- Research article
- Open Access
Propofol inhibited autophagy through Ca2+/CaMKKβ/AMPK/mTOR pathway in OGD/R-induced neuron injury
Molecular Medicine volume 24, Article number: 58 (2018)
The neuroprotective role of propofol (PPF) in cerebral ischemia-reperfusion (I/R) has recently been highlighted. This study aimed to explore whether the neuroprotective mechanisms of PPF were linked to its regulation of Ca2+/CaMKKβ (calmodulin-dependent protein kinase kinase β)/AMPK (AMP-activated protein kinase)/mTOR (mammalian target of rapamycin)/autophagy pathway.
Cultured primary rat cerebral cortical neurons were treated with oxygen-glucose deprivation and re-oxygenation (OGD/R) to mimic cerebral I/R injury in vitro.
Compared with the control neurons, OGD/R exposure successfully induced neuronal I/R injury. Furthermore, OGD/R exposure notably caused autophagy induction, reflected by augmented LC3-II/LC3-I ratio and Beclin 1 expression, decreased p62 expression, and increased LC3 puncta formation. Moreover, OGD/R exposure induced elevation of intracellular Ca2+ concentration ([Ca2+]i). However, PPF treatment significantly antagonized OGD/R-triggered cell injury, autophagy induction, and [Ca2+]i elevation. Further investigation revealed that both autophagy induction by rapamycin and [Ca2+]i elevation by the Ca2+ ionophore ionomycin significantly reversed the PPF-mediated amelioration of OGD/R-triggered cell injury. Importantly, ionomycin also significantly abrogated the PPF-mediated suppression of autophagy and CaMKKβ/AMPK/mTOR signaling in OGD/R-exposed neurons. Additionally, activation of CaMKKβ/AMPK/mTOR signaling abrogated the PPF-mediated autophagy suppression.
Our findings demonstrate that PPF antagonized OGD/R-triggered neuronal injury, which might be mediated, at least in part, via inhibition of autophagy through Ca2+/CaMKKβ/AMPK/mTOR pathway.
Cerebral ischemia-reperfusion (I/R) injury is characterized by an insufficient oxygen supply and restoration of blood flow and serves as the main cause for the aggravation of cerebral injury and functional impairment (He et al. 2016). This injury involves complex and multi-factorial mechanisms, including intracellular Ca2+ overload and damage to oxidative stress (Chen et al. 2017; Liu et al. 2011). Interestingly, it has been shown that several anesthetic drugs, including isoflurane and propofol (PPF), exert neuroprotective influence on cerebral I/R injury (Li et al. 2013; Wang et al. 2016).
PPF (2, 6-diisopropylphenol) is an intravenous sedative-hypnotic agent and has been extensively utilized in general anesthesia and sedation (Wahr et al. 2000). In addition to its sedative and hypnotic effects, the neuroprotective role of PPF in transient global and focal cerebral I/R has recently been highlighted in both animal and cell models (Wang et al. 2016; Wang et al. 2011). The mechanisms responsible for the neuroprotection of PPF involve the inhibition of apoptosis (Tao et al. 2016), Ca2+ overload (Wang et al. 2016), oxidative stress injury (Yu et al. 2018), and so forth.
Recent studies concerning the neuroprotective mechanisms of PPF have focused on autophagy (Cui et al. 2012; Noh et al. 2010). Autophagy is a basic catabolic mechanism which degrades intracellular components and damaged organelles to maintain intracellular homeostasis (Choi et al. 2013). At present, the exact role of autophagy in ischemic brain injury remains controversial (Peng et al. 2018; Hua et al. 2018; Zheng et al. 2018). It has been demonstrated that increased autophagy acts as a compensatory protective mechanism for I/R injury (Su et al. 2014). In contrast, another study has suggested that inhibition of autophagy reduces infarct volume, brain edema, and motor deficits, in a rat model of permanent focal cerebral ischemia (Wen et al. 2008). Of note, PPF has been shown to prevent cerebral ischemia-triggered autophagy activation and cell death in the rat hippocampus after a cerebral I/R insult (Cui et al. 2013). Recent studies have emphasized the correlation between autophagy and Ca2+. It has been demonstrated that accumulation of intracellular Ca2+ concentration ([Ca2+]i) activates CaMKKβ (calmodulin-dependent protein kinase kinase β)/AMPK (AMP-activated protein kinase) signaling cascade, leading to mTOR (mammalian target of rapamycin) signaling inhibition, and thus autophagy induction (Shi et al. 2018; Zhang et al. 2015; Lee et al. 2012).
Based on the aforementioned studies, we hypothesized that PPF might play a neuroprotective role in cerebral I/R injury through inactivation of Ca2+/CaMKKβ/AMPK/mTOR/autophagy pathway. To test this hypothesis, cultured primary rat cerebral cortical neurons were treated with oxygen-glucose deprivation and re-oxygenation (OGD/R) to mimic cerebral I/R injury in vitro. We first explored the effects of PPF on OGD/R-induced neuronal injury in rat primary cerebral cortical neurons. Afterwards, we verified whether the neuroprotective mechanisms of PPF were associated with the regulation of Ca2+/CaMKKβ/AMPK/mTOR/autophagy pathway.
All animal-related experiments in this study were approved by the Ethics Committee for Animal Experimentation of Xiangya Hospital, Central South University and were performed in accordance with the guidelines for the Care and Use of Laboratory Animals of the National Institutes of Health.
Primary culture of cerebral cortical neurons
Primary rat cerebral cortical neurons were isolated from the cerebral cortex of fetal Sprague-Dawley rats at embryonic day 17 as previously described (Liu et al. 2018), with some alterations. Briefly, the dissected cortices were dissociated with 0.125% trypsin (Gibco, Grand Island, NY, USA) under sterile conditions at 37 °C for 10 min. Neurons were suspended in Dulbecco’s Modified Eagle’s Medium (DMEM, Gibco, Thermo Fisher Scientific, Inc., Waltham, MA, USA) containing 10% fetal bovine serum (FBS, Gibco) to inactivate the trypsin, and then filtered through a cell strainer. Afterwards, cells were seeded into 6-well plates or coverslips those were pre-coated with poly-D-lysine (Sigma-Aldrich, St. Louis, MO, USA). After 24 h of incubation, the medium was replaced with Ca2+-free and serum-free Neurobasal medium supplemented with 2% B27 and 0.5 mM glutamine (Gibco), and half of the medium was changed every 2–3 days. Cells were maintained in humidified air with 5% CO2 at 37 °C. All experiments were performed on neurons after 10 days in culture. To determine the purity of neurons, cerebral cortical neurons were subjected to neuron-specific enolase (NSE) staining under fluorescent microscopy (Leica, DMI 4000 B, Japan) at day 10 after the culture.
Neuronal I/R injury model induced by OGD/R and drug treatment
To mimic cerebral I/R in vitro, oxygen-glucose deprivation/reperfusion (OGD/R) was performed as described previously (Liu et al. 2018). Oxygen-glucose deprivation (OGD): Primary cerebral cortical neurons were washed twice with phosphate-buffered saline (PBS, pH 7.4) and then refreshed with the glucose-free DMEM (Gibco). After that, cell cultures were transferred into a hypoxia chamber (containing a gas mixture of 5% CO2 and 95% N2) at 37 °C to produce OGD condition in cultured neurons.
Reperfusion (R): After 4 h of incubation in the hypoxic chamber (the above-mentioned OGD process), the neurons were incubated again in Neurobasal medium containing 2% B27 and 0.5 mM glutamine and then returned to the normoxic incubator (95% air/5% CO2) for 24 h at 37 °C. Cells without any treatment served as the control group.
For PPF treatment, cultured cortical neurons (5 × 105) were treated with different doses of PPF (0, 0.01, 0.03 and 0.05 mM in 0.1% DMSO; Sigma-Aldrich, St. Louis, MO, USA) during the period of OGD/R.
Cell viability and LDH secretion
Cell viability and LDH leakage assays were performed to evaluate neuronal damage as previously described (Liu et al. 2018). After OGD/R treatment, primary cultured cortical neurons were incubated with Cell Counting Kit-8 (CCK-8; Sigma-Aldrich) solution for another 4 h. Absorbance was measured using a microplate reader at 450 nm to assess cell viability. In addition, an LDH-Cytotoxicity Assay Kit (Sigma-Aldrich) was used to assess the activity of LDH. Briefly, the culture media of cortical neurons were collected after exposure to OGD/R and then centrifuged to obtain the supernatant. The cells were lysed with 1% Triton X-100 (Sigma-Aldrich) and centrifuged to remove cellular debris. After that, the culture supernatant and cell lysates were respectively incubated with LDH reaction mixture at 37 °C for 15 min. The absorbance was read at 490 nm when the reaction was stopped, and LDH release was expressed as a percentage of total LDH.
Cell apoptosis assay
An annexin V-fluorescein isothiocyanate (FITC)/propidium iodide (PI) cell apoptosis kit was used according to the instructions (Invitrogen, Thermo Fisher Scientifc, Inc., Waltham, MA, USA) to quantify cell apoptosis. After exposure to OGD/R, the primary rat cortical neurons were collected by trypsinization and washed twice with cold phosphate buffered saline (PBS). After centrifugation at 1,500 rpm for 5 min, the cells were resuspended in binding buffer and then incubated with FITC-labeled Annexin V and PI in the dark for 15 min. Cells were analyzed using the FACScan flow cytometry (BD Biosciences).
Western blot was performed to detect protein expression as previously described (Yuan et al. 2012). Briefly, total proteins from primary rat cortical neurons were isolated using the protein buffer (Beyotime, Shanghai, China). Proteins were then separated by 10% SDS-PAGE and transferred onto PVDF membranes. After being blocked with 5% fat-free milk, the membranes were incubated at 4 °C overnight with primary antibodies against p62 (1:1,000, Abcam, Cambridge, MA, USA), Beclin-1 (1:1,000, Abcam), microtubule-associated protein 1 light chain 3 (LC3-I and LC3-II, both from Anti-LC3B antibodies, 1:1,000, Sigma-Aldrich), CaMKKβ (1:1,000, Abcam), AMPK (1:1,000, Cell Signaling Technology Inc., Danvers, MA, USA), phospho (p)-AMPK (1:1,000, Cell Signaling Technology Inc.), mTOR (1:1,000, Cell Signaling Technology Inc.), and p-mTOR (1:1,000, Cell Signaling Technology Inc.). Subsequently, membranes were incubated for 2 h at room temperature with horseradish peroxidase (HRP)-secondary antibodies in TBST. The protein was visualized using the ECL detection system (Beyotime, Shanghai, China). The band intensity was quantified with Image-Pro Plus 6.0 software.
Green fluorescent protein (GFP)-LC3 immunofluorescence
Transfection of GFP-LC3 was performed according to the manufacturer’s instructions (Genomeditech, Shanghai, China). Culture medium was removed, washed three times with PBS, and then fixed with 5% paraformaldehyde for 10 min at room temperature. Coverslips were again washed three times with PBS, permeabilized with 0.3% Triton-X for 5 min, and stained with DAPI for 3 min. Finally, the coverslips were washed three times with PBS, once with ddH2O, and mounted on tissue slides with mounting medium (Thermo Fisher Scientific, Inc.). Fluorescence images were captured and analyzed under a fluorescence microscope (Nikon Corporation, Tokyo, Japan).
Intracellular Ca2+ concentration assessment
The intracellular Ca2+ concentration ([Ca2+]i) was assessed using fluorescent dye Fluo-3 AM/Pluronic F127 as previously described (Wang et al. 2016). After the indicated treatment, primary rat cortical neurons were seeded on a cover glass and incubated with 5 μM Fura-3/AM and 0.05% Pluronic F-127 (Invitrogen) for 45 min at 37 °C. The coverslips were then equilibrated in Hanks solution. After incubation at 37 °C for 30 min, the samples were determined by a laser scanning confocal microscope under the excitation 488 nm and emission 525 nm to detect fluorescence intensity.
The CaMKKβ cDNA fragment was cloned into pcDNA 3.1, generating pcDNA3.1- CaMKKβ. Cultured primary rat cortical neurons were transfected with pcDNA3.1- CaMKKβ using Lipofectamine 2000 (Invitrogen, USA) according to the manufacturer’s instructions.
All statistical analyses were performed using SPSS statistical software package standard version 16.0 (SPSS, Inc., Chicago, IL, USA). The data are presented as the mean ± standard deviation (SD) from three independent experiments. The unpaired Student’s t-test was used to analyze differences between two groups. One-way analysis of variance (ANOVA) followed by Tukey’s post hoc test was used to analyze differences among multiple groups. p < 0.05 was considered to indicate a statistically significant difference.
Neuronal I/R injury model was successfully induced by OGD/R
After being cultured for 10 days, rat primary cortical neurons exhibited plump cell body, apparent halo, and complete neural network (Fig. 1a), with a high purity indicated by NSE immunohistochemistry staining (Fig. 1b). The cultured primary cerebral cortical neurons were then subjected to oxygen-glucose deprivation for 4 h followed by 24 h of reoxygenation (OGD/R) to mimic cerebral I/R injury in vitro. Afterwards, cell viability and LDH secretion were performed to evaluate the neuronal injury. Data revealed that OGD/R-exposed cortical neurons exhibited notably increased LDH leakage rate and decreased cell viability, as compared with the control cells without OGD/R exposure (Fig. 1c and d). Collectively, these results indicated that OGD/R exposure successfully induced a model of neuronal I/R injury in cerebral cortical neurons.
PPF antagonized OGD/R-triggered cell injury, autophagy induction and [Ca2+]i elevation
PPF (0.03 and 0.05 mM) significantly antagonized OGD/R-triggered cell injury indicated by inhibition of OGD/R-induced LDH release and restoration of OGD/R-suppressed cell viability by PPF treatment, in a dose-dependent manner (Fig. 2a and b). Furthermore, as shown in Fig. 2c and d, OGD/R exposure greatly induced an increase in protein expression of Beclin-1, LC3-II but induced a decrease in p62. Moreover, the LC3-II/LC3-I ratio, which is indicative of the status of autophagy, was also upregulated by OGD/R exposure. In addition, immunofluorescence images showed strong GFP-LC3 puncta and increased the percentage of GFP-LC3 cells in cortical neurons under OGD/R exposure compared with the control cells (Fig. 2f). These results suggested that OGD/R exposure induced autophagy. However, PPF dose-dependently diminished the OGD/R-induced autophagy level (Fig. 2c, d and f). Moreover, PPF notably reduced the OGD/R-induced intracellular Ca2+ concentration ([Ca2+]i), as manifested by decreased fluorescence intensity of Ca2+ dyed with the explorer Fluo-3, AM and Pluronic F-127 (Fig. 2e).
Autophagy induction abolished the PPF-mediated amelioration of OGD/R-triggered cell injury
To address the role of autophagy in the PPF-mediated amelioration of OGD/R-triggered neuronal injury, we pre-treated OGD/R-exposed neurons with autophagy activator rapamycin, followed by PPF treatment (30 μM in 0.1% DMSO). As indicated in Fig. 3a and b, rapamycin significantly restored the PPF-suppressed autophagy level in OGD/R-exposed neurons, as manifested by an increase in LC3II and Beclin-1 expression, LC3II/LC-I ratio and a decrease in p62 expression. Importantly, activation of autophagy by rapamycin significantly reversed the PPF-mediated inhibition of LDH leakage and cell apoptosis, plus induction of cell viability in OGD/R-exposed neurons (Fig. 3c-e), indicating the involvement of autophagy in the PPF-mediated amelioration of OGD/R-triggered cell injury.
[Ca2+]i abrogated the PPF-mediated amelioration of OGD/R-triggered cell injury
To determine the role of [Ca2+]i in the PPF-mediated amelioration of OGD/R-triggered neuronal injury, we pre-treated OGD/R -exposed neurons with a Ca2+ ionophore (ionomycin, 0.3 μM) or an intracellular calcium chelator (BAPTA, 5 μM), followed by PPF treatment (30 μM in 0.1% DMSO). Ionomycin is a calcium ionophore that dose-dependently increases intracellular calcium (Natoli et al. 2014). As expected, ionomycin pre-treatment significantly restored the PPF-suppressed [Ca2+]i in OGD/R-exposed neurons, as evidenced by an increase in Ca2+ fluorescence intensity (Fig. 4a). Importantly, ionomycin, similar to the autophagy activator rapamycin, significantly reversed the PPF-mediated inhibition of LDH leakage and cell apoptosis, plus induction of cell viability in OGD/R-exposed neurons (Fig. 4b-d). On the other hand, pre-treatment with BAPTA alone, which has been generally used to block intracellular calcium, significantly alleviated OGD/R-triggered cell injury, as indicated by reduced LDH leakage (Additional file 1: Figure S1A) and induced cell viability (Additional file 1: Figure S1B) by BAPTA when compared with the vehicle DMSO group. Furthermore, BAPTA pre-treatment enhanced the PPF-mediated amelioration of OGD/R-triggered cell injury, indicating the [Ca2+]i suppression in attenuating OGD/R-triggered cell injury (Additional file 1: Figure S1). Together, these results suggested that [Ca2+]i elevation abrogated the PPF-mediated amelioration of OGD/R-triggered cell injury.
[Ca2+]i elevation abolished the PPF-mediated suppression of autophagy in OGD/R-exposed neurons
We then investigated the role of [Ca2+]i in the PPF-mediated suppression of autophagy in OGD/R-exposed neurons. The results demonstrated that elevation of [Ca2+]i by ionomycin significantly abrogated the PPF-mediated suppression of autophagy in OGD/R-exposed neurons, as indicated by an increase in LC3II and Beclin-1 protein expression (Fig. 5a and b) and GFP-LC3 puncta (Fig. 5c), plus a decrease in p62 (Fig. 5a and b) compared with the PPF alone-treated group.
Ca2+/CaMKKβ/AMPK/mTOR signaling was involved in the PPF-mediated suppression of autophagy
Finally, we explored the potential mechanism by which PPT suppressed autophagy. It has been reported that CaMKKβ activates AMPK by phosphorylation in response to increased [Ca2+]i, and that AMPK activates autophagy by down-regulating the activity of mTOR (Shi et al. 2018; Zhang et al. 2015; Lee et al. 2012; Zhang et al. 2017). As indicated in Fig. 6a, PPF significantly decreased the OGD/R-induced increase in protein expression of CaMKKβ and phosphorylation level of AMPK. In contrast, PPF obviously increased the OGD/R-mediated decrease in the phosphorylation level of mTOR. However, elevation of [Ca2+]i by ionomycin significantly abolished the effects of PPF on the expression of these proteins, indicating the involvement of [Ca2+]i in the PPF-mediated regulation of CaMKKβ/AMPK/mTOR signaling. Of note, overexpression of CaMKKβ or activation of AMPK pathway by AICAR significantly abrogated the PPF-mediated decrease in CaMKKβ protein expression and p-AMPK/AMPK ratio plus the increase in p-mTOR/mTOR ratio (Fig. 6b and c).
Subsequently, we investigated the effects of activation of CaMKKβ/AMPK/mTOR pathway on the PPF-mediated suppression of autophagy. Data revealed that activation of CaMKKβ/AMPK/mTOR pathway by overexpression of CaMKKβ and AICAR treatment significantly abolished the PPF-mediated autophagy suppression, as evidenced by an increase in LC3-II and Beclin-1 protein expression plus GFP-LC3 puncta, and a decrease in p62 compared with the PPF alone-treated group (Fig. 6d-e).
Collectively, these results indicated that Ca2+/CaMKKβ/AMPK/mTOR signaling was involved in the PPF-mediated suppression of autophagy in OGD/R-exposed neurons.
PPF has been widely used in anesthesia induction, maintenance, and intensive care. In addition to its sedative and hypnotic effects, PPF has also been shown to exert neuroprotective effects on cerebral I/R injury (Li et al. 2013; Wang et al. 2016). Of note, PPF could reduce both cerebral blood flow and cerebral metabolic rate of oxygen, whereas could not cause the risk of increasing intracranial pressure compared with other anesthetic drugs. A previous study demonstrated that PPF (1–50 μM) which was added during OGD/R period exerted a neuroprotective effect against OGD/R-induced cell injury in primary hippocampal neurons (a model of cerebral I/R in vitro), whereas PPF (100–200 μM) caused a more severe injury compared with OGD/R group (Wang et al. 2016). In accordance with this, our study also shows that PPF treatment (0.03 and 0.05 mM) during OGD/R period significantly antagonized OGD/R-triggered cell injury in primary rat cerebral cortical neurons (a model of cerebral I/R in vitro).
Recent studies concerning the neuroprotective mechanisms of PPF have focused on autophagy (Cui et al. 2012; Noh et al. 2010). Blood reperfusion following cerebral ischemia often leads to inflammation, oxidative stress, and endoplasmic reticulum stress, which can induce autophagy (T Y, 2013). OGD/R exposure is generally used to induce cerebral I/R injury and has been shown to induce autophagy in cultured cortical neurons (Qin et al. 2015). Basal autophagy plays an important role in the removal of excess proteins in neurons, but abnormal basal autophagy is related to neurodegenerative diseases (Tammineni & Cai, 2017). In ischemic brain injury, autophagy is a double-edged sword and has controversial functions (Peng et al. 2018; Hua et al. 2018; Zheng et al. 2018). It has been shown that increased autophagy acts as a compensatory protective mechanism for I/R injury (Su et al. 2014). For example, (Peng et al. 2018) showed that mitofusin 2, a mitochondrial fusion protein, could ameliorate cerebral I/R injury mainly through promoting autophagy in primary cultured neurons. In contrast, (Zheng et al. 2018) proposed that Bilobalide, an active component of Ginkgo biloba extract, inhibited autophagy and promoted angiogenesis following focal cerebral I/R, and thereby may be a potential agent for improving self-repair after ischemic stroke. Furthermore, (Wen et al. 2008) suggested that inhibition of autophagy by 3-methyladenine (3-MA) and bafliomycin A1 (BFA) reduced infarct volume, brain edema, and motor deficits in a rat model of permanent focal cerebral ischemia. (Li et al. 2017) also stated that inhibition of autophagy played a beneficial role in modulating neurological deficits after I/R observed under conditions of a lower level of estradiol.
Anesthetic agents have been shown to modulate autophagy in cardiac, neuronal, and other cell types. Autophagy is a process that must be carefully regulated as too much or too little autophagy may lead to cellular death. In some cases, upregulated autophagy was beneficial, whereas in others the opposite is true. The vast majority of studies demonstrate that anesthetic modulation of autophagy is beneficial for cell survival (Ye & Zuo, 2017). For example, (Zhou et al. 2016) showed that sevoflurane treatment activates autophagy, which antagonizes sevoflurane-induced apoptosis in H4 human neuroglioma cells. (Kwon et al. 2015) demonstrated that remifentanil protects human keratinocytes against hypoxia-reoxygenation injury through activation of autophagy. (Rao et al. 2017) proposed that isoflurane preconditioning alleviated murine liver I/R injury by restoring AMPK/mTOR-mediated autophagy. However, the findings of this study revealed that PPF antagonized OGD/R-triggered neuronal injury, which might be mediated, at least in part, via inhibition of autophagy. Our results were in agreement with the study, which showed that PPF prevented cerebral ischemia-triggered autophagy activation and cell death in the rat hippocampus after a cerebral I/R insult (Cui et al. 2013). Another study, which demonstrated that PPF exerted protective effects on neuronal PC12 cells after OGD injury via inhibition of autophagy, also confirmed the beneficial role of autophagy inhibition in cerebral I/R injury (Cui et al. 2012). However, unlike the protection of autophagy inhibition by PPF described above, a more recent study has been shown that PPF postconditioning protects H9c2 cardiac myoblast cells from hypoxia/reoxygenation injury by inducing autophagy (Li et al. 2018). The reasons for this discrepancy in the role of autophagy modulation by anesthetics are unclear but could relate to the degree to which autophagy is upregulated, or during when the autophagy cycle regulation occurs. Moreover, the controversial role of PPT in modulating autophagy may be attributed to the difference in cell type and setting, and ways of drug treatment.
Intracellular Ca2+ overload has been shown to be closely associated with I/R-induced apoptosis (Halestrap, 2006; Ren et al. 2017). (Wang et al. 2016) have stated that PPF could effectively reduce OGD/R-induced neuronal death in rat primary hippocampal neurons at 20 h after the injury for partially reducing calcium-overload during I/R injury. In this study, we found that PPF treatment significantly antagonized OGD/R-triggered [Ca2+]i elevation. Furthermore, [Ca2+]i elevation by the Ca2+ ionophore ionomycin significantly reversed the PPF-mediated amelioration of OGD/R-triggered cell injury. Recent studies have emphasized the correlation between Ca2+ and autophagy. It has been reported that an increase in [Ca2+]i activates CaMKKβ/AMPK signaling cascade, leading to the inhibition of mTOR signaling, and thus induction of autophagy (Shi et al. 2018; Zhang et al. 2015; Lee et al. 2012). (Hoyer-Hansen & Jaattela, 2007) have stated that an increase in free cytosolic Ca2+ induces autophagy via the CaMKKβ/AMPK/TSC1/2 (tuberous sclerosis complex 1 and 2)-Rheb-mTORC1 (mammalian target of rapamycin complex 1) signaling pathway. (Shi et al. 2018) have demonstrated that Saikosaponin-d, a sarcoplasmic/endoplasmic reticulum Ca2+ ATPase pump (SERCA) inhibitor, inhibits proliferation by up-regulating autophagy via the CaMKKβ/AMPK/mTOR pathway in ADPKD (autosomal dominant polycystic kidney disease) cells. (Zhang et al. 2015) reported that up-regulation of TRPC4 increased [Ca2+]i, which, in turn, activated the Ca2+/CaMKKβ/AMPK pathway, leading to mTOR inhibition and autophagy induction in vascular endothelial cells. Consistent with this, our mechanistic studies revealed that [Ca2+]i elevation by ionomycin significantly abrogated the PPF-mediated autophagy suppression in OGD/R-exposed neurons. Furthermore, ionomycin significantly abolished the PPF-mediated inhibition of CaMKKβ/AMPK/mTOR signaling. Additionally, activation of CaMKKβ/AMPK/mTOR signaling abrogated the PPF-mediated autophagy suppression.
In summary, our findings demonstrate that PPF antagonized OGD/R-triggered neuronal injury, which might be mediated, at least in part, via inhibition of autophagy through Ca2+/CaMKKβ/AMPK/mTOR pathway. Our study provides novel insight into the mechanism underlying the neuroprotection of PPF in cerebral I/R injury.
One-way analysis of variance
Cell Counting Kit-8
Dulbecco’s Modified Eagle’s Medium
fetal bovine serum
Green fluorescent protein
oxygen-glucose deprivation and re-oxygenation
Chen J, et al. Deletion of TRPC6 attenuates NMDA receptor-mediated ca entry and ca-induced neurotoxicity following cerebral ischemia and oxygen-glucose deprivation. Front Neurosci. 2017;11:138.
Choi AM, Ryter SW, Levine B. Autophagy in human health and disease. N Engl J Med. 2013;368:651–62.
Cui D, et al. Propofol prevents Autophagic cell death following oxygen and glucose deprivation in PC12 cells and cerebral ischemia-reperfusion injury in rats. PLoS One. 2012;7:e35324.
Cui DR, et al. Propofol prevents cerebral ischemia-triggered autophagy activation and cell death in the rat hippocampus through the NF-κB/p53 signaling pathway. Neuroscience. 2013;246:117–32.
Halestrap AP. Calcium, mitochondria and reperfusion injury: a pore way to die. Biochem Soc Trans. 2006;34:232–7.
He G, et al. Gadd45b prevents autophagy and apoptosis against rat cerebral neuron oxygen-glucose deprivation/reperfusion injury. Apoptosis : an international journal on programmed cell death. 2016;21:390–403.
Hoyer-Hansen M, Jaattela M. AMP-activated protein kinase: a universal regulator of autophagy? Autophagy. 2007;3:381–3.
Hua R, et al. cPKCγ-modulated sequential reactivation of mTOR inhibited Autophagic flux in neurons exposed to oxygen glucose deprivation/reperfusion. Int J Mol Sci. 2018;19.
Kwon JY, et al. Remifentanil protects human keratinocytes against hypoxia-reoxygenation injury through activation of autophagy. PLoS One. 2015;10:e0116982.
Lee CR, et al. Cyclosporin a suppresses prostate cancer cell growth through CaMKKbeta/AMPK-mediated inhibition of mTORC1 signaling. Biochem Pharmacol. 2012;84:425–31.
Li H, et al. Isoflurane postconditioning reduces ischemia-induced nuclear factor-kappaB activation and interleukin 1beta production to provide neuroprotection in rats and mice. Neurobiol Dis. 2013;54:216–24.
Li H, et al. Propofol postconditioning protects H9c2 cells from hypoxia/reoxygenation injury by inducing autophagy via the SAPK/JNK pathway. Mol Med Rep. 2018.
Li L, et al. Effects of estradiol on autophagy and Nrf-2/ARE signals after cerebral ischemia. Cellular Physiology & Biochemistry International Journal of Experimental Cellular Physiology Biochemistry & Pharmacology. 2017;41:2027.
Liu R, et al. Protection by borneol on cortical neurons against oxygen-glucose deprivation/reperfusion: involvement of anti-oxidation and anti-inflammation through nuclear transcription factor κappaB signaling pathway. Neuroscience. 2011;176:408–19.
Liu X, Ma Y, Wei X, Fan T. Neuroprotective effect of licochalcone a against oxygen-glucose deprivation/reperfusion in rat primary cortical neurons by attenuating oxidative stress injury and inflammatory response via the SIRT1/Nrf2 pathway. J Cell Biochem. 2018;119:3210–9.
Natoli RM, et al. Intracellular Na+ and Ca2+ modulation increases the tensile properties of developing engineered articular cartilage. Arthritis & Rheumatology. 2014;62:1097–107.
Noh HS, et al. Propofol protects the autophagic cell death induced by the ischemia/reperfusion injury in rats. Molecules & Cells. 2010;30:455–60.
Peng C, et al. Mitofusin 2 exerts a protective role in ischemia reperfusion injury through increasing autophagy. Cell Physiol Biochem. 2018;46:2311–24.
Qin H, et al. 15d-prostaglandin J2 protects cortical neurons against oxygen-glucose deprivation/reoxygenation injury: involvement of inhibiting autophagy through upregulation of Bcl-2. Cell Mol Neurobiol. 2015;35:303–12.
Rao Z, et al. Isoflurane preconditioning alleviated murine liver ischemia and reperfusion injury by restoring AMPK/mTOR-mediated autophagy. Anesth Analg. 2017;125:1355–63.
Ren Z, et al. Ferulic acid exerts neuroprotective effects against cerebral ischemia/reperfusion-induced injury via antioxidant and anti-apoptotic mechanisms in vitro and in vivo. Int J Mol Med. 2017;40:1444–56.
Shi W, et al. Saikosaponin-d inhibits proliferation by up-regulating autophagy via the CaMKKbeta-AMPK-mTOR pathway in ADPKD cells. Mol Cell Biochem. 2018.
Su J, Zhang T, Wang K, Zhu T, Li X. Autophagy activation contributes to the neuroprotection of remote ischemic perconditioning against focal cerebral ischemia in rats. Neurochem Res. 2014;39:2068–77.
T Y AT. Autophagy and cell death. Essays Biochem. 2013;55:105–17.
Tammineni P, Cai Q. Defective retrograde transport impairs autophagic clearance in Alzheimer disease neurons. Autophagy. 2017;13:982–4.
Tao T, et al. Protective effects of propofol against whole cerebral ischemia/reperfusion injury in rats through the inhibition of the apoptosis-inducing factor pathway. Brain Res. 2016;1644:9–14.
Wahr J, et al. Effect of propofol with and without EDTA on haemodynamics and calcium and magnesium homeostasis during and after cardiac surgery. Intensive Care Med. 2000;26(Suppl 4):S443–51.
Wang H, Luo M, Li C, Wang G. Propofol post-conditioning induced long-term neuroprotection and reduced internalization of AMPAR GluR2 subunit in a rat model of focal cerebral ischemia/reperfusion. J Neurochem. 2011;119:210–9.
Wang H, et al. The effect of Propofol on mitochondrial fission during oxygen-glucose deprivation and reperfusion injury in rat hippocampal neurons. PLoS One. 2016;11:e0165052.
Wen YD, et al. Neuronal injury in rat model of permanent focal cerebral ischemia is associated with activation of autophagic and lysosomal pathways. Autophagy. 2008;4:762–9.
Ye F, Zuo Z. Anesthetic effects on autophagy. Med Gas Res. 2017;7:204–11.
Yu W, Gao D, Jin W, Liu S, Qi S. Propofol prevents oxidative stress by decreasing the ischemic accumulation of succinate in focal cerebral ischemia-reperfusion injury. Neurochem Res. 2018;43:420–9.
Yuan T, et al. Salubrinal protects against cigarette smoke extract-induced HBEpC apoptosis likely via regulating the activity of PERK-eIF2α signaling pathway. Arch Med Res. 2012;43:522–9.
Zhang L, et al. Novel role for TRPC4 in regulation of macroautophagy by a small molecule in vascular endothelial cells. Biochim Biophys Acta. 2015;1853:377–87.
Zhang P, et al. TRPC5-induced autophagy promotes drug resistance in breast carcinoma via CaMKKbeta/AMPKalpha/mTOR pathway. Sci Rep. 2017;7:3158.
Zheng Y, et al. By activating Akt/eNOS Bilobalide B inhibits autophagy and promotes angiogenesis following focal cerebral ischemia reperfusion. Cell Physiol Biochem. 2018;47:604–16.
Zhou Y, Wang Q, Zhou H, Chen G. Autophagy activation prevents sevoflurane-induced neurotoxicity in H4 human neuroglioma cells. Acta Pharmacol Sin. 2016;37:580–8.
This work was partly supported by National Natural Science Foundation of China (81501710).
Availability of data and materials
The datasets used and/or analysed during the current study are available from the corresponding author on reasonable request.
All animal-related experiments in this study were approved by the Ethics Committee for Animal Experimentation of Xiangya Hospital, Central South University and were performed in accordance with the guidelines for the Care and Use of Laboratory Animals of the National Institutes of Health.
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Figure S1. Block of [Ca2+]i enhanced the PPF-mediated amelioration of OGD/R-triggered cell injury. OGD/R-exposed neurons were pre-treated with an intracellular calcium chelator (BAPTA, 5 μM), followed by propofol (PPF, 30 μM in 0.1% DMSO) treatment. (A) (A) LDH release and (B) CCK-8 cell viability were performed to evaluate whether [Ca2+]i was involved in the PPF-mediated amelioration of OGD/R-triggered cell injury. Values are represented as the mean ± SD from three independent experiments. *p < 0.05 vs. Control group; #p < 0.05 vs. DMSO group; $p < 0.05 vs. PPF group.(TIF 296 kb)
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Sun, B., Ou, H., Ren, F. et al. Propofol inhibited autophagy through Ca2+/CaMKKβ/AMPK/mTOR pathway in OGD/R-induced neuron injury. Mol Med 24, 58 (2018). https://doi.org/10.1186/s10020-018-0054-1
- Oxygen-glucose deprivation and re-oxygenation