|Year : 2018 | Volume
| Issue : 4 | Page : 231-236
Exposure to enriched environment restores altered passive avoidance learning and ameliorates hippocampal injury in male albino Wistar rats subjected to chronic restraint stress
Raju Suresh Kumar1, Sareesh Naduvil Narayanan2, Naveen Kumar3, Satheesha Nayak3
1 Department of Basic Sciences, College of Science and Health Professions, King Saud Bin Abdulaziz University for Health Sciences, Jeddah, Saudi Arabia
2 Department of Physiology, RAK College of Medical Sciences, RAK Medical and Health Sciences University, Ras Al Khaimah, UAE
3 Department of Anatomy, Melaka Manipal Medical College Manipal Academy of Higher Education, Karnataka, India
|Date of Submission||24-Nov-2017|
|Date of Acceptance||22-May-2018|
|Date of Web Publication||20-Nov-2018|
Dr. Raju Suresh Kumar
College of Science and Health Professions, King Saud Bin Abdulaziz University for Health Sciences, National Guard Health Affairs, Jeddah
Source of Support: None, Conflict of Interest: None
| Abstract|| |
Aims: The aim of the study was to investigate the effects of exposure to enriched environment (EE) on passive avoidance learning and hippocampal cellular morphology in rats exposed to chronic restraint stress. Materials and Methods: Adult male albino Wistar rats were assigned into the following groups: normal control (NC) remained undisturbed in their home cages; stressed group (S) subjected to restrained stress (6 h/day) followed by housing in standard housing for 21 days; And stressed + EE (S + EE) subjected to restrained stress followed by housing in EE for 21 days. On 22nd day, six animals from each of the three groups were exposed to passive avoidance test. The remaining animals were sacrificed. Hippocampus was isolated and processed for cellular morphology using cresyl violet staining. Statistical Analysis Used: Data were analyzed using one-way analysis of variance followed by Tukey's multiple comparison test (post hoc). Results: Stressed rats exposed to EE showed significant improvement in passive avoidance learning test compared to NC. Quantification of the surviving neurons in the hippocampal subfields and their cellular morphology revealed significant neuroprotection in S + EE in cornu ammonis-2 (CA2) neurons and CA3 hippocampal neurons. No significant changes were found in CA1 hippocampal subfield. Conclusions: The outcome of this study makes us to think the possibilities of adopting EE as an alternative strategy in brain diseases where there is chronic stress and to minimize the impairment in learning and memory.
Keywords: Chronic-restraint stress, cresyl violet staining, enriched environment, hippocampus, passive avoidance test
|How to cite this article:|
Kumar RS, Narayanan SN, Kumar N, Nayak S. Exposure to enriched environment restores altered passive avoidance learning and ameliorates hippocampal injury in male albino Wistar rats subjected to chronic restraint stress. Int J App Basic Med Res 2018;8:231-6
|How to cite this URL:|
Kumar RS, Narayanan SN, Kumar N, Nayak S. Exposure to enriched environment restores altered passive avoidance learning and ameliorates hippocampal injury in male albino Wistar rats subjected to chronic restraint stress. Int J App Basic Med Res [serial online] 2018 [cited 2020 Jul 8];8:231-6. Available from: http://www.ijabmr.org/text.asp?2018/8/4/231/245814
| Introduction|| |
Stress is defined as a perturbation of either physiological or psychological homeostasis. Repeated exposures to stress are known to cause long-term detrimental effects in brain including neuronal atrophy and death of neuron that in turn results in behavioral abnormalities and memory impairments., Stress is thought to exacerbate several affective disorders including depression and posttraumatic stress disorder. It causes activation of the hypothalamo–pituitary–adrenocortical (HPA) axis, which results in the secretion of steroid hormones from the adrenal cortex. The hippocampus is one of the crucial brain structures involved in memory processing. It provides negative feedback regulation of the HPA axis and intercepts uncontrolled stress response, which could be maladaptive. In Mammalian brain, hippocampus has been shown to have the presence of highest density of glucocorticoid receptors when compared to any other parts of the brain. Hence, this brain structure receives special emphasis not only because of its role in regulation of the HPA axis but also of its susceptibility to stress-related damage which might lead to this inhibitory control being disrupted. If stress persists for longer duration, the hippocampus begins to falter in its ability to control the release of stress hormones. It has been reported that chronic exposure of rodents to physical stress or exposure of nonhuman primates to psychosocial stress results in atrophy of cornu ammonis-3 (CA3) pyramidal neurons in the hippocampus. Stress markedly impairs hippocampal long-term potentiation, a cellular substrate for learning and memory. The importance of the environmental factors in the regulation of brain, and behavior has long been recognized by the researchers. The brain responds to a variety of stimuli that it received from the environment. These include modalities of sensations such as tactile, visual, or auditory stimuli. Enriched environment (EE) is an experimental paradigm, first described in a neuroscientific context by Donald Hebb in early 1947. It refers to special housing conditions, in which the experimental animals could facilitate sensory, cognitive, and motor stimulation in them when compared to the standard housing conditions. Majority of EE experimental paradigms comprise various articles of different colors, shapes, and sizes for visual stimulation, wooden or plastic objects of different textures for sensory stimulation, plastic tunnels of different shapes that guide spatial navigations, ladders, and running wheels to enhance their motor activity. Animals also get a chance for social interactions, when they are exposed to such an environmental condition. Exposure to EE has been shown to induce neural plasticity in the normal rat brain. This includes structural modification, improvements in cognitive function, and mostly favorable alterations in brain chemistry. The neuronal changes on exposure to EE include dendritic pruning, addition of spines on dendrites, and increased involvement of new neurons in the of the brain areas such as the hippocampus and the olfactory bulb. Enhanced neurogenesis was observed in the hippocampus of adult mice that were exposed to EE, primarily in the subgranular zone of the dentate gyrus. It has been reported that short-term EE rescues adult neurogenesis and memory deficits in transgenic mouse model of Alzheimer's disease. Yang et al. reported the beneficial effects of using EE in improving the memory of rats that were undergone chronic cerebral hypoperfusion. Although stress-induced impairment in learning and memory has been extensively studied, there are no studies reported in the literature that correlates the effects of exposure of EE on passive avoidance learning and hippocampal cellular morphology in rats that are exposed to chronic-restraint stress. The present study was undertaken to evaluate the effects of EE on passive avoidance learning and hippocampal cellular morphology in adult male albino Wistar rats subjected to chronic-restraint stress.
| Materials and Methods|| |
Three-month-old adult male albino Wistar rats (weighing 200–250 g) were obtained from Central Animal Research Facility (CARF) of the university. To minimize the variation in study, all animals were bred in-house. Adult male albino Wistar rats belonging to six different litter sizes were used in this study. They were distributed by random allocation method to each of the experimental groups. Three rats were maintained in each cage to minimize the stress caused by overcrowding. Rats were housed in standard polypropylene cages (dimension 41 cm × 28 cm × 14 cm). All rats were fed with filtered tap water and food except during the stress procedure, with a standard rodent pellet. All animals were handled once daily to reduce the possible anxiety associated with human handling. They were housed in the institutional CARF in a 12:12 h light: dark environment (24°C ± 1°C). All procedures were approved by the Institutional Animal Ethics Committee and were done in accordance with the Guide for Care and Use of Laboratory Animals published by the United States National Institutes of Health (Publication No. 85–23, revised 1985). All efforts were made to minimize the number of animals used in the study.
Rats were divided into three groups with 12 animals in each group (n = 12).
Normal control (NC) – Remained undisturbed in the home cage throughout the experimental period. Restraint stress (S) – These rats were stressed in wire mesh restrainers, 6 h/day, for 21 days. Stressed rats exposed to EE (S + EE) – subjected to restraint stress for 6 h/day. Following this, they were housed in EE. This procedure continued for 21 days. On 22nd day, six rats from each group were tested individually for the avoidance learning (n = 6 in each group); remaining rats were killed (n = 6 in each group); hippocampus was dissected out from the brain and processed for cresyl violet staining. Cellular morphology of neurons in CA1, CA2, and CA3 hippocampal subfields and quantification of the surviving neurons in these areas were investigated.
Rats were subjected to restraint stress using a wire mesh restrainer, 6 h/day for 21 days as described in a previous study. Stress procedures were carried out in the Institutional Animal Research Facility (24°C ± 1°C) between 10.00 h and 16.00 h each day. Restrained rats were housed in a separate room, in the Institutional Animal House away from the nonstressed control rats. This was to prevent any possible behavioral change induced by odor or sound between the experimental groups.
The housing for providing EE was made out of wood 70 cm (L) × 70 cm (B), 45 cm (H) as described by Carughi et al., which contained a variety of objects. The objects include climbing ladders, tunnels, colored balls, and marbles. Every alternate day, these objects were replaced with a new set of objects to avoid behavioral habituation, thereby providing novelty for tactile, visual, and motor stimulation to the animals. At a time, six rats were placed in each of the EE housing. Food and water were made available inside the housing during the period of enrichment. The room temperature was maintained at 24°C ± 1°C.
Passive avoidance testing
Passive avoidance apparatus (Panlab, Barcelona, Spain) was used in this study. It was connected to a computer installed with Shut-avoid software (Panlab, Barcelona Spain) and an inbuilt shock generator. The animal's position in each compartment was detected by the high-sensitive weight transducers incorporated inside the apparatus. The experiment included three parts such as (I) exploration, (II) an aversive stimulation and learning, and (III) retention test. The experimental procedure was carried out as reported earlier by Kumar et al.
Histological analysis of hippocampus
Cresyl violet is a basic dye, which is used for the staining of nucleoproteins and Nissl substance. It is used to identify the functional regions of brain and to obtain a detailed view of the cell bodies. At the end of 21 days, the set of animals assigned for histological study were perfused transcardially with 100 ml ice-cold phosphate-buffered saline [PBS] 0.1 M pH 7.4) followed by 4% paraformaldehyde in cold PBS (0.1 M pH 7.4). Brains were removed quickly and postfixed with same fixative solution for 48 h. The tissue was then blocked in paraffin using an L block over the tissue embedder. Care was taken to orient the tissue properly. Coronal section (5 μm thick) of brain through hippocampus was cut using a rotary microtome (Leica; model: RM2155, Germany). The sections were then spread in water bath at 50°C. Twenty sections from each animal were selected and mounted on gelatinized slides. After draining water from the sections, they were fixed to the slide by gentle warming on Leica hot plate at 50°C for 1–2 min. Hundred milligrams of cresyl violet (Sigma Chemicals, USA) was dissolved in 100 ml of distilled water. To this, 0.5 ml of 10% acetic acid was added to give a pH of 3.5–3–8. The stain was filtered and then used. After staining, slides were coded for subsequent blind analysis. Neurons were quantified by direct visual counting for viable neurons using a light microscope (Leica, Germany) at a magnification of ×400. Cresyl violet-stained sections were observed for any morphological changes such as cell shrinkage, cell size, cell number, Nissl substance distribution, and nuclear size and position. Twelve sections from each rat were chosen for quantification analysis. The sections were distributed evenly along the septotemporal axis of the hippocampal formation. Pyramidal neurons in the CA1, CA2, and CA3 subfields of dorsal hippocampus were counted over 125 μm length and were expressed as the number of cells per unit length of the cell field (cells/125 μm) as reported earlier by Wood et al.
Data were analyzed using one-way analysis of variance followed by Tukey's multiple comparison test (post hoc). All results were expressed in mean ± standard error of the mean; the significance level was fixed at P < 0.05. GraphPad Prism 5.0 (GraphPad Software, Inc., San Diego, CA) (California, USA), statistical software package, was used for the analysis.
| Results|| |
Passive avoidance learning
[Figure 1] shows that retention test performed after 24 h and 48 h, respectively, showing the latency to enter the dark compartment of passive avoidance apparatus. Retention test performed after 24 h indicated a decreased latency time taken by the stressed group (7.66 ± 2.5 s) to enter the dark compartment in comparison with NC (60.25 ± 1.7 s) group (P < 0.001). S + EE could significantly increase the time latency (39 ± 2.21 s) when compared to the stressed group (P < 0.001) [Figure 1].
|Figure 1: Retention test performed after 24 h and 48 h respectively showing the latency to enter the dark compartment of passive avoidance apparatus. NC versus S, #P < 0.001; NC versus S + enriched environment, £P < 0.001; S versus S + enriched environment, $P < 0.001 after 24 h. NC versus S, #P < 0.001; S versus S + enriched environment, $P < 0.001 after 48 h|
Click here to view
Retention test performed after 48 h: stressed group showed a shorter latency (3.20 ± 2 s) to enter dark compartment when compared to NC group (20.48 ± 2.59 s) (P < 0.001). Exposure to EE significantly enhanced the time latency in S + EE (14.67 ± 1.39 s) (P < 0.001) compared to the stressed group [Figure 1].
Hippocampal cellular quantification
Quantification of viable neurons in the CA1 hippocampal subfield revealed no significant differences between any of the three groups [Table 1]. Upon evaluating CA2 and CA3 hippocampal subfields among the three groups, we could identify the presence of increased surviving neurons in CA2 hippocampal subfields of S + EE group in comparison with stressed group (P < 0.01). On evaluating the CA3 hippocampal subfields, we could identify more viable neurons in S + EE group (P < 0.001) compared to the stressed group. These results indicate that the exposure to EE could significantly protect the hippocampal neuron survival in CA2 and CA3 hippocampal subfields nearing to NC.
|Table 1: Number of viable hippocampal neurons counted from Cornu Ammonis-1, Cornu Ammonis-2, and Cornu Ammonis-3 hippocampal subfields of rat brain|
Click here to view
Hippocampal cellular morphology
[Figure 2] shows the photomicrograph of CA1 region in hippocampal subfield. The CA1 neurons in the stressed group are more widely dispersed and show the presence of more darkly stained degenerated neurons as indicated by the black arrows [Figure 2]. Note the intact neuronal arrangement of CA1 subfield in the NC and S + EE groups. The presence of minimum degenerating neurons can be noted in S + EE.
|Figure 2: Photomicrograph of cornu ammonis-1 region of the hippocampal subfield (×400, Scale bar: 20 μm)|
Click here to view
[Figure 3] shows the photomicrograph of CA2 region in the hippocampal subfield. Note the minimum degenerated neurons in S + EE group compared to S [Figure 3]. The cells are more widely dispersed and show the presence of darkly stained degenerated neurons (indicated by black arrows) in S. Exposure to EE enhanced the cell survival rate of the CA2 neurons as indicated in [Table 1] when compared to the stressed group (P < 0.01).
|Figure 3: Photomicrograph of cornu ammonis-2 region of the hippocampal subfield (×400, Scale bar: 20 μm)|
Click here to view
[Figure 4] shows the photomicrograph of CA3 region in the hippocampal subfield. Quantification of CA3 neurons revealed a significant loss of neurons [Table 1] in the S compared to NC (P < 0.001). Loss of neurons was minimized [Figure 4] in S + EE group (P < 0.001). Note the presence of more darkly stained degenerated neurons (indicated by black arrows) in S.
|Figure 4: Photomicrograph of cornu ammonis-3 region of the hippocampal subfield (×400, Scale bar: 20 μm)|
Click here to view
| Discussion|| |
Hippocampus is a brain structure located in temporal lobe which plays a key role in spatial and episodic memory. It is also reported to be involved in avoidance learning, anxiety, and contextual fear conditioning. This brain structure is also known to undergo structural plasticity modulated by a variety of stimulus.
Chronic-restraint stress model has been extensively used in investigating hippocampal-dependent behaviors such as spatial memory. It has been reported that male Sprague-Dawley rats exposed to chronic-restraint stress (6 h/day for 21 days) resulted in spatial memory deficits and hippocampal damage. In the present study, cresyl violet staining of hippocampus revealed significant damage at CA3 and CA2 neurons in stressed rats without having noticeable effects on the CA1 neurons. Our findings are in line with a previous report which showed extensive damage to CA3 neurons in primates after repeated glucocorticoid exposure. Magariños et al. reported that daily injections of corticosterone for 3 weeks in adult rats induced atrophy of apical dendrites in CA3 pyramidal neurons and did not have any effect on CA1 or granule cells. The selective susceptibility of CA3 hippocampal area to damage in the above research is comparable with our present study. We could observe selective damages in CA3 hippocampal area without having significant cell damage on CA1 area. The cause for this selective vulnerability of CA3 hippocampal neurons is believed to be due to the lack of calcium-binding proteins, namely calbindin-D28K and parvalbumin. The presence of an oxidative imbalance in brain regions such as hippocampus has been highlighted as one of the possible components of stress-mediated neurodegeneration. This could be one of the reasons liable for the observed memory loss in stressed animals.
The interactions between an organism and its environment are known to influence and evoke neurobehavioral changes. Researchers have been trying to identify the use of EE to induce these changes in both intact and in injured central nervous systems. Zhang et al. reported the beneficial effects of using EE in rats having temporal lobe epilepsy. Their study revealed enhanced hippocampal neurogenesis, improved cognitive impairments, and decreased long-term seizure activity in epileptic rats after exposure to EE. In the present study, exposure of stressed rats to EE effectively minimized the behavioral deficits in passive avoidance task and could provide significant neuroprotection to the hippocampal neurons. Avoidance learning behavior in passive avoidance task was positively enhanced in stressed rats after exposure to EE. N-methyl-D-aspartate receptor (NMDA) receptors are believed to play a major role in hippocampal synaptic plasticity. Interestingly, one of the mechanisms involved in chronic stress-induced hippocampal dendritic retraction is proposed to be mediated through CA3 NMDA receptors. Exposure to EE is also reported to increase the functional response of presynaptic NMDA receptors in rodent hippocampus. One study suggests that exposure to EE could effectively prevent the alterations in hippocampal brain-derived neurotropic factor (BDNF), which is an essential molecule required for learning and memory.
All above-mentioned suggested factors could be considered as the possible mechanisms that could have helped in improving the avoidance learning and hippocampal neuroprotection in stressed animals that were exposed to EE. With the existing data, it is difficult to pinpoint the exact neural mechanism for the improved avoidance learning in stressed rats after exposure to EE. However, when we correlate the results of avoidance learning and hippocampal morphology in rats that were exposure to EE, definitely, it gives us some valuable clues regarding the usefulness of EE in chronic stress. We assume that the mechanisms responsible for improved memory observed in our experiment could be of multifactorial origin. Involvement of oxidative stress pathways, NMDA receptor modulation, alterations in the hippocampal BDNF expression, variations in nerve growth factors, and hippocampal neurogenesis are some aspects that need to be investigated. Therefore, further investigation of this project is warranted.
| Conclusion|| |
The findings of this study demonstrates the ameliorative effects of environmental enrichment on stress induced alterations in learning and hippocampal morphology in rats. It also believed to throw light and pave way for developing alternative strategies like environmental enrichment in learning and memory impairments caused by chronic stress.
Financial support and sponsorship
This study was financially supported by Manipal University, Manipal India.
Conflicts of interest
There are no conflicts of interest.
| References|| |
Kim JJ, Yoon KS. Stress: Metaplastic effects in the hippocampus. Trends Neurosci 1998;21:505-9.
McEwen BS. The neurobiology of stress: From serendipity to clinical relevance. Brain Res 2000;886:172-89.
Herman JP, McKlveen JM, Ghosal S, Kopp B, Wulsin A, Makinson R, et al.
Regulation of the hypothalamic-pituitary-adrenocortical stress response. Compr Physiol 2016;6:603-21.
McEwen BS. Neurobiological and systemic effects of chronicstress. Chronic Stress (Thousand Oaks) 2017;1:1-11.
Kim EJ, Pellman B, Kim JJ. Stress effects on the hippocampus: A critical review. Learn Mem 2015;22:411-6.
Kuipers SD, Bramham CR, Cameron HA, Fitzsimons CP, Korosi A, Lucassen PJ, et al.
Environmental control of adult neurogenesis: From hippocampal homeostasis to behavior and disease. Neural Plast 2014;2014:808643.
Nithianantharajah J, Hannan AJ. Enriched environments, experience-dependent plasticity and disorders of the nervous system. Nat Rev Neurosci 2006;7:697-709.
Hickmott PW, Ethell IM. Dendritic plasticity in the adult neocortex. Neuroscientist 2006;12:16-28.
Segal M. New building blocks for the dendritic spine. Neuron 2001;31:169-71.
Gould E. How widespread is adult neurogenesis in mammals? Nat Rev Neurosci 2007;8:481-8.
Garthe A, Roeder I, Kempermann G. Mice in an enriched environment learn more flexibly because of adult hippocampal neurogenesis. Hippocampus 2016;26:261-71.
Valero J, España J, Parra-Damas A, Martín E, Rodríguez-Álvarez J, Saura CA, et al.
Short-term environmental enrichment rescues adult neurogenesis and memory deficits in APP(Sw, Ind) transgenic mice. PLoS One 2011;6:e16832.
Yang Y, Zhang J, Xiong L, Deng M, Wang J, Xin J, et al.
Cognitive improvement induced by environment enrichment in chronic cerebral hypoperfusion rats: A result of upregulated endogenous neuroprotection? J Mol Neurosci 2015;56:278-89.
Kumar RS, Narayanan SN, Nayak S. Ascorbic acid protects against restraint stress-induced memory deficits in wistar rats. Clinics (Sao Paulo) 2009;64:1211-7.
Carughi A, Carpenter KJ, Diamond MC. Effect of environmental enrichment during nutritional rehabilitation on body growth, blood parameters and cerebral cortical development of rats. J Nutr 1989;119:2005-16.
Kaur C, Pal I, Saini S, Jacob TG, Nag TC, Thakar A, et al.
Comparison of unbiased stereological estimation of total number of cresyl violet stained neurons and parvalbumin positive neurons in the adult human spiral ganglion. J Chem Neuroanat 2017. pii: S0891-0618(17)30037-6.
Wood ER, Mumby DG, Pinel JP, Phillips AG. Impaired object recognition memory in rats following ischemia-induced damage to the hippocampus. Behav Neurosci 1993;107:51-62.
Mamad O, Stumpp L, McNamara HM, Ramakrishnan C, Deisseroth K, Reilly RB, et al.
Place field assembly distribution encodes preferred locations. PLoS Biol 2017;15:e2002365.
Cominski TP, Jiao X, Catuzzi JE, Stewart AL, Pang KC. The role of the hippocampus in avoidance learning and anxiety vulnerability. Front Behav Neurosci 2014;8:273.
Arias N, Méndez M, Arias JL. The importance of the context in the hippocampus and brain related areas throughout the performance of a fear conditioning task. Hippocampus 2015;25:1242-9.
Leuner B, Gould E. Structural plasticity and hippocampal function. Annu Rev Psychol 2010;61:111-40, C1-3.
McLaughlin KJ, Gomez JL, Baran SE, Conrad CD. The effects of chronic stress on hippocampal morphology and function: An evaluation of chronic restraint paradigms. Brain Res 2007;1161:56-64.
Sapolsky RM, Uno H, Rebert CS, Finch CE. Hippocampal damage associated with prolonged glucocorticoid exposure in primates. J Neurosci 1990;10:2897-902.
Magariños AM, McEwen BS. Stress-induced atrophy of apical dendrites of hippocampal CA3c neurons: Comparison of stressors. Neuroscience 1995;69:83-8.
Sloviter RS. Calcium-binding protein (calbindin-D28k) and parvalbumin immunocytochemistry: Localization in the rat hippocampus with specific reference to the selective vulnerability of hippocampal neurons to seizure activity. J Comp Neurol 1989;280:183-96.
Krolow R, Arcego DM, Noschang C, Weis SN, Dalmaz C. Oxidative imbalance and anxiety disorders. Curr Neuropharmacol 2014; 12:193-204.
Zhang X, Liu T, Zhou Z, Mu X, Song C, Xiao T, et al
. Enriched environment altered aberrant hippocampal neurogenesis and improved long-term consequences after temporal lobe epilepsy in adult rats. J Mol Neurosci 2015;56:409-21.
Christian KM, Miracle AD, Wellman CL, Nakazawa K. Chronic stress-induced hippocampal dendritic retraction requires CA3 NMDA receptors. Neuroscience 2011;174:26-36.
Grilli M, Zappettini S, Zanardi A, Lagomarsino F, Pittaluga A, Zoli M, et al.
Exposure to an enriched environment selectively increases the functional response of the pre-synaptic NMDA receptors which modulate noradrenaline release in mouse hippocampus. J Neurochem 2009;110:1598-606.
Ahmadalipour A, Sadeghzadeh J, Vafaei AA, Bandegi AR, Mohammadkhani R, Rashidy-Pour A, et al.
Effects of environmental enrichment on behavioral deficits and alterations in hippocampal BDNF induced by prenatal exposure to morphine in juvenile rats. Neuroscience 2015;305:372-83.
[Figure 1], [Figure 2], [Figure 3], [Figure 4]