An In-silico Approach to Explore the Possible Multifunctional Neuroprotective Efficacy of Violacein against Ischemic Stroke

Verma S1 and Pandey AK2*

1Department of Biotechnology, Institute of Engineering and Technology, Dr. APJ Abdul Kalam Technical University, Lucknow, UP, India

2Department of Biotechnology Engineering, Institute of Engineering and Technology, Bundelkhand University, Jhansi, UP, India

*Corresponding Author:
Pandey AK
Assistant Professor
Department of Biotechnology Engineering
Institute of Engineering and Technology
Bundelkhand University Jhansi
UP, India
Tel: +91 9030961817
E-mail: [email protected]

Received Date: May 16, 2017; Accepted Date: June 8, 2017; Published Date: June 15, 2017

Citation: Verma S, Pandey AK (2017) An In-silico Approach to Explore the Possible Multifunctional Neuroprotective Efficacy of Violacein against Ischemic Stroke. J In Silico In Vitro Pharmacol 3:17 doi: 10.21767/2469-6692.100017

 
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Abstract

Introduction: Cerebral ischemia arise due to insufficient/ interrupted blood supply to brain and is accompanied by pathologies like degradation of extracellular matrix resulting in blood brain barrier disruption, intra cranial haemorrhage, activation of astroglial cells and hence death of neurons. In addition, oxidative stress and inflammation is common to all neurodegenerative diseases enhancing the harmful consequences of diseases.

Matrix Metalloproteinases (MMP) are normally involved in extracellular matrix remodelling and are regulated while injury and inflammation in tissue. Over expression of MMP2 and MMP9 results in progression of ischemic conditions by extracellular matrix degradation thus compromising the structural integrity of Blood Brain Barrier (BBB) proving them a potent targets for the disease.

Violacein (source: Chromobacterium violaceum), purple pigment from microbial origin is a bisindole have high anti-inflammatory, anti-oxidant, anti-bacterial, anti-cancer and anti-parasitic properties. Present study is to study the effective potential of violacein against cerebral ischemia.

Methods and findings: Violacein’s ADMET (Absorption, Distribution, Metabolism, Excretion, Toxicity), properties were calculated and structural inhibition of MMPs through molecular docking was evaluated.

Violacein resulted six H-bonds with MMP2 with high binding energy of -11.83 kcal/mol and two H-bonds with MMP9 with binding energy of -9.889 kcal/mol. The Ki values of violacein with MMP2 and MMP9 were 2.12 nM and 56.14 nM respectively which proved high affinity of violacein towards the target.

Conclusion: Violacein with its high antioxidant and anti-inflammatory property can be a potent all round treatment for cerebral ischemia and demands extensive research.

Keywords

Inflammation; Neuronal death; Docking analysis

Abbreviations

ADMET: Absorption, Distribution, Metabolism, Excretion, Toxicity; BBB: Blood Brain Barrier; MMP: Matrix Metallo Proteinase

Introduction

Cerebral ischemia ranked third leading cause of death is victimizing half a million of lives every year [1]. It develops as a result of improper blood supply to brain due to haemorrhage and occlusions, which leads to inability to meet the metabolic demand and results in decreased supply of oxygen and glucose to brain cells [2]. The prolonged prevalence of such starving conditions activates intracellular and extracellular proteolytic pathways leading neuronal death and degradation of Extracellular Matrix (ECM) [3]. This degradation progresses to break the basal lamina thus imparting leakage and destroying the structural integrity of blood brain barrier leading to oedema, haemorrhagic transformation, microglial cell activation, circulating inflammatory cells infiltration in brain and lastly neuronal death [4].

The composition of ECM mainly contains proteins like collagen, fibronectin, laminin and proteoglycans [5]. Matrix Metalloproteinases (MMP) are Zn dependent proteolytic enzymes responsible for the remodelling of ECM in conditions of development, inflammation and tissue injury [6,7]. They are activated by cytokines and are reported to hamper the integrity of ECM in ischemic conditions due to there over expression [8]. MMP2 (gelatinase A) and MMP9 (gelatinase B) plays leading role in degrading the collagen type IV protein of ECM or basal lamina thus proving themselves the most potent targets of the disease [9-11]. The increased levels of MMPs have also been reported in many diseases, like cardiovascular diseases, cancer, osteoarthritis, lung injury etc. causing degradation of extracellular matrix [6].

Many researchers have reported increase in expression of MMPs in cerebral ischemia [5,9-11]. Past researches have proved that MMP 9 knockout mouse models or application of MMP inhibitors and antibodies have shown protective effects and reduction in disease pathogenesis by decreasing the infraction size in ischemic brain [9,11]. All these findings evoke the demand to focus MMP for the contraction of disease. Although ECM degradation by MMPs is a major pathology to deal with for combating the ischemic condition, pathologies like ionic imbalance following excitotoxicity, acidosis, peri-infract depolarization, oxidative stress, inflammation, edema and apoptosis also need special attention as they contribute a lot to adverse the conditions [12,13].

In diseased state increment in free radicals generation during enzymatic conversions and formation of transient pores in mitochondria activate apoptosis in cells [14,15]. This increase in free radicals not only cause destruction of physiology of brain by apoptotic neuronal insult but also cause, lipid peroxidation by free radicals causing membrane damage and disturb cellular processes, degradation of proteins and nucleic material in turn resulting into formation of free radical [16]. This continuous cycle of free radical formation leads to oxidative stress which occurs due to the imbalance of free radical oxidant species and the anti-oxidant levels of brain [17]. The main free radicals causing oxidative stress are reactive oxygen species especially superoxide anion, hydroxyl anion, hydrogen peroxide, NO.O-2 and NO [13,14]. Oxidative stress causes degradative stress on mitochondria and endoplasmic reticulum causing neuronal death [17]. High amount of oxidative stress causing free radical also activate mitogen activated protein kinase pathways which too are involved in increasing inflammation and cellular damage [18].

Violacein[3-(1,2-dihydro-5-(5-hydroxy-1H-indol-3-yl)-2- oxo-3H-pyrrol-3-ilydene)-1,3-dihydro-2H-indol-2-one] is a bisindol made by condensation of two tryptophan residues (Figure 1).

in-silico-in-vitro-pharmacology-Structure-violacein

Figure 1: Structure of violacein.

It is mainly synthesized by Cromobacterium violaceum but is also found to be synthesized by Janthinobacterium lividum and Alteromonasluteo violacea under specific conditions [19,20]. It is a purple pigment which is insoluble in water but soluble in DMSO, methanol and ethyl acetate. It is a multifunctional compound with anti-inflammatory, anti-oxidant, anti-bacterial, anti-cancer and anti-parasitic properties [20-22]. The antioxidant property was studied by Konzen et al. for nitrogen and oxygen reactive species, 1,1-diphenyl-2-picryl hydrazyl (DPPH) and hydroxyl radical and resulted in finding the reduction of free radicals in efficient way [18]. Lipid peroxidation studies of violacein found protective effect on lipid membranes and also proved enhanced anti-oxidant property when reconstituted with membranes or liposomes as delivery systems [21,23].

Its anti-cancer property is well established in vitro due to its inhibiting potential against MMPs via cytokine inhibition in cancer cells, hence reducing tumor growth, metastasis, and angiogenesis. Also there is reduction in inflammatory chemokine secretions in turn giving anti-inflammatory effect. In a study on mice model it became evident that violacein have great potential to treat acute and chronic inflammation by supressing the cytokine production in acute inflammation and stimulating regulatory T cells in chronic inflammation [24,25]. Its antioxidant property and immune modulatory power proved it a great marine nutraceutical which is effective against cancer, rheumatoid arthiritis, cardiovascular diseases and (Table 1) many neurodegenerative disorders. All these facts encouraged us to focus violacein for its role as neuroprotection in cerebral ischemia [22,26].

SMILES Oc1ccc2c(c1)c(c[nH]2)C1=CC(=C2C(=O)Nc3c2cccc3)C(=O)N1
Formula C20H13N3O3
Molecular weight 343.34 g/mol
Number of heavy atoms 26
Number of arom. heavy atoms 15
Fraction Csp3 0
Number of rotatable bonds 1
Number of H-bond acceptors 3
Number of H-bond donors 4
Molar Refractivity 104.77
TPSA 94.22 Ų

Table 1: Physiological properties of violacein.

Our Hypothesis

In the present study we hypothesize that violacein with its anti-oxidative, anti-inflammatory and MMP inhibiting properties can be considered as a potent drug for cerebral ischemia. Efforts were made to prove this hypothesis by finding the ADMET properties of violacein and by performing molecular docking, for the disclosure of any structural inhibition of MMPs, with MMP2 and MMP9 as major targets of cerebral ischemia.

Methodology

ADMET properties of violacein

The smile notation of violacein was taken from Pubchem (Pubchem CID: 9928039). The ADME properties were measured by Swiss ADME web tool of Swiss Institute of Bioinformatics [27]. Toxicity properties like LD50 were calculated from web based tool Protox [28]. Molecular properties and bioactivity (Tables 2-8) scoring of violacin were calculated by Molinspiration Chemoinformatics web based tool.

Log S (ESOL) -3.51
Solubility 1.05e-01 mg/ml ; 3.06e-04 mol/l
Class Soluble
Log S (Ali) -3.48
Solubility 1.14e-01 mg/ml; 3.31e-04 mol/l
Class Soluble
Log S (SILICOS-IT) -6.45
Solubility 1.21e-04 mg/ml ; 3.52e-07 mol/l
Class Poorly soluble

Table 2: Water solubility of violacein.

Log Po/w (iLOGP) 1.4
Log Po/w (XLOGP3) 1.88
Log Po/w (WLOGP) 1.8
Log Po/w (MLOGP) 1.26
Log Po/w (SILICOS-IT) 3.11
Consensus Log Po/w 1.89

Table 3: Lipophilicity of violacein.

Lipinski Yes; 0 violation
Ghose Yes
Veber Yes
Egan Yes
Muegge Yes
Bioavailability Score 0.55

Table 4: Druglikeness of violacein.

PAINS 1 alert: ene_five_het_C
Brenk 1 alert: michael_acceptor_1
Leadlikeness Yes
Synthetic accessibility 3.34

Table 5: Medicinal chemistry of violacein.

GI absorption High
P-gp substrate No
CYP1A2 inhibitor Yes
CYP2C19 inhibitor No
CYP2C9 inhibitor No
CYP2D6 inhibitor No
CYP3A4 inhibitor No
Log Kp (skin permeation) -7.06 cm/s

Table 6: Pharmacokinetics of violacein.

GPCR ligand -0.17
Ion channel modulator -0.21
Kinase inhibitor 0.52
Nuclear receptor ligand 0.17
Protease inhibitor -0.28
Enzyme inhibitor 0.14

Table 7: Molinspiration bioactivity scores of violacein.

Violacein docked with Binding energy Ki value Residues
MMP2 -11.83 kcal/mol 2.12 nM TYR223, LEU197, ALA220, ALA217, GLU202 and PRO 221
MMP9 -9.89 kcal/mol 56.14 nM TYR 420 and ARG 424

Table 8: Result of molecular docking of violacein with MMP2 and MMP9.

Docking analysis

Docking analysis of violacein and MMPs was performed by using Autodock 4.0 software. The 3D crystal structure of MMP2 (PDB id 1QIB) and MMP9 (PDB id 1L6J) were obtained from RCSB (Research Collaboratory for Structural Bioinformatics) Protein Data Bank. The violacein structure was made in ACD lab by using smile notation from Pubchem (Figure 1).

The PDB file of violacein was generated by using online smile translator to get the 3Dstructure for docking analysis. All the hetero atoms, including the water molecules, except Zn were removed from PDB files of MMP2 and MMP9. In Autodock program H-atoms were added to MMP2 and MMP9 then nonpolar H-atoms were merged. Lamarck genetic algorithm which is established on adaptive local search was applied as search parameter [10].

Short range Van der walls interactions and electrostatic interactions, entropy losses, hydrogen bonding were included as autodock energy based scoring function [29]. The Lamarckian genetic algorithm parameters for this study were: Number of runs=30, maximum number of evaluations=2500000, population size 150, number of generation=27000, rate of crossover=0.8 and rate of gene mutation=0.02 [9]. Blind docking for MMP2 was performed using grid size 126,126 and 126 along X, Y and Z axis with spacing of 0.375 Å.

The grid centre was set at 72.872 (X centre), 27.271 (Y centre), 20.779 (Z centre). Blind docking for MMP9 was performed with grid size 126, 126 and 126 along X,Y and Z-axis with spacing of 0.619 Aᵒ and grid centre was set at 36.89 (X centre), 38.95 (Y centre), and 34.737 (Z centre).The kollman charges added were -87.124 for MMP2 and -207.62 for MMP9. As reported by Hu and Shelver [29], the docking analysis was done by applying charge of +0.95e on both zinc atoms for both the MMPs (MMP2 and MMP9) [30].

Results

ADMET properties

The ADMET properties and bioactivity scores of violacein are given in (Tables 1-7). This compound was found to follow Lipinski’s rule which provide evidence for violacein to be a potent drug [31].

The toxicity results showed that the compound belongs to toxicity class 4 with LD50 of 500 mg/kg. This proved its least toxicity or no toxicity if swallowed in amounts less than 300 mg/kg. Also there was no possible binding found to toxic targets suggesting it to be safe for human administration.

Docking analysis

Results of the docking study pronounced the effectiveness of violacein for treatment of cerebral ischemia. The high binding energy of -11.83 kcal/mol with Ki value of 2.12 nM for violacein-MMP2 complex gave 6 hydrogen bonds at TYR223, LEU197, ALA220, ALA217, GLU202 and PRO 221 residues (Figure 2).

in-silico-in-vitro-pharmacology-six-hydrogen

Figure 2: Violacein docked with MMP2 formed six hydrogen bonds at TYR223, LEU197, ALA220, ALA217, GLU202 and PRO 221.

Violacein also showed high binding energy when complexed with MMP9 of -9.89 kcal/mol with 2 hydrogen bonds at TYR 420 and ARG 424 residue proving its high inhibition capability against MMPs (Figure 3).

in-silico-in-vitro-pharmacology-hydrogen-bonds

Figure 3: Violacein docked with MMP9 formed two hydrogen bonds at TYR 420 and ARG 424.

The Ki value for MMP9-violacein complex is 56.14 nM. Results of the docking study are given in Table 8.

Discussion

Cerebral occlusion and haemorrhage are the leading cause of ischemic stroke resulting into an improper blood supply to brain causing reduction in oxygen and glucose level to meet the metabolic demand [32]. As it is known that brain is the highest consumer of oxygen (about 20%) hence any reduction may lead to harmful consequences. As the blood flow reduces to one fourth of the normal supply, the brain functions become impaired [33]. Existence of such conditions for long period leads to neuronal insult in core ischemic regions of brain continued by death of neurons in penumbra ischemic regions hence activating large number of death pathways [3,34]. Therapeutics to deal with this deadly condition are still lacking due to unknown aetiologies of neuronal insult. The knowledge about the mechanisms resulting into ischemic conversions and loss of neurons is limited and yell for more research. On the other hand the role of MMPs in progression of ischemic conditions is well established and their increase in pathological conditions is reported by many researchers [3,5,6]. In past study it was reported that MMP overexpression in ischemic condition is directly proportional to infraction, and reduction in infraction had been well documented when MMP inhibition was done [11]. This has encouraged promising researches to inhibit MMPs for combating ischemic conditions. As it is reported that MMP2 and MMP9 have major role in increasing the pathologies, there is great interest in finding their inhibitors for utilizing this knowledge to treat ischemia to great extent [3,8,35-37]. Till date many natural inhibitors have been reported for the inhibition of MMPs. Quercetin was reported by Lee et al. for its role in protection against BBB disruption and resulting edema [38]. Quercetin was also reported by Pandey et al. for its structural inhibition of MMPs. Resveratrol was reported by Pandey et al. in neuroprotection in cerebral ischemia by directly inhibiting MMPs [9]. Structural inhibition of MMPs by rutin was reported by Selvaraj et al. [36]. Violacein a microbial pigment is well accepted for its great antioxidant and anti-inflammatory potential [19,25]. Inhibition of MMPs is proposed by three mechanisms.

• Inhibition at transcriptional level.

• Post translational inhibition by directly attacking the active site.

• Indirect effects on endogenous activators and inhibitors that regulate MMP’s activity [8,39-41].

It was reported that violacein inhibits MMP2 and MMP9 by an indirect effect thereby reducing the expression of CXCR4 which decreases cancer progression [24]. But the inhibition of MMPs by violacein for neuroprotection has not caught much attention.

Molecular docking studies are done to predict the most stable orientation of one molecule to the other when bound to form a complex [37]. Hence, in present study docking analysis of violacein with MMP2 and MMP9 was performed to get the possibility of direct active site inhibition to treat cerebral ischemia. A study by Kiyama suggested that MMP9 consists of S1’cavity pocket with a floor board and MMP2 have S1’channel like cavity [41,42]. The S1’ pocket of MMP9 consists of Asp185 to Leu188 and Pro421 to Tyr423 residues which are effective for inhibition and substrate binding [43]. The wall of S1’ pocket contains side chain of Leu188, Leu397, Val398 His 401, and Leu418 and the main chain residues Met422 to Try423 [44]. Present study of violacein with MMP9 docking found H-bonds at Tyr 420 and Arg424 which are nearest to the active site thus proving effective inhibition.

In past studies structural inhibition of MMP2 with quercetin was found to be at residues Leu164, Ala165, Ala 217 and Ala220 with binding energy of -9.11 kcal/mol [10]. Another study on docking analysis of rutin with MMP2 found H-bonding at residue Glu202 with binding energy of -10.19 kcal/mol [37]. In this study we found that violacein forms H-bonds with Ala217, Ala220, Tyr223, Leu197, Glu202 and Pro 221 residues with a comparatively high binding energy of -11.83 kcal/mol proving high inhibition activity against MMP2 especially because of most effective inhibition residues Ala2, Ala220 and Glu202. Docking of resveratrol with MMP9 in a study gave residues Glu402, Ala417 and Arg424 to form H-bonds with binding energy of -8.75kcal/mol (-36.634 kJ/mol) [9]. Sarkar et al. [35] in their docking study of (-)-epicatechin-3- galate and (-)-epigalocatechin-3-galate for proMMP9 inhibition found Try420 as an effective residue for inhibition with high binding energies [36]. The result obtained after docking of violacein and MMP9 complex revealed H-bonds with binding energy of -9.88 kcal/mol at residues Tyr 420 and Arg424 which were already reported as efficient residues for the inhibition hence proving our compound a better inhibitor for MMP9. Additionally the low values of Ki 2.12 nM and 56.14 nM for inhibition of MMP2 and MMP9 respectively in turn proved violacein a potent inhibitor. Ki value is the concentration of compound needed for effective inhibition of target. It has direct relationship with the IC50 values which is the concentration of compound required for 50% inhibition of the target enzyme. Thus lower the Ki value, higher will be the affinity of compound for its target to be inhibited [45]. In previous researches inhibition of MMP2 and MMP9 by resveratrol in a molecular docking study evaluated Ki values of 237.25 nM and 384.27 nM respectively which are higher than our results for violacein hence proving violacein a better inhibitor than resveratrol [9]. Also inhibition of MMP2 and MMP9 with quercetin gave Ki values 210.76 nM and 343.46 nM which being greater that the Ki value of our compound provided strong support to violacein as a treatment of cerebral ischemia by inhibiting MMP2 and MMP9 with higher affinity [10].

In addition to the effective structural inhibition with high binding energies violacein is a well-established antioxidant and anti-inflammatory compound. These properties cumulatively help to reduce the pace of progression of ischemic pathologies [22]. The absorption, distribution, metabolic, excretion and toxicity analysis of violacein stood in support for its use as a drug. Hence our study conveys great scope for violacein to be an effective multifunctional drug for the treatment of cerebral ischemia. More research is anticipated to bring it in clinical trials to battle the large number of deaths due to cerebral ischemia.

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