Probiotics: protecting the intestinal ecosystem?
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Enterocolitis, Necrotizing↗
Biomedical subjects
Ricardo Caicedo
Publications and source records attributed to Ricardo Caicedo.
Alive and dead Lactobacillus rhamnosus GG decrease tumor necrosis factor-alpha-induced interleukin-8 production in Caco-2 cells.
Certain probiotic bacteria show anti-inflammatory activity after being heat killed, whereas others do not, suggesting that the gastrointestinal environment may alter the activity of probiotic bacteria. Occasionally, probiotics are provided when a patient is also being treated with oral antibiotics; this may have an effect on the probiotic activity. We hypothesized that Lactobacillus rhamnosus GG (LGG) are capable of downregulating tumor necrosis factor-alpha (TNFalpha)-induced interleukin (IL)-8 production under all 3 of these conditions, and that LGG act through the nuclear factor kappaB (NFkappaB)/inhibitor of kappaB (IkappaB) pathway. Caco-2 cells were treated with live or heat-killed LGG in doses ranging from 10(4) to 10(10) cfu/L, in the presence or absence of antibiotics and TNFalpha in the media. TNFalpha-induced production of IL-8 by Caco-2 cells was modulated by LGG under all 3 conditions. However, higher doses of live LGG without TNFalpha in the presence or absence of antibiotics in vitro induced the production of IL-8 (P = 0.001). Heat-killed LGG also blunted the TNFalpha-induced IL-8 production (P < 0.01), but by itself did not increase IL-8 production at higher doses as markedly as live LGG (P < 0.05). LGG reduced the TNFalpha-induced NFkappaB translocation to the nucleus and lessened the decrease in IkappaB in the cytoplasm (P < 0.05). LGG reduced TNFalpha-induced IL-8 production by affecting the NFkappaB/IkappaB pathway in Caco-2 cells. High doses of live LGG markedly increased IL-8 production, but heat-killed LGG caused only a slight increase in IL-8. Thus, heat-killed LGG may effectively ameliorate inflammation with a lower potential than live LGG at high doses to cause inflammation.
Caco-2 Cells↗
Using ParaPost Tenax fiberglass and ParaCore build-up material to restore severely damaged teeth.
This article describes a technique using ParaPost Tenax Fiber White, ParaPost Cement, and ParaPost ParaCore build-up material to restore a tooth with a significant loss of tooth structure. After successful root canal therapy, the posts were bonded in the canals and the core was built using ParaPost ParaCore build-up material. At that point, the tooth was prepared to receive a conventional porcelain-fused-to-metal crown.
Dental Cements↗
Treatment-dependent calcium diffusion from two sealers through radicular dentine.
This study examined how root canal irrigation with sodium hypochlorite and citric acid affected calcium diffusion, using a calcium hydroxide-based sealer and a zinc oxide eugenol-based sealer with little calcium hydroxide. Sixty-eight single-rooted, freshly extracted teeth were decrowned to 14 mm, instrumented using a crown down technique, and divided into two groups: the experimental group (irrigated with 5.25% NaOCl followed by 10% citric acid) and the control (irrigated with 5.25% NaOCl only). Both groups were divided into two subgroups, depending on the type of sealers used in obturation with gutta-percha. Coronal and apical openings were sealed and teeth were placed in water (37 degrees C). Spectrophotometry was used to measure the amount of calcium released in water through radicular dentin. For each sealer, the calcium diffused from the experimental group was significantly higher than that of the control group (p < 0.05).
Calcium↗