Abstract

Simple SummarySaccharin sodium (SS) is one of the commonly used artificial sweeteners (AS) in the food industry, but the mechanisms mediating the physiological effects of sweeteners in the gut-brain axis is still unclear. The aim of this study was to explore the regulatory effect of SS on the microbiota-gut-hypothalamus axis on guinea pigs. We found that SS treatment may alter the growth and glucose metabolism of guinea pigs by activating sweet receptor signaling in the gut and growth hormone-releasing peptide (GHRP) hormone secretion. Besides, SS treatment increased the abundance of Firmicutes and Lactobacillasceae-Lactobacillus in the ileum, and subsequently increased levels of lactic acid and short-chain fatty acids (SCFAs). Adding 1.5 mM SS to drinking water alters the growth of guinea pigs by regulating the microbiota-hypothalamus-gut axis. This conclusion has theoretical implications for the comprehensive assessment of the biological effects of appropriate SS in the food industry.The effects of saccharin, as a type of sweetener additive, on the metabolism and development of mammals are still controversial. Our previous research revealed that saccharin sodium (SS) promoted the feed intake and growth of guinea pigs. In this experiment, we used the guinea pig model to study the physiological effect of SS in the microbiota-gut-hypothalamus axis. Adding 1.5 mM SS to drinking water increased the serum level of glucose, followed by the improvement in the morphology and barrier function of the ileal villus, such as SS supplementation which increased the villus height and villus height/crypt depth ratio. Saccharin sodium (SS) treatment activated the sweet receptor signaling in the ileum and altered GHRP hormone secretion. In the hypothalamus of SS and control (CN) group, RNA-seq identified 1370 differently expressed genes (796 upregulated, 574 downregulated), enriching into the taste signaling transduction, and neuroactive ligand–receptor interaction. LEfSe analysis suggested that Lactobacillaceae-Lactobacillus was the microbe with significantly increased abundance of ileum microorganisms in the SS-treated group, while Brevinema-Andersonii and Erysipelotrichaceae-Ilebacterium were the microbes with significantly increased abundance of the control. Furthermore, SS treatment significantly enhanced the functions of chemoheterotrophy and fermentation of ileal microflora compared to the CN group. Accordingly, SS treatment increased levels of lactic acid and short-chain fatty acids (acetic acid, propionic acid and N-valeric acid) in the ileal digesta. In summary, drinking water with 1.5 mM SS activated sweet receptor signaling in the gut and altered GHRP hormone secretion, followed by the taste signaling transduction in the hypothalamus.

Highlights

  • Artificial sweeteners (AS) are widely used in food products and soft drinks

  • We aim to explore the regulatory effect of saccharin sodium (SS) on the microbiota-gut-hypothalamus axis, which can provide a theoretical basis for studying the effect of AS on adolescent development

  • The gastrointestinal tract participates in brain–gut interactions through brain–gut peptides, mainly including growth hormone-releasing peptide (GHRP), glucagonlike peptide 1 (GLP-1), cholecystokinin (CCK), peptide-YY (PYY)

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Summary

Introduction

Artificial sweeteners (AS) are widely used in food products and soft drinks. Saccharin has good hydrolysis and PH stability, which can be completely absorbed and quickly metabolized [1]. Many researchers insist that AS ingestion stimulates hunger and increases food intake via activating sweet taste receptors in the small intestine [4,5]. The importance of nutrient-induced brain-gut signaling in the regulation of animal metabolism and food intake has become increasingly obvious. Gut microflora influences intestinal function, and plays an important role in regulating brain-gut axis signals [6]. Short-chain fatty acids (SCFAs), deriving from bacteria-dependent hydrolysis of fibers, are essential to intestinal epithelial cells, which can modulate their proliferation and differentiation, to influence gut motility and to strengthen the gut barrier functions as well as host metabolism [8]. Exploring the regulatory effects of AS on mammalian growth and metabolism requires comprehensive consideration from the perspective of the microbiota-gut-brain axis. We aim to explore the regulatory effect of saccharin sodium (SS) on the microbiota-gut-hypothalamus axis, which can provide a theoretical basis for studying the effect of AS on adolescent development

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