Quantitation of polyamines in hypothalamus and pituitary of female and male developing rats

The quantitation of four polyamines in hypothalamus and pituitary is studied in male and female developing rats using an improved high-performance liquid chromatography method. In the hypothalamus, putrescine (PUT) reaches the highest concentration (nmol/mg protein) on day 6. It shows the lowest val...

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Autor principal: Thyssen, S.M
Otros Autores: Libertun, C.
Formato: Capítulo de libro
Lenguaje:Inglés
Publicado: Elsevier Ireland Ltd 2002
Acceso en línea:Registro en Scopus
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024 7 |2 scopus  |a 2-s2.0-0037134113 
024 7 |2 cas  |a agmatine, 306-60-5; eflornithine, 67037-37-0, 70052-12-9; putrescine, 110-60-1, 333-93-7; spermidine, 124-20-9, 334-50-9 
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100 1 |a Thyssen, S.M. 
245 1 0 |a Quantitation of polyamines in hypothalamus and pituitary of female and male developing rats 
260 |b Elsevier Ireland Ltd  |c 2002 
270 1 0 |m Libertun, C.; Laboratorio de Neuroendocrinologia, Inst. de Biol. y Med. Exp.-CONICET, Vuelta de Obligado 2490, 1428 Buenos Aires, Argentina; email: libertun@dna.uba.ar 
506 |2 openaire  |e Política editorial 
504 |a Contestabile, A., Facchinetti, F., Ciani, E., Sparapani, M., Virgili, M., Chronic neonatal blockade of NMDA receptor does not affect developmental polyamine metabolism but results in altered response to the excitotoxic induction of ornithine decarboxylase (1994) Neurochem. Int., 24, pp. 549-554 
504 |a Flores, H.E., Galston, A.W., Analysis of polyamines in higher plants by high performance liquid chromatography (1982) Plant Physiol., 69, pp. 701-706 
504 |a Gilad, G.M., Gilad, V.H., Polyamine uptake, binding and release in rat brain (1991) Eur. J. Pharmacol., 193, pp. 41-46 
504 |a Gilad, G.M., Dornay, M., Gilad, V.H., Polyamines induce precocious development in rats. Possible interaction with growth factors (1989) Int. J. Dev. Neurosci., 7, pp. 641-653 
504 |a He, Y., Suziki, T., Kashiwagi, K., Igarashi, K., Antizyme delays the restoration of growth of polyamine-deficient cells through its negative regulation of polyamine transport (1994) Biochem. Biophys. Res. Commun., 203, pp. 608-614 
504 |a Hockl, P.F., Thyssen, S.M., Libertun, C., An improved HPLC method for identification and quantitation of polyamines and related compounds as benzoylated derivatives (2000) J. Liq. Chromatogr. Rel. Technol., 23, pp. 693-703 
504 |a Khan, N.A., Quemener, V., Moulinoux, J.P., Polyamine membrane transport regulation (1991) Cell Biol. Int. Rep., 15, pp. 9-24 
504 |a Li, G., Regunathan, S., Barrow, C.J., Eshraghi, J., Cooper, R., Reis, D.J., Agmatine: An endogenous clonidine-displacing substance in the brain (1994) Science, 263, pp. 966-969 
504 |a Lowry, O.H., Rosebrough, N.H., Farr, A.L., Randall, R.J., Protein measurement with Folin phenol reagent (1951) J. Biol. Chem., 193, pp. 265-275 
504 |a Morgan, D.M.L., (1998) Polyamine Protocols, pp. 1-186. , Humana Press, Totowa, NJ 
504 |a Morrison, L.D., Becker, L., Ang, L.C., Kish, S.J., Polyamines in human brain: Regional distribution and influence of aging (1995) J. Neurochem., 65, pp. 636-642 
504 |a Najm, I., Vanderklish, P., Lynch, G., Baudry, M., Effect of treatment with α-difluoromethylornithine on polyamine and spectrin breakdown levels in neonatal rat brain (1991) Dev. Brain Res., 63, pp. 287-289 
504 |a Pegg, A.E., Recent advances in the biochemistry of polyamines in eukaryotes (1986) Biochem. J., 234, pp. 249-262 
504 |a Sastre, M., Regunathan, S., Galea, E., Reis, D.J., Agmatinase activity in rat brain: A metabolic pathway for the degradation of agmatine (1996) J. Neurochem., 67, pp. 1761-1765 
504 |a Scalabrino, G., Lorenzini, E.C., Polyamines and mammalian hormones. Part II: Paracrine signals and intracellular regulators (1991) Mol. Cell. Endocrinol., 77, pp. 37-56 
504 |a Scalabrino, G., Lorenzini, E.C., Ferioli, M.E., Polyamines and mammalian hormones. Part I: Biosynthesis, interconversion and hormone effects (1991) Mol. Cell. Endocrinol., 77, pp. 1-35 
504 |a Seiler, N., Pharmacological properties of the natural polyamines and their depletion by biosynthesis inhibitors as a therapeutic approach (1991) Prog. Drug Res., 37, pp. 107-160 
504 |a Sltokin, T.A., Bartolome, J., Role of ornithine decarboxylase and the polyamines in nervous system development: A review (1986) Brain Res. Bull., 17, pp. 307-320 
504 |a Thyssen, S.M., Libertun, C., α-Difluoromethylornithine modifies FSH secretion and puberty onset in the female rat (1996) Proc. Soc. Exp. Biol. Med., 211, pp. 76-80 
504 |a Thyssen, S.M., Becu-Villalobos, D., Lacau-Mengido, I.M., Libertun, C., α-Difluoromethylornithine modifies gonadotropin-releasing hormone release and follicle-stimulating hormone secretion in the immature female rat (1997) Proc. Soc. Exp. Biol. Med., 215, pp. 192-197 
520 3 |a The quantitation of four polyamines in hypothalamus and pituitary is studied in male and female developing rats using an improved high-performance liquid chromatography method. In the hypothalamus, putrescine (PUT) reaches the highest concentration (nmol/mg protein) on day 6. It shows the lowest value in comparison with any other polyamine. Spermidine (SPD) is high during the first postnatal days. Spermine (SPM) fluctuates, and agmatine (AGM) is highest during the first week. SPD, SPM and AGM are lower in females. In the pituitary, PUT, SPD and AGM are high during the first week. SPM remains constant and it is higher in males. AGM is higher in males only on day 1. PUT shows the lowest concentration of all. Concentrations of PUT, SPD and SPM are higher in the pituitary; AGM is higher in the hypothalamus. α-Difluoromethylornithine (a specific and irreversible inhibitor of ornithine decarboxylase) decreases PUT and SPD, increased SPM and AGM remain unchanged in the hypothalamus and pituitary. Thus, each polyamine has its own pattern in hypothalamus and in pituitary during development in males and females; these changes could be related to the hypothalamic control of pituitary secretion of hormones related to reproduction in mammals. © 2002 Elsevier Science Ireland Ltd. All rights reserved.  |l eng 
536 |a Detalles de la financiación: Agencia Nacional de Promoción Científica y Tecnológica, BID 802 OC AR PICT 0043 
536 |a Detalles de la financiación: Consejo Nacional de Investigaciones Científicas y Técnicas 
536 |a Detalles de la financiación: Universidad de Buenos Aires 
536 |a Detalles de la financiación: This work was supported by grants from Consejo Nacional de Investigaciones Cientı́ficas y Técnicas (CONICET), Agencia Nacional de Promoción Cientı́fica y Tecnológica (ANPCyT; BID 802 OC AR PICT 0043), Universidad de Buenos Aires and Ministerio de Salud Pública, Argentina. 
593 |a Laboratorio de Neuroendocrinología, Instituto de Biología y Medicina Experimental-CONICET, Buenos Aires, Argentina 
593 |a Department of Physiology, University of Buenos Aires Medical School, Buenos Aires, Argentina 
593 |a Laboratorio de Neuroendocrinolog, Instituto de Biologa y Medicina Experimental-CONICET, Vuelta de Obligado 2490, 1428 Buenos Aires, Argentina 
690 1 0 |a DEVELOPMENT 
690 1 0 |a HYPOTHALAMUS 
690 1 0 |a PITUITARY 
690 1 0 |a POLYAMINES 
690 1 0 |a RAT 
690 1 0 |a SEXES 
690 1 0 |a Α-DIFLUOROMETHYLORNITHINE 
690 1 0 |a AGMATINE 
690 1 0 |a EFLORNITHINE 
690 1 0 |a ORNITHINE DECARBOXYLASE INHIBITOR 
690 1 0 |a POLYAMINE DERIVATIVE 
690 1 0 |a PUTRESCINE 
690 1 0 |a SPERMIDINE 
690 1 0 |a ANIMAL EXPERIMENT 
690 1 0 |a ARTICLE 
690 1 0 |a CONTROLLED STUDY 
690 1 0 |a DIAGNOSTIC VALUE 
690 1 0 |a DOSE RESPONSE 
690 1 0 |a FEMALE 
690 1 0 |a HIGH PERFORMANCE LIQUID CHROMATOGRAPHY 
690 1 0 |a HYPOPHYSIS 
690 1 0 |a HYPOPHYSIS FUNCTION 
690 1 0 |a HYPOTHALAMUS 
690 1 0 |a MALE 
690 1 0 |a MAMMAL 
690 1 0 |a NONHUMAN 
690 1 0 |a PERINATAL PERIOD 
690 1 0 |a PRIORITY JOURNAL 
690 1 0 |a QUANTITATIVE ANALYSIS 
690 1 0 |a RAT 
690 1 0 |a REPRODUCTION 
700 1 |a Libertun, C. 
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