The main glutamate transporter GLT-1 is responsible for clearing synaptically released glutamate from the extracellular space and contributes to shape glutamatergic transmission. Recently, it has been shown that ceftriaxone (CEF)-induced GLT-1 up-regulation is associated to an impairment of the prepulse inhibition (PPI) of the startle reflex, a simple form of information processing that is reduced in schizophrenia, and determines a strong reduction of hippocampal mGluR2/3-dependent long term depression (LTD). Here, we tested the hypothesis that administration of the mGluR2/3 agonist LY379268 blocks the effect of GLT-1 up-regulation on PPI of the startle. We showed that LY379268 (1 mg/Kg) administration prevented PPI alterations associated to GLT-1 up-regulation, suggesting that CEF-induced PPI impairment was mGluR2/3-dependent. In addition, we demonstrated that CEF-induced GLT-1 up-regulaton did not alter the expression of mGluR2/3, and that it occurred at sites of mGluR2/3 expression. These results indicate a novel mechanism by which GLT-1 up-regulation modulates PPI of the startle.
The mGluR2/3 agonist LY379268 blocks the effects of GLT-1 up-regulation on prepulse inhibition of the startle reflex in adult rats
Bellesi MPrimo
;
2010-01-01
Abstract
The main glutamate transporter GLT-1 is responsible for clearing synaptically released glutamate from the extracellular space and contributes to shape glutamatergic transmission. Recently, it has been shown that ceftriaxone (CEF)-induced GLT-1 up-regulation is associated to an impairment of the prepulse inhibition (PPI) of the startle reflex, a simple form of information processing that is reduced in schizophrenia, and determines a strong reduction of hippocampal mGluR2/3-dependent long term depression (LTD). Here, we tested the hypothesis that administration of the mGluR2/3 agonist LY379268 blocks the effect of GLT-1 up-regulation on PPI of the startle. We showed that LY379268 (1 mg/Kg) administration prevented PPI alterations associated to GLT-1 up-regulation, suggesting that CEF-induced PPI impairment was mGluR2/3-dependent. In addition, we demonstrated that CEF-induced GLT-1 up-regulaton did not alter the expression of mGluR2/3, and that it occurred at sites of mGluR2/3 expression. These results indicate a novel mechanism by which GLT-1 up-regulation modulates PPI of the startle.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.
