Literature DB >> 18501350

The L-amino acid carrier inhibitor 2-aminobicyclo[2.2.1]heptane-2-carboxylic acid (BCH) reduces L-dopa-elicited responses in dopaminergic neurons of the substantia nigra pars compacta.

Luca Sebastianelli1, Ada Ledonne, Maria Cristina Marrone, Giorgio Bernardi, Nicola B Mercuri.   

Abstract

It is not yet clear how L-dopa, that is the most effective drug for the treatment of Parkinson's disease, enters into the dopaminergic neurons to be transformed into dopamine. It is suggested that L-dopa is mainly transported into cells by a group of L-amino acid carriers named "System L". Since these carriers are selectively inhibited by 2-aminobicyclo[2.2.1]heptane-2-carboxylic acid (BCH), we have applied this compound to electrophysiologically recorded dopaminergic neurons of the rat substantia nigra pars compacta to examine the possible modulation of the effects of L-dopa by System L. We have observed that BCH reduced, in a concentration-dependent manner, the membrane hyperpolarization/outward current caused by L-dopa. Interestingly, the actions of dopamine were not changed by this System L inhibitor, suggesting that the reducing effects on L-dopa are not due to a BCH-induced unspecific block of dopamine-mediated events. Therefore, our electrophysiological data that an l-type amino acid carrier, possibly System L, is involved in the transport of L-dopa into dopaminergic neurons.

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Year:  2008        PMID: 18501350     DOI: 10.1016/j.expneurol.2008.04.005

Source DB:  PubMed          Journal:  Exp Neurol        ISSN: 0014-4886            Impact factor:   5.330


  3 in total

Review 1.  Neurophysiology of the brain stem in Parkinson's disease.

Authors:  Cecilia Bove; R Alberto Travagli
Journal:  J Neurophysiol       Date:  2019-03-27       Impact factor: 2.714

2.  L-Dopa activates histaminergic neurons.

Authors:  Yevgenij Yanovsky; Sha Li; Boris P Klyuch; Qiaoling Yao; Patrizio Blandina; M Beatrice Passani; Jian-Sheng Lin; Helmut L Haas; Olga A Sergeeva
Journal:  J Physiol       Date:  2011-01-17       Impact factor: 5.182

3.  Synthesis and transformations of di-endo-3-aminobicyclo-[2.2.2]oct-5-ene-2-carboxylic acid derivatives.

Authors:  Márta Palkó; Pál Sohár; Ferenc Fülöp
Journal:  Molecules       Date:  2011-09-07       Impact factor: 4.411

  3 in total

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