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Pulse probiotic administration induces repeated small intestinal Muc3 expression in rats.
Copyright policy )Upon ingestion, probiotics may act to protect the host through a number of protective mechanisms including modulation of genes involved in intestinal innate mucosal defense such as epithelial cell-derived mucin glycoproteins and inhibitor of apoptosis proteins. To determine the specificity of effect and sustainability of response in vivo, Lactobacillus plantarum 299v (Lp299v), Lactobacillus rhamnosus R0011 (LrR0011), and Bifidobacterium bifidum R0071 (BbR0071) were added repeatedly or intermittently to the drinking water of Sprague-Dawley rats. After killing the rats via CO2 suffocation, Muc2, Muc3, neuronal apoptosis inhibitor protein (NAIP), human inhibitor of apoptosis protein 1/cellular inhibitor of apoptosis 2 (HIAP1/cIAP2), and human inhibitor of apoptosis protein 2/cellular inhibitor of apoptosis 1 (HIAP2/cIAP1) mRNA and protein levels were analyzed via RT-PCR and immunohistochemistry. Live Lp299v, BbR0071, and LrR0011 increased Muc3 protein and mRNA expression in jejunum and ileum. Heat-killed and a nonadherent derivative of Lp299v failed to induce Muc3 expression. Lp299v did induce expression of HIAP2/cIAP1 and NAIP expression. Muc3 mucin expression was elevated for 5 d after oral administration of Lp299v; however, this effect was not sustained despite ongoing daily ingestion of a probiotic. Intermittent pulse ingestion of probiotics, however, was found to repeatedly increase Muc3 expression. We conclude that selected probiotics can induce protective genes of mucosal intestinal epithelial cells, an effect that is reproducible with pulse probiotic administration.
Microsoft Academic Graph classification: Inhibitor of apoptosis Small intestine medicine.anatomical_structure medicine Bifidobacterium bifidum ved/biology.organism_classification_rank.species ved/biology Lactobacillus rhamnosus biology.organism_classification biology Mucin Gene expression Oral administration Immunology Pharmacology NAIP
Animals, Bifidobacterium, Gene Expression, Humans, Intestine, Small, Lactobacillus plantarum, Lacticaseibacillus rhamnosus, Male, Mucin-2, Mucin-3, Probiotics, Rats, Rats, Sprague-Dawley, Up-Regulation, Pediatrics, Perinatology and Child Health
Animals, Bifidobacterium, Gene Expression, Humans, Intestine, Small, Lactobacillus plantarum, Lacticaseibacillus rhamnosus, Male, Mucin-2, Mucin-3, Probiotics, Rats, Rats, Sprague-Dawley, Up-Regulation, Pediatrics, Perinatology and Child Health
Microsoft Academic Graph classification: Inhibitor of apoptosis Small intestine medicine.anatomical_structure medicine Bifidobacterium bifidum ved/biology.organism_classification_rank.species ved/biology Lactobacillus rhamnosus biology.organism_classification biology Mucin Gene expression Oral administration Immunology Pharmacology NAIP
- University of Ottawa Canada
- Children's Hospital of Eastern Ontario Canada
- Lund University Sweden
- Malmö University Sweden
- University of Ottawa Canada
- Children's Hospital of Eastern Ontario Canada
- Lund University Sweden
- Malmö University Sweden
Upon ingestion, probiotics may act to protect the host through a number of protective mechanisms including modulation of genes involved in intestinal innate mucosal defense such as epithelial cell-derived mucin glycoproteins and inhibitor of apoptosis proteins. To determine the specificity of effect and sustainability of response in vivo, Lactobacillus plantarum 299v (Lp299v), Lactobacillus rhamnosus R0011 (LrR0011), and Bifidobacterium bifidum R0071 (BbR0071) were added repeatedly or intermittently to the drinking water of Sprague-Dawley rats. After killing the rats via CO2 suffocation, Muc2, Muc3, neuronal apoptosis inhibitor protein (NAIP), human inhibitor of apoptosis protein 1/cellular inhibitor of apoptosis 2 (HIAP1/cIAP2), and human inhibitor of apoptosis protein 2/cellular inhibitor of apoptosis 1 (HIAP2/cIAP1) mRNA and protein levels were analyzed via RT-PCR and immunohistochemistry. Live Lp299v, BbR0071, and LrR0011 increased Muc3 protein and mRNA expression in jejunum and ileum. Heat-killed and a nonadherent derivative of Lp299v failed to induce Muc3 expression. Lp299v did induce expression of HIAP2/cIAP1 and NAIP expression. Muc3 mucin expression was elevated for 5 d after oral administration of Lp299v; however, this effect was not sustained despite ongoing daily ingestion of a probiotic. Intermittent pulse ingestion of probiotics, however, was found to repeatedly increase Muc3 expression. We conclude that selected probiotics can induce protective genes of mucosal intestinal epithelial cells, an effect that is reproducible with pulse probiotic administration.