Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: UMLS:C0038187 (starvation)
 24,951 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

1. In the first experiment D-xylose, L-arabinose, D-galacturonic and D-glucuronic acids were fed ad libitum to young chicks for 2 weeks at 200 g/kg of diet and weight gains and food consumption were recorded. 2. L-arabinose and D-xylose did not depress food consumption in the first week but prolonged feeding caused food consumption to decrease and weight gain to be adversely affected. 3. D-galacturonic acid and D-glucuronic acid caused severe growth retardation as early as the first week of feeding, primarily because of voluntary starvation. 4. Apparent metabolisable energy values for the diets were obtained when chicks were 19 to 21 d of age and were 14.04 +/- 0.52, 12.03 +/- 0.61, 11.77 +/- 1.21, 11.68 +/- 0.34 and 11.66 +/- 0.45 KJ/g for the basal diet with glucose, xylose, arabinose, galacturonic and glucuronic acids respectively. 5. True metabolisable energy values for the diets were obtained from adult cockerels and were 15.07 +/- 0.16, 13.45 +/- 0.16, 13.12 +/- 0.37, 12.29 +/- 0.26 and 12.69 +/- 0.23 KJ/g for basal diet with glucose, xylose, arabinose, galacturonic and glucuronic acids respectively. 6. In the second experiment D-galactose, D-xylose, L-arabinose, D-galacturonic and D-glucuronic acid were fed ad libitum to young chicks for 3 weeks at 50 g/kg of diet and weight gains and food consumption were recorded. 7. Chicks grew and ate well on all diets. 8. The digestibilities of sugars and uronic acids were obtained by measurement of these constituents in diets and digesta using titanium dioxide as a marker. The digestibilities were 1.000 +/- 0.0, 0.997 +/- 0.002, 0.936 +/- 0.041, 0.628 +/- 0.103, 0.588 +/- 0.059, and 0.645 +/- 0.089 for D-glucose, D-galactose, D-xylose, L-arabinose, D-galacturonic and D-glucuronic acids respectively. 9. Both at 200 and 50 g/kg dietary inclusion there was noticeable caecal fermentation from L-arabinose, D-galacturonic and D-glucuronic acid. Only at 200 g/kg dietary inclusion did D-xylose produce significant evidence of caecal fermentation.
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PMID:Digestibility of pentose sugars and uronic acids and their effect on chick weight gain and caecal size. 340 82

Photoaffinity labeling with [3H]cytochalasin B detects two D-glucose-sensitive proteins in the chicken embryo fibroblast (CEF) plasma membrane, which accumulate under conditions of glucose starvation and are probably involved in the glucose transport system (Pessin, J.E., et al. (1982) Proc. Natl. Acad. Sci. U.S. 79, 2286-2290). The two labeled components, designated as peak I (Mr 45,000) and II (Mr 52,000) components, were separated by preparative gel electrophoresis in the presence of sodium dodecyl sulfate. The fractions were digested with S. aureus V8 or papain, and the radioactive products were analyzed by one-dimensional gel electrophoresis. The peptide maps showed that they have different peptide structures. Peptide maps of authentic actin, a possible contaminant of the peak I fractions, were quite different from those of the peak I component. Rous sarcoma virus-transformed CEF have two components similar as to apparent molecular size and peptide maps to those present in glucose-starved cells. The peak I and II components show minimal affinity to agarose-bound Ricinus communis agglutinin which binds the human erythrocyte glucose transporter quite well. The peak II component was more susceptible to proteolysis than the peak I one or the human erythrocyte glucose transporter. However, the peptide maps of the peak II component were similar to those of the human erythrocyte glucose transporter.
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PMID:Separation and proteolytic mapping of the two [3H]cytochalasin B photoaffinity labeled D-glucose-sensitive proteins in the chicken embryo fibroblast plasma membrane. 351 90

Fed and 48-h starved rats were infused on day 21.5 of gestation for 20 min through the left uterine artery with [U-14C-]-D-glucose, [U-14C]-glycerol, or [U-14C]-L-alanine. The mother and fetuses from both uterine horns were processed separately for radioactivity measurements in plasma and liver. Differences in radioactivity values between fetuses from the left and the right sides are used as indexes of placental transference of the infused tracers prior to their distribution and transformation in the maternal circulation. After infusion of [U-14C]-D-glucose, [U-14C]-glycerol, or [U-14C]-L-alanine, plasma radioactivity values and specific activities corresponding to the respective infused tracer appeared much higher in fetuses from the left than the right uterine side. Plasma 14C-lactate values also were higher in the left than the right fetuses indicating that fetoplacental structures produced lactate from those placentally transferred 14C-metabolites. No difference in plasma 14C-glucose between left and right uterine horn fetuses was observed after maternal infusion with either [U-14C]-glycerol or [U-14C]-L-alanine, either in fed or 48-h starved rats. In the mother both [U-14C]-glycerol and [U-14C]-L-alanine were efficiently converted to 14C-glucose, and this process was significantly enhanced with starvation. 14C-fatty acids present in fetal liver after maternal infusions with either [U-14C]-D-glucose or [U-14C]-glycerol were decreased by starvation whereas no fatty acid synthesis from [U-14C]-L-alanine was detected.(ABSTRACT TRUNCATED AT 250 WORDS)
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PMID:Lactate production and absence of gluconeogenesis from placental transferred substrates in fetuses from fed and 48-H starved rats. 362 73

The effect of Ep on radioactive glucose and methyl-alpha-D-glucoside transport by rat erythrocytes and bone marrow cells were studied. There is initial linearity followed by saturation kinetics of [14C]glucose transport by the erythrocytes of starved and starved plus Ep-treated rats at different concentrations of glucose. Starvation caused slight inhibition of glucose transport which increased markedly on Ep administration to starved rats. Normal animals failed to show any significant change in glucose transport after Ep treatment. Methyl-alpha-D-glucoside inhibited the Ep-stimulated glucose transport significantly. Ep also stimulated the transport of radioactive methyl-alpha-D-glucoside which was competitively inhibited in presence of D-glucose. Glucose transport in erythrocytes was found to be sensitive to metabolic inhibitors like azide and DNP. A sulfhydryl reagent and ouabain also inhibited the transport process. Ep stimulated glucose and methyl-alpha-D-glucoside transport in the bone marrow cells of starved rats. The sugar analog competitively inhibited the glucose transport in bone marrow cells and vice versa.
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PMID:Effect of erythropoietin on the glucose transport of rat erythrocytes and bone marrow cells. 367 16

The regulation of hexose transporters of cultured fibroblasts was investigated by exposing chicken embryo fibroblasts (CEF) to hypertonic culture medium, a condition known to enhance hexose transport activity. The effects of hypertonicity and the role of protein synthesis were examined with CEF in the basal (glucose fed) and transport enhanced (glucose starved) states. Glucose-fed CEF exposed to hypertonic conditions developed four-fold enhancement of hexose transport activity within 4 hrs; this declined in the following 20 hrs to a level slightly higher than the fed control. Protein synthesis was required in part for this effect, since the presence of cycloheximide during hypertonic exposure of fed CEF blocked the increase in of transport by almost 50%. Although the increased transport produced by glucose starvation was not further enhanced by hypertonicity, hypertonic treatment of starved CEF during glucose refeeding largely prevented the loss of transport activity to the basal, fed state. The hypertonic effects were concentration dependent (240mOsm optimal) and could be elicited with NaCl, KCl, or sucrose. Hypertonic treatment typically led to a greater than 50% decline in the incorporation of [3H]leucine into acid-insoluble fractions. The changes in transport were evident at the plasma membrane level, and studies of membrane vesicles prepared from hypertonically treated fed CEF showed a doubling of both [3H]cytochalasin B binding and the Vmax of D-glucose transport. These findings indicate that exposure of CEF to hypertonic conditions has some effects similar to those produced by glucose starvation and suggest that protein synthesis is to some extent involved in the regulation of hexose transporters in CEF.
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PMID:Effect of hypertonicity on hexose transporter regulation in chicken embryo fibroblasts. 368 Mar 95

Treatment of glucose-grown L6 rat myoblasts with rabbit or sheep anti-(L6-rat myoblast) antibody for 35 min or glucose starvation for at least 8 h results in a 2-fold increase in the Vmax. of 2-deoxy-D-glucose (dGlc) and 3-O-methyl-D-glucose uptake. In both cases, apparent transport affinities were not affected. Furthermore, once stimulation has occurred, further increases in hexose uptake could not be produced. Assays of antibody binding to whole cells suggested that the antibody is not internalized but remains bound on the cell surface. To elucidate the site and mechanism of antibody action, plasma-membrane vesicles from L6 cells were prepared. Anti-L6 antibody was found to cause a time- and dosage-dependent stimulation of dGlc transport in these vesicles. Maximum activation was achieved after 30 min exposure. This antibody-mediated activation could be inhibited by treatment of vesicles with various proteinase inhibitors. Treatment of vesicles with trypsin was also found to activate dGlc transport to levels observed with antibody. These results are virtually identical with those obtained with whole cells and suggest that antibody-mediated activation of hexose transport results from interaction of antibody with a specific membrane component(s).
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PMID:Stimulation of hexose transport in L6 rat myoblasts by antibody and by glucose starvation. 380 Sep 63

Hexose transport in plasma membrane vesicles prepared from L6 rat myoblasts was shown to be stereospecific, activated by glucose starvation and occurred by both high and low affinity systems. Transport by the high affinity system was shown to occur by an active transport process. Furthermore, the high affinity system was shown to be defective in vesicles prepared from F72 cells (hexose transport mutant). These results indicate that the high affinity hexose transport system is retained in the plasma membrane vesicles. Thus plasma membrane vesicles could be of value in further characterization of the L6 high affinity hexose transport system, without interference from the various metabolic events occurring in whole cells.
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PMID:Hexose transport in plasma membrane vesicles prepared from L6 rat myoblasts. 380 Sep 90

The relationship between circulating fibronectin concentration and nutritional status was examined in eight healthy male (31 +/- 1 yr old) volunteers in three nutritional states: the postabsorptive state, after 10 days of protein-caloric starvation, and during the 10th day of refeeding by total parenteral nutrition. Plasma fibronectin was significantly decreased from 330 +/- 22 to 154 +/- 11 micrograms/ml (p less than 0.001) from the postabsorptive to starved state which was accompanied by appropriate changes in body weight, anthropometric measurements, and nitrogen balance. Plasma fibronectin levels were restored to 402 +/- 39 micrograms/ml following 10 days of total parenteral nutrition. The plasma fibronectin response was greater (p less than 0.05) during total parenteral nutrition with dextrose as the nonprotein calorie source as compared to a 50% dextrose/50% lipid regimen. These results suggest that the calorie source must be considered during interpretation of plasma fibronectin levels in patients undergoing parenteral nutrition.
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PMID:The response of fibronectin to differing parenteral caloric sources in normal man. 392 16

The blood-brain barrier (BBB) transport and brain phosphorylation of glucose were assessed in conscious rats subjected to 2 days of starvation. Although plasma glucose decreased, no significant changes in brain blood flow, BBB glucose transport, or 2-deoxy-D-glucose phosphorylation were observed. The data suggest that adaptive changes of brain glucose metabolism previously observed in starvation are located beyond the initial steps of brain entry and phosphorylation.
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PMID:Two-day starvation does not alter the kinetics of blood--brain barrier transport and phosphorylation of glucose in rat brain. 397 22

We have previously demonstrated that Sindbis virus infection of Chinese hamster ovary (CHO) cells altered the protein glycosylation machinery of the cell, so that both normal, full-size (nine mannose-containing) oligosaccharides and abnormal, "truncated' (five mannose-containing) oligosaccharides are transferred from lipid-linked precursors to newly synthesized viral membrane glycoproteins. In the present studies, we have examined the precursor oligosaccharides on viral glycoproteins that were pulse-labelled with [3H]mannose in the presence or absence of glucose, since glucose starvation of uninfected CHO cells has been reported to induce synthesis of truncated precursor oligosaccharides. Pulse-labelling in the absence of glucose led to a greater than 10-fold increase in the relative amount of the truncated precursor oligosaccharides being transferred to the newly synthesized viral glycoproteins and to an apparent underglycosylation of some precursor viral polypeptides, with some asparaginyl sites not acquiring covalently linked oligosaccharides. The mature virion glycoproteins from CHO cells which were pulse-labelled in the absence of glucose and then 'chased' in the presence of glucose contained proportionately more unusual Man3GlcNAc2-size oligosaccharides. These small neutral-type oligosaccharides were apparently not as good a substrate for further processing into complex acidic-type oligosaccharides as the normal Man5GlcNAc2 intermediate that results from the full-size precursor oligosaccharides.
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PMID:Sindbis virus glycoproteins are abnormally glycosylated in Chinese hamster ovary cells deprived of glucose. 402 Mar 47


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