Research Breakdown on Boerhaavia diffusa
Boerhaavia diffusa (Family Nyctinaceae) is a tropical plant that has been used in Ayurveda under the name of 'Punarnava' for jaundice, dyspepsia, and menstrual symptoms. It is a creeping weed and readily grows in the Indian region, and it is usually eaten as a vegetable (West Bengal Tribes, Assam state of India).
Boerhaavia Diffusa tends to contain:
Punarnavine at 0.01% and its glycoside Punernavoside
Rotenoid compounds known as Boeravinones (A-J), with B (0.2-0.22% dry weight) and E (0.05-0.06%; one report stating 0.32%) being major constituents. Other Boeravinones are G (7.5mg/kg), H (5.2mg/kg), and D (6.4mg/kg)
Boeravinone J is slightly different as a coumaronochromones molecule with a 5-carbon ring (B ring) rather than 6-carbon in the other Boeravinones
Coccineone B and E
6-O-demethylberavinone H, 10-demethylboeravinone C, and 9-O-methyl-10-hydroxycoccineone B
Borhavine (Xanthone) and Borhavone (Flavonoid)
Caffeoyltartaric Acid at 503.32+/-6.77mg/kg in the roots, with no detectable levels in the leaves
Eupalitin as 3-O-galactoside (2198.73+/-126.49mg/kg in leaves, none in roots) and as 3-O-galactosyl(1→2)-glucoside at 1066.07+/-7.87mg/kg in the leaves and 61.38+/-3.23mg/kg in the roots
Sitosterol, Stigmasterol, and Campesterol (84:13:3 ratios)
Overall phenolic content varies depending on the part used, with leaves having a higher phenolic content (10441.3mg/kg) than the roots (1049.1mg/kg). Organic acids show a reverse trend in the leaves (23,600.5mg/kg) and roots (50,916.7mg/kg) which consisted mostly of Oxalic acid (45-58.55%), Fumaric acid (25.5-28.7%), and Quinic acid in the roots only (24%).
Punarnavine itself, and the Rotenoid class of molecules (Boeravinones) are commonly seen as the main active ingredients The IC50 values of inhibition were 0.7+/-0.07μM and 2.5+/-0.47μM, respectively, and caused mitoxantrone accumulation in cells 92+/-6.5% and 68+/-6.1%, respectively. As the benefits of the juice extract (more potent than dry powder) were inhibited by naloxone, these effects appear to be mediated by opioids.
Putative pain-reducing effects Liriodendrin does not alter resting membrane potential of a neuron while attenuating the height and length of a slow response, and at 1mM reduced the amplitude of ICa to 40% of control and was found to be dose-dependent and reversible, with no influence on activation threshold or reversal potential of the neuron. Roots of Boerhaavia appear to have some historical use for treatment of Epilepsy (Nigerian folk medicine), and injections of the methanolic extract itself (500-2000mg/kg) and one with a higher concentration of the Calcium-Channel Blocker Liridendrin (10-40mg/kg) showed dose-dependent inhibition of PTZ-induced seizures and BAY k-8644 induced seizures. The lower doses tested (10mg/kg Liriodendrin fraction, 500mg/kg methanolic) showed potency similar to 1mg/kg Diazepam while the higher doses showed dose-dependent benefit, but no Boerhaavia group managed to abolish seizures like 4mg/kg Diazepam did. However, 20mg/kg Liriodendrin-rich fraction and 1mg/kg Diazepam showed synergism and outperformed 4mg/kg Diazepam.
Appears to have efficacy in reducing the onset of seizures, but at a higher dose than normally taken in rats and with less efficacy than reference drugs. Possible synergism with Diazepam Another test on α-amylase with Boerhaavia outright failed to inhibit this enzyme, as was Ashwagandha ineffective.
Some inhibitory effects on carbohydrate absorption, but selective and not enough evidence to suggest it is potent No significant effects were noted on non-diabetic rats, and benefits appeared to build up over the 4 weeks. Another intervention with 200mg/kg of the leaf hot water extract (tea) for 4 weeks in alloxan-induced diabetes was able to reduce circulating glucose 50.5% and plasma insulin by 52.6% (relative to alloxan control), which was a potency similar to Glibenclamide at 600mcg/kg; slight reduction of blood glucose and insulin were noted in the healthy control. This study also noted a reduction of HbA1c (47%) similar to Glibenclamide and reduction in triglycerides and total cholesterol were also similar. Other studies have also noted anti-diabetic effects at this dose and in this animal model of diabetes, and another study using the same dose Glibenclamide as reference drug has replicated how the above doses are not significantly different from each other. Boerhaavia has outperformed Glibenclamide in response to an oral glucose tolerance test, with the response 120 minutes after ingestion of glucose (2g/kg) not significant different than non-diabetic control. A separate study using Punarvarine has noted increases in antibody dependent cell death and antibody dependent complement mediated cell death (10.63% to 41.57% and 14% to 26%, respectively); this study was, however, conducted in a mouse model of metastasis which influences the results. However, eupalitin (a flavonoid) involved with Boerhaavia appears to potently suppress antigen-induced PMBC proliferation with a large (500mcg/mL) concentration of the leaf ethanolic extract suppressing 88% proliferation in vitro and up to 98% with pure eupalitin glycoside. Similar suppression was seen in lymphocyte proliferation, and a lesser degree of inhibition was noted in LPS-induced macrophages (500mcg/mL of the ethanolic extract and isolated eupalitin glycoside only inhibiting 36% and 67% respectively); a wide variety of cells are suppressed under the influence of the root ethanolic extract including monocytes, macrophages (mouse and human), lymphocytes, erythroleukemic, human T-cells, and a few organ cells (BNLCL.2 liver cells, HEK293 kidney cells, and L929 Fibroblast).
Cells involved in adaptive immunity appear to be enhanced under the influence of the isolated compound, Punarvarine. The overall extract, however, appears to have immunosupressive potential on a large variety of cell typesA mouse model on Natural Killer (NK) Cells has shown that NK cell activity has increase from a peak 6.98% in control (in a model of melanoma metastasis) to 32.46% at 1mg per animal (40-50mg/kg). An inhibition of NK cell activity has been noted with an ethanolic extract of the herb, yet further testing failed to find any influence from eupalitin or its glycoside; suggesting a currently unknown molecule in Boerhaavia may suppress NK cell activity, which may be concentrated in the chloroform extract (more suppressive than ethanolic). Suppression has been noted elsewhere with an ethanolic extract of the roots.
Natural Killer Cell activity may be enhanced by Punarvarine, but practical significance is unknown as another compound in the herb may suppress NK cell activityIn this same mouse model, the cytokines that were measured noted attenuation (IL-1β, TNF-α, IL-6) or induction (IL-2, IFN-γ) following 40-50mg/kg Punarvarine injections for 5 days following tumor implantation, this study is duplicated in Medline. Reductions in TNF-α production have been noted in vivo with eupalitin glycoside (flavonoid) secondary to suppressing macrophage activation; this may be downstream from NF-kB and AP-1 inhibition. This inhibition of TNF-α has been noted elsewhere with the ethanolic root extract.
A beneficial trend of cytokines (more anti-inflammatory than pro-inflammatory, as a general statement) appears to result after injections of Punarvarine. The immunosuppressive compounds in the herb (currently not known) could simply just reduce all cytokines except perhaps IFN-γ This was accompanied by increased survival in all groups and a trend to normalize some serum parameters associated with metastasis (hexosamine, uronic acid, sialic acid) as well as suppression of VEGF, MMP2, and MMP9. Another study using similar methodology noted increases in TIMP-1 alongside the reduction in metastasis, and noted that these observed effects may be due to the immune system (due to increases in NK cells and increase in antigen-mediated cytotoxicity), and a third study has confirmed reduced metastatic potential of implanted melanoma cells in this mouse line with a concomitant increase of survival from 35.1+/-5.4 days in control (tumor bearing) and enhancing lifespan by 240-257% of control.
In mice, appears to reduce metastasis of melanoma cells possibly secondary to the immune system An increase of cells with fragmented DNA existed at 10mcg/mL from 2% to 71% (reducing cell counts in all other cell cycle phases relatively) and this concentration was accompanied by 53.6% inhibition of proliferation. A reduction of pro-survival Bcl-2 was noted in these cancer cells with 10mcg/mL Punarnavine. Three subunits of NF-kB also had their nuclear translocation reduced by 71.8% (p65), 78.6% (p50), and 80.2% (C-Rel), suggesting anti-inflammatory effects.
Limited evidence, but appears to be more anti-proliferative than inherently cytotoxic This was seen with an increase of G0/G1 cell population from 69.1% to 75.8%. Subsequently, ethanolic extract of Boerhaavia were tested and one (BDF5) exerted 55% cell death (24 hours) and 85% cell death (72h) at 300mcg/mL incubation, with nonsignificant cell death 24 hours after 100mcg/mL but 64% after 72 hours; dose and time-dependent cytotoxicity with an IC50 of 250mcg/mL at 48 hours. Boerhaavia also reduced proliferation and increased DNA fragmentation in HeLa cancer cells, while increasing the cell population in S and G2+M phases.Vitamin C at 122.0, although another study notes that the DPPH activity of Boerhaavia leaf extract (ethanolic) has less anti-oxidant activity at 78.32+/-2.41% that of Vitamin C. Interactions in the DPPH assay are stronger in the leaves than the roots, with another study noting respective IC25 values of 41μg/mL and 1234μg/mL, respectively. These effects are probably reflective of the flavonoid content of Boerhaavia, which are concentrated in the leaf water extract. Similar effects were seen for sequestering Nitric Oxide in a dose-dependent manner, with IC50 values being higher in the leaves than roots with IC25 values of 155 and 217μg/mL, respectively. Relative to other plants, Boerhaavia is relatively weak (outperforming Ginkgo Biloba, but being outperformed by 16/25 tested herbs in this study including Holy Basil). In superoxide radical tests, the roots appear to be more potent than the leaves with IC50 values of 45 and 297ug/mL, respectively. That being said, more potent anti-oxidant effects are seen with Boeravinone G. Although the Boeravinones D, G, and H are seen as the more potent ones, Boeravinone G was able to scavenge 65.9+/-3.3% of hydroxyl radicals (0.5mg/mL in a Electron spin resonance spectroscopy test), and at a concentration of 1ng/mL abolished lipid peroxidation in vitro, approximately halved intracellular ROS, and almost normalized oxidant-induced DNA damage; Boeravinone showed no pro-oxidative properties on its own, and normalized NF-kB expression induced by oxidation.
Quite potent anti-oxidant effects in general, with Boeravinone G being remarkably potent in vitro using cell cultures (Benefits after oral consumption hard to extrapolate from this)
Independent of Boeravinone G, the flavonoid component appears to also exert direct anti-oxidative properties (like most plants, with this aspect not being too remarkable) TBARS (a measure of lipid peroxidation) was also normalized at doses exceeding 100mg/kg of both ethanolic and water extracts, suggesting anti-oxidant properties underlied the liver protection. 20mg/kg injections of the hydroalcholic extract of Boerhaavia has also shown protective effects against oxidation induced by radiation, where White Blood Cell count (decreased by gamma-radiation) was effectively preserved to control levels and both lipid peroxidation and plasma ALP were reduced.
Anti-oxidant effects appear to exist in vivo after oral ingestion, but Boeravinone G has not been tested in isolation nor is the practical relevance of these studies meaningful yet; preliminary research When tested in precontracted mouse tracheal rings, Boerhaavia was able to induce relaxation at 30mcg/mL with the water extract (EC25 94+/-19mcg/mL), 50-70% relaxation with 1mg/mL ethanolic extract (EC25 533+/-233mcg/mL), and the methanolic extract inducing 55% relaxation at 20mcg/mL (EC25 12+/-3mcg/mL).
May relax the trachea; unknown practical significance or mechanisms COD crystals are considered less urolithic than COM crystals. Another test showed that it was ineffective against Monosodium Urate Monohydrate crystals. In rats administered ethylene glycol to induce hyperoxaluria (subsequently, inducing renal damage and calcium-oxalate kidney stones) given 100-200mg/kg water extract of Boerhaavia was able to reduce the size and content of kidney stone crystals in rat urine in a dose-dependent manner and normalized kidney histology (indicative of kidney damage) in a similar dose-dependent manner. Normalization of anti-oxidant enzymes and markers (MDA, Glutathione, Catalase, etc.) occured in both treated groups. This same protocol was tested with the nutraceutical formulation Urex (Boerhaavia and Tribulus Terrestris) at 200mg/kg or 400mg/kg acted to normalize serum parameters of kidney function (BUN, Creatinine) while reducing urinary salts, although neither dose was able to normalize parameters measured. In regards to diuresis (urination), the increase of urination associated with kidney stones (79.47%) was further increased by 72.3% and 220% after ingestion of 100 and 200mg/kg aqueous extract of Boerhaavia, respectively. This has been noted elsewhere where urine totals reached 133% more than control animals with 200mg/kg Urex (Boerhaavia and Tribulus). Diuretic effects are due to compounds that are present in both the leaves and roots, with minimal efficacy when using the stem.
Boerhaavia appears to be kidney protective and reduce formation of kidney stones at 100-200mg/kg (estimated human conversion dose of 16-32mg/kg)
Appears to be a diuretic, but not compared to any reference drugs (and thus unknown practical relevance) used as an indicator of estrogenicity in MCF-7.
Potent anti-estrogenic effects on the receptor when looking at the genome, yet doesn't appear to be fully explained by the receptor level antagonism (which is somewhat weak) 250mg/kg Boerhaavia ethnaolic extract in pregnant rats has failed to show teratogenic effects.
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