Abstract
Taurine is a simple sulfur-containing amino acid ubiquitously distributed in the tissues of most animals. It is involved in a wide range of physiological processes including osmoregulation, lipid metabolism, intracellular calcium regulation, neuronal development, neuromodulation and cell protection. Using in vivo model of acute ethanol intoxication (5 g/kg) in 7-day-old mice we have found that taurine treatment at total dose 2 g/kg has saved about 50 % of dying neurons from ethanol-induced apoptosis in the internal (Taranukhin et al, 2009, 2010) and the external (Taranukhin et al, 2012) granular layers of developing cerebellum. However, any further increase in taurine doses (4-6 g/kg) aiming to protect more neurons against alcohol-induced apoptosis poses to threat to the whole organism and kills 7-day-old mice thus treated. Since the high doses of taurine alone or ethanol alone did not lead to animal death, lethality appears to be due to ethanol and taurine combined toxicity. We reveal the 50 % and 100 % lethal doses of taurine and ethanol combination for developing (7-day-old), adult (5-6-month-old) and old (12-13-month-old) mice and can conclude that the toxicity of ethanol and taurine combination is age-dependent. A dramatic drop in blood glucose levels observed in 25 % of 7-day-old and 40 % of elderly mice treated with taurine and ethanol suggests that one of the reason of animal death may be hypoglycemia (Taranukhin et al., 2013, 2015). Based on the results obtained we conclude that taurine may have beneficial effects in protecting brain cells against the apoptosis induced by alcohol. However, our finding on the toxicity of combined taurine and ethanol prompts serious concern particularly for young people mixing taurine-containing energy drinks with alcohol.
Highlights
Alzheimer’s disease (AD) is an incurable neurodegenerative disease characterized by progressive dementia
The results of the present study indicate that development of the neuronal hypoxic tolerance induced by the three-trial, in contrast to one-trial, mild hypoxic preconditioning is apparently largely associated with the activation of CREB, as well as brain-derived neurotrophic factor (BDNF) and Bcl-2 overexpression
No significant differences in serum level of Solubile form of RAGE (sRAGE) where found between rapidly progressing and slow progressing subgroup of multiple sclerosis (MS) patients.Our results suggest for the role of sRAGE in MS ethiopathogenesis, but we did not find any association of sRAGE in serum with the rate of MS disability progression
Summary
Alzheimer’s disease (AD) is an incurable neurodegenerative disease characterized by progressive dementia. The aim of the study was to characterize the effects of streptozocin (STZ)-indced diabetes on learning and memory of 5XFAD and wild-type (WT) mice in Morris water maze (MWM) at ages 2 and 6 months and on brain amyloid load. Existing evidence suggests GABAergic system is involved in pathophysiology of Alzheimer’s disease (AD) via inhibitory interneuron deficits (Verret et al, 2012) and decrease in functional GABAA receptors (Limon et al, 2012). Our concept: low doses of muscimol may prevent learning/memory deficits in intracerebroventricular (icv) streptozocin (STZ)-induced AD nontransgenic rat model. The Sigma-1 receptor is a chaperone protein that modulates intracellular calcium signalling of the endoplasmatic reticulum and is involved in learning and memory processes.The aim of the present study was to compare in vitro Ca2+ concentration modulating activity and in vivo behavioural effects of enantiomers of methylphenylpiracetam, a novel positive allosteric modulator of Sigma-1 receptors
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.