Neuroprotective effects of salidroside administration in a mouse model of Alzheimer's disease

Introduction

Alzheimer's disease (AD) is a progressive neurodegenerative disorder, which is characterized by severe memory loss and behavioral disturbances (1–3). AD is a multifactorial disease and is affected by genetic risk factors, aging and oxidative stresses (4,5). The impairment of memory and cognition in patients with AD is caused by synaptic loss, enhanced inflammatory signaling, progressive deposition of senile plaques, neurofibrillary tangles and neurodegeneration (6–8). Additionally, amyloid-β (Aβ) peptides, as well as the tau protein, in the form of neurofibrillary tangles, are implicated in the pathogenesis of AD (9). In addition to the tau-amyloid signature, oxidative damage, neuroinflammation, widespread synaptic loss and neuronal death are considered hallmark features of AD (9).

With an aging population, AD is on the increase, and there are currently no effective treatments or cures. Therefore, the pursuit of novel disease-modifying therapeutics for AD is the subject of intense investigation.

Salidroside is a type of traditional Chinese medicine, which is extracted from rhodiola medical plants, named Rhodiolasa chinensis A Bor. Salidroside has numerous pharmacological activities, such as anti-anoxia (10), anticancer (11,12), anti-fatigue (13), and anti-toxin effects (14). Furthermore, numerous studies have suggested that salidroside may also improve cognitive functioning in disease models (15,16); however, the mechanisms were not determined. In this study, the potential therapeutic effect of salidroside in APPswe/PS1ΔE9 mice and its underlying mechanisms were investigated.

Materials and methods

Experimental animals

All the experiments were performed with the approval of the Ethics Committee of the Tianjin Medical University (Tianjin, China). APPswe/PS1ΔE9 mice (n=20; 3 months, male, 26–30 g) and C57BL/6J mice (n=20; 3 months, male, 23–26 g) in clean grade were obtained from Beijing Huafukang Biological Technology company (Beijing, China) and raised in the temperature of 25±2°C, relative humidity 70% and in a 12-h light/dark room at with free access to food and water. Following 1 week of adaption, all APPswe/PS1ΔE9 mice were randomly divided into either the AD model group or the salidroside + AD model group (n=10 in each group). C57BL/6J mice were also randomly divided into either the normal control (NC) group or the salidroside + NC group (n=10 in each group). The mice in the salidroside + NC and salidroside + AD model groups were administered salidroside (30 mg/kg) orally once daily for 3 consecutive months. Following treatment, behavioral tests and biochemical experiments were performed.

Morris water maze (MWM)

Following the 3 months of salidroside treatment, the cognitive behavior of all of the mice was investigated using MWM (17), which measures spatial learning and memory ability. The animals were subjected to a daily session of four training trials for 4 consecutive days. In each training session, mice were placed into the pool at four different starting points (different quadrants). The mice were then permitted to find the platform within a maximum time period of 120 sec and following that the mice were allowed to remain on the platform for a further 30 sec. If a mouse was unable to find the platform within the 120 sec time period, the mouse would then be guided to the platform by the experimenter, and the escape latency was recorded as 120 sec. At day 5 of spatial testing, the platform was removed and mice were placed into water at any starting point. The time period that the mouse remained in the quadrant where the platform had previously been placed was then recorded.

Terminal deoxynucleotidyl-transferase-mediated dUTP nick end labeling (TUNEL) assay

Detection of hippocampal neuronal apoptosis was carried out using the TUNEL assay. The hippocampal tissue was fixed in 4% formalin at 4°C for 48 h and then embedded in paraffin wax. Apoptosis rates were detected using the In Situ Cell Death Detection kit (Roche Applied Science, Rotkreuz, Switzerland) according to the manufacturer's instructions. Apoptotic rate changes were measured via a light microscope (Olympus Corporation, Tokyo, Japan). Hippocampal tissue was fixed in 4% paraformaldehyde for 48 h at 4°C and embedded into paraffin wax. In Situ Cell Death Detection kit was used to detect the apoptosis according to the manufacturer's instructions. The images were taken using a light microscope (Olympus Corporation). Apoptotic rates were then determined according to the method previously detailed by Soslow et al (18). A positive expression rate of 0–1% was defined as score 0 (negative), 1–10% as score 1 (weakly positive), 10–50% as score 2 (positive), 50–80% as score 3 (medium positive) and 80–100% as score 4 (strongly positive). Three sections were used for each group, and five fields were randomly selected from each section (magnification, ×400).

Superoxide dismutase (SOD) and malondialdehyde (MDA) measurements

Following the MWM test, all of the mice were anaesthetized, immediately sacrificed, and brain tissues were quickly isolated. Following this, the brains were separated into two cerebral hemispheres via incision along the midline. Hippocampal tissue of CA1 region was then isolated from one of the cerebral hemispheres of each animal and then immediately frozen in liquid nitrogen for subsequent SOD and MDA testing. Hippocampal SOD (cat. no. ab65354) and MDA (cat. no. ab65354) (both from Abcam, Cambridge, UK) activity were then detected usinga microplate reader (wavelength, 210 nm).

Nitrate assay

Colorimetric reaction using Griess reagent was used to investigate the nitrate concentration in the hippocampal tissue of the mouse. The Nitric Oxide Assay kit was purchased from Abcam, and all procedures were performed out in accordance with the manufacturer's instructions. The results of the hippocampal nitrate concentrations of the different groups were expressed as µg/mg protein.

Determination of glutathione (GSH) concentration

Firstly, the hippocampal rat samples were precipitated by the addition of 5% sulfosalicylic acid and protein-free supernatant was removed by centrifugation at 2,000 × g for 10 min. A sample of 100 µl protein-free supernatant of the cell lysate was then added to 800 µl 0.3 mM Na2HPO4 and 100 µl 0.04% 5,5′-dithiobis-2-nitrobenzoic acid (DTNB) in 0.1% sodium citrate at 4°C overnight. Following this, the absorbance of DTNB was monitored using a spectrophotometer at 412 nm for 5 min. A standard curve of GSH was established, and the sensitivity of measurement was determined to be between 1–100 µM. The results of the GSH concentrations in the samples were expressed as µg/mg protein.

Determination of tumor necrosis factor-α (TNF-α) and interleukin-6 (IL-6) concentrations in tissue homogenate by ELISA

The concentrations of TNF-α and IL-6 in the hippocampal tissue of the mice were determined using ELISA. ELISA kits for TNF-α (cat. no. ab46070) and IL-6 (cat. no. ab100772) were purchased from Abcam. All procedures were performed in accordance with the manufacturer's instructions. The results of the determined hippocampal concentrations of TNF-α and IL-6 were expressed as µg/mg protein.

Statistical analysis

Statistical analysis was performed using SPSS 17.0 (SPSS, Inc., Chicago, IL, USA). All data were expressed as the mean ± standard deviation of the mean. One-way analysis of variance was used to compare differences among three or more groups, and this was followed by Student Newman-Keuls-test for multiple comparisons. P<0.05 was considered to indicate a statistically significant difference.

Results

Administration of salidroside improves the spatial learning and memory abilities of AD mice

MWM was used to investigate the effects of salidroside administration on the learning and memory abilities of mice. As revealed in Fig. 1A, the escape latency time of the AD group was longer than that of the normal group, and there was no significant difference between the normal and the salidroside + NC groups. Furthermore, the escape latency of the mice in the salidroside + AD model group was significantly reduced compared with the escape latency of the AD model group. As demonstrated in Fig. 1B, the time period that the AD model group spent in the target quadrant was significantly less than that spent by the normal group. Additionally, there was no significant difference in the time period spent in the target quadrant between the NC and the salidroside + NC groups. Furthermore, the time period that the mice of the salidroside + AD model group spent in the target quadrant was significantly higher than the time spent by the AD group, but significantly less than the time spent by the NC group. Results in the salidroside + AD group, the escape latency was significantly shortened, the time of swim in the platform quadrant significantly increased, suggesting that mice significantly improved learning and memory to escape the incubation period (P<0.05; Fig. 1).

Figure 1. Salidroside administration improves the spatial learning and memory abilities of the AD animals (n=10). Results are presented as (A) escape latency and (B) time spent in target quadrant. *P<0.05 vs. normal control (NC) group; #P<0.05 vs. AD group. AD, Alzheimer's disease; NC, normal control.

Salidroside administration mitigates the rate of neuronal apoptosis in the CA1 hippocampal region in AD mice

As revealed by Fig. 2, the number of neurons undergoing apoptosis in the CA1 hippocampal region was significantly increased in the AD group compared with the other groups. However, the administration of salidroside reduced this effect, as there was a significant reduction in neuronal apoptotic rates between the salidroside + AD group and the AD group.

Figure 2. Salidroside administration mitigates the rate of neuronal apoptosis in the CA1 hippocampal region in AD mice. n=5/group. Three sections were used for each group, and five fields of view were randomly selected from each section to be viewed under a microscope. (A) NC group, (B) salidroside + NC group, (C) AD model, (D) salidroside + AD group. (E) Quantification data of the cellular apoptotic rate in different groups. *P<0.05 vs. NC group; #P<0.05 vs. AD group. AD, Alzheimer's disease; NC, normal control.

Salidroside administration increases the concentration of GSH and the activity of SOD in the hippocampus of AD mice

The activity of SOD and the concentration of GSH in hippocampal tissue were investigated. As demonstrated in Fig. 3A, the relative SOD activity was significantly decreased in the AD group compared with the NC group; whereas SOD activity was upregulated in the salidroside + AD group compared with the AD group. Furthermore, there was no significant difference between the SOD activity of the NC group and of the salidroside + NC group. Compared with the NC group, the GSH concentration was decreased in the AD group; whereas GSH concentration was upregulated in the salidroside + AD group compared with the AD group. In addition, there was no significant difference between the GSH concentration of the NC group and the salidroside + NC group (Fig. 3B).

Figure 3. Hippocampal SOD activity and GSH concentration in the four different groups (mean ± standard deviation, n=5). Results are displayed as (A) SOD activity, and (B) GSH concentration. Statistical analysis was performed using one-way analysis of variance with Student-Newman-Keuls test. *P<0.05 vs. NC group; #P<0.05 vs. AD group. SOD, superoxide dismutase; GSH, glutathione; NC, normal control; AD, Alzheimer's disease.

Salidroside administration reduces the concentrations of MDA and nitrate in the hippocampus of AD mice

The hippocampal concentrations of MDA and GSH in mice were also investigated. As revealed in Fig. 4, in comparison with the NC group, MDA and nitrate concentrations were both increased in the AD group; whereas both MDA and nitrate concentrations were downregulated in the salidroside + AD group compared with the AD group. Furthermore, there was no significant difference between the MDA and nitrate concentrations of the NC group and the salidroside + NC group.

Figure 4. Hippocampal MDA and nitrate concentrations in the four different groups (mean ± standard deviation; n=5). Results are displayed as (A) MDA concentration, and (B) nitrate concentration. Statistical analysis was performed using one-way analysis of variance with Student-Newman-Keuls test. *P<0.05 vs. NC group; #P<0.05 vs. AD group. MDA, malondialdehyde; NC, normal control; AD, Alzheimer's disease.

Salidroside administration decreases the expression of TNF-α and IL-6 in the hippocampus of AD mice

The effects of salidroside administration with regards to induced inflammation were investigated. The expressions of TNF-α and IL-6 inflammatory factors decreased significantly in the hippocampus of the salidroside + AD group compared with mice belonging to the AD group (Fig. 5). There was no significant difference between the expression levels of TNF-α and IL-6 of the NC group and the salidroside + NC group.

Figure 5. Hippocampal concentrations of IL-6 and TNF-α in the four different groups (mean ± standard deviation; n=5). Results are displayed as (A) concentration of IL-6, and (B) concentration of TNF-α. Statistical analysis was performed using one-way analysis of variance with Student-Newman-Keuls test. *P<0.05 vs. NC group, #P<0.05 vs. AD group. IL-6, interleukin-6; TNF-α, tumor necrosis factor-α, NC, normal control; AD, Alzheimer's disease.

Discussion

The number of people with AD worldwide is increasing as a result of the aging population. Previous research has revealed that 46.8 million people worldwide suffer from dementia, and further research has indicated that this number may increase 2–3-fold by 2030 (19). AD is a severe neurodegenerative disease of the central nervous system, which results in learning and memory impairment. The rising rate of senile dementia is of serious concern to global healthcare systems and causes serious economic burdens to affected families and wider society. AD is a neurologically complex disorder, and thus it is likely that a combinatorial therapeutic approach will be needed for effective treatment.

Chinese herbology has been heavily used globally and is regarded as an importance source of medicines. Salidroside is a component of Rhodiolarosea, and possesses medicinal properties, such as anti-inflammatory (20,21), antioxidative (14) and neuroprotective effects (22). In the present study, it was demonstrated that salidroside administration attenuates the memory impairment exhibited in the AD rat model.

Previous studies have reported that one of the major brain regions affected by AD-induced neurogenesis is the hippocampus, which is a vital brain region for learning and memory (23). Hippocampal neuronal damage adversely affects neural plasticity and synaptic regulation, and thus is heavily implicated in the pathogenesis of AD (24). In the present study, it was revealed that the rate of hippocampal neuronal apoptosis was significantly increased in the rat AD model. Furthermore, it was demonstrated that the rate of apoptotic neurons in the CA1 hippocampal region was clearly increased in the AD group, and that administration of salidroside could attenuate this effect. In addition, the results of this study suggest that the administration of salidroside improves cognitive function in the AD model via suppression of the rate of apoptosis of hippocampal neurons.

It has previously been reported that salidroside, a potent antioxidant, ameliorates memory impairment via anti-oxidative damage activity. The decline of learning and memory function in rodents and humans has previously been linked to excessive oxidative stress, which may lead to neuronal death. There is a growing body of research suggesting that oxidative stress is implicated in AD pathogenesis, along with increased levels of lipid peroxidation, and oxidation of both DNA and protein in the brains of AD sufferers (25,26). SOD is an important neural antioxidant enzyme that can remove excess free radicals (27). In addition, oxidative damage may also cause damage to components of the antioxidant system, such as MDA (28,29). The present study demonstrated that oxidative damage downregulated the activity of SOD and increased MDA concentration in rat hippocampal tissue. Furthermore, it was revealed that in the AD rat model with memory deficit, these adverse effects were greatly attenuated when salidroside was administered.

IL-6 is a cytokine that is secreted by T cells and macrophages, and acts as both a pro-inflammatory and as an anti-inflammatory in order to stimulate an immune response (30,31). TNF-α can promote T cells to produce a variety of inflammatory factors, and therefore trigger inflammatory reactions (32,33). In the present study, salidroside administration significantly decreased the expression of TNF-α and IL-6 cytokine inflammatory factors.

In conclusion, the present study demonstrated that salidroside administration may improve cognitive function in AD mice. The protective effects maybe associated with alteration of the levels of free radicals in the hippocampus.

Acknowledgements

The present study was supported by a grant from Natural Science Foundation of Tianjin Municipal Science and Technology Commission (grant no. 13JCYBJC22700).

Glossary

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References