MORPHOMETRIC CHANGES OF PREFRONTAL CORTEX NEURONS IN WHITE LABORATORY RATS UNDER CONDITIONS OF THE EATING OF THE PROTEIN-DEFICIENCY FOOD AFTER ACUTE SOUND STRESS
https://doi.org/10.20340/mv-mn.2021.29(4).608
Abstract
Morphometric changes in neurons in the prefrontal cortex of white laboratory rats under conditions of protein deficiency in food after acute sound exposure remain unexplored. Purpose: morphometry of neurons in the prefrontal cortex of sexually mature white laboratory rats after acute sound exposure in conditions of low-protein food. The experiments were carried out on 64 sexually mature nonlinear white laboratory male rats weighing 180-230 g (8 - intact, 56 - experimental). After a single continuous sound exposure with an intensity of 120 dB for 120 seconds, 56 rats were divided into 2 groups: with balanced food (control - 28) and low-protein food (main food - 28); with two subgroups in each: stress-resistant (12) and stress-nonresistant (16). The animals were removed from the experiment on days 10, 20, 30 and 40 after the start of the experiment. Samples of prefrontal cortex preparations were examined histologically, immunohistochemically, and morphometrically. After acute sound exposure, the indicators of the area of the cytoplasm, nucleus and nucleoli of neurons in the prefrontal cortex of white laboratory rats change. Chromatolysis of Nissl's substance occurs in most neurons of the II-III layers of neurons. During all periods of observation, morphometric changes were most pronounced in stress-nonresistant animals of the main group of experiments, especially in the first 10 days after exposure. Chromatolysis in neurons of the prefrontal cortex persists until the end of the experiment, which indicates incomplete repair of the intracellular protein-synthesizing functional system after acute sound stress. Thus, an acute sound effected causes morphometric changes in neurons and initiates chromatolysis of Nissl's substance in them in layers II-III of the cortex of the prefrontal region of the brain of white laboratory rats. Chromatolysis in animals with low-protein food after acute sound exposure in the II-III layers of the prefrontal cortex is irreversible, remains statistically significantly high and can be regarded as a manifestation of decompensation of structural changes in animals under conditions of protein deficiency in food.
About the Author
Maya Elkhan qisi SultanlyAzerbaijan
Junior Researcheress
Competing Interests:
The author declares that she did not have any conflicts of interest in the planning, implementation, financing and use of the results of this study
References
1. Euston DR, Gruber AJ and McNaughton BL. The role of medial prefrontal cortex in memory and decision making. Neuron. 2012;76:1057–1070. DOI: 10.1016/j.neuron.2012.12.002
2. Schwedhelm P, Baldauf D & Treue S. The lateral prefrontal cortex of primates encodes stimulus colors and their behavioral relevance during a match-to-sample task. Scientific Reports;10:Article number: 4216. DOI: 10.1038/s41598-020-61171-3
3. Dalley JW, Cardinal RN, Robbins TW. Prefrontal executive and cognitive functions in rodents: neural and neurochemical substrates. Neurosci. Biobehav. Rev. 2004;28(7):771-784
4. De Bruin JP, Feenstra MG, Broersen LM, van Leeuwen M, Arens C, De Vries S, et al. Role of the prefrontal cortex of the rat in learning and decision making: effects of transient inactivation. Prog. Brain Res. 2000;126:103–113. DOI: 10.1016/s0079-6123(00)26010-x
5. Farrell MR, Sengelaub DR, and Wellman CL. Sex differences and chronic stress effects on the neural circuitry underlying fear conditioning and extinction. Physiol. Behav. 2013;122:208–215. DOI: 10.1016/j.physbeh.2013.04.002
6. Bloss EB, Janssen WG, McEwen BS, and Morrison JH. Interactive effects of stress and aging on structural plasticity in the prefrontal cortex. J. Neurosci. 2010;30:6726–6731. DOI: 10.1523/jneurosci.0759-10.2010
7. Amy FT Arnsten, Murray A Raskind, Fletcher B Taylor, Daniel F Connor. The effects of stress exposure on prefrontal cortex: Translating basic research into successful treatments for post-traumatic stress disorder. Neurobiology of Stress. 2015;1:89-99. DOI: 10.1016/j.ynstr.2014.10.002.
8. Liu WZ, Zhang WH, Zheng ZH et al. Identification of a prefrontal cortex-to-amygdala pathway for chronic stress-induced anxiety. Nat Commun. 2020;11:2221. DOI: 10.1038/s41467-020-15920-7
9. Goldwater DS, Pavlides C, Hunter RG, Bloss EB, Hof PR, McEwen BS et al. Structural and functional alterations to rat medial prefrontal cortex following chronic restraint stress and recovery. Neuroscience. 2009;164:798–808. DOI: 10.1016/j.neuroscience.2009.08.053
10. Sarah M Brown, Shannon Henning, Cara L Wellman. Mild, Short-term Stress Alters Dendritic Morphology in Rat Medial Prefrontal Cortex. Cerebral Cortex. 2005;15(11):1714–1722. DOI: 10.1093/cercor/bhi048
11. Pivina SG, Rakitskaya VV, Smolenskii IV, Akulova VK, Ordyan NE. Modification of expression of neurohormones in hypothalamus of prenatally stressed male rats in model of posttraumatic stress disorder. Journal of Evolutionary Biochemistry and Physiology. 2014;4(50):345–352
12. Mironova VI, Rakitskaya VV, Pivina SG, Ordyan NE. Stress-Induced Changes in Corticoliberin and Vasopressin Expression in the Hypothalamus of Female Rats in a Model of Post-Traumatic Stress Disorder. Neuroscience and Behavioral Physiology. 2017;4(47):449–455
13. V'yushina AV, Pritvorova AV, Flerov MA. Vliyanie prenatal'nogo stressa na okislitel'nuyu modifikaciyu belkov golovnogo mozga krys v ontogeneze. Nejrohimiya. 2012;3(29):240. In Russian
14. Kuznetsova GD. Audiogennye sudorogi u krys raznyh geneticheskih linij. Zhurnal VND. 1998;48(1):143-152. In Russian
15. Nikinorov M, Urbanek-Karlowska B, Karlowska K. Protein deficient diets. Activity of selected enzymes of protein and carbohydrate metabolism. Toxicology.1973;1:263-276
16. Guidelines for accommodation and care of animals (article 5 of the convention) approved by the multilateral consultation. Strasbourg, 15 June 2006, Cons. 123
17. Watson C, Paxinos G. The Rat Brain in stereotaxic coordinates. London-San Diego: Academic Press, 2007.- 456 рp.
18. Dey P. Basic and Advanced Laboratory Techniques in Histopathology and Cytology. Singapore: Springer, 2018.- 275 pp.
19. Lin F, Prichard J (Eds). Handbook of Practical Immunohistochemistry. New York: Springer Science + Business Media, 2015.- 764 pp.
20. Yunkerov VI, Grigor'ev SG, Rezvancev MV. Matematiko-statisticheskaya obrabotka dannyh medicinskih issledovanij. Sankt-Peterburg: VmedA, 2011.- 318s. In Russian
21. Uylings HB, van Eden CG. Qualitative and quantitative comparison of the prefrontal cortex in rat and in primates, including humans. Prog Brain Res. 1990;85:31-62
22. Kanari L, Ramaswamy S, Shi Y, Morand S et al. Objective morphological classification of neocortical pyramidal cells. Cereb. Cortex. 2019;29(4):1719-1735. DOI: 10.1093/cercor/bhy339
The author has shown that a single sound exposure (audio stress) causes long-term irreversible changes in neurons of the prefrontal cortex during feeding with protein-deficient food in laboratory rats
Review
For citations:
Sultanly M.E. MORPHOMETRIC CHANGES OF PREFRONTAL CORTEX NEURONS IN WHITE LABORATORY RATS UNDER CONDITIONS OF THE EATING OF THE PROTEIN-DEFICIENCY FOOD AFTER ACUTE SOUND STRESS. Morphological newsletter. 2021;29(4):17-24. (In Russ.) https://doi.org/10.20340/mv-mn.2021.29(4).608