About the Authors:
Peiqi Wang
Contributed equally to this work with: Peiqi Wang, Jiangbei Cao
Affiliation: Department of Anesthesiology and Operation Center, Chinese PLA, General Hospital, Beijing, China
Jiangbei Cao
Contributed equally to this work with: Peiqi Wang, Jiangbei Cao
Affiliation: Department of Anesthesiology and Operation Center, Chinese PLA, General Hospital, Beijing, China
Na Liu
Affiliations Department of Anesthesiology and Operation Center, Chinese PLA, General Hospital, Beijing, China, Department of Anesthesiology, Affiliated Hospital of Chengde Medical University, Chengde, China
Li Ma
Affiliations Department of Anesthesiology and Operation Center, Chinese PLA, General Hospital, Beijing, China, Department of Anesthesiology, Beijing Military General Hospital of the Chinese People’s Liberation Army, Beijing, China
Xueyue Zhou
Affiliation: Department of Anesthesiology and Operation Center, Chinese PLA, General Hospital, Beijing, China
Hong Zhang
* E-mail: [email protected] (HZ); [email protected] (YW)
¶‡ These authors also contributed equally to this work.
Affiliation: Department of Anesthesiology and Operation Center, Chinese PLA, General Hospital, Beijing, China
Yongan Wang
* E-mail: [email protected] (HZ); [email protected] (YW)
¶‡ These authors also contributed equally to this work.
Affiliation: State Key Laboratory of Toxicology and Medical Countermeasures, Academy of Military Medical Sciences, Beijing, China
Abstract
Postoperative cognitive dysfunction (POCD) is a clinical syndrome characterized by cognitive declines in patients after surgery. Previous studies have suggested that surgery contributed to such impairment. It has been proven that neuroinflammation may exacerbate surgery-induced cognitive impairment in aged rats. The free radical scavenger edaravone has high blood brain barrier permeability, and was demonstrated to effectively remove free radicals from the brain and alleviate the development of POCD in patients undergoing carotid endarterectomy, suggesting its potential role in preventing POCD. For this reason, this study was designed to determine whether edaravone is protective against POCD through its inhibitory effects on inflammatory cytokines and oxidative stress. First, Sprague Dawley adult male rats were administered 3 mg/kg edaravone intraperitoneally after undergoing a unilateral nephrectomy combined with lipopolysaccharide injection. Second, behavioral parameters related to cognitive function were recorded by fear conditioning and Morris Water Maze tests. Last, superoxide dismutase activities and malondialdehyde levels were measured in the hippocampi and prefrontal cortex on postoperative days 3 and 7, and microglial (Iba1) activation, p-Akt and p-mTOR protein expression, and synaptic function (synapsin 1) were also examined 3 and 7 days after surgery. Rats that underwent surgery plus lipopolysaccharide administration showed significant impairments in spatial and working memory, accompanied by significant reductions in hippocampal-dependent and independent fear responses. All impairments were attenuated by treatment with edaravone. Moreover, an abnormal decrease in superoxide dismutase activation, abnormal increase in malondialdehyde levels, significant increase in microglial reactivity, downregulation of p-Akt and p-mTOR protein expression, and a statistically significant decrease in synapsin-1 were observed in the hippocampi and prefrontal cortices of rats at different time points after surgery. All mentioned abnormal changes were totally or partially reversed by edaravone. To our knowledge, few reports have shown greater protective effects of edaravone on POCD induced by surgery plus lipopolysaccharide administration from its anti-oxidative stress and anti-inflammatory effects, as well as maintenance of Akt/mTOR signal pathway activation; these might be closely related to the therapeutic effects of edaravone. Our research demonstrates the potential use of edaravone in the treatment of POCD.
Figures
Fig 7
Fig 1
Fig 2
Fig 3
Fig 4
Fig 5
Fig 6
Fig 7
Fig 1
Fig 2
Fig 3
Citation: Wang P, Cao J, Liu N, Ma L, Zhou X, Zhang H, et al. (2016) Protective Effects of Edaravone in Adult Rats with Surgery and Lipopolysaccharide Administration-Induced Cognitive Function Impairment. PLoS ONE 11(4): e0153708. https://doi.org/10.1371/journal.pone.0153708
Editor: Zhongcong Xie, Massachusetts General Hospital, UNITED STATES
Received: February 7, 2016; Accepted: April 3, 2016; Published: April 26, 2016
Copyright: © 2016 Wang et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Data Availability: All relevant data are within the paper and its Supporting Information files.
Funding: This study was supported by a grant in the special subject of health care from the General Logistics Department (13BJZ38) and a Military Medical Scientific and Technological Project for the “Twelfth Five-year Plan” (AWS15J007, BWS12J042).
Competing interests: The authors have declared that no competing interests exist.
1. Introduction
Postoperative cognitive dysfunction (POCD) refers to varying degrees of cognitive function decline in patients after surgery. It covers a wide range of cognitive functions including working memory, long term memory, information processing, attention, and cognitive flexibility [1, 2]. POCD adversely affects quality of life, social dependence, and mortality [3]. Oxidative stress, surgery, general anesthesia/anesthetics, and neuroinflammation are believed to increase the risk of POCD [4–6].
Certain tissues can be damaged as a result of oxidative stress, especially during an operation [7]. The free radical scavenger edaravone, which crosses the blood brain barrier, can effectively remove free radicals from the brain [8]. Evidence has shown that oxidative factors were harmful to cognitive function [9–10]. However, edaravone can improve the cholinergic system and protect neurons from oxidative toxicity, alleviate Alzheimer’s disease-type pathologies, and cognitive deficits [11, 12]. Other studies demonstrated that edaravone inhibited the progression of cerebral infarction and ischemia [13, 14]. Most importantly, the effects of edaravone on the development of POCD have been proven in patients undergoing carotid endarterectomy[15] In short, previous studies suggest that edaravone might improve cognitive impairment in patients after surgery by scavenging free radicals.
Lipopolysaccharide (LPS) is a major bacterial TLR4 ligand that activates the immune response to infections [16]. Recent reports have demonstrated that surgery accompanied by LPS treatment triggered more severe neurodegeneration in adult rats [17]; The interaction between oxygen free radicals and inflammatory factors would exacerbate postoperative cognitive dysfunction[18,19].They both would destroy cell membrane function, break the balance of homeostasis, cause oxidative phosphorylation in a mess[20]. The normal activation of the Akt/mTOR signal pathway was the phosphorylation[21]. a subsequent increase in activated microglial cells and inhibition of activation of the Akt/mTOR signal pathway were also observed, finally leading to declines in learning and memory [22, 23]. Also, mTOR was involved in regulating synaptic plasticity, which affected the function of memory and cognitive [24,25]. Based on previous reports, we hypothesized that in a rat model of surgery associated with LPS administration, edaravone might improve POCD by alleviating oxidative toxicity, inhibiting microglial activation, and maintaining normal function of activation of the Akt/mTOR signal pathway. The results obtained in this study may provide new insights into the potential roles of edaravone in the treatment of POCD, as well as its mechanisms of action.
2. Materials and Methods
2.1 Animals
Adult male Sprague Dawley rats (n = 80) aged 8 weeks and weighing 220–250 g were purchased from Vital River Laboratories Animal Technology Co. Ltd. (Beijing, China. Permit Number: SCXK (JING) 2012–0001). All rats were housed under controlled conditions with a 12-h light/dark cycle and ad libitum access to food and water for 7 days before the experiment. The procedures on animal experimentation were approved by the Animal Care Committee of the Chinese People’s Liberation Army General Hospital (Beijing, China). The maintenance and handling of the rats were consistent with the guidelines of the National Institutes of Health, and adequate measures were taken to minimize animal discomfort. The rats were divided into four groups randomly (20 rats per group): the control plus placebo group (C-P), control plus edaravone group (C-E), surgery plus placebo group (S-P), and surgery plus edaravone group (S-E). Each group was divided into two subgroups randomly (10 rats per group): the 3-day postoperative group and 7-day postoperative group. The C-P and S-P groups received a placebo (0.3 mL of saline by intraperitoneal [i.p.] injection), and the C-E and S-E groups received 3 mg/kg of edaravone (Cat: 80–131003, Simcere, Nanjing, China) in 0.3 mL of saline by i.p. injection.
2.2 Surgical Procedures
After undergoing the Morris Water Maze (MWM) test and fear conditioning training for 5 consecutive days, animals in the S-P and S-E groups underwent LPS administration of 100 μg/kg i.p. (Sigma, St. Louis, MO, USA). The dosage of LPS was determined according to a previous report [17]. After 1 h, the LPS-treated groups underwent a left nephrectomy under pentobarbital sodium anesthesia (1% and 40 mg/kg) (Fig 1A). A longitudinal incision was made in the back where the wounds were not accessible to the rats to avoid self-inflicted bite trauma. We considered this surgery model to mimic a standardized organ removal in humans with sub-clinical infection [8]. During the operation, the rats’ body temperature were maintained at 36.5°C to 37.5°C. All rats received 50μl of 0.2% ropivacaine subcutaneously for the post-operative analgesia. Rats were allowed to recover in an incubator at 37°C and were then returned to their cages. Later, the C-P and S-P groups received saline (i.p.), whereas the C-E and S-E groups received edaravone (i.p.) each day until days 3 and 7 after surgery, respectively(Fig 1B). Each rat would be weighted every day after operation, all rats were put on weight with days. We sterilized the wound of rats at the day 1,2,3,5,7 after surgery. Then, the animals were sacrificed with the lethal dose of pentobarbital sodium i.p. at 3 days and 7 days postoperatively, and the brains of five rats in each group were immediately removed and fixed in 4% paraformaldehyde for 48 h for histological analysis. The hippocampi and prefrontal cortices of the other rats were rapidly dissected, removed, and stored at -80°C until analysis.
[Figure omitted. See PDF.]
Fig 1. The schematic outline of the experimental protocol and the timeline of LPS and edaravone administration.
(A)Schematic outline of the experimental protocol. (B) Timeline of LPS and edaravone administration. MWM, Morris water maze; FCS, Fear conditioning test;C-P, sham surgery plus placebo; C-E, sham surgery plus edaravone; S-P, surgery plus placebo; S-E, surgery plus edaravone.
https://doi.org/10.1371/journal.pone.0153708.g001
2.3 Behavior tests
2.3.1 MWM test.
The MWM test (EthoVision, The Netherlands) was performed to assess spatial learning, spatial memory, and cognitive flexibility in the rats [26]. The water maze consisted of a round container (180 cm × 60 cm) made of black plastic and filled with water (25 ± 1°C). The pool was placed in a room with several visual cues for orientation in the maze. The maze was divided into four quadrants: the first, second, third, and fourth quadrants. An invisible platform (10 cm × 10 cm) was placed 1 cm below the water surface in the first quadrant (target quadrant). All rats underwent repeated training for 5 consecutive days. Every day, they were released successively into the water facing the wall of the pool from the first quadrant to the fourth quadrant. The rats were trained to find the hidden platform and climb onto it within 60 s. The animals were allowed to stay on the platform for at least 10 s after each trial. When the rats failed to reach the escape platform within 60 s, they were gently guided towards the platform and left there for 10 s. After the completion of four trials, the rat was dried with a towel and returned to its cage. The animals’ movements were recorded with a video camera.
On postoperative day 3, probe tests were conducted on all the treated groups by removing the platform and releasing the rats in the third quadrant (opposite to the first quadrant). Latency, the number of crossings over the former location of the platform, and time spent in each quadrant were measured in a single 60-s trial. Then, working memory was tested; both the platform and rat were randomly placed in novel positions to assess trial-dependent learning and working memory [27]. Animals underwent one more training session to ensure that all rats learned the new platform location. After 15 s, each rat was released from the same location as in the above training; the rat would swim a shorter path to the platform in the second trial if it recalled the first trial. The escape latency to the platform in the second trial was taken as measure of temporary or working memory. All of the 7-day postoperative groups underwent the same trials on postoperative day 7.
2.3.2 Fear conditioning.
Fear conditioning is used to detect associative learning and memory function [28]. Different groups of rats were trained for fear conditioning 1 day before the operation. Rats were subjected to an inescapable electric foot shock provided via the grid floor of a testing chamber. The chamber in which training occurred was lit with fluorescent bulbs. The total training time was 330 s for each rat. Each animal was allowed to explore the chamber for 60 s before the presentation of 3 tone-foot shock pairings (tone: 2000 Hz, 85 dB, 30 s; foot shock: 0.9 mA, 2 s) with an intertribal interval of 60 s. Then, the animal was removed from the test chamber 60 s after conditioning training.
Different groups underwent the context test and tone test on postoperative days 3 and 7, respectively. The rats were tested in the context and tone test. Each animal was placed into the chamber for 330 s either in a context test (without a tone or shock) or a tone test (without a shock). Episodes of freezing were recorded by a digital camera. These tests assessed hippocampi-dependent (context-related) and hippocampi-independent (tone-related) learning and memory functions [29]. They were expressed as the percentage of freezing time using software analysis.
2.4 Biochemical analysis
2.4.1 Malondialdehyde (MDA).
MDA is one of the lipid peroxides. The concentration of MDA indicates how severely tissue is attacked by free radicals. This method is based on thibabituric acid (TBA). The color reaction was measured at 532 nm. The levels of MDA in the hippocampi and prefrontal cortices of rats were measured using commercial assay kits (Nanjing Jiancheng Bioengineering Institute, Nanjing, China) according to the manufacturer’s instructions.
2.4.2 Superoxide dismutase (SOD) activity.
The method was based on the ability of SOD to inhibit the superoxide anion free radical O2-. The color reaction was measured at 550 nm. The SOD activity of tissue was also measured using commercial assay kits (Nanjing Jiancheng Bioengineering Institute, Nanjing, China).
2.5 Immunofluorescence staining
A cerebral block containing the hippocampi and prefrontal cortex was fixed in 10% neutral-buffered formalin overnight and then embedded in paraffin. Coronal 10-μm sections were prepared and subjected to immunofluorescence staining. First, paraffin sections were dewaxed and placed in EDTA buffer (pH 8.0) to repair antigens. Second, sections were washed in 0.01% Triton X-100 in phosphate-buffered saline (PBS-T) and blocked with 3% bovine serum albumin (BSA) for 30 min at room temperature. Then, they were incubated overnight at 4°C in appropriate primary antibodies: anti-Iba1 (1:100; WAKO) and anti-synapsin-1 (1:100; Cell Signaling). Next, the sections were incubated with the appropriate secondary antibodies including anti-rabbit IgG (1:400; Jackson) and anti-mouse IgG (1:400, Jackson) for 2 h at room temperature. The number of positively stained microglial cells was counted by fluorescence microscopy at 400× magnification and the mean density of the synapses was also calculated by fluorescence microscopy at 400× magnification.
2.6 Western blot
The hippocampal and prefrontal cortical tissues were homogenated in RIPA buffer (50 mmol/L Tris–HCl, pH 6.8, 150 mmol/L NaCl, 5 mmol/L EDTA, 0.5% sodium deoxycholate, 0.5% NP-40, and supplemented with a cocktail containing protease and phosphatase inhibitors). The total lysates were centrifuged at 12000 rpm for 30 min at 4°C. Protein concentrations were determined by a BCA Protein Assay reagent kit (Pierce, Rockford, IL, USA). Equal amounts of the sample (30 μg of protein) were separated by SDS-PAGE and analyzed by Western blot using the following primary antibodies: rabbit polyclonal anti-Akt and anti-p-Akt (1:1000, Cell Signaling), rabbit polyclonal anti-p-mTOR (1:1000, Cell Signaling), and mouse monoclonal anti-β-actin polyclonal antibody (1:3000; Abcam). Appropriate secondary antibodies were used. Each experiment was repeated no less than four times. Relative expression was normalized to β-actin.
2.7 Statistical analysis
All data were analyzed by an observer who was blinded to the experimental protocol. Statistical calculations were performed using SPSS 16.0 (SPSS Science, Inc., Chicago, IL, USA). We analyzed multiple group means by a two-way analysis of variance followed by Dunnett’s post hoc test wherever appropriate. Values of p < 0.05 were considered significant.
3. Results
3.1 Edaravone attenuated unilateral nephrectomy plus LPS administration-induced learning and memory impairment
Previous work has demonstrated that a nephrectomy plus an LPS injection could lead to POCD [17]. Therefore, the protective effects of edaravone on POCD were examined in this model. As shown in Fig 2A, in the MWM test, the escape latency in all groups was significantly shorter during the last training session when compared to the first training session (p < 0.001), yet no difference was observed between the groups, indicating that all animals were able to learn where the platform was located. On postoperative day 3, the well time in the target quadrant in the first MWM probe trial in the S-P group was decreased notably compared to the other groups (p < 0.05), and the number of crossings also showed a decreasing tendency, although it did not reach significance (Fig 2B and 2C). In the working memory test, the escape latency needed to reach the new platform was increased obviously (p < 0.05) in the S-P group compared to the C-P and S-E groups (Fig 2D). During the probe test, there were no significant difference in swimming speed between the groups, suggesting that the poorer performance of the S-P group was not a result of reduced motor ability (Fig 2E). On postoperative day 7, there was no statistical difference between the S-P group and other groups in dwelling time in the target quadrant, number of crossings, or escape latency, although rats in the S-P group presented a decreasing tendency in dwelling time in the target quadrant and an increasing tendency in escape latency.
[Figure omitted. See PDF.]
Fig 2.
Edaravone attenuated behavioral performance after unilateral nephrectomy plus LPS administration in rats (A) Spatial learning in the MWM. Average escape latency (s) is shown for the five training sessions in the maze. (B) Dwelling time in the target quadrant in the first MWM probe trial on day 3 after surgery. (C) The number of crossings on postoperative day 3. (D) Average escape latency (s) during the MWM reversal trials on day 3 after surgery. (E) Average swimming speed (m/s) in the first MWM probe trial. **P< 0.01 vs. the first day since training; *P< 0.05 vs. C-P group; #P <0.05 vs. S-P group. C-P, sham surgery plus placebo; C-E, sham surgery plus edaravone; S-P, surgery plus placebo; S-E, surgery plus edaravone.
https://doi.org/10.1371/journal.pone.0153708.g002
In the fear conditioning test, hippocampal-dependent memory was assessed in a novel context and revealed highly significant impairment in the S-P group when compared to the C-P group on postoperative days 3 (p < 0.01) and 7 (p < 0.05) (Fig 3A and 3B). Compared to the C-P group, the freezing time in the S-P group was significantly decreased (p < 0.01). This decrease was reversed obviously in the S-E group (p < 0.05/0.01), indicating the protective effects of edaravone on the development of POCD. During the tone-related fear conditioning test (hippocampal-independent memory) on postoperative day 3, as shown in Fig 3C, the freezing time percentage was notably decreased in the S-P group when compared to the C-P group (p < 0.05); this decrease was significantly prevented by edaravone (p < 0.05). On postoperative day 7, freezing responses to the tone were not significantly different between any of the groups (Fig 3D).
[Figure omitted. See PDF.]
Fig 3.
Cognitive impairment after surgery in the fear conditioning test (A) The hippocampal-dependent memory test on day 3 after surgery. (B) The hippocampal-dependent memory test on day 7 after surgery. (C) The hippocampal-independent memory test on postoperative day 3. (D) The hippocampal-independent memory test on postoperative day 7. *P< 0.05, **P< 0.01 vs. C-P group; #P <0.05, ##P <0.01 vs. S-P group. C-P, sham surgery plus placebo; C-E, sham surgery plus edaravone; S-P, surgery plus placebo; S-E, surgery plus edaravone.
https://doi.org/10.1371/journal.pone.0153708.g003
3.2 Edaravone increased SOD activities and reduced MDA levels in the hippocampi and prefrontal cortex in rats after surgery plus LPS administration
As demonstrated in Fig 4A and 4B, compared to the C-P group, the SOD activities of the hippocampi and prefrontal cortex were significantly decreased on postoperative day 3 (p < 0.01/0.001), but showed no change on postoperative day 7 in the S-P group; this abnormal decrease in SOD activities was largely prevented by edaravone (p < 0.05). Likewise, edaravone significantly attenuated abnormally increased MDA levels in the hippocampi of the S-P group 3 days after the operation (p < 0.01) (Fig 4C). No difference was observed between the groups regarding MDA level in the prefrontal cortex on postoperative day 3 (Fig 4D) or day 7, although the MDA level in the S-P group also showed an increasing tendency without a statistical difference.
[Figure omitted. See PDF.]
Fig 4.
Edaravone increased SOD activities and reduced hippocampal and prefrontal cortex MDA levels after surgery (A) SOD activities in the hippocampi on postoperative day 3. (B) SOD activities in the prefrontal cortex on postoperative day 3. (C) The MDA level in the hippocampi on postoperative day 3. (D) The MDA level in the prefrontal cortex on postoperative day 3. *P< 0.05, **P< 0.01, ***P< 0.001 vs. C-P group; #P <0.05 vs. S-P group. C-P, sham surgery plus placebo; C-E, sham surgery plus edaravone; S-P, surgery plus placebo; S-E, surgery plus edaravone.
https://doi.org/10.1371/journal.pone.0153708.g004
3.3 Edaravone prevented microglial activation after surgery plus LPS administration
Using immunofluorescence, the effects of edaravone on ionized calcium binding adapter molecule 1 (Iba1) were investigated. As shown in Fig 5A–5X, the total counted number of Iba1-positive cells on hippocampal (Fig 5Y; p < 0.001) and prefrontal cortical (Fig 5Z; p < 0.01) sections in the S-P group was much higher than in the C-P group and S-E group on postoperative day 3, yet there were no significant difference among the treated groups on postoperative day 7.
[Figure omitted. See PDF.]
Fig 5.
Edaravone attenuated surgery plus LPS-induced microglial (green) activation (A-X) Representative images of Iba1-labeled activated microglia in the hippocampi and prefrontal cortex. (A-D) Activated microglia and cell nuclei in the hippocampi on postoperative day 3 under a 200× magnification fluorescence microscope. (E-H) Activated microglia and cell nuclei in the hippocampi on postoperative day 3 under a 400× magnification fluorescence microscope. (I-L) Activated microglia in the hippocampi on postoperative day 3 under a 400× magnification fluorescence microscope. (M-P) Activated microglia and cell nuclei in the prefrontal cortex on postoperative day 3 under a 200× magnification fluorescence microscope. (Q-T) Activated microglia and cell nuclei in the prefrontal cortex on postoperative day 3 under a 400× magnification fluorescence microscope. (U-X) Activated microglia in the prefrontal cortex on postoperative day 3 under a 400× magnification fluorescence microscope. (Y) The number of hippocampal Iba1-positive cells on postoperative day 3. (Z) The number of prefrontal cortical Iba1-positive cells on postoperative day 3. Scale bars: A-D and M-P, 100 μm; E-L and Q-X, 50 μm. *P< 0.05, **P< 0.01, ***P< 0.001 vs. C-P group; #P <0.05, ##P <0.01 vs. S-P group. C-P, sham surgery plus placebo; C-E, sham surgery plus edaravone; S-P, surgery plus placebo; S-E, surgery plus edaravone.
https://doi.org/10.1371/journal.pone.0153708.g005
3.4 Edaravone attenuated surgery plus LPS administration-induced neuroinflammation
To further investigate the mechanism of edaravone in preventing microglial activation, Akt/mTOR signal pathway-related protein expression was tested by western blot. As shown in Fig 6A–6F, on day 3 after the operation, protein levels of p-Akt and p-mTOR in the rats’ hippocampi and prefrontal cortices were largely decreased in the S-P group compared to the C-P group (p < 0.05/0.01); this abnormal decrease was significantly attenuated (p < 0.05) by edaravone. On postoperative day 7, no difference in protein expression was observed between any of the groups.
[Figure omitted. See PDF.]
Fig 6.
Effects of edaravone on protein expression in rats with LPS-induced hippocampal and prefrontal cortical impairment (A) The expression of related protein in the hippocampi on day 3 after surgery. (B) The ratio of p-Akt/Akt in the hippocampi on day 3 after surgery. (C) The ratio of p-mTOR/actin in the hippocampi on day 3 after surgery. (D) The expression of related protein in the prefrontal cortex on postoperative day 3. (E) The ratio of p-Akt/Akt in the prefrontal cortex on postoperative day 3. (F) The ratio of p-mTOR/actin in the prefrontal cortex on postoperative day 3. *P< 0.05, **P< 0.01 vs. C-P group; #P <0.05 vs. S-P group. C-P, sham surgery plus placebo; C-E, sham surgery plus edaravone; S-P, surgery plus placebo; S-E, surgery plus edaravone.
https://doi.org/10.1371/journal.pone.0153708.g006
3.5 Edaravone improved surgery plus LPS administration-induced synaptic function depression
To further evaluate the protective effects of edaravone on surgery plus LPS administration-induced cognitive function impairment, the synaptic protein SYN was examined. On postoperative day 3, a significant reduction in SYN intensity was observed in hippocampi from group S-P (p < 0.001) (Fig 7A–7L), and this reduction was partially reversed (p < 0.01) by edaravone(Fig 7Y). On postoperative day 7, the SYN intensities in the hippocampi showed no difference. Different from the hippocampi, the expression of SYN in the prefrontal cortex was not different between any of the groups on postoperative day 3 (Fig 7M–7X and 7Z) or day 7.
[Figure omitted. See PDF.]
Fig 7.
Edaravone protected hippocampal and prefrontal cortical synaptic (red) integrity after surgery plus LPS administration (A-L) Representative images of SYN-labeled synapses in the hippocampi. (A-D) Synaptic protein and cell nuclei in the hippocampi on postoperative day 3 under a 200× magnification fluorescence microscope. (E-H) Synaptic protein and cell nuclei in the hippocampi on postoperative day 3 under a 400× magnification fluorescence microscope. (I-L) Synaptic protein in the hippocampi on postoperative day 3 under a 400× magnification fluorescence microscope. (M-P) Synaptic protein and cell nuclei in the prefrontal cortex on postoperative day 3 under a 200× magnification fluorescence microscope. (Q-T) Synaptic protein and cell nuclei in the prefrontal cortex on postoperative day 3 under a 400× magnification fluorescence microscope. (U-X) Synaptic protein in the prefrontal cortex on postoperative day 3 under a 400× magnification fluorescence microscope (Y) The density of hippocampal synaptic protein on postoperative day 3. (Z) The density of prefrontal cortical synaptic protein on postoperative day 3. Scale bars: A-D, 100 μm; E-L, 50 μm. ***P< 0.001 vs. C-P group; ##P <0.01 vs. S-P group. C-P, sham surgery plus placebo; C-E, sham surgery plus edaravone; S-P, surgery plus placebo; S-E, surgery plus edaravone.
https://doi.org/10.1371/journal.pone.0153708.g007
4. Discussion
This paper shows that surgery plus LPS injection can induce POCD in rats, and that the resulting cognitive impairment can be largely prevented by edaravone. Moreover, the protective effects of edaravone on the development of POCD in rats may be related to its antioxidant effects, inhibiting microglial activation, and maintaining normal activation of the Akt/mTOR signal pathway.
Recent studies revealed that surgery can lead to cognitive decline by triggering systemic and hippocampal inflammation [5, 30, 31]. Systemic infection increases the levels of pro-inflammatory cytokines in the brain that contribute to subsequent impairment of the consolidation of memory in rats [32]. LPS, the major component of the outer membrane of Gram-negative bacteria, is known to trigger a powerful immune response [16]. Priming the immune system with a subclinical dose of LPS can amplify the pro-inflammatory response caused by surgery [33]. In clinical practice, it is very common for patients to have sub-clinical infection before or after an operation [17]. For this reason, based on the reported studies, we chose the dosage of LPS (100 μg/kg) to mimic sub-clinical infection. The chosen dose has been tested and has the ability to sensitize the immune system and augment the severity of unilateral nephrectomy-induced impairment of cognition [17].
The MWM test was chosen as a robust and reliable test that is strongly correlated with hippocampal-dependent memory [34–35]. It consists of two parts: the spatial reference memory test and reversal test. In the spatial reference memory test, obviously inherent memory impairment was observed in the S-P group, and this inherent memory injury was significantly alleviated by edaravone. In the MWM reversal task, a method was used to evaluate cognitive flexibility, which is independent of hippocampal function [36]. The obvious reduction in learning ability and short-term memory were shown in the S-P group, and this cognitive impairment after the operation was also prevented by edaravone. In the novel context test of fear conditioning, hippocampal-dependent cognitive dysfunction was sustained on postoperative day 7, whereas hippocampal-independent cognitive decline occurred after postoperative day 3, but did not last to postoperative day 7. Edaravone administration also prevented cognitive decline and accelerated cognitive recovery in the fear conditioning test.
In the context fear conditioning test, the cognitive dysfunction was sustained on postoperative day 7, while the spatial reference memory in the MWM test on postoperative day 7 was not changed in surgery plus LPS group. It maybe related to rats form different memory with different regions of hippocampi, and the damage degree of hippocampal regions which surgery plus LPS induced was different. Although spatial memory and contextual fear memory were hippocampal-dependent, the formation of memory depended on different brain regions[37].The spatial memory rely on hippocampi, corpus striatum, basal forebrain, cerebellum and other regions participation, any damage of above tissues will induce memory impairment[38]. The impairment of dorsal hippocampi was more serious than the impairment of ventral hippocampi for spatial memory decline[39].Fear conditioning test formed cortex memory, it relied mainly on CA1 region of hippocampi[40]. Especially, the activity of RA1 was associated with the fear cortex memory[41].
Previous studies have shown that cognitive impairment was obvious in water maze and fear conditioning tests in unilateral nephrectomy-treated aged rodents [42, 43]. Meanwhile, systemic inflammation is believed to increase the levels of pro-inflammatory cytokines in the brain and aggravate POCD [17, 32]. Edaravone, a known antioxidant, has been demonstrated to antagonize POCD in patients [15]. However, to our knowledge, few studies have examined the protective effect of edaravone in POCD induced by surgery plus LPS injection. Our study is the first to demonstrate the potential role of edaravone in the treatment of cognitive impairment caused by surgery plus LPS injection.
Previous studies have indicated that surgery contributed to the inflammatory response and oxidative stress by activating the immune system [44,45], and systemic infection would result in more inflammatory cytokines in the brain [32]. Both inflammation and oxygen free radicals were believed to take part in the onset and maintenance of POCD [46, 47]. Moreover, inflammation also promoted the entrance of oxygen free radicals into the central nervous system [29] and then exacerbated the injurious effects of oxidative stress on cognitive function [18]. For these reasons, the antioxidant and anti-neuroinflammation effects of edaravone were further investigated in rats that underwent surgery plus an LPS injection.
Abnormal changes in the activities of SOD and the levels of MDA in brain tissues were thought to relate to dysfunction and damage to the structure of the cell membranes, mitochondria, and lysosomes, as well as cell autolysis related to POCD [46]. In addition, the overexpression of inflammatory cytokines was often accompanied by an increased number of activated microglial cells [48, 49], which were characterized by an acute increase in Iba1. In this paper, decreased activities of SOD and increased levels of MDA, as well as a significant increase in Iba1, were shown at different time points after the operation (days 3 and 7 for SOD and MDA, and day 3 for Iba1) in the hippocampi and prefrontal cortices of S-P group animals. All the above-mentioned abnormal changes were partially reversed by edaravone, further suggesting that the protective effects of edaravone on POCD might be related to its antioxidant and anti-neuroinflammation effects.
In addition to attenuating oxidative stress and neuroinflammation, maintaining the activation of the Akt/mTOR signal pathway to prevent POCD induced by surgery by inhibiting inflammation was thought to be a reliable method [50]. The reason was that the Akt/mTOR signal pathway has been shown to play a crucial role in the induction of key anti-inflammatory and immunomodulatory cytokines [50, 51]. In addition, the activation of the Akt/mTOR signal pathway could be inhibited by oxidative stress [52, 53]. Most importantly, known drugs with greater protective effects against POCD, such as acetylcholinesterase, were found to have the ability to activate the Akt/mTOR pathway [54]. In order to investigate the relationship between the protective effects of edaravone on POCD and activation of the Akt/mTOR pathway, the protein expressions of p-Akt and p-mTOR, as well as SYN intensity, were also tested.
In general, p-Akt participates in regulating cell apoptosis, stimulating cell proliferation, and many other physiological processes [27]. Inflammatory factors such as TNF-a, IL-6, and oxidative factors can inhibit the activation of the Akt/mTOR signal pathway via downregulating the expression of p-Akt protein [55, 56]. mTOR, the main downstream signaling factor in the Akt/mTOR signal pathway, was proven to have a close correlation with cognitive dysfunction such as in Alzheimer’s disease [57]. Moreover, it has also been demonstrated to partially influence synaptic plasticity and memory [24, 25] through regulating the synthesis of certain protein-associated with reshaping of the synapse [58, 59]. Synaptic plasticity was proven to be the biological basis for maintaining learning and memory under normal conditions [60], and SYN-1 intensity was regarded to be involved in regulating the number of synaptic vesicles and contributed to the synaptic function. In the S-P group, the downregulation of expressions of p-Akt and p-mTOR proteins, accompanied by a reduction in SYN intensity in the hippocampi and prefrontal cortex, was observed in the rats; these effects were largely reversed by edaravone, indicating that edaravone could also maintain normal activation of the Akt/mTOR signal pathway by preventing the downregulation of p-Akt and p-mTOR proteins. As a result, neuroinflammation caused by surgery was largely inhibited and synaptic plasticity was maintained, which finally led to the significant attenuation of POCD induced by an operation plus LPS injection.
5. Conclusions
In summary, obvious cognitive impairment was shown in rats that underwent a unilateral nephrectomy plus LPS administration. The known antioxidant edaravone could effectively attenuate cognitive impairment; its protective mechanism may be related to its antioxidant and anti-inflammatory effects, as well as its ability to maintain activation of the Akt/mTOR signaling pathway. Although the details of how edaravone improves cognitive function are not yet clear, this paper may provide a new strategy to counter POCD caused by operations.
Supporting Information
[Figure omitted. See PDF.]
S1 File.
Table A. Average escape latency(s) in the spatial learning of the MWM. Table B. MWM test index on day 3 after surgery. Table C. Fear conditioning test index. Table D. SOD activity (U/mg protein) and MDA concentration (nmol/mg protein) on postoperative day 3. Table E. Data5 Number of Iba1-positive cells on postoperative day 3. Table F. Ratio of related protein on day 3 after surgery. Table G. Density of synaptic protein on postoperative day 3.
https://doi.org/10.1371/journal.pone.0153708.s001
(DOC)
Author Contributions
Conceived and designed the experiments: HZ JC. Performed the experiments: PW. Analyzed the data: NL. Contributed reagents/materials/analysis tools: LM XZ. Wrote the paper: PW YW.
Citation: Wang P, Cao J, Liu N, Ma L, Zhou X, Zhang H, et al. (2016) Protective Effects of Edaravone in Adult Rats with Surgery and Lipopolysaccharide Administration-Induced Cognitive Function Impairment. PLoS ONE 11(4): e0153708. https://doi.org/10.1371/journal.pone.0153708
1. Moller JT, Cluitmans P, Rasmussen LS, Houx P, Rasmussen H, Canet J, et al. Long-term postoperative cognitive dysfunction in the elderly ISPOCD1 study. ISPOCD investigators. International Study of Post-Operative Cognitive Dysfunction. Lancet. 1998;351(9106):857–61. pmid:9525362
2. Hovens IB, Schoemaker RG, van der Zee EA, Heineman E, Izaks GJ, van Leeuwen BL. Thinking through postoperative cognitive dysfunction: How to bridge the gap between clinical and pre-clinical perspectives. Brain Behav Immun. 2012;26(7):1169–79. pmid:22728316
3. Steinmetz J, Christensen KB, Lund T, Lohse N, Rasmussen LS, Group I. Long-term consequences of postoperative cognitive dysfunction. Anesthesiology. 2009;110(3):548–55. pmid:19225398
4. Krenk L, Rasmussen LS, Kehlet H. New insights into the pathophysiology of postoperative cognitive dysfunction. Acta Anaesthesiol Scand. 2010;54(8):951–6. pmid:20626359
5. Zhang X, Xin X, Dong Y, Zhang Y, Yu B, Mao J, et al. Surgical incision-induced nociception causes cognitive impairment and reduction in synaptic NMDA receptor 2B in mice. J Neurosci. 2013;33(45):17737–48. pmid:24198365
6. Lin D, Zuo Z. Isoflurane induces hippocampal cell injury and cognitive impairments in adult rats. Neuropharmacology. 2011;61(8):1354–9. pmid:21864548
7. Choopankareh S, Vafaee F, Shafei MN, Sadeghnia HR, Salarinia R, Zarepoor L, et al. Effects of melatonin and theanine administration on pentylenetetrazole-induced seizures and brain tissue oxidative damage in ovariectomized rats. Turk J Med Sci. 2015;45(4):842–9. pmid:26422856
8. Hara N, Chijiiwa M, Yara M, Ishida Y, Ogiwara Y, Inazu M, et al. Metabolomic Analyses of Brain Tissue in Sepsis Induced by Cecal Ligation Reveal Specific Redox Alterations-Protective Effects of the Oxygen Radical Scavenger Edaravone. Shock. 2015;44(6):578–84. pmid:26529662
9. Xia SF, Xie ZX, Qiao Y, Li LR, Cheng XR, Tang X, et al. Differential effects of quercetin on hippocampus-dependent learning and memory in mice fed with different diets related with oxidative stress. Physiol Behav. 2015;138:325–31. pmid:25447470
10. Peng S, Zhao S, Yan F, Cheng J, Huang L, Chen H, et al. HDAC2 selectively regulates FOXO3a-mediated gene transcription during oxidative stress-induced neuronal cell death. J Neurosci. 2015;35(3):1250–9. pmid:25609639
11. Yang R, Wang Q, Li F, Li J, Liu X. Edaravone injection ameliorates cognitive deficits in rat model of Alzheimer's disease. Neurol Sci. 2015.
12. Jiao SS, Yao XQ, Liu YH, Wang QH, Zeng F, Lu JJ, et al. Edaravone alleviates Alzheimer's disease-type pathologies and cognitive deficits. Proc Natl Acad Sci U S A. 2015;112(16):5225–30. pmid:25847999
13. Dohare P, Hyzinski-Garcia MC, Vipani A, Bowens NH, Nalwalk JW, Feustel PJ, et al. The neuroprotective properties of the superoxide dismutase mimetic tempol correlate with its ability to reduce pathological glutamate release in a rodent model of stroke. Free Radic Biol Med. 2014;77:168–82. pmid:25224033
14. Sun YY, Li Y, Wali B, Li Y, Lee J, Heinmiller A, et al. Prophylactic Edaravone Prevents Transient Hypoxic-Ischemic Brain Injury: Implications for Perioperative Neuroprotection. Stroke. 2015;46(7):1947–55. pmid:26060244
15. Ogasawara K, Yamadate K, Kobayashi M, Endo H, Fukuda T, Yoshida K, et al. Effects of the free radical scavenger, edaravone, on the development of postoperative cognitive impairment in patients undergoing carotid endarterectomy. Surg Neurol. 2005;64(4):309–13; discussion 13–4. pmid:16182000
16. Banoub JH, El Aneed A, Cohen AM, Joly N. Structural investigation of bacterial lipopolysaccharides by mass spectrometry and tandem mass spectrometry. Mass Spectrom Rev. 2010;29(4):606–50. pmid:20589944
17. Fidalgo AR, Cibelli M, White JP, Nagy I, Maze M, Ma D. Systemic inflammation enhances surgery-induced cognitive dysfunction in mice. Neurosci Lett. 2011;498(1):63–6. pmid:21575676
18. Ullah F, Ali T, Ullah N, Kim MO. Caffeine prevents d-galactose-induced cognitive deficits, oxidative stress, neuroinflammation and neurodegeneration in the adult rat brain. Neurochem Int. 2015;90:114–24. pmid:26209154
19. Godbout JP, Chen J, Abraham J, Richwine AF, Berg BM, Kelley KW, et al. Exaggerated neuroinflammation and sickness behavior in aged mice following activation of the peripheral innate immune system. FASEB J. 2005;19(10):1329–31. pmid:15919760
20. Sun J, Ling Z, Wang F, Chen W, Li H, Jin J, et al. Clostridium butyricum pretreatment attenuates cerebral ischemia/reperfusion injury in mice via anti-oxidation and anti-apoptosis. Neurosci Lett. 2016;613:30–5. pmid:26733300
21. Lee J, Banu SK, McCracken JA, Arosh JA. Early pregnancy modulates survival and apoptosis pathways in the corpus luteum in sheep. Reproduction. 2016;151(3):187–202. pmid:26585285
22. He HJ, Wang Y, Le Y, Duan KM, Yan XB, Liao Q, et al. Surgery upregulates high mobility group box-1 and disrupts the blood-brain barrier causing cognitive dysfunction in aged rats. CNS Neurosci Ther. 2012;18(12):994–1002. pmid:23078219
23. Terrando N, Eriksson LI, Ryu JK, Yang T, Monaco C, Feldmann M, et al. Resolving postoperative neuroinflammation and cognitive decline. Ann Neurol. 2011;70(6):986–95. pmid:22190370
24. Ehninger D, Han S, Shilyansky C, Zhou Y, Li W, Kwiatkowski DJ, et al. Reversal of learning deficits in a Tsc2+/- mouse model of tuberous sclerosis. Nat Med. 2008;14(8):843–8. pmid:18568033
25. Kempermann G, Song H, Gage FH. Neurogenesis in the Adult Hippocampus. Cold Spring Harb Perspect Med. 2015;5(7):a018812.
26. Morris R. Developments of a water-maze procedure for studying spatial learning in the rat. J Neurosci Methods. 1984;11(1):47–60. pmid:6471907
27. Vorhees CV, Williams MT. Morris water maze: procedures for assessing spatial and related forms of learning and memory. Nat Protoc. 2006;1(2):848–58. pmid:17406317
28. Inoue T, Tsuchiya K, Koyama T. Regional changes in dopamine and serotonin activation with various intensity of physical and psychological stress in the rat brain. Pharmacol Biochem Behav. 1994;49(4):911–20. pmid:7886107
29. Kim JJ, Fanselow MS. Modality-specific retrograde amnesia of fear. Science. 1992;256(5057):675–7. pmid:1585183
30. Qiao Y, Feng H, Zhao T, Yan H, Zhang H, Zhao X. Postoperative cognitive dysfunction after inhalational anesthesia in elderly patients undergoing major surgery: the influence of anesthetic technique, cerebral injury and systemic inflammation. BMC Anesthesiol. 2015;15:154. pmid:26497059
31. Patel N, Minhas JS, Chung EM. Risk Factors Associated with Cognitive Decline after Cardiac Surgery: A Systematic Review. Cardiovasc Psychiatry Neurol. 2015;2015:370612. pmid:26491558
32. Barrientos RM, Frank MG, Hein AM, Higgins EA, Watkins LR, Rudy JW, et al. Time course of hippocampal IL-1 beta and memory consolidation impairments in aging rats following peripheral infection. Brain Behav Immun. 2009;23(1):46–54. pmid:18664380
33. Wang Y, Cui Y, Cao F, Qin Y, Li W, Zhang J. Ganglioside GD1a suppresses LPS-induced pro-inflammatory cytokines in RAW264.7 macrophages by reducing MAPKs and NF-kappaB signaling pathways through TLR4. Int Immunopharmacol. 2015;28(1):136–45. pmid:26054879
34. Dong Z, Bai Y, Wu X, Li H, Gong B, Howland JG, et al. Hippocampal long-term depression mediates spatial reversal learning in the Morris water maze. Neuropharmacology. 2013;64:65–73. pmid:22732443
35. Brandeis R, Brandys Y, Yehuda S. The use of the Morris Water Maze in the study of memory and learning. Int J Neurosci. 1989;48(1–2):29–69. pmid:2684886
36. D'Hooge R, De Deyn PP. Applications of the Morris water maze in the study of learning and memory. Brain Res Brain Res Rev. 2001;36(1):60–90. pmid:11516773
37. Cain DP, Saucier D. The neuroscience of spatial navigation: focus on behavior yields advances. Rev Neurosci. 1996;7(3):215–31. pmid:8916293
38. Clausen F, Lewen A, Marklund N, Olsson Y, McArthur DL, Hillered L. Correlation of hippocampal morphological changes and morris water maze performance after cortical contusion injury in rats. Neurosurgery. 2005;57(1):154–63; discussion -63. pmid:15987551
39. Moser MB, Moser EI, Forrest E, Andersen P, Morris RG. Spatial learning with a minislab in the dorsal hippocampus. Proc Natl Acad Sci U S A. 1995;92(21):9697–701. pmid:7568200
40. Gao Y, Dickerson JB, Guo F, Zheng J, Zheng Y. Rational design and characterization of a Rac GTPase-specific small molecule inhibitor. Proc Natl Acad Sci U S A. 2004;101(20):7618–23. pmid:15128949
41. Diana G, Valentini G, Travaglione S, Falzano L, Pieri M, Zona C, et al. Enhancement of learning and memory after activation of cerebral Rho GTPases. Proc Natl Acad Sci U S A. 2007;104(2):636–41. pmid:17202256
42. Al Banchaabouchi M, Marescau B, D'Hooge R, Van Marck E, De Deyn PP. Biochemical, histological and behavioral consequences of nephrectomy in young and aged mice. Nephron. 2001;89(1):90–100. pmid:11528238
43. Chen C, Cai J, Zhang S, Gan L, Dong Y, Zhu T, et al. Protective Effect of RNase on Unilateral Nephrectomy-Induced Postoperative Cognitive Dysfunction in Aged Mice. PLoS One. 2015;10(7):e0134307. pmid:26225860
44. Di Vita G, Patti R, D'Agostino P, Caruso G, Arcara M, Buscemi S, et al. Cytokines and growth factors in wound drainage fluid from patients undergoing incisional hernia repair. Wound Repair Regen. 2006;14(3):259–64. pmid:16808804
45. Kobbe P, Vodovotz Y, Kaczorowski DJ, Mollen KP, Billiar TR, Pape HC. Patterns of cytokine release and evolution of remote organ dysfunction after bilateral femur fracture. Shock. 2008;30(1):43–7. pmid:18562923
46. Pasechnik IN, Meshcheriakov AA, Kontarev SI, Lozenko SP. [The oxidant-antioxidant system and cognitive functions in patients undergoing elective abdominal operations under various general anesthesia modes]. Anesteziol Reanimatol. 2009(4):50–4. pmid:19827202
47. Wan Y, Xu J, Ma D, Zeng Y, Cibelli M, Maze M. Postoperative impairment of cognitive function in rats: a possible role for cytokine-mediated inflammation in the hippocampus. Anesthesiology. 2007;106(3):436–43. pmid:17325501
48. Hirsch EC, Hunot S. Neuroinflammation in Parkinson's disease: a target for neuroprotection? Lancet Neurol. 2009;8(4):382–97. pmid:19296921
49. Tansey MG, McCoy MK, Frank-Cannon TC. Neuroinflammatory mechanisms in Parkinson's disease: potential environmental triggers, pathways, and targets for early therapeutic intervention. Exp Neurol. 2007;208(1):1–25. pmid:17720159
50. Ramirez-Sanchez J, Simoes Pires EN, Nunez-Figueredo Y, Pardo-Andreu GL, Fonseca-Fonseca LA, Ruiz-Reyes A, et al. Neuroprotection by JM-20 against oxygen-glucose deprivation in rat hippocampal slices: Involvement of the Akt/GSK-3beta pathway. Neurochem Int. 2015;90:215–23. pmid:26361722
51. Li L, McBride DW, Doycheva D, Dixon BJ, Krafft PR, Zhang JH, et al. G-CSF attenuates neuroinflammation and stabilizes the blood-brain barrier via the PI3K/Akt/GSK-3beta signaling pathway following neonatal hypoxia-ischemia in rats. Exp Neurol. 2015;272:135–44. pmid:25585014
52. Calvino E, Estan MC, Simon GP, Sancho P, Boyano-Adanez Mdel C, de Blas E, et al. Increased apoptotic efficacy of lonidamine plus arsenic trioxide combination in human leukemia cells. Reactive oxygen species generation and defensive protein kinase (MEK/ERK, Akt/mTOR) modulation. Biochem Pharmacol. 2011;82(11):1619–29. pmid:21889928
53. Huang CS, Lin AH, Yang TC, Liu KL, Chen HW, Lii CK. Shikonin inhibits oxidized LDL-induced monocyte adhesion by suppressing NFkappaB activation via up-regulation of PI3K/Akt/Nrf2-dependent antioxidation in EA.hy926 endothelial cells. Biochem Pharmacol. 2015;93(3):352–61. pmid:25541286
54. Kalb A, von Haefen C, Sifringer M, Tegethoff A, Paeschke N, Kostova M, et al. Acetylcholinesterase inhibitors reduce neuroinflammation and -degeneration in the cortex and hippocampus of a surgery stress rat model. PLoS One. 2013;8(5):e62679. pmid:23671623
55. Tarassishin L, Suh HS, Lee SC. Interferon regulatory factor 3 plays an anti-inflammatory role in microglia by activating the PI3K/Akt pathway. J Neuroinflammation. 2011;8:187. pmid:22208359
56. Dong H, Zhang X, Dai X, Lu S, Gui B, Jin W, et al. Lithium ameliorates lipopolysaccharide-induced microglial activation via inhibition of toll-like receptor 4 expression by activating the PI3K/Akt/FoxO1 pathway. J Neuroinflammation. 2014;11:140. pmid:25115727
57. Oddo S. The role of mTOR signaling in Alzheimer disease. Front Biosci (Schol Ed). 2012;4:941–52.
58. Puighermanal E, Marsicano G, Busquets-Garcia A, Lutz B, Maldonado R, Ozaita A. Cannabinoid modulation of hippocampal long-term memory is mediated by mTOR signaling. Nat Neurosci. 2009;12(9):1152–8. pmid:19648913
59. Hoeffer CA, Klann E. mTOR signaling: at the crossroads of plasticity, memory and disease. Trends Neurosci. 2010;33(2):67–75. pmid:19963289
60. C ON. PI3-kinase/Akt/mTOR signaling: impaired on/off switches in aging, cognitive decline and Alzheimer's disease. Exp Gerontol. 2013;48(7):647–53. pmid:23470275
You have requested "on-the-fly" machine translation of selected content from our databases. This functionality is provided solely for your convenience and is in no way intended to replace human translation. Show full disclaimer
Neither ProQuest nor its licensors make any representations or warranties with respect to the translations. The translations are automatically generated "AS IS" and "AS AVAILABLE" and are not retained in our systems. PROQUEST AND ITS LICENSORS SPECIFICALLY DISCLAIM ANY AND ALL EXPRESS OR IMPLIED WARRANTIES, INCLUDING WITHOUT LIMITATION, ANY WARRANTIES FOR AVAILABILITY, ACCURACY, TIMELINESS, COMPLETENESS, NON-INFRINGMENT, MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE. Your use of the translations is subject to all use restrictions contained in your Electronic Products License Agreement and by using the translation functionality you agree to forgo any and all claims against ProQuest or its licensors for your use of the translation functionality and any output derived there from. Hide full disclaimer
© 2016 Wang et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
Abstract
Postoperative cognitive dysfunction (POCD) is a clinical syndrome characterized by cognitive declines in patients after surgery. Previous studies have suggested that surgery contributed to such impairment. It has been proven that neuroinflammation may exacerbate surgery-induced cognitive impairment in aged rats. The free radical scavenger edaravone has high blood brain barrier permeability, and was demonstrated to effectively remove free radicals from the brain and alleviate the development of POCD in patients undergoing carotid endarterectomy, suggesting its potential role in preventing POCD. For this reason, this study was designed to determine whether edaravone is protective against POCD through its inhibitory effects on inflammatory cytokines and oxidative stress. First, Sprague Dawley adult male rats were administered 3 mg/kg edaravone intraperitoneally after undergoing a unilateral nephrectomy combined with lipopolysaccharide injection. Second, behavioral parameters related to cognitive function were recorded by fear conditioning and Morris Water Maze tests. Last, superoxide dismutase activities and malondialdehyde levels were measured in the hippocampi and prefrontal cortex on postoperative days 3 and 7, and microglial (Iba1) activation, p-Akt and p-mTOR protein expression, and synaptic function (synapsin 1) were also examined 3 and 7 days after surgery. Rats that underwent surgery plus lipopolysaccharide administration showed significant impairments in spatial and working memory, accompanied by significant reductions in hippocampal-dependent and independent fear responses. All impairments were attenuated by treatment with edaravone. Moreover, an abnormal decrease in superoxide dismutase activation, abnormal increase in malondialdehyde levels, significant increase in microglial reactivity, downregulation of p-Akt and p-mTOR protein expression, and a statistically significant decrease in synapsin-1 were observed in the hippocampi and prefrontal cortices of rats at different time points after surgery. All mentioned abnormal changes were totally or partially reversed by edaravone. To our knowledge, few reports have shown greater protective effects of edaravone on POCD induced by surgery plus lipopolysaccharide administration from its anti-oxidative stress and anti-inflammatory effects, as well as maintenance of Akt/mTOR signal pathway activation; these might be closely related to the therapeutic effects of edaravone. Our research demonstrates the potential use of edaravone in the treatment of POCD.
You have requested "on-the-fly" machine translation of selected content from our databases. This functionality is provided solely for your convenience and is in no way intended to replace human translation. Show full disclaimer
Neither ProQuest nor its licensors make any representations or warranties with respect to the translations. The translations are automatically generated "AS IS" and "AS AVAILABLE" and are not retained in our systems. PROQUEST AND ITS LICENSORS SPECIFICALLY DISCLAIM ANY AND ALL EXPRESS OR IMPLIED WARRANTIES, INCLUDING WITHOUT LIMITATION, ANY WARRANTIES FOR AVAILABILITY, ACCURACY, TIMELINESS, COMPLETENESS, NON-INFRINGMENT, MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE. Your use of the translations is subject to all use restrictions contained in your Electronic Products License Agreement and by using the translation functionality you agree to forgo any and all claims against ProQuest or its licensors for your use of the translation functionality and any output derived there from. Hide full disclaimer