Neurotoxicity of aluminium chloride and okadaic acid in zebrafish: unravelling Alzheimer's disease model via learning and memory function evaluation

• Main Authors: Raduan, Siti Zaleha, Ahmed, Qamar Uddin, Ahmad Rusmili, Muhamad Rusdi, Mohmad Sabere, Awis Sukarni, Haris @ Harith, Muhammad Salahuddin, Shaikh, M.F., W. Sulaiman, W.A., Mahmood, M.H.
• Format: Article
• Language: English
• Published: Spanish Society of Neurology (Elsevier) 2024
• Subjects: QD Chemistry; RM147 Administration of Drugs and Other Therapeutic Agents; RS Pharmacy and materia medica
• Online Access: http://irep.iium.edu.my/115838/7/115838_Neurotoxicity%20of%20aluminium.pdf; http://irep.iium.edu.my/115838/; https://www.sciencedirect.com/science/article/pii/S2667049624000371?via%3Dihub; https://doi.org/10.1016/j.neurop.2024.100180

Introduction/objectives: Alzheimer's disease (AD) is characterised by a progressive decline in cognitive abilities, especially learning and memory. To validate the zebrafish as a suitable model organism for AD, the study examined the effects of 2 neurotoxin agents, aluminium chloride (AlCl3) and okadaic acid (OKA). In the full experimental design, both neurotoxins were administered intraperitoneally at 3 distinct doses (low, medium, and high) twice weekly for 21 days. At 3 time-points, behavioural tasks were conducted on day 7 (short duration), day 14 (moderate duration), and day 21 (long duration). The behavioural tasks consisted of a novel tank test lasting 6 min, followed by a T-maze tank test lasting 5 min. Methods: In this article, the T-maze tank test was discussed in detail to evaluate which neurotoxins and their optimal dosages are impactful in developing a zebrafish AD model towards learning and memory functions. This evaluation measured four parameters: the amount of time spent in the wrong arm, the total distance travelled in the deeper chamber, and the 3-h and 24-h inflexion ratios. Results: In summary, a 100 nM dosage of OKA with a maximum of 21 days of evaluation resulted in significant (P< .05) outcomes in all parameters evaluated. The longest duration was spent in the wrong arm, accompanied by a reduction in the total distance travelled in the deeper chamber and a decreasing pattern in the 3-h and 24-h inflexion ratios. Conclusion: These observations suggest that OKA is the optimal choice of neurotoxin for a validated and optimised zebrafish AD model.