Function of SERCA mediated calcium uptake and expression of SERCA3 in cerebral cortex from young and old rats

Research output: Contribution to journalArticlepeer-review

Abstract

Previous work on peripheral sympathetic neurons indicated that a decline in sarco/endoplasmic reticulum calcium ATPase (SERCA) function occurs with advancing age. Therefore, an age-related decline in mechanisms controlling intracellular calcium homeostasis could contribute to altered neuronal function and/or degeneration. In this study we sought to extend the findings on peripheral neurons and to detect possible age-related declines in SERCA function and expression of SERCA3 in central neurons from cerebral cortex from young (6-month) and old (20-month) rats. Functional studies compared ATP-dependent 45Ca2+-uptake into microsomes and plasma membrane vesicles (PMVs). We and found no significant difference in 45Ca2+-uptake between microsomes or PMVs between young and old animals. On the other hand expression of SERCA3 mRNA in rat cerebral cortex showed a significant decline with advancing age. However, comparison of SERCA3 protein content did not reveal a corresponding decline; implying that SERCA mRNA turnover rates may be greater in the younger group. Although the present work with rat cerebral cortex does not indicate an age-related decline in SERCA function, previous work from our laboratory on sympathetic nerves and by others on the hippocampus indicate such a decline. In light of our previous and current studies, aging may affect calcium homeostatic mechanisms in central and peripheral autonomic neurons differently.

Original languageEnglish
Pages (from-to)57-65
Number of pages9
JournalBrain Research
Volume914
Issue number1-2
DOIs
StatePublished - Sep 28 2001

ASJC Scopus Subject Areas

  • General Neuroscience
  • Molecular Biology
  • Clinical Neurology
  • Developmental Biology

Keywords

  • Ageing
  • Calcium regulation
  • Cerebral cortex
  • Microsoms
  • Sarco/endoplasmic reticulum calcium ATPase
  • Superior cervical ganglion
  • Rats, Inbred F344
  • Male
  • Protein Isoforms/genetics
  • Thapsigargin/pharmacology
  • Enzyme Inhibitors/pharmacology
  • Calcium/metabolism
  • Aging/physiology
  • RNA, Messenger/drug effects
  • Intracellular Fluid/drug effects
  • Microsomes/drug effects
  • Cell Membrane/drug effects
  • Rats
  • Cerebral Cortex/cytology
  • Neurons/cytology
  • Sarcoplasmic Reticulum Calcium-Transporting ATPases
  • Transport Vesicles/drug effects
  • Calcium-Transporting ATPases/genetics
  • Gene Expression Regulation, Enzymologic/physiology
  • Homeostasis/genetics
  • Nerve Degeneration/enzymology
  • Animals
  • Subcellular Fractions/drug effects

Cite this