Abstract
Long-term potentiation (LTP) and depression (LTD) are potential cellular mechanisms involved in learning and memory. Group I metabotropic glutamate receptors (mGluR), which are linked to heterotrimeric G-proteins of the Gq family (Gq and G11), have been reported to facilitate both hippocampal LTP and LTD. To evaluate their functional role in synaptic plasticity, we studied LTD and LTP in the CA1 region of the hippocampus from wild-type, Gαq(-/-), and Gα11(-/-) mice. Basic parameters of the synaptic transmission were not altered in Gαq(-/-) and Gα11(-/-) mice. Moreover, these mice showed normal LTP in response to a strong tetanus and to a weak tetanus. However, LTD induced either by a group I mGluRs agonist or by paired-pulse low-frequency stimulation (PP-LFS) was absent in Gαq(-/-) mice. Moreover, PP-LFS caused potentiation of the synaptic transmission in these mice that was not affected by the NMDAR antagonist AP-5. These results show that Gq plays a crucial role in the mGluR-dependent LTD, whereas hippocampal LTP is not affected by the lack of a single member of the Gq family.
Original language | English |
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Pages (from-to) | 4943-4948 |
Number of pages | 6 |
Journal | Journal of Neuroscience |
Volume | 21 |
Issue number | 14 |
DOIs | |
State | Published - 15 Jul 2001 |
Keywords
- GTP-binding protein
- Gene targeting
- Hippocampus
- Metabotropic glutamate receptor
- Mouse
- Synaptic plasticity