Protective effect of bilobalide on learning and memory impairment in rats with vascular dementia
- Authors:
- Published online on: July 8, 2013 https://doi.org/10.3892/mmr.2013.1573
- Pages: 935-941
Abstract
Introduction
Vascular dementia (VD) occurs as a result of ischemic injury or oligemia to brain areas, which leads to a progressive cognition decline, functional ability impairment and behavioral problems (1). VD is considered the second most common dementia and prevalence of VD is increased, accompanied by a corresponding increase in elderly population. Currently, there is no effective cure for VD, thus investigators have focused on preventing further brain damage.
The standardized Ginkgo biloba extract, EGb 761, has been reported to have neuroprotective effects against various neurological disorders, such as Alzheimer's disease, ischemia and depression (2–4). Although these results suggest the possibility of using the Ginkgo biloba extract as an anti-dementia drug, the properties of each constituent of the extract should be analyzed to develop an optimally effective anti-dementia drug. EGb 761 contains two groups of bioactive constituents, the flavonoids (24%) and the terpenoids (6%), which have been actively investigated for their neuroprotective and neuromodulatory activities (5). It has been reported that the effectiveness of the Ginkgo biloba extract EGb 761 in a middle cerebral artery occlusion (MCAO) model was exclusively due to the presence of bilobalide (BB), a sesquiterpene lactone that constitutes 2.9–3.2% of the extract (6,7). Accumulating evidence suggest that BB has neuroprotective effects (2,8,9). Optimum efficacy usually requires extracts at high doses (50–200 mg/kg), while using lower doses of BB may result in an equally high efficacy.
Chronic cerebral hypoperfusion is mimicked in animals by bilateral common carotid artery occlusion (2-vessel occlusion, 2-VO), resulting in the establishment of a suitable model for investigating the mechanisms of VD (10). The aim of the present study was to investigate the effects of BB, a specific constituent of the Ginkgo biloba extract EGb 761, on VD rats. Consequently, we investigated the effects of BB on the learning and memory dysfunction in VD rats. BB was hypothesized to improve the learning and memory dysfunction in VD rats due to its antioxidant and antiapoptotic properties. Furthermore, we investigated the effects of BB on oxidative injury, neuronal apoptosis and the expression of tumor necrosis factor-α (TNF-α) in VD rats.
Materials and methods
Drugs and reagents
Bilobalide (content of BB, >98%; Fig. 1) was obtained from the Creative Pharmaceutical Technology Co., Ltd. (Hefei, China). Streptavidin-biotin complex and diaminobenzidine (DAB) staining kits were purchased from ZSGB-BIO (Beijing, China). Antibody against TNF-α was purchased from Beijing Biosynthesis Biotechnology Co., Ltd. (China). Drugs were dissolved in distilled water, and all the additional chemicals were of the highest analytical grade available.
Animals and treatment
The rodent experiments were appropriately performed to minimize animal suffering and were in accordance with the animal protocols approved by the local authorities in Anhui, China. Adult male Sprague Dawley rats (2 to 3-month-old, 180–200 g) were obtained from the Center of Laboratory Animal of Anhui, China (Grade II, Certificate no. SCXK 2005-001). The rats were housed under conditions of controlled lighting (12-h light/dark cycle) and temperature (25°C). All the animals were allowed ad libitum access to food and water, and were allowed to acclimatize for ≥3 days prior to experimentation.
The rats were randomly divided into 7 groups: the sham-surgery, model, BB (2, 4 and 8 mg/kg), Nimotop (Nimo, 10.5 mg/kg) and Huperzine A (Hupa, 0.047 mg/kg) groups. Nimo and Hupa, which are standard drugs for dementia treatment, were used as positive controls. The animals were anesthetized with 10% chloral hydrate [3 ml/kg, intraperitoneally (i.p.)]. Surgical operation was conducted as previously described (11). Briefly, through a midline cervical incision, the bilateral common carotid arteries of each rat were carefully separated from the cervical sympathetic and vagal nerves. The bilateral common carotid arteries were then exposed and ligated with 4-0 silk sutures in the permanent 2-VO group. The rats of the sham-operated group underwent the same surgical operation without carotid artery ligations. Mean body temperature (taken rectally) was maintained during surgery at 37.0±0.5°C. The rats of the BB (2, 4 and 8 mg/kg), Nimo (10.5 mg/kg) and Hupa (0.047 mg/kg) groups were treated with the respective drugs [intragastric (i.g.) administration] for 60 days from day 1 following surgery. The rats of the sham-surgery group were administered equivalent volumes of vehicle.
Morris water maze test
The Morris water maze (MWM) consists of a black 1.6-m diameter circular pool. The pool was divided into 4 equal hypothetical quadrants and filled with water (24°C; depth, 30 cm). In the middle of a certain quadrant, there was a submerged escape platform (10 cm in diameter), which was placed 2 cm below the surface of the water. The water maze apparatus, rat handling, and general testing procedure have been previously described (12).
All the rats were released into water (facing the wall) at 4 distinct starting quadrant points and were given 4 trials/day (90 sec/trial) from 56 to 59 days following surgery, for 4 consecutive days. Using an on-line image video tracking system, escape latency (sec) was recorded to determine changes in learning dysfunction. On day 60, following completion of all the learning trials for all the rats, the platform was removed from the pool, and each rat received one 90-sec swim probe trial. The time of swimming in the quadrant of platform (STP) and the number of rats crossing the platform (NCP) were recorded to determine changes in memory dysfunction. Behavioral data were analyzed using analysis of variance.
Detection of superoxide dismutase (SOD), nitric oxide synthase (NOS) activity, and malondialdehyde (MDA) glutathione (GSH) content
Following MWM testing, 8 rats from each group were anesthetized and sacrificed by decapitation. The brain of each rat was dissociated and stored at −80°C until assessment. Superoxide dismutase (SOD) and nitric oxide synthase (NOS) activity, as well as malondialdehyde (MDA) and glutathione (GSH) content were determined using the appropriative detection kits (Nianjing Jiancheng Bioengineering Institute, Nanjing, China).
Histological examination
Following MWM testing, 5 rats from each group were anesthetized with 10% chloral hydrate (3.0 ml/kg). Following animal sacrifice, the brain of each rat was removed, fixed in 4% paraformaldehyde and embedded in paraffin. The brain tissues were sliced (5-μm) using a section cutter (Leica Biosystems, Wetzlar, Germany). The sections were then stained with hematoxylin and eosin (H&E) and examined under a light microscope.
Hoechst 33258 staining
For nuclear staining, paraffin sections were dehydrated through a gradient of xylene and ethanol, and then rinsed with phosphate-buffered saline (PBS). The sections were incubated with 25 mM Hoechst 33258 (ZSGB-BIO) for 15 min at 37°C, washed with PBS (pH 7.2–7.5), mounted onto slides using antifade mounting medium, and then examined using fluorescence microscopy (Ex/Em, 352/461 nm) (Olympus Optical, Tokyo, Japan).
Immunohistochemistry
Paraffin sections were cut (5-μm) and fixed to slides to ensure adhesion. The sections were incubated with hydrogen peroxide (3%) to inactivate endogenous peroxidase, and non-immune goat serum was used as a blocking agent. The sections were incubated with the primary antibody against TNF-α (1:100) overnight at 4°C. Immunostaining was visualized by the peroxidase method with a biotinylated anti-rabbit secondary antibody and DAB oxidation. The sections were resin-mounted and examined using a fluorescence microscope (Nikon, Japan). The immunoreactive neurons which were stained brown were observed, and images were captured under the microscope. Five sections/group and the three high-power fields of the hippocampal CA1 region and the brain cortex/section of the same magnification (x400) were used for quantitative analysis. The mean optical density of positive neurons in each section was measured using the Image-Pro Plus 6.0 analysis system to determine TNF-α expression.
Statistical analysis
Intergroup differences were analyzed using one-way ANOVA. The Student's t-test was used to determine significant differences between groups. Results were expressed as the mean ± SD. P<0.05 was considered to indicate a statistically significant difference.
Results
Effects of BB on the learning and memory ability of VD rats
MWM was used to determine the learning and memory ability of rats. In the memory training experiment, the mean escape latencies in the rats of all the groups were significantly reduced with increasing time. The mean escape latencies in the VD rats of the model group were significantly increased compared with the model group (P<0.01). The mean escape latencies were differently decreased following BB (2, 4 and 8 mg/kg), Nimo and Hupa treatment (P<0.05 or <0.01) (Table I). In addition, NCP and STP in the rats of the model group were also significantly reduced compared with the sham-surgery group (P<0.05 or <0.01). NCP (P<0.05) and STP (P<0.05 or <0.01) in the rats of the BB (2, 4 and 8 mg/kg), Nimo and Hupa groups were differentially decreased compared with the model group (Table II).
Effects of BB on neuronal morphology in the brain cortex and hippocampal CA1 region
H&E and Hoechst 33258 staining were used to investigate the neuronal morphology and apoptosis of the brain cortex and the hippocampal CA1 region of the rats. H&E staining indicated that there were no significant neuronal abnormalities in the brain cortex and the hippocampal CA1 region of the rats in the sham-surgery group (Fig. 2A). However, the rats in the model group exhibited acidophilia degeneration, nuclear condensation and disorder of the array of neurons in these regions (Fig. 2B). Neuronal degeneration was alleviated in the rats of the BB (4 and 8 mg/kg), Nimo and Hupa groups compared with the model group (Fig. 2).
We examined the neuronal apoptosis of the brain cortex and the hippocampal CA1 region of rats using Hoechst 33258 staining. The average number of apoptotic cells in these regions, which appear smaller than normal and in which the chromatin appears to be condensed, were counted (n=5). The percentage of nuclear condensation in the brain cortex and the hippocampal CA1 region in the rats of the model group was significantly increased compared with sham-surgery group (P<0.05 or <0.01). The percentage of nuclear condensation in the brain cortex and the hippocampal CA1 region in the rats of the BB (4 and 8 mg/kg), Hupa and Nimo groups was differentially decreased compared with the model group (P<0.05 or <0.01; Fig. 3).
Effects of BB on brain tissue SOD, NOS activities and MDA, GSH contents
SOD activity and GSH content were significantly decreased (P<0.01), while the MDA content and NOS activity were clearly increased (P<0.01) in the rats of the model group compared with the sham-surgery group. BB 2, 4 and 8 mg/kg), Nimo and Hupa treatment differentially increased SOD activity and GSH content (P<0.05 or <0.01), but decreased MDA content and NOS activity in VD rats compared with the rats in the model group (P<0.05 or <0.01) (Tables III and IV).
Effect of BB on the expression of TNF-α in the brain cortex and the hippocampal CA1 region
The effect of BB on TNF-α immunoreactivity in the brain cortex and the hippocampal CA1 region in VD rats was investigated. Under normal conditions, immunoreactive cells are abundant and appear brown in color following immunohistochemistry. Many TNF-α immunoreactive neuronal cells were observed in the brain cortex and the hippocampal CA1 region in the rats of the model group compared with the sham-surgery group. However, the number of TNF-α immunoreactive cells in the BB (4 and 8 mg/kg), Nimo and Hupa-treated rats was significantly decreased compared with the model group (Fig. 4).
The mean optical density of the brain cortex and the hippocampal CA1 region in the rats of the model group was significantly increased compared with the sham-surgery group (P<0.01). BB (4 and 8 mg/kg), Nimo and Hupa treatment obviously decreased the expression of TNF-α in these regions of VD rats (P<0.05) (Fig. 4).
Discussion
The 2-VO rat is a suitable model for investigating the pathophysiology of learning and memory impairment in human dementia, as well as for assessing the therapeutic potential and/or exploring possible mechanisms of putative anti-dementia drugs (13). BB, a sesquiterpene trilactone constituent of Ginkgo biloba leaf extracts, has been suggested to exert protective and trophic effects on neurons (8,9,14). MWM has been proven to be an effective method for the ethological evaluation of rats, and has been used to evaluate the spatial learning and memory abilities of rats (15). In the present study, the spatial learning and memory abilities of rats were decreased in the model group, while they were found to be improved following BB (4 and 8 mg/kg) treatment. These results suggest that daily administration of BB rescues cognitive deficits in VD rats.
The mechanism underlying the permanent occlusion of both common carotid arteries responsible for inducing learning and memory deficits is intricate. Neuronal apoptosis has been found to be related to deficits in spatial learning and memory in rats induced by chronic cerebral hypoperfusion (16). Hippocampus plays an important role in learning and memory processing, and is highly sensitive to ischemic insults (11,17). Cerebral ischemia inducing neuronal degeneration has also been observed in other structures, such as striatum, brain cortex and thalamus (18,19). In the present study, histological changes and neuronal apoptosis in the brain cortex and the hippocampal CA1 region of rats were investigated. Histological examination plays an important role in the evaluation of neuronal damage and drug action (20). H&E and Hoechst 33258 staining showed that the number of apoptotic cells was significantly increased in the rats of the model group, and that BB (4 and 8 mg/kg) treatment alleviated the neuronal impairment and apoptosis. These results suggest that BB has an antiapoptotic activity.
Oxidative stress is involved in neuronal apoptosis (21). It is well known that free radicals participate in the regulation of neuron degeneration and apoptosis, and are potentially involved in the pathogenesis of neurodegenerative diseases such as VD (22,23). MDA is an important biomarker of lipid peroxidation that is induced by reactive oxygen species. Specific quantification of MDA is able to determine the extent of lipid damage as a result of oxidative stress in a variety of lipid systems, such as plasma, organs and cell membranes (24). Free radicals cause oxidative damage to important biological molecules. Consequently, organisms exhibit increased SOD, catalase and glutathione peroxidase activities in response to oxidative stress (25). Increased SOD activity could be regarded as an indication that the antioxidant mechanism of the brain is activated in response to oxidative stress (26). Free radicals directly damage antioxidant enzymes and reduce their activities (27). In the present study, GSH content was found to be significantly decreased in VD rats. Therefore, the increment in MDA content and SOD activity found in the rats of the model group suggests an obviously increased oxidative process, while the decrease in the GSH content indicates the presence of deficiencies in the endogenous antioxidant ability. Nitric oxide (NO) might exacerbate the damage by enhancing the post-ischemic release of excitatory neurotransmitters (28). Changes in the level of NO produced by NOS occur in acute cerebral ischemia and Alzheimer's disease (AD) (29). In the present study, BB (2, 4 and 8 mg/kg) significantly increased SOD activity and GSH content, and decreased MDA content and NOS activity in VD rats. Previous studies have demonstrated that agents with antioxidant and radical scavenger properties have been effective in the treatment of VD in animals or in clinical trials (30–32). In the present study, learning and memory dysfunction is suggested to have been alleviated by BB due to its antioxidant properties, since oxidative stress in all cases plays an important role in 2-VO-induced neurodegenerative processes (33).
TNF-α, a pro-inflammatory cytokine that is produced by macrophages, adipocytes and astrocytes, appears to be an unspecific but potent factor in the development of several psychiatric diseases, including depression and dementia. Elevated TNF-α levels have been found in the cerebrospinal fluid of patients with AD and VD, suggesting an important role of TNF-α production by the central nervous system in dementia (34). TNF-α has been shown to induce neuronal death in several neurodegenerative disorders including AD and VD (35). The results of the present study have shown that BB (4 and 8 mg/kg) significantly decreased the expression of TNF-α in the brain cortex and the hippocampal CA1 region of VD rats. This suggests that the inhibitory effect of BB on neuronal apoptosis is associated with the regulation of TNF-α expression by BB.
In conclusion, the present study has demonstrated that BB has a potential antioxidant activity, inhibits neuronal apoptosis and reduces the expression of TNF-α in the brain cortex and the hippocampal CA1 region of VD rats. These effects might be related to its antioxidant and antiapoptotic activities. However, additional studies are needed for the elucidation of the detailed mechanism between the two activities of BB.
Acknowledgements
This study was supported by the Doctor Foundation of Anhui Medical University (XJ201011) and the Teaching Quality Project of Anhui Higher Education (20101941). The authors thank Dake Huang, Shan Huang and Li Gui (Synthetic Laboratory of Basic Medicine College, Anhui Medical University, Hefei, China) for their excellent technical assistance.
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