Modulatory effects of probenecid on the nitroglycerin-induced changes in the rat caudal trigeminal nucleus

Four hours after systemic administration of the nitric oxide donor nitroglycerin (10 mg/kg bodyweight, s.c.), the neurons of the rat caudal trigeminal nucleus are activated, the area covered by calcitonin gene-related peptide (CGRP)-immunoreactive fibres is decreased and the neuronal nitric oxide sy...

Teljes leírás

Elmentve itt :
Bibliográfiai részletek
Szerzők: Vámos Enikő
Párdutz Árpád
Fejes-Szabó Annamária
Tajti János
Toldi József
Vécsei László
Dokumentumtípus: Cikk
Megjelent: 2009
Sorozat:EUROPEAN JOURNAL OF PHARMACOLOGY 621 No. 1-3
doi:10.1016/j.ejphar.2009.08.034

mtmt:1277503
Online Access:http://publicatio.bibl.u-szeged.hu/9963
Leíró adatok
Tartalmi kivonat:Four hours after systemic administration of the nitric oxide donor nitroglycerin (10 mg/kg bodyweight, s.c.), the neurons of the rat caudal trigeminal nucleus are activated, the area covered by calcitonin gene-related peptide (CGRP)-immunoreactive fibres is decreased and the neuronal nitric oxide synthase (nNOS)- and the calmodulin-dependent protein kinase II alpha (CamKII alpha)-immunopositive neurons in the same area are increased. Probenecid is a non-selective inhibitor of multidrug-resistance associated proteins and organic anion transporters thus it can modulate the transport functions in the central nervous system influencing nociception. Accordingly, the aim of the present experiments was to examine the effects of probenecid administration on the nitroglycerin-induced expressions of nNOS, CamKII alpha and CGRP in the rat caudal trigeminal nucleus. Probenecid (200 mg/kg bodyweight, i.p.) pretreatment proved to mitigate the nitroglycerin-induced changes in expression in the rat caudal trigeminal nucleus. The data suggest that the changes caused by nitroglycerin in the expressions of CGRP, nNOS and CamKII alpha can be influenced by probenecid modulating the inflammatory functions in the nervous system. These data may be of relevance for the pathogenesis of migraine headache. (C) 2009 Elsevier B.V. All rights reserved.
Terjedelem/Fizikai jellemzők:33-37
ISSN:0014-2999