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 inJournal of periodontal research Vol. 58; no. 5; pp. 1006 - 1019
Main Authors Moreira, André L. G., Silva, Giselle A., Silva, Pedro H. F., Salvador, Sérgio L., Vicente, Raphael M., Ferreira, Graziele C., Tanus‐Santos, Jose E., Mayer, Marcia P. A., Ishikawa, Karin H., de Souza, Sérgio Luís Scombatti, Furlaneto, Flávia A. C., Messora, Michel R.
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LanguageEnglish
Published United States Wiley Subscription Services, Inc 01.10.2023
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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.
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.
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  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
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  givenname: Pedro H. F.
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  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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  givenname: Sérgio L.
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  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
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  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
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  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
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  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
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  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
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  givenname: Sérgio Luís Scombatti
  surname: de Souza
  fullname: de Souza, Sérgio Luís Scombatti
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  givenname: Flávia A. C.
  surname: Furlaneto
  fullname: Furlaneto, Flávia A. C.
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  givenname: Michel R.
  orcidid: 0000-0001-8485-9645
  surname: Messora
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  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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Keywords Bifidobacterium lactis
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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
URI https://www.ncbi.nlm.nih.gov/pubmed/37482954
https://www.proquest.com/docview/2862036042
https://www.proquest.com/docview/2841401481
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