Effect of environmental enrichment exposure on neuronal morphology of streptozotocin-induced diabetic and stressed rat hippocampus

Background: Environmental enrichment (EE) exposure is known to influence the structural changes in the neuronal network of hippocampus. In the present study, we evaluated the effects of EE exposure on the streptozotocin (STZ)-induced diabetic and stressed rat hippocampus. Methods: Male albino rats...

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Main Authors: Narendra Pamidi, Satheesha Nayak
Format: Article
Language:English
Published: Elsevier 2014-08-01
Series:Biomedical Journal
Subjects:
Online Access:http://www.biomedj.org/article.asp?issn=2319-4170;year=2014;volume=37;issue=4;spage=225;epage=231;aulast=Pamidi
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author Narendra Pamidi
Satheesha Nayak
author_facet Narendra Pamidi
Satheesha Nayak
author_sort Narendra Pamidi
collection DOAJ
description Background: Environmental enrichment (EE) exposure is known to influence the structural changes in the neuronal network of hippocampus. In the present study, we evaluated the effects of EE exposure on the streptozotocin (STZ)-induced diabetic and stressed rat hippocampus. Methods: Male albino rats of Wistar strain (4-5 weeks old) were grouped into normal control (NC), vehicle control (VC), diabetes (DI), diabetes + stress (DI + S), diabetes + EE (DI + E), and diabetes + stress + EE (DI + S + E) groups (n = 8 in each group). Rats were exposed to stress and EE after inducing diabetes with STZ (40 mg/kg). Rats were sacrificed on Day 30 and brain sections were processed for cresyl violet staining to quantify the number of surviving neurons in the CA1, CA3, and dentate hilus (DH) regions of hippocampus. Results: A significant (p < 0.001) decrease in the number of survived neurons was noticed in DI (CA1, 34.06 ± 3.2; CA3, 36.1 ± 3.62; DH, 9.83 ± 2.02) as well as DI + S (CA1, 14.03 ± 3.12; CA3, 20.27 ± 4.09; DH, 6.4 ± 1.21) group rats compared to NC rats (CA1, 53.64 ± 2.96; CA3, 62.1 ± 3.34; DH, 21.11 ± 1.03). A significant (p < 0.001) increase in the number of survived neurons was observed in DI + E (CA1, 42.3 ± 3.66; CA3, 46.73 ± 4.74; DH, 17.03 ± 2.19) and DI + S + E (CA1, 29.69 ± 4.47; CA3, 36.73 ± 3.89; DH, 12.23 ± 2.36) group rats compared to DI and DI + S groups, respectively. Conclusions: EE exposure significantly reduced the amount of neuronal damage caused by complications of diabetes and stress to the neurons of hippocampus.
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spelling doaj.art-5ea0821cae774c9eb2c3d4e8cbad2d392022-12-22T04:27:47ZengElsevierBiomedical Journal2319-41702320-28902014-08-0137422523110.4103/2319-4170.125651Effect of environmental enrichment exposure on neuronal morphology of streptozotocin-induced diabetic and stressed rat hippocampusNarendra Pamidi0Satheesha Nayak1Department of Anatomy, Faculty of Medicine, Jeffrey Cheah School of Medicine and Health Sciences, Monash University, Sunway Campus, Kuala Lumpur, MalaysiaDepartment of Anatomy, Melaka Manipal Medical College, Manipal, Karnataka, IndiaBackground: Environmental enrichment (EE) exposure is known to influence the structural changes in the neuronal network of hippocampus. In the present study, we evaluated the effects of EE exposure on the streptozotocin (STZ)-induced diabetic and stressed rat hippocampus. Methods: Male albino rats of Wistar strain (4-5 weeks old) were grouped into normal control (NC), vehicle control (VC), diabetes (DI), diabetes + stress (DI + S), diabetes + EE (DI + E), and diabetes + stress + EE (DI + S + E) groups (n = 8 in each group). Rats were exposed to stress and EE after inducing diabetes with STZ (40 mg/kg). Rats were sacrificed on Day 30 and brain sections were processed for cresyl violet staining to quantify the number of surviving neurons in the CA1, CA3, and dentate hilus (DH) regions of hippocampus. Results: A significant (p < 0.001) decrease in the number of survived neurons was noticed in DI (CA1, 34.06 ± 3.2; CA3, 36.1 ± 3.62; DH, 9.83 ± 2.02) as well as DI + S (CA1, 14.03 ± 3.12; CA3, 20.27 ± 4.09; DH, 6.4 ± 1.21) group rats compared to NC rats (CA1, 53.64 ± 2.96; CA3, 62.1 ± 3.34; DH, 21.11 ± 1.03). A significant (p < 0.001) increase in the number of survived neurons was observed in DI + E (CA1, 42.3 ± 3.66; CA3, 46.73 ± 4.74; DH, 17.03 ± 2.19) and DI + S + E (CA1, 29.69 ± 4.47; CA3, 36.73 ± 3.89; DH, 12.23 ± 2.36) group rats compared to DI and DI + S groups, respectively. Conclusions: EE exposure significantly reduced the amount of neuronal damage caused by complications of diabetes and stress to the neurons of hippocampus.http://www.biomedj.org/article.asp?issn=2319-4170;year=2014;volume=37;issue=4;spage=225;epage=231;aulast=Pamididiabetesenrichmenthippocampusneuronsstreptozotocinstress
spellingShingle Narendra Pamidi
Satheesha Nayak
Effect of environmental enrichment exposure on neuronal morphology of streptozotocin-induced diabetic and stressed rat hippocampus
Biomedical Journal
diabetes
enrichment
hippocampus
neurons
streptozotocin
stress
title Effect of environmental enrichment exposure on neuronal morphology of streptozotocin-induced diabetic and stressed rat hippocampus
title_full Effect of environmental enrichment exposure on neuronal morphology of streptozotocin-induced diabetic and stressed rat hippocampus
title_fullStr Effect of environmental enrichment exposure on neuronal morphology of streptozotocin-induced diabetic and stressed rat hippocampus
title_full_unstemmed Effect of environmental enrichment exposure on neuronal morphology of streptozotocin-induced diabetic and stressed rat hippocampus
title_short Effect of environmental enrichment exposure on neuronal morphology of streptozotocin-induced diabetic and stressed rat hippocampus
title_sort effect of environmental enrichment exposure on neuronal morphology of streptozotocin induced diabetic and stressed rat hippocampus
topic diabetes
enrichment
hippocampus
neurons
streptozotocin
stress
url http://www.biomedj.org/article.asp?issn=2319-4170;year=2014;volume=37;issue=4;spage=225;epage=231;aulast=Pamidi
work_keys_str_mv AT narendrapamidi effectofenvironmentalenrichmentexposureonneuronalmorphologyofstreptozotocininduceddiabeticandstressedrathippocampus
AT satheeshanayak effectofenvironmentalenrichmentexposureonneuronalmorphologyofstreptozotocininduceddiabeticandstressedrathippocampus