2012, Number 5
<< Back Next >>
Salud Mental 2012; 35 (5)
La hormona liberadora de tirotropina (TRH) del núcleo paraventricular hipotalámico y sistema límbico como reguladora de la homeostasis energética y de la conducta alimentaria en animales con ayuno, restricción alimentaria y anorexia
de Gortari P, González-Alzati ME, Jaimes-Hoy L, Estrada A, Mancera K, García-Luna C, Amaya MI
Language: Spanish
References: 63
Page: 385-393
PDF size: 119.92 Kb.
ABSTRACT
TRH expression and release from hypothalamic paraventricular nucleus
(PVN) change with environmental stimuli. Fasted and food-restricted
animals present decreased TRH synthesis and release, decelerating
metabolic rate and utilization of energy stores, which is an advantageous
adaptation of animals with nutrient deficit. Comparing thyroid
axis function between prepuberal
vs. adult male fasted animals, we
found a greater body weight reduction than in adults (30% vs.11%)
and TRH release was not decreased; TRH degradation by pituitary
PPII enzyme decreased, which maintained energy waste. TRH content
of fasted-prepuberal animals changed in hippocampus and nucleus
accumbens, and in amygdala of adults
vs.ad libitum fed animals.
PVN TRH role in food-avoiding behavior was studied by comparing its
expression levels and of adolescent, adult females and male animals
with anorexic conduct when drinking 2.5% of NaCl solution (AN)
vs. a group forced to ingest the amount of food consumed by AN
(FFR); also
vs. a control group fed
ad libitum (C). PVN TRH mRNA
and TSH serum levels increased in AN
vs. C; both decreased in FFR,
supporting the putative anorexigenic role for the peptide. TRH content
differentially changed in hippocampus and in frontal cortex of AN
and FFR, suggesting its participation in taste perception and memory
association. Orexinergic and NPYergic pathways are inactive in anorexic
animals. Blocking corticotrophin-releasing hormone signal by
an antagonist of CRH-R2 in the PVN reverses TRH high expression and
TSH serum levels in AN.
REFERENCES
Schwartz MW, Woods SC, Porte D, Seeley RJ et al. Central nervous system control of food intake. Nature 2000;404:661-671.
Ikemoto S. Dopamine reward circuitry: two projection systems from the ventral midbrain to the nucleus accumbens-olfactory tubercle complex. Brain Res Rev 2007;56:27-78.
Ikemoto S, Wise R. Mapping of chemical trigger zones for reward. Neuropharmacology 2004;47:190-201.
Rolls E. Brain mechanisms underlying flavour and appetite. Philos Trans R Soc Lond B Biol Sci 2006;361:1123-1136.
Shils M, Olson J, Shike M, Ross A. Nutrición en salud y enfermedad. 9 ed. Nueva York: Lippincott Williams & Wilkins; 2002.
Gibson E. Emotional influences on food choice: sensory, physiological and psychological pathways. Physiol Behav 2006;89:53-61.
Torres S, Nowson C. Relationship between stress, eating behavior, and obesity. Nutrition 2007;23:887-894.
Serlachius A, Hamer M, Wardle J. Stress and weight change in university students in the United Kingdom. Physiol Behav 2007;92:548-553.
Gottfried JA, O’Doherty J, Dolan RJ. Encoding predictive reward value in human amygdala and orbitofrontal cortex. Science 2003;301:1104-1107.
Smith PM, Ferguson AV. Neurophysiology of hunger and satiety. Dev Disabil Res Rev 2008;14:96-104.
Sawchenko PE, Swanson LW. The organization of forebrain afferents to the paraventricular and supraoptic nuclei of the rat. J Comp Neurol 1983;218:121-144.
Potter E, Sutton S, Donaldson C, Chen R et al. Distribution of corticotropin- releasing factor receptor mRNA expression in the rat brain and pituitary. Neurobiology 1994;91:8777-8781.
Arase K, York D, Shimizu H, Shargill N et al. Effects of corticotropinreleasing factor on food intake and brown adipose tissue thermogenesis in rats. Am J Physiol 1988;255:E255-E259.
Boler J, Enzmann F, Folkers K, Bowers CY et al. The identity of chemical and hormonal properties of the thyrotropin releasing hormone and pyroglutamyl-histidyl-proline amide. Biochem Biophys Res Commun 1969;37:705-710.
Burgus R, Dunn T, Desiderio D, Guillemin R. Molecular structure of the hypothalamic hypophysiotropic TRF factor of ovine origin: mass spectrometry demonstration of the PCA-His-Pro-NH2 sequence. C R Acad Sci Hebd Seances Acad Sci D 1969;269:226-228.
Lechan RM, Segerson TP. Pro-TRH gene expression and precursor peptides in rat brain. Observations by hybridization analysis and immunocytochemistry. Ann N Y Acad Sci 1989;553:29-59.
Lechan R.M. Update on thyrotropin-releasing hormone. Thyroid Today 1993;16:1-11.
O’Leary R, O’Connor B. Thyrotropin-releasing hormone. J Neurochem 1995;65:953-963.
Freeman ME, Kanyicska B, Lerant A, Nagy G. Prolactin: structure, function, and regulation of secretion. Physiol Rev 2000;80:1523-1631.
Lanni A, Moreno M, Lombardi A, Goglia F. Thyroid hormone and uncoupling proteins. FEBS Lett 2003;543:5-10.
Yen PM. Physiological and molecular basis of thyroid hormone action. Physiol Rev 2001;81:1097-1142.
Nikrodhanond AA, Ortiga-Carvalho TM, Shibusawa N, Hashimoto K et al. Dominant role of thyrotropin-releasing hormone in the hypothalamic- pituitary-thyroid axis. J Biol Chem 2006;281:5000-5007.
Fekete C, Lechan RM. Negative feedback regulation of hypophysiotropic thyrotropin-releasing hormone (TRH) synthesizing neurons: role of neuronal afferents and type 2 deiodinase. Front Neuroendocrinol 2007;28:97-114.
Ponce G, Charli JL, Pasten JA, Aceves C et al. Tissue-specific regulation of pyroglutamate aminopeptidase II activity by thyroid hormones. Neuroendocrinology 1988;48:211-213.
Bauer K. Adenohypophyseal degradation of thyrotropin releasing hormone regulated by thyroid hormones. Nature 1987;330:375-377.
Baskin DG, Wilcox BJ, Figlewicz DP, Dorsa DM. Insulin and insulinlike growth factors in the CNS. Trends Neurosci 1988;11:107-111.
Baskin D, Breininger J, Schwartz M. Leptin receptor mRNA identifies a subpopulation of neuropeptide Y neurons activated by fasting in rat hypothalamus. Diabetes 1999;48:828-833.
Fekete C, Mihaly E, Luo LG, Kelly J et al. Association of cocaine- and amphetamine- regulated transcript-immunoreactive elements with thyrotropin- releasing hormone-synthesizing neurons in the hypothalamic paraventricular nucleus and its role in the regulation of the hypothalamic- pituitary-thyroid axis during fasting. J Neurosci 2000;20:9224-9234.
Christoffolete MA, Ribeiro R, Singru P, Fekete C et al. Atypical expression of type 2 iodothyronine deiodinase in thyrotrophs explains the thyroxine-mediated pituitary thyrotropin feedback mechanism. Endocrinology 2006;147:1735-1743.
Cheung CC, Clifton DK, Steiner RA. Proopiomelanocortin neurons are direct targets for leptin in the hypothalamus. Endocrinology 1997;138:4489-4492.
Joseph-Bravo P. Hypophysiotropic thyrotropin-releasing hormone neurons as transducers of energy homeostasis. Endocrinology 2004;145: 4813-4815.
Fekete C, Sarkar S, Rand WM, Harney JW et al. Neuropeptide Y1 and Y5 receptors mediate the effects of neuropeptide Y on the hypothalamic- pituitary-thyroid axis. Endocrinology 2002;143:4513-4519.
Fekete C, Sarkar S, Rand WM, Harney JW et al. Agouti-related protein (AGRP) has a central inhibitory action on the hypothalamic-pituitarythyroid (HPT) axis; comparisons between the effect of AGRP and neuropeptide Y on energy homeostasis and the HPT axis. Endocrinology 2002;143:3846-3853.
Raptis S, Fekete C, Sarkar S, Rand WM et al. Cocaine- and amphetamine- regulated transcript co-contained in thyrotropin-releasing hormone (TRH) neurons of the hypothalamic paraventricular nucleus modulates TRH-induced prolactin secretion. Endocrinology 2004;145:1695-1699.
de Gortari P, González-Alzati M, Cisneros M, Joseph-Bravo P. Effect of Fasting on the Content of Thyrotropin-releasing Hormone and its mRNA in the Central Nervous System and Pyroglutamyl Peptidase II Activity in the Anterior Pituitary of Post-Weaned and Adult Rats. Nutritional Neuroscience 2000;3:255-265.
Blake NG, Eckland DJ, Foster OJ, Lightman SL. Inhibition of hypothalamic thyrotropin-releasing hormone messenger ribonucleic acid during food deprivation. Endocrinology 1991;129:2714-2718.
van Haasteren GA, Linkels E, Klootwijk W, van Toor H et al. Starvation- induced changes in the hypothalamic content of prothyrotrophinreleasing hormone (proTRH) mRNA and the hypothalamic release of proTRH-derived peptides: role of the adrenal gland. J Endocrinol 1995;145:143-153.
van Haasteren GA, Linkels E, van Toor H, Klootwijk W et al. Effects of long-term food reduction on the hypothalamus-pituitary-thyroid axis in male and female rats. J Endocrinol 1996;150:169-178.
Vargas MA, Joseph-Bravo P, Charli JL. Thyrotropin-releasing hormone downregulates pyroglutamyl peptidase II activity in adenohypophyseal cells. Neuroendocrinology 1994;60:323-330.
Sun Y, Lu X, Gershengorn M. Thyrotropin-releasing hormone receptors - similarities and differences. J Molec Endocrinol 2003;30:97-
Vargas M, Cisneros M, Herrera J, Joseph-Bravo P et al. Regional distribution of pyroglutamyl peptidase II in rabbit brain, spinal cord, and organs. Peptides 1992;13:255-260.
Sattin A, Pekary A, Lloyd R. TRH in therapeutic vs. nontherapeutic seizures: affective and motor functions. Pharmacol Biochem Behav 1999;62:575-583.
Yamamura M, Kinoshita K, Nakagawa H, Ishida R. Pharmacological study of TA-0910, a new thyrotropin-releasing hormone (TRH) analog (II): Involvement of the DA system in the locomotor stimulating action of TA-0910. Jpn J Pharmacol 1991;55:57-68.
Ballard T, Hunter A, Bennett G. Effect of a thyrotropin-releasing hormone analogue, RX77368, on AMPA-induced septal-hippocampal lesioned rats in an operant delayed non-matching to position test. Psychopharmacology 1996;127:265-275.
Legradi G, Emerson CH, Ahima RS, Flier JS et al. Leptin prevents fasting- induced suppression of prothyrotropin-releasing hormone messenger ribonucleic acid in neurons of the hypothalamic paraventricular nucleus. Endocrinology 1997;138:2569-2576.
Jaimes-Hoy L, Joseph-Bravo P, de Gortari P. Differential response of TRHergic neurons of the hypothalamic paraventricular nucleus (PVN) in female animals submitted to food-restriction or dehydration-induced anorexia and cold exposure. Horm Behav 2008;53:366-377.
de Gortari P, Mancera K, Cote-Velez A, Amaya MI et al. Involvement of CRH-R2 receptor in eating behavior and in the response of the HPT axis in rats subjected to dehydration-induced anorexia. Psychoneuroendocrinology 2009;34:259-272.
Watts AG. Dehydration-associated anorexia: development and rapid reversal. Physiol Behav 1999;65:871-878.
Watts AG, Sanchez-Watts G, Kelly AB. Distinct patterns of neuropeptide gene expression in the lateral hypothalamic area and arcuate nucleus are associated with dehydration-induced anorexia. J Neurosci 1999;19:6111-6121.
Gutierrez-Mariscal M, de Gortari P, Lopez-Rubalcava C, Martinez A et al. Analysis of the anxiolytic-like effect of TRH and the response of amygdalar TRHergic neurons in anxiety. Psychoneuroendocrinology 2008;33:198-213.
Aguilar-Valles A, Sanchez E, de Gortari P, Balderas I et al. Analysis of the stress response in rats trained in the water-maze: differential expression of corticotropin-releasing hormone, CRH-R1, glucocorticoid receptors and brain-derived neurotrophic factor in limbic regions. Neuroendocrinology 2005;82:306-319.
Rolls E. The orbitofrontal cortex and reward. Cereb Cortex 2000;10:284- 294.
O’Doherty J, Rolls E, Francis S, Bowtell R et al. Representation of pleasant and aversive taste in the human brain. J Neurophysiol 2001;85:1315-1321.
Rolls E, Verhagen J, Kadohisa M. Representations of the texture of food in the primate orbitofrontal cortex: neurons responding to viscosity, grittiness, and capsaicin. J Neurophysiol 2003;90:3711-3724.
Strupp B, Levitsky D. Early brain insult and cognition: a comparison of malnutrition and hypothyroidism. Dev Psychobiol 1983;16:535-549.
Rosenblum K, Berman D, Hazvi S, Lamprecht R et al. NMDA receptor and the tyrosine phosphorylation of its 2B subunit in taste learning in the rat insular cortex. J Neurosci 1997;17:5129-5135.
Hanamori T, Kunitake T, Kato K, Kannan H. Responses of neurons in the insular cortex to gustatory, visceral, and nociceptive stimuli in rats. J Neurophysiol 1998;79:2535-2545.
Peyron C, Tighe DK, van den Pol AN, de Lecea L et al. Neurons containing hypocretin (orexin) project to multiple neuronal systems. J Neurosci 1998;18:9996-10015.
Garcia-Luna C, Amaya MI, Alvarez-Salas E, de Gortari P. Preproorexin and feeding-related peptide receptor expression in dehydration- induced anorexia. Regul Pept 2010;159:54-60.
Eckert E, Pomeroy C, Raymond N, Kohler P et al. Leptin in anorexia nervosa. J Clin Endocrinol Metab 1998;83:791-795.
Aguilera G, Millan M, Hauger R, Catt K. Corticotropin-releasing factor receptors; distribution and regulation in brain, pituitary, and peripheral tissues. Ann N Y Acad Sci 1987;512:48-66.
Bale T, Contarino A, Smith G, Chan R et al. Mice deficient for corticotropin- releasing hormone receptor-2 display anxiety-like behaviour and are hypersensitive to stress. Nat Genet 2000;24:410-414.
Chalmers D, Lovenberg T, DeSouza E. Localization of novel corticotropin- releasing factor receptor (CRF2) mRNA expression to specific subcortical nuclei in rat brain: comparison with CRF1 receptor mRNA expression. J Neurosci 1995;15:6340-6350.