2008
DOI: 10.1152/ajpheart.00699.2007
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Acute ethanol exposure disrupts VEGF receptor cell signaling in endothelial cells

Abstract: Radek KA, Kovacs EJ, Gallo RL, DiPietro LA. Acute ethanol exposure disrupts VEGF receptor cell signaling in endothelial cells.

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Cited by 58 publications
(64 citation statements)
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“…However, higher dose at 10% EtOH inhibit angiogenesis. Inhibition of angiogenesis has also been reported in studies carried out on chick embryo and on wound healing (Radek, Matthies et al 2005;Radek, Kovacs et al 2008). This suggests that EtOH inhibit the angiogenesis at higher doses.…”
Section: Discussionmentioning
confidence: 74%
“…However, higher dose at 10% EtOH inhibit angiogenesis. Inhibition of angiogenesis has also been reported in studies carried out on chick embryo and on wound healing (Radek, Matthies et al 2005;Radek, Kovacs et al 2008). This suggests that EtOH inhibit the angiogenesis at higher doses.…”
Section: Discussionmentioning
confidence: 74%
“…Relevant murine models demonstrate that acute alcohol consumption decreases the expression of VEGF receptors and reduces nuclear expression of HIF-1α in endothelial cells, thereby affecting angiogenesis and the proliferative phase of wound healing [69,70]. There are also studies showing that inappropriate alcohol consumption has an adverse effect on the physiologic reepithelialisation and collagen production [69][70][71][72].…”
Section: Inappropriate Alcohol Consumption Is Linked To Non-physiologmentioning
confidence: 99%
“…AAA leads to insufficient immune system responses to infections; such deficiency was observed both in organ-specific [67][68][69] and systemic infections [70][71][72] . Acute alcohol intoxication impairs the ability of the host to counteract hemorrhagic shock [73] , augments corticosteroid release [74] and delays wound healing [75][76][77][78] , thus contributing to higher morbidity and mortality [79] and prolonged recovery from trauma [80] . The pathogenesis of AAA effects on human health is not fully understood.…”
Section: Aaa: Biomedical Impactmentioning
confidence: 99%
“…For example, if the desired alcohol concentration in the cell culture is 25 mmol/L, a Petri dish with 2 × the alcohol amount (50 mmol/L) was placed on the bottom of the chamber to ensure the saturation of the gas in the chamber); such conditions maintain the initial alcohol concentration ± 15% over a 24 h period [139] . However, depending on the scientific question of the study, the declining alcohol levels in vitro may be desired to mimic the alcohol elimination in vivo; in these situations the in vitro experiments are disadvantaged by the absence/limitation of alcohol metabolism [76,134] . The in vitro AAA model offers the possibility of primary in vitro exposure of alcohol-naive cells to alcohol alone or its combinations with diverse pharmacological or naturally-derived substances [24, but also the investigation of the effects of in vivo exposure to alcohol followed by ex vivo exposure to other stimulants [110,113,115] or vice versa.…”
Section: In Vitro Aaa Modelmentioning
confidence: 99%