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Effects of histidine, a precursor of histamine, on pentylenetetrazole-induced seizures in rats.

  
@article{APS7525,
	author = {Zhong CHEN and Wei-Dong LI and Li-Jun ZHU and Ying-Jie SHEN and Er-Qing WEI},
	title = {Effects of histidine, a precursor of histamine, on pentylenetetrazole-induced seizures in rats.},
	journal = {Acta Pharmacologica Sinica},
	volume = {23},
	number = {4},
	year = {2016},
	keywords = {},
	abstract = {AIM: The effect of histidine on pentylenetetrazole-induced seizures was
investigated in rats.
METHODS: Chemical kindling was elicited by repeated ip injection a subconvulsant 
dose of pentylenetetrazole (35 mg/kg) once every 48 h until the occurrence of
seizure stages 4-5, and seizure activity of kindling was recorded for 30 min.
RESULTS: In the kindling development process, ip injection of histidine (200, 500
mg/kg), a precursor of histamine, prolonged latency for the onset of myoclonic
jerks and the clonic generalized seizure, and inhibited seizure stage in a
dose-dependent manner. In the kindling challenge process, histidine (500, 1000
mg/kg) and H3 antagonist thioperamide (10, 20 microg) al so showed a significant 
anticonvulsant effect. The inhibitory action of histidine was enhanced
significantly by thioperamide (5 microg), however, was antagonized by both alpha 
fluoromethylhistidine (20 microg), a selective histidine decarboxylase inhibitor 
and H1 ant agonist pyrilamine (2, 5 mg/kg), dose-dependently and significantly.
In addition, H2 antagonist zolantidine appeared no appreciable effect, even at a 
dose of 10 mg/kg.
CONCLUSION: These results indicated that brain endogenous histamine may play
certain important role in protect against generalized clonic seizures, its action
may via presynaptic H3-receptors and postsynaptic H1-receptors.},
	issn = {1745-7254},	url = {http://www.chinaphar.com/article/view/7525}
}