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Campo DC | Valor | Idioma |
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dc.creator | Azzi, Diana Vilela | - |
dc.creator | Pereira, Andressa Naira de Jesus | - |
dc.creator | Silva, Viviam de Oliveira | - |
dc.creator | Foureaux, Renata de Carvalho | - |
dc.creator | Lima, Andressa Ribeiro Veiga | - |
dc.creator | Barducci, Robson Sfaciotti | - |
dc.creator | Albuquerque, Adriana Silva | - |
dc.creator | Reis, Gabriel Lasmar | - |
dc.creator | Oliveira, Raphael Ricon de | - |
dc.creator | Andrade, Eric Francelino | - |
dc.creator | Zangeronimo, Márcio Gilberto | - |
dc.creator | Chalfun Júnior, Antonio | - |
dc.creator | Pereira, Luciano José | - |
dc.date.accessioned | 2022-01-24T20:28:50Z | - |
dc.date.accessioned | 2023-06-27T19:57:04Z | - |
dc.date.available | 2022-01-24T20:28:50Z | - |
dc.date.available | 2023-06-27T19:57:04Z | - |
dc.date.issued | 2021-10 | - |
dc.identifier.citation | AZZI, D. V. et al. Dose-response effect of prebiotic ingestion (β-glucans isolated from Saccharomyces cerevisiae) in diabetic rats with periodontal disease. Diabetology & Metabolic Syndrome, [S. I.], v. 13, 2021. DOI: https://doi.org/10.1186/s13098-021-00729-1. | pt_BR |
dc.identifier.uri | http://repositorio.ufla.br/jspui/handle/1/57802 | - |
dc.description.abstract | Background: Periodontal disease is one of the most frequent comorbidities in diabetic patients and can contribute to poor blood glucose control. Objective: To evaluate the efects of ingesting diferent doses of beta-glucans (BG) isolated from Saccharomyces cer‑ evisiae on alveolar bone loss (ABL) and infammatory/metabolic parameters in normal and diabetic rats with ligatureinduced periodontal disease (PD). Design: Sixty male rats were assigned into two groups: non-diabetic or diabetic (i.p. 70 mg/kg streptozotocin) with PD. Then, groups were subdivided into fve subgroups according BG doses: 0 mg/Kg; 10 mg/Kg; 20 mg/Kg; 40 mg/Kg or 80 mg/Kg. Animals received BG for 28 days and ligatures were placed on lower frst molars during the last 14 days. Results: ABL of diabetic and non-diabetic animals receiving BG 40 mg/kg (1.33 ± 0.03 mm and 0.77 ± 0.07 mm, respectively) and 80 mg/kg (1.26 ± 0.07 mm and 0.78 ± 0.05 mm, respectively) doses was lower (p < 0.05) in com‑ parison to respective controls (1.59 ± 0.11 mm and 0.90 mm ±0.08). COX-2 (Control: 1.66 ± 0.12; 40 mg/kg: 1.13 ± 0.07; 80 mg/kg: 0.92 ± 0.18) and RANKL expressions (Control: 1.74 ± 0.34; 40 mg/kg: 1.03 ± 0.29 ;80 mg/kg: 0.75 ± 0.21), together with the RANKL/OPG ratio (Control: 1.17 ± 0.08; 40 mg/kg: 0.67 ± 0.09; 80 mg/kg: 0.63 ± 0.28) were attenuated above the same dose (p < 0.05). BG did not infuence (p > 0.05) metabolic parameters in non-diabetic rats. In diabetic animals, doses above 40 mg/kg reduced IL-1β (Control: 387 ± 66; 40 mg/kg: 309 ± 27; 80 mg/kg: 300 ± 14) and TNF-α (Control: 229 ± 19; 40 mg/kg: 128 ± 53; 80 mg/kg: 71 ± 25), blood glucose levels (Control: 402 ± 49; 40 mg/kg: 334 ± 32; 80 mg/kg: 287 ± 56), total cholesterol (Control: 124 ± 8; 40 mg/kg: 120 ± 10; 80 mg/kg: 108 ± 9), LDL-c + VLDL-c (Control: 106 ± 8; 40 mg/kg: 103 ± 10; 80 mg/kg: 87 ± 10) and triacylglycerols (Control: 508 ± 90; 40 mg/kg: 301 ± 40; 80 mg/kg: 208 ± 61), whereas increased HDL-c (Control: 18 ± 0.5; 40 mg/kg: 19 ± 1; 80 mg/kg: 21 ± 1) (p < 0.05). Optimal dose needed to reduce ABL was higher in diabetic animals with PD. | pt_BR |
dc.language | en | pt_BR |
dc.publisher | Springer Nature | pt_BR |
dc.rights | Attribution 4.0 International | * |
dc.rights | acesso aberto | pt_BR |
dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | * |
dc.source | Diabetology & Metabolic Syndrome | pt_BR |
dc.subject | Periodontitis | pt_BR |
dc.subject | Diabetes mellitus | pt_BR |
dc.subject | Bone loss | pt_BR |
dc.subject | Inflammatory status | pt_BR |
dc.subject | β-glucans | pt_BR |
dc.subject | Periodontite | pt_BR |
dc.subject | Perda óssea | pt_BR |
dc.subject | Status inflamatório | pt_BR |
dc.subject | β-glucanos | pt_BR |
dc.subject | Prebióticos | pt_BR |
dc.title | Dose-response effect of prebiotic ingestion (β-glucans isolated from Saccharomyces cerevisiae) in diabetic rats with periodontal disease | pt_BR |
dc.type | Artigo | pt_BR |
Aparece nas coleções: | DMV - Artigos publicados em periódicos |
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