Genistein is a naturally occurring plant-derived phytoestrogen, present in the human diet, known to possess some beneficial effects. The present study investigated the effect of genistein on neuroprotection evaluated through electroencephalographic and behavioural correlates in a model of global cerebral ischemia in gerbils. Over the dose range tested, genistein (3 and 10 mg/kg), given 5 min after recirculation antagonized the ischemia-induced electroencephalographic total spectral power decrease 7 days after ischemia; fully prevented ischemia-induced hyperlocomotion evaluated 1 day after ischemia; reversed ischemia-induced memory impairment evaluated through both nest building behaviour and object recognition test; decreased malondialdehyde overproduction in the brain, evaluated 7 days after reperfusion; and fully promoted the survival of pyramidal cells in the CA(1) hippocampal subfield. The selective antagonist for estrogen receptor-β (ERβ), 4-[2-phenyl-5,7-bis(trifluoromethyl) pyrazolo[1,5-a]pyrimidin-3-yl]phenol (PHTPP) given 30 min before carotid occlusion, fully prevented the neuroprotective effect of genistein at the dose of 3 mg/kg. These results demonstrate the neuroprotective effect of genistein through the activation of ERβ and provide further grounds for the growing interest concerning the true potential of phytoestrogens as compounds to beneficially affect brain injury without having the disadvantages of estrogens.

Neuroprotective effects of genistein in mongolian gerbils : estrogen receptor-β involvement / A. Donzelli, D. Braida, A. Finardi, V. Capurro, A.E. Valsecchi, M. Colleoni, M. Sala. - In: JOURNAL OF PHARMACOLOGICAL SCIENCES. - ISSN 1347-8613. - 114:2(2010 Oct), pp. 158-167. [10.1254/jphs.10164FP]

Neuroprotective effects of genistein in mongolian gerbils : estrogen receptor-β involvement

A. Donzelli
Primo
;
D. Braida
Secondo
;
A. Finardi;V. Capurro;A.E. Valsecchi;M. Colleoni
Penultimo
;
M. Sala
Ultimo
2010

Abstract

Genistein is a naturally occurring plant-derived phytoestrogen, present in the human diet, known to possess some beneficial effects. The present study investigated the effect of genistein on neuroprotection evaluated through electroencephalographic and behavioural correlates in a model of global cerebral ischemia in gerbils. Over the dose range tested, genistein (3 and 10 mg/kg), given 5 min after recirculation antagonized the ischemia-induced electroencephalographic total spectral power decrease 7 days after ischemia; fully prevented ischemia-induced hyperlocomotion evaluated 1 day after ischemia; reversed ischemia-induced memory impairment evaluated through both nest building behaviour and object recognition test; decreased malondialdehyde overproduction in the brain, evaluated 7 days after reperfusion; and fully promoted the survival of pyramidal cells in the CA(1) hippocampal subfield. The selective antagonist for estrogen receptor-β (ERβ), 4-[2-phenyl-5,7-bis(trifluoromethyl) pyrazolo[1,5-a]pyrimidin-3-yl]phenol (PHTPP) given 30 min before carotid occlusion, fully prevented the neuroprotective effect of genistein at the dose of 3 mg/kg. These results demonstrate the neuroprotective effect of genistein through the activation of ERβ and provide further grounds for the growing interest concerning the true potential of phytoestrogens as compounds to beneficially affect brain injury without having the disadvantages of estrogens.
English
CA1; Electroencephalography (EEG); Estrogen receptor-β; Ischemia; Phytoestrogen
Settore BIO/14 - Farmacologia
Articolo
Sì, ma tipo non specificato
ott-2010
Japanese Pharmacological Society
114
2
158
167
Periodico con rilevanza internazionale
info:eu-repo/semantics/article
Neuroprotective effects of genistein in mongolian gerbils : estrogen receptor-β involvement / A. Donzelli, D. Braida, A. Finardi, V. Capurro, A.E. Valsecchi, M. Colleoni, M. Sala. - In: JOURNAL OF PHARMACOLOGICAL SCIENCES. - ISSN 1347-8613. - 114:2(2010 Oct), pp. 158-167. [10.1254/jphs.10164FP]
none
Prodotti della ricerca::01 - Articolo su periodico
7
262
Article (author)
no
A. Donzelli, D. Braida, A. Finardi, V. Capurro, A.E. Valsecchi, M. Colleoni, M. Sala
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/148638
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