Related Experiment Video
Updated: Mar 6, 2026

Autofluorescence Imaging to Evaluate Cellular Metabolism
Published on: November 15, 2021
Assessment of Cellular Redox State Using NAD(P)H Fluorescence Intensity and Lifetime
Thomas S Blacker1, Tunde Berecz2, Michael R Duchen2
1Consortium for Mitochondrial Research, Department of Cell & Developmental Biology, University College London, London, United Kingdom; Department of Physics & Astronomy, University College London, London, United Kingdom.
Abstract:
NADH and NADPH are redox cofactors, primarily involved in catabolic and anabolic metabolic processes respectively. In addition, NADPH plays an important role in cellular antioxidant defence. In live cells and tissues, the intensity of their spectrally-identical autofluorescence, termed NAD(P)H, can be used to probe the mitochondrial redox state, while their distinct enzyme-binding characteristics can be used to separate their relative contributions to the total NAD(P)H intensity using fluorescence lifetime imaging microscopy (FLIM). These protocols allow differences in metabolism to be detected between cell types and altered physiological and pathological states.

