Assessing Genotoxic Potential of Cotinus Coggygria Scop: Using the Mussel Micronucleus Test

Introduction: Cotinus coggygria Scop. is widely used in ethnopharmacology such as antiseptic, anti-inflammatory, antimicrobial, hepatoprotective, as well as for countering diarrhea, gastric and duodenal ulcers. Total phenols, flavonoids and tannins were determined as the main group of biologically active compounds. Tannins, however, have proven mutagenic in different studies. Also, methanol extract of C. coggygria induced sex-linked recessive lethal mutations on the X-chromosome of Drosophila melanogaster males. Materials and methods: In our study, genotoxic potential of aqueous extract of C. coggygria leaves was assessed using the mussel micronucleus test. The test is based on the formation of micronuclei which indicates chromosomal DNA damage occurring as a result of either chromosome breakage or chromosome mis-segregation during mitosis. It is an easy-to-perform test which has proven sensitive to tannins or tannin containing extracts. Results and conclusions: The aqueous extract had high hydrolysable tannin content but did not elucidate significant mutagenic effect. Our result might give an indication on the safe use of the plant. Citation: Eck-Varanka B, Kováts N, Horváth E, et al. (2019) Assessing Genotoxic Potential of Cotinus Coggygria Scop: Using the Mussel Micronucleus Test. J Bot Res 2(1):57-59 Eck-Varanka et al. J Bot Res 2019, 2(1):57-59 Open Access | Page 58 | microscope slide and allowed to dry. Slides were fixed in 80% methanol, air dried and stained with 5% Giemsa in distilled water for 20 minutes. Photos were taken by a Zeiss Axio Scope A1 microscope with an Axio Cam ICC1 camera and Zen 2011 program at 400 × magnification. 1000 cells/specimen were counted, micronuclei (MN) were identified according to Bolognesi and Fenech [12]. Robust ANOVA of Welch with Tamahane T2 post hoc test was used to compare the mean MN numbers between the treatments. The difference in mean MN numbers of control and C. coggygria extract was determined using Students t-test. Total tannin concentration was determined from air dried plant material [15]. Finely ground plant material (100 mg) was extracted with 5 ml of 70% acetone, after 1 hour 0.5 ml of supernatant was collected, and 0.5 ml distilled water was added. Then 5 ml of Na2CO3 2% w/v (in 0.1 N NaOH), and after 5 min 0.5 ml Folin-Ciocalteu reagent was added. After 120 min absorbance was measured at 760 nm. Hydrolysed tannin concentration was determined from aqueous extracts [16]. 50 ml extract (1 g/l) was mixed with 1 ml Folin-phenol reagent and 10 ml carbonatetartrate. 30 min at 4 °C was allowed for colour development. Absorbance was measured at 700 nm. In both measurements tannic acid solutions were used as standards. Results and Discussions Total tannin and hydrolysable tannin content of the dried water by shaking for 24 h at room temperature. In the micronucleus test, Unio pictorum (painter’s mussel) specimens with length of 5-8 cm were used. Mussels were collected in Lake Balaton (Hungary) and were acclimatized for 1 month prior to the test. During acclimatisation, they were kept in a flow-through aquarium at the facility of the Balaton Limnological Research Centre. In the flow-through aquarium, Lake Balaton water was used, therefore continuous food supply was also provided. Treatments were performed in aquaria of 3l volume, in 3 replicates. Each aquarium contained 10 specimens. Aquaria were aerated during the experiment; temperature was set at 22 °C). In the first experiment, 6 g/l concentration was used, but this concentration proved to be lethal. Further on, 1 g/l and 0.1 g/l concentrations were applied. Exposure was 4 days. As in our previous tests plant extracts proved to be highly degradable [14], semi-static test was conducted: Sample was renewed after 2 days. After the pre-set exposure, haemolymph was taken from the posterior adductor. 1 ml of haemolymph was mixed with 0.3 ml 10% acetic acid in methanol as a fixative and centrifuged at 1000 rpm for 5 minutes. The supernatant was discarded and the rest was fixed in 1 ml 80% ethanol. This ensures that the sample can be kept refrigerated for several weeks. When processing the samples, refrigerated samples are centrifuged again at 1000 rpm for 5 minutes. For assessing the micronucleus ratio, the sample was smeared onto a


Introduction
Cotinus coggygria Scop. (Rhus Cotinus L). (smoke tree, family Anacardiaceae) is a widely distributed shrub. Its area extends from, the Mediterranean, Moldova and the Caucasus, to central China and the Himalayas [1]. In recent ethnopharmacology, it is used for counteringdiarrhea, paradontosis, and gastric and duodenalulcers [2], healing skin disorders [3] or as mouth wash [4]. When testing antibacterial capacity of home-made mouthwash from C. coggygria, Ferazzano, et al. [5] demonstrated strong antimicrobial activity against selected oral pathogenic bacterial strains such as Streptococcus sobrinus or S. mutans. In vitro studies have proven its antibacterial capacity against pathogenic bacteria such as Staphylococcus aureus [6].
Total phenols, flavonoids and tannins were determined as the main group of biologically active compounds in ethyl-acetate and methanol extracts of various parts of the plant [7]. There are studies available reporting on the direct genotoxic effect of tannins [8]. Although C. coggygria has been long used as a medicinal herb, its potential genotoxicity has only recently been addressed [9,10]. While in recent decades there has been a growing public interest in the use of herbs and herbal medicinal products both in developing and developed countries, the toxicity of several traditional medicinal herbs has not been completely and comprehensively evaluated. Sponchiado, et al. [11] for example discuss that some plants frequently used in folk medicine have already proven potentially genotoxic requiring the evaluation of genotoxicity. As such, the aim of the study was to assess the genotoxic potential of C. coggygria aqueous extract using the mussel micronucleus test (MNT). This test is based on the formation of micronuclei which indicates chromosomal DNA damage occurring as a result of either chromosome breakage or chromosome mis-segregation during mitosis [12]. The test is cost-efficient, easy-to-perform and found sensitive to tannins or plant extracts with high tannin content in genotoxicological studies [13,14]. microscope slide and allowed to dry. Slides were fixed in 80% methanol, air dried and stained with 5% Giemsa in distilled water for 20 minutes. Photos were taken by a Zeiss Axio Scope A1 microscope with an Axio Cam ICC1 camera and Zen 2011 program at 400 × magnification. 1000 cells/specimen were counted, micronuclei (MN) were identified according to Bolognesi and Fenech [12]. Robust ANOVA of Welch with Tamahane T2 post hoc test was used to compare the mean MN numbers between the treatments. The difference in mean MN numbers of control and C. coggygria extract was determined using Students t-test.
Total tannin concentration was determined from air dried plant material [15]. Finely ground plant material (100 mg) was extracted with 5 ml of 70% acetone, after 1 hour 0.5 ml of supernatant was collected, and 0.5 ml distilled water was added. Then 5 ml of Na 2 CO 3 2% w/v (in 0.1 N NaOH), and after 5 min 0.5 ml Folin-Ciocalteu reagent was added. After 120 min absorbance was measured at 760 nm.
Hydrolysed tannin concentration was determined from aqueous extracts [16]. 50 ml extract (1 g/l) was mixed with 1 ml Folin-phenol reagent and 10 ml carbonate-tartrate. 30 min at 4 °C was allowed for colour development. Absorbance was measured at 700 nm. In both measurements tannic acid solutions were used as standards.

Results and Discussions
Total tannin and hydrolysable tannin content of the dried water by shaking for 24 h at room temperature.
In the micronucleus test, Unio pictorum (painter's mussel) specimens with length of 5-8 cm were used. Mussels were collected in Lake Balaton (Hungary) and were acclimatized for 1 month prior to the test. During acclimatisation, they were kept in a flow-through aquarium at the facility of the Balaton Limnological Research Centre. In the flow-through aquarium, Lake Balaton water was used, therefore continuous food supply was also provided.
Treatments were performed in aquaria of 3l volume, in 3 replicates. Each aquarium contained 10 specimens. Aquaria were aerated during the experiment; temperature was set at 22 °C). In the first experiment, 6 g/l concentration was used, but this concentration proved to be lethal. Further on, 1 g/l and 0.1 g/l concentrations were applied. Exposure was 4 days. As in our previous tests plant extracts proved to be highly degradable [14], semi-static test was conducted: Sample was renewed after 2 days. After the pre-set exposure, haemolymph was taken from the posterior adductor. 1 ml of haemolymph was mixed with 0.3 ml 10% acetic acid in methanol as a fixative and centrifuged at 1000 rpm for 5 minutes. The supernatant was discarded and the rest was fixed in 1 ml 80% ethanol. This ensures that the sample can be kept refrigerated for several weeks. When processing the samples, refrigerated samples are centrifuged again at 1000 rpm for 5 minutes. For assessing the micronucleus ratio, the sample was smeared onto a aerial part was 150.03 mg/g and 66.35 mg/g, respectively. However, aqueous extract of C. coggygria had no significant micronuclei induction, number of micronuclei/1000 cells was 2.1 in the control, 1.8 in the 0.1 g/l and 3.3 in the 1 g/l extract (Welch-ANOVA: df = 2, F = 1.3424, p = 0.2787, t-test: p = 0.8655 between the control and the 0.1 g/l, p = 0.112 between the control and the 1 g/l and p = 0.0697 between the 0.1 g/l and the 1 g/l concentration) (Figure 1). It has been reported that methanol extract of C. coggygria in a concentration of 5% was clearly genotoxic, inducing sex-linked recessive lethal mutations on the X-chromosome of Drosophila melanogaster males [9,10]. On the other hand, post-treatment with lower concentration (2%) of the methanol extract was effective in reducing genotoxicity [10]. Drosophila melanogaster has been widely used in a number of studies on genotoxicity of various compounds, including plant extracts, due to the similarity of metabolic pathways between Drosophila and mammals [17].
Similar pattern was experienced by Labieniec, et al. [13], using U. tumidus as test organism. It was demonstrated that tannin concentrations of 1 and 5 µM significantly decreased the amount of lesions induced by H 2 O 2 while higher concentrations triggered single strand breaks in the DNA of the digestive gland of the mussels. Similar concentrationdependency was reported in a further study [8]. Azqueta and Collins [18] in their review discuss the effect of polyphenols and conclude that in general, while low concentrations can decrease DNA damage, high concentrations might themselves induce DNA damage. It should be noted, however, that all the above mentioned studies used methanol extract; therefore no data are available on the potential genotoxicity of the aqueous extract of C. coggygria.

Conclusion
The World Health Organisation [19] recommends the safety monitoring of herbal medicines/traditional medicines. In our study aqueous extract was used, somewhat mimicking the mode of preparation when C. coggygria is used as a tea or infusion. Our result might give an indication on the safe use of the plant.