Effects of chronic food stress on morphometry and expression of nuclear organizing regions in the adult rats hippocampus Chronic food stress on morphometry and expression of agnor in the rats hippocampus / Efeitos do estresse alimentar crônico na morfometria e expressão das regiões de organização nuclear nos ratos adultos hipocampo Testemunho crônico de alimentação sobre morfometria e expressão do agnor no hippocampus das taxas
DOI:
https://doi.org/10.34119/bjhrv3n4-277Keywords:
Neuron, Hippocampus, Stress, Food restriction, Morphometry.Abstract
The aim of this study was to verify the immediate and late effects of chronic food stress on the expression of Nuclear Organizing Regions (NORs) in hippocampal neurons. Twenty Wistar rats were separated into two groups: test (n = 10) and control (n = 10). Food stress started from the 60th day of life and lasted for a month. After this time the animals were anesthetized, euthanized and had their hippocampus dissected. The obtained hippocampus were histologically processed, stained by the HE technique for morphological description and by the AgNOR technique for NOR analysis. From each image the total number of neurons, the number of neurons with NOR in Dispersion (NND), the total number of NORs (NNOR), and then performed a ratio of NNOR by the total number of neurons to obtain the number Of NOR by neuron (NNN). Of the analyzed variants, the number of neurons was higher (p <0.001) in the stressed group (41.98 ± 17), when compared with the control group (33.57 ± 14). In addition, NND was also higher in the stressed group (4.523 ± 4.04) than the control group (1.4 ± 2.20) with p <0.001. Thus, we have that chronic food stress increases the number of granular neurons in the hippocampus in rats as well as increases the number of NOR in dispersion.
References
Azuma, S; Yamamoto, T; Kawamura, Y (1958). Studies on gustatory responses of amyg-daloid neurons in rats. Exp Brain Res, 56, 1, 12-22. doi: 10.1007/BF00237437
Bruce-Keller, AJ; Umberger, G; Mcfall, R; Mattson, MP (1999). Food restriction reduces brain damage and improves behavioral outcome following excitotoxic and metabolic insults. Annals of Neurology, 45, 8-15. doi: 10.1002/1531-8249(199901)45:1<8::AID-ART4>3.0.CO;2-V
Cain, DP (1975). Effects of insulin injection on responses of olfactory bulb and amygdala single units to odors. Brain Res, 99, 1, 69-83. doi: 10.1016/0006-8993(75)90609-5
Cain, DP & Bindra, D (1972). Responses of amygdala single units to odors in the rat. Exp Neurol, 35, 1, 98-110. doi: 10.1016/0014-4886(72)90062-3
Cameron, HA; Hazel, TG; Mckay, RD (1998). Regulation of neurogenesis by growth factors and neurotransmitters. Journal of Neurobiology, 36, 2, 287–306. doi: 10.1002/(SICI)1097-4695(199808)36:2<287::AID-NEU13>3.0.CO;2-B
Corwin, RL; Avena, NM; Boggiano, MM (2011). Feeding and reward: perspectives from three rat models of binge eating. Physiolgy & Behaviour, 104, 87-97. doi: 10.1016/j.physbeh.2011.04.041
Cifani, C; Polidori, C; Melotto, S; Ciccocioppo, R; Massi, M (2009). A preclinical model of binge eating elicited by yo-yo dieting and stressful exposure to food: effect of sibutramine, fluoxetine, topiramate, and midazolam. Psychopharmacology, 204, 113-25. doi: 10.1007/s00213-008-1442-y
Dallman, MF; Pecoraro, N; Akana, SF; La Fleur, SE; Gomez, F; Houshyar, H; et al (2003). Chronic stress and obesity: a new view of "comfort food". Proc Natl Acad Sci, 100, 20, 11696-11701. doi: 10.1073/pnas.1934666100
Derenzini, M; Trere, D; Pessin, A; Givoni, M; Sirri, V; Chieco, P (2000). Nucleolar size indicates the rapidity of cell proliferation in cancer tissues. Journal of Pathology, 191, 181-186. doi: 10.1002/(SICI)1096-9896(200006)191:2<181::AID-PATH607>3.0.CO;2-V
Freund, J; Brandmaier, AM; Lewejohann, L; Kirste, I; Kritzler, M; Krüger, A; et al (2015). Association between exploratory activity and social individuality in genetically identical mice living in the same enriched environment. Neuroscience, 309, 140-152. doi: 10.1016/j.neuroscience.2015.05.027
Gos, T; Krell, D; Bielau, H; Steiner, J; Mawrin, C; Trübner, K; et al (2010). Demonstration of disturbed activity of the lateral amygdaloid nucleus projection neurons in depressed patients by the AgNOR staining method. J Affect Disord, 126, 3, 402-410. doi: 10.1016/j.jad.2010.04.006
Hagan, MM; Wauford, PK; Chandler, PC; Jarrett, LA; Rybak, RJ; Blackburn, K (2002). A new animal model of binge eating: key synergistic role of past caloric restriction and stress. Physiol Behav, 77, 1, 45-54. doi: 10.1016/S0031-9384(02)00809-0
Healy-Stoffel, M; Ahmad, SO; Stanford, JA; et al (2012). A novel use of combined tyrosine hydroxylase and silver nucleolar staining to determine the effects of a unilateral intrastriatal 6-hydroxydopamine lesion in the substantia nigra: a stereological study. J Neurosci Methods, 210, 187–194. doi: 10.1016/j.jneumeth.2012.07.013
Herman, JP & Cullinan, WE (1997). Neurocircuitry of stress: central control of the hypothalamus-pituitary-adrenal axis. Trends Neuroscience, 20, 78-84. doi: 10.1016/S0166-2236(96)10069-2
Herman, JP & Muller, NK (2006). Role of the ventral subiculum in stress integration. Behav Brain Res, 174, 2, 215-24. doi: 10.1016/j.bbr.2006.05.035
Joels, M (2008). Functional actions of corticosteroids in the hippocampus. Eur J Pharmacol, 583, 2-3, 312–321. doi: 10.1016/j.ejphar.2007.11.064
Kumar, S; Parkash, J; Kataria, H; Kaur, G (2009). Interactive effect of excitotoxic injury and dietary restriction on neurogenesis and neurotrophic factors in adult male rat brain. Neuroscience Research, 65, 4, 367-374. doi: 10.1016/j.neures.2009.08.015
Lathe, R (2001). Hormone and hippocampus. J Endocrinol, 169, 205-31. doi: 10.1677/joe.0.1690205
Lavezzi, AM; Alfonsi, G; Pulsiol, T; Maturri, L (2016). Decreased argyrophilic nucleolar organiser region (AgNOR) expression in Purkinje cells: first signal of neuronal damage in sudden fetal and infant death. J Clin Pathol, 69, 1, 58-63. doi: 10.1136/jclinpath-2015-202961
Récamier-Carballo, S; Estrada-Camarena, E; Lopes-Rubalcava, C (2017). Maternal separation induces long-term effects on monoamines and brain-derived neurotrophic factor levels on the frontal cortex, amygdala, and hippocampus: differential effects after a stress challenge. Behavioural Pharmacology, 28, 7, 545-557. doi: 10.1097/FBP.0000000000000324
Manzzanero, S; Erion, JR; Santro, T; Steyn, FJ; Chen, C; Arumugam, TV; Stranahan, AM (2014). Intermittent Fasting Attenuates Increases in Neurogenesis after Ischemia and Reperfusion and Improves Recovery. Journal of Cerebral Blood Flow & Metabolism, 897–905. doi: 10.1038/jcbfm.2014.36
Monteiro, BM; Moreira, FA; Massensini, AR; Moraes, MF; Pereira, GS (2013). Enriched environment increases neurogenesis and improves social memory persistence in socially isolated adult mice. Hippocampus, 24, 2, 239-248. doi: 10.1002/hipo.22218
Mineur, YS; Belzung, C; Crusio, WE (2007). Functional implications of decreases in neurogenesis following chronic mild stress in mice. Neuroscience, 150, 251–259. doi: 10.1016/j.neuroscience.2007.09.045
Nicola, D; Hanson, A; Michael, J; Owens, A; Katherinea Boss-Williams, A; Jay, M; Weiss, A; Charles, N (2011). Several stressors fail to reduce adult hippocampal neurogenesis. Psychoneuroendocrinology, 36, 10, 1520-1529. doi: 10.1016/j.psyneuen.2011.04.006
Nishijo, H; Uwano, T; Tamura, R; Ono, T (1998). Gustatory and multimodal neuronal responses in the amygdala during licking and discrimination of sensory stimuliin awake rats. J Neurophysiol, 79, 1, 21-36. PMID: 9425173
Ortolani, D; Garcia, MC; Melo-Thomas, L; Spadari-Bratfisch, RC (2014). Stress-induced endocrine response and anxiety: the effects of comfort food in rats. Stress, 17, 3, 211-218. doi: 10.3109/10253890.2014.898059
Schoenfeld, TJ & Gould, E (2011). Stress, stress hormones, and adult neurogenesis. Experimental Neurology, 233, 1, 12-21. doi: 10.1016/j.expneurol.2011.01.008
Scwabe, L; Joels, M; Roozendaal, B; Wolf, OT; Oitzl, MS (2011). Stress effects on memory: An update and integration. Neuroscience and Biobehavioral Reviews, 36, 7, 1740-1747. doi: 10.1016/j.neubiorev.2011.07.002
Sharma, S & Kaur, G (2005). Neuroprotective potential of dietary restriction against Kainate-induced excitotoxicity in adult male wistar rats. Brain Research Bullitin, 67, 482–493. doi: 10.1016/j.brainresbull.2005.07.015
Yang, D; Li, Q; Fang, L; Cheng, K; Zhang, R; Zheng, P; et al (2011). Reduced neurogenesis and pre-synaptic dysfunction in the olfactory bulb of a rat model of depression. Neuroscience, 192, 609-618. doi: 10.1016/j.neuroscience.2011.06.043
Zeeni, N; Daher, C; Fromentin, G; Tomé, D; Darcel, N; Chaumontet, C (2013). A cafeteria diet modifies the response to chronic variable stress in rats. Stress, 16, 2, 211-219. doi: 10.3109/10253890.2012.708952


