Chronic treatment with taurine after intracerebroventricular streptozotocin injection improves cognitive dysfunction in rats by modulating oxidative stress, cholinergic functions and neuroinflammation.
Study Design
- Studientyp
- In Vitro
- Population
- Male Wistar rats with ICV-STZ cognitive impairment
- Dauer
- 4 weeks
- Intervention
- Chronic treatment with taurine after intracerebroventricular streptozotocin injection improves cognitive dysfunction in rats by modulating oxidative stress, cholinergic functions and neuroinflammation 40, 60, 120 mg/kg taurine
- Vergleichsgruppe
- vehicle control
- Primärer Endpunkt
- cognitive performance (Morris water maze)
- Wirkungsrichtung
- Positive
- Verzerrungsrisiko
- Moderate
Abstract
The present study investigated the neuroprotective effects of taurine, an essential amino acid for growth and development of central nervous system. Intracerebroventricular streptozotocin (ICV-STZ) model of cognitive impairment was used in male Wistar rats (270 ± 20 g). Morris water maze, elevated plus maze and passive avoidance paradigm were used to assess cognitive performance. Taurine (40, 60 and 120 mg/kg) was administered orally for 28 days following STZ administration on day 1. Oxidative stress parameters (malondialdehyde, glutathione, nitric oxide and superoxide dismutase) and cholinesterases (acetylcholinesterase and butyrylcholinesterase) activity were measured at end of the study in the cortex and hippocampus. Levels of TNF-α, IL-1β, expression of rho kinase-II (ROCK-II), glycogen synthase kinase-3β (GSK-3β) and choline acetyltransferase (ChAT) were studied in cortex and hippocampus. STZ caused significant cognitive impairment as compared to normal control. Chronic administration of taurine attenuated STZ-induced cognitive impairment. Increased oxidative stress and increased levels of TNF-α, IL-1β induced by STZ were also significantly attenuated by taurine. Taurine significantly (p < 0.05) decreased the STZ-induced increased expression of ROCK-II in cortex and hippocampus. Further, STZ-induced increased activity of cholinesterases was significantly (p < 0.001) mitigated by taurine. STZ decreased the expression of ChAT in hippocampus which was significantly (p < 0.05) reversed by taurine. However, GSK-3β expression was not altered by either STZ or taurine. The present study indicates that taurine exerts a neuroprotective role against STZ-induced cognitive impairment in rats. This effect is probably mediated by modulating oxidative stress, cholinesterases, inflammatory cytokines and expression of ROCK-II. Thus, this study suggests a potential of chronic taurine administration in cognitive impairment of Alzheimer's type.
Zusammenfassung
It is indicated that taurine exerts a neuroprotective role against STZ‐induced cognitive impairment in rats, probably mediated by modulating oxidative stress, cholinesterases, inflammatory cytokines and expression of ROCK‐II.
Used In Evidence Reviews
Similar Papers
Alcohol (Fayetteville, N.Y.) · 2015
Assessment and treatment of insomnia in adult patients with alcohol use disorders.
British journal of clinical pharmacology · 2014
The clinical pharmacology of acamprosate.
Life sciences · 2019
Roles of taurine in cognitive function of physiology, pathologies and toxication.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association · 2014
Taurine ameliorates neuropathy via regulating NF-κB and Nrf2/HO-1 signaling cascades in diabetic rats.
Frontiers in aging · 2023
The dual face of microglia (M1/M2) as a potential target in the protective effect of nutraceuticals against neurodegenerative diseases.
Frontiers in bioscience (Scholar edition) · 2015