2017
DOI: 10.1016/j.anifeedsci.2016.11.013
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Effect of Silybum marianum fruit constituents on the health status of rabbits in repeated 42‐day fattening experiment

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Cited by 18 publications
(14 citation statements)
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“…Our local population showed a similar average daily gain than other local populations [ 24 , 29 ]. However, the average daily gain was 19% higher in the synthetic line, but it was still lower than gains of different reported in other lines such as Hyla line (−16%) [ 30 ], New Zealand rabbits (−6%) [ 31 ], and V line (−11%) [ 28 ]. On the other side, although daily feed intake was similar in both groups, feed ratio conversion was better in the synthetic line (3.92) than the local population (4.81) due to a better feed efficiency in this line [ 23 ].…”
Section: Discussioncontrasting
confidence: 53%
“…Our local population showed a similar average daily gain than other local populations [ 24 , 29 ]. However, the average daily gain was 19% higher in the synthetic line, but it was still lower than gains of different reported in other lines such as Hyla line (−16%) [ 30 ], New Zealand rabbits (−6%) [ 31 ], and V line (−11%) [ 28 ]. On the other side, although daily feed intake was similar in both groups, feed ratio conversion was better in the synthetic line (3.92) than the local population (4.81) due to a better feed efficiency in this line [ 23 ].…”
Section: Discussioncontrasting
confidence: 53%
“…It is believed that silymarin is mainly effective due to its anti-inflammatory and antioxidant effects, thereby stimulating hepatocyte regeneration [ 36 ]. For example, Kosina et al [ 37 ] used milk thistle seed cakes in their experiment with rabbits containing 27% crude protein, 35% crude fiber, 10% fat, 6% starch and 4% of total flavonolignans (at 92% dry matter). This seed cakes contained more crude protein, more crude fiber and more total flavonolignans compared to ours.…”
Section: The Seed Cakes As a Feedmentioning
confidence: 99%
“…Flavonolignans determination was performed according to Kosina et al (2017). 1 g of homogenized sample was combined with 10 mL of the extraction mixture (H 2 O:ACN:MeOH in the ratio 10:50:40, v / v / v); the sample in the presence of the extraction mixture was vortexed for 1 min, sonicated in an ultrasonic bath for 30 min and then macerated for 12 h at room temperature in the dark.…”
Section: Determination Of Amino Acids Flavonolignans and Mycotoxin Cmentioning
confidence: 99%