Cell specificity of molecular changes during memory storage

J Neurochem. 1993 Feb;60(2):646-51. doi: 10.1111/j.1471-4159.1993.tb03196.x.

Abstract

The aeolid nudibranch, Hermissenda crassicornis, exhibits Pavlovian conditioning to paired light and rotational stimuli and it has been suggested that protein kinase C(PKC) may play a critical role in the cellular mechanism for this conditioned behavioral response in the B-cell photoreceptor. The present study was designed to further examine learning-specific PKC involvement in identified cellular areas, particularly those in the visual-vestibular network, of the Hermissenda nervous system after Pavlovian conditioning. As used in previous vertebrate studies, the highly specific PKC radioligand, [3H]phorbol-12,13-dibutyrate ([3H]-PDBU), was used to determine the binding characteristics of the molluscan protein receptor considered to be PKC. The binding was specific, saturable, and could be displaced by a soluble diacylglycerol analogue. The binding activity was distributed evenly between the cytosol and the membrane. All of these analyses suggest that [3H]PDBU binds primarily to PKC in Hermissenda as it does in many other systems. Computerized grain image analysis was then used to determine the cellular localization of PKC as a function of Pavlovian conditioning. The medial and intermediate B photoreceptor and the optic ganglion showed significantly increased [3H]PDBU binding in conditioned animals. The present results provide the first report of an associative learning change of a key signal transduction component in identified neurons.

MeSH terms

  • Animals
  • Autoradiography
  • Binding Sites
  • Conditioning, Psychological
  • Diglycerides / pharmacology
  • Kinetics
  • Memory / physiology*
  • Mollusca
  • Nervous System / drug effects
  • Nervous System / metabolism*
  • Phorbol 12,13-Dibutyrate / metabolism*
  • Photic Stimulation
  • Tritium
  • Visual Perception

Substances

  • Diglycerides
  • Tritium
  • Phorbol 12,13-Dibutyrate
  • 1-oleoyl-2-acetylglycerol