scholarly journals The effect of free glycerol intake on cerebral glycerol concentration

2021 ◽  
Vol 122 (01) ◽  
pp. 24-27
Author(s):  
J. Adamkov ◽  
P. Poczos ◽  
M. Kanta ◽  
J. Habalova ◽  
M. Bartos ◽  
...  
2018 ◽  
Vol 789 ◽  
pp. 87-91
Author(s):  
Harry Marareza ◽  
Rochmadi ◽  
Sarto

Shellac is a natural product which has been presumed as a fragile polymer due to itschemical properties. The objective of this study was to improve chemical properties of shellac by themodification with different concentration of glycerol and acrylic acid. Shellac was reacted withglycerol at various temperature and amounts of glycerol. The intermediate product was reacted withacrylic acid at different concentration. Acid value, hydroxyl groups, and free glycerol concentrationof modified shellac was determined. The result showed that acid value gradually decrease alongincreasing temperature for each ratio of glycerol and acrylic acid to shellac. The concentration ofhydroxyl groups rise as temperature and ratio increases. Furthermore, free glycerol concentration felldown along with the rise temperature. Modification chemical properties of shellac with glycerol andacrylic acid can be applied for the further study to enhance shellac properties.


1995 ◽  
Vol 41 (4) ◽  
pp. 619-620 ◽  
Author(s):  
M Nauck ◽  
K Winkler ◽  
R Siekmeier ◽  
N Marangos ◽  
B Richter ◽  
...  

Abstract High concentrations of glycerol in plasma may result in overestimation of triglycerides in chemical and enzymatic assays. Known causes of increased glycerol concentrations in blood include glycerol-contaminated blood-collector tubes and pseudohypertriglyceridemia, a condition caused by genetic defects in the gene for glycerol kinase. We report a patient with sudden hearing loss who presented with an increased blood glycerol concentration after undergoing an oral glycerol test.


2020 ◽  
Vol 58 (8) ◽  
pp. 1257-1264 ◽  
Author(s):  
Carla van Heerden ◽  
Agnes Magwete ◽  
Dineo Mabuza

AbstractBackgroundThe accurate and precise measurement of triglycerides is important due to the adverse effects associated with hypertriglyceridaemia. Most laboratory methods are based on enzymatic hydrolysis of triglycerides with measurement of the total glycerol. An elevated free glycerol concentration may result in overestimation of triglyceride concentrations. The removal of free glycerol by blanking may therefore be of clinical importance. The aim of this study was to compare the glycerol blanking and non-glycerol blanking triglyceride methods.MethodsThis was a method comparison study of 1518 samples from both in-patients and out-patients at Charlotte Maxeke Johannesburg Academic Hospital. Triglycerides were measured in each sample using both the blanking and the non-blanking methods. Analytical performance was assessed based on the National Cholesterol Education Program (NCEP) goals. Clinical impact was assessed according to the NCEP Adult Treatment Program III (ATP III) risk classification.ResultsThe method median was significantly higher in the non-blanking compared to the blanking method (1.33 vs. 1.12 mmol/L, p < 0.0001) in all patients. The average bias was above the total allowable error of 15% across all groups. There was a significant change in NCEP ATP III risk classification, with fewer patients classified as normal (67.6% vs. 74.6%, p < 0.0001) with the non-blanking method compared to the blanking method.ConclusionsThere was a significant error when glycerol blanking for triglyceride determination was not performed. The non-blanking triglyceride method overestimates triglyceride concentrations. This does not only exceed analytical performance goals, but also impacts on patient categorisation and clinical decision making in all patients.


2021 ◽  
Vol 5 (3) ◽  
Author(s):  
James R Vinyard ◽  
Efstathios Sarmikasoglou ◽  
Sarah L Bennett ◽  
Jose A Arce-Cordero ◽  
Glen Aines ◽  
...  

Abstract The objective of this study was to adapt existing in vitro methodologies to determine the extent of intestinal digestion of corn oil (CO), canola oil (CA), and beef tallow (BT) via manipulation of incubation length and concentrations of lipase, bile, and calcium within a buffer solution. Unless otherwise stated, 0.5 g of each lipid source were incubated separately and in triplicate, with triplicate batch culture runs for each treatment in 40 mL of 0.5 M KH2PO4 (pH = 7.6) for 24 h with pancreatin (8 g/L), bovine bile (2.5 g/L), and CaCl2 (10 mM). Individually, concentrations of pancreatin, bile, and CaCl2, as well as incubation length were tested. To examine the use of this assay to estimate in vitro total tract digestion, a KH2PO4 solution with concentrated amounts to reach the same final concentrations of pancreatin, bile, and Ca were used as the third step in a three-step total tract digestibility procedure. Free glycerol and free fatty acid (FFA) concentrations were measured using colorimetric assays as indicators of digestion. Data wereanalyzed as a completely randomized block design (block = run), using the Glimmix procedure of SAS. For each lipid source, free glycerol increased with increasing pancreatin; however, FFA was lowest at 0 g/L pancreatin but was similar at 6, 8, and 10 g/L. Both glycerol and FFA were greater for 2.5 and 5 g/L of bile than for 0 g/L for each lipid source. Calcium concentration did not affect glycerol or FFA for either CO or CA; however, glycerol and FFA for BT were greater when calcium was included at 5 and 10 mM than at 0 mM. For all fat sources, free glycerol and FFA increased after 1 h until 12 h, but did not increase from 12 to 24 h. When a concentrated mixture was used following fermentation and acidification steps, digestibility using FFA concentration increased as compared to just adding buffer; however, free glycerol concentration was indeterminable. Thus, free glycerol and FFA can be used as indicators of lipid digestion when a lipid source is incubated for at least 12 h in a buffer solution containing 8 g/L pancreatin, 2.5 g/L bile, and 5 mM Ca when only estimating in vitro intestinal digestion; however, when utilizing this assay in a three-step in vitro total tract digestibility procedure, only FFA can be used.


2006 ◽  
Vol 18 (2) ◽  
pp. 192
Author(s):  
H. Men ◽  
Y. Agca ◽  
L. K. Riley ◽  
R. S. Prather ◽  
J. K. Critser

The sensitivity of porcine embryos to cryopreservation is largely due to their high level of intracellular lipid content (Polge and Willadsen 1978 Cryobiology 15, 370-373). Delipation through centrifugation and micromanipulation resulted in a significant proportion of porcine embryos produced in vivo being able to survive cryopreservation and produce live births (Nagashima et al. 1995 Nature 374, 416). However, due to the intense resources needed for delipation via micromanipulation, this approach has limited practical value. In this experiment, we tested the hypothesis that delipation can be achieved through chemical stimulation of intracellular lipolysis in porcine embryos produced in vitro. Day 6 porcine blastocysts cultured in the presence of 10 �M forskolin, a lipolytic agent (Ho and Shi 1982 Biochem. Biophys. Res. Commun. 107, 157-164), in a group of 101-202 blastocysts per 50 �L of NCSU-23 + 4 mg/mL BSA (Sigma-Aldrich, St. Louis, MO, USA) yielded approximately 125 000-250 000 cells/mL (Zalatan et al. 2001 Endocrinology 142, 3783-3790). Blastocysts cultured in 50 �L NCSU-23 + 4 mg/mL BSA without the supplementation of forskolin served as control. Samples (12 �L) of the media were taken from culture at 0, 3, and 6 h and frozen at -20�C for lipolytic assay. Because the major content of intracellular lipids in porcine embryos is triacylglycerol and the hydrolysis of triacylglycerol results in the production of fatty acid and glycerol, therefore, the lipolytic activity in porcine blastocysts was measured by detection of glycerol concentration in the culture media. A commercially available Free Glycerol Regent (Sigma) was used with modifications. This kit only measures free glycerol released into the media as a result of endogenous lipase activity because the kit itself doesn't contain lipase. Ten �L of sample medium was mixed with 80 �L of Free Glycerol Regent and incubated in a 37�C water bath for 5 min. The resulting samples were read using a Cary 50 UV Spectrophotometer (Varian, Inc., Palo Alto, CA, USA). The actual concentration of glycerol in the culture medium was calculated using the glycerol standard curve. The glycerol concentration at 0 h was regarded as 0 for both the treatment group and the control group. The glycerol concentrations at other time points were calculated accordingly. The measurement was conducted four times for the treatment group and three times for the control group. The data were analyzed using a Student's t-test. Glycerol concentrations in the treatment group at 3 h and 6 h were 5.99 � 1.74 (mean � SEM) �M, and 10.49 � 0.81 �M, respectively, and both values were significantly different from their counterparts in the control group, which were 0.95 � 0.62 �M and 4.43 � 1.31 �M, respectively. These results indicate that the hydrolysis of intracellular lipids in porcine embryos can be stimulated by lipolytic agents and result in the partial reduction of the intracellular lipid content. This approach may be used for designing a better protocol for the cryopreservation of porcine embryos produced in vitro. This project was supported by a grant from the National Institutes of Health (U42 RR 018877).


2015 ◽  
Vol 308 (8) ◽  
pp. E680-E687 ◽  
Author(s):  
Mahmoud A. Mohammad ◽  
Patricia Maningat ◽  
Agneta L. Sunehag ◽  
Morey W. Haymond

The human mammary gland is capable of de novo synthesis of glucose and galactose (hexoneogenesis); however, the carbon source is incompletely understood. In this study, we investigated the role of acetate, glutamine, lactate and glycerol as potential carbon sources for hexoneogenesis. Healthy breastfeeding women were studied following a 24-h fast on two occasions separated by 1–3 wk. Five women were infused with [U-13C]lactate or [1,2-13C2]glutamine and five women with [U-13C]glycerol or [1,2-13C2]acetate. Enrichments of 13C in plasma and milk substrates were analyzed using GC-MS. Infusion of labeled lactate, glycerol, glutamine, and acetate resulted in plasma glucose being 22.0 ± 3.7, 11.2 ± 1.0, 2.5 ± 0.5, and 1.3 ± 0.2% labeled, respectively. Lactate, glutamine, or acetate did not contribute to milk glucose or galactose (0–2%). In milk, 13C-free glycerol enrichment was one-fourth that in plasma but free glycerol concentration in milk was fourfold higher than in plasma. Using [U-13C]glycerol and by accounting for tracer dilution, glycerol alone contributed to 10 ± 2 and 69 ± 11% of the hexoneogenesis of milk glucose and galactose, respectively. During [U-13C]glycerol infusion, the ratio of M3 enrichment on 4–6 carbons/M3 on 1–3 carbons of galactose was higher ( P < 0.05, 1.22 ± 0.05) than those of glucose in plasma (1.05 ± 0.03) and milk (1.07 ± 0.02). Reanalysis of samples from a previous study involving [U-13C]glucose infusion alone suggested labeling a portion of galactose consistent with pentose phosphate pathway (PPP) activity. We conclude that, although lactate contributed significantly to gluconeogenesis, glycerol alone provides the vast majority of substrate for hexoneogenesis. The relative contribution of the PPP vs. the reversal Embden-Meyerhof pathway to hexoneogenesis within the human mammary gland remains to be determined.


1996 ◽  
Vol 90 (6) ◽  
pp. 453-456 ◽  
Author(s):  
Jaswinder S. Samra ◽  
Cate L. Ravell ◽  
Sarah L. Giles ◽  
Peter Arner ◽  
Keith N. Frayn

1. The suggestion that the interstitial glycerol concentration in both adipose tissue and skeletal muscle is around 3 mmol/l (Maggs DG, Jacob R, Rife F, et al. J Clin Invest 1995; 96: 370–7), rather than close to the blood concentration as previously supposed, was tested by independent methods. 2. Free glycerol was infused, as part of a triacylglycerol emulsion, into six normal subjects and the arteriovenous difference for glycerol across the forearm was measured. In addition the relative interstitial glycerol concentration in subcutaneous adipose tissue was assessed simultaneously in four of the subjects by microdialysis. 3. During glycerol infusion the arterialized glycerol concentration rose from 52 ± 5 μmol/l to 250–300 μmol/l (P < 0.001) in a square wave fashion. The net arteriovenous difference for glycerol across the forearm changed from negative (output) to positive (uptake) (P < 0.01). In subcutaneous adipose tissue the interstitial glycerol concentration rose during glycerol infusion (P < 0.001). 4. These observations are most easily explained by the movement of glycerol from plasma to interstitial fluid down a concentration gradient. We conclude that the interstitial glycerol concentration in skeletal muscle and adipose tissue is closer to the arterial concentration than to 3 mmol/l.


2020 ◽  
Vol 2 (2) ◽  
Author(s):  
Musdar Musdar ◽  
Lukmanul Hakim ◽  
Juliani Juliani ◽  
Jailani Jailani

White sweet potato starch (Ipomea batatas L.) and avocado seed starch (Parsea americana Mill) derived from local plants have the potential to be developed as agricultural products. Starch is a hydrocolloid compound as a potential local resource to be utilized. Glycerol function as an anti-freezing which is hygroscopic. This study aims to determine the ratio of white sweet potato starch with avocado seed starch and the concentration of glycerol for making edible film. This study was an experiment using a completely randimized factorial design with 2 (two) main factor consisting of a comparison of white sweet potato starch and avocado seed with 3 levels: P1 = 35%:65%., P2=50%:50%., P3=65%:35% and glycerol concentration with 3 levels: G1=1%., G2=2%., G3=3%. The best result reasearch were content of 23.03% (tratment P1G1), solubility of 55.57% (treatment P3G2)., swelling test of 9.83% (treatment P2g3)., elongation of 8.18% (treatment P3G2)


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