Bifidobacterium animalis subspecies lactis HN019 can reduce the sequelae of experimental periodontitis in rats modulating intestinal parameters, expression of lipogenic genes, and levels of hepatic steatosis
To determine whether Bifidobacterium animalis subspecies lactis HN019 (B. lactis HN019) can reduce the sequelae of experimental periodontitis (EP) in rats modulating systemic parameters. This study evaluated the effects of probiotic therapy (PROB) in the prevention of local and systemic damage resul...
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Published in | Journal of periodontal research Vol. 58; no. 5; pp. 1006 - 1019 |
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Abstract | To determine whether Bifidobacterium animalis subspecies lactis HN019 (B. lactis HN019) can reduce the sequelae of experimental periodontitis (EP) in rats modulating systemic parameters.
This study evaluated the effects of probiotic therapy (PROB) in the prevention of local and systemic damage resulting from EP.
Forty-eight rats were allocated into four groups: C (control), PROB, EP, and EP-PROB. PROB (1 × 10
CFU/mL) administration lasted 8 weeks and PE was induced on the 7th week by placing ligature on the animals' lower first molars. All animals were euthanized in the 9th week of the experiment. Biomolecular analyses, RT-PCR, and histomorphometric analyses were performed. The data obtained were analyzed statistically (ANOVA, Tukey, p < .05).
The EP group had higher dyslipidemia when compared to the C group, as well as higher levels of insulin resistance, proteinuria levels, percentages of systolic blood pressure, percentage of fatty hepatocytes in the liver, and expression of adipokines was up-regulated (LEPR, NAMPT, and FABP4). All these parameters (except insulin resistance, systolic blood pressure, LEPR and FABP4 gene expression) were reduced in the EP-PROB group when compared to the EP group. The EP group had lower villus height and crypt depth, as well as a greater reduction in Bacteroidetes and a greater increase in Firmicutes when compared to the EP-PROB group. Greater alveolar bone loss was observed in the EP group when compared to the EP-PROB group.
Bifidobacterium lactis HN019 can reduce the sequelae of EP in rats modulating intestinal parameters, attenuating expression of lipogenic genes and hepatic steatosis. |
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AbstractList | To determine whether Bifidobacterium animalis subspecies lactis HN019 (B. lactis HN019) can reduce the sequelae of experimental periodontitis (EP) in rats modulating systemic parameters.
This study evaluated the effects of probiotic therapy (PROB) in the prevention of local and systemic damage resulting from EP.
Forty-eight rats were allocated into four groups: C (control), PROB, EP, and EP-PROB. PROB (1 × 10
CFU/mL) administration lasted 8 weeks and PE was induced on the 7th week by placing ligature on the animals' lower first molars. All animals were euthanized in the 9th week of the experiment. Biomolecular analyses, RT-PCR, and histomorphometric analyses were performed. The data obtained were analyzed statistically (ANOVA, Tukey, p < .05).
The EP group had higher dyslipidemia when compared to the C group, as well as higher levels of insulin resistance, proteinuria levels, percentages of systolic blood pressure, percentage of fatty hepatocytes in the liver, and expression of adipokines was up-regulated (LEPR, NAMPT, and FABP4). All these parameters (except insulin resistance, systolic blood pressure, LEPR and FABP4 gene expression) were reduced in the EP-PROB group when compared to the EP group. The EP group had lower villus height and crypt depth, as well as a greater reduction in Bacteroidetes and a greater increase in Firmicutes when compared to the EP-PROB group. Greater alveolar bone loss was observed in the EP group when compared to the EP-PROB group.
Bifidobacterium lactis HN019 can reduce the sequelae of EP in rats modulating intestinal parameters, attenuating expression of lipogenic genes and hepatic steatosis. To determine whether Bifidobacterium animalis subspecies lactis HN019 (B. lactis HN019) can reduce the sequelae of experimental periodontitis (EP) in rats modulating systemic parameters.OBJECTIVETo determine whether Bifidobacterium animalis subspecies lactis HN019 (B. lactis HN019) can reduce the sequelae of experimental periodontitis (EP) in rats modulating systemic parameters.This study evaluated the effects of probiotic therapy (PROB) in the prevention of local and systemic damage resulting from EP.BACKGROUNDThis study evaluated the effects of probiotic therapy (PROB) in the prevention of local and systemic damage resulting from EP.Forty-eight rats were allocated into four groups: C (control), PROB, EP, and EP-PROB. PROB (1 × 1010 CFU/mL) administration lasted 8 weeks and PE was induced on the 7th week by placing ligature on the animals' lower first molars. All animals were euthanized in the 9th week of the experiment. Biomolecular analyses, RT-PCR, and histomorphometric analyses were performed. The data obtained were analyzed statistically (ANOVA, Tukey, p < .05).METHODSForty-eight rats were allocated into four groups: C (control), PROB, EP, and EP-PROB. PROB (1 × 1010 CFU/mL) administration lasted 8 weeks and PE was induced on the 7th week by placing ligature on the animals' lower first molars. All animals were euthanized in the 9th week of the experiment. Biomolecular analyses, RT-PCR, and histomorphometric analyses were performed. The data obtained were analyzed statistically (ANOVA, Tukey, p < .05).The EP group had higher dyslipidemia when compared to the C group, as well as higher levels of insulin resistance, proteinuria levels, percentages of systolic blood pressure, percentage of fatty hepatocytes in the liver, and expression of adipokines was up-regulated (LEPR, NAMPT, and FABP4). All these parameters (except insulin resistance, systolic blood pressure, LEPR and FABP4 gene expression) were reduced in the EP-PROB group when compared to the EP group. The EP group had lower villus height and crypt depth, as well as a greater reduction in Bacteroidetes and a greater increase in Firmicutes when compared to the EP-PROB group. Greater alveolar bone loss was observed in the EP group when compared to the EP-PROB group.RESULTSThe EP group had higher dyslipidemia when compared to the C group, as well as higher levels of insulin resistance, proteinuria levels, percentages of systolic blood pressure, percentage of fatty hepatocytes in the liver, and expression of adipokines was up-regulated (LEPR, NAMPT, and FABP4). All these parameters (except insulin resistance, systolic blood pressure, LEPR and FABP4 gene expression) were reduced in the EP-PROB group when compared to the EP group. The EP group had lower villus height and crypt depth, as well as a greater reduction in Bacteroidetes and a greater increase in Firmicutes when compared to the EP-PROB group. Greater alveolar bone loss was observed in the EP group when compared to the EP-PROB group.Bifidobacterium lactis HN019 can reduce the sequelae of EP in rats modulating intestinal parameters, attenuating expression of lipogenic genes and hepatic steatosis.CONCLUSIONBifidobacterium lactis HN019 can reduce the sequelae of EP in rats modulating intestinal parameters, attenuating expression of lipogenic genes and hepatic steatosis. ObjectiveTo determine whether Bifidobacterium animalis subspecies lactis HN019 (B. lactis HN019) can reduce the sequelae of experimental periodontitis (EP) in rats modulating systemic parameters.BackgroundThis study evaluated the effects of probiotic therapy (PROB) in the prevention of local and systemic damage resulting from EP.MethodsForty‐eight rats were allocated into four groups: C (control), PROB, EP, and EP‐PROB. PROB (1 × 1010 CFU/mL) administration lasted 8 weeks and PE was induced on the 7th week by placing ligature on the animals' lower first molars. All animals were euthanized in the 9th week of the experiment. Biomolecular analyses, RT‐PCR, and histomorphometric analyses were performed. The data obtained were analyzed statistically (ANOVA, Tukey, p < .05).ResultsThe EP group had higher dyslipidemia when compared to the C group, as well as higher levels of insulin resistance, proteinuria levels, percentages of systolic blood pressure, percentage of fatty hepatocytes in the liver, and expression of adipokines was up‐regulated (LEPR, NAMPT, and FABP4). All these parameters (except insulin resistance, systolic blood pressure, LEPR and FABP4 gene expression) were reduced in the EP‐PROB group when compared to the EP group. The EP group had lower villus height and crypt depth, as well as a greater reduction in Bacteroidetes and a greater increase in Firmicutes when compared to the EP‐PROB group. Greater alveolar bone loss was observed in the EP group when compared to the EP‐PROB group.ConclusionBifidobacterium lactis HN019 can reduce the sequelae of EP in rats modulating intestinal parameters, attenuating expression of lipogenic genes and hepatic steatosis. |
Author | Vicente, Raphael M. Mayer, Marcia P. A. de Souza, Sérgio Luís Scombatti Salvador, Sérgio L. Tanus‐Santos, Jose E. Ishikawa, Karin H. Messora, Michel R. Ferreira, Graziele C. Silva, Pedro H. F. Furlaneto, Flávia A. C. Moreira, André L. G. Silva, Giselle A. |
Author_xml | – sequence: 1 givenname: André L. G. surname: Moreira fullname: Moreira, André L. G. organization: Department of Oral and Maxillofacial Surgery and Periodontology, School of Dentistry of Ribeirão Preto University of São Paulo – USP Ribeirão Preto, São Paulo Brazil – sequence: 2 givenname: Giselle A. surname: Silva fullname: Silva, Giselle A. organization: Department of Oral and Maxillofacial Surgery and Periodontology, School of Dentistry of Ribeirão Preto University of São Paulo – USP Ribeirão Preto, São Paulo Brazil – sequence: 3 givenname: Pedro H. F. orcidid: 0000-0002-7583-7046 surname: Silva fullname: Silva, Pedro H. F. organization: Department of Oral and Maxillofacial Surgery and Periodontology, School of Dentistry of Ribeirão Preto University of São Paulo – USP Ribeirão Preto, São Paulo Brazil – sequence: 4 givenname: Sérgio L. orcidid: 0000-0002-4867-7294 surname: Salvador fullname: Salvador, Sérgio L. organization: Department of Clinical Analyses, School of Pharmaceutical Sciences of Ribeirão Preto University of São Paulo – USP Ribeirão Preto, São Paulo Brazil – sequence: 5 givenname: Raphael M. surname: Vicente fullname: Vicente, Raphael M. organization: Department of Oral and Maxillofacial Surgery and Periodontology, School of Dentistry of Ribeirão Preto University of São Paulo – USP Ribeirão Preto, São Paulo Brazil – sequence: 6 givenname: Graziele C. surname: Ferreira fullname: Ferreira, Graziele C. organization: Department of Pharmacology, Ribeirão Preto Medical School University of São Paulo – USP Ribeirão Preto, São Paulo Brazil – sequence: 7 givenname: Jose E. surname: Tanus‐Santos fullname: Tanus‐Santos, Jose E. organization: Department of Pharmacology, Ribeirão Preto Medical School University of São Paulo – USP Ribeirão Preto, São Paulo Brazil – sequence: 8 givenname: Marcia P. A. orcidid: 0000-0002-5910-8433 surname: Mayer fullname: Mayer, Marcia P. A. organization: Department of Microbiology, Institute of Biomedical Sciences University of São Paulo São Paulo Brazil – sequence: 9 givenname: Karin H. orcidid: 0000-0003-3926-3572 surname: Ishikawa fullname: Ishikawa, Karin H. organization: Department of Microbiology, Institute of Biomedical Sciences University of São Paulo São Paulo Brazil – sequence: 10 givenname: Sérgio Luís Scombatti surname: de Souza fullname: de Souza, Sérgio Luís Scombatti organization: Department of Oral and Maxillofacial Surgery and Periodontology, School of Dentistry of Ribeirão Preto University of São Paulo – USP Ribeirão Preto, São Paulo Brazil – sequence: 11 givenname: Flávia A. C. surname: Furlaneto fullname: Furlaneto, Flávia A. C. organization: Department of Oral and Maxillofacial Surgery and Periodontology, School of Dentistry of Ribeirão Preto University of São Paulo – USP Ribeirão Preto, São Paulo Brazil – sequence: 12 givenname: Michel R. orcidid: 0000-0001-8485-9645 surname: Messora fullname: Messora, Michel R. organization: Department of Oral and Maxillofacial Surgery and Periodontology, School of Dentistry of Ribeirão Preto University of São Paulo – USP Ribeirão Preto, São Paulo Brazil |
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Snippet | To determine whether Bifidobacterium animalis subspecies lactis HN019 (B. lactis HN019) can reduce the sequelae of experimental periodontitis (EP) in rats... ObjectiveTo determine whether Bifidobacterium animalis subspecies lactis HN019 (B. lactis HN019) can reduce the sequelae of experimental periodontitis (EP) in... |
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SubjectTerms | Alveolar bone Bifidobacterium animalis Blood pressure Bone loss Complications Dyslipidemia Fatty liver Gene expression Gum disease Hepatocytes Insulin resistance Intestine Molars Periodontitis Probiotics Proteinuria Steatosis Villus |
Title | Bifidobacterium animalis subspecies lactis HN019 can reduce the sequelae of experimental periodontitis in rats modulating intestinal parameters, expression of lipogenic genes, and levels of hepatic steatosis |
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