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Piroli, G.G., Manuel, A.M., Walla, M.D., Jepson, M.J., Brock, J.W., Rajesh, M.P., Tanis, R.M., Cotham, W.E. and Frizzell, N. (2014) Identification of Protein Succination as a Novel Modification of Tubulin. Biochemical Journal, 462, 231-245.
http://dx.doi.org/10.1042/BJ20131581

has been cited by the following article:

• TITLE: Insulin Age-Dependently Modulates Synaptic Transmission and AMPA Receptor Trafficking in Region CA1 of the Rat Hippocampus

  AUTHORS: Shayna A. Wrighten, Gerardo G. Piroli

  KEYWORDS: Insulin, Synaptic Plasticity, Synaptic Transmission, Long-Term Depression (LTD)

  JOURNAL NAME: Open Journal of Molecular and Integrative Physiology, Vol.6 No.2, May 31, 2016

  ABSTRACT: Insulin induces long-term depression (insulin-LTD) in the CA1 region of the rat juvenile hippocampus. This insulin-LTD may be due in part to internalization of the GluA2 subunit of the AMPA receptor (AMPAR) events that haven’t been studied in the mature rat hippocampus. In our studies, we used hippocampal preparations from juvenile (14 - 25 days) and mature (60 - 90 days) rats to assess insulin modulation of CA1 synaptic transmission and AMPAR trafficking and phosphorylation. Using field potential electrophysiology, we observed that insulin induced LTD in the juvenile hippocampus (as previously reported) in the presence and absence of phosphoinositide 3-kinase (PI3K) activity, but produced no significant long-term changes in the mature hippocampus in the presence of PI3K activity. Interestingly, during PI3K inhibition, insulin did produce LTD in the mature hippocampus. Additionally, insulin induced a long-term decrease in plasma membrane expression of the GluA2 and GluA1 subunits of the AMPAR in the juvenile, but not mature hippocampus. Furthermore, there was a long-term decrease in GluA1 phosphorylation at Serine 845 in the juvenile, but not mature hippocampus. These data reveal that insulin modulation of synaptic plasticity and AMPAR modulation within the hippocampus is age-dependent, suggesting that insulin-regulated behaviors may also show age-dependence. These findings are important largely due to the increased use of insulin as a therapeutic throughout the lifespan. Our data suggest that additional work should be done to determine how this use of insulin throughout different stages of life might affect synaptic function and development.