Changes in the Cellular Composition of the Cerebral Cortex in Rats with Different Levels of Cognitive Functions Under Cerebral Hypoperfusion
https://doi.org/10.18499/2225-7357-2019-8-4-22-29
Abstract
The aim of study was to investigate characteristics of neurodystrophic changes in neurons and glia of the motor cortex in rats with different levels of cognitive functions under bilateral ligation of the common carotid arteries.
Material and methods. The study included 136 Wistar rats. All animals were divided into two subgroups based on the results of the Morris water maze test: with high and low level of ability to spatial learning. Animals of the experimental group were removed from the experiment on the 1st, 6th, 14th, 21st, 35th, 60th and 90th days after bilateral ligation of both carotid arteries. Histological sections of the motor cortex were studied using Nissl and hematoxylin-eosin staining.
Results. In 1, 6 and 8 days after ischemia, the number of neurons with irreversible changes and dead cells reached their maximum for the entire time of observation. On the 8th day of study, compact groups of glial cells appeared near the vessels. Heterochrony was noted: in animals with high level of cognitive ability, an increase in the number of neurons with irreversible changes followed the peak of cell death; in animals with low level, on the contrary, the maximum number of dead cells was observed on the 6th day, and the maximum number of neurons with irreversible changes – on the 1st. On the 14th, 21st, and 28th days there was observed a gradual stabilization of indicators characterizing damage to the cerebral cortex. Average values of the perikarya area and neurons nuclei increased, the nuclear-cytoplasmic ratio decreased, and intracellular swelling was noted. After 35 days, areas of the cortex depleted in bodies of neurons and glia appeared; the number of neurons with irreversible changes increased, to a greater extent, in animals with high level of cognitive abilities. Typical trends of the first month of study are as follows: a decrease in the nuclear-cytoplasmic ratio and a number of neurons without irreversible changes, and an increase in the neuroglial index continued to progress on the 60th and 90th days of study. The apical dendrites of the pyramidal neurons obtained a corkscrew course. Compact groups of glial cells disappeared.
Conclusion. During the first week of cerebral hypoperfusion, irreversible changes in neurons predominated, in the second and third weeks, the morphological criteria of their functional activity decreased. In the fourth and fifth weeks incomplete adaptation developed in the form of an increased number of neurons near the vessels of the hemocirculatory bed and an increased number of satellite gliocytes by immersing them in the cytoplasm of neurons. In 2-3 months after cerebral hypoperfusion, signs of acute hypoxia reappeared. Animals with high level of cognitive ability were characterized by large damage to the structures of the neuroglial ensemble.
About the Authors
V. V. KrishtopRussian Federation
Ivanovo.
V. G. Nikonorova
Russian Federation
Ivanovo.
T. А. Rumyantseva
Russian Federation
Yaroslavl.
References
1. Vasil'ev YuG. Morfologiya neiro-glio-sosudistykh otnoshenii mlekopitayushchikh (sravnitel'noe i ontogeneticheskoe issledovanie). avtoref. dis… dokt. med.nauk. Saransk; 2001. 40 (in Russian).
2. Durov RA. Kadrovyi potentsial promyshlennogo razvitiya Rossii. The Humanities and social sciences. 2013; (3):2–8 (in Russian).
3. Zadnipryany IV, Sataieva TP. Application of antihypoxants in the correction of antenatal hypoxia based on its morphological and functional data. Journal of Clinical and Experimental Medical Research. 2013; 1(1):13–21 (in Russian).
4. Ivlieva AL, Petritskaya EN, Rogatkin DA, Demin VA. Methodical features of the application of morris water maze for estimation of cognitive functions in animals. Russian Journal of Physiology. 2016; 102(1):3–17 (in Russian).
5. Chrishtop VV, Pakhrova OA, Rumyantseva TA. Dynamics of permanent cerebral hypoxia of rats depending on individual features of higher nervous activity and sex. Medical News of North Caucasus. 2018; 13(4):654–9 (in Russian).
6. Monid MV, Droblenkov AV, Sosin DV, Shabanov PD. Reactive morphological changes of the rat brain anterior cingulate cortex after acute hypoxia. Vestnik Smolenskoy Gosudarstvennoy Meditsinskoy Akademii. 2013; 12(4):31–4 (in Russian).
7. Sergeev AV. Immunomorfologicheskaya i morfometricheskaya kharakteristika tormoznykh i vozbuzhdayushchikh neironov kory golovnogo mozga cheloveka v norme i pri khronicheskoi ishemii: avtoref. dis... kand. med. nauk. Novosibirsk; 2014. 23 (in Russian).
8. Stepanov AS, Akulinin VA, Mysik AV, Stepanov SS, Avdeev DB. Neuro-Glio-Vascular Complexes of the Brain After Acute Ischemia. General Reanimatology. 2017 Jan 1;13(6):6–17 (in Russian). doi: 10.15360/1813-9779-2017-6-6-17
9. Charriaut-Marlangue C, Margaill I, Represa A, Popovici T, Plotkine M, Ben-Ari Y. Apoptosis and Necrosis after Reversible Focal Ischemia: An in Situ DNA Fragmentation Analysis. Journal of Cerebral Blood Flow & Metabolism. 1996 Mar;16(2):186–94. doi:10.1097/00004647-199603000-00002
10. Farkas E, Luiten PGM, Bari F. Permanent, bilateral common carotid artery occlusion in the rat: A model for chronic cerebral hypoperfusion-related neurodegenerative diseases. Brain Research Reviews. 2007 Apr;54(1):162–80. doi: 10.1016/j.brainresrev.2007.01.003
11. Ishida K, Shimizu H, Hida H, Urakawa S, Ida K, Nishino H. Argyrophilic dark neurons represent various states of neuronal damage in brain insults: some come to die and others survive. Neuroscience. 2004 Jan;125(3):633–44. doi: 10.1016/j.neuroscience.2004.02.002
12. Liu J, Jin D-Z, Xiao L, Zhu X-Z. Paeoniflorin attenuates chronic cerebral hypoperfusion-induced learning dysfunction and brain damage in rats. Brain Research. 2006 May;1089(1):162–70. doi: 10.1016/j.brainres.2006.02.115
13. Ohtaki H, Fujimoto T, Sato T, Kishimoto K, Fujimoto M, Moriya M, et al. Progressive expression of vascular endothelial growth factor (VEGF) and angiogenesis after chronic ischemic hypoperfusion in rat. Acta neurochirurgica. Supplement. 2006;(96):283–7. doi: 10.1007/3-211-30714-1_61
14. Schoenfeld R, Schiffelholz T, Beyer C, Leplow B, Foreman N. Variants of the Morris water maze task to comparatively assess human and rodent place navigation. Neurobiology of Learning and Memory. 2017 Mar;139:117–27. doi: 10.1016/j.nlm.2016.12.022
15. Turtzo L, Lescher J, Janes L, Dean DD, Budde MD, Frank JA. Macrophagic and microglial responses after focal traumatic brain injury in the female rat. Journal of Neuroinflammation. 2014;11(1):82: 82. doi: 10.1186/1742-2094-11-82
Review
For citations:
Krishtop V.V., Nikonorova V.G., Rumyantseva T.А. Changes in the Cellular Composition of the Cerebral Cortex in Rats with Different Levels of Cognitive Functions Under Cerebral Hypoperfusion. Journal of Anatomy and Histopathology. 2019;8(4):22-29. (In Russ.) https://doi.org/10.18499/2225-7357-2019-8-4-22-29