Evidence map›Paper›PMID 19675291›Full record

ArticleJournal of neurophysiology2009

Enhanced calcium buffering in F344 rat cholinergic basal forebrain neurons is associated with age-related cognitive impairment.

David Murchison, Angelika N McDermott, Candi L Lasarge, Kathryn A Peebles, Jennifer L Bizon, William H Griffith

Abstract read
In one paragraph

Article in Journal of neurophysiology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

21 citing papers in PubMed.

  1. Glial Cells Response in Stroke.Cellular and molecular neurobiology · 2023
    Review
  2. Article
  3. Article
  4. CaCells · 2020
    Review
  5. Review
  6. Article
  7. 20 Years of Secretagogin: Exocytosis and Beyond.Frontiers in molecular neuroscience · 2019
    Article
  8. Article
  9. Calcium's role as nuanced modulator of cellular physiology in the brain.Biochemical and biophysical research communications · 2017
    Review
  10. Article
  11. Article
  12. Review
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

David Murchison1Department of Neuroscience and Experimental Therapeutics, Texas A&M Health Science Center, College Station, Texas77843-1114, USA.
Angelika N McDermott
Candi L Lasarge
Kathryn A Peebles
Jennifer L Bizon
William H Griffith

Funding

PHYSIOLOGY OF CHOLINERGIC BASAL FOREBRAIN NEURONSR01AG007805 · NIA · TEXAS A&M UNIVERSITY HEALTH SCIENCE CTR · PI GRIFFITH, WILLIAM H · 1989 to 2007
$1.6M
NIA NIH HHS AG-007805
6 · The paper itself

Abstract

Alterations in neuronal Ca(2+) homeostasis are important determinants of age-related cognitive impairment. We examined the Ca(2+) influx, buffering, and electrophysiology of basal forebrain neurons in adult, middle-aged, and aged male F344 behaviorally assessed rats. Middle-aged and aged rats were characterized as cognitively impaired or unimpaired by water maze performance relative to young cohorts. Patch-clamp experiments were conducted on neurons acutely dissociated from medial septum/nucleus of the diagonal band with post hoc identification of phenotypic marker mRNA using single-cell RT-PCR. We measured whole cell calcium and barium currents and dissected these currents using pharmacological agents. We combined Ca(2+) current recording with Ca(2+)-sensitive ratiometric microfluorimetry to measure Ca(2+) buffering. Additionally, we sought changes in neuronal firing properties using current-clamp recording. There were no age- or cognition-related changes in the amplitudes or fractional compositions of the whole cell Ca(2+) channel currents. However, Ca(2+) buffering was significantly enhanced in cholinergic neurons from aged cognitively impaired rats. Moreover, increased Ca(2+) buffering was present in middle-aged rats that were not cognitively impaired. Firing properties were largely unchanged with age or cognitive status, except for an increase in the slow afterhyperpolarization in aged cholinergic neurons, independent of cognitive status. Furthermore, acutely dissociated basal forebrain neurons in which choline acetyltransferase mRNA was detected had the electrophysiological profiles of identified cholinergic neurons. We conclude that enhanced Ca(2+) buffering by cholinergic basal forebrain neurons may be important during aging.

Indexed as

AgingAction PotentialsAnimalsBariumCalciumCholine O-AcetyltransferaseCognition DisordersCohort StudiesMaleMaze LearningMembrane PotentialsNeuronsNeuropsychological TestsPatch-Clamp TechniquesProsencephalonRatsBariumCalciumCholine O-AcetyltransferaseRNA, Messenger

Identifiers

PMID19675291
PMCPMC2775378

What OpenQuestion holds

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Read underepoch 390

Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.