Ramos-Morales Eva, de la Fuente Gabriel, Duval Stephane, Wehrli Christof, Bouillon Marc, Lahmann Martina, Preskett David, Braganca Radek, Newbold Charles J
Institute of Biological, Environmental and Rural Sciences, Aberystwyth University Aberystwyth, UK.
DSM Nutritional Products Ltd., Centre de Recherche en Nutrition Animale Saint Louis Cedex, France.
Front Microbiol. 2017 Mar 16;8:399. doi: 10.3389/fmicb.2017.00399. eCollection 2017.
The antiprotozoal effect of saponins is transitory, as when saponins are deglycosylated to the sapogenin by rumen microorganisms they become inactive. We postulated that the substitution of the sugar moiety of the saponin with small polar residues would produce sapogen-like analogs which might be resistant to degradation in the rumen as they would not be enzymatically cleaved, allowing the antiprotozoal effect to persist over time. In this study, we used an acute assay based on the ability of protozoa to break down [C] leucine-labeled and a longer term assay based on protozoal motility over 24 h to evaluate both the antiprotozoal effect and the stability of this effect with fifteen hederagenin -esters esterified with two identical groups, and five cholesterol and cholic acid based derivatives carrying one to three succinate residues. The acute antiprotozoal effect of hederagenin derivatives was more pronounced than that of cholesterol and cholic acid derivatives. Modifications in the structure of hederagenin, cholesterol, and cholic acid derivatives resulted in compounds with different biological activities in terms of acute effect and stability, although those which were highly toxic to protozoa were not always the most stable over time. Most of the hederagenin -esters, and in particular hederagenin -succinate (TSB24), hederagenin -betainate dichloride (TSB37) and hederagenin -adipate (TSB47) had a persistent effect against rumen protozoa , shifting the fermentation pattern toward higher propionate and lower butyrate. These chemically modified triterpenes could potentially be used in ruminant diets as an effective defaunation agent to, ultimately, increase nitrogen utilization, decrease methane emissions, and enhance animal production. Further trials or in long term rumen simulators are now needed to confirm the observations presented.
皂苷的抗原生动物作用是短暂的,因为当皂苷被瘤胃微生物去糖基化成为皂苷元时,它们就会失去活性。我们推测,用小的极性残基取代皂苷的糖部分会产生类似皂苷元的类似物,这些类似物可能在瘤胃中抗降解,因为它们不会被酶切,从而使抗原生动物作用能持续一段时间。在本研究中,我们使用了基于原生动物分解[C]亮氨酸标记能力的急性试验,以及基于原生动物24小时运动能力的长期试验,来评估15种用两个相同基团酯化的常春藤皂苷元酯、5种带有1至3个琥珀酸残基的胆固醇和胆酸基衍生物的抗原生动物作用及其稳定性。常春藤皂苷元衍生物的急性抗原生动物作用比胆固醇和胆酸衍生物更明显。常春藤皂苷元、胆固醇和胆酸衍生物结构的修饰导致化合物在急性作用和稳定性方面具有不同的生物活性,尽管那些对原生动物毒性高的化合物并不总是随时间最稳定的。大多数常春藤皂苷元酯,特别是常春藤皂苷元琥珀酸酯(TSB24)、常春藤皂苷元甜菜碱二氯化物(TSB37)和常春藤皂苷元己二酸酯(TSB47)对瘤胃原生动物有持续作用,使发酵模式向更高的丙酸和更低的丁酸转变。这些化学修饰的三萜类化合物有可能作为有效的除虫剂用于反刍动物日粮中,最终提高氮利用率、减少甲烷排放并提高动物生产性能。现在需要进一步试验或在长期瘤胃模拟器中进行试验以证实所呈现的观察结果。