Exposure to high fat during early development impairs adaptations in dopamine and neuroendocrine responses to repeated stress

References

• Abercrombie ED, Keefe KA, DiFrischia DS, Zigmond MJ. (1989). Differential effect of stress on in vivo dopamine release in striatum, nucleus accumbens, and medial frontal cortex. J Neurochem 52(5):1655–8
   PubMed Web of Science ®Google Scholar
• Antonopoulos J, Dori I, Dinopoulos A, Chiotelli M, Parnavelas JG. (2002). Postnatal development of the dopaminergic system of the striatum in the rat. Neuroscience 110(2):245–56
   PubMedGoogle Scholar
• Benes FM, Taylor JB, Cunningham MC. (2000). Convergence and plasticity of monoaminergic systems in the medial prefrontal cortex during the postnatal period: implications for the development of psychopathologies. Cerebral Cortex 10:1014–27
   PubMedGoogle Scholar
• Bhatnagar S, Huber R, Nowak N, Trotter P. (2002). Lesions of the posterior paraventricular thalamus block habituation of hypothalamic--pituitary--adrenal responses to repeated restraint. J Neuroendocrinol 14(5):403–10
   PubMedGoogle Scholar
• Brake WG, Noel MB, Boksa P, Gratton A. (1997). Influence of perinatal factors on the nucleus accumbens dopamine response to repeated stress during adulthood: an electrochemical study in the rat. Neuroscience 77(4):1067–76
   PubMedGoogle Scholar
• Brake WG, Zhang TY, Diorio J, Meaney MJ, Gratton A. (2004). Influence of early postnatal rearing conditions on mesocorticolimbic dopamine and behavioural responses to psychostimulants and stressors in adult rats. Eur J Neurosci 19(7):1863–74
   PubMed Web of Science ®Google Scholar
• Budygin EA, Park J, Bass CE, Grinevich VP, Bonin KD, Wightman RM. (2012). Aversive stimulus differentially triggers subsecond dopamine release in reward regions. Neuroscience 201:331–7
   PubMed Web of Science ®Google Scholar
• Buwembo A, Long H, Walker CD. (2012). Participation of endocannabinoids in rapid suppression of stress responses by glucocorticoids in neonates. Neuroscience, epub ahead of print. DOI: 10.1016/j.neuroscience.2012.10.057
   Google Scholar
• Cabib S, Puglisi-Allegra S. (2012). The mesoaccumbens dopamine in coping with stress. Neurosci Biobehav Rev 36(1):79–89
   PubMedGoogle Scholar
• Chen Y, Hatalski CG, Brunson KL, Baram TZ. (2001). Rapid phosphorylation of the CRE binding protein precedes stress-induced activation of the corticotropin releasing hormone gene in medial parvocellular hypothalamic neurons of the immature rat. Brain Res Mol Brain Res 96(1–2):39–49
   PubMedGoogle Scholar
• Copeland BJ, Neff NH, Hadjiconstantinou M. (2005). Enhanced dopamine uptake in the striatum following repeated restraint stress. Synapse 57(3):167–74
   PubMedGoogle Scholar
• D’Asti E, Long H, Tremblay-Mercier J, Grajzier M, Cunnane S, Di Marzo V, Walker C-D. (2010). Maternal dietary fat determines metabolic profile and the magnitude of endocannabinoid inhibiton of the stress response in neonatal rat offspring. Endocrinology 151(4):1685–94
   PubMed Web of Science ®Google Scholar
• Doell RG, Dallman MF, Clayton RB, Gray GD, Levine S. (1981). Dissociation of adrenal corticosteroid production from ACTH in water-restricted female rats. Am J Physiol 241(1):R21–4
   Google Scholar
• Doherty MD, Gratton A. (1992). High-speed chronoamperometric measurements of mesolimbic and nigrostriatal dopamine release associated with repeated daily stress. Brain Res 586(2):295–302
   PubMedGoogle Scholar
• Doherty MD, Gratton A. (1996). Medial prefrontal cortical D1 receptor modulation of the meso-accumbens dopamine response to stress: an electrochemical study in freely-behaving rats. Brain Res 15(1–2):86–97
   Google Scholar
• El-Khodor BF, Boksa P. (2002). Birth insult and stress interact to alter dopamine transporter binding in rat brain. Neuroreport 13(2):201–6
   PubMedGoogle Scholar
• Fernandes GA, Perks P, Cox NK, Lightman SL, Ingram CD, Shanks N. (2002). Habituation and cross-sensitization of stress-induced hypothalamic--pituitary--adrenal activity: effect of lesions in the paraventricular nucleus of the thalamus or bed nuclei of the stria terminalis. J Neuroendocrinol 14(7):593–602
   PubMedGoogle Scholar
• Francis DD, Diorio J, Plotsky PM, Meaney MJ. (2002). Environmental enrichment reverses the effects of maternal separation on stress reactivity. J Neurosci 22(18):7840–3
   PubMed Web of Science ®Google Scholar
• Gresch PJ, Sved AF, Zigmond MJ, Finlay JM. (1994). Stress-induced sensitization of dopamine and norepinephrine efflux in medial prefrontal cortex of the rat. J Neurochem 63(2):575–83
   PubMed Web of Science ®Google Scholar
• Grissom N, Bhatnagar S. (2009). Habituation to repeated stress: get used to it. Neurobiol Learn Mem 92(2):215–24
   PubMed Web of Science ®Google Scholar
• Heydendael W, Sharma K, Iyer V, Luz S, Piel D, Beck S, Bhatnagar S. (2011). Orexins/hypocretins act in the posterior paraventricular thalamic nucleus during repeated stress to regulate facilitation to novel stress. Endocrinology 152(12):4738–52
   PubMedGoogle Scholar
• Imperato A, Angelluci L, Casolini P, Zocchi A, Puglisi-Allegra S. (1992). Repeated stressful experiences differently affect limbic dopamine release during and following stress. Brain Res 577(2):194–9
   PubMedGoogle Scholar
• Jankord R, Herman JP. (2008). Limbic regulation of hypothalamo--pituitary--adrenocortical function during acute and chronic stress. Ann N Y Acad Sci 1148:64–73
   PubMed Web of Science ®Google Scholar
• Kovács KJ, Sawchenko PE. (1996). Sequence of stress-induced alterations in indices of synaptic and transcriptional activation in parvocellular neurosecretory neurons. J Neurosci 16(1):262–73
   PubMedGoogle Scholar
• Levin BE. (2006). Metabolic imprinting: critical impact of the perinatal environment on the regulation of energy homeostasis. Philos Trans R Soc Lond B Biol Sci 361(1471):1107–21
   PubMed Web of Science ®Google Scholar
• Liu D, Diorio J, Tannenbaum B, Caldgi C, Francis D, Freedman A, Sharma S, et al. (1997). Maternal care, hippocampal glucocorticoid receptors, and hypothalamic--pituitary--adrenal responses to stress. Science 277(5332):1659–62
   PubMed Web of Science ®Google Scholar
• Lupinsky D, Moquin L, Gratton A. (2010). Interhemispheric regulation of the medial prefrontal cortical glutamate stress response in rats. J Neurosci 30(22):7624–33
   PubMedGoogle Scholar
• Mansi JA, Rivest S, Drolet G. (1998). Effect of immobilization stress on transcriptional activity of inducible immediate-early genes, corticotropin-releasing factor, its type 1 receptor, and enkephalin in the hypothalamus of borderline hypertensive rats. J Neurochem 70(4):1556–66
   PubMedGoogle Scholar
• Naef L, Moquin L, Gratton A, Walker CD. (2012). Reduced anticipatory dopamine responses to food in rats exposed to high-fat during early development. Int J Obes, epub ahead of print. DOI: 10.1038/ijo.2012.153
   Google Scholar
• Naef L, Moquin L, Dal Bo G, Giros B, Gratton A, Walker CD. (2011). Maternal high-fat intake alters presynaptic regulation of dopamine in the nucleus accumbens and increases motivation for fat rewards in the offspring. Neuroscience 176:225–36
   PubMed Web of Science ®Google Scholar
• Naef L, Srivastava L, Gratton A, Hendrickson H, Owens SM, Walker CD. (2008). Maternal high fat diet during the perinatal period alters mesocorticolimbic dopamine in the adult rat offspring: reduction on the behavioral responses to repeated amphetamine administration. Psychopharmacology 197:83–94
   PubMed Web of Science ®Google Scholar
• Nesse RM, Bhatnagar S, Young E. (2007). The evolutionary origins and functions of the stress response. In: Fink G, editor, The encyclopedia of stress. 2nd ed. New York: Academic Press
   Google Scholar
• Nicniocaill B, Gratton A. (2007). Medial prefrontal cortical alpha1 adrenoreceptor modulation of the nucleus accumbens dopamine response to stress in Long-Evans rats. Psychopharmacology 191(3):835–42
   PubMedGoogle Scholar
• Pascucci T, Ventura R, Latagliata EC, Cabib S, Puglisi-Allegra S. (2007). The medial prefrontal cortex determines the accumbens dopamine response to stress through the opposing influences of norepinephrine and dopamine. Cereb Cortex 17(12):2796–804
   PubMedGoogle Scholar
• Patel S, Hillard CJ. (2008). Adaptations in endocannabinoid signaling in response to repeated homotypic stress: a novel mechanism for stress habituation. Eur J Neurosci 27(11):2821–9
   PubMedGoogle Scholar
• Paxinos G, Watson C. (1998). The rat brain in stereotaxic coordinates, 4th ed. New York: Academic Press
   Google Scholar
• Pierce RC, Bari AA. (2001). The role of neurotrophic factors in psychostimulant-induced behavioral and neuronal plasticity. Rev Neurosci 12(2):95–110
   PubMed Web of Science ®Google Scholar
• Proulx K, Clavel S, Nault G, Richard D, Walker CD. (2001). High neonatal leptin exposure enhances brain GR expression and feedback efficacy on the adrenocortical axis of developing rats. Endocrinology 142(11):4607–16
   PubMed Web of Science ®Google Scholar
• Puglisi-Allegra S, Imperato A, Angelucci L, Cabib S. (1991). Acute stress induces time-dependent responses in dopamine mesolimbic system. Brain Res 554(1–2):217–22
   PubMedGoogle Scholar
• Rougé-Pont F, Deroche V, Le Moal M, Piazza PV. (1998). Individual differences in stress-induced dopamine release in the nucleus accumbens are influenced by corticosterone. Eur J Neurosci 10(12):3903–7
   PubMed Web of Science ®Google Scholar
• Sullivan RM, Gratton A. (2002). Prefrontal cortical regulation of hypothalamic--pituitary--adrenal function in the rat and implications for psychopathology: side matters. Psychoneuroendocrinology 27(1–2):99–114
   PubMedGoogle Scholar
• Tannenbaum BM, Brindley DN, Tannenbaum GS, Dallman MF, McArthur MD, Meaney MJ. (1997). High-fat feeding alters both basal and stress-induced hypothalamic--pituitary--adrenal activity in the rat. Am J Physiol 3(6 Pt 1):E1168–77
   Google Scholar
• Teegarden SL, Scott AN, Bale TL. (2009). Early life exposure to a high fat diet promotes long-term changes in dietary preferences and central reward signaling. Neuroscience 162(4):924–32
   PubMedGoogle Scholar
• Tozuka Y, Kumon M, Wada E, Onodera M, Mochizuki H, Wada K. (2010). Maternal obesity impairs hippocampal BDNF production and spatial learning performance in young mouse offspring. Neurochem Int 57(3):235–47
   PubMed Web of Science ®Google Scholar
• Trottier G, Koski KG, Brun T, Toufexis DJ, Richard D, Walker C-D. (1998). Increased fat intake during lactation modifies hypothalamic--pituitary--adrenal responsiveness in developing rat pups: a possible role for leptin. Endocrinology 139(9):3704–11
   PubMed Web of Science ®Google Scholar
• Vucetic Z, Kimmel J, Totoki K, Hollenbeck E, Reyes TM. (2010). Maternal high-fat diet alters methylation and gene expression of dopamine and opioid-related genes. Endocrinology 1(10):4756–64
   Google Scholar
• Walker C-D, Anand KJS, Plotsky PM. (2001). Ontogeny of the hypothalamus--pituitary--adrenal axis and the stress response. In: McEwen BS, Goddman HM, editors. Handbook of Physiology section 7: the endocrine system: coping with the environment: neural and endocrine mechanisms. New York: Oxford Press. p 237
   Google Scholar
• Walker C-D, Naef L, d’Asti E, Long H, Xu Z, Moreau A, Azeddine B. (2008). Perinatal maternal fat intake affects metabolism and hippocampal function in the offspring: a potential role for leptin. Annals NY Acad Sciences 1144:189–202
   PubMed Web of Science ®Google Scholar
• Weinberg MS, Girotti M, Spencer RL. (2010). Medial prefrontal cortex activity can disrupt the expression of stress response habituation. Neuroscience 168(3):744–56
   PubMed Web of Science ®Google Scholar
• Zhang TY, Chretien P, Meaney MJ, Gratton A. (2005). Influence of naturally occurring variations in maternal care on prepulse inhibition of acoustic startle and the medial prefrontal cortical dopamine response to stress in adult rats. J Neurosci 25(6):1493–502
   PubMed Web of Science ®Google Scholar