SUBJECT: REVIEW METHODS OF DETECTING SUGAR IN A SAMPLE

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Inas Hasan AL-Khafaji, . (2024). SUBJECT: REVIEW METHODS OF DETECTING SUGAR IN A SAMPLE. The American Journal of Interdisciplinary Innovations and Research, 6(01), 50–59. https://doi.org/10.37547/tajiir/Volume06Issue01-08
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Abstract

The sugar is a simple type of carbohydrate and represents the main source of energy to power the biological and physical activities in the body. However, it has been reported that over weight gain, imperfect metabolic processes and heart diseases are mainly related to excess sugar intake, which causes diabetic complains. This has raised the demand of having reliable test methods for quantifying sugar amount in different samples to both monitor sugar levels and to study the biological effects of carbohydrates. This provides valuable information in various fields, including food science, biochemistry, and medicine. Several test methods have been applied to detect the presence of sugar in a biological sample. Conventional tests imply using special chemical reagents. Two well known tests are discussed briefly in this report, namely Molich’s and Fehling's tests. The chemical reagents, test procedures, precaution as well as advantages and limitations were comprehensively discussed. A comparison between the two tests has been thoroughly addressed.   

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References

Lehninger Principles of Biochemistry by David L. Nelson and Michael M. Cox

Biochemistry by Lubert Stryer

Biochemistry by Jeremy M. Berg, John L. Tymoczko, and Lubert Stryer

Principles of Biochemistry by Albert L. Lehninger, David L. Nelson, and Michael M. Cox

Biochemistry: The Molecular Basis of Life by Trudy McKee and James R. McKee

Parikka P et al. Prevention of type 2 diabetes mellitus by changes

in lifestyle among subjects with impaired glucose tolerance. N Engl J Med 2001; 344: 1343–1350

Iezzi M, Kouri G, Fukuda M, Wollheim CB. Synaptotagmin V and IX isoforms control Ca2+ -dependent insulin exocytosis. J Cell Sci 2004; 117 (Pt 15): 3119–3127.

Cabrera O, Berman DM, Kenyon NS, Ricordi C, Berggren PO, Caicedo A. The unique cytoarchitecture of human pancreatic islets has implications for islet cell function. Proc Natl Acad Sci USA 2006; 103:2334–2339.

Freychet L, Rizkalla SW, Desplanque N, Basdevant A, Zirinis P, Tchobroutsky G et al. Effect of intranasal glucagon on blood glucose levels in healthy subjects and hypoglycaemic patients with insulin-dependent diabetes. Lancet 1988; 1:1364–1366.

Komatsu M, Takei M, Ishii H, Sato Y. Glucose-stimulated insulin secretion: a newer perspective. JDiabetes Investig 2013; 4:511–516.

Khan AH, Pessin JE. Insulin regulation of glucose uptake: a complex interplay of intracellular signalling pathways. Diabetologia 2002; 45: 1475–1483.

Kohn AD, Summers SA, Birnbaum MJ, Roth RA. Expression of a constitutively active Akt Ser/Thr kinase in 3T3-L1 adipocytes stimulates glucose uptake and glucose transporter 4 translocation. JBiol Chem 1996; 271: 31372–31378.

Zisman A, Peroni OD, Abel ED, Michael MD, Mauvais-Jarvis F, Lowell BB et al. Targeted disruption of the glucose transporter 4 selectively in muscle causes insulin resistance and glucose intolerance. Nat Med 2000; 6: 924–928.

Sibrowski W, Seitz HJ. Rapid action of insulin and cyclic AMP in the regulation of functional messenger RNA coding for glucokinase in rat liver. JBiol Chem 1984; 259:343–346.

Kim SY, Kim HI, Kim TH, Im SS, Park SK, Lee IK et al. SREBP-1c mediates the insulin-dependent hepatic glucokinase expression. JBiol Chem 2004; 279: 30823–30829.

Aiston S, Hampson LJ, Arden C, Iynedjian PB, Agius L. The role of protein kinase B/Akt in insulin-induced inactivation of phosphorylase in rat hepatocytes. Diabetologia 2006; 49:174–182.

Syed NA, Khandelwal RL. Reciprocal regulation of glycogen phosphorylase and glycogen synthase by insulin involving phosphatidylinositol-3 kinase and protein phosphatase-1 in HepG2 cells. Mol Cell Biochem 2000; 211:123–136.

Miller TB Jr, Larner J. Mechanism of control of hepatic glycogenesis by insulin. JBiol Chem 1973; 248:3483–3488.

Akpan JO, Gardner R, Wagle SR. Studies on the effects of insulin and acetylcholine on activation of glycogen synthase and on glycogenesis in hepatocytes. Biochem Biophys Res Commun 1974; 61: 222–229.

Stalmans W, De Wulf H, Hue L, Hers HG. The sequential inactivation of glycogen phosphorylase and activation of glycogen synthetase in liver after the administration of glucose to mice and rats. The mechanism of the hepatic threshold to glucose. Eur J Biochem 1974; 41:127–134.

O'Brien RM, Lucas PC, Forest CD, Magnuson MA, Granner DK. Identification of a sequence in the PEPCK gene that mediates a negative effect of insulin on transcription. Science 1990; 249:533–537.

Streeper RS, Svitek CA, Chapman S, Greenbaum LE, Taub R, O'Brien RM. A multicomponent insulin response sequence mediates a strong repression of mouse glucose-6-phosphatase gene transcription by insulin. J Biol Chem 1997; 272: 11698–11701.

Duong DT, Waltner-Law ME, Sears R, Sealy L, Granner DK. Insulin inhibits hepatocellular glucose production by utilizing liver-enriched transcriptional inhibitory protein to disrupt the association of CREB-binding protein and RNA polymerase II with the phosphoenolpyruvate carboxykinase gene promoter. J Biol Chem 2002; 277: 32234–32242.

Nakae J, Kitamura T, Silver DL, Accili D. The forkhead transcription factor Foxo1 (Fkhr) confers insulin sensitivity onto glucose-6-phosphatase expression. JClin Invest 2001; 108:1359–1367.

Schmoll D, Walker KS, Alessi DR, Grempler R, Burchell A, Guo S et al. Regulation of glucose-6-phosphatase gene expression by protein kinase Balpha and the forkhead transcription factor FKHR. Evidence for insulin response unit-dependent and -independent effects of insulin on promoter activity. JBiol Chem 2000; 275: 36324–36333.

Lochhead PA, Coghlan M, Rice SQ, Sutherland C. Inhibition of GSK-3 selectively reduces glucose-6-phosphatase and phosphatase and phosphoenolypyruvate carboxykinase gene expression. Diabetes 2001; 50:937–946.

Walton PE, Etherton TD. Stimulation of lipogenesis by insulin in swine adipose tissue: antagonism by porcine growth hormone. JAnimSci 1986; 62:1584–1595.

McTernan PG, Harte AL, Anderson LA, Green A, Smith SA, Holder JC et al. Insulin and rosiglitazone regulation of lipolysis and lipogenesis in human adipose tissue in vitro. Diabetes 2002; 51:1493–1498.

Biolo G, Declan Fleming RY, Wolfe RR. Physiologic hyperinsulinemia stimulates protein synthesis and enhances transport of selected amino acids in human skeletal muscle. JClin Invest 1995; 95:811–819.

Ashcroft FM, Proks P, Smith PA, Ammala C, Bokvist K, Rorsman P. Stimulus-secretion coupling in pancreatic beta cells. JCell Biochem 1994; 55 Suppl:54–65.

Henquin JC. Triggering and amplifying pathways of regulation of insulin secretion by glucose. Diabetes 2000; 49:1751–1760.

Cerasi E, Luft R. The plasma insulin response to glucose infusion in healthy subjects and in diabetes mellitus. Acta Endocrinol (Copenh) 1967; 55:278–304.

Porte D Jr, Pupo AA. Insulin responses to glucose: evidence for a two pool system in man. JClin Invest 1969; 48:2309–2319.

Curry DL, Bennett LL, Grodsky GM. Dynamics of insulin secretion by the perfused rat pancreas. Endocrinology 1968; 83:572–584.

Hao M, Li X, Rizzo MA, Rocheleau JV, Dawant BM, Piston DW. Regulation of two insulin granule populations within the reserve pool by distinct calcium sources. J Cell Sci 2005; 118(Pt 24): 5873–5884.

Olofsson CS, Gopel SO, Barg S, Galvanovskis J, Ma X, Salehi A et al. Fast insulin secretion reflects exocytosis of docked granules in mouse pancreatic B-cells. Pflugers Arch 2002; 444:43–51.

Thurmond DC. Regulation of Insulin Action and Insulin Secretion by SNARE-Mediated Vesicle Exocytosis. Landes Bioscience: Austin, TX, USA, 2000.

Chapman ER, An S, Barton N, Jahn R. SNAP-25, a t-SNARE which binds to both syntaxin and synaptobrevin via domains that may form coiled coils. JBiol Chem 1994; 269:27427–27432.

Fasshauer D, Otto H, Eliason WK, Jahn R, Brunger AT. Structural changes are associated with soluble N-ethylmaleimide-sensitive fusion protein attachment protein receptor complex formation. JBiol Chem 1997; 272: 28036–28041.

Voets T, Toonen RF, Brian EC, de Wit H, Moser T, Rettig J et al. Munc18-1 promotes large dense-core vesicle docking. Neuron 2001; 31: 581–591.

Lam PP, Ohno M, Dolai S, He Y, Qin T, Liang T et al. Munc18b is a major mediator of insulin exocytosis in rat pancreatic beta-cells. Diabetes 2013; 62:2416–2428.

Foster LJ, Yeung B, Mohtashami M, Ross K, Trimble WS, Klip A. Binary interactions of the SNARE proteins syntaxin-4, SNAP23, and VAMP-2 and their regulation by phosphorylation. Biochemistry 1998; 37: 11089–11096.

Ravichandran V, Chawla A, Roche PA. Identification of a novel syntaxin- and synaptobrevin/VAMP-binding protein, SNAP-23, expressed in non-neuronal tissues. JBiolChem 1996; 271:13300–13303.

Leung YM, Kwan EP, Ng B, Kang Y, Gaisano HY. SNAREing voltage-gated K+ and ATP-sensitive K+ channels: tuning beta-cell excitability with syntaxin-1A and other exocytotic proteins. Endocr Rev 2007; 28: 653–663.

Regazzi R, Wollheim CB, Lang J, Theler JM, Rossetto O, Montecucco C et al. VAMP-2 and cellubrevin are expressed in pancreatic beta-cells and are essential for Ca(2+)-but not for GTP gamma S-induced insulin secretion. EMBO J 1995; 14:2723–2730.

Zhu D, Koo E, Kwan E, Kang Y, Park S, Xie H et al. Syntaxin-3 regulates newcomer insulin granule exocytosis and compound fusion in pancreatic beta cells. Diabetologia 2013; 56:359–369.

Zhu D, Zhang Y, Lam PP, Dolai S, Liu Y, Cai EP et al. Dual role of VAMP8 in regulating insulin exocytosis and islet beta cell growth. Cell Metab 2012; 16:238–249.

Gustavsson N, Han W. Calcium-sensing beyond neurotransmitters: functions of synaptotagmins in neuroendocrine and endocrine secretion. Biosci Rep 2009; 29:245–259.

Gut A, Kiraly CE, Fukuda M, Mikoshiba K, Wollheim CB, Lang J. Expression and localisation of synaptotagmin isoforms in endocrine beta-cells: their function in insulin exocytosis. J Cell Sci 2001; 114(Pt 9): 1709–1716.

Gustavsson N, Wei SH, Hoang DN, Lao Y, Zhang Q, Radda GK et al. Synaptotagmin-7 is a principal Ca2+ sensor for Ca2+ -induced glucagon exocytosis in pancreas. JPhysiol 2009; 587(Pt 6): 1169–1178.

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