2005
DOI: 10.1016/j.exger.2005.01.005
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Differential effects of alcohol upon gluconeogenesis from lactate in young and old hepatocytes

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Cited by 7 publications
(4 citation statements)
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“…[ 72 ] showed that the in vitro inhibitory effect of gluconeogenesis by alcohol was especially noted in matured hepatocytes, than in young ones. [ 72 ] Hence, it would be expected that the effect of alcohol consumption on gluconeogenesis would be more pronounced for the older humans, compared to young adults. This issue of the age differences in alcohol action on liver gluconeogenesis needs further attention.…”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…[ 72 ] showed that the in vitro inhibitory effect of gluconeogenesis by alcohol was especially noted in matured hepatocytes, than in young ones. [ 72 ] Hence, it would be expected that the effect of alcohol consumption on gluconeogenesis would be more pronounced for the older humans, compared to young adults. This issue of the age differences in alcohol action on liver gluconeogenesis needs further attention.…”
Section: Resultsmentioning
confidence: 99%
“…In this study, two parallel data sources were utilized: Our research data;[ 18 ] and peer-reviewed articles from scientific databases. [ 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60 61 62 63 64 65 66 67 68 69 70 71 72 73 74 75 76 77 ]…”
Section: Materials and Methods Of Literature Searchmentioning
confidence: 99%
“…4a). The liver is the major organ involved in biotransforming galactose into glucose (Xu and Purcell 2006), and this function is retained in liver spheroids; furthermore, glucose can be synthesized from other sources such as pyruvate , lactate (Sumida et al 2005), as well as from a range of glucogenic amino acids such as serine, threonine, glutamine, etc. through gluconeogenesis (Brosnan 2003).…”
Section: Discussionmentioning
confidence: 99%
“…Before entering the liver, the perfusate was sequentially filtered through a nylon mesh, oxygenated (95%:5%, O 2 :CO 2 ), and then passed through a bubble trap. Hepatocytes were isolated as previously reported by our laboratory (Sumida et al, 2005b) where calcium-free Krebs-Hensleit bicarbonate buffer and fresh thoroughly washed bovine red blood cells (hematocrit of 13-15%) perfused the liver (single-pass) for 10 minutes at a rate of 35 ml/min. Collagenase was added to the perfusate and the system was switched to a recirculation mode with the flow rate adjusted to ∼2 ml/min × g liver −1 .…”
Section: Isolation Of Hepatocytes and Experimentsmentioning
confidence: 99%