g a surgical blade in aseptic condition. The rats were then placed in the sterotaxis frame and the Bregma was first identified. The surgical techniques used were essentially the same as those described previously by Hashimoto et al. (2002)  (Figure 2). Two holes (right and left, relative to Bregma; 0.8 mm posterior, 1.4 mm lateral) were drilled onto the exposed skull
Figure 2. Surgical procedures for Alzheimer’s disease (AD) model rats. 1: Rat before surgery. 2: Hair is shaved and antiseptic liquid is treated on the shaved region. 3: Rat is placed on the stereotaxic frame. 4: Skull is opened and cleaned. 5: Bregma is identified. 6: Right and left ventricles are identified. Ventricles are 0.8 mm posterior and 1.2 mm lateral to the Bergsma. 7: Two pinholes are drilled by using microdriller. 8: Two holes are seen onto skull just above the brain’s left and right ventricles. 9: Infusion of AlCl3 into the right ventricle is being carried out. 10: Infusion of Aβ1-40 is being carried out into the left ventricle. 11: After the infusion (of AlCl3 and Aβ1-40) is completed, the holes of the skull are closed by bone-cement. 12: After stitching, the rats are kept at 37˚C in the hotplate incubator. 13: Incision has been recovered (healed) after surgery. 14: The skull’s condition after 5 - 7-days of surgery, indicating a complete recovery from surgery.
according to the Atlas of Paxinos and Watson (1986)  using a stereotaxic frame (Narishige, Tokyo, Japan). About 8.0 nmol of Aβ1-40 (in 5 μl solvent) was infused 3.5 mm deep into the left ventricle of the brain for about 5 min with a cannula by using a 10-μl Hamilton syringe. Then, 0.5 μg AlCl3 (in 5 μl volume) was infused 3.5 mm deep into the right ventricle of all rats using a Hamilton syringe according to Oka et al. (1999)  with slight modification. After complete recovery from surgery, the AD model rats were fed either with saline or S. cumini extract (Figure 3).
2.2. Behavioral Analysis
2.2.1. Adaptation Trials of the Rats
The animals were habituated with the experimenter and radial maze (once per day for 7 days prior to the memory experiment). An eight-arm radial maze used for the estimation of learning ability and set at 60 cm elevation above floor level, consisted of an octagonal center platform surrounded by eight equally spaced radial arms (50 cm long and 11 cm wide). Food cups, 1.5 cm deep and 2.5 cm in diameter, were located at the end of each arm. Then, for five days, the rats were familiarized with the apparatus, where the reward pellets were scattered through-out the maze. In this way, the rats were habituated to explore the reward (food pellet) placed in food cups at the end of the radial arm.
2.2.2. Data Collection for Learning Ability
After familiarization of the 8-arm maze, the rats were subjected to test trials, as previously described  . A trial consisted of baiting only four arms with reward pellet and placing the rat in the center platform facing a randomly selected arm. Here, the same four arms were baited consistently for any one animal. The testing continued for five weeks and involved two parameters of memory function:
Figure 3. Experimental design.
reference memory error (RME), entry into unbaited arms; and working memory error (WME), repeated entry into arms that had already been visited within a trial. A 5 minutes trial to collect the pellets was allowed for each rat. The experimenter maintained a constant position beside the maze and observed the behavior of the rats.
2.3. Brain Tissue Preparation
After the behavioral studies for memory evaluation were completed, the rats were anesthetized with sodium pentobarbital (65 mg/kg BW, i.p.) to collect blood, and the hippocampus and cerebral cortex were separated on ice as described previously  . Tissues were either first stored at −80˚C or immediately homogenized in ice-cold 0.32 M sucrose buffer (pH 7.4) containing 2 mM EDTA, and 0.2 mM phenylmethylsufonyl fluoride using a Polytron homogenizer (PCU 2-110; Kinematica GmbH, Steinhofhale, Switzerland). The homogenates were also centrifuged to prepare cytosolic fraction, which was stored at −80˚C until analyses were performed.
2.4. Lipid Peroxide (LPO) Assay
The oxidative stress in the plasma and brain tissues was evaluated by determining the levels of lipid peroxide (LPO). LPO was determined by estimating the thiobarbituric acid reactive substances (TBARs) according to the method Hashimoto et al., (2002)  . The samples (plasma and/or whole homogenate, 0.1 ml) were added to 0.1 ml of 8.1% (w/v) sodium dodecylsulphate, 2 ml of 0.4% thiobarbituric acid in 20% acetic acid (pH 3.5) and 0.1 ml distilled water. Each tube was tightly capped and heated at 95˚C for one hour. After cooling, 2 ml of n-butanol-pyridine (15:1, v/v) was added to tube and shaken vigorously for about 10 min. The tubes were then centrifuged at 1200 ×g for 10 min at room temperature (Digital centrifuge; DSC-1512SD). The absorbance of the supernatant fraction was measured at 532 nm. TEP (1,1,3,3-tetraethoxypropane) was utilized as standard. The levels of LPO were expressed as nmol/mg of protein.
2.5. ELISA for Aβ1-40 and Aβ1-40 Oligomers
The levels of Aβ1-40 were determined by following the methods of Hashimoto et al., (2005)  . The levels of Aβ1-40 oligomers were determined as previously described by Hossain et al. (2009)  . The level of Aβ1-40 was determined from the detergent-insoluble membrane fraction (DIF) by indirect ELISA with beta amyloid 1 - 40 rabbit recombinant oligoclonal antibody [Novex by life Technologies, Catalog # 710174]. The levels of Aβ1-40 oligomers were determined from the cytosolic fraction by the conformation-specific antibody [Invitrogen, rabbit polyclonal anti-oligomer antibody (A11), Cat # AHB0052] that recognizes the amino acid sequence-independent oligomers of the peptides. In brief, the multiwell plates were coated with detergent-insoluble fraction (DIF) or cytosolic fraction in a volume of 100 μl/well of carbonate buffer (pH 9.6) and incubated overnight at 4˚C. After three washes, the wells were blocked with 100 μl/well 3% BSA in Tris-buffered saline (TBS) at room temperature for 1 h. Following three washes with TBS, primary antibodies, each of which was diluted at a ratio of 1:1000, were added to respective wells and incubated overnight at 4˚C. After three washes with TBS, the plates were incubated with 100 μl of HRP-conjugated anti-rabbit antibody (Biosource International, Inc., Camarillo, CA, USA) for 1 h at room temperature. After final three washes with TBS, the reaction was developed with tetramethylbenzidine for 30 min and stopped with HCl and absorbance was recorded at 450 nm. The absorbance of the samples was 4 - 5-fold higher than that of the background (blank). Aβ1-40 concentrations in the cortex or hippocampus were determined by comparison with the Aβ1-40 standard curve and expressed as picograms of Aβ1-40 per milligram of total protein. However, the relative concentrations of Aβ1-40 oligomers in the Aβ1-40 + S. cumini samples were calculated by considering the absorbance of the control (Aβ1-40-alone) well as 100%. All values were normalized to total protein concentrations.
2.6. TNFα, PSD-95, SNAP-25, BDNF and TrkB Assay
The levels of TNFα, PSD-95, SNAP-25, BDNF and TrkB proteins were determined by using indirect ELISA as previously described  . In brief, the multiwell plates were coated with 50 μg of cytosolic protein in a volume of 100 μl/well of carbonate buffer (pH 9.6) and incubated overnight at 4˚C. After three washes, the wells were blocked with 1% BSA in Tris-buffered saline (TBS) at room temperature for 1 h. Following three washes with TBS, primary anti-TNFα-antibody, primary anti-PSD-95 antibody, primary anti-SNAP-25 antibody, primary anti-BDNF antibody and primary anti-TrkB antibody, each of which was diluted at a ratio of 1:1000, were added to respective wells and incubated at 4˚C overnight. Again, after three washes with TBS, the plates were incubated with 100 μl of HRP-conjugated anti-rabbit secondary antibody for 1 h at room temperature. After final three washes with TBS, the color was developed with tetramethylbenzidine for 30 min and the reaction was stopped with HCl, and absorbance was recorded at 450 nm (ErbaLisascan II, Mannheim, Germany). The absorbance of the samples was 4 - 5-fold higher than that of the background (blank).However, the relative concentrations of TNFα, PSD-95, SNAP-25, BDNF and TrkB in the Aβ1-40 + S. cumini samples were calculated by considering the absorbance of the control (Aβ1-40-alone) well as 100%. Finally, all absorbance values were normalized to per mg of protein.
2.7. In Vitro Anti-LPO (Lipid Peroxide) Study
The brain tissues from normal old rats were homogenized in phosphate buffer (50 mM, pH 7.4) using Dounce glass homogenizer (the USA). The homogenates were adjusted to a final concentration of 100 mg of tissue/ml of buffer. Briefly, 100 μl whole homogenate containing 100 μg of protein from each brain was treated with Fenton’s reagent [H2O2 (45 mM) + FeSO4 (2.0 mM)] in the absence or presence of S. cumini seed extract. Controls and extract-alone homogenates were treated at identical conditions without the addition of Fenton’s reagents. The reaction mixtures were then incubated at room temperature for 4 hours. At the end of incubation, the levels of LPO were determined as described above for those of the plasma  .
2.8. In Vitro Free Radical Scavenging Activity of S. cumini Seed Extract
Antioxdative power of the S. cumini seed extract also was analyzed by its DPPH radical scavenging activity, as described previously  . Briefly, the antioxidant activity of the extract was studied at several concentrations (0 - 1.0 mM GAE, gallic acid equivalent). Aliquots of DPPH solution in ethanol (0.4 mM, 100 μl) and each extract solution (100 μl) or standard solutions of BHT (0 - 1.0 mM, 100 μl) and quercetin (0 - 1.0 mM, 100 μl) were mixed in the wells of 96-well plate. The plate was then sealed, shaken for 10 s and placed in the dark for 30 min. Afterwards, the plate was carried out at room temperature, again shaken for 10 s, and then absorbance was taken at 515 nm. Data were reported as the average of three measurements. The IC50 value was expressed as the concentration of extract or standards (BHT and quercetin) required to decrease the absorbance of DPPH (0.2 mM, final concentration) by 50%. The value can be determined graphically by plotting the absorbance against the used extract or standard concentrations.
In addition, to directly visualize the antioxidant activity of the extract, aliquots of 8 μl 0.4 mM DPPH solution were subjected to thin layer chromatographic (TLC) plate. After air drying, 8 μl of the extract and standards (BHT and quercetin) were re-applied onto the DPPH spots. After 30 min of incubation, the spots were photographed and analyzed by Image J.
2.9. Total Polyphenol/Flavonoid Contents of S. cumini Extract
To estimate total polyphenol content of S. cumini extract gallic acid was used as standard, as described previously by Hossain et al. (2012)  . Briefly, the calibration curve was generated using different concentrations of gallic acid (0 - 0.2 mM) in the reaction mixture of Folin-Ciocalteu’s reagent (FCR) in total volume 200 μl in micro well plate. These solutions were incubated at room temperature for 40 min. The absorbance was recorded at 710 nm using ELISA plate reader. Total polyphenol content was expressed as μmol of gallic acid equivalents per 100 mg of dry powder (GAE/100 mg of dry powder). Total flavonoid content of the S. cumini extract was estimated following aluminum chloride colorimetric assay described by Chang et al. (2001)  . Quercetin was used as standard. Total flavonoid content was expressed as μmol of quercetin equivalents per 100 mg of dry powder (μmol of QE/100 mg of dry powder).
2.10. Statistical Analysis
Results were expressed as mean ± SEM (standard error of means). Behavioral data were analyzed by a 2-factor (group and session) randomized block factorial ANOVA (expressed as mean ± SD (standard deviations), and all other parameters were analyzed for intergroup differences by unpaired students t-test and/or one-way ANOVA. Statistical programs used were GB-STAT© 6.5.4 (Dynamic Microsystems, Inc., Silver Spring, MD, USA), and STATVIEW v4.01 (MindVision Software, Abacus Concepts, Inc., Berkeley, CA, USA). A level of P < 0.05 was considered statistically significant.
3.1. Effects of S. cumini Administration on the BW of Aβ-Infused AD Model Rats
No significant differences were observed in body weight or food intake, measured after 12 wks, between Control (Aβ1-40 + Vehicle-administered) and S. cumini seed extract-administered AD model rats (P < 0.05). The body weight of Aβ1-40 infused rats was increased to the extent of 139% as compared to 135.5% increase in weight of Aβ1-40 + S. cumini seed extract-administered rats. Average daily food intake in Control was 15.60 gm/rat and in S. cumini seed extract rats was 16.13 gm/rat.
3.2. Effects of S. cumini Administration on the Memory of Aβ-Infused AD Model Rats
Figure 4(A) shows the effect of chronic administration of S. cumini seed extract on reference memory-related learning ability in AD rats. The score is expressed as mean number of reference memory errors (REMs) with data averaged over blocks of six trials.
A randomized block two-way ANOVA (block and group) was conducted based on the scores. The analysis revealed a significant main effect of blocks of trials (F5, 41 = 5.96; P < 0.0001) and group (F1, 5 = 17.3; P < 0.0002) on the
Figure 4. Effects of oral administration of S. cumuni extract on reference memory error (RME) (A) and working memory error (B). Data are the mean ± SD for each block of six trials showing the number of reference memory error until the rat acquired all the rewards. Data were analyzed by randomized block two-way (block and group) ANOVA.
number of RME. The analysis also revealed a significant block-group interaction (F5, 205 = 2.403; P = 0.038).
The effect of oral administration of S. cumini on working memory related learning abilities of the AD rats is shown in Figure 4(B). The score is expressed as mean number of working memory errors (WMEs) with data averaged over blocks of six days. A randomized block two-way ANOVA (block and group) was conducted based on the scores. The analysis revealed a significant main effect of blocks of trials (F5, 41 = 10.76; P < 0.0001) and groups (F1, 5 = 17.3; P < 0.0001) on the number of WME. The analysis did not reveal a significant block-group interaction (F5, 205 = 1.02; P = 0.40).
3.3. Effects of S. cumini Administration on the Plasma and Brain LPO of AD Model Rats
The levels of LPO significantly decreased by ~28% in the plasma of the S. cumini-fed (Aβ1-40 + S. cumini) rats, when compared to those of Aβ1-40 alone infused AD control rats. The levels LPO also decreased both in the cerebral cortex (by~26.5%) and hippocampus (by~33%) of the S. cumini seed extract-administered AD model (Aβ1-40 + S. cumini) rats (Figure 5), as compared to those of the Aβ1-40-infused AD control rats.
3.4. Effects of S. cumini Administration on the Levels of Aβ1-40 in the Brains of AD Model Rats
The levels of Aβ peptide1?40, as determined by indirect ELISA, significantly decreased in the detergent-insoluble fraction (DIF) of cortex (~18%) and hippocampus (>20%) homogenates of (Aβ1-40 + S. cumini) rats. This suggest that S. cumini extract, by somehow decreased the amyloid burden in the brains of Alzheimer’s disease model rats (Figure 6).
Figure 5. Effects of oral administration of S. cumini seed extract (SC) on the plasma (A), cerebral cortex (B) and hippocampus (C) lipid peroxide (LPO) levels of the Aβ1-40-infused Alzheimer’s disease (AD) model rats. Results are mean ± SEM for 7-9 rats each with duplicate determinations. Bars with different notations are significantly different at P < 0.05.
Figure 6. Effects of oral administration of S. cumini seed extract on the levels of Aβ1-40 in the detergent-insoluble membrane fractions (DIF) of cortex and hippocampus. DIF was prepared as described previously  . Each bar represents the mean ± SEM (n = 7 - 8). The data were analyzed by unpaired student’s t-test. *P < 0.005.
3.5. Effects of S. cumini Administration on the Levels of Aβ1-40 Oligomers in the Brains of AD Model Rats
The relative levels of Aβ oligomers, the most toxic species of Aβ1-40 also significantly decreased in the cortex of S. cumini-fed Alzheimer’s disease (AD) model (Aβ1-40 + S. cumini) rats (Figure 7). This suggests that the components in S. cumini might have reduced the brainamyloid Aβ1-40 burden by inhibiting at the stages of oligomer formation.
3.6. Effects of S. cumini on the TNFα, BDNF, TrKB, PSD-95, SNAP-25 of AD Model Rats
The oral administration of S. cumini decreased the levels of proinflammatory TNFα and invariably increased the levels of the brain cognition/synaptic plasticity-related proteins (Figure 8). The levels of pro-inflammatory TNFα decreased by 18%, BDNF increased by 37%, TrKB increased by 14%, PSD-95 increased by 31% and SNAP-25 increased by 44% in the cortex of S. cumini-administered AD model rats, as compared those of the Aβ1-40-infusedalone AD rats. (Figure 8, upper panel).
The levels of pro-inflammatory TNFα decreased by 17%, BDNF increased by 27%, TrKB increased by 24%, PSD-95 increased by 45% and SNAP-25increased by 28% in the hippocampus of S. cumini-administered AD model (Aβ1-40 + S. cumini) rats, as compared those of the Aβ1-40-alone infused AD rats. (Figure 8, lower panel).
3.7. Effects of S. cumini Extract on the Fenton’s Reagent-Induced Oxidative Stress of the Brain Tissues Homogenates (in Vitro Anti-LPO Effects)
The levels of LPO significantly incresed (>70%) in the homogenates of Fenton’s reagents (FR)-incubated brain samples. This indicates a successful induction of oxidative stress (OS) in the FR+ homogenate samples, when compared to those
Figure 7. Effects of oral administration of S. cumini seed extract on the levels of Aβ1-40 oligomers of in the cortex of AD model rats. The mean absorbance value, normalized to one mg of protein, of the control (Aβ1-40-alone) samples was considered as 100%. Each bar represents the mean ± SEM (n = 7 - 8). The data were analyzed by unpaired student’s t-test. *P < 0.005.
Figure 8. Upper panel: Effects of oral administration of S. cumini seed extract on the levels of (A) TNFα, (B) BDNF, (C) TrKB, (D) PSD-95 and (E) SNAP-25 in the cortex of AD model rats. Lower panel: Effects of oral administration of S. cumini seed extract on the levels of (F) TNFα, (G) BDNF, (H) TrKB, (I) PSD-95 and (J) SNAP-25 in the hippocampus of AD model rats. Each bar represents the mean ± SEM (n = 7 - 8). The data were analyzed by unpaired student’s t-test. *P < 0.05.
of the control homogenate alone (Figure 9). However, if the oxidative stress was instigated in the presence of S. cumini, the levels of LPO were significantly suppressed (28% as compared to those of the control). This suggests that S. cumini extract significantly withstood the oxidative stress, as indicated by the reductions of the levels of LPO in the S. cumini-incubated brain homogenates (Figure 9). S. cumini alone also decreased the levels of LPO.
Figure 9. In vitro effects of seed extract on the oxidatve stress (OS)-induced production of lipid peroxide (LPO) in the brain tissues of the rats. Results are expressed as mean ± SEM. Bars that do not share a common alphabet are significantly different at P < 0.05 (Two-way ANOVA). Con = Control homogenate. OS = Oxidative stress was induced in the homogenate samples by Fenton’s reagents. SC = Homogenate samples incubated with the S. cumini extract alone. OS + SC = OS was induced in the S. cumini extract-preincubated samples.
3.8. In Vitro Free-Radical Scavenging Effects of S. cumini Seed Extract
The DPPH-scavenging activities of S. cumini seed extract versus BHT and quercetin are shown in the Figure 10. The non-linear analyses revealed IC50 of 0.12 ± 0.03 mM, 0.014 ± 0.001 mM and 0.006 ± 0.0.001 mM GAE, respectively, for BHT, quercetin and the S. cumini seed extract (Figure 10(a)). The seed extract or standards dose-dependently (0 - 0.1 mM) decolorized the DPPH spots (Figure 10(b)). Therefore, the intensity, as evaluated by ImajeJ, of the DPPH spots gradually decreased with the concentrations of the extract and standards (Figure 10(c)). This indicates an anti-oxidative potential of the S. cumini extract.
3.9. Total Polyphenol and Flavonoid Contents of S. cumini Extract
We determined the total polyphenol/flavonoid contents of S. cumini seed extract. S. cumini seed contained 8.11 ± 0.10 μmol GAE/100 mg of dry powder. Total flavonoid content was 2.3 ± 0.07 μmol QE/100 mg of dry powder.
The aim of the present study was to investigate whether the chronic oral pre-administration of S. cumini seed extract improves the memory-related learning impairments of Alzheimer’s disease (AD) model rats, suppresses the levels of oxidative stress, pro-inflammatory TNFα and elevates important brain cognition-related proteins, such as BDNF, TrKB, PSD-95 and SNAP-25. On the basis of quantitative lipid peroxidation assays, amyloid peptide assays (for amyloid
Figure 10. (A): DPPH-free radical scavenging effects of butylated hydroxytoluene (BHT), quercetin (QCTN) and S. cumini seed extract. Each symbol represents the mean ± SEM of triplicate determinations. Data were subjected to nonlinear regression analysis with the hyperbola equiation [Y = Bmax*X = /(Kd + X)], where Bmax is the maximal inhibition and Kd is the concentrations required to reach half maximal inhibition (IC50). (B): DPPH staining of TLC plate in the absence or presence of BHT, QCTN and S. cumini seed extract. The scavenging effects were dose dependent. (C): The intensity of the color of the DPPH-spots of Figure (B) was 3-D digitized by using ImageJ analyzer.
Aβ1-40 burden and amyloid oligomer levels in the brains), our study clearly demonstrates that the oral administration of S. cumini seed extract improves the memory impairments of the AD model rats. The improvements might relate to the decreases in the amyloid burdens in the brains of S. cumini-administered AD model rats, as indicated by the decreased levels of Aβ1-40 fibers and Aβ1-40 oligomers in these rats. Amyloid burden associated with theneuritic plaques and tau-hyperphosphorylatedneurofibrillar tangles is the pathological hall mark of Alzheimer’s brains. Aβ passes through diverse stages, including α-helix to β-sheet transformation, nucleation of β-sheet into oligomers, beading of oligomers into fibrills (fibrillation) and coalescence of fibrils into larger fibers, leading to matured amyloid aggregates  . These molecular transitions are typically associated with neuronal loss and cognitive deficits in AD. Therefore, the principal strategy for preventing AD is to inhibit the amyloid deposition in the brains of the AD patients. Although the accumulation of amyloid fibrous deposits is one of the important characteristic features of AD, the pathological significance of fibrillar plaques is still a matter of great debate   . Rather, the levels of amyloid oligomers better correlate with the status of dementia in the AD patients  . Klyubin et al. (2005)  reported that oligomer decreases learning and memory by inhibiting the long-term potentiation. Oral administration of S. cumini extract decreased the amyloid burden in the brains of the AD model rats (Figure 6), however, the mechanism through which S. cumini decreased the amyloid burden from the AD rats remains to be known clearly. We speculate that the components of the S. cumini extract might have inhibited the amyloid oligomers, hence the amount of Aβ1-40 deposits in the brains. Otherwise, the levels of Aβ1-40 could have not been reduced (Figure 6) in the brains of S. cumini-fed AD rats. Infusion of Aβ into the brain ventricle reduced the learning-related memory of AD model rats, when compared to that of the control rats   , thus suggesting a clear evidence of the detrimental effect of infused-Aβ on the memory of AD model rats. In the present investigation, we thus infer that S. cumini ameliorated the cognitive deficits of AD rats by decreasing the amyloid burden/oligomerconcentrations from the brains of AD rats. The results are also consistent with our previous reports  that the S. cumini not only ameliorates the memory dficts of eldely rats but also those of the Alzheimer’s disease model rats.
The increases in the oxidative stress, as indicated by the increased levels of lipid peroxide, are attributed to the neurodegenerative loss of neurons and related cognitive loss in the Alzheimers’s disease   . In our investigation, the memory-deficits in the AD rats were also associated with increases in the levels of LPO both in the plasma and brain cortico-hippocampal tissues (Figure 5). The oral administration of S. cumini significantly reduced the levels of LPO both in the plasma and brain tissues (Figure 5). Therefore it is conceiveable that S. cumini-induced decreases in the oxidative stress contributed to the amelioration of the cognitive deficits of AD model rats. The speculation is consistrent with the in vitro anti-LPO effect, DPPH-free radical scavenging effect, concurrently with the presence of subtantial amounts of total polyphenols/flavonoids in the extract of S. cumini seeds.
Neurodegeneration of Alzheimer’s disease is also characterized by inflammation in the brain. Pathophysiology and associated inflammation of the AD brain thus might help to elucidate potential therapeutic and preventative options  . Neuro-inflammation driven by glial activation contributes to the damage of neurons  . These reports are well consistent with the increased levels of TNFa in the AD model rats of the present study. Whatever the mechanism is, our results provide a clear evidence that the induction of AD through ventricular infusion of Aβ in the rat brains resulted in an increase of the level of proinflammatory TNFα. Furthermore, the prescription of non-steroidal anti-inflmmatory (NSAID) drugs have been shown to benefit the AD symptoms   . S. cumini-induced decreases in the levels of TNFα (Figure 8) are thus consistent with these reports and that the ameoliration of proinflammatory TNFα might have contributed to the improvement of memory impairments of AD model rats in the present investigation.
Next, we evaluated whether the oral administration of S. cumini extract could affect the brain synaptogenesis-marker proteins, namely PSD-95 and SNAP-25. PSD-95 binds to and co-localizes with NMDA receptor (NMDAR) at postsynaptic sites for downstream signal transductions. Intraventricular infusion of Aβ peptides leads to memory impairments in rats, with a corresponding lower levels of synaptic transmission and plasticity-related proteins like BDNF and PSD-95    . Our resuts are thus consistent with these reports. The levels of brain-derived neurotrophic factor (BDNF) and TrkB (the receptor of BDNF) decreased significantly inour Aβ1-40-infused AD rats. BDNF mediates neuroprotective activities through various intracellular signaling pathways triggered by activating the TrkB. BDNF and its receptor TrkB are critical regulators of neuronal survival, synapse formation, neuronal plasticity of brain   . The levels of BDNF in cortex and hippocampus also decreased in post-mortem AD patients   . Therefore, the decreased levels of these proteins might impair the functions such as memory in the Aβ1-40-infused AD rats, which after feeding with S. cumini exhibited a better memory performance.
The reduction in the level of PSD-95 in the brains of the Aβ1-40-infusedAD model rats would be expected to alter the PSD95-NMDAR complex formation at post-synaptic membrane sites and related downstream signals, and finally disturb brain cognitions. Furthermore, the presyanptic protein SNAP-25, a component of the SNARE complex, is linked to the triggering of calcium-mediated exocytosis  and plays an important role in presynaptic neuro-transmitter release  . The levels of SNAP-25 proteins also decreased in the brains of the AD model rats. Therefore, the reductions in the levels of both PSD-95 and SNAP-25 proteins might affect the release and synaptic transmission to the postsynaptic neurons in the brains of the AD rats. The increased levels of PSD95 and SNAP-25 are thus consistent with the positive effects of S. cumini extract on the neurotransmitter packaging/release/synaptic connectivity, and finally on amelioration of memory S. cumini-fed AD rats.
The oral administration of S. cumini seed extract significantly ameliorated the learning-related memory impairments of Aβ1-40-infused AD model rats. The ameliorative effects were associated with suppressions of the levels of LPO both in the brains and plasma of Aβ1-40 + S. cumini rats. The effects could be attributed to antioxidative potentials of S. cumini seed extract. The levels of proinflammatory TNFα decreased and the levels of brain cognition/synaptic transmission-related proteins, including BDNF, TrKB, PSD-95 and SNAP-25 rose after oral administration of S. cumini to AD model rats. Finally, it is concluded that S. cumini could be used as prophylaxis in the neurodegenerative diseases, such as Alzheimer’s disease. However, the exact mechanism of action(s) of S. cumini extract on the BDNF, TrKB, PSD-95 and SNAP-25 proteins remains to be investigated. Thus, further experimentation is a must.
This work was supported in part by Grants for Advanced Research in Science, from the Ministry of Education, Govt. of the People’s Republic of Bangladesh (to S.H.).
The authors declare no conflict of interest.