570 research outputs found
Actions taken and future considerations due to findings of Echinococcus multilocularis in two Scandinavian countries
Wastewater treatment with <em>Moringa oleifera</em> seed extract: Impact on turbidity and sedimentation of <em>Cryptosporidium parvum</em> oocysts
Antiparasitic activity of chicory (Cichorium intybus) and its natural bioactive compounds in livestock: a review
Increasing drug resistance in gastrointestinal (GI) parasites of livestock and concerns about chemical residues in animal products and the environment are driving the development of alternative control strategies that are less reliant on the use of synthetic drugs. An increasingly investigated approach is the use of bioactive forages with antiparasitic properties as part of the animal’s diet (nutraceuticals) or as potential sources of novel, natural parasiticides. Chicory (Cichorium intybus) is a multi-purpose crop and one of the most promising bioactive forages in temperate regions, and numerous in vivo trials have explored its potential against parasitic nematodes in livestock. However, it is unclear whether chicory can induce a direct and broad activity against various GI parasites in different livestock species, and the levels of chicory in the diet that are required to exert an efficient antiparasitic effect. Moreover, the mechanisms leading to the reported parasiticidal activity of chicory are still largely unknown, and its bioactive phytochemicals have only recently been investigated. In this review, we summarise the progress in the study of the antiparasitic activity of chicory and its natural bioactive compounds against GI parasites in livestock, through examination of the published literature. The available evidence indicates that feeding chicory can reduce faecal egg counts and/or worm burdens of abomasal nematodes, but not infections with intestinal worms, in ruminants. Highly chicory-rich diets (≥ 70% of chicory dry matter in the diet) may be necessary to directly affect abomasal parasitism. Chicory is known to synthesise several bioactive compounds with potential antiparasitic activity, but most research has been devoted to the role of sesquiterpene lactones (SL). Recent in vitro studies have confirmed direct and potent activity of SL-rich extracts from chicory against different GI helminths of livestock. Chicory SL have also been reported to exhibit antimalarial properties and its potential antiprotozoal activity in livestock remains to be evaluated. Furthermore, the detailed identification of the main antiparasitic metabolites of chicory and their pharmacokinetics need further confirmation. Research gaps and perspectives on the potential use of chicory as a nutraceutical forage and a source of bioactive compounds for parasite control in livestock are discussed
Occurrence of <em>Cryptosporidium</em> spp. oocysts in low quality water and on vegetables irrigated with low quality water in Kumasi, Ghana
Transport and survival of <em>Cryptosporidium parvum</em> oocysts in soil columns following applications of raw and separated liquid slurry
Tarapacol 15-Acetate, a New Diterpenoid from Grindelia tarapacana Phil.
In the title compound, 15-acetoxy-14(S)-hydroxy-13-epi-manoyl oxide {IUPAC systematic name: 2-(dodecahydro-3,4a,7,7,10a-pentamethyl-1H-naphtho[2,1-b]pyran-3-yl)-2-hydroxyethyl acetate}, C22H38N4, rings A and B have chair conformations. Ring C adopts a boat conformation with the 16-methyl group in an axial position and the bulky glycol monoacetate group in an equatorial position. Ring systems A/B and B/C (conventional IUPAC labdane diterpenoid nomenclature) are trans fused about the C(5)-C(10) and C(8)-C(9) bonds, respectively. The present study establishes the relative stereochemistry at the C(14) position.This work was supported by a grant to the American Association for the Advancement of Science from the John D. and Catherine T. MacArthur Foundation, awarded to BNT. The structure was determined in the Molecular Structure Laboratory of the Department of Chemistry as a special class project in Chemistry 517
Gastrointestinal parasites of cats in Denmark assessed by necropsy and concentration McMaster technique
Electron impact excitation cross sections for allowed transitions in atoms
We present a semiempirical Gaunt factor for widely used Van Regemorter
formula [Astrophys. J. 136, 906 (1962)] for the case of allowed transitions in
atoms with the LS coupling scheme. Cross sections calculated using this Gaunt
factor agree with measured cross sections to within the experimental error.Comment: RevTeX, 3 pages, 10 PS figures, 2 PS tables, submitted to Phys. Rev.
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