Table 1.
Confirmed Biological Activity | Extract Type | Probable Active Compounds | Method Applied | Results | Source |
---|---|---|---|---|---|
Anticancer potential |
Dried extracts obtained by extraction with water, 70% ethanol, isopropanol, acetone, and chloroform | May be attributed to ursolic acid as a constituent component | In vitro using primary human myeloid leukemia cell line patient samples, in vivro on mice engrafted with C1498 cells | This study demonstrated that extracts can exert anti-AML activity | [9] |
Antidiabetic | Dried extracts obtained by extraction with 80% ethanol | Polyphenols | In vitro using the Caco-2 human enterocytic cell line and in vivo using an oral glucose tolerance test (OGTT) |
These studies indicate a decrease in glucose absorption during an OGTT in normoglycemic rats and a significant decrease in the protein expression of SGLT1 and GLUT2 in CaCo2/15 cells | [10] |
Antidiabetic potential | Dried extracts obtained by extraction with 80% ethanol | Chlorogenic acid, catechins, taxifolin, and quercetin glycosides | Using potentiation of basal and insulin-stimulated glucose uptake by skeletal muscle cells (C2C12) and adipocytes (3T3-L1), potentiation of glucose-stimulated insulin secretion by pancreatic b cells (bTC), potentiation of adipogenesis in 3T3-L1 cells, protection against glucose toxicity and glucose deprivation in PC12-AC neuronal precursor cells, and DPPH oxygen free radical scavenging |
The present study revealed that Rh. tomentosum exhibits a promising profile of antidiabetic potential and is a good candidate for more in-depth evaluation |
[11] |
Antioxidant and anti-inflammatory activities | Extract obtained by extraction with 70% ethanol and was fractionated by EtOAc |
Unknown | Antioxidant by DPPH and ABTS assay. The anti-inflammatory activities by the inhibitory activity against NO, PGE2, TNF-α, IL-1β, and IL-6 production on LPS-stimulated raw 264.7 macrophages | Extracts have high antioxidant activities similar to vitamin C, and the low concentration of extracts have high anti-inflammatory activities | [12] |
Analgesic and anti-inflammatory activities | Essential oil, methanol extract, and aqueous extract | Flavonoid components | In vivo using model of acetic acid-induced writhing response and anti-inflammatory effect by using model of lambda-carrageenan-induced paw adema in mice | The analgesic and anti-inflammatory effects of methanol extract | [13] |
Anti-inflammatory effect | Novogalene agent Ledum 50 obtained by 50% ethanol | Polyphenolic compounds | In vivo model of acute bronchitis initiated by endotracheal administration of 1% formalin solution | Normalization of the histostructure of the respiratory system | [14] |
Anti-inflammatory activity | Dried extracts obtained by extraction with water | Unknown | In vitro using evaluation of inhibitory activity on prostaglandin biosynthesis and platelet-activating factor (PAF)-induced exocytosis | High inhibition was obtained, prostaglandin inhibition 50 ± 4%, PAF–exocytosis inhibition 71 ± 3% | [15] |
Toxic, antioxidant, and antifungal activity | Essential oils obtained by hydrodistillation | The major compounds were palustrol, ledol, ascaridol isomers, myrcene, and cyclocolorenone isomers | The toxic activity using a brine shrimp (Artemia sp.) bioassay, DPPH and ABTS assay, and antifungal activity by agar disc diffusion assay (Candida parapsilosis) | Notable toxic activity of essential oils, high abilities to scavenge radicals, possess potential antifungal activity | [16] |
Antioxidant and antimicrobial activities | Essential oil obtained by hydrodistillation and methanol extracts | The major compounds sabinene, terpinen-4-ol, myrtenal, α-pinen, β-selinene, α-selinene, and γ-elemene | Antioxidant activity by TBARS, NBT, and DPPH assay and inhibition of lipid peroxide formation. Antimicrobial activity by MIC (minimum inhibitory concentration) test and disc diffusion method | The methanol extract and essential oil showed antioxidant activity. The oil showed antimicrobial activity against Streptococcus pneumoniae, Clostridium perfringens, Candida albicans, Mycobacterium smegmatis, Acinetobacter lwoffii, and Candida krusei, while the methanolic extracts exhibited slight or no activity | [17] |
Antioxidant activities | Essential oil obtained by hydrodistillation, extract obtained by extraction with 70% ethanol | The major compounds 4-thujene, α-thujenal, and (-)-4-terpineolwhile. In the ethanol extract were α-farnesene, n-tetradecane, hexadecanoic acid, oblivon c, and lilac aldehyde | DPPH and ABTS assay | Ethanol extract showed stronger antioxidant activities than the essential oil | [18] |
Antimicrobial activities | Essential oil obtained by steam distillation, CO2 by supercritical carbon dioxide | The main compounds EO palustrol, myrcene, and ledol. In scCO2 extract, the major components palustrol and ledol, and myrcene absent | Using modified agar well diffusion methods against S. aureus, P. aeruginosa, C. albicans, A. niger, C. cladosporioides, and P. venetum | All the EOs and scCO2 extracts showed a broad spectrum of antimicrobial activities against the selected microbes | [19] |
Antibacterial activity | Essential oil was isolated by subcritical fluid extraction technology with butane as a solvent | The main constituents α-thujenal, bicyclocompounds, β-phellandrene, benzene,1-methyl-3-(1-methylethyl, propanal,2-methyl-3-phenyl, and β-terpineol | Using the modified disc method |
Extract expressed good antibacterial activity against the marine pathogen V. parahaemolyticus | [20] |
Insecticidal activity on mosquitoes, moths, and flies | Essential oil obtained by hydrodistillation | The main constituents p-cymene, isoascaridole, and cis-ascaridole | Culex quinquefasciatus larvae, M. domestica adults, S. littoralis early 3rd instar larvae. Toxicity on the nontarget aquatic microcrustacean Daphnia magna and soil organisms Eisenia fetida. Toxicity keratinocytes cell line (HaCaT), primary human fibroblast cell line (NHF A12), and MTT assay | Essential oil showed significant mortality on the larvae of C. quinquefasciatus and S. littoralis and adults of M. domestica, with little or no impact on beneficial organisms such as aquatic microcrustacean and earthworms and moderate toxicity on human fibroblasts and keratinocytes | [21] |
Mosquito repellent |
Volatile compounds were collected by solid phase microextraction, essential oil was obtained by steam distillation, extracts were extracted with hexane, ethyl acetate, or methanol | The volatile fraction of an ethyl acetate extract has the major compounds p-cymene, terpinyl acetate, sabinene, p-pinene, bornyl acetate, α pinene, β-phellandrene, camphene, Z-ocimene, and γ-terpinene | Repellency bioassays were carried out using cages made of mosquito netting and field experiment | Ethyl acetate extracts significantly reduced the probing activity of Aedes aegypti (L.) and reduced biting by mosquitoes | [22] |
Repellency activity | Oil, 10%, diluted in acetone | Compounds of essential oil | A repellency bioassay on I. ricinus nymphs | Exhibited 95% repellency | [23] |
Antihyperuricmic | Mother tincture Ledum palustre L., potency 30c and 1M | Homeopathy | Potassium oxonate induced rat model | The present study indicated marked hypouricemic effects; however, clear conclusion of hypouricemic potential of Ledum palustre required replication of experiment | [24] |
Antihyperuricmic | Mother tincture Ledum palustre L. | Homeopathy | Randomized single-blind experimental design was applied to the study (200 humans). For analysis of uric acid in blood samples, the enzymatic method was selected | The value of reduction in serum uric acid in males was 4.3 ± 0.3, in females was 4.6 ± 0.4 | [25] |