2003
DOI: 10.2310/6650.2003.39201
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Effects of Hyperbaric Oxygen on Proliferative and Apoptotic Activities and Reactive Oxygen Species Generation in Mouse Fibroblast 3T3/J2 Cell Line

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Cited by 34 publications
(18 citation statements)
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“…In contrast, exposure of cultured fibroblasts to HBO 2 at pressures ranging from 1.5 to 3.0 ATA for 90 to 120 minutes inhibits the cell growth rate, 35 suppresses collagen synthesis, 36 and accelerates cell death. 37 Our results showed that daily HBO 2 treatment at 2.5 ATA for 90 minutes on 3 consecutive days significantly suppressed BrdU incorporation, indicating a reduced proliferation rate in fibroblasts cultured with normal DME medium. HBO 2 exposure also caused more cell death (Figure 4) and an overall significant decrease in total cell survival.…”
Section: Discussionsupporting
confidence: 48%
See 1 more Smart Citation
“…In contrast, exposure of cultured fibroblasts to HBO 2 at pressures ranging from 1.5 to 3.0 ATA for 90 to 120 minutes inhibits the cell growth rate, 35 suppresses collagen synthesis, 36 and accelerates cell death. 37 Our results showed that daily HBO 2 treatment at 2.5 ATA for 90 minutes on 3 consecutive days significantly suppressed BrdU incorporation, indicating a reduced proliferation rate in fibroblasts cultured with normal DME medium. HBO 2 exposure also caused more cell death (Figure 4) and an overall significant decrease in total cell survival.…”
Section: Discussionsupporting
confidence: 48%
“…A small amount of ROS production may trigger mechanisms leading to endothelial proliferation and neovascularization. 18 Conconi et al 37 demonstrated that exposure of cultured fibroblasts to a short period of HBO 2 increased proliferation, whereas prolonged HBO 2 exposure inhibited cell growth. These findings suggest that oxygen tension is the critical factor determining the direct effects of oxygen on fibroblasts whose proliferation is suppressed by exposure to a high glucose concentration.…”
Section: Discussionmentioning
confidence: 99%
“…This study has shown that survival in vitro of 3 T3 fibroblast cultures was not impaired, and that IEC cells incubated with oxygen-producing sutures, and cultured under hypoxic conditions, had contractility responses comparable to those of cells cultured under normoxia. These results confirm the findings of an earlier study 22 that demonstrated a proliferative effect of hyperbaric oxygen (HBO) on murine 3 T3 fibroblasts, in spite of enhanced ROS production. However, ROS were demonstrated to play a beneficial key role in intestinal wound healing by stimulating cell attraction, migration and adhesion, and immune cell activation, effects that appear to be potentiated by the presence of commensal bacteria 23,24 .…”
Section: Discussionsupporting
confidence: 91%
“…As an overall effect, at least in rodents, hyperbaric oxygenation appears to be antiinflammatory since it increases the susceptibility to respiratory infections [23,24] and delays allograft rejection [25][26][27]. While hyperbaric oxygenation may inhibit apoptosis in models of ischemic brain injury [28,29] and ischemic wound healing [30] possibly due to limiting tissue hypoxia, a single exposure to high partial oxygen pressure was observed to enhance apoptosis mouse fibroblasts [31], Jurkat-T-cells, HL-60 cells, murine thymocytes [32] and NCI-H929 [33].…”
Section: Introductionmentioning
confidence: 98%