibodies

Anti-A1AR antibody (ab82477), anti-active caspase-3 (ab2302), Chk pAb to albumin (ab106582), Rb pAb to MAPKAP2 (ab131531), Rb pAb to phosphor MAPKAP2 (ab63378), Ms mAb to Hsp27 (ab2790), Rb pAb to phosphor Hsp27 (ab5594), Rb mAb to NeuN (ab177487), anti-ERK1 (phospho T202) + ERK2 (phospho T185) antibody (ab201015), anti-ERK1 + ERK2 antibody (ab17942), anti-JNK1 (phospho T183) antibody (ab47337), anti-JNK1 antibody (ab110724), anti-GFAP antibody (ab10062), and Ms mAb to NeuN (ab104224) were purchased from abcam. Anti-A2aAR antibody (sc-32261), anti-A2bAR antibody (sc-28996), anti-A3AR antibody (sc-13938), β-actin (sc-47778), and GAPDH (sc-365062) were purchased from Santa Cruz. Rb pAb to P38, phosphor P38 was purchased from Cell Signaling.

Establishing the ICH model

Adult male SD rats (0–300 g) were anesthetized with 4 % chloral hydrate, which was injected intraperitoneally at a dose of 1 mL per 100 g. After the rat was fully anesthetized, it was fixed in a stereotactic apparatus frame (Shanghai Ruanlong Science and Technology Development Co., Ltd., Shanghai, China). Extra chloral hydrate was injected if needed based on responses to tail pinches. The rat was then placed supine on a heating pad, which maintained temperature at approximately 27–35 °C. The experimental ICH model was produced using stereotaxic insertion of a needle with a rounded tip and a side hole into the basal ganglia [51, 52]. The position of basal ganglia was 3.5 mm lateral to the midline, 0.2 mm posterior to bregma, and 5.5 mm ventral to the cortical surface. After the microinjector was in position, collagenase IV was injected over 5 min, and the needle was left in the brain for 5 min. Bone wax was used as needed to block the burr hole to prevent loss of CSF and blood from the midline vessels. Next, we sutured the scalp and returned the rat to its cage where it had free access to food and water. Representative brain slices from the ICH model are shown in Fig. 6d. Assessment of SBI was performed at 48 h after ICH onsets.

Western blot analysis

After brain tissues were collected, the brain tissue from each rat was separately homogenized and lysed in ice-cold RIPA lysis buffer (P0013; Beyotime, Shanghai, China). After centrifuging at 12,500 × g for 15 min at 4 °C, the supernatants were collected. A standard BCA (Beyotime, P0012) method was used to determine protein concentration. Then, protein samples (100 mg/lane) were loaded onto a 10 % SDS polyacrylamide gel, separated, and electrophoretically transferred to a PVDF membrane (IPVH00010; Millipore, Billerica, MA, USA). The membrane was blocked in 5 % nonfat milk for 2 h at 37 °C. Next, the membrane was incubated with the primary antibody overnight at 4 °C and then with the horseradish peroxidase-linked secondary antibody for 1.5 h at 37 °C. The membrane was washed with PBST and visualized using enhanced chemiluminesence detection (3100 Mini; Clinx Science Instruments Co.). The relative quantities of proteins were analyzed using Image J software.

Immunofluorescence microscopy

We performed double labeling for A1AR, A2aAR, A2bAR, and A3AR with NeuN, to detect expression of A1AR, A2aAR, A2bAR, and A3AR in neurons. The sections were incubated with primary antibody, including antibodies for A1AR, A2aAR, A2bAR, A3AR, and NeuN antibody-neuronal cell marker (all diluted 1:100), overnight at 4 °C. Then, secondary antibodies were added, followed by washing 3 times with PBS. Secondary antibodies were Alexa Fluor 488 donkey anti-rabbit IgG antibody and Alexa Fluor 555 donkey anti-mouse IgG antibody (Life Technologies, Carlsbad, CA, USA, 1:300 dilution). After a final wash, sections were coverslipped with an anti-fading mounting medium containing 4,6-diamino-2-phenyl indole (DAPI, SouthernBiotech, Birmingham, AL, USA). Normal rabbit IgG and normal mouse IgG were used as negative controls for immunofluorescence assays (data not shown). Sections were observed with a fluorescence microscope (Olympus, BX50/BX-FLA/DP70, Olympus Co., Japan). The relative fluorescence intensity was analyzed using Image J.

TUNEL staining

Brain tissues embedded in paraffin were used for TUNEL staining. The sections were deparaffinized, dehydrated by heating at 75 °C in an oven for 60 min, and then rehydrated through xylenes and graded ethanol solutions to water. The sections were then incubated in Triton X-100 for 10 min. After 3 washes in PBS (5 min per wash), the sections were incubated with the TUNEL reaction mixture for 1 h at 37 °C. Sections were once again washed 3 times in PBS (5 min per wash). After the final wash, sections were coverslipped with an anti-fading mounting medium containing DAPI. The number of TUNEL-positive neurons in each millimeter length was counted carefully per sample. Cell counts from the brain were averaged to provide the mean value.

FJB

Cell necrosis in brain tissue was detected by FJB. FJB procedures were identical to those for TUNEL. Sections were deparaffinized, dehydrated in an oven, rehydrated through xylenes and graded ethanol solutions to water, and permeabilized in 0.04 % Triton X-100. Sections were then incubated in FJB dye solution. The sections were visualized by a fluorescence microscope (Olympus BX50/BXFLA/DP70; Olympus). The FJB-positive cells were counted by an observer who was blind to the experimental groups. To evaluate the extent of cell necrosis, the necrotic index was defined as the average number of FJB-positive cells in each section counted in 6 microscopic fields (×400 magnification).

Brain edema

Rats were randomly divided into 4 groups: sham, ICH, R-PIA (7.5 g dissolved in 1.5 mL DMSO and NaCl solution) [53], 8-PT(0.9 mg dissolved in 4 mL DMSO and NaCl solution) [54]. The index of brain edema was evaluated using the wet/dry method. Briefly, after brain tissue was removed, the samples were collected and weighed immediately (wet weight), dried at 100 °C for 72 h, and then weighed again (dry weight). The percentage of water content was calculated as [(wet weight-dry weight)/wet weight] × 100 %.

EB detection

BBB injury was determined by EB (Sigma-Aldrich, St Louis, MO, USA) extravasation. Briefly, EB (2 % in Normal saline, 2 mL/kg) was injected into the rat through the femoral vein 48 h after ICH, and it was allowed to remain in circulation for 1 h. Animals were then reanesthetized and perfused using PBS to wash intravascular EB dye. A 3 mm of the brain tissue (coronal plane) were taken and it was divided into four parts: left cortical, right cortical, left basal, right basal. The samples were incubated in 5 % TCA and centrifuged at 15,000 rpm for 10 min. The supernatant was collected and mixed with ethanol. Absorbance at 620 nm was measured in a spectrophotometer.

Primary neuron-enriched cultures

Whole brains of 1-day-old pups (from pregnant SD rats) were used to prepare primary neuron-enriched cultures. We tried as much as possible to minimize the number of pups used and their suffering. In brief, we first removed the meninges and blood vessels of the brain. The brain tissues were then digested with 0.% trypsin for 5 min, and the digestion was terminated by washing the tissue 3 times with PBS. The brain tissue suspension was centrifuged at 500 × g for 5 min, and the pellet was resuspended in DMEM/F12 medium containing 10 % heat-inactivated fetal bovine serum, 1 mM sodium pyruvate, 2 mM L-glutamine, 100 mM nonessential amino acids, 50 U/mL penicillin, and 50 mg/mL streptomycin (all from GIBCO, Carlsbad, CA, USA). Finally, cells were seeded in 150-cm² culture flasks in fresh medium. Afterwards, half of the medium was changed every 2 d. In general, approximately 2 weeks after the initial seeding, a confluent monolayer of neurons was achieved. Neurons were separated from the brain tissue by shaking the flask for 4 h at 150 rpm, collected by centrifugation, and re-seeded in 12-well plates with fresh DMEM/F12 medium.

Treatments of neurons

Enriched neurons were divided into 5 groups: control, OxyHb, OxyHb + vehicle (DMSO, Sigma-Aldrich), OxyHb + R-PIA (Sigma-Aldrich), and OxyHb + 8-PT (Sigma-Aldrich). Forty-eight hours after neuron re-seeding, cells were treated with OxyHb (at a final concentration of 10 μM), DMSO (volume equal to R-PIA and 8-PT), R-PIA (at a final concentration of 100 nM) [39], or 8-PT (at a final concentration of 100 nM) in fresh medium. After incubation for 48 h (37 °C, 5 % CO₂), the cell medium was removed. Cells were then washed 3 times in PBS and fixed with 4 % paraformaldehyde.

Statistical analysis

Values are presented as means ± SEM. SPSS 11.5 (SPSS Inc., Chicago, IL, U.S.) was used for statistical analysis. The Mann–Whitney U test was used to compare behavior and activity scores among groups. Statistical comparisons between groups were performed using one-way analysis of variance followed by either a Dunnett’s or a Tukey’s post hoc test, the former for comparisons to a single control group, the latter to compare across multiple groups. Mortality was compared with a w2 test. A probability of P < 0.05 was considered statistically significant.

Abbreviations

ICH, intracerebral hemorrhage; SBI, secondary brain injury; ARs, adenosine receptors; A1AR, A1 adenosine receptor; R-PIA, N(6)-cyclohexyladenosine; 8-PT, 8-phenyl-1,3-dipropylxanthine; TUNEL, terminal deoxynucleotidyl transferase-mediated dUTP nick end labeling; FJB, Fluoro-Jade B; EB, Evans blue; BBB, blood–brain barrier; SD, Sprague–Dawley; OxyHb, oxyhemoglobin; ERK1/2, extracellular signal-regulated kinase; PI3-K/AKT, phosphatidylinositol 3-kinase

References

1.
Rodriguez-Yanez M, Castellanos M, Freijo MM, Lopez Fernandez JC, Marti-Fabregas J, Nombela F, et al. Clinical practice guidelines in intracerebral haemorrhage. Neurologia. 2013;28:236–49.
CAS Article PubMed Google Scholar
2.
van Asch CJ, Luitse MJ, Rinkel GJ, van der Tweel I, Algra A, Klijn CJ. Incidence, case fatality, and functional outcome of intracerebral haemorrhage over time, according to age, sex, and ethnic origin: a systematic review and meta-analysis. Lancet Neurol. 2010;9:167–76.
Article PubMed Google Scholar
3.
Cannon JR, Xi G, Keep RF. Recent research on changes in genomic regulation and protein expression in intracerebral haemorrhage. Int J Stroke. 2007;2:265–9.
Article PubMed Google Scholar
4.
Qureshi AI, Mendelow AD, Hanley DF. Intracerebral haemorrhage. Lancet. 2009;373:1632–44.
Article PubMed PubMed Central Google Scholar
5.
Schlunk F, Greenberg SM. The Pathophysiology of Intracerebral Hemorrhage Formation and Expansion. Transl Stroke Res. 2015;6:257–63.
CAS Article PubMed Google Scholar
6.
Qureshi AI, Tuhrim S, Broderick JP, Batjer HH, Hondo H, Hanley DF. Spontaneous intracerebral hemorrhage. N Engl J Med. 2001;344:1450–60.
CAS Article PubMed Google Scholar
7.
Behrouz R. Re-exploring Tumor Necrosis Factor Alpha as a Target for Therapy in Intracerebral Hemorrhage. Transl Stroke Res. 2016;7:93–6.
CAS Article PubMed Google Scholar
8.
Gebel Jr JM, Jauch EC, Brott TG, Khoury J, Sauerbeck L, Salisbury S, et al. Relative edema volume is a predictor of outcome in patients with hyperacute spontaneous intracerebral hemorrhage. Stroke. 2002;33:2636–41.
Article PubMed Google Scholar
9.
Gebel Jr JM, Jauch EC, Brott TG, Khoury J, Sauerbeck L, Salisbury S, et al. Natural history of perihematomal edema in patients with hyperacute spontaneous intracerebral hemorrhage. Stroke. 2002;33:2631–5.
Article PubMed Google Scholar
10.
Qureshi AI, Ling GS, Khan J, Suri MF, Miskolczi L, Guterman LR, et al. Quantitative analysis of injured, necrotic, and apoptotic cells in a new experimental model of intracerebral hemorrhage. Crit Care Med. 2001;29:152–7.
CAS Article PubMed Google Scholar
11.
Xiong XY, Yang QW. Rethinking the roles of inflammation in the intracerebral hemorrhage. Transl Stroke Res. 2015;6:339–41.
Article PubMed Google Scholar
12.
Chen S, Yang Q, Chen G, Zhang JH. An update on inflammation in the acute phase of intracerebral hemorrhage. Transl Stroke Res. 2015;6:4–8.
CAS Article PubMed Google Scholar
13.
Hua Y, Nakamura T, Keep RF, Wu J, Schallert T, Hoff JT, et al. Long-term effects of experimental intracerebral hemorrhage: the role of iron. J Neurosurg. 2006;104:305–12.
CAS Article PubMed Google Scholar
14.
Lee ST, Chu K, Sinn DI, Jung KH, Kim EH, Kim SJ, et al. Erythropoietin reduces perihematomal inflammation and cell death with eNOS and STAT3 activations in experimental intracerebral hemorrhage. J Neurochem. 2006;96:1728–39.
CAS Article PubMed Google Scholar
15.
Zhang YL, Lautt WW. Release and regulation of endogenous adenosine during hemorrhage. Pharmacology. 1994;48:265–72.
CAS Article PubMed Google Scholar
16.
Correia-de-Sa P, Ribeiro JA. Adenosine uptake and deamination regulate tonic A2a receptor facilitation of evoked [3H] acetylcholine release from the rat motor nerve terminals. Neuroscience. 1996;73:85–92.
CAS Article PubMed Google Scholar
17.
Lindquist BE, Shuttleworth CW. Spreading depolarization-induced adenosine accumulation reflects metabolic status in vitro and in vivo. J Cereb Blood Flow Metab. 2014;34:1779–90.
CAS Article PubMed PubMed Central Google Scholar
18.
Durmaz R, Ozkara E, Kanbak G, Arslan OC, Dokumacioglu A, Kartkaya K, et al. Nitric oxide level and adenosine deaminase activity in cerebrospinal fluid of patients with subarachnoid hemorrhage. Turk Neurosurg. 2008;18:157–64.
PubMed Google Scholar
19.
Chen JF, Sonsalla PK, Pedata F, Melani A, Domenici MR, Popoli P, et al. Adenosine A2A receptors and brain injury: broad spectrum of neuroprotection, multifaceted actions and “fine tuning” modulation. Prog Neurobiol. 2007;83:310–31.
CAS Article PubMed Google Scholar
20.
Lin CL, Dumont AS, Tsai YJ, Huang JH, Chang KP, Kwan AL, et al. 17Beta-estradiol activates adenosine A(2a) receptor after subarachnoid hemorrhage. J Surg Res. 2009;157:208–15.
CAS Article PubMed Google Scholar
21.
Lin CL, Su YF, Dumont AS, Shih HC, Lieu AS, Howng SL, et al. The effect of an adenosine A1 receptor agonist in the treatment of experimental subarachnoid hemorrhage-induced cerebrovasospasm. Acta Neurochir (Wien). 2006;148:873–9. discussion 879.
CAS Article Google Scholar
22.
Schulte G, Fredholm BB. Human adenosine A(1), A(2A), A(2B), and A(3) receptors expressed in Chinese hamster ovary cells all mediate the phosphorylation of extracellular-regulated kinase 1/2. Mol Pharmacol. 2000;58:477–82.
CAS PubMed Google Scholar
23.
Dickenson JM, Blank JL, Hill SJ. Human adenosine A1 receptor and P2Y2-purinoceptor-mediated activation of the mitogen-activated protein kinase cascade in transfected CHO cells. Br J Pharmacol. 1998;124:1491–9.
CAS Article PubMed PubMed Central Google Scholar
24.
Seidel MG, Klinger M, Freissmuth M, Holler C. Activation of mitogen-activated protein kinase by the A(2A)-adenosine receptor via a rap1-dependent and via a p21(ras)-dependent pathway. J Biol Chem. 1999;274:25833–41.
CAS Article PubMed Google Scholar
25.
Sexl V, Mancusi G, Holler C, Gloria-Maercker E, Schutz W, Freissmuth M. Stimulation of the mitogen-activated protein kinase via the A2A-adenosine receptor in primary human endothelial cells. J Biol Chem. 1997;272:5792–9.
CAS Article PubMed Google Scholar
26.
Gao Z, Chen T, Weber MJ, Linden J. A2B adenosine and P2Y2 receptors stimulate mitogen-activated protein kinase in human embryonic kidney-293 cells. cross-talk between cyclic AMP and protein kinase c pathways. J Biol Chem. 1999;274:5972–80.
CAS Article PubMed Google Scholar
27.
Brust TB, Cayabyab FS, Zhou N, MacVicar BA. p38 mitogen-activated protein kinase contributes to adenosine A1 receptor-mediated synaptic depression in area CA1 of the rat hippocampus. J Neurosci. 2006;26:12427–38.
CAS Article PubMed Google Scholar
28.
Chen Z, Xiong C, Pancyr C, Stockwell J, Walz W, Cayabyab FS. Prolonged adenosine A1 receptor activation in hypoxia and pial vessel disruption focal cortical ischemia facilitates clathrin-mediated AMPA receptor endocytosis and long-lasting synaptic inhibition in rat hippocampal CA3-CA1 synapses: differential regulation of GluA2 and GluA1 subunits by p38 MAPK and JNK. J Neurosci. 2014;34:9621–43.
Article PubMed Google Scholar
29.
Kenakin T. Differences between natural and recombinant G protein-coupled receptor systems with varying receptor/G protein stoichiometry. Trends Pharmacol Sci. 1997;18:456–64.
CAS Article PubMed Google Scholar
30.
Jeong HK, Jou I, Joe EH. Absence of Delayed Neuronal Death in ATP-Injected Brain: Possible Roles of Astrogliosis. Exp Neurobiol. 2013;22:308–14.
Article PubMed PubMed Central Google Scholar
31.
Lee HT, Kim M, Jan M, Penn RB, Emala CW. Renal tubule necrosis and apoptosis modulation by A1 adenosine receptor expression. Kidney Int. 2007;71:1249–61.
CAS Article PubMed Google Scholar
32.
Aronowski J, Zhao X. Molecular pathophysiology of cerebral hemorrhage: secondary brain injury. Stroke. 2011;42:1781–6.
Article PubMed PubMed Central Google Scholar
33.
Jeong HK, Ji KM, Kim B, Kim J, Jou I, Joe EH. Inflammatory responses are not sufficient to cause delayed neuronal death in ATP-induced acute brain injury. PLoS One. 2010;5:e13756.
Article PubMed PubMed Central Google Scholar
34.
Zimmermann H, Zebisch M, Strater N. Cellular function and molecular structure of ecto-nucleotidases. Purinergic Signal. 2012;8:437–502.
CAS Article PubMed PubMed Central Google Scholar
35.
Chen J, Zhao Y, Liu Y. The role of nucleotides and purinergic signaling in apoptotic cell clearance - implications for chronic inflammatory diseases. Front Immunol. 2014;5:656.
PubMed PubMed Central Google Scholar
36.
Junger WG. Immune cell regulation by autocrine purinergic signalling. Nat Rev Immunol. 2011;11:201–12.
CAS Article PubMed PubMed Central Google Scholar
37.
Lin CL, Shih HC, Lieu AS, Lee KS, Dumont AS, Kassell NF, et al. Attenuation of experimental subarachnoid hemorrhage--induced cerebral vasospasm by the adenosine A2A receptor agonist CGS 21680. J Neurosurg. 2007;106:436–41.
Article PubMed Google Scholar
38.
Sehba FA, Flores R, Muller A, Friedrich V, Chen JF, Britz GW, et al. Adenosine A(2A) receptors in early ischemic vascular injury after subarachnoid hemorrhage. Laboratory investigation. J Neurosurg. 2010;113:826–34.
Article PubMed PubMed Central Google Scholar
39.
Kim M, Chen SW, Park SW, Kim M, D’Agati VD, Yang J, et al. Kidney-specific reconstitution of the A1 adenosine receptor in A1 adenosine receptor knockout mice reduces renal ischemia-reperfusion injury. Kidney Int. 2009;75:809–23.
CAS Article PubMed PubMed Central Google Scholar
40.
Leshem-Lev D, Hochhauser E, Chanyshev B, Isak A, Shainberg A. Adenosine A(1) and A (3) receptor agonists reduce hypoxic injury through the involvement of P38 MAPK. Mol Cell Biochem. 2010;345:153–60.
CAS Article PubMed Google Scholar
41.
Nayak GH, Prentice HM, Milton SL. Neuroprotective signaling pathways are modulated by adenosine in the anoxia tolerant turtle. J Cereb Blood Flow Metab. 2011;31:467–75.
CAS Article PubMed Google Scholar
42.
Yang T, Gao X, Sandberg M, Zollbrecht C, Zhang XM, Hezel M, et al. Abrogation of adenosine A1 receptor signalling improves metabolic regulation in mice by modulating oxidative stress and inflammatory responses. Diabetologia. 2015;58:1610–20.
CAS Article PubMed Google Scholar
43.
Tofovic SP, Salah EM, Smits GJ, Whalley ET, Ticho B, Deykin A, et al. Dual A1/A2B Receptor Blockade Improves Cardiac and Renal Outcomes in a Rat Model of Heart Failure with Preserved Ejection Fraction. J Pharmacol Exp Ther. 2016;356:333–40.
Article PubMed Google Scholar
44.
Carroll R, Yellon DM. Delayed cardioprotection in a human cardiomyocyte-derived cell line: the role of adenosine, p38MAP kinase and mitochondrial KATP. Basic Res Cardiol. 2000;95:243–9.
CAS Article PubMed Google Scholar
45.
Van Why SK, Mann AS, Ardito T, Thulin G, Ferris S, Macleod MA, et al. Hsp27 associates with actin and limits injury in energy depleted renal epithelia. J Am Soc Nephrol. 2003;14:98–106.
Article PubMed Google Scholar
46.
Huot J, Houle F, Marceau F, Landry J. Oxidative stress-induced actin reorganization mediated by the p38 mitogen-activated protein kinase/heat shock protein 27 pathway in vascular endothelial cells. Circ Res. 1997;80:383–92.
CAS Article PubMed Google Scholar
47.
Concannon CG, Orrenius S, Samali A. Hsp27 inhibits cytochrome c-mediated caspase activation by sequestering both pro-caspase-3 and cytochrome c. Gene Expr. 2001;9:195–201.
CAS Article PubMed Google Scholar
48.
Concannon CG, Gorman AM, Samali A. On the role of Hsp27 in regulating apoptosis. Apoptosis. 2003;8:61–70.
CAS Article PubMed Google Scholar
49.
Zhao L, Liu X, Liang J, Han S, Wang Y, Yin Y, et al. Phosphorylation of p38 MAPK mediates hypoxic preconditioning-induced neuroprotection against cerebral ischemic injury via mitochondria translocation of Bcl-xL in mice. Brain Res. 2013;1503:78–88.
CAS Article PubMed Google Scholar
50.
Wu H, Wu T, Li M, Wang J. Efficacy of the lipid-soluble iron chelator 2,2’-dipyridyl against hemorrhagic brain injury. Neurobiol Dis. 2012;45:388–94.
CAS Article PubMed Google Scholar
51.
Wang J, Fields J, Zhao C, Langer J, Thimmulappa RK, Kensler TW, et al. Role of Nrf2 in protection against intracerebral hemorrhage injury in mice. Free Radic Biol Med. 2007;43:408–14.
Article PubMed PubMed Central Google Scholar
52.
Nascimento FP, Figueredo SM, Marcon R, Martins DF, Macedo Jr SJ, Lima DA, et al. Inosine reduces pain-related behavior in mice: involvement of adenosine A1 and A2A receptor subtypes and protein kinase C pathways. J Pharmacol Exp Ther. 2010;334:590–8.
CAS Article PubMed Google Scholar
53.
Rosim FE, Persike DS, Nehlig A, Amorim RP, de Oliveira DM, Fernandes MJ. Differential neuroprotection by A(1) receptor activation and A(2A) receptor inhibition following pilocarpine-induced status epilepticus. Epilepsy Behav. 2011;22:207–13.
Article PubMed Google Scholar
54.
Mayne M, Fotheringham J, Yan HJ, Power C, Del Bigio MR, Peeling J, et al. Adenosine A2A receptor activation reduces proinflammatory events and decreases cell death following intracerebral hemorrhage. Ann Neurol. 2001;49:727–35.
CAS Article PubMed Google Scholar

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Acknowledgements

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Funding

This work was supported by Suzhou Key Medical Center (Szzx201501), grants from the National Natural Science Foundation of China (No. 81571115, 81422013, and 81471196), Scientific Department of Jiangsu Province (No. BL2014045), Suzhou Government (No. LCZX201301, SZS201413, and SYS201332), and A Project Funded by the Priority Academic Program Development of Jiangsu Higher Education Institutions.

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Authors’ contributions

WZ carried out the experiments. DC participated in the design of the study and performed the statistical analysis. HS helped to draft the manuscript. ZC participated in the acquisition of data. HL carried out analysis and interpretation of data. ZY participated in the design of the study. GC drafted the manuscript. All authors read and approved the final manuscript.

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The authors declare that they have no competing interests.

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Ethics approval and consent to participate

All animal experiments are strictly in accordance with the guideline of Soochow University institutional Animal Care and Use Committee.

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Department of Neurosurgery & Brain and Nerve Research Laboratory, The First Affiliated Hospital of Soochow University, 188 Shizi Street, Suzhou, 215006, China
Weiwei Zhai, Dongdong Chen, Haitao Shen, Zhouqing Chen, Haiying Li, Zhengquan Yu & Gang Chen

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Weiwei Zhai
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Dongdong Chen
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Haitao Shen
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Zhouqing Chen
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Haiying Li
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Zhengquan Yu
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Gang Chen
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Correspondence to Zhengquan Yu or Gang Chen.

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Zhai, W., Chen, D., Shen, H. et al. A1 adenosine receptor attenuates intracerebral hemorrhage-induced secondary brain injury in rats by activating the P38-MAPKAP2-Hsp27 pathway. Mol Brain 9, 66 (2016). https://doi.org/10.1186/s13041-016-0247-x

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Received: 14 March 2016
Accepted: 02 June 2016
Published: 14 June 2016
DOI: https://doi.org/10.1186/s13041-016-0247-x

Keywords

Adenosine A1 receptor
Intracerebral hemorrhage, P38, MAPKAP2, Hsp27

A1 adenosine receptor attenuates intracerebral hemorrhage-induced secondary brain injury in rats by activating the P38-MAPKAP2-Hsp27 pathway

Abstract

Background

Methods

Results

Conclusions

Background

Results

Time course

A1AR activation suppressed caspase-3 activation and albumin extravasation

A1AR decreased neuronal death and degeneration and relieved brain edema

A1AR increased phosphorylation levels of P38, MAPKAP2, and Hsp27

Blocking P38 or Hsp27 inhibited the neuroprotective effect of A1AR

Discussion and Conclusions

Methods

Study design and experimental groups

Antibodies

Establishing the ICH model

Western blot analysis

Immunofluorescence microscopy

TUNEL staining

FJB

Brain edema

EB detection

Primary neuron-enriched cultures

Treatments of neurons

Statistical analysis

Abbreviations

References

Acknowledgements

Funding

Availability of data and material

Authors’ contributions

Authors’ information

Competing interests

Consent for publication

Ethics approval and consent to participate

Author information

Affiliations

Corresponding authors

Rights and permissions

About this article

Cite this article

Keywords

Molecular Brain

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