Juvenile Lobster (Homarus americanus) Do Not Require Dietary Ascorbic Acid

1985 ◽  
Vol 42 (2) ◽  
pp. 368-370 ◽  
Author(s):  
J. C. Kean ◽  
J. D. Castell ◽  
D. J. Trider
Keyword(s):  
Ascorbic Acid ◽  
De Novo ◽  
Homarus Americanus ◽  
De Novo Synthesis ◽  
Experimental Conditions ◽  
Deficient Diet ◽  
Significant Difference ◽  
Dry Diet ◽  
Dietary Treatments ◽  
Ascorbic Acid Supplementation

We found no dietary ascorbic acid requirement for juvenile lobsters (Homarus americanus) (37–42 mg). The lobsters were fed semipurified diets containing 0, 0.6, 1.2, 2.4, or 12 g L-ascorbic acid/kg dry diet for 20 wk. At termination, the hepatopancreases were removed and assayed for ascorbic acid. There was no significant difference in growth or mortality among any of the dietary treatments. Lobsters fed the deficient diet had hepatopancreatic ascorbic acid levels that were not significantly different from animals fed the supplemented diets. Juvenile lobster, therefore, did not require dietary ascorbic acid under these experimental conditions. We suggest that juvenile lobsters do not require ascorbic acid supplementation in the diet and may be capable of de novo synthesis of this vitamin.

scholarly journals Chemical Stability of Ascorbic Acid Integrated into Commercial Products: A Review on Bioactivity and Delivery Technology

Antioxidants ◽  
2022 ◽  
Vol 11 (1) ◽  
pp. 153
Author(s):  
Xin Yin ◽  
Kaiwen Chen ◽  
Hao Cheng ◽  
Xing Chen ◽  
Shuai Feng ◽  
...  
Keyword(s):  
Ascorbic Acid ◽  
Active Site ◽  
De Novo ◽  
Food Matrix ◽  
De Novo Synthesis ◽  
Nutritional Characteristics ◽  
Gulonolactone Oxidase ◽  
Key Enzyme ◽  
Commercial Applications ◽  
Delivery Technology

The L-enantiomer of ascorbic acid is commonly known as vitamin C. It is an indispensable nutrient and plays a key role in retaining the physiological process of humans and animals. L-gulonolactone oxidase, the key enzyme for the de novo synthesis of ascorbic acid, is lacking in some mammals including humans. The functionality of ascorbic acid has prompted the development of foods fortified with this vitamin. As a natural antioxidant, it is expected to protect the sensory and nutritional characteristics of the food. It is thus important to know the degradation of ascorbic acid in the food matrix and its interaction with coexisting components. The biggest challenge in the utilization of ascorbic acid is maintaining its stability and improving its delivery to the active site. The review also includes the current strategies for stabilizing ascorbic acid and the commercial applications of ascorbic acid.

151 EFFECT OF ASCORBIC ACID ON OXIDATIVE STRESS AND ITS THERMOPROTECTANT ROLE ON IN VITRO EMBRYONIC DEVELOPMENT OF BUFFALO (BUBALUS BUBALIS) EMBRYOS

2017 ◽  
Vol 29 (1) ◽  
pp. 184
Author(s):  
M. Roshan ◽  
D. Dua ◽  
N. Saini ◽  
A. Sharma ◽  
T. Sharma ◽  
...  
Keyword(s):  
Oxidative Stress ◽  
Heat Treatment ◽  
Ascorbic Acid ◽  
Heat Stress ◽  
Significant Difference ◽  
Blastocyst Rate ◽  
Stress Related Genes ◽  
Nonsignificant Decrease ◽  
Ascorbic Acid Supplementation

The most important factors that lead to stress in farm animals are oxidative and thermal stress, leading to reduced reproductive efficiency. Oxidative stress leads to an increase in proportion of reactive oxygen species, whereas heat stress affects the physiology of animals, which lowers the conception rates of dairy cattle. In vitro culture systems have been enhanced by manipulating media with various supplements such as vitamins, growth factors, and antioxidants that have overcome these problems. Ascorbic acid has been shown to play an antioxidant role in many species such as sheep, goat, and pigs. Keeping this in mind, this study was conducted to investigate the effect of supplementation of in vitro-matured (IVM) and/or in vitro-cultured (IVC) media with ascorbic acid and evaluate its antioxidant role in in vitro development of buffalo embryos. Immature oocytes were collected from visible surface follicles (2 to 8 mm in diameter) in slaughterhouse buffalo ovaries and subjected to IVM, IVF, and IVC in a humidified CO2 incubator at 38.5°C. Ascorbic acid was supplemented to IVM [TCM-199 + 10% featl bovine serum (FBS) + 1 µg mL−1 oestradiol-17β + 5 µg mL−1 pFSH + 0.81 mM sodium pyruvate + 0.68 mM l-glutamine + 50 µg mL−1 gentamicin sulfate] at 50 or 100 µM or IVC (mCR2aa + 0.6% BSA + 10% FBS+ 50 µg mL−1 gentamicin sulfate) at 50 µM or both IVM and IVC media at 50 µM. Oocytes without ascorbic acid were treated as the control group. Cleavage and blastocyst rate was improved when 50 µM (66.67 ± 2.27; 16.67 ± 1.26%) ascorbic acid was supplemented to IVM medium but no significant difference (P < 0.05) was observed at 100 µM (54.04 ± 2.20; 6.16 ± 0.37%) as compared with the control (62.77 ± 2.71; 10.67 ± 0.24%), respectively. When 50 µM ascorbic acid was supplemented in IVM, IVC, or both media, though cleavage rate (66.67 ± 2.27; 69.09 ± 3.22; 66.67 ± 2.23%) was similar in 3 groups, a significant increase was observed in blastocyst rate (16.67 ± 1.26; 20.18 ± 0.86; 28.57 ± 0.37%) when both media were supplemented, respectively. To evaluate the thermoprotectant effect, 4 groups were taken: group 1 without and group 2 with ascorbic acid supplementation, oocytes were given heat treatment at 39.5°C initially for 12 h during IVM; group 3 without and group 4 with ascorbic acid supplementation, oocytes were given heat treatment at 40.5°C initially for 12 h during IVM. No significant difference in developmental rate was observed at elevated temperature of 39.5°C or 40.5°C as compared with the control. Relative mRNA abundance of heat stress-related genes, HSP 70.1 and HSP 70.2, was nonsignificantly higher in oocytes matured at 39.5°C or 40.5°C after supplementation with ascorbic acid as compared to control. Relative mRNA abundance of BAX decreased at 50 µM and increased at 100 µM ascorbic acid compared with control, whereas BID showed similar results between control and treatment. Regarding anti-apoptotic gene expression, significantly higher expression was observed in MCL1 for 50 µM and lower for 100 µM ascorbic acid, and a similar nonsignificant trend was observed for BCL-XL. Developmental genes GDF9 and BMP15 showed a nonsignificant increase in 50 µM, and a nonsignificant decrease in the 100 µM supplemented group as compared with the control. Oxidative stress-related genes SOD and GPX showed a nonsignificant decrease in treated groups as compared to control. From above results, it was concluded that ascorbic acid had an anti-oxidant as well as thermoprotectant role in developmental competence that increased the potential for generation of large domestic animal in vitro embryos for research and applied technologies such as cloning and transgenesis.

Enhanced RNA and protein synthesis in adipose tissue of rats adapted to periodic hyperphagia

1968 ◽  
Vol 46 (6) ◽  
pp. 903-906 ◽  
Author(s):  
L. Kazdová ◽  
T. Braun ◽  
P. Fábry ◽  
R. Poledne
Keyword(s):  
Protein Synthesis ◽  
Adipose Tissue ◽  
Rna Synthesis ◽  
De Novo ◽  
Specific Activity ◽  
De Novo Synthesis ◽  
Experimental Conditions ◽  
Rna And Protein Synthesis ◽  
Meal Feeding ◽  
The Difference

RNA synthesis measured by the incorporation of orotic acid-6-14C into RNA was investigated in isolated adipose tissue of control rats and of rats adapted to periodic hyperphagia, evoked by meal-feeding (a single 2-h meal per day). Both groups were fasted for 22 h and subsequently fed a measured test meal for another 2 h. It was revealed that 2 and 4 h after feeding there was no significant change in comparison with values during fasting, whereas in tissue of meal-fed rats the specific activity of RNA gradually increased by 22% and 41% respectively. The difference between controls and meal-fed rats was even much more marked if the specific activity of RNA in fat cells, isolated after incubation of the tissue, was measured. A significantly greater response of meal-fed rats was found when protein synthesis and lipogenesis in adipose tissue were assessed under the same experimental conditions. The possibility is discussed that the enhanced RNA and protein synthesis in adipose tissue of meal-fed rats is associated with de novo synthesis of enzymes involved in adaptive hyperlipogenesis.

SUPPLEMENTAL VALUE OF ASCORBIC ACID DURING LATE GESTATION ON PIGLET SURVIVAL AND EARLY GROWTH

1983 ◽  
Vol 63 (3) ◽  
pp. 683-687 ◽  
Author(s):  
E. R. CHAVEZ
Keyword(s):  
Ascorbic Acid ◽  
Vitamin C ◽  
Late Gestation ◽  
Dietary Vitamin ◽  
Control Group ◽  
Plasma Vitamin ◽  
Significant Difference ◽  
Vitamin C Supplementation ◽  
Dietary Treatments ◽  
Piglet Survival

Twenty-six pregnant sows were included in four different dietary treatments as follows: (1) Control group with no vitamin C supplementation; (2) vitamin-C-supplemented group receiving 1 g/day ascorbic acid provided in a gelatin capsule; or (3) vitamin-C-supplemented group receiving 1 g/day ascorbic acid in a powder form spread on the top of the pelleted meal; (4) as (3) but receiving 10 g/day ascorbic acid. Vitamin-C-supplemented sows in treatments 2 and 4 showed a significant (P < 0.05) increase in blood plasma vitamin C prefarrowing. Pregnant sows receiving 10 g/day vitamin C supplement showed a significantly (P < 0.05) higher concentration of this vitamin in the urine than either control or sows receiving 1 g/day vitamin C supplementation. Sows in treatment 4 showed a significantly higher (P < 0.05) vitamin C content in colostrum than control animals. During lactation, no significant difference in vitamin C content in milk was observed between control and animals receiving 10 g/day vitamin C supplement. The vitamin C content in the plasma of the piglets at birth indicated that supplementing vitamin C to the mothers, significantly (P < 0.05) increased the concentration of this vitamin in the newborn piglet compared to control animals. However, the piglet survival and growth up to weaning at 3 wk of age was not significantly affected by dietary vitamin C supplementation of the mothers' diet. Key words: Ascorbic acid, gestation, piglet survival, Vitamin C

Über eine in-vivo-Methode zur Herstellung radioaktiv markierter Phosphatide mit Sojabohnen / A Method for Preparing Radioactive Labeled Phosphatides Using Soybeans in-Vivo

1971 ◽  
Vol 26 (5) ◽  
pp. 425-434 ◽  
Author(s):  
J. Hölzl ◽  
H. Wagner
Keyword(s):  
Fatty Acids ◽  
Oleic Acid ◽  
Phosphatidic Acid ◽  
Stearic Acid ◽  
Palmitic Acid ◽  
De Novo ◽  
Specific Radioactivity ◽  
De Novo Synthesis ◽  
Experimental Conditions

Germinating soybeans, when incubated for 20-30 hours under an illumination at 25°-30° temp, with labeled 32P-phosphate, 14C-acetate, 14C-glycerol and 14C-choline, radioactivity ranging from 2 to 14% is incorporated into the main phosphatides lecithin (PC), phosphatidylethanolamine (PE) and monophosphoinositide (MPI). The incorporation of 32P-phosphate in these phosphatides depending on light and temperature, increases to its maximum (3.7 mCi/1 g soybeans) almost running linear and continues further even in the absence of any further germination due to intensive exposure to radiation.14C-acetate is incorporated almost exclusively into fatty acids of the phospholipids during germination as a result of which highest specific radioactivity was seen in the stearic acid followed by oleic acid and palmitic acid. Linol- and linolenic acid under these experimental conditions are weakly or not labeled, 14C-choline is incorporated only in PC. As the PC after 14C-(methyl) -methionine-incubation does not exhibit any significant labeling, one can exclude the pathway of PC-biosynthesis through PE-methylation. The utilization of 14C-glycerol proves that the incorporation of all the compounds under consideration here is effected not by a mere exchange but by a de novo synthesis. This procedure of labeling is suitable for preparing 3H-, 14C- and 32P-PC, -PE, -MPI and phosphatidic acid (PA).

Antagonism by Clopyralid of Picloram-Induced Ethylene Biosynthesis in Rapeseed Plants

1991 ◽  
Vol 46 (11-12) ◽  
pp. 957-962
Author(s):  
J. Christopher Hall ◽  
Mira Soni
Keyword(s):  
Carboxylic Acid ◽  
De Novo ◽  
Subsequent Development ◽  
Acc Synthase ◽  
Ethylene Biosynthesis ◽  
De Novo Synthesis ◽  
Ethylene Evolution ◽  
Significant Difference ◽  
Acc Conversion ◽  
Stimulation Of

The effect of clopyralid pretreatment (500 g/ha) on picloram-induced ethylene, ACC (1-aminocyclopropane-l-carboxylic acid), and MACC [l-(malonylamino)-cyclopropane-1-carboxylic acid] was measured in rapeseed plants that were treated with 50 or 100 g/ha of picloram. In contrast to plants that did not receive a clopyralid pretreatment, ethylene biosynthesis was significantly reduced in plants pretreated with clopyralid prior to picloram. Picloram- induced levels of ACC also were significantly reduced in plants receiving pretreatment with clopyralid. In contrast, there was no difference between the levels of MACC in plants that were and were not pretreated with clopyralid. Therefore, the mechanism by which clopyralid pretreatment interferes with picloram-induced synthesis of both ACC and ethylene may be manifested through the blocking of de novo synthesis of ACC synthase normally stimulated by picloram. The lack of significant difference in MACC levels between plants that were and were not pretreated with clopyralid precludes the stimulation of enhanced ACC conversion to MACC as an exclusive mechanism of clopyralid’s antidoting activity. It is likely that the rate of picloram-induced ACC synthesis by plants receiving pretreatment is within their capacity to convert ACC to MACC, thereby limiting the substrate available for conversion to ethylene. In contrast, it appears that the extent of ACC synthesis by plants receiving no pretreatment supersedes their capacity for conversion to MACC. thereby resulting in greatly enhanced rates of ethylene evolution and subsequent development of injury symptoms.

Antagonism by Clopyralid of Picloram-Induced Ethylene Biosynthesis in Rapeseed Plants

1991 ◽  
Vol 46 (9-10) ◽  
pp. 957-962 ◽  
Author(s):  
J. Christopher Hall ◽  
Mira Soni
Keyword(s):  
Carboxylic Acid ◽  
De Novo ◽  
Subsequent Development ◽  
Acc Synthase ◽  
Ethylene Biosynthesis ◽  
De Novo Synthesis ◽  
Ethylene Evolution ◽  
Significant Difference ◽  
Acc Conversion ◽  
Stimulation Of

Abstract The effect of clopyralid pretreatment (500 g/ha) on picloram-induced ethylene, ACC (1-aminocyclopropane-1-carboxylic acid), and MACC [1-(malonylamino)-cyclopropane-1-carboxylic acid] was measured in rapeseed plants that were treated with 50 or 100 g/ha of picloram. In contrast to plants that did not receive a clopyralid pretreatment, ethylene biosynthesis was significantly reduced in plants pretreated with clopyralid prior to picloram. Piclo­ram-induced levels of ACC also were significantly reduced in plants receiving pretreatment with clopyralid. In contrast, there was no difference between the levels of MACC in plants that were and were not pretreated with clopyralid. Therefore, the mechanism by which clopyralid pretreatment interferes with picloram-induced synthesis of both ACC and ethylene may be manifested through the blocking of de novo synthesis of ACC synthase normally stimulated by picloram. The lack of significant difference in MACC levels between plants that were and were not pretreated with clopyralid precludes the stimulation of enhanced ACC conversion to MACC as an exclusive mechanism of clopyralid’s antidoting activity. It is likely that the rate of picloram-induced ACC synthesis by plants receiving pretreatment is within their capacity to convert ACC to MACC, thereby limiting the substrate available for conversion to ethylene. In contrast, it appears that the extent of ACC synthesis by plants receiving no pretreatment su­persedes their capacity for conversion to MACC, thereby resulting in greatly enhanced rates of ethylene evolution and subsequent development of injury symptoms.

Relevance Predictability in Information Retrieval Systems

1967 ◽  
Vol 06 (02) ◽  
pp. 45-51 ◽  
Author(s):  
A. Kent ◽  
J. Belzer ◽  
M. Kuhfeerst ◽  
E. D. Dym ◽  
D. L. Shirey ◽  
...  
Keyword(s):  
Information Retrieval ◽  
Experimental Conditions ◽  
Treatment Groups ◽  
Retrieval Systems ◽  
Significant Difference ◽  
Information Retrieval Systems ◽  
High Predictability ◽  
Intermediate Response ◽  
Quantitative Indicators ◽  
Level Of Processing

An experiment is described which attempts to derive quantitative indicators regarding the potential relevance predictability of the intermediate stimuli used to represent documents in information retrieval systems. In effect, since the decision to peruse an entire document is often predicated upon the examination of one »level of processing« of the document (e.g., the citation and/or abstract), it became interesting to analyze the properties of what constitutes »relevance«. However, prior to such an analysis, an even more elementary step had to be made, namely, to determine what portions of a document should be examined.An evaluation of the ability of intermediate response products (IRPs), functioning as cues to the information content of full documents, to predict the relevance determination that would be subsequently made on these documents by motivated users of information retrieval systems, was made under controlled experimental conditions. The hypothesis that there might be other intermediate response products (selected extracts from the document, i.e., first paragraph, last paragraph, and the combination of first and last paragraph), that would be as representative of the full document as the traditional IRPs (citation and abstract) was tested systematically. The results showed that:1. there is no significant difference among the several IRP treatment groups on the number of cue evaluations of relevancy which match the subsequent user relevancy decision on the document;2. first and last paragraph combinations have consistently predicted relevancy to a higher degree than the other IRPs;3. abstracts were undistinguished as predictors; and4. the apparent high predictability rating for citations was not substantive.Some of these results are quite different than would be expected from previous work with unmotivated subjects.

Characterization of Monocyte-Associated Factor V

1993 ◽  
Vol 70 (02) ◽  
pp. 273-280 ◽  
Author(s):  
Janos Kappelmayer ◽  
Satya P Kunapuli ◽  
Edward G Wyshock ◽  
Robert W Colman
Keyword(s):  
Monoclonal Antibody ◽  
Light Chain ◽  
Peripheral Blood ◽  
De Novo ◽  
Factor V ◽  
Blood Monocytes ◽  
De Novo Synthesis ◽  
Hep G2 ◽  
Hep G2 Cells ◽  
Peripheral Blood Monocytes

SummaryWe demonstrate that in addition to possessing binding sites for intact factor V (FV), unstimulated peripheral blood monocytes also express activated factor V (FVa) on their surfaces. FVa was identified on the monocyte surface by monoclonal antibody B38 recognizing FVa light chain and by human oligoclonal antibodies H1 (to FVa light chain) and H2 (to FVa heavy chain) using immunofluorescence microscopy and flow cytometry. On Western blots, partially cleaved FV could be identified as a 220 kDa band in lysates of monocytes. In addition to surface expression of FVa, monocytes also contain intracellular FV as detected only after permeabilization by Triton X-100 by monoclonal antibody B10 directed specifically to the Cl domain not present in FVa. We sought to determine whether the presence of FV in peripheral blood monocytes is a result of de novo synthesis.Using in situ hybridization, no FV mRNA could be detected in monocytes, while in parallel control studies, factor V mRNA was detectable in Hep G2 cells and CD18 mRNA in monocytes. In addition, using reverse transcriptase and the polymerase chain reaction, no FV mRNA was detected in mononuclear cells or in U937 cells, but mRNA for factor V was present in Hep G2 cells using the same techniques. These data suggest that FV is present in human monocytes, presumably acquired by binding of plasma FV, and that the presence of this critical coagulation factor is not due to de novo synthesis.

Platelets Stimulate Thromboplastin Synthesis in Human Endothelial Cells

1983 ◽  
Vol 49 (02) ◽  
pp. 069-072 ◽  
Author(s):  
U L H Johnsen ◽  
T Lyberg ◽  
K S Galdal ◽  
H Prydz
Keyword(s):  
Endothelial Cells ◽  
De Novo ◽  
Umbilical Vein ◽  
Time Dependent ◽  
De Novo Synthesis ◽  
Human Endothelial Cells ◽  
Tumor Promotor ◽  
Coagulation Assay ◽  
Platelet Aggregates ◽  
Umbilical Vein Endothelial Cells

SummaryHuman umbilical vein endothelial cells in culture synthesize thromboplastin upon stimulation with phytohaemagglutinin (PHA) or the tumor promotor 12-O-tetradecanoyl-phorbol-13-acetate (TPA). The thromboplastin activity is further strongly enhanced in a time dependent reaction by the presence of gel-filtered platelets or platelet aggregates. This effect was demonstrable at platelet concentrations lower than those normally found in plasma, it may thus be of pathophysiological relevance. The thromboplastin activity increased with increasing number of platelets added. Cycloheximide inhibited the increase, suggesting that de novo synthesis of the protein component of thromboplastin, apoprotein III, is necessary.When care was taken to remove monocytes no thromboplastin activity and no apoprotein HI antigen could be demonstrated in suspensions of gel-filtered platelets, platelets aggregated with thrombin or homogenized platelets when studied with a coagulation assay and an antibody neutralization technique.

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