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Curti 1997 Neurosci Lett

From Bioblast
Publications in the MiPMap
Curti D, Rognoni F, Gasparini L, Cattaneo A, Paolillo M, Racchi M, Zani L, Bianchetti A, Trabucchi M, Bergamaschi S, Govoni S (1997) Oxidative metabolism in cultured fibroblasts derived from sporadic Alzheimer's disease (AD) patients. Neurosci Lett 236:13-6.

» [ PMID: 9404940]

Curti D, Rognoni F, Gasparini L, Cattaneo A, Paolillo M, Racchi M, Zani L, Bianchetti A, Trabucchi M, Bergamaschi S, Govoni S (1997) Neurosci Lett

Abstract: Fibroblasts from Alzheimer's disease (AD) patients displayed decreased cytochrome c oxidase (complex IV) activity (P < 0.05). The basal oxygen consumption rate (QO2) and the response to an uncoupler of oxidative phosphorylation did not differ between AD and control fibroblasts. The QO2 of AD fibroblasts was more susceptible (P < 0.05) to inhibition by azide in the range 0.5-5 mM. The basal intracellular pH (pHi) in AD fibroblasts was significantly more acidic than in control ones. The results support the hypothesis that subtle dysfunctions of oxidative energy-producing processes are present in fibroblasts from sporadic AD patients. The alterations observed scantly influence the fibroblasts functioning even in stressful conditions; however in tissues, such as the brain, that rely heavily on oxidative metabolism for their function, similar alterations may trigger molecular mechanisms leading to cell damage.

Bioblast editor: Gnaiger E


Labels: MiParea: Respiration  Pathology: Aging;senescence 

Organism: Human  Tissue;cell: Heart  Preparation: Intact organism 


Coupling state: LEAK  Pathway:



  • The basal QO2 in fibroblasts from controls (3.57±0.33 nmol O2/min per mg of protein)
  • After ‘in vitro’ addition of FCCP: 6.59±0.95 nmol O2/min per mg of protein