Journal of Biomedical Engineering

Research Article

Assessment of Beans as Functional Food for Control of Oxidative Stress Borne Diseases

**Savita Chaurasia* and Saloni Gupta**

Department of Biotechnology, IMS Engineering College, Ghaziabad, Dr. APJ Abdul Kalam Technical University, India

Submission: March 29, 2017; Published: May 30, 2017

*Corresponding author: Dr. Savita Chaurasia, Department of Biotechnology, IMS Engineering College, NH-24, Adyatmik Nagar, Ghaziabad 201009, UP, India, Tel: +911207945555; Email: drsav16@gmail.com

How to cite this article: Savita C, Saloni G. Assessment of Beans as Functional Food for Control of Oxidative Stress Borne Diseases. Curr Trends Biomedical Eng & Biosci. 2017; 5(1): 555652. DOI: 10.19080/CTBEB.2017.05.555652.

Abstract

Increased oxidative stress has been postulated in the diabetic state. Oxygen free radical activity can initiate peroxidation of lipids, which in turn stimulates glycation of protein, inactivation of enzymes and alterations in the structure and function of collagen, basement and other membranes and play a role in the long team complications of diabetes. Oxidative stress in diabetes coexists with a reduction in the antioxidant status, which can increase the deleterious effects of free radicals. It has also been known that alloxan induces its diabetogenic activity mainly by inducing oxygen free radicals and thereby damaging the pancreas. Supplementation with non-toxic antioxidants may have a chemoprotective role in the diabetes.

The study was undertaken to evaluate antioxidant potential of beans namely moth bean (Vigna aconitifolia), mung bean (Vigna radiata) and soybean (Glycine max). Water and methanol extracts were examined for antioxidant activity by DPPH radical scavenging assay, total phenol and flavanoid content were determined in both cases which showed maximum percentage of antioxidant activity in water extract of moth beans followed by soy and mung due to the presence of water soluble phenols and radicals more than that in methanol. The extracts also possess mild antibacterial property. Several physiological and biochemical parameters such as moisture content, seedling vigor, germination percent, total sugar and reduced sugar content during different period of germination showed gradual increment. Therefore, utilization of these legumes in the development of functional foods with increased therapeutic value would be a significant step toward health promotion and wellness.

Keywords: Legumes; Oxidative stress; Antioxidant potential; DPPH radical scavenging; Phenol; Flavanoid; Free radicals

Introduction

Nature has bestowed on us a very rich botanical wealth and a large number of diverse types of plants grow in different parts of the country. In India many of the plant species are known to have medicinal value. Herbal plants continue to be a major source of drugs and natural products on the basis of their therapeutics [1] in virtually all cultures [2]. The plants possess potent bioactive compounds capable of preventing and treating most oxidative related diseases [3] and have often been used in folkloric medicine [4]. In developing countries, the use of medicinal plants in the treatment of infectious disease is rife and reasons include the high cost of effective drugs [5]. However, potential indigenous plants exploited for medicinal purposes have to undergo basic phytochemical screening and bioassay as first step towards the ultimate development of drugs.

In search of natural antioxidants, we have studied the antioxidant activity, total phenols, flavonoids, metal chelating and radical scavenging properties of different varieties of Fabaceae (beans) in fresh condition. After getting positive results, study was extended with methanolic extracts. Findings of the study may be beneficial for mankind, as beans forms the major dietary component and can be treated as food supplement to overcome the oxidative stress due to present lifestyle, pollution, radiations, smoking, and certain pesticides etc. Academic, government and private research institutes around the globe are devoting substantial efforts to identify how functional foods and food ingredients might help prevent chronic disease or optimize health, thereby reducing healthcare costs and improving the quality of life for many consumers. The acceptance of biotechnology by consumers will be important if the potential of this powerful methodology is to be realized. Therefore, the present study aims at investigating the potentials of beans as a functional food for nutritional and therapeutic control of oxidative stress borne diseases.

Materials and Methods

Plant material

The mung beans (Vigna radiata), moth beans (Vigna aconitifolia) and soy beans (Glycine max) were procured from local market of Ghaziabad, India.

Chemicals

Gallic acid and aluminium chloride hexahydrate were procured from Titan Biotech Ltd., Bhiwadi, India; folin- ciocalteu's phenol reagent was obtained from Sisco Research laboratories, Pvt. Ltd., Mumbai, India; Quercitin dihydrate and DPPH (1,1-diphenyl-2-picrylhydrazyl) were purchased from HIMEDIA laboratories Pvt. Ltd., Mumbai, India; Potassium thiocyanate and 2,2'- bipyridyl, potassium ferricyanide were obtained from Central Drug House Pvt. Ltd., New Delhi, India.

Other chemicals like ethanol, sodium carbonate, ascorbic acid, phosphate buffer, trichloroacetic acid, hydrogen peroxide, ferric chloride, ferrous sulphate, potassium acetate, EDTA used in the study were of analytical grade.

Preparation of extracts

50g of dried powder was taken in 500ml of solvent (water or methanol) in a conical flask, plugged with cotton wool and kept on a rotatory shaker at 190-200rpm for 24h. After that the extracts were centrifuged at 5000g for 10min. The extract was filtered and was re-extracted by the same process until plant materials were exhausted. From the collected supernatant, solvents were evaporated and the dry extracts were stored at 4 °C in air tight bottle [6].

Antioxidant Screening: DPPH radical scavenging assay

The method of Mensor et al. [7] with slight modification was used. 1ml of 0.3mM DPPH in methanol was added to 2ml of each sample solutions (different concentration of extracts in methanol as per protocol) and allowed to react at room temperature in the dark for 30 minutes. The blank was prepared with 2ml sample solution and 1ml methanol while the negative control was 1ml DPPH solution and 2ml methanol. The decrease in absorbance was measured at 517nm.

These were converted to % AA (antioxidant activity) using the formula:

/1/%AA=100-{[(As-Ab)*100]/Ac}

Where, as was the absorbance sample, Ab was the absorbance of the blank and Ac was the absorbance of the control.

Antioxidant Potential

Determination of total phenolic content

Total phenolic contents were determined by the Folin- Ciocalteau method [8]. In brief, 0.1ml of each extract was mixed with 4.9ml distilled water, 0.5ml of Folin Ciocalteu reagent was added to the mixture. After incubation of 5min, 5ml of 7% of aqueous Na₂CO₃ solution was added. The mixture was allowed to stand for 30 minutes and the absorbance was measured at 760nm using a UV-Vis spectrophotometer (Systronics, model no. 2202). The standard curve was prepared by gallic acid (0.1mg/ ml) in methanol: water (50:50,v/v). Total phenolic content was expressed as of gallic acid equivalent |ig GAE/g fresh weight.

Determination of flavonoid content

Aluminium chloride method was used for flavonoid content determination [8]. Briefly, 0.1mL of each extract was mixed with 1.9ml distilled water, then 0.1ml 10% alluminium chloride hexa hydrate, 0.1ml 1M potassium acetate and 2.8ml of distilled water were added. The reaction mixture was incubated at room temperature for 40 minutes. The absorbance of the reaction mixture was measured at 415nm. Quercitin (0.2mg/ml) was used as a standard. Total flavonoid content was expressed as |ig QE/g fresh weight.

Screening of Metal Chelating Activity

Fe²⁺ chelation

The concentration of ferrous ion was estimated by 2,2'- bipyridyl-Fe²⁺ complex. The reaction mixture contained 0.01g of FeSO₄, 1ml of 1mM NaCl (pH 7.0). Reaction mixture was incubated for 30min at room temperature. At the end of incubation time, 2ml of 2,2'-bipyridal was added and absorbance of 2,2'-bipyridal-Fe²⁺ complex was measured at 525nm in final volume of 3ml [9].

Fe3+ chelation

Iron (III) reacts with thiocyanate and gives an intensely red colour compound which remains in true solution. In the spectrometric determination a large excess of thiocynate should be used, since this increases the intensity and also the stability of the colour [9]. 0.01g of FeCl₃ without or with different concentrations of extracts was taken. They were incubated for 30 min at room temperature. At the end of incubation time 1ml potassium thiocyanate was added. Absorbance was measured at 450nm in final 3ml solution. For both the forms of iron EDTA-Na₂ was used as the standard.

/2/%(Fe²⁺/Fe³⁺)chelation=(Ac-As)/Ac*100

Where, Ac is the absorbance of the control and as is the absorbance of the sample.

Results and Disscusion

Percent yield

Water extracts showed higher percent yield than methanol extracts ( Table 1).

DPPH scavenging assay

The antioxidants react with the stable free radical DPPH (deep violet color) and convert it to 1,1-diphenyl-2-picryl hydrazine resulting in decoloration. The scavenging effect of extracts was expressed as (%AA) percentage activity given in Table 2 & 3. Vigna aconitifolia showed highest scavenging activity in water extracts followed by Vigna radiata which? indicates that they contain more water soluble phenolic content than methanol. Data infers approx 90% antioxidant activity for moth and mung in water extracts. There was no significant effect of methanol on DDPH radical scavenging of beans.

Antioxidant Potential for Water and Methanol Extracts

Total phenolic content

Phenolic compounds are a class of antioxidant compounds which act as free radical terminators [10]. The water and methanol extracts of four varieties of beans were studied for their contents of total phenols. Table 3 shows the total phenolic content of extracts measured by Folin-Ciocalteau reagent in terms of gallic acid equivalent (GAE). The highest phenolic content was observed in Vigna aconitifolia and same pattern was found for the methanol extracts. The water extracts showed higher phenolic content which indicates water soluble phenols are dominant over methanol extracts (Figure 1).

Total flavonoid content

The mechanisms of action of flavonoids are through scavenging or chelating process [11]. The flavonoid content of extracts was calculated as quercetin equivalent (QE) using alluminium chloride method as shown in Table 3. Vigna aconitifolia and Vigna radiata both contained highest flavonoid content for water extracts while the lowest was found in Glycine max in both conditions (Figure 2).

Metal chelation activity

The main strategy to avoid free radical (ROS) generation that is associated with redox active metal catalysis involves chelating of the metal ions. Fe³⁺ with thiocyanate and Fe²⁺ with bipyridal forms complex giving red and pink colour respectively. In the presence of chelating agents, the complex formation is disrupted such that the colour of the complex is decreased. Measurement of reduction in color given by the decrease in absorbance therefore, allows the estimation of the chelating activity of the coexisting chelator. Both water and methanol extracts showed chelation towards the two forms of iron. Figure 3 & 4 shows that affinity of all the extracts towards Fe³⁺ was higher.

Conclusion

These beans can be considered as good sources of antioxidants as shown by their flavanoid and phenol contents. Vigna aconitifolia found to be most potent antioxidant with highest phenolic content and antioxidant activity. A significant correlation was observed between antioxidant activity and phenolic content indicating that phenolic compounds contribute significantly to antioxidant activity of the investigated beans in water extracts due to presence of more water soluble phenols than methanol soluble phenols. Hence these beans may be utilized as functional food for the control of oxidative stress borne diseases in the form of nutraceuticals but further in vitro and in vivo studies are required to claim the same.