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Chronic treatment with taurine after intracerebroventricular streptozotocin injection improves cognitive dysfunction in rats by modulating oxidative stress, cholinergic functions and neuroinflammation.
Reeta, K H; Singh, Devendra; Gupta, Y K.
Affiliation
  • Reeta KH; Department of Pharmacology, All India Institute of Medical Sciences, New Delhi, India. Electronic address: reetakh@gmail.com.
  • Singh D; Department of Pharmacology, All India Institute of Medical Sciences, New Delhi, India.
  • Gupta YK; Department of Pharmacology, All India Institute of Medical Sciences, New Delhi, India.
Neurochem Int ; 108: 146-156, 2017 Sep.
Article in En | MEDLINE | ID: mdl-28284975
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-1ß, expression of rho kinase-II (ROCK-II), glycogen synthase kinase-3ß (GSK-3ß) 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-1ß 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-3ß 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.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Taurine / Choline O-Acetyltransferase / Streptozocin / Oxidative Stress / Inflammation Mediators / Cognitive Dysfunction Limits: Animals Language: En Journal: Neurochem Int Year: 2017 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Taurine / Choline O-Acetyltransferase / Streptozocin / Oxidative Stress / Inflammation Mediators / Cognitive Dysfunction Limits: Animals Language: En Journal: Neurochem Int Year: 2017 Document type: Article
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