The thermal stability of several crystal polymorphs in polyamide 11 (PA11) and polyamide 6 (PA6) has been investigated by means of in situ X-ray experiments. In the case of PA11, δ′ and α′ phases display a Brill transition far below the melting point. Both phases transform into a (pseudo)-hexagonal HT δ phase above 100 °C. The latter turns back into the most stable α′ phase upon cooling. PA6 exhibits similar thermally induced crystal transitions. In situ X-ray investigations refute the occurrence of a β → α transition upon heating, whereas the existence of a pseudohexagonal HT phase is suggested as in PA11. For both polymers, the present study underlines the major role of crystal perfection of the most stable α phase on the existence of a Brill transition. The combination of in situ structural information with thermal analysis allows to propose a thermodynamic scheme to describe the Brill transition in both polyamides.

Hippocampal interneurons synchronize the activity of large neuronal ensembles during memory consolidation. Although the latter process is manifested as increases in synaptic efficacy which require new protein synthesis in pyramidal neurons, it is unknown whether such enduring plasticity occurs in interneurons. Here, we uncover a long-term potentiation (LTP) of transmission at individual interneuron excitatory synapses which persists for at least 24 h, after repetitive activation of type-1 metabotropic glutamate receptors [mGluR1-mediated chemical late LTP (cL-LTP mGluR1 )]. cL-LTP mGluR1 involves presynaptic and postsynaptic expression mechanisms and requires both transcription and translation via phosphoinositide 3-kinase/mammalian target of rapamycin and MAP kinase kinaseextracellular signal-regulated protein kinase signaling pathways. Moreover, cL-LTP mGluR1 involves translational control at the level of initiation as it is prevented by hippuristanol, an inhibitor of eIF4A, and facilitated in mice lacking the cap-dependent translational repressor, 4E-BP. Our results reveal novel mechanisms of long-term synaptic plasticity that are transcription and translation-dependent in inhibitory interneurons, indicating that persistent synaptic modifications in interneuron circuits may contribute to hippocampaldependent cognitive processes.

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