The sliding threshold of modification hypothesis: application to the effect of hypothyroidism or chronic psychosocial stress and nicotine on synaptic plasticity

Neurosci Lett. 2008 Jan 17;430(3):203-6. doi: 10.1016/j.neulet.2007.10.043. Epub 2007 Nov 6.

Abstract

The Bienenstock, Cooper, and Munro (BCM) theory or the sliding threshold model can be used to explain the changes in synaptic plasticity related to learning and memory, namely long-term potentiation (LTP) and depression (LTD). In this study, we applied synaptic plasticity changes induced by either chronic psychosocial stress or hypothyroidism, and their restoration by chronic nicotine treatment, to the sliding threshold model. Psychosocial stress- or hypothyroidism-induced changes in synaptic plasticity generated a shift in the sliding threshold of modification (theta(m)) toward LTD. In addition, chronic nicotine treatment restored the theta(m) to the normal position by normalizing psychosocial stress- or hypothyroidism-induced impairment of LTP and enhancement of LTD. The data correlate with our previous findings: a shift in the balance of kinase/phosphatase toward phosphatase during psychosocial stress or hypothyroidism, which is restored by chronic nicotine treatment.

MeSH terms

  • Animals
  • Chronic Disease
  • Disease Models, Animal
  • Hippocampus / drug effects
  • Hippocampus / physiology*
  • Hypothyroidism / physiopathology*
  • Long-Term Potentiation / drug effects
  • Long-Term Potentiation / physiology
  • Long-Term Synaptic Depression / drug effects
  • Long-Term Synaptic Depression / physiology
  • Male
  • Models, Neurological
  • Neuronal Plasticity / drug effects
  • Neuronal Plasticity / physiology*
  • Nicotine / pharmacology*
  • Nicotinic Agonists / pharmacology
  • Phosphoric Monoester Hydrolases / metabolism
  • Phosphotransferases / metabolism
  • Rats
  • Rats, Wistar
  • Stress, Psychological / physiopathology*
  • Synaptic Transmission / drug effects
  • Synaptic Transmission / physiology*
  • Thyroid Hormones / metabolism

Substances

  • Nicotinic Agonists
  • Thyroid Hormones
  • Nicotine
  • Phosphotransferases
  • Phosphoric Monoester Hydrolases