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Taurine can Decrease Phosphorylated Tau Protein Levels in Alzheimer's Model Rats' Brains
M Jahanshahi1, E Nikmahzar1, S Gorgani1
1Neuroscience Research Center, Golestan University of Medical Sciences, Gorgan, Iran.
Kathmandu University Medical Journal (KUMJ)
|November 25, 2021
Summary
Taurine pretreatment significantly reduced scopolamine-induced increases in phosphorylated tau protein in rat brains. Taurine shows neuroprotective potential, especially when administered before neurotoxic insults.
Area of Science:
- Neuroscience
- Biochemistry
- Pharmacology
Background:
- Microtubule formation is regulated by Tau proteins, crucial for neuronal structure.
- Hyperphosphorylated Tau leads to neuron starvation and cell death, implicated in neurodegenerative diseases.
- Taurine, an amino acid abundant in the brain, exhibits known neuroprotective properties.
Purpose of the Study:
- To investigate the neuroprotective effects of Taurine on phosphorylated Tau protein levels in the cerebellum and prefrontal cortex.
- To determine if Taurine administration, before or after scopolamine induction, can mitigate Tau hyperphosphorylation.
Main Methods:
- Adult male Wistar rats were divided into nine groups.
- Taurine (25, 50, 100 mg/kg/day) was administered before or after scopolamine injection for two weeks.
- Phosphorylated Tau protein levels were quantified using ELISA in brain tissues.
Main Results:
- Taurine pretreatment at all doses significantly reduced scopolamine-induced Tau hyperphosphorylation in both cerebellum and prefrontal cortex (p < 0.001).
- High-dose Taurine (100 mg/kg/day) administered post-scopolamine also significantly decreased phosphorylated Tau levels (cerebellum: p < 0.01; prefrontal cortex: p < 0.05).
- Lower Taurine doses (25, 50 mg/kg/day) after scopolamine showed no significant effect on Tau phosphorylation.
Conclusions:
- Taurine effectively attenuates scopolamine-induced increases in phosphorylated Tau protein in rat brain regions.
- Taurine administration, particularly as a pretreatment, offers a promising strategy for neuronal protection against Tau pathology.

