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Relevance of sedative-tranquilizing effect of l-tetra-hydropalmatine to brain monoaminergic neurotransmitters

  
@article{APS8471,
	author = {Guo-zhang Jin and Jian Xu and Fu-tian Zhang and Lei-ping Yu and Jian-hua Li and Xiao-li Wang},
	title = {Relevance of sedative-tranquilizing effect of l-tetra-hydropalmatine to brain monoaminergic  neurotransmitters},
	journal = {Acta Pharmacologica Sinica},
	volume = {4},
	number = {1},
	year = {2016},
	keywords = {},
	abstract = {l-Tetrahydropalmatine  (l-THP) possessed a marked tranquilizing effect. The brain levels of NA and 5-HT were hardly influenced by l-THP 100 mg/kg,  and the striatal level of DA was slightly reduced (P>0.05). But reserpine reduced the levels of 5-HT, NA and DA markedly.  Hence l-THP, in contrast with the action of reserpine, did not deplete the stored monoamines.      The stereotyped behavior induced by apomorphine or  benserazide +l-dopa +de-prenyl in rats and the  rotational  activity induced by apomorphine or amphetamine in 6-OH-DA lesioned rats were all anta-gonized by l-THP (50 mg/kg)  as  halope-ridol did. Thus l-THP blocked post-synap-tic DA receptor. In rats, the hyperactivi-ty evoked by p-chloro-N-methylamphe-tamine (PCMA). scopolamine or atropine was antagonized by l-THP 10-15 mg/kg.     l-THP did not antagonize the convul-sions produced by picrotoxin and bicucul-line which are the selective blocking a-gents of GABA receptor. In contrast with l-THP, AOAA and diazepam antagonized the convulsion effectively.       It is concluded that the blockade of DA-receptor is an important mechanism of the tranquilizing action of l-THP,  not involving the depletion of stored monoa-mines or augmentation of GABA function.},
	issn = {1745-7254},	url = {http://www.chinaphar.com/article/view/8471}
}