Effects of artificial sweeteners on feed palatability and performance in weaned pigs

Author:

Lee Chang Hee12,Yun Won12,Lee Ji Hwan12,Kwak Woo Gi12,Oh Han Jin12,An Ji Seon12,Liu Shu Dong12,Cho Jin Ho12

Affiliation:

1. Division of Food and Animal Sciences, Chungbuk National University, Cheongju 28644, South Korea

2. Division of Food and Animal Sciences, Chungbuk National University, Cheongju 28644, South Korea.

Abstract

In experiment 1, a total of 30 weaning pigs were allotted to three dietary treatments to check the palatability of the dietary feed. Diet treatments were as follows: reference diets = basal diets + 0.05% saccharin (50% Saccharin-natrium), TRT1 = 0.03% saccharin–neotame mix (50% Saccharine-natrium + 2% Neotame), TRT2 = 0.02% neotame (10% Neotame), and TRT3 = 0.02% saccharin–neotame mix (10% Saccharine-natrium + 10% Neotame). TRT2 group was significantly higher than other treatments in palatability (P < 0.05). In experiment 2, a total of 52 weaning pigs were allotted to four dietary treatments. In the average daily gain and average daily feed intake over 1 wk, the TRT2 group was significantly higher than the TRT1 and TRT3 groups (P < 0.05). The concentration of triglyceride in the blood was highest in the TRT1 treated group and the lowest in the TRT2 group (P < 0.05). The Lactobacillus was significantly higher in the TRT2 and TRT3 treatments compared with 0.05% saccharin (50% Saccharine-natrium) (P < 0.05). There was no significant difference in the number of Escherichia coli (P < 0.05). In conclusion, diets supplemented with neotame could improve palatability, and artificial sweeteners can affect nutrient digestibility, blood characteristic, and fecal microbiota.

Publisher

Canadian Science Publishing

Subject

Animal Science and Zoology,Food Animals

Reference44 articles.

1. Association of Official Analytical Chemists (AOAC). 2007. Official method of analysis. 18th ed. AOAC, Washington, DC, USA.

2. The artificial sweetener acesulfame potassium affects the gut microbiome and body weight gain in CD-1 mice

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