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Free Radical Scavenging Activities and Neuro-protective Effects of Extracts from Juniperus rigida Sieb. Fruit

Hyun Woo Kang*, Sang Jae Kwak

Department of Korean Food & Culinary Arts, Youngsan University, Busan, 48015, Korea

Abstract: The antioxidative activity of extracts from Juniperus rigida Sieb. Fruit (JRSF) was evaluated by measuring 1,1-diphenyl-2-picrylhydrazyl (DPPH), hydroxyl and alkyl radical scavenging activity using an electron spin resonance (ESR) spectrometer. The free radical scavenging activity of the extract was dose dependant manner, and the IC₅₀ value on DPPH, hydroxyl and alkyl radical at 16.84, 82.35 and 52.27 μg/mL respectively. In addition, evaluated the protection effect on H₂O₂-induced oxidative damage in PC-12 cells via propidium iodide (PI) staining using a flow cytometer. JRSF extract decreased cell death in PC-12 cells due to H₂O₂-induced oxidative damage in a dose-dependent manner. These results suggest that JRSF extract exhibit antioxidative activity against oxidative stress on PC-12 cells.

Keywords: Juniperus rigida Sieb. fruit, antioxidant, free radical, PC-12 cells, flow cytometer

Received December 12, 2018; Revised January 19, 2019; Accepted March 02, 2019

Citation: Hyun Woo Kang, Sang Jae Kwak, Free Radical Scavenging Activities and Neuro-protective Effects of Extracts from Juniperus rigida Sieb. Fruit. Journal of Food and Nutrition Research, 7 (3). 187-190. January 2019. doi:10.12691/jfnr-7-3-2

1. Introduction

Reactive oxygen-mediated modification of DNA, proteins, lipids and small cellular molecules is associated with a number of pathological processes, including atherosclerosis, arthritis, diabetes, cataractogenesis, muscular dystrophy, pulmonary dysfunction, inflammatory disorders, ischemia-reperfusion tissue damage and neurological disorders such as Alzheimer’s disease [1]. Free radical scavenger is a preventive antioxidant. The term antioxidant is defined as any substance that, when present at low concentrations compared to that of an oxidizable substrate, significantly delays or inhibits oxidation of that substrate [2]. Antioxidants can act at different levels in an oxidative sequence. This may be illustrated by considering one of the many mechanisms by which oxidative stress can cause damage by stimulating the free radical chain reaction of lipid peroxidation [3]. Free radical chain reactions within a material could be inhibited by adding chemicals that retard the formation of free radicals, by introducing substances that retard the formation of free radicals or by introducing substances that compete for the existing radicals and remove them from the reaction medium [3]. Many synthetic antioxidants such as butylated hydroxyanisole (BHA), butylated hydroxytoluene (BHT), tertiary-butylhydroquinone (t-BHQ) and propyl gallate (PG) may be used to retard lipid peroxidation in a lot of fields [3,4]. Therefore, search for natural antioxidants as alternatives to synthetic ones is of great interest among researchers.

Juniperus rigida Sieb. (JRS), is mainly grown in Asia [5,6]. The fruits and leaves of this tree have been traditionally used in folk medicine for the treatment of neuralgia, dropsy, and gout [7]. Pharmacologically, the phenolic compounds have been reported to inhibit NO production in LPS-induced RAW264.7cells [8]. However, the free radical scaveingin antivities of JRSF has not been evaluated until now.

Thus, the present study aimed to investigate the free radical scavenging activities of extracts from JRSF by ESR spectroscopy and their possible protective effects on PC-12 cells against oxidative stress.

2. Materials and Methods

2.1. Materials

Juniperus rigida Sieb. Fruit (JRSF) was purchased from a local market (). 1,1-diphenyl-2-picrylhydrazyl (DPPH), 5,5-Dimethyl-1-pyrroline N-oxide (DMPO), 2,2-azobis (2-amidinopropane) hydrochloride (AAPH), (4-pyridyl-1-oxide)-N-tert-butylnitrone (4-POBN) were purchased from Sigma Chemical Co. (St Louis, USA), and pBR 322 DNA was procurred from Fermentas (Hanover, MD). Dulbecco’s modified Eagle’s medium (DMEM), fetal bovine serum (FBS), penicillin, and streptomycin were purchased from Hyclone (Logan, UT, USA). All other reagents were of the highest grade available commercially.

2.2. DPPH Radical Scavenging Activity

DPPH radical scavenging activity was measured using the method described by Nanjo et al. [9]. An ethanol solution of 60 µL of each sample (or ethanol itself as control) was added to 60 µL of DPPH (60 mM) in ethanol solution. After mixing vigorously for 10 s, the solution was then transferred into a 100 mL quartz capillary tube, and the scavenging activity of JRSF extract on DPPH radical was measured using a JES-FA ESR spectrometer (JEOL Ltd., ). ESR spectrum was measured on an ESR spectrometer exactly 2 min later. Experimental conditions were as follows: central field, 3475 G; modulation frequency, 100 kHz; modulation amplitude, 2 G; microwave power, 5 mW; gain, 6.3×10⁵ and temperature, 298 K.

2.3. Hydroxyl Radical Scavenging Activity

Hydroxyl radicals were generated by iron-catalyzed Haber-Weiss reaction (Fenton driven Haber-Weiss reaction) and the generated hydroxyl radicals rapidly reacted with nitrone spin trap DMPO [10]. The resultant DMPO-OH adducts was detectable with an ESR spectrometer. JRSF extract (0.2 mL) with various concentrations was mixed with DMPO (0.3 M, 0.2 mL), Fe₂SO₄ (10 mM, 0.2 mL) and H₂O₂ (10 mM, 0.2 mL) in a phosphate buffer solution (pH 7.2), and then transferred into a 100 mL quartz capillary tube. After 2.5 min, the ESR spectrum was recorded using an ESR spectrometer. Experimental conditions were as follows: central field, 3475 G; modulation frequency, 100 kHz; modulation amplitude, 2 G; microwave power, 1 mW; gain, 6.3×10⁵ and temperature, 298 K.

2.4. Alkyl Radical Scavenging Activity

Alkyl radicals were generated by AAPH. The PBS (pH 7.4) reaction mixtures containing 40 mM AAPH, 40 mM 4-POBN and indicated concentrations of tested samples, were incubated at 37°C in a water bath for 30 min, and then transferred to a 60 µL Teflon capillary tube. The spin adduct was recorded on an ESR spectrometer. Measurement conditions were as follows: central field, 3475 G; modulation frequency, 100 kHz; modulation amplitude, 2 G; microwave power, 1 mW; gain, 6.3×10⁵ and temperature, 298 K [11].

2.5. Cell Culture

PC-12 cells were cultured and maintained in DMEM supplemented with penicillin (100 U/mL), streptomycin (100 µg/mL) and FBS (10%) and maintained at 37°C under a humidified atmosphere with 5% CO₂. All the treatments were performed at 30% confluence.

2.6. Apoptosis Analysis

The PC-12 cells were seeded at 2 × 10⁵ cells/well in 6-well plates in a complete medium, DMEM with 10% FBS. After 24 h incubation in a humidified 5% (v/v) CO₂/air environment at 37°C, 990 μL of the extract solution in DMEM was transferred to the well to give a final concentration of mg/mL. Following 1 h incubation with the extracts, 10 μL of 100 mM hydrogen peroxide was added the medium. After 24 h the cell was harvested, and the harvested cells were suspended in ethanol with 0.5% Tween-20 and left for 24 h at 4°C. The cells were then harvested by centrifugation and re-suspended in 1.0 mL of PBS with 0.05 mg/mL of propidium iodide and 10 μg/mL of RNase A and incubated at 37°C for 30 min. The analysis of apoptotic cell death was performed by measuring the hypodiploid DNA contents using a flow cytometer (FACS-caliber, Becton Dickinson, NJ) [12].

2.7. Statistical Analysis

Study data are expressed as mean ± standard error of mean (SEM). Statistical analyses of differences between treatment groups were conducted using Student’s t-test for paired data, and p < 0.05 was considered to have statistical significance. All analyses were carried out in triplicate using Graph Pad Prism software version 4.00 (Graph Pad Software Inc., San Diego, CA).

3. Results and Discussion

DPPH radical is a stable free radical, which has been used to evaluate free radical scavenging activity of natural antioxidants. In this study, the DPPH radical scavenging activity of extract from JRSF was shown in Figure 1A. JRSF extract was observed scavenging activity of 42.36, 66.82 and 81.35 at the concentrations of 15.625, 31.25 and 62.5 μg/mL on DPPH radical, respectively, In addition, the IC₅₀ values was 16.84 μg/mL. Hydroxyl radicals generated in the Fe²⁺/H₂O2 system were trapped by DMPO, forming a spin adduct detected by an ESR spectrometer. Here. the extract from JRSF was observed that the hydroxyl radical scavenging activities were 27.61, 40.29 and 77.76% at 31.25, 62.5 and 125 μg/mL, respectively, and the IC50 value was 82.35 μg/mL (Figure 1B). The alkyl radical spin adduct of 4-POBN/free radicals was generated from AAPH at 37℃ for 30 min, and the decrease of ESR signals was observed with the dose increment of the extract from JRSF. alkyl radical scavenging activities of the extract from JRSF were 36.50, 56.11 and 88.66% at 31.25, 62.5 and 125 μg/mL, respectively, and the IC₅₀ value was 52.27 μg/mL (Figure 1C). In recent, there is a continuing search for better and more effective antioxidants, expecially those from natural sources. There is a close association between chronic inflammation and cancer. Evidence for this comes from epidemiological studies, linking reactive species overload diseases to high cancer risk [13]. At a molecular level, free radicals produced during chronic inflammation, can induce deleterious gene mutation and post-translational modifications of key cancer-related proteins [14]. The pro-cancerous outcome of chronic inflammation is increased DNA damage. A critical mechanism toward cancer associated with reactive species overload diseases is the attack of cancer genes and proteins, RNA, and lipids by reactive nitrogen and oxygen species [14]. Therefore, a key treatment strategy is to reduce the free radical load to diminish these pro-cancerous mechanisms. Free radicals are atoms or groups of atoms with an odd (unpaired) number of electrons and can be formed when oxygen interacts with certain molecules. Once formed these highly reactive radicals can start a chain reaction, like dominoes. These results indicate that the extract from JRSF possess scavenging activity against DPPH, hydroxyl and alkyl radicals. The neuroprotective effect of JRSF extracts was determined by apoptosis analysis using a flow cytometer. The cells were treated with the extracts prior 1.0 mM hydrogen peroxide, the percentage of apoptotic cells was observed 35.31% at 1.0 mM hydrogen peroxide, while the percentages of JRSF extracts treated cells were 27.55 and 19.36% at 62.5 and 125 μg/mL, respectively (Figure 2).

Figure 1. DPPH (A), hydroxyl (B), and alkyl (C) radical scavenging activity (left) and spectra (right) of extract from JRSF using ESR spectroscopy. Means±SD of determinations were acquired from triplicate experiments Data are presented as mean ± S.E.M. (n = 3) for three independent experiments. жNot significantly different from that of the control group. Significance was determined by Student’s t-test. *p < 0.05.

Figure 2. Cell death and cell cycle of PC-12 cells after treatment with extract of JRSF prior to hydrogen peroxide (1 mM) treatment. Means±SD of determinations were made in triplicate experiments. *(p<0.05) and **(p<0.01) are significantly different as analyzed by paired t-test that compared the oxidative stress group with the extract of JRSF treated group

The result of this study suggests that JRSF extract could be utilised to develop physiologically functional foods. In addition, it is expected that this will contribute to increase interest and potential applications of bioactive materials.

4. Conclusions

In the present study, we focused on natural water-soluble free radical scavenger from ectract of JRSF. Their free radical scavenging activities were evaluated in different reactive oxygen species assays including DPPH, hydroxyl and Alkyl radical scavenging assays by an ESR spectrophotometer. Also, JRSF extract protect neuronal cells against hydrogen peroxide-induced oxidative damage. Overall, this natural product has the potential to be developed into new biomaterials.

Acknowledgments

This research was supported by Youngsan University in 2018.

References

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