Enhanced Neurophysiological Benefits of Magnesium-Acetyl-Taurate Over Magnesium-L-Threonate: A Comparative...

The study examines how magnesium compounds, especially Magnesium-L-Threonate (MLT) and Magnesium-Acetyl-Taurate (MAT), affect neurophysiological functions in adult Wistar rats. Magnesium is essential for many cellular processes in the brain & peripheral system, such as neurotransmitter regulation, muscle function, and energy metabolism. Tissue Mg²⁺ levels were defined as the primary endpoint of the study, as they directly reflect the central objective of evaluating magnesium-based interventions. All other outcomes, including behavioral, biochemical, and molecular parameters, were considered secondary endpoints. This research aimed to compare the brain effectiveness of MLT (115 mg/kg and 450 mg/kg) and MAT (150 mg/kg and 500 mg/kg) in raising magnesium levels in biological samples like blood plasma, cerebrospinal fluid (CSF), muscles and brain tissues. The aim is to examine the effect of Magnesium compounds (MLT, MAT & combination treatment) on modulation and alterations in all the biological markers for neuroinflammation, synaptic plasticity, neurotransmission balance, oxidative stress & mitochondrial functioning. MAT showed better Mg²⁺, resulting in more notable improvements in cognitive functions, neuromuscular strength, and motor coordination compared to MLT. Behavioral tests indicated that MAT and the combined therapy of MLT and MAT significantly improved spatial learning, memory, and anxiety-related behaviors. These improvements correlated with increased expression of key proteins, including brain-derived neurotrophic factor (BDNF), cAMP response element-binding protein (CREB), Nrf2, HO-1, cAMP, and synaptic proteins such as synaptophysin and PSD-95, which are crucial for synaptic plasticity and cognition. Additionally, MAT treatment was associated with alteration inantioxidant markers, including superoxide dismutase (SOD), glutathione (GSH), catalase, and coenzyme Q10 (CoQ10), indicating better cellular defense against oxidative stress. Moreover, the upregulation of Mitochondrial ETC complexes by MAT and the combination therapy of MLT and MAT suggest improved mitochondrial function inside cells. Levels of Threonate, Taurine, and Mg²⁺ were also significantly higher in the MAT, MLT, and combined treatment groups. Neurotransmitters such as Dopamine, GABA & Glutamate, as well as complete blood count, have also been estimated. Morphological and histological analyses showed that MAT and the combination therapy significantly enhanced neuronal myelination and structural integrity across various brain regions. These results suggest that MAT & MLT + MAT could serve as a promising neurotherapeutic agent due to its ability to improve better magnesium bioavailability, stimulate neurogenesis, enhance cognitive functions & overall brain functioning. Future research should focus on refining methods for higher-brain bioavailable magnesium salt supplementation and investigating the combined effects of such magnesium salts with other neuroprotective compounds for treating cognitive decline, neurodegenerative diseases & other neurological conditions.