PUBLICATION

Neuroprotective role of taurine on MK-801-induced memory impairment and hyperlocomotion in zebrafish

Authors
Franscescon, F., Müller, T.E., Bertoncello, K.T., Rosemberg, D.B.
ID
ZDB-PUB-200229-9
Date
2020
Source
Neurochemistry international   135: 104710 (Journal)
Registered Authors
Keywords
glutamate excitotoxicity, inhibitory avoidance task, memory deficits, neuroprotection, schizophrenia, zebrafish.
MeSH Terms
  • Animals
  • Dizocilpine Maleate/toxicity*
  • Dose-Response Relationship, Drug
  • Excitatory Amino Acid Antagonists/toxicity
  • Female
  • Gait Disorders, Neurologic/chemically induced
  • Gait Disorders, Neurologic/physiopathology
  • Gait Disorders, Neurologic/prevention & control*
  • Male
  • Memory Disorders/chemically induced
  • Memory Disorders/physiopathology
  • Memory Disorders/prevention & control*
  • Neuroprotective Agents/pharmacology
  • Neuroprotective Agents/therapeutic use*
  • Taurine/pharmacology
  • Taurine/therapeutic use*
  • Zebrafish
PubMed
32105720 Full text @ Neurochem. Int.
Abstract
Schizophrenia is a neuropsychiatric condition that reaches around 1% of people worldwide. Because taurine exerts a neuroprotective role in the brain, this molecule is a promising candidate to reduce schizophrenia-like symptoms. Here, we investigated a possible neuroprotector role of taurine against MK-801-induced memory deficit and hyperlocomotion in zebrafish using the inhibitory avoidance task and the novel tank diving test, respectively. First, we assessed the influence of different MK-801 doses (0.1, 0.3, 0.5, 1 and 2 mg/kg, i.p.) on memory consolidation. Although all MK-801 doses tend to reduce the retention index, only 2 mg/kg MK-801 showed robust amnesic effects. Then, we evaluated whether taurine pretreatments (42, 150 and 400 mg/L for 60 min) prevent MK-801-induced cognitive impairment. Immediately after the training, animals were exposed to non-chlorinated water or taurine and subsequently challenged with 2 mg/kg MK-801, i.p. The test session was performed 24 hours after training. Although taurine alone did not change memory retention when compared with control, taurine pretreatments prevented MK-801-induced memory deficit. Importantly, no locomotor changes were observed 24 h after the training session. In the novel tank diving test, MK-801 induced hyperlocomotion and disrupted vertical activity, while 400 mg/L taurine pretreatment prevented these effects. Overall, our novel findings indicate a neuroprotective role of taurine against MK-801-induced memory deficit and hyperlocomotion, reinforcing the growing utility of zebrafish models to investigate the beneficial effects of different compounds against glutamate excitotoxicity.
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