Evidence-Based Complementary and Alternative Medicine

Volume 2013 (2013), Article ID 759615, 7 pages

http://dx.doi.org/10.1155/2013/759615

Research Article

Citrus bergamia Risso Elevates Intracellular Ca²⁺ in Human Vascular Endothelial Cells due to Release of Ca²⁺ from Primary Intracellular Stores

Purum Kang,¹ Seung Ho Han,² Hea Kyung Moon,¹ Jeong-Min Lee,³ Hyo-Keun Kim,³ Sun Seek Min,² and Geun Hee Seol¹

¹Department of Basic Nursing Science, School of Nursing, Korea University, 145 Anam-ro, Seongbuk-gu, Seoul 136-701, Republic of Korea

²Department of Physiology and Biophysics, School of Medicine, Eulji University, Youngdu-dong, Jung-gu, Daejeon 301-746, Republic of Korea

³KT&G Research Institute, Daejeon 305-805, Republic of Korea

Received 26 June 2013; Revised 28 October 2013; Accepted 28 October 2013

Academic Editor: Mohamed Eddouks

Copyright © 2013 Purum Kang et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract.

The purpose of the present study is to examine the effects of essential oil of Citrus bergamia Risso (bergamot, BEO) on intracellular Ca²⁺ in human umbilical vein endothelial cells. Fura-2 fluorescence was used to examine changes in intracellular Ca²⁺ concentration . In the presence of extracellular Ca²⁺, BEO increased , which was partially inhibited by a nonselective Ca²⁺ channel blocker La³⁺. In Ca²⁺-free extracellular solutions, BEO increased in a concentration-dependent manner, suggesting that BEO mobilizes intracellular Ca²⁺. BEO-induced increase was partially inhibited by a Ca²⁺-induced Ca²⁺ release inhibitor dantrolene, a phospholipase C inhibitor U73122, and an inositol 1,4,5-triphosphate (IP₃)-gated Ca²⁺ channel blocker, 2-aminoethoxydiphenyl borane (2-APB). BEO also increased in the presence of carbonyl cyanide m-chlorophenylhydrazone, an inhibitor of mitochondrial Ca²⁺ uptake. In addition, store-operated Ca²⁺ entry (SOC) was potentiated by BEO. These results suggest that BEO mobilizes Ca²⁺ from primary intracellular stores via Ca²⁺-induced and IP3-mediated Ca²⁺ release and affect promotion of Ca²⁺ influx, likely via an SOC mechanism.

1. Introduction

Bergamot essential oil (BEO) is obtained from bergamot (Citrus bergamia Risso), a roughly pear-shaped citrus fruit. BEO is widely used in aromatherapy to alleviate symptoms of stress-induced anxiety, mild mood disorders, and cancer pain [1] and it has anxiolytic [2] and analgesic [1, 3, 4] effects in rodents.

Besides these effects of BEO, bergamottin, isolated from nonvolatile fraction of BEO, significantly decreased the typical electrocardiographic signs of coronary arterial spasm, the force of the contraction and the incidence of cardiac arrhythmias induced by vasopressin in the guinea pig [5]. Given the potential roles of bergamottine in cardiovascular function, it is of interest to know the roles of BEO in Ca²⁺ mobilization in endothelial cells. Vasorelaxant effect of BEO may involve Ca²⁺ mobilization from intracellular stores and/or from the extracellular pool in endothelial cells. Several studies demonstrating the relationship between endothelial cells and smooth muscle relaxation have been reported. Our previous study implicated that a change in cytosolic Ca²⁺ levels during stimulation of endothelial cells was a basic mechanism by which endothelial cells modulate vasomotor activity [6]. Another report indirectly supports this view, demonstrating that the vasorelaxant effect of the essential oil of Ocimum gratissimum is partly dependent on the integrity of the vascular endothelium [7].

Up till now, the effects of BEO on in endothelial cells and the mechanisms by which BEO modulates the intracellular Ca²⁺ concentration () are not revealed. In the present study, we investigate the intracellular Ca²⁺-regulating properties of BEO in endothelial cells and present evidence that BEO increases via release from intracellular Ca²⁺ stores and through store-operated Ca²⁺ entry (SOC).

2. Materials and Methods

2.1. Human Vascular Endothelial Cell Culture

A human endothelium-derived cell line EA.hy926 was purchased from the American Type Culture Collection (Manassas, VA, USA) [8]. EA cells were grown in Dulbecco’s Modified Eagle Medium (DMEM) containing 20% fetal bovine serum (FBS) and 10% hypoxanthine-aminopterin-thymidine 50 supplement (Life Technologies). Cell cultures were maintained at 37°C in a fully humidified 95% air 5% CO₂ atmosphere. The media were removed and replaced with fresh medium three times in a week. The cells were detached by exposure to trypsin, reseeded on gelatin-coated coverslips, and maintained in culture for 2 to 4 days before use. Measurements were performed on subconfluent cells.

2.2. Cell Viability Assays

The thiazolyl blue tetrazolium bromide (MTT) assay was used to determine the effects of BEO on cell viability. EA cells were cultured using DMEM with 100% (v/v) FBS (Gibco Invitrogen), 100 units/mL penicillin, 100 μg/mL streptomycin (Gibco Invitrogen), and MEM nonessential amino acids (Invitrogen) in 96-well plates (Nunclon, Denmark) for 48 h until 80–90% confluence has been reached. To evaluate the effect of BEO, cells were for 15 min with varying concentrations (0.001, 0.005, 0.01, 0.05, or 0.1% [v/v in DMSO]) of the BEO and 0.25% DMSO. Then cells were washed with fresh PBS and replaced with serum-free media. In addition, cells were loaded with 10 μL MTT (5 mg/mL) and incubated at 37°C for 3 h. MTT solution was removed and replaced with 100 μL DMSO in a dark place for 2 h. The change in color was read at 540 nm using a plate reader.

2.3. Ca²⁺ Measurements

Cells were loaded with fura-2 AM, and was measured using a microfluorometer system consisting of an inverted microscope (IX71, Olympus, Japan) and a PTI Filter Scan power illuminator system (Photon Technology International). Fura-2 AM (2 μM) was added to the bath and the cells were incubated for 25 min at 37°C. The cells were illuminated alternatively at wavelengths of 340 and 380 nm through a chopper wheel (frequency = 50 Hz). Fluorescence was measured at 510 nm, and autofluorescence was subtracted from the signals obtained. The Ca²⁺-free concentration was calculated from the ratio of the fluorescence signals emitted at each excitation wavelength. The calibration procedure was identical to that described previously [9].

2.4. Solutions and Chemicals

The external solution contained the following (in mM): 150 NaCl, 6 KCl, 1.5 CaCl₂, 1 MgCl₂, 10 HEPES, and 10 glucose; pH was adjusted to 7.4 with NaOH. Ca²⁺-free solution contained 5 mM EGTA in place of Ca²⁺. The osmolarity of this solution, as measured with a vapor pressure osmometer (FISKE, USA), was 320 ± 5 mOsm. ATP, 2-aminoethoxydiphenyl borane (2-APB), 2,5-di-t-butyl-1,4-benzohydroquinone (BHQ), carbonyl cyanide m-chlorophenylhydrazone (CCCP), dantrolene, U73122, and MTT were purchased from Sigma; Fura-2 AM was obtained from molecular probes. BHQ, U73122, and essential oil (0.001%, 0.005%, 0.01%, 0.05%, 0.1%, or 0.2% v/v) were applied from a stock solution in dimethyl sulfoxide (DMSO). Final concentration of DMSO was less than 1%. 2-APB was applied from a stock solution in ethanol. The final concentrations of DMSO and ethanol were less than 0.05%. BEO (batch no. 110824) was purchased from Aromarant Co. Ltd., Röttingen, Germany, and came from locally cultivated plants in Italy.

2.5. Statistical Analysis

Pooled data are presented as means ± SEMs and significant differences were determined using paired t-test or ANOVA followed by Scheffe’s post-hoc analysis. A value of was considered significant.

3. Results

3.1. Cell Viability

The MTT assay was used to determine explored effect of varying concentrations of BEO in EA cells. Each cell was treated with media (control), DMSO (vehicle, 0.25% [v/v]), or BEO (0.001%, 0.005%, 0.01%, 0.05%, or 0.1% [v/v in DMSO]) for 15 min (Figure 1). Differences between groups were analyzed using the ANOVA followed by Scheffe’s post-hoc analysis. There was no significant effect to the percentage of viable cells at all concentrations of BEO in EA cells (, ).

Figure 1: The cell survival percentage measured using MTT assay after 15 min posttreatment of bergamot essential oil, one-way ANOVA followed by Scheffe’s post hoc test ().

3.2. Elevation of by BEO in Human Vascular Endothelial Cells

BEO increased in a concentration-dependent manner in EA cells (Figure 2(a)). The concentration-response relationship for mobilization of Ca²⁺ from intracellular stores by BEO is summarized in Figure 2(b). The concentration of BEO was nonlinearly related to the increase in as revealed by fitting the Hill equation type dose-response curve. The half maximal increase in (EC₅₀) was obtained at %. DMSO (0.25% v/v) itself did not change intracellular Ca²⁺ levels. The cells showed no morphological change after treatment with BEO. Then we investigated whether BEO changed in the presence of extracellular Ca²⁺ in EA cells. Application of BEO increased to  μM, which was partially and reversibly inhibited by the non-selective Ca²⁺ channel blocker La³⁺ (1 μM). was reduced to  μM by La³⁺ (, , Figures 2(c) and 2(d)), indicating that BEO induces Ca²⁺ influx from extracellular pool and Ca²⁺ release from intracellular stores.

(a)

(b)

(c)

(d)

Figure 2: Application of BEO increased in a concentration-dependent manner (a). Summary data describing the concentration-response relationship for BEO effects on (b). Data are means ± SEMs. Applications of BEO or drugs are indicated by upper or bottom lines. Effects of BEO on in human vascular endothelial cells. In the presence of extracellular Ca²⁺, application of BEO (0.1% v/v) induced an increase in that was significantly inhibited by La³⁺ (1 μM) ((c), (d)). * compared to the BEO group; = 10~13 cells/group.

3.3. Ca²⁺ Release from Endoplasmic Reticulum and Mitochondrial Ca²⁺ Stores by BEO

We next performed experiments to determine which of the two main dynamic intracellular Ca²⁺ stores, namely, the endoplasmic reticulum (ER) and mitochondria, is affected by BEO in EA cells. Ca²⁺ release from the ER depends on two mechanisms: Ca²⁺-induced Ca²⁺ release (CICR), involving ryanodine receptors, and IP₃-induced Ca²⁺ release (IICR), involving inositol 1,4,5-triphosphate (IP₃) receptors [10]. BEO-induced intracellular Ca²⁺ increase was significantly and reversibly inhibited by the CICR inhibitor, dantrolene (, , Figure 3(a)). These data indicate that BEO elevates in part by the release of Ca²⁺ from intracellular stores via a CICR mechanism. To determine whether BEO releases Ca²⁺ from intracellular Ca²⁺ stores via IICR, we tested the effects of BEO in the presence of U73122, the specific inhibitor of phospholipase C (PLC) [11], to inhibit IP₃ synthesis, or 2-APB, a membrane-permeable inhibitor of IP₃-gated ER Ca²⁺ channels [12]. BEO-induced intracellular Ca²⁺ increase was significantly inhibited by both U73122 (, , Figure 3(b)) and 2-APB (, , Figure 3(c)). These data indicate that PLC-mediated synthesis of IP₃ and IP₃ binding to IP₃-gated Ca²⁺ channels in the ER contribute to BEO-induced Ca²⁺ release from intracellular stores.

(a)

(b)

(c)

Figure 3: Involvement of CICR and IICR on BEO-induced intracellular Ca²⁺ release. Effects of CICR inhibitor, dantrolene (10 μM) on BEO-induced intracellular Ca²⁺ release. Application of dantrolene partially attenuated increase in by BEO (the first upper line) (a). Involvement of IICR pathways in BEO-induced intracellular Ca²⁺ release ((b), (c)). Increased by BEO was significantly inhibited by inhibitors of PLC (U73122, 10 μM) or IP₃ receptors (2-APB, 10 μM).

A portion of Ca²⁺ released from the ER is taken up by proximate mitochondria, which can also release Ca²⁺ and thereby regulate . To determine whether mitochondria participate in the reuptake of BEO-induced Ca²⁺ release, we examined the effects of BEO on in a Ca²⁺-free solution in the presence of BHQ (an SR/ER Ca²⁺-ATPase inhibitor) and CCCP (a mitochondrial Ca²⁺ uptake inhibitor). In cells treated with BHQ and/or CCCP, transiently increased and then decreased slowly to a steady state, suggesting that an SR/ER Ca²⁺-ATPase and mitochondrial Ca²⁺ uptake participate in the regulation of under basal conditions (Figure 4(a)). Increase in in EA cells by subsequent application of BEO in the presence of BHQ and CCCP was higher than that in the presence of BHQ only. An area under the curve in each condition was and arbitrary unit, respectively. The difference between two conditions was arbitrary unit, suggesting that mitochondrial Ca²⁺ stores may contribute to the regulation of the BEO-induced increase in .

(a)

(b)

Figure 4: Involvement of mitochondrial Ca²⁺ uptake and SOC pathway on BEO-induced Ca²⁺ release. Inhibition of mitochondrial Ca²⁺ uptake and SR/ER Ca²⁺-ATPase on BEO-induced Ca²⁺ release with CCCP (20 μM) and BHQ (30 μM), respectively (a). Increase in by subsequent application of BEO in the presence of BHQ and CCCP (black trace a) was higher than that in the presence of BHQ only (gray trace b). Effects of SOC pathway in BEO-induced intracellular Ca²⁺ release. SOC was induced by reintroduction of extracellular Ca²⁺ following SR/ER Ca²⁺-ATPase inhibition with BHQ (b). Intracellular Ca²⁺ levels were further enhanced by subsequent addition of BEO. Data are means ± SEMs. **; cells/group. Applications of BEO or drugs are indicated by upper or bottom lines.

Considering the inhibitory effect of La³⁺, noted above, it is suggested that Ca²⁺-entry pathway(s) is (are) activated by BEO. Thus, we next examined whether BEO modulated Ca²⁺ entry via an SOC mechanism. Exposure of EA cells to the BHQ in a Ca²⁺-free solution induced a transient increase in , which then decreased slowly to a steady state (Figure 4(a)). Reapplication of extracellular Ca²⁺ following emptying of intracellular Ca²⁺ stores with BHQ caused an increase in , indicating activation of an SOC mechanism. When BEO was applied after SOC was evoked, SOC was further enhanced, suggesting that BEO also activates Ca²⁺ influx through an SOC pathway (Figure 4(b)). However, using this protocol alone in this experiment does not rule out that other calcium entry pathways may be activated by BEO.

4. Discussion

In the present study, we firstly demonstrate that BEO mobilized Ca²⁺ from extracellular and intracellular sources in endothelial cells. Our present results also suggest that BEO increased intracellular Ca²⁺ level through both mobilization of intracellular Ca²⁺ stores, ER and mitochondria, and promotion of Ca²⁺ influx, via an SOC mechanism. These findings will provide insight into the physiological mechanisms involved in Ca²⁺ regulation in endothelial cells following exposure to BEO.

Some essential oils contain photoactive molecules like furocoumarins. For instance, essential oil of Citrus bergamia contains psoralens which bind to DNA under ultraviolet A light exposure producing mono- and biadducts that are cytotoxic and highly mutagenic [13]. Therefore, the results observed in the present study may be results from the effects of photoirritation of BEO. Since, however, intracellular Ca²⁺ level rapidly returned to a baseline level after washing out of BEO and cell viability was normal in doses tested, we think that phototoxic or cytotoxic effect is little on intracellular Ca²⁺ level by BEO. In addition, in vitro studies have shown that BEO reduces glutamate receptor-mediated cell death induced by N-methyl-D-aspartate [14]. Nevertheless, further researches are necessary to evaluate phototoxic potential of BEO in endothelial cells.

BEO has been reported to decrease the blood pressure in healthy human and have dilating effect on mouse artery [15, 16]. In the recent study, limonene, one of the major components of BEO (37.26%), increased cytosolic Ca²⁺ concentration by the direct activation of adenosine receptors [17]. In endothelium, an adenosine receptor has an important role in NO release. Adenosine receptor induced NO-dependent vasodilation by intracellular Ca²⁺ increase [18]. Thus, we suggest that the effect of BEO may be attributable to limonene by activation of adenosine receptors.

Contraction and relaxation of smooth muscle are regulated not only by changes in cytoplasmic calcium concentration but also by other important signaling mechanisms, that is, independent of the changes in , known as Ca²⁺ sensitization [19]. Although the increase in initiates smooth muscle contraction via activating myosin light chain kinase, Ca²⁺ sensitization mediates smooth muscle contraction by modulating myosin light chain phosphatase [20]. The increase in in endothelial cell plays a role in synthesis and the release of vasoactive compounds such as nitric oxide or prostaglandins [21], thereby altering Ca²⁺ sensitization in smooth muscle cells. It has been reported that linalyl acetate, one of the main components of BEO, induces relaxation of the smooth muscle via partially endothelium-dependent pathway [22]. Further research will be needed to reveal the mechanism by which the calcium releasing actions by BEO in endothelial cells regulate to the vasodilator action.

In conclusion, before BEO can be considered for use in treating vascular-related diseases, further studies are necessary to define the Ca²⁺-elevating pathways enlisted by BEO under pathological conditions.

Conflict of Interests

The authors declare they have no conflict of interests.

Authors’ Contribution

Purum Kang, Seung Ho Han, and Hea Kyung Moon contributed equally to this work.

Acknowledgment

This work was supported by the National Research Foundation of Korea (NRF) grant funded by the Korean government (MEST) (2012-0004065, 2012-007145).

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