Sucralose and stevia consumption leads to intergenerational alterations in body weight and intestinal expression of histone deacetylase 3

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC
Francisca Concha Celume Ph.D. , Francisco Pérez-Bravo Ph.D. , Martin Gotteland Ph.D.
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引用次数: 0

Abstract

Objectives

It is unclear whether parental consumption of non-nutritive sweetener (NNS) can affect subsequent generations. The aim of this study was to determine whether chronic parental consumption of sucralose and stevia in mice affects body weight gain and liver and intestinal expression of histone deacetylase 3 (Hdac3) in these animals and in the subsequent first filial (F1) and second filial (F2) generations.

Methods

Male and female mice (n = 47) were divided into three groups to receive water alone or supplemented with sucralose (0.1 mg/mL) or stevia (0.1 mg/mL) for 16 wk (parental [F0] generation). F0 mice were bred to produce the F1 generation; then, F1 mice were bred to produce the F2 generation. F1 and F2 animals did not receive NNSs. After euthanasia, hepatic and intestinal expression of Hdac3 was determined by quantitative reverse transcription polymerase chain reaction.

Results

Body weight gain did not differ between the three groups in the F0 generation, but it was greater in the F1 sucralose and stevia groups than in the control group. Consumption of both NNSs in the F0 generation was associated with lower Hdac3 expression in the liver and higher in the intestine. Hepatic Hdac3 expression was normalized to the control values in the F1 and F2 animals of the sucralose and stevia groups. Intestinal expression was still higher in the F1 generations of the sucralose and stevia groups but was partially normalized in the F2 generation of these groups, compared with control.

Conclusions

NNS consumption differentially affects hepatic and intestinal Hdac3 expression. Changes in hepatic expression are not transmitted to the F1 and F2 generations whereas those in intestinal expression are enhanced in the F1 and attenuated in the F2 generations.

Abstract Image

食用三氯蔗糖和甜菊糖会导致体重和肠道组蛋白去乙酰化酶-3表达的代际变化
目的 目前尚不清楚亲代食用非营养性甜味剂(NNS)是否会影响后代。本研究旨在确定小鼠亲代长期食用三氯蔗糖和甜菊糖是否会影响其体重增加以及肝脏和肠道组蛋白去乙酰化酶 3 (Hdac3) 的表达,并影响其后的第一代孝子 (F1) 和第二代孝子 (F2)。方法将雄性和雌性小鼠(n = 47)分为三组,分别在16周内(亲代[F0])单独饮水或补充蔗糖素(0.1 mg/mL)或甜菊糖(0.1 mg/mL)。F0 小鼠经繁殖产生 F1 代;然后,F1 小鼠经繁殖产生 F2 代。F1 和 F2 动物不接受 NNS。安乐死后,通过逆转录聚合酶链式反应定量测定肝脏和肠道中 Hdac3 的表达。F0 代食用这两种 NNS 与肝脏中较低的 Hdac3 表达量和肠道中较高的 Hdac3 表达量有关。蔗糖素(三氯蔗糖)组和甜叶菊组的 F1 和 F2 动物的肝脏 Hdac3 表达与对照组的值基本一致。与对照组相比,三氯蔗糖和甜菊糖组 F1 代动物的肠道表达量仍然较高,但这些组的 F2 代动物的肠道表达量已部分恢复正常。肝脏表达的变化不会传递到 F1 代和 F2 代,而肠道表达的变化在 F1 代中增强,在 F2 代中减弱。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
7.20
自引率
4.30%
发文量
567
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