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日粮可消化钙浓度对体重11至22千克、采食不同可消化磷浓度日粮的仔猪生长性能、骨矿化、血浆钙以及肠道钙吸收相关基因丰度的影响。

Influence of the concentration of dietary digestible calcium on growth performance, bone mineralization, plasma calcium, and abundance of genes involved in intestinal absorption of calcium in pigs from 11 to 22 kg fed diets with different concentrations of digestible phosphorus.

作者信息

Lagos L Vanessa, Lee Su A, Fondevila Guillermo, Walk Carrie L, Murphy Michael R, Loor Juan J, Stein Hans H

机构信息

1Division of Nutritional Sciences, University of Illinois, Urbana, IL 61801 USA.

2Department of Animal Sciences, University of Illinois, Urbana, IL 61801 USA.

出版信息

J Anim Sci Biotechnol. 2019 May 28;10:47. doi: 10.1186/s40104-019-0349-2. eCollection 2019.

DOI:10.1186/s40104-019-0349-2
PMID:31149337
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6537374/
Abstract

BACKGROUND

A 21-day experiment was conducted to test the hypothesis that Ca requirements to maximize growth performance expressed as the standardized total tract digestible (STTD) Ca to STTD P ratio is less than 1.40:1. The second hypothesis was that increasing dietary Ca increases plasma Ca concentration and downregulates abundance of genes related to Ca absorption (, , and ) in the duodenum, and tight junction proteins (, , and ) in the duodenum and ileum.

METHODS

Twenty corn-soybean meal diets were formulated using a 4 × 5 factorial design with diets containing 0.16%, 0.33%, 0.42%, or 0.50% STTD P, and 0.14%, 0.29%, 0.44%, 0.59%, or 0.74% STTD Ca. Six hundred and forty pigs (initial weight: 11.1 ± 1.4 kg) were allotted to 20 diets and 5 blocks in a randomized complete block design. On day 21, weights of pigs and feed left in feeders were recorded and blood, duodenal tissue, ileal mucosa, and the right femur were collected from 1 pig per pen. Abundance of mRNA was determined in duodenal and ileal tissue via quantitative RT-PCR. Data were analyzed using a response surface model.

RESULTS

The predicted maximum ADG (614 g), G:F (0.65), and bone ash (11.68 g) was obtained at STTD Ca:STTD P ratios of 1.39:1, 1.25:1, and 1.66:1, respectively, when STTD P was provided at the requirement (0.33%). If dietary STTD P was below the requirement, increasing dietary Ca resulted in reduced ( < 0.05) ADG and G:F. However, if dietary STTD P was above the requirement, negative effects ( < 0.05) on ADG and G:F of increasing STTD Ca were observed only if dietary STTD Ca exceeded 0.6%. Plasma Ca concentration was positively affected by STTD Ca over the range studied (quadratic,  < 0.01) and negatively affected by increasing STTD P (linear,  < 0.01). There was a linear negative effect ( < 0.05) of STTD Ca on the abundance of , , , and in duodenum, and and in ileum.

CONCLUSIONS

The STTD Ca:STTD P ratio needed to maximize growth performance of 11- to 25-kg pigs is less than 1.40:1, if P is at the estimated requirement. Increasing dietary Ca reduces transcellular absorption of Ca and increases paracellular absorption of Ca.

摘要

背景

进行了一项为期21天的试验,以验证以下假设:以标准化全肠道可消化(STTD)钙与STTD磷的比例表示,使生长性能最大化的钙需求量小于1.40:1。第二个假设是,增加日粮钙会提高血浆钙浓度,并下调十二指肠中与钙吸收相关基因(、和)以及十二指肠和回肠中紧密连接蛋白(、和)的丰度。

方法

采用4×5析因设计配制20种玉米-豆粕型日粮,日粮中STTD磷含量分别为0.16%、0.33%、0.42%或0.50%,STTD钙含量分别为0.14%、0.29%、0.44%、0.59%或0.74%。640头猪(初始体重:11.1±1.4 kg)按照随机完全区组设计分配到20种日粮和5个区组中。在第21天,记录猪的体重和料槽中剩余的饲料量,并从每栏中选取1头猪采集血液、十二指肠组织、回肠黏膜和右侧股骨。通过定量RT-PCR测定十二指肠和回肠组织中mRNA的丰度。数据采用响应面模型进行分析。

结果

当按照需求量(0.33%)提供STTD磷时,预测的最大日增重(614 g)、料重比(0.65)和骨灰含量(11.68 g)分别在STTD钙与STTD磷比例为1.39:1、1.25:1和1.66:1时获得。如果日粮STTD磷低于需求量,增加日粮钙会导致日增重和料重比降低(<0.05)。然而,如果日粮STTD磷高于需求量,仅当日粮STTD钙超过0.6%时,才会观察到增加STTD钙对日增重和料重比产生负面影响(<0.05)。在所研究的范围内,血浆钙浓度受到STTD钙的正向影响(二次效应,<0.01),并受到STTD磷增加的负向影响(线性效应,<0.01)。STTD钙对十二指肠中、、、以及回肠中和的丰度有线性负向影响(<0.05)。

结论

如果磷含量为估计需求量,使11至25千克猪生长性能最大化所需的STTD钙与STTD磷比例小于1.40:1。增加日粮钙会减少钙的跨细胞吸收,并增加钙的细胞旁吸收。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/15c7/6537374/25e175ec37ef/40104_2019_349_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/15c7/6537374/8e1cf9ea4cca/40104_2019_349_Fig1_HTML.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/15c7/6537374/c6a269eff3e7/40104_2019_349_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/15c7/6537374/d9083a3b053d/40104_2019_349_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/15c7/6537374/ac6b4a2c1ba2/40104_2019_349_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/15c7/6537374/25e175ec37ef/40104_2019_349_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/15c7/6537374/8e1cf9ea4cca/40104_2019_349_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/15c7/6537374/a994f72c2405/40104_2019_349_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/15c7/6537374/c6a269eff3e7/40104_2019_349_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/15c7/6537374/d9083a3b053d/40104_2019_349_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/15c7/6537374/ac6b4a2c1ba2/40104_2019_349_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/15c7/6537374/25e175ec37ef/40104_2019_349_Fig6_HTML.jpg

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