Introduction

Many medical conditions of central nervous system are potentially life threatening, and subarachnoid hemorrhage (SAH) is one of them. The World Health Organization (WHO) reported an incidence of 22.5 cases of SAH in 100,000 individuals each year1. Due to the poor outcomes of SAH, extensive research has been conducted to better understand the disease. One highly influential factor identified previously is early brain injury (EBI)2. Individuals presented with EBI following an event of SAH typically experience abnormally enhanced inflammatory response, oxidative stress, cerebral vasospasm, and cell death3.

One key factor that influences the development of EBI following SAH is apoptosis, or cell death, and neural growth factor (NGF) and TP53 are believed to be two of the most important regulators of cell apoptosis4. If NGF is knocked out, the neuron will be destined to undergo the apoptosis5. Neural growth factor is believed to suppress apoptosis of neurons by activating phosphatidylinositol 3-kinase (PI3K)/Akt signaling. This subsequently promoted the expression of pro-apoptotic Bcl-2 family members6. TP53 is the overall most important factor in initiating the apoptosis process in response to ischemia, hypoxia, or severely damaged DNA, and it has been well studied as a tumor suppressor7.

Long non-coding RNAs (lncRNAs) is a class of non-coding RNA that is composed of more than 200 nucleotides (nt) that regulate the expression of gene(s) at transcriptional and post-transcriptional levels8. Long non-coding RNAs do not have any particular open reading frame or coding sequence9. Meanwhile, microRNAs (miRNAs) is a class of single-stranded, small non-coding RNAs consisting of between 21 and 24 nt, and they are involved in the control of multiple cellular activities such as proliferation, differentiation, and apoptosis by regulating the expression of genes at the post-transcriptional or translational level10. MicroRNA-675 (miR-675) has been reported to be a derivative of H1911. MiR-675 has been reported to suppress placental growth and promote differentiation or regeneration of skeletal muscle cells11,12. Meanwhile, let-7a has been known to be involved in regulating the apoptosis of the cells13.

Some studies have indicated that MT may be useful in ameliorating EBI, and thereby could have a protective role in the management of SAH14. In addition, MT has also been found to be able to prevent vasospasm, decrease mortality, and reduce apoptosis of neurons15,16. It has also been indicated that it can alleviate focal cerebellum injury17,18. Melatonin has been reported to protect brain against post-SAH injury19. It has been also found that administration of MT could alter the expression of lncRNA and H19, and H19 has been shown to host miR-675, and miR-675 has been found to be a negative regulator of P5320,21. In another study, H19 was found to be a competing non-coding RNA for let-7a, and let-7a was found to be a virtual regulator of NGF by using an online miRNA database (www.mirdb.org)22. In this study, we established animal model of SAH, which was treated with MT, and the possible involvement of H19-miR-675-P53-apoptosis and H19-let-7a-NGF-apoptosis signaling pathway was investigated in those animals.

Materials and methods

Animals

Healthy adult male C57BL/6J mice were used in this study. The mice were purchased from the experimental animal center of our institute and weighed between 22 and 25 g. All the experiments were carried out under the guidance of the Guide for the Care and Use of Laboratory Animals which was published by NIH and was approved by the Ethics Committee of our institute.

SAH model

The endovascular perforation method was used to establish animal model of SAH. Pentobarbital sodium (50  mg/kg) was injected to perform anesthetization. A heat blanket was used to maintain the rectal temperature at 37 ± 0.5 °C. The internal carotid artery, external carotid artery, and left common carotid artery were exposed after a midline incision at the neck. Ligation and cut at the left external carotid was finished to leave a 3-mm stump. Insertion of a nylon suture into the left internal carotid artery was accompanied to perforate the artery at the bifurcation of the anterior and middle cerebral artery. The identical procedures were performed on Sham-operated mice except the artery perforation.

Experimental protocol

The mice were assigned into the groups listed below: (1) SAH group (n = 12), (2) sham group (n = 12), (3) SAH + MT group (n = 12). Melatonin was dissolved in 1% ethanol in 1 ml saline, then Mel was intraperitoneally injected at a dose of 150 mg/kg 2 and 12 h after SAH.

Neurological score

Neurological deficits were assessed with an 18-point system from six tests at 24 h after SAH; the six tests are: forelimbs outstretching (0–3), spontaneous activity (0–3), climbing (1–3), symmetry in the movements of all limbs (0–3), response to vibrissae touch (1–3), and body proprioception (1–3). A higher score indicates an elevated function.

Brain water content

The standard wet–dry method was used to measure the brain water content. Briefly, mice were killed, and mice brains were immediately isolated and separated into the right and left cerebellum, cerebral hemispheres and brain stem; these parts were weighed respectively to obtain wet weight. Then, brain sections were dried for 24 h at 105 °C and weighed to obtain the dry weight. Finally, the brain water content was inferred as follows: (wet weight -dry weight)/wet weight × 100.

RNA isolation and real-time PCR

Total RNA extraction was performed on ancerous/non-cancerous specimens or cell lines with TRIzol® reagent (Invitrogen) following instructions indicated by the supplier. Reverse transcription of the total RNA into TP53 or NGF cDNA was accompanied with the reverse transcription kit with random primers (Invitrogen). Primers specific to H19, TUG1, SNHG14, MEG3, let-7a, miR-675, TP53 mRNA, NGF mRNA were designed and used to evaluate the expression level of these genes by real-time qPCR with SYBR® Green real-time PCR kit (Toyobo, Co., Ltd., Osaka, Japan). Each reaction contains 10 μl of PCR mix, 5 pmol of forward and reverse primers, 1 μl cDNA template and proper volume of water to achieve a 20 μl total reaction volume. Each reaction was replicated for at least three times. The reaction was performed on a Roche 480 system under conditions listed as follows: initial denaturation at 94 ˚C for 3 min; 45 cycles of denaturation at 94 ˚C for 20 s, annealing at 60 ˚C for 60 s, and elongation at 72 ˚C for 45 s; and final elongation at 72 ˚C for 3 min. The 2−ΔΔCT method was used to calculate the relative expression of genes and miRNA, including H19, TUG1, SNHG14, MEG3, let-7a, miR-675, TP53 mRNA, NGF mRNA.

Cell culture and transfection

U87 and U251 cells were cultured in DMEM high glucose medium containing 10% Fetal Bovine Serum(FBS) and maintained at 37 °C in a humidified incubator with 5 % CO2. Cells were seeded into six-well dishes and treated with MT at a final concentration of 100 nm, 1 μm, and 10 μm, respectively. When the cells were grown to 70–80% confluence, lipofectamine2000 transfection reagent (Invitrogen, California, USA) was used to transfect the U87 and U251 cells with let-7a or miR-675 based on the standard protocol by the supplier. All experiments were carried out three times.

Cell proliferation assay

The cells were seeded in a 12-well dish and incubated overnight, and the cells were incubated with or without MT for 48 h. The proliferation rates of the cells were measured with MTT assay (Sigma-Aldrich, Inc., St. Louis, MO, USA) according to the manufacturer’s instructions. Briefly, 50 mg MTT was used to treat cells in each well, dimethyl sulfoxide (DMSO) was used to dissolve the formazan, then a plate reader was used to measure the absorbance at 590 nm. The experiments were repeatedly carried out for three times.

Vector construction and mutagenesis, and luciferase assay

3′UTRs of TP53 and NGF were cloned using primers specific to these fragments. Site-directed mutagenesis of miR-675 binding sites in the 3′UTR of TP53 and let-7a binding sites in the 3′UTR of NGF was performed by using site-Directed Mutagenesis Kit (SBS Genetech). The wild-type and mutant 3′UTRs of TP53 or NGF was cloned into pGL3 at the downstream of the firefly luciferase reporter gene. U87 and U251 cells were seeded in a 24-well plate, co-transfection of miR-675, the luciferase expressing plasmid pRL-TK and TP53 reporter plasmids containing wild-type or mutant 3′UTR were performed. Similarly, co-transfection of let-7a and NGF reporter plasmids was carried out in cells. After 48 h incubation, the cells were harvested and the assay was performed using D-20/20 luminometer (Turner Biosystems).

Vector construction and mutagenesis and luciferase assay

Full fragment of the promoters of H19, TUG1, SNHG14 or MEG3 was amplified using PCR. The products were inserted into pGL3 at the upstream of the firefly luciferase reporter gene. U87 and U251 cells were seeded in a 24-well plate, and transfected with constructs containing the promoters of H19, TUG1, SNHG14 or MEG3. U87 and U251 cells were subjected to treatment with MT at a final concentration of 100 nm, 1 μm, and 10 μm, respectively. Luciferase activity of H19, TUG1, SNHG14 or MEG3 was determined using D-20/20 luminometer (Turner Biosystems).

Western blot analysis

To detect and compare the expression of TP53 and NGF protein levels, U87 and U251 cells were collected and lysed in lysis buffer (1 mm EDTA, 50 mm Tris pH 7.4, 250 mm NaCl, 0.1% NP40, 5 mm sodium fluoride (NaF), 0.5 mm NaVO3 pepstatin, benzamidine, aprotinin, phenylmethanesulfonylfluoride or phenylmethylsulfonyl fluoride (PMSF), leupeptin). The cell extracts were mixed with 0.01% bromophenol blue and 5% 2-Mercaptoethanol and boiled in a water bath. A total amount of 40 mg proteins were separated by PAGE:sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS)-PAGE and further transferred onto polyvinylidene difluoride (PVDF) membrane. phosphate buffered saline-tween (PBS-T)-dissolved 5% fat-free milk was used to block the membranes for 2 h in darkness, following which the primary antibodies against TP53 at a dilution of 1:2000 (Santa Cruz Biotechnology, CA, USA) or NGF at a dilution of 1:5000 (Santa Cruz Biotechnology, CA, USA) were incubated with the membranes at 4 ℃ for 12 h. Monoclonal anti-β-actin (Cell Signaling) was selected as the loading control. Visualization of the immune complexes was further detected with horseradish peroxidase-conjugated antiserums (Santa Cruz Biotechnology). The photographed with Chemi- Doc™ XRS System (BIO-RAD, USA) and immobilon western chemiluminescent HRP Substrate (Millipore, Billerica, MA, USA) were used to visualize the immune-complexes.

Immunohistochemistry

The immunoreactivity of TP53 and NGF is determined by using immunohistochemistry. Briefly, the sections were firstly deparaffinized and rehydrated in ethanol of graded concentrations to water. Five-minute treatment of 3% H2O2 was conducted to block the endogenous peroxidase activity, followed by water rinse and PBS washing for 15 min. Sections were further placed in citrate buffer and heated for 30 min at 95 °C in microwave oven, then cooled at RT for 20 min and rinsed in PBS. Forty-minute incubation with 5% horse serum was performed to block the nonspecific protein binding. Primary antibodies for TP53 (diluted 1:500; Santa Cruz Biotechnology) and NGF (diluted 1:500; Santa Cruz Biotechnology) were diluted and incubated with the sections at RT for 1 h. Followed by PBS washing and incubation with HRP-conjugated IgG (1:1000 dilution; Santa Cruz Biotechnology) at RT for 1 h. Hematoxylin was used to perform counterstaining with 3'-diaminobenzidine (DAB) as chromogen.

Terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL)

The apoptosis status of the brain cortex was evaluated using TUNEL assay following the instructions provided by the manufacturer. The ratio was calculated as number of TUNEL-positive neurons /total neurons.

Statistical analysis

All data analyses were performed with SPSS 21.0 software (IBM, Chicago, IL), and Chi square test, t-test, or one-way ANOVA were used to examine the difference of the study targets among the groups. P < 0.05 was considered statically significant.

Results

Melatonin affected H19 level by influencing H19 promoter transcription efficiency

Real-time PCR and luciferase assay were utilized to explore the effect of MT on H19 transcriptional efficiency. Different doses of MT (100 nm, 1 μm, 10 μm) were utilized to treat U87 cells and U251 cells. Then real-time PCR was performed to examine and compare the expression level of candidate lncRNAs including H19, TUG1, SNHG14, MEG3 between MT treated and untreated groups. As shown in Fig. 1, MT-treated U87 cells (Fig. 1a) and U251 (Fig. 1b) cells showed a stepwise increase in H19 level as the concentration of MT increased, while TUG1, SNHG14, MEG3 levels in MT-treated U87 (Fig. 1a) and U251 (Fig. 1b) showed no obvious difference between the two groups. Furthermore, luciferase assay was conducted to confirm whether MT affected H19 level by influencing H19 transcriptional efficiency, and luciferase activity of H19 in MT-treated U87 cells (Fig. 1c) or U251 cells (Fig. 1d) was increased in a concentration-dependent manner in comparison with the control.

Fig. 1: MT modulated H19 level by affecting H19 promoter transcription efficiency (*P < 0.05 compared with the control)
figure 1

a Only H19 among H19, TUG1, SNHG14, MEG3 was increased following MT treatment, and under a concentration manner in U87 cells. b Only H19 among H19, TUG1, SNHG14, MEG3 was dose-dependently increased following MT treatment in U215 cells. c Only luciferase activity of H19 among H19, TUG1, SNHG14, MEG3 was dose-dependently upregulated subsequent to treatment with MT in U87 cells. d Only luciferase activity of H19 among H19, TUG1, SNHG14, MEG3 was dose-dependently upregulated subsequent to treatment with MT in U251 cells

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MiR-675 or let-7a directly targeted P53 or NGF, respectively

Both miR-675 and let-7a have been reported to be functionally associated with H19, and we further search the online miRNA database for the potential target of the miRNAs. We identified P53 or NGF as the candidate target gene of miR-675 or let-7a respectively with the “seed sequence” in the 3′UTR. And luciferase assay results showed that miR-675 suppressed luciferase activity of wild-type but not that of mutant P53 3′UTR in either U87 cells (Fig. 2a) or U251 cells (Fig. 2b) compared to that in the control. Meanwhile, let-7a suppressed luciferase activity of wild-type but not that of mutant NGF 3′UTR in either U87 cells (Fig. 2c) or U251 cells (Fig. 2d) compared to that in the control, suggesting that P53 was a direct target gene of miR-675, and NGF was a direct target gene of let-7a.

Fig. 2: P53 or NGF was candidate gene of miR-675 or let-7a, respectively (*P < 0.05 compared with the control)
figure 2

a miR-675 evidently inhibited luciferase activity of wild-type P53 3′UTR but not that of mutant P53 3′UTR in U87 cells. b miR-675 evidently inhibited luciferase activity of wild-type P53 3′UTR but not that of mutant P53 3′UTR in U251 cells. c Luciferase activity of wild-type but not mutant NGF 3′UTR in U87 cells transfected with let-7a mimic was much lower. d Luciferase activity of wild-type but not mutant NGF 3′UTR in U251 cells transfected with let-7a mimic was much lower

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MT affected cell apoptosis, H19, miR-675, let-7a, TP53, NGF levels

To verify the protective role of MT against apoptosis, sub-lethal concentration of H2O2 (<200 μm), or H2O2 along with various doses of MT was utilized to treat U87 and U251 cells. As shown in Figs. 3a and 4a, the number of SA-b-gal (senescence-associated b-galactosidase)-positive U87 (Fig. 3a) and U251 (Fig. 4a) cells treated with H2O2 were greater than control, while 1 μm and 10 μm of MT inhibited premature senescence of U87 cells (Fig. 3a) and U251 cells (Fig. 4a). Co-culture with H2O2 obviously upregulated expressions of H19 (Figs. 3b and 4b), miR-675 (Figs. 3c and 4c), NGF (Figs. 3e and 4e) in U87 cells (Fig. 3) and U251 cells (Fig. 4), as well as the viability of U87 cells (Fig. 3g) and U251 cells (Fig. 4g), which were partly restored by the administration of MT. By contrast, H2O2 remarkably inhibited expressions of let-7a (Figs. 3d and 4d), TP53 (Figs. 3f and 4f) in U87 cells (Fig. 3) and U215 cells (Fig. 4), as well as the apoptosis of U87 cells (Fig. 3h) and U251 cells (Fig. 4h), and the inhibition of H2O2 on let-7a, TP53, and cell apoptosis were partly abrogated by co-culture with MT.

Fig. 3: MT regulated cell apoptosis, H19, miR-675, let-7a, TP53, NGF levels in U87 cells (*P < 0.05 compared with the control)
figure 3

a H2O2 treatment increased number of SA-b-gal, which was restored by 1 and 10 μm of MT administration. b H19 level in H2O2 treatment group was much lower than H2O2 plus MT treatment group; both of them were much lower than control. c miR-675 level in H2O2 plus MT treatment group was much lower than control, and was even lower in H2O2 treatment group. d let-7a level in H2O2 treatment group was much higher than H2O2 plus MT treatment group; both of them were much higher than control. e NGF level in H2O2 plus MT treatment group was much lower than control, and was even lower in H2O2 treatment group. f TP53 level in H2O2 treatment group was much higher than H2O2 plus MT treatment group; both of them were much higher than control. g Treating with H2O2 or H2O2 plus MT inhibited proliferation of U87 cell, but the inhibition effect of H2O2 was much stronger than H2O2 plus MT. h Treating with H2O2 or H2O2 plus MT promoted apoptosis of U87 cell, but the promotion effect of H2O2 was much stronger than H2O2 plus MT

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Fig. 4: MT regulated cell apoptosis, H19, miR-675, let-7a, TP53, NGF levels in U251 cells (*P < 0.05 compared with the control)
figure 4

a H2O2 treatment increased number of SA-b-gal, which was restored by 1 and 10 μm of MT administration. b H19 level in H2O2 treatment group was much lower than H2O2 plus MT treatment group; both of them were much lower than control. c miR-675 level in H2O2 plus MT treatment group was much lower than control, and was even lower in H2O2 treatment group. d let-7a level in H2O2 treatment group was much higher than H2O2 plus MT treatment group; both of them were much higher than control. e NGF level in H2O2 plus MT treatment group was much lower than control, and was even lower in H2O2 treatment group. f TP53 level in H2O2 treatment group was much higher than H2O2 plus MT treatment group; both of them were much higher than control. g Treating with H2O2 or H2O2 plus MT inhibited proliferation of U251 cell, but the inhibition effect of H2O2 was much stronger than H2O2 plus MT. h Treating with H2O2 or H2O2 plus MT promoted apoptosis of U251 cell, but the promotion effect of H2O2 was much stronger than H2O2 plus MT

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Melatonin provided the brain relief from edema and neurological deficits after SAH

We further established the animal models of SAH, which were treated with administration of MT, and the brain water content and neurological scores were examined within 24 h following the SAH. We found that the mice in the SAH group displayed an evident decline in neurological score (Fig. 5a), as well as an obvious increase in water content of different anatomical brain structure including (Fig. 5b−e). We also noticed MT treatment improved the neurological deficits (Fig. 5a) and attenuated the brain swelling (Fig. 5b−e) 24 h following SAH event.

Fig. 5: The effects of MT on water content of brain and neurological deficits (*P < 0.05 compared with the sham group)
figure 5

a SAH group displayed a lower level of water content in brain, and MT treatment improved neurological score. b Evident increase in brain swelling, including left, right, cerebellum, and brain stem (b−e) in the SAH group, which was improved by MT treatment

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MT inhibited apoptosis of neuronal in the brain cortex caused by SAH

TUNEL assay was utilized to evaluate the apoptosis of the neurons. As shown in Fig. 6, evident increase in apoptotic index in the SAH group compared with the sham group. MT treatment remarkably repressed apoptosis of neurons in the brain 24 h after SAH.

Fig. 6: MT suppressed apoptosis of neuronal in the brain cortex induced by SAH
figure 6

a Apoptosis status in the sham group, b apoptosis status in the SAH group, c apoptosis status in the SAH group treated with MT, d summary and comparison between the sham group, SAH group, and SAH + MT group (*P < 0.05 compared with the sham group)

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Determination of the effect of MT on H19, miR-675, let-7a, TP53, and NGF

Real-time polymerase chain reaction(PCR) and western blot analysis were utilized to detect the effect of MT on H19, miR-675, let-7a, TP53, and NGF expressions. As shown in Fig. 7, levels of H19 mRNA (Fig. 7a), miR-675 mRNA (Fig. 7b), NGF mRNA, and protein (Fig. 7d) were much higher in the SAH  +  MT group than in the sham group, while the SAH group displayed even higher levels of H19 (Fig. 7a), miR-675 (Fig. 7b), and NGF (Fig. 7d). However, levels of let-7a mRNA (Fig. 7c), TP53 mRNA, and protein (Fig. 7e) were much lower in the SAH + MT group than in the sham group, while the SAH group displayed even lower levels of let-7a and TP53.

Fig. 7: Effects of MT on H19, miR-675, let-7a, TP53, and NGF expressions were detected using real-time PCR and western blot analysis (*P < 0.05 compared with the sham group)
figure 7

a H19 level in the SAH group was much lower than in the SAH  +  MT treatment group; both of them were much lower than the sham group. b miR-675 level in the SAH  +  MT treatment group was much lower than control, and was even lower in the SAH group. c let-7a level in the SAH group was much higher than in the SAH  +  MT treatment group; both of them were much higher than the sham group. d NGF level in the SAH  +  MT treatment group was much lower than the sham group, and was even lower in the SAH group. e TP53 level in the SAH group was much higher than in the SAH  +  MT treatment group; both of them were much higher than the sham group

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Differential levels of TP53 and NGF among different groups

Immunohistochemistry was conducted to measure protein levels of TP53 and NGF among the sham, SAH, and SAH  +  MT groups. As shown in Fig. 8, NGF protein level (Fig. 8a−c) in the SAH group was much lower than in the SHA + MT group, and both were much lower than the sham group; meanwhile, TP53 protein level (Fig. 8d−f) in the SAH group was much higher than in the SHA + MT group, and both of them were much higher than the sham group.

Fig. 8: Levels of TP53 and NGF were different among different groups
figure 8

a−c NGF protein level in the SAH  +  MT treatment group was much lower than in the sham group, and was even lower in the SAH group. d−f TP53 protein level in the SAH group was much higher than in the SAH  +  MT treatment group; both of them were much higher than the sham group

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Discussion

Melatonin has been reported to be used to treat neurological diseases, and the majority of this study has been focused on its ability to scavenger free radicals by promoting production of anti-oxidant enzymes and further initiating the synthesis of glutathione23,24,25,26. The focus of this present study was to explore its ability to attenuate signals of apoptosis, thereby preventing EBI following an event of SAH, by its interaction with non-coding RNA as well as their target genes. It has been shown that MT administration could alter the expression of H19, an lncRNA, that has been reported to be involved in the control of cellular apoptosis27. Recent studies have revealed that expression of H19 was substantially upregulated in response to a cerebral I/R injury28. In this study, we performed real-time polymerase chain reaction(PCR) and luciferase assay to investigate the effect of MT on transcriptional efficiency of H19 promoter, and we found that MT treatment upregulated H19 expression level, possibly by enhancing the transcriptional efficiency of H19 promoter.

Matouk et al. reported that the expression of Let-7a is up-regulated in the development of cerebral I/R brain29. If the upregulation was restored, the apoptosis as well as subsequent inflammation would be attenuated, lessening the injury to the nervous system30. Some studies have suggested that lincRNA is a precursor to other RNAs, which are notably smaller, with regulatory functionality. An example of a small RNA would be miRNAs. As it is understood that H19 is involved in apoptosis, it is not surprising that exon 1 is home to an miRNA. Closer examination of this miRNA indicates that there is a hairpin within it, providing a template for miR-675-5p and miR-675-3P31. In line with this, we confirmed that upregulation of H19 increased the expression of miR-675 in our study. Meanwhile, we also found that H19 is an endogenous competing RNA of let-7a by using luciferase reporter system. Furthermore, we searched the online miRNA database for the potential target of the H19-associated miRNAs (miR-675 and let-7a), and identified P53 or NGF as the virtual target gene of miR-675 or let-7a, respectively with the “seed sequence” in the 3′UTR, and the results of the following luciferase assay confirmed such regulatory association between the miRNAs and targets.

Accumulating evidence has indicated that SAH or other types of hemorrhage exposure inevitably induces cell death in human brains, and others have highlighted that inflammation occurring following the initial SAH could be a significant factor in the cell death that follows32. Our hypothesis was that MT treatment could ameliorate EBI by suppressing the apoptosis of neurons following an event of SAH by alternating the expression of the associated miRNAs such as miR-675 and let-7a.

Nerve growth factor is a neurotrophic factor and a neuropeptide that is primarily involved in the control of various functions including formation of synapses, and development, plasticity, growth, maintenance, apoptosis, and viability of neurons33. Neural growth factor has been shown to protect neurons against apoptosis by its ability to interact with some other anti-apoptotic genes such as PI3K, extracellular signal-related kinase/mitogen-activated protein kinase and phospholipase C pathways33. In addition, NGF has also been reported to protect the neurons against oxidative stress and toxin-induced apoptosis33. Another study indicated that NGF is capable of counteracting apoptosis, regardless of the causal factor34.

P53 is a known key tumor suppressor as it is a central hub where stress pathways are signaled. Therefore, it is effectively the region that controls the fate of human cells35. Apoptosis, or cell death, is valuable to maintain homeostasis when it is executed appropriately. For example, chemotherapeutic drugs and radiation are intended to place cellular stress on cancer cells and actively promote apoptosis35. Recent research indicated that p53 promoted the apoptosis via mitochondrial pathway, and this research is further supported by studies demonstrating that activation of Bax was mediated by suppressing p5340. Furthermore, activation of Bcl-2 protected against the apoptosis. It is also suggested that inhibiting Caspase 3 may be effective in preventing apoptosis, which would help to minimize the risk of EBI following an event of SAH36. In this study, we established the animal models of SAH, and found that MT treatment improved the neurological score and caused an evident decline in the brain swelling. Using TUNEL assay, we showed that MT inhibited apoptosis of neuronal in the brain cortex caused by SAH. Furthermore, the H19, miR-675, and NGF were decreased in response to SAH, while let-7a and TP53 were increased during this same process. Administration of MT to the SAH animal model partially, but significantly, restored the alternation of those ncRNAs and genes.

Conclusion

Our study revealed for the first time that H19 regulates brain injury after SAH via microRNA -675 and let-7a by interacting with apoptosis induced by P53 and NGF. In this study, we found that administration of MT upregulated expression of H19, and H19 was shown to host miR-675, and miR-675 has been found to be a negative regulator of P53; meanwhile H19 was found to be a competing non-coding RNA for let-7a, and let-7a was found to be a virtual regulator of NGF. P53 and NGF were two important modulators of cell apoptosis, and finally influencing progression of brain injury after SAH. Our study revealed the involvement of H19-miR-675-P53-apoptosis and H19-let-7a-NGF-apoptosis signaling pathway in brain injury after SAH38,39,40.