Home | About PR | Editorial board | Search | Ahead of print | Current Issue | Archives | Instructions | Subscribe | Advertise | Contact us |   Login 
Pharmacognosy Magazine
Search Article 
Advanced search 

 Table of Contents 
Year : 2012  |  Volume : 4  |  Issue : 4  |  Page : 230-233  

Flower extract of Nyctanthes arbor-tristis modulates glutathione level in hydrogen peroxide treated lymphocytes

Cancer Genetics and Chemoprevention Research Group, Department of Molecular Biology and Biotechnology, Tezpur University, Tezpur, Assam, India

Date of Submission04-Apr-2012
Date of Decision09-Jun-2012
Date of Web Publication11-Oct-2012

Correspondence Address:
Anand Ramteke
Cancer Genetics and Chemoprevention Research Group, Department of Molecular Biology and Biotechnology, Tezpur University, Tezpur, Assam - 784 028
Login to access the Email id

Source of Support: None, Conflict of Interest: None

DOI: 10.4103/0974-8490.102272

Rights and Permissions

Background: Nyctanthes arbor-tristis Linn (Oleaceae) is a well-known traditional medicinal plant used throughout the India as an herbal remedy for treating various infectious and non-infectious diseases. Objective: To evaluate the antioxidative activity of hydro-alcoholic extract of flower in the lymphocytes exposed to oxidative stress induced by H 2 O 2 . Materials and Methods: Isolated lymphocytes were treated in vitro with extract or extract+H 2 O 2, and the level of reduced glutathione (GSH) as well as the activity of glutathione-S-transferase (GST) and lactate dehydrogenase (LDH) were measured. Results: Treatment of lymphocyte with flower extract (50, 100, and 200 μg/ ml) significantly increased the level of GSH and decreased the activity of GST. The LDH activity measured in the cell-free medium decreased significantly. Pre-treatment of lymphocyte with flower extract protects the lymphocyte from the H 2 O 2 induced oxidative stress by significantly increasing the levels of GSH as compared to the cells treated only with H 2 O 2 . Pre-treatment also reduced the activity of LDH significantly as compared to the cells treated only with H 2 O 2 . The LDH activity in cell-free medium is associated with membrane damage, the decreased levels of LDH activity reflects the reduced level of membrane damage due to H 2 O 2 . Conclusion: The present findings suggest the protective role of the hydro-alcoholic extracts of the flower of Nyctanthes arbor-tristis against membrane damage induced by H 2 O 2 . The results also suggest that the extract might be rich in phytochemicals with antioxidant/radical scavenging potentials, which might find application in antioxidant therapy.

Keywords: Nyctanthes arbor-tristis, oxidative stress, reduced glutathione

How to cite this article:
Hussain A, Ramteke A. Flower extract of Nyctanthes arbor-tristis modulates glutathione level in hydrogen peroxide treated lymphocytes. Phcog Res 2012;4:230-3

How to cite this URL:
Hussain A, Ramteke A. Flower extract of Nyctanthes arbor-tristis modulates glutathione level in hydrogen peroxide treated lymphocytes. Phcog Res [serial online] 2012 [cited 2021 Jun 22];4:230-3. Available from: http://www.phcogres.com/text.asp?2012/4/4/230/102272

   Introduction Top

Reactive oxygen species (ROS) are generated as a metabolic by product in biological system during normal metabolism of oxygen and plays vital role in cell signaling homeostasis for maintaining normal functioning of cells. [1] In the stress conditions, either intrinsic or extrinsic, ROS levels increase dramatically, resulting imbalance in between oxidants and antioxidants that leads to various forms of damage of micro and macromolecules and finally contributes into the manifestation of disease such as sickle cell anemia, atherosclerosis, Parkinson's disease, heart failure, myocardial infarction, Alzheimer's disease, schizophrenia, cancer etc. [2],[3],[4],[5]

Biological systems inherently have antioxidant system to scavenge and/or neutralize ROS generated under oxidative stress. Cellular antioxidant system (AOEs) consisting of mainly superoxide dismutase (SOD), catalase, reduced glutathione (GSH), glutathione peroxidase (GPx), reduced glutathione (GSH) etc. [6] These biological AOEs function as cascade manner to neutralize or eliminate the ROS and failure of which contributes the diseases manifestation. For effective management of reactive species, antioxidants have been supplemented, and several botanicals and synthetic compounds such as BHT, BHA have been studied for potent source of antioxidants. However, in real, biological state of radical scavenging and subsequent reduction of disease manifestation is still challenging area. [7]

Nyctanthes arbor-tristis Linn (commonly known as Night-flowering Jasmine), belonging to the family Oleaceae, is known for its extensive traditional medicinal use by the rural, mainly tribal people of India along with its use in Ayurveda, Sidha, and Unani systems of medicines. [8] Traditionally, whole plants and different parts have used as an herbal remedy for treating sciatica, arthritis, malaria, enlargement of spleen and as blood purifier. The beautiful white flowers are bitter in taste and are used as stomachic, carminative, astringent to bowel, anti-bilious, expectorant, hair tonic and in the treatment of piles and various skin diseases. [9] Recent pharmacological studies showed anti-spasmodic, antioxidant, anthelmintic, cytoprotective, anti-diabetic, anti-leishmanial, CNS depressant activity of the flower extract. [9] However, very few reports are available regarding antistress or stress scavenging activity or antioxidant activity of the flower extract of this plant. Therefore, the present study was aimed to assess the modulatory response of flower extract of Nyctanthes arbortristis on the cellular antioxidant status in lymphocytes exposed to oxidative stress induced by hydrogen peroxide (H 2 O 2 ) and tried to correlate with oxidative stress induced membrane damage.

   Materials and Methods Top

Preparation of Modulator

The flowers of Nyctanthes arbor-tristis were collected from healthy plants, cleaned properly, and dried at shade at room temperature. The dried plant materials were finely powdered and macerated thrice with 80% (v/v) ethanol in shaking condition for 7 days at room temperature. The extract thus obtained were filtered and concentrated by air drying and stored at 4° C. The resulting extract was dissolved in Dimethyl sulfoxide (DMSO) with final concentration of 2.5 mg/ml.

Lymphocytes Isolation, culture, and treatment

Anti-coagulated chicken blood, collected from source, was diluted with PBS (1:1, v/v), layered 6 ml into 6 ml Histopaque (1.077 gm/ml), centrifuged at 400 g for 30 minutes, and lymphocytes were isolated from the buffy layer. Isolated lymphocytes were then washed with 2 ml PBS and 2 ml RPMI media separately through centrifugation for 10 minutes at 250 g. [10],[11] Pelleted lymphocytes were then suspended in RPMI, and viability was checked by Trypan blue exclusion method using hemocytometer. [12] Lymphocytes with viability more than 90% were used for subsequent study.

Isolated lymphocytes (200 μl) were seeded in 96 well culture plate in RPMI supplemented with 10% heat inactivated fetal bovine serum (FBS). Lymphocytes were treated with extract (for 4 hr), and extract+H 2 O 2 (1 hr+4 hr) as per experimental requirements and maintained at 37° C and 5% CO 2 in CO 2 incubator. After incubation, lymphocytes were centrifuged and washed with PBS and homogenized in PBS. The cell homogenates were used for assaying level of GSH, GST activity, and total protein content while cell free media were used for assaying LDH activity.

Reduced glutathione (GSH) Estimation

Level of reduced glutathione was estimated as total non-protein sulphydryl group in the cell homogenates after precipitating the proteins by 5% tricholoroacetic acid (TCA). The supernatant was mixed with 0.2 M phosphate buffer (pH 8) and 0.6 M 5, 5′-dithio-bis (2-nitrobenzoic acid) and allowed to stand for 8-10 min at room temperature. The absorbance was recorded at 412 nm using a spectrophotometer (Thermo Scientific, UV 10), and level was calculated as nMole of -SH content/mg protein from standard curve made with reduced glutathione (GSH) and finally expressed as percentage change of GSH level. [13]

Glutathione- S -transferase (GST) activity

The specific activity of cytosolic GST was determined spectrophotometricaly (Cecil Aquarius, 7000 series) by measuring the CDNB-GSH conjugates formation at 340 nm for 3 min. The reaction mixture (1 ml) was prepared by mixing 0.1 M phosphate buffer (pH 6.5), 1 mM CDNB in 95% ethanol, and 1 mM GSH followed by incubation at 37° C for 5 min prior to measuring OD. The specific activity of GST was calculated using the extinction coefficient 9.6 mM -1 cm -1 at 340 nm and expressed in terms of percentage change of μ mole of CDNB-GSH conjugates formed/ min/mg proteins. [14]

Lactate Dehydrogenase (LDH) activity

The specific activity of lactate dehydrogenase (LDH) released into the medium was assayed by measuring the rate of oxidation of NADH at 340 nm using a spectrophometer (Cecil Aquarius, 7000 series). Briefly, assay mixture consists of 50 mM potassium phosphate buffer (pH 7.5), 0.5 mM sodium pyruvate, 0.1 mM NADH, and enzyme sample. The enzyme activity was calculated using extinction coefficient 6.22 mM -1 Cm -1 and finally expressed as percentage change of LDH activity. [15]

Protein Estimation

The amounts of protein present in the sample were estimated using bovine serum albumin (BSA) as standard by using Folin reagent. [16]

Statistical Analysis

All the results are expressed as means±SD. Results were statistically analyzed by student's t test for significance difference between group mean using GraphPad software.

   Results and Discussion Top

The use of natural products in the form of crude preparation and active principle as a therapeutic regime has been widely established. Several medicinal plants have been studied for their potentials to modulate cellular antioxidants and free radicals, and a numbers of active principles have also isolated from plants with anti-oxidative efficacy. [17],[18] But, there is still lack of magic principle with maximum efficacy and least toxicity. The present study explores the anti-oxidative activity of flower extract of Nyctanthes arbor-tristis, a traditional medicinal plant of India against H 2 O 2 -treated lymphocytes.

H 2 O 2 is weak oxidizing agent and can easily cross cell membranes and inside the cell, H 2 O 2 probably reacts with Fe 2+ and Cu 2+ ions to forms hydroxyl radicals. [19] Increased level of hydroxyl radicals in the cell subsequently cause damage to the cells by interacting with micro and macro molecules. It also inactivate enzymes directly, usually by oxidation of essential thiol (-SH) groups. [20] Our previous study established the detrimental effects of H 2 O 2 . Treatment of lymphocyte with H 2 O 2 decreases the viability of cells by lowering cellular antioxidant, reduced glutathione (GSH). [21]

In the present study, the level of GSH increased significantly when lymphocytes were treated with flower extract of Nyctanthes arbor-tristis for 4 hours, and at 200 μg/ml of treatment, 1.22-fold increase was observed in comparison to untreated lymphocytes [Table 1]. In contrast to GSH, the specific activity of glutathione-S-transferase, an important constituent of phase II drug metabolizing enzymes declined; however, the decline was non-significant [Table 1]. For the similar treatment condition, the specific activity of lactate dehydrogenase (LDH), marker of membrane damage was significantly declined in comparison to untreated lymphocytes [Table 1]. This decrease in the activity of LDH suggests non-toxic effect of the extract on the cellular system; rather it might have decreased the endogenous cellular injury (as a part of normal cellular metabolism). [22],[23] These data clearly showed the anti-oxidative property of the crude extract used for the current study.
Table 1: Modulatory effects of the flower extract of Nyctanthes arbor-tristis

Click here to view

Increased level of cellular antioxidants is known to provide protection against oxidative stress. [24] Here, in our study, pre-treatment of lymphocytes with the flower extract (50, 100, and 200 μg/ml) for 1 h significantly restored the depleted GSH level in the 1% H 2 O 2 -treated lymphocytes (4 h) [Table 2]. The restoration of GSH level at 200 μg/ ml treatment condition [Table 2] was above the untreated lymphocyte (P<0.001). As expected, the specific activity of GST decreased significantly as compared to the cells treated with H 2 O 2 [Table 2]. GSH is co-factor of GST and is responsible for the redox status of cell. The rise in the levels of GSH is due to decreased GST activity. [25],[26] The significant decrease in the activity of LDH was observed in the lymphocytes pre-treated with flower extract followed by H 2 O 2 treatment. The significant decline in the activity of LDH suggests protective function of the extract against membrane damage induced by the H 2 O 2 . [27]
Table 2: Protective effects of flower extract of Nyctanthes arbor-tristis in H2O2 (1%) treated lymphocytes

Click here to view

In conclusion, the results of the present study clearly indicate the anti-oxidative and protective role of hydro-alcoholic extract of Nyctanthes arbor-tristis against the oxidative stress induced by H 2 O 2 . The encouraging results shown by the hydro-alcoholic extract might be due to the presence of high content of phytochemicals and merits detail pharmacological investigation in suitable model to identify and characterize the active principle responsible for the observed activity.

   Acknowledgement Top

The authors expressed their gratitude to Prof. S K Borthakur (Dept of Botany, Gauhati University, Gauhati, Assam, India) for his help in the identification of the plant specimen. The author AH is thankful to DST, Govt. of India for financial support in the form of INSPIRE JRF.

   References Top

1.Wijeratne SS, Cuppett SL, Schlegel V. Hydrogen peroxide induced oxidative stress damage and antioxidant enzyme response in Caco-2 human colon cells. J Agric Food Chem 2005;53:8768-74.  Back to cited text no. 1
2.Matés JM, Sánchez-Jiménez FM. Role of reactive oxygen species in apoptosis: Implications for cancer therapy. Int J Biochem Cell Biol 2000;32:157-70.  Back to cited text no. 2
3.Dash DK, Yeligar VC, Nayak SS, Ghosh T, Rajalingam D, Sengupta P, et al. Evaluation of hepatoprotective and antioxidant activity of Ichnocarpus frutescens (Linn) R.Br. on paracetamol-inuduced hepatotoxicity in rats. Trop J Pharm Res 2007;6:755-65.  Back to cited text no. 3
4.Nordberg J, Arnér ES. Reactive oxygen species, antioxidants and the mammalian thioredoxin system. Free Radic Biol Med 2001;31:1287-312.  Back to cited text no. 4
5.Waris G, Ahsan H. Reactive oxygen species: Role in the development of cancer and various chronic conditions. J Carcinog 2006;5:14-22.  Back to cited text no. 5
[PUBMED]  Medknow Journal  
6.Valko M, Leibfritz D, Moncol J, Cronin MT, Mazur M, Telser J. Free radicals and antioxidants in normal physiological functions and human disease. Int J Biochem Cell Biol 2007; 39:44-84.  Back to cited text no. 6
7.Hazarika N, Singh P, Hussain A, Das S. Phenolics content and antioxidant activity of crude extract of Oldenlandia corymbosa and Bryophyllum pinnatum. Res J Pharm Biol Chem Sci 2012;3:297-303.  Back to cited text no. 7
8.Sasmal D, Das S, Basu SP. Phytoconstituents and therapeutic potential of Nyctanthes arbor-tristis Linn. Pharmacogn Rev 2007;1:344-9.  Back to cited text no. 8
9.Sandhar HK, Kaur M, Kumar B, Prasher S. An update on Nyctanthes arbor-tristis Linn. Int Pharm Sci 2011;1:77-86.  Back to cited text no. 9
10.Winchester RJ, Ross G. Methods for enumerating lymphocyte populations. Man Clin Immunol 1976:64-76.  Back to cited text no. 10
11.Thorsby E, Bratlie A. A rapid method for preparation of pure lymphocyte suspensions. Histocompat Test 1970:665-6.  Back to cited text no. 11
12.Lechón MJ, Iborra FJ, Azorín I, Guerri C, Piqueras JR. Cryopreservation of rat astrocytes from primary cultures. Methods Cell Sci 1992;14:73-7.  Back to cited text no. 12
13.Moron MS, Depierre JW, Mannervik B. Levels of glutathione, glutathione reductase and glutathione S-transferase activities in rat lung and liver. Biochim Biophys Acta 1979;582:67-78.  Back to cited text no. 13
14.Habig WH, Pabst MJ, Jakoby WB. Glutathione S-transferases. The first enzymatic step in mercapturic acid formation. J Biol Chem 1974;249:7130-9.  Back to cited text no. 14
15.Bergmeyer HU, Bent E. Methods of Enzymatic Analysis. Vol. II. Verlag: Academic Press; 1971. p. 5574-9.  Back to cited text no. 15
16.Lowry OH, Rosebrough NJ, Farr AL, Randall RJ. Protein measurement with the Folin phenol reagent. J Biol Chem 1951; 193:265-75.  Back to cited text no. 16
17.Miguel MG. Antioxidant activity of medicinal and aromatic plants. A review. Flavour Fragr J 2010;25:291-312.  Back to cited text no. 17
18.Krishnaiah D, Sarbatly R, Nithyanandam R. A review of the antioxidant potential of medicinal plant species. Food Bioprod Process 2011;89:217-33.  Back to cited text no. 18
19.Halliwell B, Gutterridge JMC. Free Radicals in Biology and Medicine. Clarendon: Oxford; 1993. p. 419.  Back to cited text no. 19
20.Yermilov V, Rubio J, Becchi M, Friesen MD, Pignatelli B, Ohshima H. Formation of 8-nitroguanine by the reaction of guanine with peroxynitrite in vitro. Carcinogenesis 1995; 16:2045-50.  Back to cited text no. 20
21.Ramteke A, Hussain A, Kaundal S, Kumar G. Oxidative Stress and modulatory effects of the root extract of Phlogacanthus tubiflorus on the activity of Glutathione-S-Transferase in Hydrogen Peroxide treated Lymphocyte. J Stress Physiol Biochem 2012;8:5-11.  Back to cited text no. 21
22.Dahiru D, William ET, Nadro MS. Protective effect of Ziziphus mauritiana leaf extract on carbon tetrachloride-induced liver injury. Afr J Biotechnol 2005;4:1177-9.  Back to cited text no. 22
23.Pardhasaradhi BV, Reddy M, Ali AM, Kumari AL, Khar A. Differential cytotoxic effects of Annona squamosa seed extracts on human tumour cell lines: Role of reactive oxygen species and glutathione. J Biosci 2005;30:237-44.  Back to cited text no. 23
24.Salganik RI. The benefits and hazards of antioxidants: Controlling apoptosis and other protective mechanisms in cancer patients and the human population. J Am Coll Nutr 2001;20:464S-472S.  Back to cited text no. 24
25.Rouach H, Fataccioli V, Gentil M, French SW, Morimoto M, Nordmann R. Effect of chronic ethanol feeding on lipid peroxidation and protein oxidation in relation to liver pathology. Hepatology 1997;25:351-5.  Back to cited text no. 25
26.Ramteke A, Prasad SB, Kumar S, Borah S, Das RK. Leaf extract of extract of Phlogacanthus tubiflorus Nees modulates glutathione level in CCl 4 treated chicken lymphocyte. J Assam Science Society 2007;47:20-4.  Back to cited text no. 26
27.Dash R, Acharya C, Bindu PC, Kundu SC. Antioxidant potential of silk protein sericin against hydrogen peroxide-induced oxidative stress in skin fibroblasts. BMB Rep 2008; 41:236- 41.  Back to cited text no. 27


  [Table 1], [Table 2]


    Similar in PUBMED
   Search Pubmed for
   Search in Google Scholar for
 Related articles
    Access Statistics
    Email Alert *
    Add to My List *
* Registration required (free)  

  In this article
    Materials and Me...
    Results and Disc...
    Article Tables

 Article Access Statistics
    PDF Downloaded45    
    Comments [Add]    

Recommend this journal