Arginine effects on in vivo glucose-induced insulin secretion in mice and hamsters

Arginine effects on in vivo glucose-induced insulin secretion in mice and hamsters

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Title: Arginine effects on in vivo glucose-induced insulin secretion in mice and hamsters
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Article_Title: Arginine effects on in vivo glucose-induced insulin secretion in mice and hamsters
Authors: Ioana Trandaburu, Dorina Mirancea, Mirela Simionescu, Tiberiu Trandaburu
Affiliation: 1 Centre of Cytobiology, Institute of Biology, Bucharest
2 Laboratory of Histology and Embriology, Faculty of Sciences, University of Pitesti
Abstract: Alterations of the biphasic pattern of insulin secretion and of glycemia induced with glucose were described for the first time in hamsters after the sole i.p. injection of a mixture of glucose (3,3 g glucose/kg body weight) and L-arginine (7,16g arginine/kg body weight) or after 10 min. delayed injections of identical amounts of the same hexose and amino acid . With the exception of several minor, species-specific differences, the monophasic hyperglycemic profiles evoked by both experimental variants pledge undoubtedly for a stimulatory effect of arginine on the glucose induced insulin secretion (time-dependent potentiation; TDP), much less expressed in mice than in hamsters. Taking into account, however, the quantitative fluctuations of the B-cells granular contents evinced histochemically is rather likely to presume the co-existence and successive exercise of both potentiation and inhibition states (TDP, TDI) of the glucose-induced insulin secretion in the two rodents species studied. The above results obtained “in vivo” are discussed in connection with the findings reported in other mammalian species.
Keywords: in vivo time-course, insulin secretion and glycemia, arginine and glucose, mice and hamsters
References: Zawalich W.S., Zawalich K.C. Species differences in the induction of time-dependent potentiation of
insulin secretion. Endocrinology 1996;137: 1664-9.
Thams P, Capito K. L-arginine stimulation of glucoseinduced insulin secretion through membrane
depolarization and independent of nitric oxide. Eur.J.Endocrinol.,1999;140: 87-93.
Zawalich W.S., Yamazaky H., Zawalich K.C., Cline G. Comparative effects of amino acids and glucose
on insulin secretion from isolated rat or mouse islets. J.Endocrinol., 2004;183: 309-19.
Nesher R., Cerasi E. Modeling phasic insulin release: immediate and time-dependent effects of
glucose. Diabetes 2002;51, supl 1: 53-9.
Nesher R., Tuch B., Hage C., Levy J., Cerasi E. Timedependent inhibition of insulin release:
suppression of the arginine effect by hyperglycaemia. Diabetologia 1984a;26: 142-5.
Nesher R., Waldman L., Cerasi E. Time-dependent inhibition of insulin release: glucose-arginine
interactions in the perfused rat pancreas. Diabetologia 1984b;26: 146-9.
Henquin J.C., Ishiyama N., Nenquin M., Ravier M.A., Jonas J.C. Signals and pools underlyining
biphasic insulin secretion. Diabetes 2002;51, suppl 1: 60-7.
Nunemaker C.S., Wasserman D.H., McGuinness O.P., Sweet I.R., Teague J.C., Satin L.S. Insulin
secretion in the conscious mouse is biphasic and pulsatile. Am.J.Physiol.Endocrinol.Metab.
2006;290: E523-9.
Coalson R.E. Pseudoisocyanine-staining of insulin and specificity of empirical islets cell stains. Stain Technol. 1966;41: 121-131.
Epple A. Islet cytology in urodele amphibians. Gen.Comp.Endocrinol. 1966;7: 207-14.
Trandaburu I., Mirancea D., Argint M., Trandaburu T. Biphasic dynamic of the “in vivo” glucoseinduced insulin secretion in mice and hamsters. Rom. J.Biol.- Zool. 2006; 51 in print
Lucotti P., Setola E., Monti L.D., Gallucio E., Costa S., Sandoli E.P., Rabaiotti G., Gatti R., Piatti P. Beneficial effects of oral L-arginine treatment added to a hypocaloric diet and exercise training program in obese, insulin resistant type 2 diabetic patients. Am.J.Physiol.Endocrinol.Metab. 2006; 29:E906-12.
Ishiyama N., Ravier M.A., Henquin J.C. Dual mechanism of the potentiation by glucose of insulin secretion induced by arginine and tolbutamide in mouse islets. Am.J.Physiol.Endocrinol.Metab. 2006;
290:E540-9.
Zawalich W.S. Zawalich K.C., Tesz G.I., Sterpka J.A., Philbrick W.M. Insulin secretion and IP levels
in two distant lineages of the genus Mus: comparisons wit rat islets. Am.J.Physiol.Endocrinol.Metab.,280:E720-9, 2001
Rorsman P., Eliasson L., Renstrőm E., Gromada J., Barg S., Gőpel S.The cell physiology of biphasic insulin secretion.News Physiol. Sci. 15, pp. 72-77, 2005
Straub S.G., Sharp G.W.G. Hypothesis: one rate limiting step controls the magnitude of both
phases of glucose-stimulated insulin secretion. Am.J.Physiol.Endocrinol.Metab. 287, pp. 565-71, 2004
Read_full_article: pdf/18-2008/SU08Trandaburu.pdf
Correspondence: Ioana TRANDABURU, Institute of Biology, no. 296 Spl. Independenţei, 060031, Bucharest, e-mail: itrandaburu@yahoo.com; ioana.trandaburu@ibiol.ro

Read full article
Article Title: Arginine effects on in vivo glucose-induced insulin secretion in mice and hamsters
Authors: Ioana Trandaburu, Dorina Mirancea, Mirela Simionescu, Tiberiu Trandaburu
Affiliation: 1 Centre of Cytobiology, Institute of Biology, Bucharest
2 Laboratory of Histology and Embriology, Faculty of Sciences, University of Pitesti
Abstract: Alterations of the biphasic pattern of insulin secretion and of glycemia induced with glucose were described for the first time in hamsters after the sole i.p. injection of a mixture of glucose (3,3 g glucose/kg body weight) and L-arginine (7,16g arginine/kg body weight) or after 10 min. delayed injections of identical amounts of the same hexose and amino acid . With the exception of several minor, species-specific differences, the monophasic hyperglycemic profiles evoked by both experimental variants pledge undoubtedly for a stimulatory effect of arginine on the glucose induced insulin secretion (time-dependent potentiation; TDP), much less expressed in mice than in hamsters. Taking into account, however, the quantitative fluctuations of the B-cells granular contents evinced histochemically is rather likely to presume the co-existence and successive exercise of both potentiation and inhibition states (TDP, TDI) of the glucose-induced insulin secretion in the two rodents species studied. The above results obtained “in vivo” are discussed in connection with the findings reported in other mammalian species.
Keywords: in vivo time-course, insulin secretion and glycemia, arginine and glucose, mice and hamsters
References: Zawalich W.S., Zawalich K.C. Species differences in the induction of time-dependent potentiation of
insulin secretion. Endocrinology 1996;137: 1664-9.
Thams P, Capito K. L-arginine stimulation of glucoseinduced insulin secretion through membrane
depolarization and independent of nitric oxide. Eur.J.Endocrinol.,1999;140: 87-93.
Zawalich W.S., Yamazaky H., Zawalich K.C., Cline G. Comparative effects of amino acids and glucose
on insulin secretion from isolated rat or mouse islets. J.Endocrinol., 2004;183: 309-19.
Nesher R., Cerasi E. Modeling phasic insulin release: immediate and time-dependent effects of
glucose. Diabetes 2002;51, supl 1: 53-9.
Nesher R., Tuch B., Hage C., Levy J., Cerasi E. Timedependent inhibition of insulin release:
suppression of the arginine effect by hyperglycaemia. Diabetologia 1984a;26: 142-5.
Nesher R., Waldman L., Cerasi E. Time-dependent inhibition of insulin release: glucose-arginine
interactions in the perfused rat pancreas. Diabetologia 1984b;26: 146-9.
Henquin J.C., Ishiyama N., Nenquin M., Ravier M.A., Jonas J.C. Signals and pools underlyining
biphasic insulin secretion. Diabetes 2002;51, suppl 1: 60-7.
Nunemaker C.S., Wasserman D.H., McGuinness O.P., Sweet I.R., Teague J.C., Satin L.S. Insulin
secretion in the conscious mouse is biphasic and pulsatile. Am.J.Physiol.Endocrinol.Metab.
2006;290: E523-9.
Coalson R.E. Pseudoisocyanine-staining of insulin and specificity of empirical islets cell stains. Stain Technol. 1966;41: 121-131.
Epple A. Islet cytology in urodele amphibians. Gen.Comp.Endocrinol. 1966;7: 207-14.
Trandaburu I., Mirancea D., Argint M., Trandaburu T. Biphasic dynamic of the “in vivo” glucoseinduced insulin secretion in mice and hamsters. Rom. J.Biol.- Zool. 2006; 51 in print
Lucotti P., Setola E., Monti L.D., Gallucio E., Costa S., Sandoli E.P., Rabaiotti G., Gatti R., Piatti P. Beneficial effects of oral L-arginine treatment added to a hypocaloric diet and exercise training program in obese, insulin resistant type 2 diabetic patients. Am.J.Physiol.Endocrinol.Metab. 2006; 29:E906-12.
Ishiyama N., Ravier M.A., Henquin J.C. Dual mechanism of the potentiation by glucose of insulin secretion induced by arginine and tolbutamide in mouse islets. Am.J.Physiol.Endocrinol.Metab. 2006;
290:E540-9.
Zawalich W.S. Zawalich K.C., Tesz G.I., Sterpka J.A., Philbrick W.M. Insulin secretion and IP levels
in two distant lineages of the genus Mus: comparisons wit rat islets. Am.J.Physiol.Endocrinol.Metab.,280:E720-9, 2001
Rorsman P., Eliasson L., Renstrőm E., Gromada J., Barg S., Gőpel S.The cell physiology of biphasic insulin secretion.News Physiol. Sci. 15, pp. 72-77, 2005
Straub S.G., Sharp G.W.G. Hypothesis: one rate limiting step controls the magnitude of both
phases of glucose-stimulated insulin secretion. Am.J.Physiol.Endocrinol.Metab. 287, pp. 565-71, 2004
*Correspondence: Ioana TRANDABURU, Institute of Biology, no. 296 Spl. Independenţei, 060031, Bucharest, e-mail: itrandaburu@yahoo.com; ioana.trandaburu@ibiol.ro