Peroral Exposure to Cannabis Sativa Ethanol Extract Caused Neuronal Degeneration and Astrogliosis in Wistar Rats’ Prefrontal Cortex

Author:

Yinka Olatunji Sunday12,Olubunmi Ogunnaike Philip1,Zabdiel Abijo Ayodeji1ORCID,Oladele Owolabi Joshua13,Taiye Adelodun Stephen1,Ayodele Adeoye4,Adetutu Fasesan Oluwatoyin5ORCID,Afees Olanrewaju John1ORCID,Kayode Adegbite Ademola1

Affiliation:

1. Department of Anatomy, School of Basic Medical Sciences, Benjamin Carson (Snr.) College of Medical and Health Sciences, Ilishan-Remo, Ogun State Nigeria

2. Anatomy Department, Adventist School of Medicine of East-Central Africa, Adventist University of Central Africa, Kigali, Rwanda

3. Anatomy Department, Division of Basic Medical Sciences, University of Global Health Equity, Kigali, Rwanda

4. Department of Education, School of Education and Humanities, Babcock University, Ilisan-Remo, Ogun State, Nigeria

5. Department of Psychiatry, Ben Carson School of Medicine, Babcock University, Ilisan-Remo, Ogun State, Nigeria

Abstract

Background: Despite widespread concerns about its possible side effects, notably on the prefrontal cortex (PFC), which mediates cognitive processes, the use of Cannabis sativa as a medicinal and recreational drug is expanding exponentially. This study evaluated possible behavioral alterations, neurotransmitter levels, histological, and immunohistochemical changes in the PFC of Wistar rats exposed to Cannabis sativa. Purpose: To evaluate the effect of graded doses of Cannabis sativa on the PFC using behavioural, histological, and immunohistochemical approaches. Methods: Twenty-eight juvenile male Wistar rats weighing between 70 g and 100 g were procured and assigned into groups A-D ( n = 7 each). Group A served as control which received distilled water only as a placebo; rats in groups B, C, and D which were the treatment groups were orally exposed to graded doses of Cannabis sativa (10 mg/kg, 50 mg/kg, and 100 mg/kg, respectively). Rats in all experimental groups were exposed to Cannabis sativa for 21 days, followed by behavioral tests using the open field test for locomotor, anxiety, and exploratory activities, while the Y-maze test was for spatial memory assessment. Rats for biochemical analysis were cervically dislocated and rats for tissue processing were intracardially perfused following neurobehavioral tests. Sequel to sacrifice, brain tissues were excised and prefrontal cortices were obtained for the neurotransmitter (glutamate, acetylcholine, and dopamine) and enzymatic assay (Cytochrome C oxidase (CcO) and Glucose 6- Phosphate Dehydrogenase-G-6-PDH). Brain tissues were fixed in 10% Neutral Buffered Formalin (NBF) for histological demonstration of the PFC cytoarchitecture using H&E and glial fibrillary acidic protein (GFAP) for astrocyte evaluation. Results: Glutamate and dopamine levels were significantly increased ( F = 24.44, P = .0132) in groups D, and B, C, and D, respectively, compared to control; likewise, the activities of CcO and G-6-PDH were also significantly elevated ( F = 96.28, P = .0001) ( F = 167.5, P = .0001) in groups C and D compared to the control. Cannabis sativa impaired locomotor activity and spatial memory in B and D and D, respectively. All Cannabis sativa exposed groups demonstrated evidence of neurodegeneration in the exposed groups; GFAP immunoexpression was evident in all groups with a marked increase in group D. Conclusion: Cannabis sativa altered neurotransmitter levels, energy metabolism, locomotor, and exploratory activity, and spatial working memory, with neuronal degeneration as well as reactive astrogliosis in the PFC.

Publisher

SAGE Publications

Subject

General Neuroscience

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