Horm Metab Res 2014; 46(05): 322-327
DOI: 10.1055/s-0033-1361159
Endocrine Research
© Georg Thieme Verlag KG Stuttgart · New York

Neonatal Exposure to Estradiol Valerate Increases Dopamine Content in Nigrostriatal Pathway During Adulthood in the Rat

G. Cruz
1   Departamento de Fisiología, Facultad de Ciencias, Centro de Neurobiología y Plasticidad Cerebral, Universidad de ­Valparaíso, Valparaíso, Chile
,
R. Riquelme*
1   Departamento de Fisiología, Facultad de Ciencias, Centro de Neurobiología y Plasticidad Cerebral, Universidad de ­Valparaíso, Valparaíso, Chile
,
P. Espinosa*
1   Departamento de Fisiología, Facultad de Ciencias, Centro de Neurobiología y Plasticidad Cerebral, Universidad de ­Valparaíso, Valparaíso, Chile
,
P. Jara
2   Faculty of Chemistry and Biology, University of Santiago de Chile, Santiago, Chile
,
A. Dagnino-Subiabre
1   Departamento de Fisiología, Facultad de Ciencias, Centro de Neurobiología y Plasticidad Cerebral, Universidad de ­Valparaíso, Valparaíso, Chile
,
G. M. Renard
1   Departamento de Fisiología, Facultad de Ciencias, Centro de Neurobiología y Plasticidad Cerebral, Universidad de ­Valparaíso, Valparaíso, Chile
,
R. Sotomayor-Zárate
1   Departamento de Fisiología, Facultad de Ciencias, Centro de Neurobiología y Plasticidad Cerebral, Universidad de ­Valparaíso, Valparaíso, Chile
3   Millennium Science Nucleus in Stress and Addiction (NEDA), Pontificia Universidad Católica de Chile, Santiago, Chile
› Author Affiliations
Further Information

Publication History

received 08 August 2013

accepted 14 November 2013

Publication Date:
09 December 2013 (online)

Abstract

Research in programming has focused in the study of stimuli that affect sensitive periods of development such as prenatal and neonatal stage. We previously showed that exposure to estradiol valerate to female rats during the first 12 h of life increased catecholamine content in ventromedial-arcuatus hypothalamus of the adult rat. However, changes in others dopaminergic circuits have not been studied. The purpose of this work was to determine the neurotransmitters changes induced by neonatal estradiol valerate (0.1 mg/50 μl s. c. per rat) administration on nigrostriatal pathway of adult female rats. Sesame oil (50 μl s. c. per rat) was administered in a control parallel group. EV-1 adult rats presented effective markers of long-term estrogenization as decreased serum levels of progesterone and a reduction in the size of estrogen-sensitive organs. In the brain, neonatal estradiol valerate administration led to a significant increase in dopamine content in striatum, substantia nigra and ventral tegmental area. With respect to the contents of dopamine metabolites, only 3-methoxytyramine content increased in substantia nigra and ventral tegmental area. In addition, the content of noradrenaline increased only in striatum. Interestingly, estrogenized rats lacked locomotor activity induced by acute dose of amphetamine (1 mg/kg i. p.). Altogether, these results show that neonatal exposure to estradiol valerate permanently modified the content of monoamine neurotransmitters in nigrostriatal pathway and amphetamine-induced locomotor activity of adult female rats. This might imply that estrogenized rats could have changes in the expression of key proteins in dopaminergic regulation, as tyrosine hydroxylase and dopamine transporter.

* Both authors contributed equally to this work.


 
  • References

  • 1 Lucas A. Programming by early nutrition in man. Ciba Found Symp. 1991; 156: 38-50 discussion 50–5
  • 2 Koenig JI, Elmer GI, Shepard PD, Lee PR, Mayo C, Joy B, Hercher E, Brady DL. Prenatal exposure to a repeated variable stress paradigm elicits behavioral and neuroendocrinological changes in the adult offspring: potential relevance to schizophrenia. Behav Brain Res 2005; 156: 251-261
  • 3 Sotomayor-Zarate R, Dorfman M, Paredes A, Lara HE. Neonatal exposure to estradiol valerate programs ovarian sympathetic innervation and follicular development in the adult rat. Biol Reprod 2008; 78: 673-680
  • 4 Sotomayor-Zarate R, Tiszavari M, Cruz G, Lara HE. Neonatal exposure to single doses of estradiol or testosterone programs ovarian follicular development-modified hypothalamic neurotransmitters and causes polycystic ovary during adulthood in the rat. Fertil Steril 2011; 96: 1490-1496
  • 5 Kouki T, Kishitake M, Okamoto M, Oosuka I, Takebe M, Yamamnouchi K. Effects of neonatal treatment with phytoestrogens, genistein and daidzein, on sex difference in female rat brain function: estrous cycle and lordosis. Horm Behav 2003; 44: 140-145
  • 6 Dominguez R, Cruz-Morales SE, Carvalho MC, Xavier M, Brandao ML. Effect of steroid injection to newborn rats on serotonin activity in frontal cortex and raphe. Neuroreport 2003; 14: 597-599
  • 7 Sundblad C, Eriksson E. Reduced extracellular levels of serotonin in the amygdala of androgenized female rats. Eur Neuropsychopharmacol 1997; 7: 253-259
  • 8 Chavez C, Hollaus M, Scarr E, Pavey G, Gogos A, van den Buuse M. The effect of estrogen on dopamine and serotonin receptor and transporter levels in the brain: an autoradiography study. Brain Res 2010; 1321: 51-59
  • 9 Yanagihara N, Liu M, Toyohira Y, Tsutsui M, Ueno S, Shinohara Y, Takahashi K, Tanaka K. Stimulation of catecholamine synthesis through unique estrogen receptors in the bovine adrenomedullary plasma membrane by 17beta-estradiol. Biochem Biophys Res Commun 2006; 339: 548-553
  • 10 Johnson ML, Ho CC, Day AE, Walker QD, Francis R, Kuhn CM. Oestrogen receptors enhance dopamine neurone survival in rat midbrain. J Neuroendocrinol 2010; 22: 226-237
  • 11 Johnson ML, Day AE, Ho CC, Walker QD, Francis R, Kuhn CM. Androgen decreases dopamine neurone survival in rat midbrain. J Neuroendocrinol 2010; 22: 238-247
  • 12 Torrens Y, Beaujouan JC, Besson MJ, Michelot R, Glowinski J. Inhibitory effects of GABA, L-glutamic acid and nicotine on the potassium-evoked release of substance P in substantia nigra slices of the rat. Eur J Pharmacol 1981; 71: 383-392
  • 13 Abarca J, Bustos G. Differential regulation of glutamate, aspartate and gamma-amino-butyrate release by N-methyl-D-aspartate receptors in rat striatum after partial and extensive lesions to the nigro-striatal dopamine pathway. Neurochem Int 1999; 35: 19-33
  • 14 Chi JD, Odontiadis J, Franklin M. Simultaneous determination of catecholamines in rat brain tissue by high-performance liquid chromatography. J Chromatogr B Biomed Sci Appl 1999; 731: 361-367
  • 15 Cruz G, Barra R, Gonzalez D, Sotomayor-Zarate R, Lara HE. Temporal window in which exposure to estradiol permanently modifies ovarian function causing polycystic ovary morphology in rats. Fertil Steril 2012; 98: 1283-1290
  • 16 Schwarz JM, Nugent BM, McCarthy MM. Developmental and hormone-induced epigenetic changes to estrogen and progesterone receptor genes in brain are dynamic across the life span. Endocrinology 2010; 151: 4871-4881
  • 17 Morikawa H, Paladini CA. Dynamic regulation of midbrain dopamine neuron activity: intrinsic, synaptic, and plasticity mechanisms. Neuroscience 2011; 198: 95-111
  • 18 Koob GF, Volkow ND. Neurocircuitry of addiction. Neuropsychopharmacology 2010; 35: 217-238
  • 19 Tian YH, Baek JH, Lee SY, Jang CG. Prenatal and postnatal exposure to bisphenol a induces anxiolytic behaviors and cognitive deficits in mice. Synapse 2010; 64: 432-439
  • 20 Ishido M, Yonemoto J, Morita M. Mesencephalic neurodegeneration in the orally administered bisphenol A-caused hyperactive rats. Toxicol Lett 2007; 173: 66-72
  • 21 Walker QD, Johnson ML, Van Swearingen AE, Arrant AE, Caster JM, Kuhn CM. Individual differences in psychostimulant responses of female rats are associated with ovarian hormones and dopamine neuroanatomy. Neuropharmacology 2012; 62: 2267-2277
  • 22 Silverman JL, Koenig JI. Evidence for the involvement of ERbeta and RGS9-2 in 17-beta estradiol enhancement of amphetamine-induced place preference behavior. Horm Behav 2007; 52: 146-155
  • 23 Kerstetter KA, Kippin TE. Impact of Sex and Gonadal Hormones on Cocaine and Food Reinforcement Paradigms. J Addict Res Ther 2011; S4
  • 24 Dluzen DE, Ramirez VD. In vitro progesterone modulates amphetamine-stimulated dopamine release from the corpus striatum of castrated male rats treated with estrogen. Neuroendocrinology 1990; 52: 517-520
  • 25 Dluzen DE, Ramirez VD. In vitro progesterone modulation of amphetamine-stimulated dopamine release from the corpus striatum of ovariectomized estrogen-treated female rats: response characteristics. Brain Res 1990; 517: 117-122
  • 26 Cabrera R, Diaz A, Pinter A, Belmar J. In vitro progesterone effects on 3H-dopamine release from rat corpus striatum slices obtained under different endocrine conditions. Life Sci 1993; 53: 1767-1777
  • 27 Mello NK, Knudson IM, Kelly M, Fivel PA, Mendelson JH. Effects of progesterone and testosterone on cocaine self-administration and cocaine discrimination by female rhesus monkeys. Neuropsychopharmacology 2011; 36: 2187-2199