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Journal articles on the topic 'Eupatorium perfoliatum'

Author: Grafiati

Published: 4 June 2021

Last updated: 1 February 2022

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1

Maas, Mareike, and Andreas Hensel. "Eupatorium perfoliatum L." Zeitschrift für Phytotherapie 29, no. 05 (October 2008): 249–54. http://dx.doi.org/10.1055/s-0028-1102730.

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2

Vollmar, Angelika, Wolfram Schäfer, and Hildebert Wagner. "Immunologically active polysaccharides of eupatorium cannabinum and eupatorium perfoliatum." Phytochemistry 25, no. 2 (January 1986): 377–81. http://dx.doi.org/10.1016/s0031-9422(00)85484-9.

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3

Maas, Mareike, Frank Petereit, and Andreas Hensel. "Caffeic Acid Derivatives from Eupatorium perfoliatum L." Molecules 14, no. 1 (December 23, 2008): 36–45. http://dx.doi.org/10.3390/molecules14010036.

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4

Hensel, Andreas, Mareike Maas, Jandirk Sendker, Matthias Lechtenberg, Frank Petereit, Alexandra Deters, Thomas Schmidt, and Timo Stark. "Eupatorium perfoliatum L.: Phytochemistry, traditional use and current applications." Journal of Ethnopharmacology 138, no. 3 (December 2011): 641–51. http://dx.doi.org/10.1016/j.jep.2011.10.002.

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5

Hensel, Andreas, Mareike Heimink, Matthias Lechtenberg, Jandirk Sendker, Frank Petereit, Andrea Derksen, Thomas Schmidt, Joachim Kühn, and Christian Nauert. "Eupatorium perfoliatum L. - Neue Befunde zu einer alten Arzneipflanze." Zeitschrift für Phytotherapie 34, no. 02 (May 16, 2013): 90–98. http://dx.doi.org/10.1055/s-0032-1331485.

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6

Stahl, E. "Grippesymptomatik - Verdacht auf Denguefieber - Erfolgreiche Therapie mittels Eupatorium perfoliatum." Allgemeine Homöopathische Zeitung 246, no. 04 (April 4, 2007): 156–59. http://dx.doi.org/10.1055/s-2006-936768.

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7

Maas, Mareike, Andreas Hensel, Fernando Batista da Costa, Reto Brun, Marcel Kaiser, and Thomas J. Schmidt. "An unusual dimeric guaianolide with antiprotozoal activity and further sesquiterpene lactones from Eupatorium perfoliatum." Phytochemistry 72, no. 7 (May 2011): 635–44. http://dx.doi.org/10.1016/j.phytochem.2011.01.025.

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8

Habtemariam, Solomon. "Activity-guided Isolation and Identification of Free Radical-scavenging Components from Ethanolic Extract of Boneset (Leaves of Eupatorium Perfoliatum)." Natural Product Communications 3, no. 8 (August 2008): 1934578X0800300. http://dx.doi.org/10.1177/1934578x0800300815.

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Activity-directed fractionation and isolation procedures were used to identify the antioxidant components of Boneset (Eupatorium perfoliatum). Dried powdered leaves were extracted with ethanol and subsequently fractionated into light petroleum, chloroform, ethyl acetate, and n-butanol fractions. The ethyl acetate fraction, which showed the strongest antioxidant activity, reducing power and highest phenolic content, was subjected to Sephadex LH-20 chromatography followed by repetitive preparative TLC to afford protocatechuic acid as the major antioxidant constituent, together with small amounts of other antioxidants (hyperoside, quercetin and rutin). Similar treatment of the n-butanol fraction, the second most potent fraction, yielded predominantly rutin and a trace amount of hyperoside as active constituents. The identity of the compounds was established based on direct comparison of spectral data (UV, IR, 1D- and 2D-NMR and MS) with those of authentic samples and literature values.

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9

Lira-Salazar, G., E. Marines-Montiel, J. Torres-Monzón, F. Hernández-Hernández, and J. S. Salas-Benito. "Effects of homeopathic medications Eupatorium perfoliatum and Arsenicum album on parasitemia of Plasmodium berghei-infected mice." Homeopathy 95, no. 4 (October 2006): 223–28. http://dx.doi.org/10.1016/j.homp.2006.06.003.

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10

Habtemariam, Solomon, and Angela M. Macpherson. "Cytotoxicity and antibacterial activity of ethanol extract from leaves of a herbal drug, Boneset (Eupatorium perfoliatum)." Phytotherapy Research 14, no. 7 (2000): 575–77. http://dx.doi.org/10.1002/1099-1573(200011)14:7<575::aid-ptr652>3.0.co;2-1.

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11

Derksen, Andrea, Joachim Kühn, Wali Hafezi, Jandirk Sendker, Christina Ehrhardt, Stephan Ludwig, and Andreas Hensel. "Antiviral activity of hydroalcoholic extract from Eupatorium perfoliatum L. against the attachment of influenza A virus." Journal of Ethnopharmacology 188 (July 2016): 144–52. http://dx.doi.org/10.1016/j.jep.2016.05.016.

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12

Colegate, Steven M., Roy Upton, Dale R. Gardner, Kip E. Panter, and Joseph M. Betz. "Potentially toxic pyrrolizidine alkaloids in Eupatorium perfoliatum and three related species. Implications for herbal use as boneset." Phytochemical Analysis 29, no. 6 (July 2, 2018): 613–26. http://dx.doi.org/10.1002/pca.2775.

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13

Sinha, Moonmoon, Urmita Chakraborty, Anirban Kool, Mousumi Chakravarti, Souvik Das, Sandip Ghosh, Lovnish Thakur, et al. "In-vitro antiviral action of Eupatorium perfoliatum against dengue virus infection: Modulation of mTOR signaling and autophagy." Journal of Ethnopharmacology 282 (January 2022): 114627. http://dx.doi.org/10.1016/j.jep.2021.114627.

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14

Rath, Padmalaya, Bhopal Singh Arya, Anil Kumar Vichitra, and Udaiveer Singh. "Case Series of Dengue Treated with Homoeopathic Intervention." Homœopathic Links 32, no. 01 (March 2019): 031–35. http://dx.doi.org/10.1055/s-0039-1688454.

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Background Dengue is an infectious mosquito-borne disease in India and is caused by a virus named as dengue virus. It is also known as break bone fever, is a painful and sometimes fatal viral disease characterized by headache, skin rash and debilitating muscle and joint pains. In India, dengue is becoming a public health problem. The predominant dengue virus serotypes during the last few years have been DENV-2 and DENV-3. There is no specific antiviral treatment currently available for dengue fever. Time to time many dengue cases treated with homoeopathic medicine successfully have been reported. Methodology Demographic data, symptoms and laboratory findings were collected from patients with confirmed dengue infections treated from outpatient department and inpatient department of Dr. D. P. R. Central Research Institute for Homoeopathy, Noida, from September 2015 to October 2015. Results Four dengue infected patients were treated successfully by homoeopathic medicine Eupatorium perfoliatum without any complication. Conclusion Dengue requires early diagnosis and treatment. Dengue can be managed with homoeopathy. Further studies are mandatory as evidence-based data in the management of dengue are sparse.

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15

Singh, Surender, Ritu Karwasra, Prerna Kalra, Debadatta Nayak, AnilK Khurana, and RajK Manchanda. "Attenuation of Complete Freund's Adjuvant-induced arthritis by different dilutions of Eupatorium perfoliatum and Crotalus horridus and their safety evaluation." Indian Journal of Research in Homoeopathy 13, no. 2 (2019): 107. http://dx.doi.org/10.4103/ijrh.ijrh_23_19.

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16

Keddy, Paul A., and Timothy H. Ellis. "Seedling recruitment of 11 wetland plant species along a water level gradient: shared or distinct responses?" Canadian Journal of Botany 63, no. 10 (October 1, 1985): 1876–79. http://dx.doi.org/10.1139/b85-263.

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Where many different plant species occupy an environmental gradient, the responses of their offspring to that gradient could show one of two patterns. All species could have similar requirements for maximum recruitment, in which case all would show maximum germination and emergence in the same region of the gradient ("shared responses"). Alternatively, each species could have different requirements for recruitment and therefore would show maximum recruitment in different regions of the gradient ("distinct responses"). The objective of this study was to test between these two alternatives in plants occurring along a water level gradient. Seeds of 11 wetland species were allowed to germinate in sand along a gradient of water depth, ranging from 10 cm above to 5 cm below the substrate surface. Scirpus americanus, S. validus, Sagittaria latifolia, Typha angustifolia, and Lythrum salicaria showed no significant response to this gradient, while Spartina pectinata, Polygonum punctatum, Bidens cernua, Acorus calamus, Alisma plantago-aquatica, and Eupatorium perfoliatum did. However, the six species in the latter group did not exhibit shared preferences along the water depth gradient. These different recruitment patterns were consistent with adult distributions in the field. Most species showed some recruitment at all water levels examined, suggesting that they have broad tolerance limits for water level in the recruitment phase of their life history.

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17

Maas, Mareike, Alexandra M. Deters, and Andreas Hensel. "Anti-inflammatory activity of Eupatorium perfoliatum L. extracts, eupafolin, and dimeric guaianolide via iNOS inhibitory activity and modulation of inflammation-related cytokines and chemokines." Journal of Ethnopharmacology 137, no. 1 (September 2011): 371–81. http://dx.doi.org/10.1016/j.jep.2011.05.040.

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18

LeSage, Laurent. "A TAXONOMIC MONOGRAPH OF THE NEARCTIC GALERUCINE GENUS OPHRAELLA WILCOX (COLEOPTERA: CHRYSOMELIDAE)." Memoirs of the Entomological Society of Canada 118, S133 (1986): 3–75. http://dx.doi.org/10.4039/entm118133fv.

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AbstractThe taxonomy of the Nearctic genus Ophraella Wilcox is revised. Data for all known immature stages are included. Ophraella integra (LeConte) is synonymized with O. notulata (Fabricius). Ophraella dilatipennis (Jacoby) is transferred to the genus Neolochmaea Laboissière.Thirteen species are recognized, of which 6 are new : O. arctica, californiana, communa, macrovittata, nuda, and pilosa. The distribution and host plants of species are as follows : O. americana, eastern North America, on Solidago spp.; O. pilosa, transcontinental along the Canadian border, on Aster, primarily A. macrophyllus; O. cribrata, coast to coast in the United States, on Solidago of the subgenus Virgaurea; O. conferta in northeastern states, on Solidago with preference for S. canadensis and S. rugosa; O. sexvittata in southeastern states, on Solidago spp.; O. notulata in eastern US and Gulf states to Mexico, on Iva oraria; O. notata in eastern portion of the United States, on Eupatorium perfoliatum; O. macrovittata in the Gulf states, host plant unknown; O. communa in North America and Mexico, on Ambrosia artemisiifolia; O. bilineata in the Canadian Prairies and the bordering states, on Chrysopsis villosa; O. californiana in California and Mexico, on Artemisia Douglasiana; O. nuda in Alberta, host plant unknown; and O. arctica in tundra zone, on Solidago multiradiata scopulorum.The life cycles of most species are still unknown but most species probably have only 1 generation per year. The eggs are laid in clusters on the under surface of young leaves. The larvae skeletonize young leaves and live exposed. Before pupation, the larva spins a loose cocoon and attaches it to a leaf tip. Pupation lasts 1–2 weeks. The newly hatched adults are active on host plants until the early fall, when they enter the leaf litter for overwintering.

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19

Groves, R. L., J. F. Walgenbach, J. W. Moyer, and G. G. Kennedy. "The Role of Weed Hosts and Tobacco Thrips, Frankliniella fusca, in the Epidemiology of Tomato spotted wilt virus." Plant Disease 86, no. 6 (June 2002): 573–82. http://dx.doi.org/10.1094/pdis.2002.86.6.573.

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Wild plant species were systematically sampled to characterize reproduction of thrips, the vector of Tomato spotted wilt virus (TSWV), and natural sources TSWV infection. Thrips populations were monitored on 28 common perennial, biennial, and annual plant species over two noncrop seasons at six field locations across North Carolina. Sonchus asper, Stellaria media, and Taraxacum officianale consistently supported the largest populations of immature TSWV vector species. The tobacco thrips, Frankliniella fusca, was the most abundant TSWV vector species collected, comprising over 95% of vector species in each survey season. Perennial plant species (i.e., Plantago rugelii and Taraxacum officianale) were often only locally abundant, and many annual species (Cerastium vulgatum, Sonchus asper, and Stellaria media) were more widely distributed. Perennial species, including P. rugelii and Rumex crispus, remained TSWV infected for 2 years in a small-plot field test. Where these perennial species are locally abundant, they may serve as important and long-lasting TSWV inoculum sources. In random surveys across 12 locations in North Carolina, TSWV infection was documented by double antibody sandwich enzyme-linked immunosorbent assay in 35 of 72 (49%) common perennial (N = 10), biennial (N = 4), and annual (N = 21) plant species across 18 plant families. Estimated rates of TSWV infection were highest in Cerastium vulgatum (4.2%), Lactuca scariola (1.3%), Molluga verticillata (4.3%), Plantago rugelii (3.4%), Ranunculus sardous (3.6%), Sonchus asper (5.1%), Stellaria media (1.4%), and Taraxacum officianale (5.8%). Nine plant species were determined to be new host recordings for TSWV infection, including Cardamine hirsuta, Eupatorium capillifolium, Geranium carolinianum, Gnaphalium purpureum, Linaria canadense, Molluga verticillata, Pyrrhopappus carolinianus, Raphanus raphanistrum, and Triodanis perfoliata. Our findings document the relative potential of a number of common annual, biennial, and perennial plant species to act as important reproductive sites for F. fusca and as acquisition sources of TSWV for spread to susceptible crops.

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20

Nauert, C., C. Bentley, and BL Fiebich. "In-vitro-Untersuchungen zur entzündungshemmenden Wirkung von Eupatorium perfoliatum (EP)." Zeitschrift für Phytotherapie 27, S 1 (November 23, 2006). http://dx.doi.org/10.1055/s-2006-954930.

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21

Lechtenberg, M., M. Maas, B. Quandt, and A. Hensel. "Capillary electrophoresis of phenolic compounds from Eupatorium perfoliatum L. (Asteraceae)." Planta Medica 75, no. 09 (July 2009). http://dx.doi.org/10.1055/s-0029-1234664.

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22

Maas, M., F. da Costa, A. Deters, T. Schmidt, and A. Hensel. "Eupatorium perfoliatum L.: Antiinflammatory and antiplasmodial activity of the dichloromethane extract and novel sesquiterpene lactones." Planta Medica 76, no. 12 (August 24, 2010). http://dx.doi.org/10.1055/s-0030-1264249.

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23

Derksen, A., J. Sendker, W. Hafezi, C. Nauert, J. Kühn, and A. Hensel. "Bioassay-guided fractionation of Eupatorium Perfoliatum L. towards anti-Influenza A-activity leads to dicaffeoyl quinic acids." Planta Medica 78, no. 11 (July 2012). http://dx.doi.org/10.1055/s-0032-1320423.

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24

Derksen, A., W. Hafezi, J. Kühn, C. Nauert, and A. Hensel. "Bioassay-guided fractionation of Eupatorium perfoliatum L. towards anti-influenza A-activity leads to dicaffeoyl quinic acids." Zeitschrift für Phytotherapie 34, S 01 (March 1, 2013). http://dx.doi.org/10.1055/s-0033-1338201.

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