Abstract
Inositol phosphoglycan-like compounds are produced by the hydrolysis of the membrane
bound glycosyl phosphoinositides. Besides being short term mediators of insulin action,
they inhibit peroxidases and catalase, increasing the concentration of cellular hydrogen
peroxide. Although high concentrations of hydrogen peroxide are toxic, moderate increases
of its basal level are signals for different metabolic pathways. The inhibitor, localized
in the cytosol of the cell, acts on peroxidases and catalase of the same tissue (homologous
action) and of other tissues or organisms (heterologous action). The inositol phosphoglycan-like
compound inhibits peroxidases with different prosthetic groups, i.e. containing iron
such as: thyroid peroxidase, lactoperoxidase, horseradish peroxidase, soy bean peroxidase;
and containing selenium such as glutathione peroxidase and 2-cys peroxiredoxin with
no prosthetic group. Besides peroxidases, the inositol phosphoglycan-like compound
inhibits catalase, another heme enzyme. The inhibition kinetics demonstrates a noncompetitive
effect. The site of action is not the prosthetic group, given that the inhibitor does
not produce any effect on the peak in the Soret region in the presence or absence
of hydrogen peroxide. In conclusion, the inositol phosphoglycan-like compound is the
general inhibitor of peroxidases and catalase involved in the modulation of hydrogen
peroxide level that acts in different metabolic pathways as a signal transducer.
Key words
oxidoreductases - inhibitor - signal transduction - hydrogen peroxide - metabolic
pathways
References
- 1
Saltiel AR.
Second messengers of insulin actions.
Diabetes Care.
1990;
13
244-256
- 2
Larner J.
Mediators of postreceptor action of insulin.
Am J Med.
1983;
74
38-51
- 3
Jones DR, Varela-Nieto I.
The role of glycosyl-phosphatidylinositol in signal transduction.
J Int Biochem Cell Biol.
1998;
30
313-326
- 4
Varela-Nieto I, León Y, Caro HN.
Cell signalling by inositol phosphoglycans from different species.
Comp Biochem Physiol.
1996;
115B
223-241
- 5
Fonteles MC, Huang LC, Larner J.
Infusion of pH 2.0 D-chiro-inositol glycan insulin putative mediator normalizes plasma glucose in streptozotocin
diabetic rats at a dose equivalent to insulin without inducing hypoglycaemia.
Diabetologia.
1996;
39
731-734
- 6
Jones DR, Varela-Nieto I.
Diabetes and the role of inositol-containing lipids in insulin signaling.
Mol Med.
1999;
5
505-514
- 7
Krawiec L, Pizarro RA, Aphalo P, Cavanagh EMV de, Pisarev MA, Juvenal GJ, Policastro L,
Bocanera LV.
Role of peroxidase inhibition by insulin in the bovine thyroid cell proliferation
mechanism.
Eur J Biochem.
2004;
271
2607-2614
- 8
Lee SF, Huang YT, Wu WS, Lin JK.
Induction of c-jun protooncogene expression by hydrogen peroxide through hydroxyl
radical generation and p60src tyrosine kinase activation.
Free Radic Biol Med.
1996;
21
437-448
- 9
Bocanera LB, Aphalo P, Pisarev MA, Gartner R, Silberschmidt D, Juvenal GJ, Beraldi G,
Krawiec L.
Presence of a soluble inhibitor of thyroid iodination in primary cultures of thyroid
cells.
Eur J Endocrinol.
1999;
141
55-60
- 10
DeGroot LJ, Davis AM.
Studies on the biosynthesis of iodotyrosine: a soluble thyroidal iodide-peroxidase
tyrosine-iodinase system.
Endocrinology.
1962;
70
492-504
- 11
Aebi H.
Catalase in vitro.
Meth Enzymol.
1984;
105
121-126
- 12
Wolff SP.
Ferrous ion oxidation in presence of ferric ion indicator xylenol orange for measurement
of hydroperoxides.
Methods Enzymol.
1994;
233
182-189
- 13
Folch J, Lees M, Sloane-Stanley GH.
A simple method for the isolation and purification of total lipids from animal tissues.
J Biol Chem.
1957;
226
497-509
- 14
Caro HN, Kunjara S, Rademacher TW, León Y, Jones DR, Avila MA, Varela-Nieto I.
Isolation and partial characterisation of insulin-mimetic inositol phosphoglycans
from human liver.
Biochem Mol Med.
1997;
61
214-228
- 15
Lowry OH, Rosebrough NJ, Farr AL, Randall RJ.
Protein measurement with the Folin phenol reagent.
J Biol Chem.
1951;
193
265-275
- 16
Dunnet CW.
A multiple comparison procedure for comparing several treatments with a control.
J Am Statis Assoc.
1955;
50
1096-1121
- 17
Rhee SG, Chae HZ, Kim K.
Peroxiredoxins : A historical overview and speculative preview of novel mechanisms
and emerging concepts in cell signaling.
Free Rad Biol Med.
2005;
38
1543-1552
- 18
Lineweaver H, Burk D.
The determination of enzyme dissociation constants.
J Am Chem Soc.
1934;
56
658-666
- 19 Dixon M, Webb EC. Enzyme inhibition and activation. In: The Enzymes 3rd Ed. New
York, Academic Press 1979: 332-467
- 20
Pañeda C, Villar AV, Alonso A, Goñi FM, Varela F, Brodbeck U, León Y, Varela-Nieto I,
Jones DR.
Purification and characterization of insulin-mimetic inositol phosphoglycan-like molecules
from grass pea (Lathyrus sativus) seeds.
Mol Med.
2001;
7
454-460
- 21
Divi RL, Chang HC, Doerge DR.
Anti-thyroid isoflavones from soy bean.
Biochem Pharmacol.
1997;
54
1087-1096
- 22 Metzler DE. How oxygen meets the electrons with generation of ATP, and other stories. In:
Biochemistry.
The Chemical Reactions of Living Cells. New York, Academic Press 1977: 559-629
Correspondence
L. Krawiec
División Bioquímica Nuclear - Unidad de Actividad Radiobiología
Comisión Nacional de Energía Atómica
Av. del Libertador 8250
1429-Buenos Aires
Argentina
Phone: +541167 72 71 85
Fax: +541167 72 71 88
Email: krawiec@cnea.gov.ar