1976
DOI: 10.1021/jf60206a024
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Activity of tall fescue alkaloids and analogues in in vitro rumen fermentation

Abstract: The alkaloid perloline inhibited rumen fermentation in vitro at 0.04 to 1.0 mM as measured by cellulose digestion. The perlolidine moiety of perloline also inhibited cellulose digestion, but the inhibitory effect of perlolidine was equal to that of perloline only at the higher concentrations. Perloline methyl ether was less inhibitory than perlolidine. The veratrole moiety of perloline and perlolyrine did not inhibit cellulose digestion below 10 mM. Phenanthridine inhibited cellulose digestion at 0.1 to 1.0 mM… Show more

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Cited by 16 publications
(9 citation statements)
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“…The chemistry and synthesis of ergot alkaloids has been discussed in several publications over the years (Berde, 1980;Weber, 1980;Garner et al, 1993;Smith and Shappell, 2002;Hafner et al, 2008;Bush and Fannin, 2009), including the 1978 publication of the book titled Ergot Alkaloids and Related Compounds (Berde and Stürmer, 1978). Therefore, only a brief synopsis of ergot alkaloid chemistry is provided here for the convenience of the reader.…”
Section: Ergot Alkaloid Chemistrymentioning
confidence: 99%
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“…The chemistry and synthesis of ergot alkaloids has been discussed in several publications over the years (Berde, 1980;Weber, 1980;Garner et al, 1993;Smith and Shappell, 2002;Hafner et al, 2008;Bush and Fannin, 2009), including the 1978 publication of the book titled Ergot Alkaloids and Related Compounds (Berde and Stürmer, 1978). Therefore, only a brief synopsis of ergot alkaloid chemistry is provided here for the convenience of the reader.…”
Section: Ergot Alkaloid Chemistrymentioning
confidence: 99%
“…There are 3 major classes of ergot alkaloids: 1) clavine alkaloids, 2) lysergic acid and derivatives, and 3) ergopeptine alkaloids ( Figure 1; Lyons et al, 1986;Porter, 1995;Bush and Fannin, 2009). Whereas derivatives of D-lysergic acid (e.g., ergopeptines) are of concern for causing ergotism or fescue toxicosis, those of its epimer, D-isolysergic acid, have little biological effect reported in animal systems (Berde and Stürmer, 1978;Berde, 1980).…”
Section: Ergot Alkaloid Chemistrymentioning
confidence: 99%
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“…In addition to being a Lolium-Festuca amphiploid (Buckner et al, 1985), Johnstone does not contain the fungal endophyte (Acremonium coenophialum Morgan-Jones Gams) present in KY31 and most other tall fescue cultivars (Collins, 1991). Tall fescue containing the endophyte produces high concentrations of several alkaloids (Bush et al, 1976) that have significant physiological activity on ruminants consuming the grass. These alkaloids catalyze thiaminase activity leading to the breakdown of thiamine, an essential growth factor for many microorganisms and for most vertebrates.…”
mentioning
confidence: 99%