Carnosine, a precursor of histidine, ameliorates pentylenetetrazole-induced kindled seizures in rat
Carnosine, a precursor of histidine, ameliorates pentylenetetrazole-induced kindled seizures in rat
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肌肽(组氨酸的前体)可改善戊四唑诱导的大鼠癫痫发作
DOI:
10.1016/j.neulet.2006.02.031
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发表时间:
2006-05
影响因子:
2.5
通讯作者:
中科院分区:
文献类型:
--
作者:
Carnosine (β-alanyl-l-histidine) has been characterized as a putative neurotransmitter. However, so far, understanding of the role of carnosine in the brain is very limited. The objective of this study was to examine the effects of carnosine on the development of pentylenetetrazol (PTZ) kindling seizures and protection against the PTZ kindled seizures in rats. Chemical kindling was elicited by repeated intraperitoneal injection of PTZ (35mg/kg) once every 48h until the occurrence of Stage 4–5 seizures, and the seizure activity of kindling was recorded for 30min. In an acute PTZ challenge study, 60mg/kg PTZ was used to induce kindled seizure. Injection of carnosine (200, 500mg/kg, i.p.) significantly decreased seizure stage, and prolonged the latencies for myoclonic jerks, in a dose- and time-dependent manner. In the seizure development process, 500mg/kg carnosine also significantly delayed the onset of PTZ kindled seizures. In addition, carnosine significantly reversed decreased histamine levels induced by PTZ kindled seizure in the hippocampus. These results indicate that carnosine can protect against PTZ-induced seizures in both the development of kindling and the challenge process in rats. The results suggest that carnosine might be an endogenous anticonvulsant factor in the brain and can be used as a new antiepileptic drug in future.
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