Opposite changes in phosphoinositide-specific phospholipase C immunoreactivity in the left prefrontal and superior temporal cortex of patients with chronic schizophrenia

Biol Psychiatry. 1999 Dec 15;46(12):1665-71. doi: 10.1016/s0006-3223(99)00036-0.

Abstract

Background: Abnormalities in types of neurotransmitter signaling that are coupled with phosphoinositide-specific phospholipase C (PLC) have previously been reported in brains from patients with schizophrenia. PLC, a main component of this pathway, may be affected in schizophrenia.

Methods: We immunoquantified PLC beta 1, gamma 1 and delta 1 in the left prefrontal cortex and superior temporal cortex, nucleus accumbens and amygdala, and in the right superior temporal cortex of postmortem brains obtained from a total of 19 patients with schizophrenia and a total of 27 controls.

Results: PLC beta 1 immunoreactivities were increased in the particulate fraction from the prefrontal cortex (by 64%), although they were decreased in the particulate fraction from the left superior temporal cortex (by 28%), as compared with the values in controls. There was no difference in PLC beta 1 immunoreactivities in the nucleus accumbens, the amygdala or the right superior temporal cortex between schizophrenic patients and controls. PLC gamma 1 and delta 1 immunoreactivities did not differ between the two groups in any of the regions studied.

Conclusions: Changes in PLC beta 1 immunoreactivities in the prefrontal and superior temporal cortex of patients with schizophrenia may reflect abnormalities in neurotransmissions via receptors that are coupled with the Gq alpha-PLC beta 1 cascade.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amygdala / enzymology
  • Blotting, Western
  • Case-Control Studies
  • Chronic Disease
  • Female
  • Humans
  • Male
  • Middle Aged
  • Nucleus Accumbens / enzymology
  • Phosphatidylinositols / metabolism*
  • Prefrontal Cortex / enzymology*
  • Schizophrenia / enzymology*
  • Temporal Lobe / enzymology*
  • Type C Phospholipases / metabolism*

Substances

  • Phosphatidylinositols
  • Type C Phospholipases