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Publication : Absence of cerebellar long-term depression in mice lacking neuronal nitric oxide synthase.

First Author  Lev-Ram V Year  1997
Journal  Learn Mem Volume  4
Issue  1 Pages  169-77
PubMed ID  10456061 Mgi Jnum  J:42548
Mgi Id  MGI:1095972 Doi  10.1101/lm.4.1.169
Citation  Lev-Ram V, et al. (1997) Absence of cerebellar long-term depression in mice lacking neuronal nitric oxide synthase. Learn Mem 4(1):169-177
abstractText  Extensive pharmacological evidence suggests that nitric oxide (NO) is a crucial transmitter for cerebellar long- term depression (LTD), a long-lasting decrease in efficacy of the synapses from parallel fibers onto Purkinje neurons, triggered by coincident presynaptic activity and postsynaptic depolarization. We now show that LTD cannot be induced in Purkinje neurons under whole-cell patch clamp in cerebellar slices from young adult mice genetically lacking neuronal nitric oxide synthase (nNOS). This genetic evidence confirms the essentiality of NO and nNOS for LTD in young adult rodents, Surprisingly, LTD in cells from nNOS knockout mice cannot be rescued by photolytic uncaging of NO and cGMP inside Purkinje neurons, although such stimuli circumvent acute pharmacological inhibition of nNOS and soluble guanylate cyclase in normal rodents. Also slices from knockout mice show no deficit in cGMP elevation in response to exogenous NO. Therefore, prolonged absence of nNOS allows atrophy of the signaling pathway downstream of cGMP.
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