| Id |
Subject |
Object |
Predicate |
Lexical cue |
| T1 |
0-125 |
DRI_Outcome |
denotes |
Selective blockade of the mGluR1 receptor reduces traumatic neuronal injury in vitro and improvesoOutcome after brain trauma. |
| T2 |
126-334 |
DRI_Outcome |
denotes |
The effects of selective blockade of group I metabotropic glutamate receptor subtype 1 (mGluR1) on neuronal cell survival and post-traumatic recovery was examined using rat in vitro and in vivo trauma models. |
| T3 |
335-713 |
DRI_Approach |
denotes |
The selective mGluR1 antagonists (RS)-1-aminoindan-1,5-dicarboxylic acid (AIDA), 7-(hydroxyimino)cyclopropa[b]chromen-1a-carboxylate ethyl ester (CPCCOEt), and (S)-(+)-alpha-amino-4-carboxy-2-methylbezeneacetic acid (LY367385) provided significant neuroprotection in rat cortical neuronal cultures subjected to mechanical injury, in both pretreatment or posttreatment paradigms. |
| T4 |
714-818 |
DRI_Background |
denotes |
Administration of the antagonists also attenuated glutamate-induced neuronal cell death in the cultures. |
| T5 |
819-1061 |
DRI_Background |
denotes |
Coapplication of these antagonists with the N-methyl-d-aspartate (NMDA) receptor antagonist (5R,10S)-(+)-5-methyl-10,11-dihydro-5H-dibenzo[a,d]cyclohepten-5,10-imine (MK-801) had additive neuroprotective effects in glutamate injured cultures. |
| T6 |
1062-1235 |
DRI_Challenge |
denotes |
Intracerebroventricular administration of AIDA to rats markedly improved recovery from motor dysfunction after lateral fluid percussion induced traumatic brain injury (TBI). |
| T7 |
1236-1351 |
DRI_Approach |
denotes |
Treatment with mGluR1 antagonists also significantly reduced lesion volumes in rats after TBI, as evaluated by MRI. |
| T8 |
1352-1558 |
DRI_Outcome |
denotes |
It appears that these compounds mediate their neuroprotective effect through an mGluR1 antagonist action, as demonstrated by inhibition of agonist induced phosphoinositide hydrolysis in our in vitro system. |
| T9 |
1559-1723 |
DRI_Background |
denotes |
Moreover, AIDA, CPCCOEt, and LY367385, at concentrations shown to be neuroprotective, had no significant effects on the steady state NMDA evoked whole cell current. |
| T10 |
1724-1853 |
DRI_Approach |
denotes |
Taken together, these data suggest that modulation of mGluR1 activity may have substantial therapeutic potential in brain injury. |