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日粮添加发酵艾蒿对肉鸡生长性能、屠宰性能和肉品质的影响。

Effects of dietary supplementation of fermented Artemisia argyi on growth performance, slaughter performance, and meat quality in broilers.

机构信息

College of Animal Science and Veterinary Medicine, Henan Institute of Science and Technology, Xinxiang 453003, Henan, China.

College of Life Science, Xinxiang University, Xinxiang 453003, Henan, China.

出版信息

Poult Sci. 2024 Apr;103(4):103545. doi: 10.1016/j.psj.2024.103545. Epub 2024 Feb 13.

DOI:10.1016/j.psj.2024.103545
PMID:38387294
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10899031/
Abstract

Artemisia argyi (AA) is promising as a potential feed additive. Microbial fermentation is beneficial to the degradation of cell walls and the better release of bioactive compounds of AA. However, there are few reports on the application of fermented AA as a feed additive for broilers. The present study intended to evaluate the application value of fermented AA as a feed additive for broilers by examining the effects of the dietary supplementation of Aspergillus niger-fermented AA and unfermented AA on growth performance, slaughter performance, and meat quality of brokers. A total of 360 newly hatched (1-day-old) broilers with similar body weight were randomly divided into the following 5 groups: basal diet group as control (C) group, basal diet +3% unfermented AA (E1) group, basal diet + 1% fermented AA (E2) group, basal diet + 3% fermented AA (E3) group, basal diet + 5% fermented AA (E4) group. Each group included 6 replicates with 12 broilers per replicate, and the feeding trail lasted for 48 d. Body weight and feed intake were recorded every 2 wk, and the feed gain ratio was calculated to assess growth performance. At 42 d, 6 broilers from each group were slaughtered, and the carcass traits were calculated. The results showed that compared with the control group, Aspergillus Niger could effectively destroy AA fiber, which contributed to better release of AA bioactive compounds. Moreover, dietary supplementation with AA could improve the growth performance of broilers (P < 0.05), and the effect of fermented AA was better than unfermented AA, especially 3% fermented AA. From 28 to 42 d, compared with the control group, the average daily gain of broilers in the group supplementation with 3% fermented AA was significantly increased (P < 0.05), and the feed-to-gain ratio was decreased (P < 0.05). At 42 d, the dressing percentage, half-eviscerated carcass percentage, eviscerated carcass percentage, and breast muscle percentage of broilers in the groups of 1, 3, and 5% fermented AA diets were significantly improved (P < 0.05), and the thigh muscle percentage of broilers in the group with 3% fermented AA diets was significantly improved (P < 0.05). Meanwhile, the meat quality of broilers in the group with fermented AA diets was also significantly improved. Birds in AA groups had higher a* value and lower shear force of breast muscle, especially the group supplementation with 3% fermented AA (P < 0.05). In conclusion, fermented AA has good application value as a potential feed additive for broilers, dietary supplementation of fermented AA can improve the production performance and meat quality of broiler chickens, of which 3% fermented AA is more effective.

摘要

艾草(AA)作为一种有潜力的饲料添加剂具有广阔的应用前景。微生物发酵有利于 AA 细胞壁的降解和生物活性化合物的更好释放。然而,关于发酵后的 AA 作为肉鸡饲料添加剂的应用报道较少。本研究旨在通过考察黑曲霉发酵 AA 和未发酵 AA 对肉鸡生长性能、屠宰性能和肉质的影响,评估发酵 AA 作为肉鸡饲料添加剂的应用价值。

将 360 只(1 日龄)体重相近的新孵化肉鸡随机分为以下 5 组:基础日粮组(对照组,C 组)、基础日粮+3%未发酵 AA(E1 组)、基础日粮+1%发酵 AA(E2 组)、基础日粮+3%发酵 AA(E3 组)、基础日粮+5%发酵 AA(E4 组)。每组 6 个重复,每个重复 12 只肉鸡,饲养试验持续 48 天。每 2 周记录一次体重和采食量,计算饲料增重比,以评估生长性能。42 日龄时,每组随机抽取 6 只肉鸡屠宰,计算屠宰性能。

结果表明,与对照组相比,黑曲霉能有效破坏 AA 纤维,有助于 AA 生物活性化合物更好地释放。此外,日粮添加 AA 可提高肉鸡的生长性能(P<0.05),且发酵 AA 的效果优于未发酵 AA,尤其是 3%发酵 AA。从 28 日龄到 42 日龄,与对照组相比,添加 3%发酵 AA 的肉鸡平均日增重显著增加(P<0.05),料重比降低(P<0.05)。42 日龄时,1%、3%和 5%发酵 AA 日粮组肉鸡的屠宰率、半净膛率、全净膛率和胸肌率均显著提高(P<0.05),3%发酵 AA 日粮组肉鸡的腿肌率显著提高(P<0.05)。同时,发酵 AA 日粮组肉鸡的肉质也得到了显著改善。AA 组鸡的 a*值较高,胸肌剪切力较低,尤其是添加 3%发酵 AA 的组(P<0.05)。

综上所述,发酵 AA 作为一种有潜力的肉鸡饲料添加剂具有良好的应用价值,日粮添加发酵 AA 可提高肉鸡的生产性能和肉质,其中 3%发酵 AA 效果更显著。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc7d/10899031/b2d94438aa90/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc7d/10899031/8b5581bf11a5/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc7d/10899031/8f757f068afa/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc7d/10899031/b2d94438aa90/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc7d/10899031/8b5581bf11a5/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc7d/10899031/8f757f068afa/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc7d/10899031/b2d94438aa90/gr3.jpg

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