3. Ethnopharmacological Usage
Of the more than 150 species of the genus, few appear in the scientific literature, and even fewer are mentioned from an ethnopharmacological perspective. Notwithstanding,
Tragia species are a part of traditional medicinal systems of East Africa and the Indian subcontinent, such as Siddha and Ayurveda
[11][19], with documented uses of
T. involucrata appearing as early as the 1st century CE
[12][20] and with only a handful of mentions of
Tragia species in the New World pharmacopoeia, concerning mostly topical applications. There is concern over an excessive use of
Tragia species, e.g.,
Tragia bicolor, which poses a conservation hazard
[13][14][21,22].
Most of the interest in this genus has been focused on four species:
Tragia involucrata,
Tragia spathulata,
Tragia plukenetii and
Tragia benthamii [15][23], with the bulk of the research focused on
T. involucrata. Nevertheless, several more species and their medicinal uses appear in literature.
According to the ATC classification, the most frequent ethnopharmacological uses of
Tragia spp. in ethnopharmacology are: genitourinary system and sex hormones, with 19% of occurrences (15 of 77); nervous system, with 12%; and alimentary tract and metabolism, anti-infective for systemic use and antineoplastic and immunomodulating agents with 10% of occurrences each. The “various” classification presents 17% of occurrences, which include non-specified and vague uses, such as “toxic” or “medicinal”.
As for the morphological structures used per species, the most common are the leaves, 38%; followed by “not specified”, 33%; whole plant, 15%; roots, 13% and a single occurrence of endophytes (3%).
4. Biological Activity
Biological activity tests of
Tragia, both in vitro and in vivo, are performed mostly with plant extracts and to a much lesser degree with essential oils: leaf, root or the whole plant, although ethnopharmacological uses mostly employ the plant via infusions, decoctions or ashes
[15][16][23,35]. Different solvents and solvent mixtures have been used for the extracts, mainly methanol and ethanol. Due to the presence of
Tragia in ethnomedical traditions in Africa and Asia, there is a team of research about the bioactivity of Old World
Tragia extracts that have confirmed their activity and potency in some cases. Not all the health claims or traditional uses recorded have been validated through research. Again, the bulk of the research is centered on
T. involucrata.
4.1. In Vitro Activity
Extracts of
T. benthamii,
T. brevipes,
T. involucrata,
T. pungens and
T. spatulatha have been tested to ascertain their in vitro activity for a variety of uses.
In vitro biological activity tests devote the most attention to leaves (36%), with whole plant and root used to a lesser extent, with both 14%. Extraction solvents are methanol (47%), DCM (5%), Ethyl acetate (10%), water (6%), chloroform (5%), petroleum ether (5%), ethanol (5%) and acetone (5%). This solvent usage supports the assumption that most active compounds are moderately polar and are thus extracted with polar solvents.
Testing centers on antibacterial (41%) and antifungal (18%) activity of the extracts, with antiproliferative (12%) and antidiabetic, antiurolithiatic, radioprotective, immunomodulatory and cytotoxic effects (6% each) behind. This is a different profile than what was found in the ethnomedicinal claims, which centers on the genitourinary system and sex hormones. This is justified because aphrodisiacs do not have the expected properties
[17][92].
4.2. In Vivo Activity
Besides in vitro activity testing, research has been done in animal models, mostly mice and also chicks, with at least one clinical trial performed in humans.
Most of the research (73%) centers on
T. involucrata, with
T. plukenetii (18%),
T. benthamii (9%) and
T. furialis (5%) behind. In vivo assay extracts were obtained from leaves (29%), whole plant (25%), root (21%) and aerial parts (8%). Solvents used are methanol (48%), ethanol (26%) and water (13%), which shows that most active compounds are polar and are thus extracted with polar solvents.
For both in vitro and in vivo testing, the most common effect is antibacterial and antimicrobial with 22% of the reviewed studies. This is higher than the 10% reported in the ethnopharmacological uses. Effects having to do with cancer prevention and treatment—antiproliferative, antitumor, cytotoxic immunomodulatory and radioprotective—add up to 17% of the reported effects, which makes it the second most frequent use. Analgesic and anti-inflammatory activity is equally reported in 10% of the tests.
The findings reported in literature validate several medicinal use cases for
Tragia species and dismiss some claims, e.g.,
T. meyeriana as an antineoplastic
[18][60].
5. Phytochemical Composition
Phytochemical studies allow for the identification, separation and isolation of compounds of interest
[19][109]. Based on phytochemical screenings published in the literature, the main secondary metabolites found in
Tragia species extracts are alkaloids, glycosides, flavonoids, and sterols
[15][20][23,110].
Some compounds found in plants belonging to the
Tragia genus, classified according to their chemical nature, are listed in
Table 1. Where applicable, the biological activity of the identified compound has been mentioned.
Table 1. Compounds isolated/identified in Tragia extracts and oils and their biological effect.
No. |
Compound |
Identified |
Isolated |
Methodology Used |
Species |
Collection area |
Plant Organ Used |
Use |
Effect |
Reference |
Acetal |
1 |
1,1-diethoxy-2- methylpropane |
X |
|
Ethanol extract GC, MS |
T. plukenetii |
NS |
Whole plant |
NS |
NS |
[21][111] |
|
|
|
|
Aldehydes |
2 |
16-heptadecenal |
X |
|
Ethanol extract GC, MS |
T. plukenetii |
NS |
Whole plant |
NS |
NS |
[21][111] |
3 |
Hexanal |
X |
|
Hydrodistillation GC/GC-MS |
T. benthamii |
Ibadan, Nigeria |
Leaves |
NS |
NS |
[22][112] |
|
|
|
|
Alkaloid |
4 |
(E)-4-(1-hydroxypropyl)-7,8-dimethyl-9-(prop-1-en-1-yl)-[1,3] dioxolo [4,5-g]quinolin-6(5 | H | )-one |
X |
X |
Acidified ethanol extract GC, MS, LC |
T. plukenetii |
NS |
Whole plant |
NS |
NS |
[21] | [111] |
Esters |
5 |
4-oxo-4H-pyran-2,6-dicarboxylic acid bis-[6-methyl-heptyl] ester |
X |
X |
Ethanol extract IR 1H, 13C NMR, MS |
T. involucrata |
Salem, India |
Roots |
Antidiabetic |
Blood glucose reduction |
[23][86] |
6 |
Ethyl linoleate |
X |
X |
Ethanol extract GC, MS |
T. plukenetii |
NS |
Whole plant |
NS |
NS |
[21][111] |
7 |
Ethyl palmitate |
X |
X |
Ethanol extract GC, MS |
T. plukenetii |
NS |
Whole plant |
NS |
NS |
[21][111] |
|
|
|
|
Ether |
8 |
Vinyl hexyl ether |
X |
X |
Aqueous extract GC, MS |
T. involucrata |
Tamil Nadu, India |
Leaf |
Antibacterial
| Escherichia coli |
| Proteus vulgaris |
| Staphylococcus aureus |
MBC 12.25 μg/mL |
[24][25] | [98,113] |
Flavonoids |
9 |
3-(2,4-dimethoxyphenyl)-6,7-dimethoxy-2,3-dihydrochromen-4-one |
X |
X |
Ethyl acetate extract FTIR, MS, 1H NMR |
T. involucrata |
Odisha, India |
Root |
Antibacterial Fungicidal |
MIC 1.25-12.5 μg/mL |
[26][53] |
10 |
Iridin |
X |
X |
Ethyl acetate extract FTIR, MS, 1H NMR |
T. involucrata |
Odisha, India |
Root |
Toxic |
|
[26][53] |
11 |
Quercetin |
X |
X |
Ethyl acetate extract FTIR, MS, 1H NMR |
T. involucrata |
Odisha, India |
Root |
Antioxidant |
|
[26][53] |
12 |
Rutin |
X |
X |
Ethyl acetate extract FTIR, MS, | 1 | H NMR |
T. involucrata |
Odisha, India |
Root |
Antioxidant |
|
[26] | [53] |
Heterocycle |
13 |
2,5-dithia-3,6-diazabicyclo[2.2.1]heptane |
X |
X |
95% aqueous ethanol extraction
| 1 | H, | 13 | C NMR |
T. benthamii |
Ibadan, Nigeria |
Whole plant |
NS |
|
[27] | [114] |
Hydrocarbons |
14 |
2,6-dimethylheptane |
X |
X |
Aqueous extract GC, MS |
T. involucrata |
Tamil Nadu, India |
Leaf |
Antibacterial Proteus vulgaris |
MBC 10 μg/mL |
[24][98] |
15 |
2,4-dimethylhexane |
X |
X |
Aqueous extract GC, MS |
T. involucrata |
Tamil Nadu, India |
Leaf |
Antibacterial Staphylococcus aureus |
MBC 12.25 μg/mL |
[24][98] |
16 |
2-methylnonane |
X |
X |
Aqueous extract GC, MS |
T. involucrata |
Tamil Nadu, India |
Leaf |
Antibacterial Escherichia coli Proteus vulgaris Staphylococcus aureus |
MIC 5.0 μg/mL |
[24][98] |
17 |
Shellsol (2-methyldecane) |
X |
X |
Aqueous extract GC, MS |
T. involucrata |
Tamil Nadu, India |
Leaf |
Antibacterial Proteus vulgaris Staphylococcus aureus |
MBC 25.0 μg/mL |
[24][98] |
18 |
3,5-di-tert-butyl-4-hydroxyanisole |
X |
X |
95% aqueous ethanol extraction 1H, 13C NMR |
T. benthamii |
Ibadan, Nigeria |
Whole plant |
Antioxidant |
|
[27][114] |
19 |
5-hydroxy-1-methylpiperdin-2-one |
X |
X |
Methanol extract IR, | 1 | H, | 13 | C RMN, LC |
T. involucrata |
Kerala, India |
Leaf |
Antihistamine |
Muscle relaxant, bronchodilating and anti-allergic effects |
[28] | [115] |
Polyols |
20 |
Erythritol |
X |
X |
95% aqueous ethanol extraction 1H, 13C NMR |
T. benthamii |
Ibadan, Nigeria |
Whole plant |
NS |
NS |
[27][114] |
21 |
Glycerol |
X |
X |
95% aqueous ethanol extraction
| 1 | H, | 13 | C NMR |
T. benthamii |
Ibadan, Nigeria |
Whole plant |
NS |
NS |
[27] | [114] |
Terpenoids |
22 |
10,13-dimethoxy-17-(6-methylheptan-2-yl)-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[α]phenanthrene. |
X |
X |
Ethyl acetate extract FTIR, MS, 1H NMR |
T. involucrata |
Odisha, India |
Root |
NS |
NS |
[26][53] |
23 |
Stigmasterol |
X |
|
Aqueous extract GC, MS |
T. involucrata |
|
Leaf |
NS |
NS |
[24][98] |
24 |
Caryophyllene |
X |
|
Hydrodistillation GC/GC-MS |
T. benthamii |
Ibadan, Nigeria |
Leaves |
Anti inflammatory |
|
[22][112] |
25 |
Citronellal |
X |
X |
Ethanol extract IR, 1H RMN, LC |
T. ramosa |
Maharashtra, India |
Leaves |
Antibacterial |
|
[29][71] |
26 |
Clerodane |
X |
X |
Ethanol extract IR, 1H RMN, LC |
T. ramosa |
Maharashtra, India |
Leaves |
NS |
NS |
[29][71] |
27 |
Geranylacetone |
X |
|
Hydrodistillation GC/GC-MS |
T. benthamii |
Ibadan, Nigeria |
Leaves |
NS |
NS |
[22][112] |
28 |
Neophytadiene (2-(4,8,12-Trimethyltridecyl) buta-1,3-diene) |
X |
X |
Ethanol extract GC, MS |
T. plukenetii |
NS |
Whole plant |
NS |
NS |
[21][111] |
29 |
Phytol |
X |
X |
95% aqueous ethanol extraction 1H, 13C NMR |
T. benthamii |
Ibadan, Nigeria |
Whole plant |
NS |
NS |
[27][114] |
30 |
Squalene (all trans) |
X |
X |
Ethanol extract GC, MS |
T. plukenetii |
NS |
Whole plant |
NS |
NS |
[21][111] |
31 |
α-terpinene |
X |
X |
Ethanol extract IR, | 1 | H RMN, LC |
T. ramosa |
Maharashtra, India |
Leaves |
Antiinflammatory, Antimicrobial |
NS |
[29] | [71] |
Identification of the compounds relies heavily on spectroscopic and spectrometric methods
[19][109], and chromatography retention times and comparison with the literature are also used for tentative identification.
A strength of the genus is its diversity and its pantropical distribution, which makes it readily available in most tropical countries. A weakness would be that, despite the interest shown concerning
T. involucrata and other traditionally medicinal species, there appear to be no drugs derived from plants of these species, remaining in the realm of herbal remedies and plant extracts, entailing less medicinal interest than other genera of the
Euphorbiaceae family, notably
Euphorbia [7][8]. This can be attributed to the stage of research, with most work performed in vitro or in vivo and with a single clinical trial
[30][52]. Hopefully the current research will advance into new drugs.