Autor(es):
Cesar-Tognoli, Lilian M. M. [UNESP] ; Salamoni, Simone D. ; Tavares, Andrea A. ; Elias, Carol F. ; Da Costa, Jaderson C. ; Bittencourt, Jackson C. ; Palma, Mario Sergio [UNESP]
Data: 2014
Identificador Persistente: http://hdl.handle.net/11449/20015
Origem: Oasisbr
Assunto(s): 6-hydroxytrypargine; fos protein; immunohistochemistry; hypothalamus; hippocampus; epilepsy; NMDA; neurotoxicity; 6-hydroxytrypargine; 6-hydroxytrypargine; fos protein; fos protein; immunohistochemistry; immunohistochemistry; hypothalamus; hypothalamus; hippocampus; hippocampus; epilepsy; epilepsy; NMDA; NMDA; neurotoxicity; neurotoxicity
Descrição
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Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
The 6-hydroxytrypargine (6-HT) is an alkaloidal toxin of the group of tetrahydro-beta-carbolines (TH beta C) isolated from the venom of the colonial spider Parawixia bistriata. These alkaloids are reversible inhibitors of the monoamine-oxidase enzyme (MAO), with hallucinogenic, tremorigenic and anxiolytic properties. The toxin 6-HT was the first TH beta C chemically reported in the venom of spiders; however, it was not functionally well characterized up to now. The action of 6-HT was investigated by intracerebroventricular (i.c.v.) and intravenous (i.v.) applications of the toxin in adult male Wistar rats, followed by the monitoring of the expression of fos-protein, combined with the use of double labeling immunehistochemistry protocols for the detection of some nervous receptors and enzymes related to the metabolism of neurotransmitters in the central nervous system (CNS). We also investigated the epileptiform activity in presence of this toxin. The assays were carried out in normal hippocampal neurons and also in a model of chronic epilepsy obtained by the use of neurons incubated in free-magnesium artificial cerebro-spinal fluid (ACSF). Trypargine, a well known TH beta C toxin, was used as standard compound for comparative purposes. Fos-immunoreactive cells (fos-ir) were observed in hypothalamic and thalamic areas, while the double-labeling identified nervous receptors of the sub-types rGlu2/3 and NMR1, and orexinergic neurons. The 6-HT was administrated by perfusion and ejection in brain slices of hippocampus, inducing epileptic activity after its administration; the toxin was not able to block the epileptogenic crisis observed in the chronic model of the epilepsy, suggesting that 6-HT did not block the overactive GluRs responsible for this epileptic activity.
São Paulo State Univ UNESP, Inst Biosci, CEIS, Dept Biol,Lab Struct Biol & Zoochem, BR-13506900 Rio Claro, SP, Brazil
Pontif Catholic Univ Rio Grande Sul PUCRS, Inst Biomed Res, Neurosci Lab, BR-90619900 Porto Alegre, RS, Brazil
Univ São Paulo, Inst Biomed Sci, Lab Chem Neuroanat, Dept Anat, BR-05508900 São Paulo, Brazil
Pontif Catholic Univ Rio Grande Sul PUCRS, Brain Inst InsCer, BR-90619900 Porto Alegre, RS, Brazil
São Paulo State Univ UNESP, Inst Biosci, CEIS, Dept Biol,Lab Struct Biol & Zoochem, BR-13506900 Rio Claro, SP, Brazil
FAPESP: 04/07942-2
FAPESP: 06/57122-7
