DSpace

RI UFBA >
Instituto de Ciências da Saúde - ICS >
Artigos Publicados em Periódicos (ICS) >

Please use this identifier to cite or link to this item: http://repositorio.ufba.br/ri/handle/ri/5245

Title: Alkaloids from Prosopis juliflora leaves induce glial activation, cytotoxicity and stimulate NO production
Other Titles: Toxicon
Authors: Silva, Andre Mario Mendes da
Silva, Ana Rita
Pinheiro, Alexandre Moraes
Freitas, Sandra Regina Villas Bôas de
Silva, Victor Diogenes Amaral da
Souza, Cleide dos Santos
Hughes, Juliana Bentes
El-Bachá, Ramon dos Santos
Costa, Maria de Fátima Dias
Velozo, Eudes da Silva
Tardy, Marcienne Bloch
Costa, Silvia Lima
Keywords: Prosopis juliflora;Alkaloids;Astrocytes;Microglia;GFAP;Nitric oxide
Issue Date: 2007
Abstract: Prosopis juliflora is used for feeding cattle and humans. Intoxication with the plant has been reported, and is characterized by neuromuscular alterations and gliosis. Total alkaloidal extract (TAE) was obtained using acid/basicmodified extraction and was fractionated. TAE and seven alkaloidal fractions, at concentrations ranging 0.03–30 mg/ml, were tested for 24 h on astrocyte primary cultures derived from the cortex of newborn Wistar rats. The MTT test and the measure of LDH activity on the culture medium, revealed that TAE and fractions F29/30, F31/33, F32 and F34/35 were cytotoxic to astrocytes. The EC50 values for the most toxic compounds, TAE, F31/33 and F32 were 2.87 2.82 and 3.01 mg/ml, respectively. Morphological changes and glial cells activation were investigated through Rosenfeld’s staining, by immunocytochemistry for the protein OX-42, specific of activated microglia, by immunocytochemistry and western immunoblot for GFAP, the marker of reactive and mature astrocytes, and by the production of nitric oxide (NO). We observed that astrocytes exposed to 3 mg/ml TAE, F29/30 or F31/33 developed compact cell body with many processes overexpressing GFAP. Treatment with 30 mg/ml TAE and fractions, induced cytotoxicity characterized by a strong cell body contraction, very thin and long processes and condensed chromatin. We also observed that when compared with the control (71.34%), the proportion of OX-42 positive cells was increased in cultures treated with 30 mg/ml TAE or F29/30, F31/33, F32 and F34/35, with values raging from 7.27% to 28.74%. Moreover, incubation with 3 mg/ml F32, 30 mg/ml TAE, F29/30, F31/33 or F34/35 induced accumulation of nitrite in culture medium indicating induction of NO production. Taken together these results show that TAE and fractionated alkaloids from P. juliflora act directly on glial cells, inducing activation and/or cytotoxicity, stimulating NO production, and may have an impact on neuronal damages observed on intoxicated animals.
Description: p.601–614
URI: http://www.repositorio.ufba.br/ri/handle/ri/5245
ISSN: 0041-0101
Appears in Collections:Artigos Publicados em Periódicos (ICS)

Files in This Item:

File Description SizeFormat
S0041010106002935-main.pdf3.03 MBAdobe PDFView/Open
View Statistics

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.

 

    Universidade Federal da Bahia

Contate-nos. Saiba mais sobre o RI/UFBA