微量元素来源和植酸酶补充剂对肉鸡钙前植酸降解和矿物质消化率、骨矿化和组织基因表达的影响

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC
ACS Applied Electronic Materials Pub Date : 2024-11-01 Epub Date: 2024-02-08 DOI:10.1007/s12011-024-04076-w
Hanna Philippi, Vera Sommerfeld, Alessandra Monteiro, Markus Rodehutscord, Oluyinka A Olukosi
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引用次数: 0

摘要

本研究的目的是确定不添加植酸酶和添加植酸酶的饲料中不同来源的锌、锰和铜如何影响肉鸡前肌醇六磷酸(InsP6)分解为肌醇(MI)、前P消化率、骨骼矿化以及空肠中矿物质转运体的表达。共有 896 只雄性肉鸡(Cobb 500)被分配到 7 种日粮中,8 个重复栏(每层栏 16 只鸡)。实验日粮从第 0 天开始饲喂至第 28 天。日粮中不添加或添加植酸酶(0 或 750 FTU/kg),并添加三种不同的微量矿物质源(TMS:硫酸盐、氧化物或螯合物),分别含有 100 mg/kg Zn、100 mg/kg Mn 和 125 mg/kg Cu。前体 InsP6 消失和钙消化率受交互作用(植酸酶 × TMS:P ≤ 0.010)的影响。在未添加植酸酶的日粮中,饲喂螯合矿物质的鸟类的钙前InsP6消失率和钙消化率均高于饲喂硫酸盐或氧化物的鸟类(P≤ 0.001)。然而,在补充植酸酶的日粮中,没有观察到 TMS 之间的差异。外源植酸酶可增加回肠中的 MI 浓度,但不同 TMS 的浓度不同(植酸酶 × TMS:P ≤ 0.050)。补充植酸酶后,胫骨灰分浓度以及胫骨灰分中的锌和锰浓度均有所增加(P 0.050)。除了锌转运体 5(植酸酶 × TMS:P = 0.024)外,空肠中检测的矿物质转运体的基因表达不受日粮影响(P > 0.050)。总之,测试的 TMS 对肉鸡消化道的内源性植酸降解影响较小。然而,在本研究的条件下,在添加植酸酶的日粮中,TMS 的选择与植酸降解无关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Impact of Trace Mineral Source and Phytase Supplementation on Prececal Phytate Degradation and Mineral Digestibility, Bone Mineralization, and Tissue Gene Expression in Broiler Chickens.

The objective of this study was to determine how different sources of Zn, Mn, and Cu in the feed without and with phytase affect prececal myo-inositol hexakisphosphate (InsP6) breakdown to myo-inositol (MI), prececal P digestibility, bone mineralization, and expression of mineral transporters in the jejunum of broiler chickens. A total of 896 male broiler chicks (Cobb 500) were distributed to 7 diets with 8 replicate pens (16 birds per floor pen). Experimental diets were fed from day 0 to 28. Diets were without or with phytase supplementation (0 or 750 FTU/kg) and were supplemented with three different trace mineral sources (TMS: sulfates, oxides, or chelates) containing 100 mg/kg Zn, 100 mg/kg Mn, and 125 mg/kg Cu. Prececal InsP6 disappearance and P digestibility were affected by interaction (phytase × TMS: P ≤ 0.010). In diets without phytase supplementation, prececal InsP6 disappearance and P digestibility were greater (P ≤ 0.001) in birds fed chelated minerals than in birds fed sulfates or oxides. However, no differences were observed between TMS in diets with phytase supplementation. Ileal MI concentration was increased by exogenous phytase but differed depending on TMS (phytase × TMS: P ≤ 0.050). Tibia ash concentration as well as Zn and Mn concentration in tibia ash were increased by phytase supplementation (P < 0.010), but the Cu concentration in tibia ash was not (P > 0.050). Gene expression of the assayed mineral transporters in the jejunum was not affected by diet (P > 0.050), except for Zn transporter 5 (phytase × TMS: P = 0.024). In conclusion, the tested TMS had minor effects on endogenous phytate degradation in the digestive tract of broiler chickens. However, in phytase-supplemented diets, the choice of TMS was not relevant to phytate degradation under the conditions of this study.

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