Isorhynchophylline Protects PC12 Cells Against Beta-Amyloid-Induced Apoptosis via PI3K/Akt Signaling Pathway

Xian, Yan-Fang; Lin, Zhi-Xiu; Mao, Qing-Qiu; Chen, Jian-Nan; Su, Zi-Ren; Lai, Xiao-Ping; Ip, Paul Siu-Po

doi:https://doi.org/10.1155/2013/163057

Evidence-Based Complementary and Alternative Medicine

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Application of Complementary and Alternative Medicine on Neurodegenerative Disorders 2013

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Volume 2013 | Article ID 163057 | https://doi.org/10.1155/2013/163057

Isorhynchophylline Protects PC12 Cells Against Beta-Amyloid-Induced Apoptosis via PI3K/Akt Signaling Pathway

Yan-Fang Xian,¹Zhi-Xiu Lin,¹Qing-Qiu Mao,¹Jian-Nan Chen,²Zi-Ren Su,²Xiao-Ping Lai,²and Paul Siu-Po Ip¹

Academic Editor: Karl Wah-Keung Tsim

Received03 Jun 2013

Revised12 Sept 2013

Accepted23 Sept 2013

Published06 Nov 2013

Abstract

The neurotoxicity of amyloid-β (Aβ) has been implicated as a critical cause of Alzheimer’s disease. Isorhynchophylline (IRN), an oxindole alkaloid isolated from Uncaria rhynchophylla, exerts neuroprotective effect against -induced neurotoxicity in vitro. However, the exact mechanism for its neuroprotective effect is not well understood. The present study aimed to investigate the molecular mechanisms underlying the protective action of IRN against -induced neurotoxicity in cultured rat pheochromocytoma (PC12) cells. Pretreatment with IRN significantly increased the cell viability, inhibited the release of lactate dehydrogenase and the extent of DNA fragmentation in -treated cells. IRN treatment was able to enhance the protein levels of phosphorylated Akt (p-Akt) and glycogen synthase kinase-3β (p-GSK-3β). Lithium chloride blocked -induced cellular apoptosis in a similar manner as IRN, suggesting that GSK-3β inhibition was involved in neuroprotective action of IRN. Pretreatment with LY294002 completely abolished the protective effects of IRN. Furthermore, IRN reversed -induced attenuation in the level of phosphorylated cyclic AMP response element binding protein (p-CREB) and the effect of IRN could be blocked by the PI3K inhibitor. These experimental findings unambiguously suggested that the protective effect of IRN against -induced apoptosis in PC12 cells was associated with the enhancement of p-CREB expression via PI3K/Akt/GSK-3β signaling pathway.

1. Introduction

Alzheimer’s disease (AD) is the most common form of neurodegenerative disorders of the brain and affects an estimated 26.6 million people across the globe in 2006 [1]. The neuropathological hallmarks of AD include massive accumulation of beta-amyloid (Aβ) in senile plaques, abnormal tau filaments in neurofibrillary tangles, and extensive neuronal loss [2, 3]. Aβ is a 39- to 43-amino acid peptide fragment derived from sequential proteolysis of amyloid precursor protein (APP) through cleavage by β-secretase and γ-secretase [4]. Recent studies have suggested that Aβ plays an important role in the pathogenesis of AD [5]. Aβ accumulation has been causatively implicated in the neuronal dysfunction and neuronal loss that underlie the clinical manifestations of AD [6]. A correlation among memory deficits, Aβ elevation, and amyloid plaques on transgenic has been reported in previous studies [7, 8]. Therefore, inhibition of Aβ-induced neuronal degeneration may provide clinical benefits to AD patients.

Isorhynchophylline (IRN, Figure 1), an oxindole alkaloid, has been identified as the main active ingredient responsible for the biological activities of Uncaria rhynchophylla [9, 10]. IRN has also been reported to protect against the ischemia- and glutamate-induced neuronal damage or death [9, 11], and inhibition of 5-HT receptor [12, 13]. Previous studies in our laboratory has demonstrated that IRN protected rat pheochromocytoma (PC12) cells against the -induced oxidative stress, mitochondrial dysfunction, apoptosis, calcium influx, and tau protein hyperphosphorylation [14, 15]. However, the molecular mechanisms underlying the protective effect of IRN against the neurotoxicity induced by have not been fully understood. In this study, we aimed to elucidate the molecular signaling pathway involved in the neuroprotective effect of IRN.

2. Materials and Methods

2.1. Chemicals and Reagents

Isorhynchophylline (IRN, purity 98%) was purchased from Chengdu Mansite Pharmaceutical Co. Ltd. (Chengdu, Sichuan, China). Its identity was confirmed by comparing its H¹ NMR spectra with the published data [16]. Nerve growth factor (NGF), LY294002 (LY), lithium chloride (LiCl), and β-amyloid peptide () were purchased from Sigma-Aldrich (St. Louis, MO, USA). Dulbecco’s modified Eagle medium (DMEM), fetal bovine serum (FBS), penicillin, and streptomycin were obtained from Gibco (Grand Island, NY, USA). Unless otherwise indicated, all other reagents were of analytical grade and were obtained from Sigma-Aldrich.

2.2. Peptide Preparation

, which is the most toxic peptide fragment derived from amyloid precursor protein, was dissolved in deionized distilled water at the concentration of 1 mM. The stock solution was diluted to desired concentrations immediately before use and added to cell culture medium.

2.3. Cell Culture and Drug Treatment

The PC12 cells were obtained from the American Type Culture Collection (Rockville, MD, USA). They were maintained in DMEM medium supplemented with penicillin (100 U/mL), streptomycin (100 μg/mL), 6% FBS, and 6% horse serum at 37°C in a humidified atmosphere of 95% air and 5% CO₂. Unless otherwise specified, the cells were seeded onto 24-well culture plate at a density of 8 × 10⁴ cells/well. PC12 cells were differentiated with 50 ng/mL NGF in serum-free DMEM for 3 days [15]. IRN and all inhibitors were dissolved in DMSO and diluted with culture medium. The final concentration of DMSO in the test solutions was less than 0.1%. The cells were incubated with different concentrations of IRN (final concentrations: 1, 10, and 50 μM) for 2 h. at a final concentration of 20 μM was then added to the culture for an additional 24 h. In experiments involving kinase inhibitors, the inhibitors LY294002 (50 μM) or LiCl (10 mM) were added 1 h prior to IRN (50 μM) and/or (20 μM) treatment.

2.4. Cell Viability Assay

Cell viability was measured using a CellTiter 96 AQ_ueous One Solution Cell Proliferation Assay (Promega, Madison, WI, USA). In brief, PC12 cells were seeded onto a 96-well culture plate at a density of 2 × 10⁴ cells/well. Cells were washed with D-Hanks solution after drug treatment. Then, 100 μL of serum-free medium and 20 μL of CellTiter 96 AQ_ueous One Solution were added into each well. The cells were incubated at 37°C for 2 h. The quantity of formazan product, which is directly proportional to the number of living cells, was measured using a FLUOstar OPTIMA microplate reader (BMG Labtech, Offenbury, Germany) at 490 nm. Cell viability was expressed as percentage of nontreated control.

2.5. Lactate Dehydrogenase (LDH) Activity Assay

LDH activity was measured using a LDH diagnostic kit (STANBIO Laboratory, Boerne, TX, USA) according to the manufacturer’s protocol. Briefly, PC12 cells were seeded onto 24-well culture plates at a density of 1 × 10⁵ cells/well. At the end of the drug treatment, the medium was collected. Subsequently, 100 μL of the medium was added to a polystyrene cuvette containing 1 mL of LDH reagent. The cuvette was placed immediately into a spectrophotometer and maintained at 30°C. After stabilization for 1 min, the absorbance at 340 nm was recorded at 1 min intervals for 3 min. The enzyme activity was expressed in unit per liter. To determine intracellular LDH activity, the cells were washed with D-Hanks solution and then scraped from the plates into 500 μL of ice-cold PBS (0.1 M, containing 0.05 mM of EDTA) and homogenized. The homogenate was centrifuged (4000 ×g) at 4°C for 30 min. The resulting supernatant was collected for the LDH assay. The total LDH activity was computed by summing the activities in the cell lysate and medium. Cellular toxicity was indicted by the percentage of LDH released from the cell.

2.6. Quantification of DNA Fragmentation

Quantification of DNA fragmentation was determined by Cell Death Detection kit (Roche Applied Sciences, Basel, Switzerland) according to the manufacturer’s protocol. In brief, the cells were washed with HBSS after drug treatment. Then, the cells were incubated with 200 μL of lysis buffer for 30 min at room temperature. The plate was centrifuged at 200 ×g for 10 min at 4°C. An aliquot (20 μL) of the supernatant from each well was transferred into a streptavidin-coated microplate and incubated with a mixture of anti-histone biotin and anti-DNA peroxidase. The apoptotic nucleosomes were captured via their histone component by the anti-histone-biotin antibody which was bound to the streptavidin-coated microplate. Simultaneously, anti-DNA peroxidase was bound to the DNA part of the nucleosomes. After removing the unbound antibodies, the amount of peroxidase retained in the immunocomplex was quantified by adding 2,2′-azinobis (3-ethylbenzthiazoline-6-sulphonic acid) (ABTS) as the substrate, and the absorbance of the reaction mixture was measured at 405 nm using a microplate reader. The absorbance is directly proportional to the number of apoptotic nucleosomes. The extent of DNA fragmentation was expressed as percentage of the control.

2.7. Western Blot Analysis

PC12 cells were seeded onto 100 mm² dish at 5 × 10⁶ cells/dish. The cells were washed twice with D-Hanks solution after drug treatment. The cells were harvested and lysed with protein lysis buffer (50 mM Tris-HCl, pH 7.5, 100 mM NaCl, 1% NP-40, 0.5% sodium deoxycholate, 0.1% SDS, 1 mM EDTA, 1 mM sodium orthovanadate, 10 mM sodium fluoride, and 100 mg/mL PMSF). Protein concentration in the supernatants was determined with the BCA protein assay. Protein samples were electrophoresed by SDS-PAGE for 2 h at 80 V. The separated proteins were transferred to polyvinylidene fluoride (PVDF) membranes using a transblotting apparatus (Bio-Rad Laboratories, Hercules, CA, USA) for 30 min at 15 V. The membranes were blocked with 5% (w/v) nonfat milk in TBS-T (Tris-buffer saline containing 0.1% Tween-20) at room temperature for 2 h and subsequently incubated at 4°C overnight with appropriate amount of primary antibodies against p-Akt (Ser 473), Akt, phosphorylation of glycogen synthase kinase-3β (p-GSK-3β, Ser9), GSK-3β, phosphorylation cyclic AMP response element binding protein (p-CREB, Ser133), CREB (Cell Signaling Technology, Beverly, MA), and β-actin (Santa Cruz Biotechnology Inc., USA) at 4°C overnight. Next, the membrane was washed with TBS-T three times and probed with horseradish peroxidase conjugated secondary antibody at room temperature for 1 h. To verify equal loading of samples, the membranes were incubated with monoclonal antibody β-actin, followed by a horseradish peroxidase conjugated goat anti-mouse IgG. The membrane again was washed with TBS-T for three times, and finally the protein bands were visualized by the ECL western blotting detection reagents (Amersham Biosciences, Buckinghamshire, UK). The intensity of each band was analyzed using Image J software (NIH Image, Bethesda, MD, USA).

2.8. Statistical Analysis

Data were expressed as mean ± SEM. Multiple group comparisons were performed using one-way analysis of variance (ANOVA) followed by Tukey’s test in order to detect intergroup differences. GraphPad Prism software (Version 4.0; GraphPad Software, Inc., San Diego, CA) was used to perform the statistical analysis. A difference was considered statistically significant if the value was less than 0.05.

3. Results

3.1. Effects of IRN on -Induced Cytotoxicity in PC12 Cells

The effect of IRN on cell viability of -treated PC12 cells was shown in Figure 2(a). Treating the cells with at 20 μM for 24 h could significantly decrease cell viability, as compared to the control group (). Pretreatment with IRN (10 and 50 μM) in the presence of 20 μM for 24 h was able to significantly increase the cell viability as compared with the -treated control ( for both concentrations).

(a)

(b)

To investigate the protective effect of IRN, a LDH assay was performed. As shown in Figure 2(b), when PC12 cells were incubated with 20 μM of for 24 h, the percentage of LDH leakage was conspicuously increased (). When the cells were pretreated with IRN (50 μM) in the presence of 20 μM of for 24 h, the percentage of LDH leakage was significantly reduced as compared with the -treated control ().

3.2. Effect of IRN on -Induced Activation of GSK-3β in PC12 Cells

To investigate the effect of IRN on the activation of GSK-3β in -treated PC12 cells, the protein levels of GSK-3β and p-GSK-3β (Ser9) were determined. As shown in Figure 3(a), the level of p-GSK-3β was significantly decreased () after treatment with 20 μM of . Interestingly, pretreatment with IRN (1, 10 and 50 μM) markedly elevated the level of p-GSK-3β (, and , resp.) when compared to the -treated control, indicating that IRN suppressed the activation of GSK-3β induced by . To show the correlation between p-GSK-3β and cell viability, LiCl, a potent GSK-3β inhibitor, was used. Results showed that pretreatment with LiCl (10 mM) could significantly accentuate cell viability (, Figure 6(a)) and the protein level of p-GSK-3β (, Figure 3(b)). The treatment also attenuated LDH leakage (, Figure 6(b)) and DNA fragmentation (, Figure 6(c)) in -treated cells.

(a)

(b)

3.3. Effect of IRN on -Induced Inactivation of PI3K/Akt Pathway

As shown in Figure 4(a), treatment with 20 μM of for 24 h significantly decreased the protein level of p-Akt (Ser473). However, pretreatment with IRN (50 μM) markedly increased the protein level of p-Akt (), indicating that IRN was able to activate PI3K/Akt signaling pathway in the -treated cells. LY294002, a potent PI3K/Akt signaling pathway inhibitor [17, 18], thoroughly abolished the effects of IRN on p-Akt and p-GSK-3β (Figures 4(b) and 4(c)). In these experiments, total protein levels of Akt and GSK-3β did not change in all groups.

(a)

(b)

(c)

3.4. Effect of IRN on the Phosphor-CREB through PI3K Activation

As shown in Figure 5, treating the cells with 20 μM of for 24 h significantly decreased protein level of p-CREB (Ser133), while pretreatment with IRN (10 and 50 μM) markedly elevated protein level of p-CREB ( and , resp.), as compared with the -treated control. The effect of IRN was completely blocked by LY294002, indicating the involvement of PI3K signal transduction.

(a)

(b)

(a)

(b)

(c)

4. Discussion

Previous studies in our laboratory demonstrated that IRN could significantly reduce the neurotoxicity induced by via inhibiting oxidative stress, calcium influx, tau protein hyperphosphorylation, and suppressing cellular apoptosis in PC12 cells [14, 15]. The present study revealed that IRN could protect PC12 cells against the -induced neurotoxicity via PI3K/Akt/GSK-3β signaling pathway.

Recent studies suggest that GSK-3β plays an important role in AD neuropathology [19] and its activity accounts for many pathological hallmarks of the disease in both sporadic and familial AD cases. Hyperactivation of GSK-3β has been reported to induce neuronal cell death [20] and abnormal tau protein hyperphosphorylation [21, 22], both of which are the cardinal pathogenesis of AD. GSK-3β genes have been identified as potential candidate susceptibility genes for dementia [23]. In addition, GSK-3β expression is elevated in APP transgenic cultures which is coincided with the development of neuronal injury in brains of AD patients [24, 25]. Unlike most protein kinases, phosphorylation of GSK-3β at Ser9 leads to the inactivation of the enzyme [26]. Therefore, upregulation of p-GSK-3β (Ser9) may confer a protective effect. Our findings showed that Aβ significantly reduced the protein level of p-GSK-3β (Ser9), while pretreatment with IRN variably elevated the protein level of p-GSK-3β (Ser9). Treating the cells with LiCl, an inhibitor of GSK-3β, produces similar effects as IRN on -induced cytotoxicity (Figure 6). However, synergistic effect was not observed between IRN and LiCl. Our previous studies demonstrated that IRN was able to reverse cellular apoptosis and tau protein hyperphosphorylation in Aβ-treated PC12 cells [14, 15]. These results suggest that the protective effect of IRN against -induced apoptosis and tau protein hyperphosphorylation may be mediated by the suppression of GSK-3β activation.

Akt is a well-known prosurvival kinase and is activated by the phosphorylation at the Ser473 via PI3K pathway [27, 28]. PI3K/Akt signaling pathway has been suggested to play a pivotal role in GSK-3β-mediated tau protein hyperphosphorylation and neuronal survival. Inhibition of PI3K/Akt signaling pathway increases GSK-3β activity, resulting in tau protein hyperphosphorylation [29]. PI3K enhances neuroprotection through regulating phosphorylation level and activation of the Akt. Akt activity can be modulated by phosphorylation either on the residue Thr308 or Ser473 [30, 31]. The activation of Akt can lead to the suppression of GSK-3β activity [32]. Our results showed that Aβ treatment significantly decreased the protein level of p-Akt (Ser473) in PC12 cells. Pretreatment with IRN could significantly reverse the effect of Aβ on p-Akt which accounted for the protective mechanism of IRN against Aβ-induced neurotoxicity. Cotreatment with LY294002, a specific inhibitor of PI3K, completely abolished the effect of IRN on p-Akt and p-GSK-3β (Figure 4). Consistent results were obtained for the interaction of LY294002 and IRN on Aβ-induced cytotoxicity and DNA fragmentation (Figure 6). These findings strongly suggested that the protective effect of IRN against the -induced neurotoxicity in PC12 cells was medicated via PI3K/Akt signaling pathway.

In addition to robustly phosphorylated tau protein, GSK-3β also acts as a key regulator of a broad array of transcriptional factors, that is, β-catenin, activator protein-1, nuclear factor kappa B (NFκB), p53, CREB, heat shock factor (HSF-1), and CCAAT/enhancer binding protein [33]. Among these factors, CREB is the most important element in regulating cell survival and death. P-CREB (Ser133) is a downstream protein of the PI3K/Akt pathway [34] and acts as a substrate for GSK-3β [35]. It participates in many vital processes, including cell survival [36]. Our data showed that treatment with markedly inhibited the content of p-CREB, while pretreatment with IRN significantly increased the content of p-CREB via PI3K activation. Recent studies revealed that Akt and CREB could promote cell survival by upregulating the expression of antiapoptotic proteins such as Bcl-2 [37, 38]. Interestingly, our previous study indicated that pretreatment with IRN could significantly enhance the expression of Bcl-2 [14]. Furthermore, our results showed that PI3K inhibitor, LY294002, could abolish the accentuating effect of IRN on the protein expression of p-CREB, suggesting that p-CREB was involved in the neuroprotective mechanism of IRN.

In summary, our results demonstrated that IRN could protect against the -induced apoptosis in PC12 cells. The protective effect of IRN was associated with the enhancement of p-CREB expression via PI3K/Akt/GSK-3β signaling pathway. The results from the present study advance our knowledge regarding the neuroprotective mechanism of IRN. More importantly, this study has laid a foundation for future clinical studies to evaluate the potential benefits of IRN on AD patients.

Acknowledgment

This study was supported by a Direct Grant of The Chinese University of Hong Kong.

References

R. Brookmeyer, E. Johnson, K. Ziegler-Graham, and H. M. Arrighi, “Forecasting the global burden of Alzheimer's disease,” Alzheimer's and Dementia, vol. 3, no. 3, pp. 186–191, 2007.
View at: Publisher Site | Google Scholar
H. L. Weiner, C. A. Lemere, R. Maron et al., “Nasal administration of amyloid-beta peptide decreases cerebral amyloid burden in a mouse model of Alzheimer’s disease,” Annals of Neurology, vol. 48, no. 4, pp. 567–579, 2000.
View at: Google Scholar
M. Bothwell and E. Giniger, “Alzheimer's disease: neurodevelopment converges with neurodegeneration,” Cell, vol. 102, no. 3, pp. 271–273, 2000.
View at: Google Scholar
D. J. Selkoe, “Alzheimer's disease: genotypes, phenotype, and treatments,” Science, vol. 275, no. 5300, pp. 630–631, 1997.
View at: Publisher Site | Google Scholar
E. Hellström-Lindahl, M. Viitanen, and A. Marutle, “Comparison of Aβ levels in the brain of familial and sporadic Alzheimer's disease,” Neurochemistry International, vol. 55, no. 4, pp. 243–252, 2009.
View at: Publisher Site | Google Scholar
M. R. Basha, M. Murali, H. K. Siddiqi et al., “Lead (Pb) exposure and its effect on APP proteolysis and Aβ aggregation,” FASEB Journal, vol. 19, no. 14, pp. 2083–2084, 2005.
View at: Publisher Site | Google Scholar
Y. Hashimoto, T. Niikura, T. Chiba et al., “The cytoplasmic domain of Alzheimer's amyloid-β protein precursor causes sustained apoptosis signal-regulating kinase 1/c-Jun NH 2-terminal kinase-mediated neurotoxic signal via dimerization,” Journal of Pharmacology and Experimental Therapeutics, vol. 306, no. 3, pp. 889–902, 2003.
View at: Publisher Site | Google Scholar
D. L. McPhie, R. Coopersmith, A. Hines-Peralta et al., “DNA synthesis and neuronal apoptosis caused by familial Alzheimer disease mutants of the amyloid precursor protein are mediated by the p21 activated kinase PAK3,” Journal of Neuroscience, vol. 23, no. 17, pp. 6914–6927, 2003.
View at: Google Scholar
T. H. Kang, Y. Murakami, H. Takayama et al., “Protective effect of rhynchophylline and isorhynchophylline on in vitro ischemia-induced neuronal damage in the hippocampus: putative neurotransmitter receptors involved in their action,” Life Sciences, vol. 76, no. 3, pp. 331–343, 2004.
View at: Publisher Site | Google Scholar
D. Yuan, B. Ma, J. Y. Yang et al., “Anti-inflammatory effects of rhynchophylline and isorhynchophylline in mouse N9 microglial cells and the molecular mechanism,” International Immunopharmacology, vol. 9, no. 13-14, pp. 1549–1554, 2009.
View at: Publisher Site | Google Scholar
Y. Shimada, H. Goto, T. Itoh et al., “Evaluation of the protective effects of alkaloids isolated from the hooks and stems of Uncaria sinensis on glutamate-induced neuronal death in cultured cerebellar granule cells from rats,” Journal of Pharmacy and Pharmacology, vol. 51, no. 6, pp. 715–722, 1999.
View at: Publisher Site | Google Scholar
H. Kanatani, H. Kohda, and K. Yamasaki, “The active principles of the branchlet and hood of Uncaria sinensis Oliv. examined with a 5-hydroxytryptamine receptor binding assay,” Journal of Pharmacy and Pharmacology, vol. 37, no. 6, pp. 401–404, 1985.
View at: Google Scholar
K. Matsumoto, R. Morishige, Y. Murakami et al., “Suppressive effects of isorhynchophylline on 5-HT2A receptor function in the brain: behavioural and electrophysiological studies,” European Journal of Pharmacology, vol. 517, no. 3, pp. 191–199, 2005.
View at: Publisher Site | Google Scholar
Y. F. Xian, Z. X. Lin, Q. Q. Mao, S. P. Ip, Z. R. Su, and X. P. Lai, “Protective effect of isorhynchophylline against β-amyloid-induced neurotoxicity in PC12 cells,” Cellular and Molecular Neurobiology, vol. 32, no. 3, pp. 353–360, 2012.
View at: Publisher Site | Google Scholar
Y. F. Xian, Z. X. Lin, Q. Q. Mao, M. Zhao, Z. Hu, and S. P. Ip, “Bioassay-guided isolation of neuroprotective compounds from uncaria rhynchophylla against beta-amyloid-induced neurotoxicity in PC12 cells,” Evidence-Based Complementary and Alternative Medicine, vol. 2012, Article ID 802625, 8 pages, 2012.
View at: Publisher Site | Google Scholar
J. Haginiwa, S. Sakai, and N. Aimi, “Studies of plants containing indole alkaloids. (II). The alkaloids of Uncaria rhynchophylla Miq,” Yakugaku Zasshi, vol. 93, no. 4, pp. 448–452, 1973.
View at: Google Scholar
K. W. Zeng, H. Ko, H. O. Yang, and X. M. Wang, “Icariin attenuates β-amyloid-induced neurotoxicity by inhibition of tau protein hyperphosphorylation in PC12 cells,” Neuropharmacology, vol. 59, no. 6, pp. 542–550, 2010.
View at: Publisher Site | Google Scholar
Z. Zhang, R. Zhao, J. Qi, S. Wen, Y. Tang, and D. Wang, “Inhibition of glycogen synthase kinase-3β by Angelica sinensis extract decreases β-amyloid-induced neurotoxicity and tau phosphorylation in cultured cortical neurons,” Journal of Neuroscience Research, vol. 89, no. 3, pp. 437–447, 2011.
View at: Publisher Site | Google Scholar
L. Sun, C. Guo, D. Liu et al., “Protective effects of bone morphogenetic protein 7 against amyloid-beta induced neurotoxicity in PC12 cells,” Neuroscience, vol. 184, pp. 151–163, 2011.
View at: Publisher Site | Google Scholar
M. Pap and G. M. Cooper, “Role of glycogen synthase kinase-3 in the phosphatidylinositol 3- kinase/Akt cell survival pathway,” Journal of Biological Chemistry, vol. 273, no. 32, pp. 19929–19932, 1998.
View at: Publisher Site | Google Scholar
G. Alvarez, J. R. Muñoz-Montaño, J. Satrústegui, J. Avila, E. Bogónez, and J. Díaz-Nido, “Regulation of tau phosphorylation and protection against beta-amyloid-induced neurodegeneration by lithium. Possible implications for Alzheimer’s disease,” Bipolar Disorders, vol. 4, no. 3, pp. 153–165, 2002.
View at: Google Scholar
F. Plattner, M. Angelo, and K. P. Giese, “The roles of cyclin-dependent kinase 5 and glycogen synthase kinase 3 in tau hyperphosphorylation,” Journal of Biological Chemistry, vol. 281, no. 35, pp. 25457–25465, 2006.
View at: Publisher Site | Google Scholar
D. H. Geschwind and B. L. Miller, “Molecular approaches to cerebral laterality: development and neurodegeneration,” American Journal of Medical Genetics, vol. 101, no. 4, pp. 370–381, 2001.
View at: Google Scholar
C. Tackenberg and R. Brandt, “Divergent pathways mediate spine alterations and cell death induced by amyloid-β, wild-type tau, and R406W tau,” Journal of Neuroscience, vol. 29, no. 46, pp. 14439–14450, 2009.
View at: Publisher Site | Google Scholar
J. J. Pei, E. Braak, H. Braak et al., “Distribution of active glycogen synthase kinase 3β (GSK-3β) in brains staged for Alzheimer disease neurofibrillary changes,” Journal of Neuropathology and Experimental Neurology, vol. 58, no. 9, pp. 1010–1019, 1999.
View at: Google Scholar
M. D. Kaytor and H. T. Orr, “The GSK3β signaling cascade and neurodegenerative disease,” Current Opinion in Neurobiology, vol. 12, no. 3, pp. 275–278, 2002.
View at: Publisher Site | Google Scholar
I. Tato, R. Bartrons, F. Ventura, and J. L. Rosa, “Amino acids activate mammalian target of rapamycin complex 2 (mTORC2) via PI3K/Akt signaling,” Journal of Biological Chemistry, vol. 286, no. 8, pp. 6128–6142, 2011.
View at: Publisher Site | Google Scholar
R. Zhao, Z. Zhang, Y. Song, D. Wang, J. Qi, and S. Wen, “Implication of phosphatidylinositol-3 kinase/Akt/glycogen synthase kinase-3β pathway in ginsenoside Rb1's attenuation of beta-amyloid-induced neurotoxicity and tau phosphorylation,” Journal of Ethnopharmacology, vol. 133, no. 3, pp. 1109–1116, 2011.
View at: Publisher Site | Google Scholar
L. Baki, J. Shioi, P. Wen et al., “PS1 activates PI3K thus inhibiting GSK-3 activity and tau overphosphorylation: effects of FAD mutations,” EMBO Journal, vol. 23, no. 13, pp. 2586–2596, 2004.
View at: Publisher Site | Google Scholar
S. F. Moore, R. W. Hunter, and I. Hers, “mTORC2 protein-mediated protein kinase B (Akt) serine 473 phosphorylation is not required for Akt1 activity in human platelets,” Journal of Biological Chemistry, vol. 286, no. 28, pp. 24553–24560, 2011.
View at: Publisher Site | Google Scholar
H. Koide, T. Asai, K. Furuya et al., “Inhibition of Akt (ser473) phosphorylation and rapamycin-resistant cell growth by knockdown of mammalian target of rapamycin with small interfering RNA in vascular endothelial growth factor receptor-1-targeting vector,” Biological and Pharmaceutical Bulletin, vol. 34, no. 5, pp. 602–608, 2011.
View at: Publisher Site | Google Scholar
J. M. Beaulieu, R. R. Gainetdinov, and M. G. Caron, “Akt/GSK3 signaling in the action of psychotropic drugs,” Annual Review of Pharmacology and Toxicology, vol. 49, pp. 327–347, 2009.
View at: Publisher Site | Google Scholar
C. A. Grimes and R. S. Jope, “The multifaceted roles of glycogen synthase kinase 3β in cellular signaling,” Progress in Neurobiology, vol. 65, no. 4, pp. 391–426, 2001.
View at: Publisher Site | Google Scholar
K. Du and M. Montminy, “CREB is a regulatory target for the protein kinase Akt/PKB,” Journal of Biological Chemistry, vol. 273, no. 49, pp. 32377–32379, 1998.
View at: Publisher Site | Google Scholar
T. R. Salas, S. A. Reddy, J. L. Clifford et al., “Alleviating the suppression of glycogen synthase kinase-3β by Akt leads to the phosphorylation of cAMP-response element-binding protein and its transactivation in intact cell nuclei,” Journal of Biological Chemistry, vol. 278, no. 42, pp. 41338–41346, 2003.
View at: Publisher Site | Google Scholar
D. W. Kim, J. H. Lee, S. K. Park et al., “Astrocytic expressions of phosphorylated Akt, GSK3β and CREB following an excitotoxic lesion in the mouse hippocampus,” Neurochemical Research, vol. 32, no. 9, pp. 1460–1468, 2007.
View at: Publisher Site | Google Scholar
L. Ji, E. Mochon, M. Arcinas, and L. M. Boxer, “CREB proteins function as positive regulators of the translocated bcl-2 allele in t(14;18) lymphomas,” Journal of Biological Chemistry, vol. 271, no. 37, pp. 22687–22691, 1996.
View at: Publisher Site | Google Scholar
Y. Takada-Takatori, T. Kume, M. Sugimoto, H. Katsuki, H. Sugimoto, and A. Akaike, “Acetylcholinesterase inhibitors used in treatment of Alzheimer's disease prevent glutamate neurotoxicity via nicotinic acetylcholine receptors and phosphatidylinositol 3-kinase cascade,” Neuropharmacology, vol. 51, no. 3, pp. 474–486, 2006.
View at: Publisher Site | Google Scholar

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Copyright © 2013 Yan-Fang Xian et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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