TY - JOUR
T1 - Acetylsalicylic acid improves cognitive performance in sleep deprived adult Zebrafish (Danio rerio) model
AU - Bishir, Muhammed
AU - Aslam, Muhammed
AU - Bhat, Abid
AU - Ray, Bipul
AU - Elumalai, Preetham
AU - Jyothi Priya, R.
AU - Rashan, Luay
AU - Yang, Jian
AU - Chang, Sulie L.
AU - Essa, Musthafa Mohamed
AU - Sakharkar, Meena Kishore
AU - Chidambaram, Saravana Babu
N1 - Publisher Copyright:
© 2021 Frontiers in Bioscience. All rights reserved.
PY - 2021/5/30
Y1 - 2021/5/30
N2 - Sleep deprivation (SD) is commonly associated with decreased attention, reduced responsiveness to external stimuli, and impaired locomotor and cognitive performances. Strong evidence indicates that SD disrupts neuroimmuno- endocrine system which is also linked to cognitive function. Recently Zebrafish have emerged as a powerful model sharing organizational and functional characteristics with other vertebrates, providing great translational relevance with rapid and reliable screening results. In the current study, we examined the effects of acetylsalicylic acid (aspirin) on cognitive and locomotor activity in sleep deprived Zebrafish model. Learning and memory were assessed by T-maze and locomotor activity was assessed by partition preference and swimming time in spinning tasks. Furthermore, brain bioavailability of aspirin was determined by high performance liquid chromatography. Following drug exposure and tasks, histopathology of the brain was performed. It was observed that three-day SD significantly reduces learning and memory and locomotion in the Zebrafish. Aspirin was found to restore SD induced cognitive decline and improve the locomotor functions. Neuroinflammation and impaired functional network connectivity is linked to cognitive defects, which implicate the possible benefits of immunotherapeutics. In the present study, aspirin decreased neutrophil infiltration, and increased spine density in dentate gyrus granular and shrinkage and basophil in the CA1 neurons of hippocampus. This hints the benefit of aspirin on neuroimmune functions in sleep deprived fish and warrants more studies to establish the clear molecular mechanism behind this protective effect.
AB - Sleep deprivation (SD) is commonly associated with decreased attention, reduced responsiveness to external stimuli, and impaired locomotor and cognitive performances. Strong evidence indicates that SD disrupts neuroimmuno- endocrine system which is also linked to cognitive function. Recently Zebrafish have emerged as a powerful model sharing organizational and functional characteristics with other vertebrates, providing great translational relevance with rapid and reliable screening results. In the current study, we examined the effects of acetylsalicylic acid (aspirin) on cognitive and locomotor activity in sleep deprived Zebrafish model. Learning and memory were assessed by T-maze and locomotor activity was assessed by partition preference and swimming time in spinning tasks. Furthermore, brain bioavailability of aspirin was determined by high performance liquid chromatography. Following drug exposure and tasks, histopathology of the brain was performed. It was observed that three-day SD significantly reduces learning and memory and locomotion in the Zebrafish. Aspirin was found to restore SD induced cognitive decline and improve the locomotor functions. Neuroinflammation and impaired functional network connectivity is linked to cognitive defects, which implicate the possible benefits of immunotherapeutics. In the present study, aspirin decreased neutrophil infiltration, and increased spine density in dentate gyrus granular and shrinkage and basophil in the CA1 neurons of hippocampus. This hints the benefit of aspirin on neuroimmune functions in sleep deprived fish and warrants more studies to establish the clear molecular mechanism behind this protective effect.
KW - Acetylsalicylic acid
KW - Cognition
KW - Neuro-immune
KW - Sleep deprivation
KW - Spinning task
KW - Tmaze
KW - Zebrafish
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UR - http://www.scopus.com/inward/citedby.url?scp=85109056590&partnerID=8YFLogxK
U2 - 10.52586/4928
DO - 10.52586/4928
M3 - Article
C2 - 34162040
AN - SCOPUS:85109056590
SN - 1093-9946
VL - 26
SP - 114
EP - 124
JO - Frontiers in bioscience (Landmark edition)
JF - Frontiers in bioscience (Landmark edition)
IS - 6
ER -