English (United Kingdom)

https://curated-unify.zendy.io/wp-json/zendy-region/v1/featured_content/oa?rat=en

https://curated-unify.zendy.io/wp-json/zendy-region/v1/highlighted_journal/

Global: Zendy Plus annual

Presents the access of premium content as premium feature

Premium Content

Presents the keyphrase highlighting as premium feature

Keyphrase Highlighting

Presents the summarisation as premium feature

Summarisation

Insights

Presents the pdf analysis as premium feature

PDF Analysis

Presents the zaia usage as premium feature

ZAIA

Global: Zendy Tools annual

Global: Zendy Free Plan

Global: Zendy Tools monthly

Global: Zendy Plus monthly

Tritiated L-leucine ((3H)L-leu) was injected into the amniotic sacs of 19-day gestation rat fetuses during a brief (4-hr) period of elevation in maternal serum ethanol. The pregnant rats received 47.5% ethanol at "high dose" (0.29 to 0.33 g/100 g body weight) or "low dose" (0.12 to 0.14 g/100 gm body weight) by intraperitoneal injection. Fetal brain and liver were removed and analyzed for tissue uptake (TU) and protein incorporation (PI) of (3H)L-leu. Relative protein synthesis, independent of alterations in TU, was expressed by the ratio PI/TU x 100. Delayed fetal effects of acute maternal ethanol exposure were studied by injecting the fetal amniotic sacs with (3H)L-leu 24 hr after maternal ethanol administration. Both TU and PI were decreased in high dose fetal brain. Liver PI, but not TU, was depressed. High dose ethanol treatment caused a reduction in protein synthesis (PI/TU x 100) in fetal brain but not liver. Low dose ethanol enhanced brain PI and both liver and brain PI/TU x 100. Utilization of (3H)L-leu was related to fourth-hour (sacrifice) maternal serum ethanol levels. Fetal brain was more strikingly affected than liver. Ethanol concentrations greater than 200 mg/dl caused a decrease in brain TU (control, 1879 +/- 185 versus ethanol, 1219 +/- 123 dpm/mg protein) and PI/TU x 100 (control, 48.9 +/- 3.3 versus ethanol, 31.5 +/- 2.9). At levels less than 100 mg/dl, PI/TU x 100 was enhanced in both brain (control, 48.9 +/- 3.3 versus ethanol, 67.3 +/- 2.8) and liver (control, 45.3 +/- 4.2 versus ethanol, 62.3 +/- 1.7). Tissue uptake of (3H)L-leu 24 hr after high dose maternal ethanol exposure was increased in fetal brain. The results support the hypothesis that a brief period of maternal/fetal ethanol exposure, similar to that found in "social" drinking humans, alters normal fetal metabolism.

Effects of Acute Ethanol Exposure upon In Vivo Leucine Uptake and Protein Synthesis in the Fetal Rat