*Corresponding Author:
N Saemram
Department of Chemistry
Faculty of Science
Ramkhamhaeng University
Bangkok 10240, Thailand
Date of Received 11 February 2020
Date of Revision 26 August 2020
Date of Acceptance 02 June 2021
Indian J Pharm Sci 2021;83(3):494-503  

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Thunbergiaalata and Thunbergiaerecta have been mostly used for ornamentation but have interesting other uses. However, toxicity and phytochemical studies of these plants are lacking. Therefore, phytochemicals of the two species were investigated by gas chromatography-mass spectrometry, cytotoxicity and genotoxicity were tested via 3-(4,5-dimethylthiazol-2yl)-2,5-diphenyltetrazolium bromide and comet assays in normal human peripheral blood mononuclear cells. Then, the extracts of the two species and their combination were applied to peripheral blood mononuclear cells poisoned with rice whisky and bathroom cleaner as toxic models in everyday life. The results showed that the major phytochemicals were 12.36 % and 24.90 % phytol in ethanol extracts of Thunbergia alata and Thunbergia erecta and 46.29 % and 43.47 % oleamide in hexane extracts of Thunbergia alata and Thunbergia erecta, respectively. Half-maximal inhibitory concentration values, which indicate toxicity in cells, were not detected for either species, but at the deoxyribonucleic acid level, the extracts induced significant deoxyribonucleic acid damage, shown by high Olive Tail Moment values in peripheral blood mononuclear cells (p<0.05). Biological activity of the extracts revealed by higher cell viability percentages and lower Olive Tail Moment values in the treatments (poisoned peripheral blood mononuclear cells treated with plant extracts) than the controls (poisoned peripheral blood mononuclear cells). Taking all the results together, Thunbergia alata and Thunbergia erecta extracts and their combination can be applied for many benefits in humans following properties that have been previously used and their phytochemicals but have limitations of doses.


Biological activity, comet assay, gas chromatography-mass spectrometry, 3-(4,5-dimethylthiazol- 2-yl)-2,5-diphenyl tetrazolium bromide assay, oleamide, phytol

Plants of the genus Thunbergia are well known in several species for medicine and ornamentation, but not for foods such as T. laurifolia, T. grandiflora, T. alata, T. erecta, T. coccinea, T. colpifera and T. fragrans. Of all of them, T. laurifolia was the first widely consumed both in traditionally and locally prepared forms for human living and the second species used was T. grandifola. Many ethnobotanical reviews and scientific publications have pointed to the indications, phytochemicals and treatments of these two species. Various compounds isolated from the leaves of T. laurifolia include iridoid glycoside, grandifloric acid, glucopyranosides and derivatives of apigenin, delphinidin and phenolic acids: chlorogenic, caffeic, gallic and protocatechuic. These substances give the plant various effects as follows: biological effects and applications as an antidote for poisons and drugs and in treating drug addiction. The plant has also been reported to have antioxidant, antidiabetic, anti-inflammatory, antipyretic, antimicrobial and hepatoprotective properties[1,2]. Additionally, T. laurifolia has reduced heavy metal on lead-induced acetylcholinesterase dysfunction and cognitive impairment in mice[3], reduced signs of toxicity and reduced organ damage caused by cadmium[4]. Toxicity has also been reported. Chivapat et al.[5] studied chronic toxicity of T. laurifolia in rats for 6 mo, which did not produce any histological alterations of visceral organs in any rat group. Another one of the species mentioned, T. grandiflora was shown to have activity and vital phytochemicals, including phenols and flavonoids. Its leaves had potential antioxidative and anticholinesterase inhibitory effects, which may be effective in treating Alzheimers disease[6]. In addition, T. grandiflora leaves had marked hypoglycemic and antioxidant activity and hepatoprotective effects in liver-damaged rats[7]. There are few scientific studies on T. alata and T. erecta. Methanol extracts of T. alata play an important inhibitory role in the modulation of severe inflammation[8]. Three phenolic compounds, caffeoylmalic, feruloylmalic and p-coumaroylmalic acids, were found in the leaves of T. alata; their concentrations were different during wounding and salicylic acid treatment and were elicited by salicylic acid[9]. The flower of T. erecta L. can be used as an alternative to commercial indicators and is more environmentally friendly[10]. T. erecta, including leaves, stems, roots and flowers, could be exploited for the green synthesis of zinc oxide nanoparticles, which can be used in the development of pharmaceutical products beneficial to mankind[11]. Bhuiyan et al.[12] researched T. erecta, a medicinal plant with many reported phytochemicals and significant medicinal value and revealed that the methanol leaf extract has hypoglycemic effects in an animal model. The most recent research reported experimental results in swiss albino mice with T. erecta, which contained phytoconstituents, flavonoids, glycosides, tannins saponin, carbohydrates and alkaloids and possessed sedative and anxiolytic activity traditionally used in insomnia, depression and anxiety management[13]. Information on the two well- known, representative species of Thunbergia mentioned above, T. laurifolia and T. grandiflora, is very important for natural methods for human health, which is a long- lived concept. There are more interesting species in the Thunbergia genus that should be focused on for their benefits to human health as a natural way to decrease public health costs and disease suffering.

This research aimed to evaluate the biological efficacy, usage and limitations of T. alata and T. erecta following phytochemicals, toxicity and biological activity testing. Additionally, the combined extract of the two species was tested to confirm the enhanced efficacy in poisoned peripheral blood mononuclear cells (PBMCs).

Materials and Methods

Leaves of the two studied plant species, T. alata and T. erecta were collected for the following tests: phytochemical analyses via gas chromatography- mass spectrometry (GC-MS), cytotoxicity and genotoxicity testing via 3-(4,5-dimethylthiazol-2yl)- 2,5-diphenyltetrazolium bromide (MTT) and comet assays. The biological activity of the plants was tested in PBMCs poisoned with bathroom cleaner (containing 8.5 % w/w hydrochloric acid and 2 % w/w ethoxylated alcohol) and rice whisky (containing 40 % alcohol).

Phytochemical extraction, extract component analysis via GC-MS, isolation of human PBMCs, cell toxicity testing by MTT assay and genotoxicity testing by comet assays were performed following Sirikhansaen et al.[14] and briefly described below.

Phytochemical composition analysis:

Dried powder of the sample was macerated in hexane or ethanol, 20 g to 100 ml, for 72 h and then filtered. The filtrates were analyzed by an Agilent Technologies GC 6890 N/5973. The relative percentage of the constituents was expressed and determined.

Extract preparation for toxicity testing:

Solvents were evaporated from the filtrates by rotary evaporation, then the dried filtrates were redissolved in dimethyl sulfoxide (DMSO) and maintained as stock extracts at -20°.

Isolation of human peripheral blood mononuclear cells (PBMCs):

Anonymous buffy coat samples were received from a blood bank and used for PBMCs isolation using Ficoll- Paque Plus (GE Healthcare). The isolated cells were suspended at a concentration of 106 cells/ml in modified RPMI-1640 medium, with 2 mM L-glutamine and 25 mM 4-(2-hydroxyethyl)-1-piperazineethanesulfonic acid (HEPES), supplemented with 10 % Fetal bovine serum (FBS), 5 μg/ml phytohemagglutinin (PHA), 100 μg/ml streptomycin and 100 U/ml penicillin.

MTT assay:

The stock extracts were serial 10-fold diluted with water, for five levels as working concentrations. The prepared cells were seeded in 96-well plates, 125 μl per well, 12.5 μl of the extract working concentrations were added to each well, the untreated cells and the cells treated with UV light for 20 min were used as negative and positive controls, respectively. The plates were incubated for 4 h at 37° with 5 % CO2. The medium was removed and then 10 μl of 0.5 mg/ml MTT (Sigma, USA) was added to each well, the plates were incubated for 4 h at 37°, in the dark. DMSO was added to each well to solubilize formazan crystals for 4 h in the dark; finally, the absorbance was read at 570 nm. If the Half-maximal inhibitory concentration (IC50) values were observed, they will be used to estimate LD50 values following World Health Organization (WHO)[15] guideline.

Comet assay:

The cells were treated with the extract concentration at IC50 value or at a maximum-treated concentration, in case no IC50 value was detected. After the treatment, the cells are applied on a gel-coated slide and subjected to electrophoresis and then the images were recorded. The comets in the images were observed; at least 150 cells (50 cells for each of triplicate slides) were examined for each experiment. Level of Deoxyribonucleic acid (DNA) damage was defined using the Olive Tail Moment (OTM), which is the relative amount of DNA in the tail of the comet multiplied by the median migration distance using the CASP software (Wroclaw, Poland). The nonparametric Mann-Whitney test was used for statistical analysis of the comet assay results, at p<0.05.

Biological activity testing:

For appropriate concentration screening, rice whisky and bathroom cleaner were serially 10-fold diluted with distilled H2O for 10 levels to get the working concentrations of 40 %–0.00000004 % (percentage of alcohol, equivalent 1000 μl/ml-0.000001 μl/ml) and 10-0.00000001 % (equivalent 100 μl/ml-0.0000001 μl/ml) for rice whisky and bathroom cleaner, respectively. The PBMCs were poisoned with each working concentration and determined for their viability by MTT assay as described above. The working concentration giving viability over 50 % were selected to poison the cells in the next steps.

The combined extract was prepared by mixing the leaf powders of T. alata and T. erecta at a ratio of 1:1. Each of the 1 mg combinations was added to 9 ml of DMSO, stirred and kept at -20° for 2 d. The upper part, clear solution defined as combination extract was used to test their biological activity on poisoned PBMCs by MTT and comet assays.

The poisoned PBMCs with five working concentrations of rice whisky and bathroom cleaner, 40–0.004 % and 10 %–0.001 % were subsequently treated with the combination extract and then MTT and comet assays were performed. The control cells were the poisoned PBMCs without plant extract treatment. Biological activity was detected by comparing cell viability percentages and OTM values between the control cells and the treatments.

Results and Discussion

Phytochemical investigation of the ethanol and hexane crude extracts of the two Thunbergia species, T. alata and T. erecta (fig. 1), which are often ornamental plants, showed several substances in the GC-MS chromatogram, as shown in Table 1 (fig. 2). The major compounds were 12.36 % phytol and 46.29 % oleamide in the ethanol and hexane extracts of T. alata and 24.90 % phytol and 43.47 % oleamide in the ethanol and hexane extracts of T. erecta, respectively.

Compounds Formula Relative content (%)
T. alata T. erecta
H** Et** H** Et**
ethyl α-d-glucopyranoside C8H16O - - - 0.75
oxazole, 5-hexyl-2,4-dimethyl- C11H19NO - - - 1.15
phytol, acetate C22H42O2 - 9.59 - 3.20
(2E)-3,7,11,15-tetramethyl-2-hexadecene C20H40 - 1.14 - 0.37
3,7,11,15-tetramethyl-2-hexadecen-1-ol C20H40O 0.15 4.83 - 1.50
hexadecanoic acid, ethyl ester C16H32O2 - 0.49 - 0.30
phytol C20H40O 0.48 12.36 2.46 24.90
methyl stearate C19H38O2 - - - 0.39
ethyl 9,12,15-octadecatrienoate C20H34O2 - 0.47 - -
hexadecanamide C16H33NO 4.47 0.61 3.35 1.24
docosane C22H46 - - 0.72 -
octadecanoic acid, ethyl ester C20H40O2 - 0.16 - -
(Z)-9-octadecenamide (oleamide) C18H35NO 46.29 7.47 43.47 13.38
octadecanamide C18H37NO 4.73 0.49 2.43 0.79
tetracosane C24H50 - - 4.27 -
glycerol β-palmitate C19H38O4 1.33 2.68 1.86 2.03
lidocaine benzyl benzoate C28H34N2O3 - 0.66 - -
benzyldiethyl-(2,6-xylylcarbamoylmethyl)-ammonium benzoate C28H34N2O3 - - - 0.74
cis-11-Eicosenamide C20H39NO 5.50   6.18 0.99
glycerin 1-monostearate C21H24O4 0.46 0.43 0.95 0.49
squalene C30H50 0.91 13.82 0.53 4.34
oxirane, 2,2-dimethyl-3-(3,7,12,16,20-pentamethyl-3,7,11,15,19-heneicosapentaenyl)-, (all-E)- C30H50 - - - 0.91
γ-tocopherol C28H48O2 - 1.08 0.56 0.93
dl-α-tocopherol C29H50O2 0.74 2.82 4.73 8.16
campesterol C28H48O 0.79 2.91 - -
stigmasterol C29H48O 2.50 8.03 7.13 16.74
γ-sitosterol C29H50O 5.88 16.60 0.38 0.87
stigmasta-5,24(28)-dien-3-ol, (3β,24Z)- C29H48O - 1.51 - 0.75
β-amyrin C30H50O - 1.12 - -
α-amyrin C30H50O - 2.14 - -
vitamin E* n/a - - - 1.20
friedelan-3-one C30H50O - - - 0.86
unknown   25.77 8.59 20.99 13.00

Table 1: Phytochemical Constituents Derived from GC-MS of the Two Studied Leaf Extracts of T. alata and T. erecta by GC-MS Analysis


Figure 1: The two studied plant species, (A). T. alata; (B). T. erecta


Figure 2: Chromatograms of ethanol and hexane crude extracts from the leaves of T. alata and T. erecta by GC-MS analysis

The primary (maximum) mass concentrations of the crude ethanol and hexane extracts of the two studied species were 0.5 and 0.7 mg/ml for T. alata and 0.7 and 0.7 mg/ml for T. erecta, respectively. The extracts were subjected to serial 10-fold dilutions and used for the MTT assay (Table 2). The results showed no IC50 values and there was no toxicity at the cellular level, with high percentages of cell viability revealed in the plotted graph between extract concentration and cell viability percentages (fig. 3). The cell viability percentages were 72.40±0.16–76.13±0.17 and 65.57±0.13–74.05±0.16 with the ethanol and hexane extracts of T. alata and 55.70±0.21–88.83±0.27 and 76.58±0.26–83.43±0.25 with the ethanol and hexane extracts of T. erecta, respectively.

Plant Extraction solvent Working extract conc. (mg/ml) IC50
Cell viability (%)
T. alata hexane 0.07-0.000007 - 65.57±0.13-74.05±0.16
ethanol 0.05-000005 - 72.40±0.16-76.13±0.17
T. erecta hexane 0.07-0.000007 - 76.58±0.26-83.43±0.25
ethanol 0.07-0.000007 - 55.70±0.21-88.83±0.27

Table 2: Working Extract Concentrations from Ethanol and Hexane Extracts of T. alata and T. erecta Leaves Diluted and Used for MTT Assay Showing Cell Viability Percentages


Figure 3: Graphs between extract concentrations and cell viability percentages resulting from MTT assay of T. alata and T. erecta leaf extracts

Because the extracts did not show IC50 values, the concentration of the first extract dilution was used as working the concentration (Table 3) and selected for further genotoxicity study via the comet assay. The results showed that the extracts of both sample species induced significant DNA damage in PBMCs (p<0.05) compared to the negative control. The level of DNA damage exhibited OTM in PBMCs (Table 3, fig. 4).

Plants Extraction Solvent Working extract conc. (mg/ml) Olive Tail Moment (OTM) p value
T. alata hexane 0.07 1.07±0.82 <0.0001
ethanol 0.05 1.04±0.45 <0.0001
negative control - 0.05±0.03 -
T. erecta hexane 0.07 0.14±0.11 0.0020
ethanol 0.07 0.30±0.14 <0.0001
negative control - 0.11±0.09 -

Table 3: The Level of DNA Damage Expressed as Olive Tail Moment (OTM) In PBMCS after Treatment with Ethanol and Hexane Extracts of T. alata and T. erecta Leaves


Figure 4: Comet assay images of PBMCs (200X); (A) negative control for T. alata; (B) positive control for T. Alata; (C) hexane T. alata leaf extract; (D) ethanol T. alata leaf extract; (E) negative control for T. erecta; (F) positive control for T. erecta; (G) hexane T. erecta leaf extract; (H) ethanol T. erecta leaf extract

Biological activity testing was performed, which included poison concentration screening for use in the test and preparing controls for experiments to compare via MTT and comet assays. The concentrations of poison, rice whisky and bathroom cleaner, were screened using the MTT method. The results (Table 4, fig. 5), the concentrations of them were selected from the first to fifth as 40 %–0.04 % and 10 %–0.001 % and the cell viability percentages were 56.26±0.12– 62.05±0.12 and 45.82±0.14–56.33±0.17 for the rice whisky and bathroom cleaner, respectively. A set of controls (PBMCs incubated with each poison), which was simultaneously analyzed with the treatments, was prepared using the same set of PBMCs as the treatments. After the experiments, the final activity results were obtained by comparing the MTT results with the cell viability percentages and the comet result with the OTM values of the control and the treatments. These treatments (poisoned PBMCs treated with extracts) had higher cell viability percentages (65.67±0.76–84.49±0.54, 68.17±0.21–80.96±0.22 and 63.34±0.54–78.63±0.52 for rice whiskey; 44.09±0.69–75.39±0.62, 36.34±0.12–72.79±0.14 and 53.63±0.41–72.36±0.38 for bathroom cleaner with the T. alata, T. erecta and combined extracts, respectively) than the controls (62.54±0.20–74.51±0.19)(Table 5, fig. 6). The combination did not show higher cell viability percentages than the two studied species.

of rice whiskey (%)
Cell viability (%) Concentration of bathroom cleaner (%) Cell viability (%)
40 56.26±0.12 10 45.82±0.14
4.0 59.10±0.12 1.0 48.42±0.18
0.4 60.74±0.12 0.1 53.74±0.17
0.04 61.04±0.12 0.01 54.09±0.18
0.004 62.05±0.12 0.001 56.33±0.17
0.0004 63.21±0.12 0.0001 57.37±0.17
0.00004 64.85±0.13 0.00001 62.49±0.17
0.000004 65.93±0.13 0.000001 65.61±0.17
0.0000004 66.64±0.13 0.0000001 67.98±0.18
0.00000004 67.74±0.14 0.00000001 69.44±0.18

Table 4: Poison Concentration Screening, Rice Whisky and Bathroom Cleaner, Indicated By Cell Viability Percentages

Experiment Rice whiskey Bathroom cleaner
Cell viability (%) Olive Tail Moment Cell viability (%) Olive Tail Moment
Controls 62.54±0.20-74.51±0.19 3.600±1.970 29.48±0.14-67.30±0.17 3.770±1.970
T. alata 65.67±0.76-84.49±0.54 0.046±0.045 44.09±0.69-75.39±0.62 0.47±0.34
T. erecta 68.17±0.21-80.96±0.22 0.047±0.041 36.34±0.12-72.79±0.14 0.55±0.47
Combination 63.34±0.54-78.63±0.52 0.055±0.046 53.63±0.41-72.36±0.38 0.58±0.42

Table 5: The Detoxifying Bioactivity Results Indicated by Cell Viability Percentages and Olive Tail Moment (OTM) from the Poisons Rice Whisky and Bathroom Cleaner in PBMCS Treated with the T. alata, T. erecta And Combined Extracts


Figure 5: Graphs of poison concentration screening showing relations between 10 level concentrations of bathroom cleaner and rice whiskey showing cell viability percentages


Figure 6: Graphs plotted between poisoned concentrations (rice whiskey, left; bathroom cleaner, right) and cell viability of the controls in red lines (poisoned PBMCs) and the treatments in blue lines (poisoned PBMCs treated with T. alata and T. erecta leaf extracts) indicating the detoxifying bioactivity results by cell viability percentages

Similarly, OTM values of the treatments, which were 0.046±0.045, 0.047±0.041, 0.055±0.038 for rice whisky (Table 5, fig. 7) and 0.47±0.34, 0.55±0.47, 0.58±0.42 for bathroom cleaner (Table 5, fig. 8) with the T. alata, T. erecta and combined extracts, respectively, were clearly shorter than the OTM values of the controls, 3.77±1.97. The combined extract also did not show shorter OTM values than the other two studied species, meaning that it was not better. The shorter OTM values indicate less DNA damage than the other OTM values.


Figure 7: Comet assay images of rice whisky-poisoned PBMCs (200×); (A) negative control; (B) the control; (C) treatment of T. alata leaf extract; (D) treatment of T. erecta leaf extract; (E) treatment of the combined extract


Figure 8: Comet assay images of bathroom cleaner-poisoned PBMCs (200×); (A) negative control; (B) positive control; (C) treatment of T. alata leaf extract; (D) treatment of T. erecta leaf extract; (E) treatment of the combined extract

Testing in both the normal and poisoned human PBMCs is in preclinical trials with animal cell and tissue culture following Doke and Dhawale[16] and the Physicians Committee for Responsible Medicine[17]. The methods selected here are reliable for in vitro and human cell and tissue, PBMCs cultures for cytotoxicity and genotoxicity with MTT and comet assays for toxicity and biological activity testing.

The two studied species and the combination showed no toxicity at the cellular level, but they induced significant DNA damage at the concentrations tested, 0.05 and 0.07 mg/ml. It means that genetic materials of the cells were destructed, can lead mutation. These two extract concentration levels may be carcinogen[18]. So, the hazardous level must be found for consumption caution of these two plants, the tested concentrations which induced significant DNA damage, 0.05 and 0.07 mg/ml were used for LD50 calculation for consumption limitation. The LD50 values were 452.915 and 513.306 mg for the extracts of T. alata and T. erecta, respectively per 1 kg rat, which are classified in the WHO[15] class II, moderately hazardous when taken orally by rat at 50–2000 mg/kg body weight. When passed through humans at approximately 50 kg of body weight, the plants can be taken up to 2500–1 00 000 mg (2.5–100 g) to reach a moderate hazard according to the WHO[15] referring that doses of T. alata and T. erecta extracts under 2.5–100 g, should be saved for consumers. Concerning these data, usages of T. erecta reported[11-13,19] in cooking, eating as a vegetable and application of its leaves for a remedy of headache, should be carefully determined for the doses. However, it is not surprise that T. alata leaf extracts can have activity against Pseudomonas aeruginosa and have significant antibacterial activity against Salmonella typhi[20], according to their biological activities including DNA damage in normal and poisoned PBMCs, which can be assumed to occur at plant concentrations.

At careful extracts doses, the presence of phytochemicals needs to be further considered for bioactivity assessments for further use in humans. The high quantity of oleamide and phytol were probable major or worked together having synergetic activity; phytol made up 12.36 % and 24.90 % in T. alata and T. erecta, while oleamide made up 46.29 % and 43.47 % in T. alata and T. erecta, respectively. Therefore, the extracts should have activities against scopolamine- induced memory loss, increase the production of the hormone acetylcholine, increasing memory function and act as a chemopreventive agent against Alzheimer’s disease, inducing deep sleep and upregulating appetite[21,22]. Additionally, the presence of phytol can be assumed as a property of plants. Phytol is derived from chlorophyll metabolism and released when plants are digested in the intestines. It is indispensable in the human body as it has important functions, including regulating blood glucose by activating enzymes that have a positive effect on the production of insulin and it may restore the metabolic functions of patients with type 2 diabetes, reducing cholesterol levels in blood, ultimately reducing blood pressure levels[23]. Moreover, phytol leads to the biosynthesis of tocopherols, a type of vitamin E[24] which is useful for cell health and can help decrease cell aging[25]. Therefore, the two studied plants, which can be assumed to be beneficial in human health, should be focused on the correct doses. Another minor substance may potentially work together with the major phytochemicals based on experiments at the preclinical trial level here.

As some synthetic drugs display several limitations, including side effects and costs, medicinal plants and their phytochemical compounds have been considered and used for many disease treatments in fresh, dried, and prepared forms, including T. alata and T. erecta. However, the dose limitations have been focused on.


This research is financially supported by Research and Academic Services, Khon Kaen University.

Conflict of interest:

Authors have no conflict of interest.