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Assessment of cytotoxicity exerted by leaf extracts from plants of the genus Rhododendron towards epidermal keratinocytes and intestine epithelial cells
© Rezk et al. 2015
Received: 3 July 2015
Accepted: 10 September 2015
Published: 15 October 2015
Rhododendron leaf extracts were previously found to exert antimicrobial activities against a range of Gram-positive bacteria. In this study, we investigated which of the extracts with these antimicrobial properties would be best suited for further exploitation. Specifically, the project aims to identify biologically active compounds that affect bacterial but not mammalian cells when applied in medical treatments such as lotions for ectopic application onto skin, or as orally administered drugs.
Different concentrations of DMSO-dissolved remnants of crude methanol Rhododendron leaf extracts were incubated for 24 h with cultured epidermal keratinocytes (human HaCaT cell line) and epithelial cells of the intestinal mucosa (rat IEC6 cell line) and tested for their cytotoxic potential. In particular, the cytotoxic potencies of the compounds contained in antimicrobial Rhododendron leaf extracts were assessed by quantifying their effects on (i) plasma membrane integrity, (ii) cell viability and proliferation rates, (iii) cellular metabolism, (iv) cytoskeletal architecture, and (v) determining initiation of cell death pathways by morphological and biochemical means.
Extracts of almost all Rhododendron species, when applied at 500 μg/mL, were potent in negatively affecting both keratinocytes and intestine epithelial cells, except material from R. hippophaeoides var. hippophaeoides. Extracts of R. minus and R. racemosum were non-toxic towards both mammalian cell types when used at 50 μg/mL, which was equivalent to their minimal inhibitory concentration against bacteria. At this concentration, leaf extracts from three other highly potent antimicrobial Rhododendron species proved non-cytotoxic against one or the other mammalian cell type: Extracts of R. ferrugineum were non-toxic towards IEC6 cells, and extracts of R. rubiginosum as well as R. concinnum did not affect HaCaT cells. In general, keratinocytes proved more resistant than intestine epithelial cells against the treatment with compounds contained in Rhododendron leaf extracts.
We conclude that leaf extracts from highly potent antimicrobial R. minus and R. racemosum are safe to use at 50 μg/mL in 24-h incubations with HaCaT keratinocytes and IEC6 intestine epithelial cells in monolayer cultures. Extracts from R. rubiginosum as well as R. concinnum or R. ferrugineum are applicable to either keratinocytes or intestinal epithelial cells, respectively. Beyond the scope of the current study, further experiments are required to identify the specific compounds contained in those Rhododendron leaf extracts that exert antimicrobial activity while being non-cytotoxic when applied onto human skin or gastrointestinal tract mucosa. Thus, this study supports the notion that detailed phytochemical profiling and compound identification is needed for characterization of the leaf extracts from specific Rhododendron species in order to exploit their components as supplementary agents in antimicrobial phyto-medical treatments.
KeywordsRhododendron Bio-active compounds Cytotoxicity Mitochondrial activity Programmed cell death
Plant extracts are commonly used in formulations of alternative and traditional medicine such as skin lotions, or when used as ingredients in dietary treatments and teas . Plant-based medications are well-accepted by patients and are often preferred over chemically produced therapeutics because of their well-known health-benefitting bio-active ingredients [2–6]. Moreover, plant-extractable compounds have also gained a lot of attention in conventional medicine. For instance, plant-based drugs are now used for therapeutic treatment of diseases such as cancer and various inflammatory disorders [7, 8]. Therefore, knowing and assessing the potentials of plant-derived bio-active compounds is important for further drug development. This notion is deducible from the increasing interest of the pharmaceutical industry in gaining the rights to identify and exploit plant-borne compounds from species-rich rainforests in countries of tropical and subtropical regions [9–11]. While there is certainly a great potential in identifying plant-derived medication, the challenges associated with this venture must also be noted. Some of the current discussion revolving around this topic are: the protection of bio-diversity, acceptance of intellectual property rights, as well as biosafety of application [12, 13]. The aim of this study is to establish and provide an experimental, cell biological platform that allows for the identification of plant species that should be characterized and assessed in more detail.
So far, roughly 6 % of all higher plant species existing worldwide have been, or are currently being, assessed for their medicinal potential. In fact, only a minor proportion of these plant species have actually been subjected to detailed phytochemical profiling [14–16]. Bio-active compounds must first be purified before they can be assessed and eventually tested in clinical trials. Of course, the overall aim of the tests would be to ensure the efficacy of the biomolecules in particular therapeutic approaches. Simultaneously, drug safety and absence of undesirable side-effects are of the highest concern . These considerations are important, regardless of whether pure compounds or crude extracts of an entire plant, or parts thereof, are used for the production of a pharmaceutically applicable plant ingredient .
The genus Rhododendron, comprising the species-richest group of wooden plants, belongs to the family Ericaceae and encompasses about one thousand species: the majority of which are indigenous to Asia . In ethno-medicine, extracts of Rhododendron have been used traditionally in treating various disorders such as inflammatory conditions, common symptoms of cold, gastrointestinal disorders, skin diseases, or as pain killers . Recent research highlighted that Rhododendron leaf extracts might be highly potent and beneficial to health due to properties they contain, such as anti-bacterial [21, 22], anti-allergic, and anti-inflammatory [23, 24] agents. The reported usefulness of crude extracts of R. ferrugineum and R. anthopogon [20, 25–27] is most likely due to the presence of terpenoids in high concentrations .
Previously, we investigated leaf extracts of 120 different Rhododendron species for their efficacy as antimicrobials in killing a variety of Gram-positive and Gram-negative bacteria . In the current study, extracts of 12 of the Rhododendron species with highest anti-bacterial potencies were applied in different concentrations to monolayer cultures of human HaCaT epidermal keratinocytes and rat intestine epithelial cell line IEC6. Intestinal epithelial cells and keratinocytes are considered to be among the first points of contact when drugs are administered orally or applied ectopically, respectively. In general, bio-active compounds are considered cytotoxic when they alter cellular morphology or metabolism, interfere with the cytoskeleton or cell adhesion, affect cell proliferation rates or cell differentiation processes, or initiate programmed cell death . Different cell types might exhibit differential responses towards a specific compound or plant extract. Consequently, it is neither sufficient to use only one cell line nor to apply just a single cytotoxicity assay in any safety assessment study.
The aim of this study was to assess possible cytotoxic effects of antimicrobial Rhododendron leaf extracts on mammalian cells in order to identify a potential candidate species for further analysis of safe use. Thus, the study contributes to on-going investigations on the bioactivity potential of plant species such as the Rhododendron. Hence, the effects of Rhododendron leaf extracts on cell survival, metabolism, and growth as well as on different cellular structures were monitored in vitro by an array of cell biological assays employing differentiated cell lines.
Collection of plant material and leaf extract preparation
List of Rhododendron species from which leaves were collected and used to prepare extracts that were screened for exhibiting cytotoxicity towards intestine epithelial cell cultures and monolayers of keratinocytes
R. ferrugineum L.
R. ambiguum Hemsley
R. anthopogon Don ssp. anthopogon Betty Graham
R. hirsutum L.
R. concinnum Hemsley
R. cinnabarinum Hooker
R. racemosum Franchet
R. rubiginosum Franchet
R. xanthostephanum Merrill
R. minus Michaux
R. polycladum Franchet
R. hippophaeoides var. hippophaeoides Hutchinson
Leaf material was frozen in liquid nitrogen and powdered using a KSW 3307 mill (Clatronic, Kempen, Germany). Crude extracts were prepared by soaking two grams of Rhododendron leaf powder in 10 mL of 80 % methanol for 24 h at 4 °C with constant shaking. Insoluble material was removed by centrifugation at 3,220 g for 30 min at 4 °C, and supernatants were stored at -20 °C for further use. Methanol was evaporated from the extracts using a Micro Modulyo lyophilizer (Edwards, Crawley, UK). Stock solutions were prepared by dissolving the residues in 100 % dimethyl sulfoxide (DMSO) (Carl Roth, Karlsruhe, Germany). Prior to the in vitro assays, the samples were mixed with the respective cell culture medium such that the final concentration of DMSO did not exceed 0.5 % (v/v), and 5, 50, or 500 μg of lyophilized powder per mL culture medium were applied to confluent IEC6 and HaCaT cell monolayers.
The normal rat small intestine epithelial cell line IEC6 [29, 30] and the human keratinocyte cell line HaCaT [31, 32], purchased from the European Collection of Cell Cultures (Salisbury, UK), were used throughout this study. IEC6 cells were grown in Dulbecco’s modified Eagle’s Medium (DMEM High Glucose) (Lonza Group, Basel, Switzerland) supplemented with 10 % fetal calf serum (FCS) (Perbio Science, Bonn, Germany) and 10 μg/mL insulin (Sigma-Aldrich, Steinheim, Germany). IEC6 cells were incubated at 37 °C in a 5 % CO2 atmosphere in an incubator (Heraeus, Osterode, Germany). HaCaT cells were cultured in DMEM containing 10 % FCS and incubated at 37 °C in an 8.4 % CO2 atmosphere. Cell cultures were passaged once per week. All experiments were performed with cultures at approx. 70 % and 95 % confluence for IEC6 and HaCaT cells, respectively.
Determination of cell viability and proliferative activity by MTT assays
Propidium iodide staining of nuclei in cells with ruptured plasma membranes
The two cell lines were grown on cover glasses in 24-well Bio-One Cellstar plates (Greiner) to reach the desired degree of confluence. Next, cells were incubated with three different concentrations of Rhododendron leaf extracts (i.e. 5, 50, or 500 μg/mL) for 24 h as described above. Subsequently, cells were washed three times with phosphate-buffered saline (PBS) before being incubated for 45 min in 2 mg/mL propidium iodide (PI) (Carl Roth) and 5 μM Draq5™ (Biostatus, Leicester, UK) in culture medium at 37 °C. After washing three times in PBS, cells were fixed in 4 % paraformaldehyde (PFA) (Carl Roth) in 200 mM HEPES (pH 7.4) at room temperature for 20 min. Cells on cover glasses were washed again in PBS and distilled water before mounting them in Mowiol for subsequent laser scanning microscopy as described previously . PI is not capable of penetrating cells with intact plasma membranes, however, if plasma membrane integrity is lost, PI gains access to the nucleus and forms complexes with the DNA. In contrast, Draq5™ serves as a nuclear counter-stain that transverses the intact plasma membrane and can therefore be used to determine the total cell number. Special care had to be taken when analyzing total cell numbers, because some plant leaf extracts could have exhibited anti-adhesive effects such that total cell numbers were significantly diminished after washing steps. Therefore, total cell numbers were determined and reported herein as a measure for anti-adhesive properties of Rhododendron-derived compounds.
Phalloidin staining of the filamentous actin cytoskeleton
IEC6 and HaCaT cells were grown on cover glasses in 24-well plates to reach 70 % and 95 % confluence, respectively, and exposed to Rhododendron leaf extracts for 24 h as described above, while 0.5 % DMSO was used as a negative control. Cells were washed three times with PBS before fixation in 4 % PFA in 200 mM HEPES (pH 7.4) at room temperature for 20 min. After fixation, cells were washed with PBS before applying 0.2 % Triton X-100 in PBS for 5 min at room temperature, followed by several washing steps in PBS. Finally, cells were stained for 30 min at room temperature with a mixture of 3 μM FITC-labeled phalloidin (Sigma Aldrich) and 5 μM Draq5™ in PBS, the latter used as a counter-stain of nuclear DNA. Cover glasses were mounted in Mowiol for subsequent inspection by laser scanning microscopy (see below).
MitoTracker® Red CMXRos staining of the mitochondrial matrix
Cells were incubated and treated as described above, before washing twice in phenol red-free HEPES-buffered culture medium for 5 min. Subsequently, the cells were incubated with phenol red-free culture medium containing 20 mM HEPES and 500 nM MitoTracker® Red CMXRos (Molecular Probes, Oregon, USA) for 45 min at 37 °C followed by several washes. The fluorescent dye accumulates in the mitochondrial matrix only when an intact membrane potential, due to active cellular metabolism, is present across the inner mitochondrial membrane. Cells were fixed with 4 % PFA in 200 mM HEPES (pH 7.4) for 20 min at room temperature, rinsed, and mounted on microscope slides as described above for subsequent microscopic inspection.
Stained cells were visualized with an LSM 510 confocal laser scanning microscope (Carl Zeiss, Jena, Germany) at excitation wavelengths of 488 nm, 543 nm and 633 nm for fluorophore excitation to visualize FITC-phalloidin, PI or MitoTracker® Red CMXRos, and Draq5™, respectively. Scans at a resolution of 1024 x1024 pixels were taken in the line averaging mode and at a pinhole setting of one airy unit. Color coding and image analysis was performed by using the LSM 510 software, release 3.2 (Carl Zeiss).
Caspase-3 activity assay
For IEC6 cells, induction of apoptosis upon incubation with R. ferrugineum and R. cinnabarinum leaf extracts at the highest concentration, i.e. 500 μg/mL, was evaluated at different time intervals ranging from 1 to 24 h. The apoptosis assay was performed using the EnzChek Caspase-3 assay kit (Invitrogen, Karlsruhe, Germany) detecting activation of procaspase-3 and other Asp-Glu-Val-Asp (DEVD)-specific proteases. Lysates of treated IEC6 cells and non-treated controls were prepared according to the manufacturer’s protocol. Following clearance by centrifugation, the samples were incubated with 5 mM Z-DEVD-R110 substrate for 30 min at 4 °C. Lysates of IEC6 cells treated for 4 h at 37 °C with apoptosis-inducing staurosporin (10 mM) (Sigma-Aldrich) were used as positive controls, whereas no treatment or incubation with the solvent served as negative controls. Additionally, staurosporin-treated cells incubated with 1 mM of Ac-DEVD-CHO for 10 min served as a negative control since caspase-3 activity is blocked under these conditions. The extent of procaspase-3 activation was determined by fluorescence of liberated rhodamine upon excitation at 496 nm and reading the emission at 520 nm, using a microplate reader (Tecan Group, Männedorf, Switzerland). The values were normalized to equal amounts of DNA in the pellets after lysis, as determined by the Burton assay .
Determination of minimum inhibitory concentrations
The minimum inhibitory concentration (MIC) was defined as the lowest concentration of Rhododendron leaf extract that inhibits visible growth of microorganisms after overnight incubation. The MIC was determined by a two-fold dilution assay in Mueller-Hinton broth (MHB) (Becton Dickinson, Heidelberg, Germany). The Bacillus subtilis strain S168 was tested against 12 Rhododendron crude extracts (Table 1) . All tests were performed in triplicates following the National Center for Clinical Laboratory Standards recommendations .
All assays were performed in triplicates and repeated at least three times in independent experiments unless stated otherwise. All data were expressed as means ± standard deviation (SD), as determined by using Origin software (MicroCal Software, Northampton, USA). The profile map shown in Fig. 9 was created using R (RStudio, Boston, USA). Levels of significance were calculated by One-Way ANOVA, and p < 0.05 was considered statistically significant. CellProfiler software  was used to determine total cell numbers (Draq5™-positive cells) versus numbers of dead cells (PI-positive cells). This software was also employed to quantify the MitoTracker® Red CMXRos and FITC-phalloidin fluorescence signal intensities as previously described by us .
Classification of Rhododendron species based on antibacterial activities
In order to group the 12 selected Rhododendron species  according to their antibacterial activities, minimum inhibitory concentration (MIC) tests were conducted against B. subtilis . Accordingly, the plant species were classified into four major groups: six Rhododendron species formed the group with the highest antibacterial activity with an MIC of 50 μg/mL: R. minus, R. racemosum, R. ferrugineum, R. rubiginosum, R. anthopogon ssp. anthopogon, and R. concinnum. Another three species formed the group with moderately active extracts, with an MIC of 100 μg/mL: R. cinnabarinum, R. hirsutum, and R. ambiguum. The remaining Rhododendron species exhibited lower antibacterial activities with R. xanthostephanum and R. polycladum having an MIC of 150 μg/mL and R. hippophaeoides var. hippophaeoides requiring 300 μg/mL to efficiently produce an inhibition zone for B. subtilis.
Cell viability and proliferation rates as quantified by the MTT assay
Analysis of plasma membrane integrity
Total cell numbers and percentages of dead cells of IEC6 and HaCaT cell cultures which were treated with three different concentrations of Rhododendron leaf extracts as indicated
Total cell numbers (Draq5™)
Dead cells (%)
Total cell numbers (Draq5™)
Dead cells (%)
R. hippophaeoides var. hippophaeoides
99 ± 46
81 ± 16
212 ± 57
0 ± 0
494 ± 188
2 ± 0.6
283 ± 123
0.2 ± 0.2
297 ± 139
1 ± 1
328 ± 138
2 ± 2
74 ± 48
79 ± 19
221 ± 86
83 ± 12
497 ± 106
0.4 ± 0.4
348 ± 113
0.4 ± 0.5
683 ± 60
0.8 ± 0.2
372 ± 155
0.8 ± 0.8
288 ± 120
97 ± 3
253 ± 122
4 ± 0.7
551 ± 147
0.9 ± 1
413 ± 197
0.9 ± 0.9
672 ± 101
0.5 ± 0.4
390 ± 41
0 ± 0
204 ± 40
100 ± 0
112 ± 23
94 ± 7
475 ± 183
0.8 ± 0.8
448 ± 77
2 ± 1
481 ± 128
1 ± 1
552 ± 68
2 ± 0.5
33 ± 11
100 ± 0
490 ± 122
85 ± 15
522 ± 62
1 ± 0.6
287 ± 109
1 ± 1
439 ± 85
2 ± 2
481 ± 59
1 ± 1
99 ± 25
100 ± 0
204 ± 62
13 ± 22
274 ± 106
1 ± 1
204 ± 72
1 ± 1
384 ± 104
0.9 ± 0.5
274 ± 26
0 ± 0
304 ± 109
100 ± 0
143 ± 58
93 ± 6
252 ± 58
45 ± 44
320 ± 66
0.5 ± 0.1
586 ± 160
0.9 ± 0.8
260 ± 108
0 ± 0
211 ± 58
12 ± 4
127 ± 56
0 ± 0
408 ± 68
0 ± 0
181 ± 70
0 ± 0
460 ± 115
0.7 ± 0.6
319 ± 89
0.3 ± 0.3
R. anthopogon ssp. anthopogon
164 ± 41
100 ± 0
196 ± 50
90 ± 4
235 ± 72
23 ± 9
370 ± 153
1 ± 1
578 ± 164
2 ± 1
395 ± 157
4 ± 5
666 ± 220
99 ± 2
179 ± 60
0 ± 0
439 ± 154
1 ± 1
327 ± 82
0.5 ± 0.6
535 ± 119
0.7 ± 0.7
357 ± 150
0 ± 0
189 ± 65
99 ± 0.6
270 ± 113
98 ± 0.7
267 ± 64
11 ± 15
258 ± 109
0.5 ± 0.1
271 ± 147
1 ± 0.5
298 ± 67
0 ± 0
224 ± 54
81 ± 23
123 ± 45
94 ± 3
400 ± 262
0.4 ± 0.6
211 ± 33
0 ± 0
471 ± 183
1 ± 0.7
225 ± 79
0 ± 0
HaCaT keratinocytes exposed to Rhododendron leaf extracts at any of the concentrations tested proved more tolerant than IEC6 cells under the same conditions. The total cell number was only significantly diminished upon incubation of HaCaT cells with 500 μg/mL leaf extracts from four Rhododendron species, i.e. R. cinnabarinum, R.concinnum, R. xanthostephanum, and R. racemosum (Fig. 2b, Additional file 2: Figure S2). Three out of those treatments followed the previously observed major trend: A combination of cell de-adhesion and plasma membrane disruption of HaCaT cells was observed when a high concentration of plant extract was applied (Table 2). Interestingly, the extract of R. xanthostephanum led to de-adhesion but not to disruption of plasma membrane integrity. Irrespective of the level of reduction in total cell number caused by 500 μg/mL of extract (Fig. 2b), five out of the 12 Rhododendron leaf extracts did not induce plasma membrane rupture in HaCaT cells (Table 2). This result indicated significant differences in the susceptibility of the two different cell types to the tested Rhododendron leaf extracts.
Effects of Rhododendron leaf extracts on mitochondrial membrane potential
IEC6 cells incubated with leaf extracts from all Rhododendron species at the highest concentration were dramatically affected with regard to the mitochondrial membrane potential as deduced from the drastically reduced MitoTracker® Red CMXRos staining although effects were somewhat milder for leaf extracts from R. hippophaeoides var. hippophaeoides, R. xanthostephanum, R. hirsutum, and R. racemosum (Fig. 3a). Alterations in mitochondrial structure of IEC6 cells treated with leaf extracts were frequently observed at all three concentration (Additional file 3: Figure S3). However, IEC6 cells treated with 5 or 50 μg/mL extracts from R. hippophaeoides var. hippophaeoides, R. xanthostephanum, R. hirsutum, and R. racemosum did not show significant differences in the metabolic activity and mitochondrial structure when compared to controls (Figs. 3a and 4a).
Effects of Rhododendron leaf extracts on mitochondrial structure and metabolic activity, i.e. staining intensities, were much less pronounced in HaCaT keratinocytes (Figs. 3b and 4b, Additional file 3: Figure S3b). Exceptions were observed when HaCaT cell cultures were treated with high concentrations of leaf extracts prepared from R. minus, R. cinnabarinum, R. ferrugineum, R. concinnum, R. anthopogon ssp. anthopogon, and R. ambiguum (Fig. 3b) with mitochondria that no longer appeared elongated but were rounded up (Fig. 4b, Additional file 3: Figure S3b).
Analysis of the actin cytoskeleton of Rhododendron extract-treated cells
Inspection of sub-cellular architecture of floating cells that detached from monolayers
The findings detailed above suggested that IEC6 and HaCaT cells remained either adherent within or to the monolayers, or that they detached upon incubation with specific Rhododendron leaf extracts. Such observations could be falsely interpreted as both cell types being able to tolerate exposure to cytotoxic agents only to some extent. Because the above assays were technically restricted to adherent cells in monolayers, we next analyzed the fraction of free-floating cells which detached during treatment with Rhododendron leaf extracts using the same staining methods as described above. Therefore, Draq5™ staining additionally served to examine the status of nuclear DNA and to identify morphological alterations of the nuclei, such as those that are typical for cells undergoing programmed cell death.
However, IEC6 cells exposed to 500 μg/mL R. ferrugineum leaf extracts became pycnotic and the actin filaments formed a ring surrounding the nucleus. In addition, IEC6 cells treated with leaf extracts from R. minus, R. rubiginosum, and R. ambiguum showed different stages of chromatin condensation and shrinkage of the nuclei (Fig. 7). Thus, five Rhododendron leaf extracts, namely R. hippophaeoides var. hippophaeoides, R. cinnabarinum, R. ferrugineum, R. xanthostephanum, and R. racemosum induced signs closely related to the classical symptoms of programmed cell death –apoptosis– where the treated cells also exhibited typical phenotypes like formation of plasma membrane blebs.
HaCaT cells too showed cellular changes indicative of cell death upon exposure to 500 μg/mL Rhododendron leaf extracts. However, these were different from the phenotypes observed in treated IEC6 cell cultures. HaCaT cells treated with leaf extracts from either R. cinnabarinum or R. ferrugineum displayed signs of the final stages of cell death, reminiscent of cornification, because they exhibited intense PI staining throughout the nuclei and the cytoplasm, while some cells had lost their nuclei altogether (Fig. 7b, G and H).
Moreover, exposure of HaCaT cells to R. minus, R. concinnum, and R. anthopogon ssp. anthopogon induced changes that featured shrinkage of nuclei and chromatin condensation (Fig. 7b, I).
Investigation of apoptotic cell death pathways through determination of procaspase-3 activation
Summarizing integration of the results achieved with a variety of cell toxicity assays
The partially complex data acquired herein with different cell toxicity analysis assays are summarized by grouping the 12 Rhododendron species according to their antibacterial effectiveness with respective MICs of 50, 100, 150, or 300 μg/ml, and qualitatively comparing their effects against both cell types (Fig. 9). In general, most Rhododendron leaf extracts exerted more pronounced effects on IEC6 intestine epithelial cells as compared to HaCaT keratinocytes, when applied at high concentrations (500 μg/mL). R. hippophaeoides var. hippophaeoides, which exhibited the lowest antibacterial effect, also proved to be least toxic towards both mammalian cell types. A total of five Rhododendron extracts with high antibacterial potential (MIC of 50 μg/mL) did not reveal cytotoxicity against the mammalian cell lines in any of the tested assays when applied at 50 μg/mL, indicating that these extracts are unlikely to harm mammalian cells while killing bacterial cells. Thus, these five extracts are the candidates to be further assessed for possibly containing bio-active compounds with antimicrobial potencies, while still proving safe to be applied onto epidermal or intestine mucosal cell monolayers. The corresponding plant species were R. minus, R. racemosum, R. ferrugineum, R. rubiginosum, and R. concinnum. Interestingly, only the extracts of R. minus and R. racemosum proved to be non-cytotoxic to both intestine epithelial cells and keratinocytes (Fig. 9), suggesting they are the most promising candidates for future investigations on the search for optimized antibiotics in bio-active plant extract and, therefore, to be used for the identification and purification of specific compounds derived from Rhododendron.
To date, there are only few medicinal formulations on the market that contain compounds derived from Rhododendron. These comprise ‘Rhomitoxin’ used to treat hypertension, and ‘Rhododendron cp paste’ used to relieve pain in arthritis . In addition, only few in vitro and in vivo studies with specific Rhododendron extracts and compounds isolated thereof have been reported that validated plant extracts as being useful in traditional remedies . Importantly, plants of the genus Rhododendron are more commonly used as alternative medicine in the geographic regions of their natural habitats, i.e., Nepal, Northeastern India, Western and Central China, or Indonesia . This may be due to the fact that the precise chemical composition of medicinal formulations is often not very well defined [40, 41]. However, Rhododendron plants are known to synthesize a large number of chemical compounds, some of which exhibit attested pharmacological activities [42–45]. Several of these chemical compounds have been identified to belong to the pro-anthocyanidins, polyphenols, or terpenoids which are typically synthesized by plants reacting in defense to pathogenic infection or inflictions caused by herbivores [46, 47].
Not surprisingly, various plant-derived compounds exert severe cytotoxic or mutagenic effects when applied to animal cells and tissues [48, 49]. Intoxication of domesticated or wild animals feeding on Rhododendron plants have been repeatedly reported and were linked to the presence of grayano-toxins [50–52]. Therefore, a comprehensive number of cytotoxicity studies involving mammalian cells or tissue cultures must be conducted before a given extract or a defined Rhododendron-derived compound can eventually be considered for testing on animal models, or even enter clinical trials [53, 54].
To the best of our knowledge, none of the previous studies had comprehensively analyzed the cytotoxicity of a group of pharmaceutically interesting Rhododendron species. Consequently, the current study introduces a multi-facetted approach, consisting of five different cytotoxicity assays, in order to investigate the effects of Rhododendron leaf extracts on cellular structure, metabolic activity, and viability of two different types of mammalian cells.
The results obtained herein show that treating IEC6 and HaCaT cells with low concentrations of leaf extracts prepared from any of the 12 Rhododendron species exhibited rather mild or no cytotoxic effects, whereas the use of high concentrations (500 μg/mL) resulted in a rather expected and remarkable cytotoxicity. A total of five Rhododendron species exhibited high antibacterial activities with MICs of 50 μg/mL and proved to be non-cytotoxic at this concentration. Interestingly, extracts of R. minus and R. racemosum were non-toxic to either cell lines, which makes them promising candidates for future studies. In contrast, incubation of either of the two cell lines with 500 μg/mL of the other Rhododendron leaf extracts resulted in severe structural and functional alterations often associated with signs of apoptosis. Our study thus confirmed that simultaneous analysis of several, albeit partially unlinked or only indirectly linked cellular parameters, is a convenient tool to separate potentially cytotoxic extracts from their ‘safe-to-use’ Rhododendron extracts counterparts, thus overcoming technical short-comings of previous studies aiming at high-throughput screening.
Our results demonstrated that the incubation of cells with high concentrations of Rhododendron leaf extracts induced apoptosis specifically in intestine epithelial cells. Interestingly, only two extracts, namely those of R. cinnabarinum and R. ferrugineum, shared a similar pattern of cytotoxicity in all assays tested in this study. Leaf extracts of these two Rhododendron species were capable of inducing procaspase-3 activation prominently in IEC6 cells. The results of this study concur with other studies that have shown several secondary metabolic compounds from Rhododendron species to induce apoptosis in cultures of different mammalian cell lines [55, 57].
Overall, keratinocytes were more resistant to cytotoxicity exerted upon incubation with Rhododendron leaf extracts than IEC6 cells. Resistance of HaCaT cells against cytotoxic agents was observed by us previously when studying dust exposure . This remarkable feature of keratinocytes might be due to the specific lipid composition of their membranes and their ability to build a stratified epithelium when exposed to air during cornification [32, 57, 58].
Using a comprehensive approach, the cytotoxicity of those Rhododendron species that had previously been shown to exhibit the highest antibacterial activities was determined. As such, we managed to continue our ongoing approach in identifying pharmaceutically feasible antibiotics or lead structures. Utilizing two tester cell lines as relevant models for the envisioned ectopic or oral treatment and applying several different cell biological assays, proved to be a suitable combination of screening tools. Two out of the 12 Rhododendron species with antibacterial properties exhibit the desired traits: the extracts of R. minus and R. racemosum were both non-cytotoxic at a concentration at where they efficiently produced an inhibition zone for B. subtilis.
Furthermore, we could conclude that Rhododendron leaf extracts induced apoptosis, as evidenced by typical alterations of the cellular phenotypes (chromatin condensation and formation of plasma membrane blebs) as well as by the increasing levels of active caspase-3 when cells were exposed to higher extract concentrations. In the future, we will extend our current study in order to determine whether the specific apoptosis-inducing effects of R. cinnabarinum and R. ferrugineum can be used to selectively target cancer cells, such as colorectal carcinoma cells.
In our future research, we will focus on phyto-chemically identifying the actual active compounds present in the leaf extracts derived from different Rhododendron species. We plan to determine the IC 50 values and to study their potential cytotoxic effects through a repertoire of different methods similar to the cell biological screening tool box laid out in the current study.
This study was financially supported by the Stiftung Bremer Rhododendronpark. The authors are particularly grateful to late Wolfgang Klunker for his enthusiastic support. We would like to thank Maren Rehders for expert help with cell culture experiments, as well as Maria Qatato and Daniel Boland for proofreading the manuscript.
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