<i>Pistacia chinensis</i> Methanolic Extract Attenuated MAPK and Akt Phosphorylations in ADP Stimulated Rat Platelets <i>In Vitro</i>

Park, Ji Young; Hong, Mei; Jia, Qi; Lee, Young-Chul; Yayeh, Taddesse; Hyun, Eujin; Kwak, Dong-Mi; Cho, Jae Youl; Rhee, Man Hee

doi:https://doi.org/10.1155/2012/895729

Evidence-Based Complementary and Alternative Medicine

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Research Article | Open Access

Volume 2012 | Article ID 895729 | https://doi.org/10.1155/2012/895729

Pistacia chinensis Methanolic Extract Attenuated MAPK and Akt Phosphorylations in ADP Stimulated Rat Platelets In Vitro

Ji Young Park,¹Mei Hong,²Qi Jia,²Young-Chul Lee,²Taddesse Yayeh,¹Eujin Hyun,²Dong-Mi Kwak,¹Jae Youl Cho,³and Man Hee Rhee¹

Academic Editor: Carlo Ventura

Received13 Feb 2012

Revised13 Jun 2012

Accepted20 Jun 2012

Published30 Jul 2012

Abstract

Pistacia chinensis (Chinese pistache) is a widely grown plant in southern China where the galls extract is a common practice in folk medicine. However, extracts from this plant have never been attempted for their cardiovascular protective effects in experimental setting. Here therefore we aimed to investigate the antiplatelet activity of Pistacia chinensis methanolic extract (PCME) in ADP stimulated rat platelets in vitro. PCME (2.5–20 g/mL) inhibited ADP-induced platelet aggregation. While PCME diminished [Ca²⁺]i, ATP, and TXA2 release in ADP-activated platelets, it enhanced cAMP production in resting platelets. Likewise, PCME inhibited fibrinogen binding to αIIbβ3 and downregulated JNK, ERK, and Akt phosphorylations. Thus, PCME contains potential antiplatelet compounds that could be deployed for their therapeutic values in cardiovascular pathology.

1. Introduction

Platelets adhere and mitigate bleeding during vascular injury through plug formation [1]; nevertheless, their dysfunctions gear toward thrombus development and subsequent cardiovascular pathology [2]. At the injured vascular site, the exposed subendothelial collagen and von Willebrand factor (vWF) initiate platelet activation marked by the secretion of prothrombotic factors like ADP, thrombin, serotonin, and thromboxane A2 (TXA2) [3]. Platelet activation is also further amplified by dense granule secretions (ADP and ATP) and α-granule adhesive molecules like fibrinogen and P-selectin [4].

ADP activates G-protein-coupled receptor (GPCR) signaling mediated by two metabotropic purinergic receptors in platelets, Gq-coupled P2Y₁ receptor activates phospholipase C whereas Gi-coupled P2Y₁₂ receptor inhibits adenylyl cyclase and activates PI-3K/Akt and ERK [5]. Adenylyl cyclase enhances cyclic adenosine monophosphoate (cAMP) which activates protein kinase (PKA) that inhibits platelet shape change, granule secretion, calcium mobilization, and aggregation [6]. However, ADP-induced adenylyl cyclase attenuation vanishes cAMP production which culminate in platelet activation. Likewise, ADP-stimulated Gi-coupled P2Y12 receptor that activates mitogen-activated protein kinases (MAPKs) (ERK, JNK, and p38) and PI-3k/Akt signaling to arrive at similar scenario of platelet activation and aggregation [7].

Pistacia chinensis (chinese pistache) is a drought resistance deciduous indigenous tree in southern China. The tree is marked by its finely divided dark green foliage with an attractive orange bark which has been used frequently for grafting the commercial Pistacia vera [8] that showed antiatherosclerosis [9], anti-inflammatory [10], and antioxidant effects [11]. Nevertheless, the antiplatelet activity of Pistacia chinensis was unattempted yet. We therefore reported that Pistacia chinensis methanolic extract (PCME) inhibited ADP stimulated rat platelet granule secretions and aggregation in vitro. Furthermore, PCME attenuated ERK, JNK, and Akt phosphorylations in ADP-stimulated platelets, while it enhanced cAMP production.

2. Materials and Methods

2.1. Materials

Fura-2/AM was obtained from Sigma (St. Louis, MO, USA). ADP was procured from Chrono-log (Havertown, PA, USA). Antibodies against phospho-p44/42, p44/42, phospho-p38, p38, phospho-SAPK/JNK, and -actin were bought from Cell Signaling (Beverly, MA, USA). ATP assay kits were purchased from Biomedical Research Service Center (Buffalo, NY, USA). TXB2 EIA was purchased from Enzo Life Sciences (Plymouth Meeting, PA, USA). cAMP enzyme immunoassay (EIA) kits were from Cayman Chemical (MI, USA). Fibrinogen Alexa Fluor 488 conjugate was obtained from Invitrogen molecular probes (Eugene, OR, USA). All other chemicals were of reagent grade.

2.2. Sample Preparation and GC Mass Spectrometry Analysis

Dr. Zhengliu Zhang identified Pistacia chinensis trunk bark collected from Sichuan, China and the voucher specimen (PLSA1301) was deposited at the Unigen Inc., till the extraction date. Trunk bark of Pistacia chinensis was dried and pulverized into powder, of which 159 g with 50% methanol/dichloromethane (MeOH/DCM) extraction yielded 11 g for silica gel fractionation to get 590 mg of subfraction. 300 mg of 500 mg was again further purified by preparative HPLC (Luna C18, 30 × 250 mm) to obtain 30 mg of fraction. PCME of the final fraction (2.5 mg) was employed in GC mass analysis indicating its polyphenolic nature replete with resorcinol (18.9%) and pyridine (2.8%) compounds with common structural moieties (Table 1 and Figure 1) except solvents like methane, DMSO, and dichloroethylene. GC mass spectrometry was performed using Agilent Technology 7890A-Gas Chromatograph system (Agilent Technologies, Santa Clara, CA, USA), coupled to XLMSD-5975C equipment operating in electrospray ionisation (EI) mode.

(a) resorcinol

(b) resveratrol

(c) quercetin

(d) catechin

2.3. Platelet Preparation and Aggregation Assay

Platelets preparations from rats were described previously [12]. Briefly, 8 weeks old male Sprague Dawely rats (240–250 g weight) were obtained from Orient Co. (Seoul, Korea) and maintained in a standard laboratory facility with ad libitum feed and water. Whole blood was collected using a 23G needle from abdominal aorta and then transferred into 15 mL test tube containing 1 mL of the anticoagulant acid/citrate/dextrose (ACD, 85 mM trisodium citrate, 83 mM dextrose, and 21 mM citric acid). Blood was centrifuged at 170 ×g for 7 min to obtain platelet-rich plasma which was further centrifuged at 120 ×g for 7 min to remove residual erythrocytes. This platelet-rich plasma was centrifuged twice at 350 ×g with a washing buffer for 10 min to remove the ACD solution, and then platelet precipitates were adjusted to (3 × 10⁸/mL) for aggregation assay in Tyrode buffer (137 mM of NaCl, 12 mM of NaHCO₃, 5.5 mM of glucose, 2 mM of KCl, 1 mM of MgCl₂, 0.3 mM of NaHPO₄, and pH 7.4). All platelet preparations were conducted at room temperature, and all experimental procedures and protocols used in this investigation were reviewed and approved by the Ethics Committee of the College of Veterinary Medicine, Kyungpook National University.

Platelet aggregation was conducted as mentioned before. Briefly, aggregation was monitored by measuring light transmission in an aggregometer (Chronolog, Havertown, PA, USA). The washed platelets were preincubated at 37°C for 2 min with either PCME or vehicle (<0.1%), and then stimulated with agonists. The reaction mixture was further incubated for 5 min, stirring at 170 ×g.

2.4. Determining [Ca²⁺]i

The [Ca²⁺]i was determined with Fura-2/AM as described previously [13]. Briefly, platelets were incubated with 5 M of Fura-2/AM for 30 min at 37°C and washed. The Fura-2-loaded platelets (3 × 10⁸/ml) were then pre-incubated with PCME for 3 min at 37°C in the presence of 1 mM CaCl₂, then stimulated with ADP for 5 min. Fluorescence signals were recorded using a Hitachi F-2500 fluorescence spectrofluorometer (F-2500, Hitachi, Japan). Fluorescence emission was determined at 510 nm, with simultaneous excitation at 340 and 380 nm, changing every 0.5 s. Fura-2 fluorescence was measured in a spectrofluorometer by the method of Schaeffer: [Ca²⁺]i in cytosol = 224 nM × ()/(), where 224 nM is the dissociation constant of the Fura-2-Ca²⁺ complex, and and represent the fluorescence intensity levels at very low and very high Ca²⁺ concentrations, respectively. In our experiment, is the fluorescence intensity of the Fura-2-Ca²⁺ complex at 510 nm after the platelet suspension containing 1 mM of CaCl₂ had been solubilized by Triton X-100 (0.1%). is the fluorescence intensity of the Fura-2-Ca²⁺ complex at 510 nm, after the platelet suspension containing 20 mM Tris/3 mM of EGTA had been solubilized by Triton X-100 (0.1%). represents the fluorescence intensity of the Fura-2-complex at 510 nm after the platelet suspension was stimulated by ADP, with and without PCME, in the presence of 1 mM CaCl₂.

2.5. ATP Release Assay

Washed platelets were pre-incubated for 2 min at 37°C with various concentrations of PCME and then platelets were stimulated with ADP for 5 min. After the reaction was terminated, samples were centrifuged and supernatants were used for ATP assay in a luminometer (GloMax 20/20, Promega, Madison, USA) using an ATP assay kit (Biomedical Research Service Center, Buffalo, USA).

2.6. Determination of Thromboxane A2 Generation

Washed platelets (3 × 10⁸/ml) were pre-incubated with or without PCME for 2 min in the presence of 1 mM CaCl₂, and then the platelets were stimulated with ADP. Reactions were terminated after 5 min by adding ice-cold 2.5 mM EDTA and 100 M indomethacin. After centrifugation at 14,000 rpm for 3 min at 4°C, the amount of TXB2 (supernatant) was determined using TXB2 EIA kit according to the manufacturer’s protocol (Enzo Life Sciences, Plymouth Meeting, PA, USA).

2.7. Measurements of cAMP

Washed platelets were pre-incubated for 2 min at 37°C with various concentrations of PCME or vehicle in the presence of 1 mM CaCl₂, and then stimulated with ADP for 5 min in a platelet aggregometer. The reaction was terminated by the addition of equal volumes of 80% ice-cold ethanol. Samples were then centrifuged at 2,000 ×g for 10 min at 4°C and the supernatant cAMP level was determined with a cyclic AMP (Ann Arbor, MI, USA).

2.8. Immunoblotting

Proteins were prepared as previously described [14]. Briefly, platelet suspensions (3 × 10⁸/mL) were pre-incubated with PCME or vehicle. Platelet activation was induced by ADP and the reaction was allowed to proceed for 5 min. After termination of the reaction, lysates were prepared by solubilizing and centrifuging platelets in sample buffer (0.125 M Tris-HCl at pH 6.8, 2% SDS, 2% -mercaptoethanol, 20% glycerol, and 0.02% bromophenol blue) in the presence of protease inhibitors (g/ml: 1 phenylmethylsulfonylfluoride (PMSF), 2 aprotinin, 1 leupeptin, and 1 pepstatin A). Protein concentration was determined using BCA Assay (PRO-MEASURE, iNtRON Biotechnology, Korea). 30 g of protein was separated in 10% SDS-PAGE and transferred to nitrocellulose membrane in transfer buffer (25 mM Tris (pH 8.5), 0.2 M glycine, and 20% methanol). Immunoblots were blocked with TBS-T containing 5% non-fat dry milk, washed, and incubated with primary antibody diluted in a blocking solution. The immunoblots were again probed with horseradish peroxidase secondary antibody, and membranes were visualized using enhanced chemiluminescence, ECL (iNtRON Biotechnology, Korea).

2.9. Fibrinogen-Binding Assay

Alexa Fluor 488-fibrinogen binding to the washed platelets was quantified by flow cytometry. Briefly, the washed platelets were pre-incubated with PCME at room temperature in the presence of 0.1 mM CaCl₂. The platelets were then stimulated by ADP for 5 min, and immediately incubated with Alexa Fluor 488-human fibrinogen (20 g/mL) for 5 min and fixed with 0.5% paraformaldehyde at 4°C for 30 min. Platelets were pelleted by centrifugation at 2000 ×g at 4°C and resuspended in 500 L PBS. Binding of fibrinogen to integrin was measured in the presence of calcium chelator EGTA 1 mM. Fluorescent intensities were determined using FACS Calibur cytometer (BD Biosciences, San Jose, UAS), and data were analyzed using CellQuest software (Becton Dickinson Immunocytometry Systems, San Jose, CA).

2.10. Statistical Analysis

One-way analysis of variance was used for data analysis followed by a post hoc Dunnett’s test for statistical significance. All data were means ± S.E.M. values less than 0.05 were considered statistically significant.

3. Results

3.1. PCME Inhibited ADP-Induced Platelet Aggregation

ADP is a well-known soluble agonist for platelet aggregation and thrombus formation [2]. Previously, we showed that ADP at 10 M induced complete platelet aggregation and, therefore, this concentration was used to induce platelet aggregation in this study. PCME (5–20 g/mL) showed a dose dependent inhibition of ADP (10 M) induced platelet aggregation in rat platelets with a potent effect observed at the highest dosage (20 g/mL) used (Figure 2).

3.2. PCME Attenuated ADP-Induced [Ca²⁺]i Elevation and ATP Release

Platelet activation is marked by the release of platelet granular contents. Therefore, we determined whether PCME used at various concentrations attenuated the release of [Ca²⁺]i and ATP from dense granules in platelets stimulated with ADP. PCME (5–20 g/mL) strongly diminished [Ca²⁺]i mobilization (Figure 3(a)), and the same inhibitory effect on ATP release was observed at a lesser degree (Figure 3(b)).

(a)

(b)

Figure 3

Inhibitory effect of PCME on ADP-induced [Ca²⁺]i mobilization and ATP release. Washed platelets were incubated with calcium fluorophore (fura-2/AM) and then stimulated with ADP as described in Section 2 for [Ca²⁺]i determination (a). For ATP assay (b), washed platelets were pre-incubated with PCME, stirred in an aggregometer for 3 min and then stimulated with ADP for 5 min. Each graph shows mean ± SEM from 3 independent experiments performed. *** was considered as statistically significant compared with agonist control.

3.3. The Effect of PCME on TXA2 and cAMP Generation in ADP-Activated Platelets

While thromboxane A2 (TXA2) is an important mediator in the amplification of platelet activation, cAMP plays an imperative role in antiplatelet activity. Therefore, we measured the intracellular level of ADP-induced TXA2 generation and the level of cAMP in unstimulated platelets pretreated with PCME in vitro. PCME (5–20 g/mL) markedly inhibited the stable form of TXA2 (i.e., TXB2) in ADP-stimulated platelets (Figure 4(a)) whereas the level of cAMP was profoundly upregulated and its level at the highest concentration of PCME (20 g/mL) was comparable with that of forskolin used at 1 M (Figure 4(b)).

(a)

(b)

Figure 4

Effect of PCME on TXA2 generation and cAMP production. ADP (10 M) evoked TXB2 production (as measure of TXA2 generation) which was measured after 5 min of ADP stimulation according to EIA Kit instructions (a). For cAMP assay (b), washed platelets were stirred with vehicle, PCME, or forskolin in an aggregometer prior to ADP stimulation for 5 min. Reaction was terminated, and then cAMP enzyme immunoassay was performed as described in Section 2. Bar graphs show mean ± SEM of 3 independent experiments performed. ** and *** considered as statistically significant compared with control.

3.4. PCME Attenuated JNK, ERK, and Akt Phosphorylations in ADP-Induced Platelets

Phosphorylations of mitogen-activated protein kinases (MAPKs) (ERK, p38, and JNK) and Akt in platelets are closely associated with platelet activation and aggregation. Hence, we determined if PCME inhibited MAPK and Akt phosphorylations in ADP stimulated platelets. Whereas p38 phosphorylation was unaffected by PCME (5–20 g/mL), ERK and JNK phosphorylations were dose-dependently suppressed in ADP-activated platelets (Figure 5(a)). Moreover, PCME totally demolished phosphorylation of Akt beyond 5 g/ml of concentration (Figure 5(b)).

(a)

(b)

3.5. PCME Inhibited Fibrinogen Binding to Integrin in ADP-Activated Platelets

Integrin activation and the subsequent fibrinogen binding to are crucial events in platelet aggregation. Thus, we determined whether fibrinogen binding to integrin was inhibited in platelets pretreated with PCME and stimulated by ADP. Our finding revealed that PCME at 10 and 20 g/mL inhibited fibrinogen binding to activated integrin in ADP-stimulated rat platelets (Figures 6(a) and 6(b)).

(a)

(b)

Figure 6

Effects of PCME on fibrinogen binding to integrin in ADP-activated platelets.Washed platelets were pretreated with PCME at 10 and 20 g/mL, and then stimulated with ADP (10 M) in Alexa Fluor 488-human fibrinogen (20 g/mL) for 5 min, fixed with 0.5% paraformaldehyde at 4°C for 30 min. Fluorescent intensity graphs indicate 4 independent experiments (a). Data exhibit mean fluorescence intensity (MFI) of fibrinogen-positive platelets. Each graph was expressed as % of gated (b). ** and *** were considered as statistically significant compared with agonist.

4. Discussion

In this study, we reported that Pistacia chinensis methanolic extract (PCME) displayed broad inhibitory effects on platelet aggregation, calcium mobilization, ATP release, TXA2 formation, and fibrinogen binding to in ADP-activated platelets. Moreover, PCME enhanced cAMP production in unstimulated platelets whereas it downregulated ADP-stimulated ERK, JNK, and Akt phosphorylations.

ADP activates two G-protein-coupled purinoceptors, P2Y₁₂ and P2Y₁, to transduce its intracellular signaling [15]. P2Y₁ receptor is linked to Gq to activate PLC with consequent formation of inositol-1,4,5-trisphosphate (IP3) and Ca²⁺ release in one side and 1,2-diacylglycerol required for protein kinase C (PKC) activation on the other. P2Y₁₂ receptor is linked to the adenylate cyclase inhibiting Gi-protein [16]. Here, therefore, we explored that PCME inhibited the rise of [Ca²⁺]i in ADP stimulated platelets (Figure 3(a)) while it upregulated the level of cAMP in resting platelets (Figure 4(b)), suggesting that ADP receptors could be among the potential targets of PCME via upregulation of cAMP which has been reviewed as inhibitor of G-protein-coupled receptors [17], albeit this needs further insightful verification. Likewise, previous reports indicated that resorcinol showed antiplatelet activity [18] mediated through COX-1 inhibition [19], implicating that the diminished release of TXA2 (Figure 4(a)) at this moment might be originated from a similar effect of resorcinol available in PCME.

Phosphoinositide 3-kinase (PI3K) and Akt play platelet activation via sequential activation of PI-3K/Akt, nitric-oxide synthase 3, soluble guanylate cyclase (sGC), and cGMP-dependent protein kinase [20]. Thus, PCME-mediated inhibition of Akt (Figure 5(b)) may unravel the potential anti-platelet activity of this extract that could be mediated through modulation of PI-3K/Akt/cGMP signaling path-way despite that cGMP has also been reported to inhibit platelet activation [17]. Moreover, a recent report indicated that PI-3Kβ plays an important role in ADP-induced ERK activation and TXA2 generation [7], implying that PCME-mediated inhibition of ERK phosphorylation and TXA2 release might indicate its potential target at P2Y₁₂/PI-3K/Akt signaling. Likewise, Adam et al. reported that JNK1^−/− platelets showed impaired platelet secretion that brought altered integrin activation and reduced platelet aggregation via a mechanism involving PKC [21]. Therefore, we speculated that the reduced fibrinogen binding to (Figures 6(a) and 6(b)) could be partly attributed to JNK1 inactivation (Figure 5(a)) that might be linked to impaired P2Y₁₂-dependent PKC function in PCME pretreated platelets.

We conclude that PCME inhibited ADP-stimulated rat platelet aggregation, JNK, ERK, and Akt phosphorylations. While PCME downregulated TXA2 release and fibrinogen binding to in activated platelets, it showed enhanced cAMP production at the resting state. Thus, PCME could be considered as a potential antiplatelet agent targeting ADP amplified second wave of platelet secretion and aggregation.

Abbreviations

PCME:	Pistacia chinensis methanolic extract
MAPK:	Mitogen-activated protein kinase
TXA2:	Thromboxane A2
GPCR:	G-protein-coupled receptor
PKA:	Protein kinase A
ADP:	Adenosine diphosphate
ERK:	Extracelluar signal-regulated kinase
JNK:	c-jun N-terminal kinase.

Acknowledgments

This research was supported by a Grant from Ministry of Food, Agriculture, Forestry and Fisheries (110109-03-2-HD110), Republic of Korea.

References

J. M. Gibbins, “Platelet adhesion signalling and the regulation of thrombus formation,” Journal of Cell Science, vol. 117, no. 16, pp. 3415–3425, 2004.
View at: Publisher Site | Google Scholar
R. T. Dorsam and S. P. Kunapuli, “Central role of the P2Y₁₂ receptor in platelet activation,” The Journal of Clinical Investigation, vol. 113, no. 3, pp. 340–345, 2004.
View at: Publisher Site | Google Scholar
J. W. M. Heemskerk, P. R. M. Siljander, E. M. Bevers, R. W. Farndale, and T. Lindhout, “Receptors and signalling mechanisms in the procoagulant response of platelets,” Platelets, vol. 11, no. 6, pp. 301–306, 2000.
View at: Google Scholar
P. Blair and R. Flaumenhaft, “Platelet α-granules: basic biology and clinical correlates,” Blood Reviews, vol. 23, no. 4, pp. 177–189, 2009.
View at: Publisher Site | Google Scholar
C. Gachet, “P2Y₁₂ receptors in platelets and other hematopoietic and non-hematopoietic cells,” Purinergic Signalling, vol. 8, no. 3, pp. 609–619, 2012.
View at: Google Scholar
Z. Li, J. Ajdic, M. Eigenthaler, and X. Du, “A predominant role for cAMP-dependent protein kinase in the cGMP-induced phosphorylation of vasodilator-stimulated phosphoprotein and platelet inhibition in humans,” Blood, vol. 101, no. 11, pp. 4423–4429, 2003.
View at: Publisher Site | Google Scholar
S. Kim and S. P. Kunapuli, “P2Y₁₂ receptor in platelet activation,” Platelets, vol. 22, no. 1, pp. 54–58, 2011.
View at: Publisher Site | Google Scholar
L. Yu and J. Lu, “Does landscape fragmentation influence sex ratio of dioecious plants? A case study of Pistacia chinensis in the Thousand-Island lake region of China,” PLoS ONE, vol. 6, no. 8, Article ID e22903, 2011.
View at: Publisher Site | Google Scholar
K. A. Marinou, K. Georgopoulou, G. Agrogiannis et al., “Differential effect of Pistacia vera extracts on experimental atherosclerosis in the rabbit animal model: an experimental study,” Lipids in Health and Disease, vol. 9, article 73, 2010.
View at: Publisher Site | Google Scholar
C. Gentile, M. Allegra, F. Angileri, A. M. Pintaudi, M. A. Livrea, and L. Tesoriere, “Polymeric proanthocyanidins from Sicilian pistachio (Pistacia vera L.) nut extract inhibit lipopolysaccharide-induced inflammatory response in RAW 264.7 cells,” European Journal of Nutrition, vol. 51, pp. 353–363, 2011.
View at: Publisher Site | Google Scholar
A. Tomaino, M. Martorana, T. Arcoraci, D. Monteleone, C. Giovinazzo, and A. Saija, “Antioxidant activity and phenolic profile of pistachio (Pistacia vera L., variety Bronte) seeds and skins,” Biochimie, vol. 92, no. 9, pp. 1115–1122, 2010.
View at: Publisher Site | Google Scholar
D.-H. Lee, H.-J. Cho, H.-Y. Kang, M. H. Rhee, and H.-J. Park, “Total saponin from Korean red ginseng inhibits thromboxane A₂ production associated microsomal enzyme activity in platelets,” Journal of Ginseng Research, vol. 36, no. 1, pp. 40–46, 2012.
View at: Publisher Site | Google Scholar
S. M. Kamruzzaman, M. Endale, W. J. Oh et al., “Inhibitory effects of Bulnesia sarmienti aqueous extract on agonist-induced platelet activation and thrombus formation involves mitogen-activated protein kinases,” Journal of Ethnopharmacology, vol. 130, no. 3, pp. 614–620, 2010.
View at: Publisher Site | Google Scholar
H. S. Lee, S. D. Kim, W. M. Lee et al., “A noble function of BAY 11-7082: inhibition of platelet aggregation mediated by an elevated cAMP-induced VASP, and decreased ERK2/JNK1 phosphorylations,” European Journal of Pharmacology, vol. 627, no. 1–3, pp. 85–91, 2010.
View at: Publisher Site | Google Scholar
J. Yang, J. Wu, H. Jiang et al., “Signaling through Gi family members in platelets: redundancy and specificity in the regulation of adenylyl cyclase and other effectors,” The Journal of Biological Chemistry, vol. 277, no. 48, pp. 46035–46042, 2002.
View at: Publisher Site | Google Scholar
L. F. Brass, K. M. Wannemacher, P. Ma, and T. J. Stalker, “Regulating thrombus growth and stability to achieve an optimal response to injury,” Journal of Thrombosis and Haemostasis, vol. 9, no. 1, pp. 66–75, 2011.
View at: Publisher Site | Google Scholar
A. Smolenski, “Novel roles of cAMP/cGMP-dependent signaling in platelets,” Journal of Thrombosis and Haemostasis, vol. 10, no. 2, pp. 167–176, 2012.
View at: Publisher Site | Google Scholar
L. M. Ostertag, N. O'Kennedy, G. W. Horgan, P. A. Kroon, G. G. Duthie, and B. de Roos, “In vitro anti-platelet effects of simple plant-derived phenolic compounds are only found at high, non-physiological concentrations,” Molecular Nutrition and Food Research, vol. 55, no. 11, pp. 1624–1636, 2011.
View at: Publisher Site | Google Scholar
L. M. Szewczuk and T. M. Penning, “Mechanism-based inactivation of COX-1 by red wine m-hydroquinones: a structure-activity relationship study,” Journal of Natural Products, vol. 67, no. 11, pp. 1777–1782, 2004.
View at: Publisher Site | Google Scholar
A. Stojanovic, J. A. Marjanovic, V. M. Brovkovych et al., “A phosphoinositide 3-kinase-AKT-nitric oxide-cGMP signaling pathway in stimulating platelet secretion and aggregation,” The Journal of Biological Chemistry, vol. 281, no. 24, pp. 16333–16339, 2006.
View at: Publisher Site | Google Scholar
F. Adam, A. Kauskot, P. Nurden et al., “Platelet JNK1 is involved in secretion and thrombus formation,” Blood, vol. 115, no. 20, pp. 4083–4092, 2010.
View at: Publisher Site | Google Scholar

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Copyright © 2012 Ji Young Park 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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Evidence-Based Complementary and Alternative Medicine

Pistacia chinensis Methanolic Extract Attenuated MAPK and Akt Phosphorylations in ADP Stimulated Rat Platelets In Vitro

Abstract

1. Introduction

2. Materials and Methods

2.1. Materials

2.2. Sample Preparation and GC Mass Spectrometry Analysis

2.3. Platelet Preparation and Aggregation Assay

2.4. Determining [Ca2+]i

2.5. ATP Release Assay

2.6. Determination of Thromboxane A2 Generation

2.7. Measurements of cAMP

2.8. Immunoblotting

2.9. Fibrinogen-Binding Assay

2.10. Statistical Analysis

3. Results

3.1. PCME Inhibited ADP-Induced Platelet Aggregation

3.2. PCME Attenuated ADP-Induced [Ca2+]i Elevation and ATP Release

3.3. The Effect of PCME on TXA2 and cAMP Generation in ADP-Activated Platelets

3.4. PCME Attenuated JNK, ERK, and Akt Phosphorylations in ADP-Induced Platelets

3.5. PCME Inhibited Fibrinogen Binding to Integrin in ADP-Activated Platelets

4. Discussion

Abbreviations

Acknowledgments

References

Copyright

2.4. Determining [Ca²⁺]i

3.2. PCME Attenuated ADP-Induced [Ca²⁺]i Elevation and ATP Release