General Model for the Molecular Events in Synapses During Learning

Any biochemical theory about the synaptic events during learning should be based on the assumption that the critical physiological phenomenon in learning is the very first activation of a previously nonfunctional synapse. Once the nonfunctional synapse has become usable, the essential event that is responsible for learning has taken place [I]. Unfortunately, most of the presented biochemical theories about learning do not propose anything about this basic physiological phenomenon in learning but are content to suggest vaguely "specific" changes in the neuronal metabolism of proteins, nucleic acids, etc. At the same time, it seems to be the opinion of many critical neurobiologists that our present state of knowledge about the neuronal metabolism is too scattered to permit the formulation of any detailed theory about the molecular events in synapses during learning. It is, however, a fact that our inability to measure directly these extremely fast chemical reactions compels us to approach the biology of learning intuitively—from a detailed theory to experiments. In this communication an effort has been made to formulate a general model for the chemical events in the activation of a previously nonfunctional synapse. The purpose of the author is not to claim this model to be ultimately the right one, but rather to show that in spite of our diversified knowledge it is possible to present a realistic detailed chemical model for this essential event in memory fixation. The present theory is a modification of a hypothesis presented previously by the author [2, 3]. The majority of the synapses in the central nervous system are probably congenitally functional [4]. This genetically determined network of neurons is the backbone of any learning, as "learning" always involves the coupling of an unconditional stimulus with a conditional stimulus [I]. Learning and memory, however, would not be possible in any form without the existence of a particular group of nonfunctional synapses which "open" only as the result of a specific unconditional stimulus from

[1]  J. Folch-Pi,et al.  SOME EFFECTS OF PHYSIOLOGICAL CATIONS ON THE BEHAVIOUR OF GANGLIOSIDES IN A CHLOROFORM‐METHANOL‐WATER BIPHASIC SYSTEM * , 1965, Journal of neurochemistry.

[2]  V. Bloch Facts and hypotheses concerning memory consolidation processes. , 1970, Brain research.

[3]  R T Schimke,et al.  Control of enzyme levels in animal tissues. , 1970, Annual review of biochemistry.

[4]  B. Agranoff Molecular basis of some aspects of mental activity: O. Walaas (Editor). (Academic Press, New York, 1967, 476 p., $19.50) , 1968 .

[5]  Georges Ungar,et al.  Molecular mechanisms in memory and learning , 1970 .

[6]  J. Jarnefelt,et al.  Regulatory Functions of Biological Membranes , 1968 .

[7]  H. Rasmussen Cell Communication, Calcium Ion, and Cyclic Adenosine Monophosphate , 1970, Science.

[8]  R. Dawson 'Phosphatido-peptide'-like complexes formed by the interaction of calcium triphosphoinositide with protein. , 1965, The Biochemical journal.

[9]  G. C. Quarton,et al.  The Neurosciences;: Second study program , 1970 .

[10]  I. T. Oliver,et al.  A translational control mechanism in mammalian protein synthesis modulated by cyclic adenosine monophosphate. Translational control of tyrosine aminotransferase synthesis in neonatal rat liver. , 1972, Biochemistry.

[11]  G. Béraud,et al.  Actinomycin-insensitive stimulation of protein synthesis in rat anterior pituitary in vitro by dibutyryl adenosine 3',5'-monophosphate. , 1971, The Journal of biological chemistry.

[12]  R. Rubin The role of calcium in the release of neurotransmitter substances and hormones. , 1970, Pharmacological reviews.