Effective components screening and anti-myocardial infarction mechanism study of the Chinese medicine NSLF6 based on "system to system" mode
© Liang et al; licensee BioMed Central Ltd. 2012
Received: 11 August 2011
Accepted: 8 February 2012
Published: 8 February 2012
Shuanglong formula (SLF), a Chinese medicine composed of panax ginseng and salvia miltiorrhiza exhibited significant effect in the treatment of myocardial infarction (MI) in clinical. Because of the complex nature and lack of stringent quality control, it's difficult to explain the action mechanism of SLF.
In this study, we present a "system to system" (S2S) mode. Based on this mode, SLF was simplified successively through bioactivity-guided screening to achieve an optimized minimal phytochemical composition (new formula NSLF6) while maintaining its curative effect for MI.
Pharmacological test combining with the study of systems biology show that NSLF6 has activity for treatment MI through synergistic therapeutic efficacies between total ginsenosides and total salvianolic acids via promoting cardiac cell regeneration and myocardial angiogenesis, antagonistic myocardial cell oxidative damage.
The present S2S mode may be an effective way for the discovery of new composite drugs from traditional medicines.
Dr. Zerhouni pointed out in NIH's Roadmap that translational medicine may evoke a great evolution of medicine in 21st century . The conventional drug (western medicine) is screened based on single entity and its interaction with single target, representing as 'point to point' (P2P) mode. However, its R&D productivity has experienced decades of decline with the greatly increased cost and lengthened time . Some of those problems of single-target-based screening may be overcome with the proposal of systems biology which believe that the body system is a holistic well-organized system composed of ordered networks including genes, proteins, metabolites, and so on. The network pharmacology based on the development of systems biology may represent an interaction mode of single (or multiple) point and biological system (point to system, P2S) . Since Translational Medicine emphasizes on exploring the synergy and interaction of various networks and combining knowledge across disparate domains, interests are arouse if Translational Medicine will impact on Traditional Chinese Medicine (TCM) and catalyze the mixing of western medicine and eastern medicine.
TCM has not been fully accepted by mainstream medicine whereas it has a long history of clinical practice in China and beyond China. Besides of the complex nature of the formulae, as well as a lack of stringent quality control, the main obstacles of understand TCM may be attributed to its holistic treatment concept representing the interaction of drug system and human system which is quite different with the "P2P" mode of western medicine .
During its thousands of years' clinical practice, TCM formulas have being developed according to the routine of "Beside-Bench-Beside" which is also similar with the proposal of Translational Medicine. Many of the TCM formulas have a proven efficacy in clinical application. The pioneering work of Prof. Cheng's group from Yale University proved the efficacy of a TCM formula (PHY906) and interpreted its mechanism by modern pharmacological study , demonstrated the necessity and rationality of TCM's combination use to the international communities, and helped the communication of Chinese traditional medicine and modern medicine.
In the past study we have introduced approaches of Chemomics and systems biology to study the composition of a chemome (e.g. a TCM formula) and the correlation between its change and biological effect [6, 7]. Prof. Sutherland from Brunel University commented that Chemomics represents an interesting synthesis of both Eastern and Western culture and provide a new "omics" approach to develop "modernized composite medicine" (MCM), where "the phytochemical composition of a herbal formula with demonstrated clinical efficacy is regarded as a global chemome, which can be simplified successively through bioactivity-guided screening to achieve an optimized chemomome with minimal phytochemical composition for further drug development, while maintaining its curative effect for a specific disease" .
Panax ginseng, Salvia miltiorrhiza, SLF and NSLF were provided by Guangzhou Xiangxue Pharmaceutical Co., Ltd. The detailed descriptions for the studies of global chemome fingerprint and quantitative fingerprint analysis together with serum pharmacochemistry were given in the Supplementary Material.
Methods of MI rat models
The animal experiments were operated in accordance with the standards established by the Guide for the Care and Use of Laboratory Animals of Beijing city and approved by the local ethics committee (IACUC#: 2010-LuoGA-SMI). Methods of isoproterenol (ISO)-induced MI rat model and coronary artery ligation-induced MI rat model were the same as before [12, 13].
Metabolomic study methods
Human Umbilical Vein Endothelial Cells (HUVECs) were routinely cultured in Medium RPMI1640 supplemented with 10% fetal bovine serum (FBS), 100 μg/ml penicillin/streptomycin. These cells were cultured in 5% CO2 at 37°C and the media were replaced at 2-day intervals.
HUVECs proliferation assay
HUVECs were grown to 70% confluence in 96-well plates and cultured with indicated concentration of GS, TSA and NSLF6. Cell proliferation was both measured using MTT assay and direct counting. Each experiment was carried out with five replicates per treatment and was independently repeated more than three times.
Effect of NSLF on HUVECs migration was studied using BD Chambers with Polycarbonate filters (8.0 μm pore). Suspended cells (5 × 104) were placed on the filter in RPMI1640 0.1% bovine serum albumin (BSA) containing indicated concentrations of NSLF. In the lower chamber RPMI1640 supplemented with 5% FBS was added. After incubated 3 h at 37°C, the filter was removed, and the upper side of the filter containing the nonmigrated cells was wiped and rinsed. The filters were fixed with 4% paraformaldehyde and stained with 4',6-diamidino-2-phenylindole (DAPI). Migration was quantified by counting cells. All groups were studied in triplicate.
The cDNA microarray hybridization was performed as previously described .
Total RNA was extracted from the cardiac tissue using TRIZOL reagent (Invitrogen) and further purified with RNeasy affinity column (MN). First-strand cDNA was synthesized using First strand cDNA synthesis Kit (Fermentas). Primers of Arnt1, Nppa and GAPDH were designed by primer 3.0 (the information of primers was shown in Additional file 1: Table S1). Each sample was measured in triplicate. Cycle threshold (Ct) value of each sample was obtained and 2-ΔΔCt. Relative quantification was used to calculate the gene expression. Each quantitative PCR was preformed twice.
Capillary-like structure formation
HUVECs (104 cells/well) were cultured on growth factor reduced-Matrigel (BD Biosciences) coated 24 plates in RPMI1640 0.1% BSA containing 10-40 μg/ml NSLF6 or vehicle. When cultured on matrigel, cells assemble into capillary-like structures. After incubated 18 h, the cord-like structures were observed by an inverted microscope.
Screening of effective components in SLF
We have reported a urine metabolomic study combined with pharmacological tests based on coronary artery ligation-induced MI rat model and concluded that SLF (in its original form) exhibited appealing therapeutic efficacies on MI .
On the one hand, the combination TGS + TSA exhibited equal pharmacological activities with the original SLF and the removal of the rest parts (RPG, RSM) had no significant effect on activities. On the other hand, absence of either/both of ginsenosides and salvianolic acids led to losing of anti-ischemic efficacy. Therefore, we took the components of ginsenosides and salvianolic acids as the indispensable effective components and equivalence contributed to the anti-MI efficacy of SLF. As a result, we obtained a new prescription with simplified compositions and maintaining efficacy, combination of TGS and TSA as the equal ratio of which present in the original formula SLF, named as "NSLF6".
Study on chemistry and activity confirmation of NSLF6
The global chromatographic fingerprint of the NSLF6 was established by UPLC/TOF-MS. A total of 20 compounds in NSLF6 were separated and identified, among of which there were 12 ginsenosides and 8 salvianolic acids. The quantitative fingerprints of total ginsenosides and total salvianolic acids were established by HPLC-DAD. As shown in Additional file 1: Table S7 and Additional file 1: Figure S4, the total contents of quantitative compounds such as ginsenosides Rb1, Rg1, Ro, salvianolic acid B, and lithospermic acid accounted for 74.4% of total solids. Thus, most of the constituents in NSLF6 have been identified and quantifiable so that we have established a stringent quality control, which provided the chemical basis for unveiling the pharmacological mechanism. Additionally, the comparative study of components in plasma of rats before and after administration of NSLF6 as well as NSLF6 was conducted by UPLC/TOF-MS. The results showed that 5 salvianolic acids including salvianolic acid B, rosmarinic acid, propanoid acid, salvianolic E, and lithospermic acid, and 7 ginsenosides concluding ginsenoside Rb1, Rb2, Re, Rd, Rf, M-Rb1, and M-Rb1 from NSLF6 were detected in plasma.
NSLF6 promotes Human Umbilical Vein Endothelial cells (HUVECs) proliferation, migration and angiogenesis
NSLF6 could significantly reduce myocardial infarction area, and one of the mechanisms might be related to promote angiogenesis and antagonize cardiomyocytes oxidative damage.
NSLF6 antagonizes cardiomyocytes oxidative damage
Study of NSLF6 based on Systems biology
Using the same MI model as above, 24 of 26 differential endogenous metabolites in urine were identified using high resolution mass spectrometry, involved in metabolic processes related to myocardial energy metabolism (myocardial energy metabolism, the citric acid cycle, and amino acid metabolism) (Additional file 1: Table S11). Among them, the levels of glucaric acid, uridine, D-Glucuronic acid 1-phosphate, deoxyadenosine monophosphate, 6-Phosphogluconic acid, and ceramide were observed significantly increased and the others were significantly decreased in model group compared with the normal control group. The observation of the differential endogenous metabolites moved to nearly normal levels in NSLF6 group indicated that NSLF6 may exert therapeutic efficacies on MI by regulating these metabolomic networks. For the study on SLF, we have indentified 17 potential biomarkers related to the effect of SLF , and we find that 13 of them are also contributed to the effect of NSLF6 and exhibit the consistent variation trend. Furthermore, the 14 differential endogenous metabolites in serum obtained from MI rats induced by ISO had the same trends as the urine metabolites (Additional file 1: Table S12).
Furthermore, the differentially expressed genes and proteins were screened through comparative genomics and comparative proteomics during the differentiation from BMMSCs into cardiomyocyte-like cells induced by NSLF6. 180 differentially expressed genes were obtained, in which 10 genes (fold change ≥ 10) were confirmed by Real-Time PCR, and obtained the functional relationship (Additional file 1: Figure S8). The differentially expressed proteins were obtained between control group and the differentiation group, and the relative signaling pathway network was obtained (Additional file 1: Figure S9). These results suggested that the MAPK, calcium binding, Rho and Wnt pathways played important roles during the BMMSCs differentiation . And NSLF6-induced differentiation was mainly attributed to the MAPK (eEF-2, Actb and Nme2), calcium binding (S100 calcium binding protein) and the Rho (Vim) signaling pathways (Additional file 1: Table S13) .
DiscussionTraditional Chinese Compound Medicine (TCCM) is known as multi-component drug capable of targeting multiple sites through multiple mechanism of action at multiple pathological steps. But these actions represent integral regulation other than the sum of individual target. Therefore, chemomics-integrated systems biology (integrative systems biology, ISB), a holistic methodology, was developed for the study of interaction between external intervention system (TCM) and biological response system (human system) based on S2S mode. The Traditional Chinese Formula is a compatible combination of raw herbs, in which indispensable components co-exist with ineffective components. For further drug development, it is necessary to remove the ineffective components while maintaining its curative effect for a specific disease. Consequently, we developed a S2S mode by which a complex formula can be simplified successively through bioactivity-guided screening to achieve a minimal effective composition with definite constituents and controllable quality, so that its mechanism can also be interpreted. In the present study, TGS and TSA were screened from SLF according to the studies of chemomics, serum pharmacochemistry, metabolomics and activity evaluation. NSLF6, the simplified prescription with components combination of TSA and TGS was obtained, and the systems study on the action mechanism of NSLF6 was conducted.
According pharmacological studies based on the MI rat model induced by ISO or the coronary artery ligation, NSLF6 can treat MI via several mechanisms such as promoting cardiomyocytes renewal, promoting angiogenesis and antagonizing cardiomyocytes oxidative damage.
It has been reported that there are stem cells existing in the heart of adult . Whether NSLF6 has the effect of promoting the differentiation of stem cells into cardiomyocytes to treat myocardial infarction? The in vivo experiments showed that SLF with bone marrow mononuclear cells (BMMCs) auto-transplanted into myocardial infarction model in swines could significantly improve the survival, differentiation and amplification of the transplanted cells in myocardial tissue, generate a raft of new cardiomyocytes and microvascular, and eventually promote lesions recovery, compared with BMMCs group . The above in vitro study proved that SAB, the effective ingredient of NSLF6, effectively induced the differentiation of mESCs into cardiomyocytes with physiological beating frequency. Except Vc and retinoic acid, there has been few drug reported to have the inducing effect on ESC differentiating into cardiomyocytes. Thus, NSLF6 has a good potential and specific advantage in the treatment of MI. The study of genomic and metabolomic above displayed the NSLF6 activity of regulating energy metabolism, transcription factors and oxide reductase activity, which was reported to be involved in the differentiation of mESCs into cardiomyocytes .
Partial angiogenesis and remodeling after MI is an important part of Cardiac Tissue Repair. Therapeutic angiogenesis is the clinical use of methods to enhance or promote the development of collateral blood vessels in ischemic tissue, and vividly described as "self-medication for heart bypass". The study of genomic and metabolomic above displayed the NSLF6 activity of regulating the energy metabolism, ion binding, MAPK and VEGF pathway which was reported to be the most Specific and powerful regulators to promote angiogenesis . Therefore, we considered that NSLF6 could promote angiogenesis through adjusting VEGF pathway, and confirmed the promoting angiogenesis of NSLF6 on HUVECs in vitro. Ginsenoside Rg1, one of ingredients in NSLF6, could stimulate the expression of VEGF to enhance the angiogenesis in previous report .
The H2O2 oxidative damage model of myocardial cells was widely used in the study of ischemia/reperfusion injury and ischemic preconditioning. It presents as the destruction of nuclear integrity and membrane permeability, increased mitochondrial membrane potential, oxygen free radicals, myocardial damage induced increase of enzyme activity, cell apoptosis, calcium overload and so on . The activities of MDA , SOD  and LDH  were closely related to the myocardial oxidative damage. The study of cardiomyocytes model based on HCS system and MI rats model based on pharmacological test suggested that NSLF6 could effectively protect cardiomyocytes via several mechanisms that act simultaneously, such as decreasing lipid peroxidation, improving the myocardial cell' ability of oxygen free radicals, and resisting apotosis.
Based on the integrative system biology mode, the traditional Chinese medicine SLF, as a clinical effective medicine, was developed to a new formula--NSLF6 with comparatively clear phytochemical composition, comparatively clear mechanism, and controllable quality. The stringent quality control system has been established using combination of fingerprint and multi-component determination. NSLF6 was proved to be effective on MI by pharmacological test (four levels of animal, tissue, cell, and molecular) combining with the study of gene, protein, and metabolite networks. The results revealed that SLF produced efficacy against MI through synergistic therapeutic efficacies between TGS and TSA. The present S2S mode may be an effective way for the discovery of new compound medicines.
point to point
point to system
system to system
Traditional Chinese Medicine
the remainder of PG
the remainder of SM
Human Umbilical Vein Endothelial cells
high content screening
Traditional Chinese Compound Medicine
bone marrow mononuclear cells
nonesterified fatty acid
Supported by Major Special Project for New Drugs (2009ZX09311-001), International Cooperation Project of Ministry of Science and Technology (2010DFA32420), National Key Technology Program (2006BAI108B04) and National Natural Science Foundation of China (20805026, 81130066).
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