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Micrographs of immunostained cells were captured using an Olympus AX70 (Olympus, Tokyo, Japan), and the length of the longest neurite on each DRG neuron was measured using NIH Image software.

The total neurite length for each imaged neuron was measured using the Neurite Tracer plug-in for the ImageJ software package.

Confocal microscope pictures were taken (Zeiss Axioplan 2, Pascal software) and total neurite outgrowth per neuron was measured using Image-Pro Plusoftwarere tracing all processes (N ~ 70/group).

Here, the mice used their whiskers to judge the location of an object by touch alone, while the electrical activity of the neurons was measured using electrodes.

Number of phospho-Tau or beta-amyloid stained pyramidal neurons was measured using Photoshop version 8.0 (Adobe System Incorporated, San Jose, CA, USA), as previously reported.

To further investigate the role of PGC-1α in cellular bioenergetics, the oxygen consumption of cultured midbrain neurons was measured using the XF-24 Analyzer (Fig.  2A D).

Net pixel intensity of PDF staining at the terminus of the dorsal projection from the ventral lateral neurons was measured using a Kodak Molecular Imaging quantification program (Carestream Health Inc., Rochester, NY, USA).

The fluorescence intensities in the time-lapse movies of the cultured neurons were measured using Imaris software (Bitplane).

Rates of lipid peroxidation in neurons were measured using C11-BODIPY.

The sizes of the perikaryon of the calbindin+ve neurons were measured using the direct moment estimation of the volume of particles, which allows the unbiased estimation of volume from single sections.

The length of DsRed-positive axonal processes from single-labeled (DsRed alone), double-labeled (DsRed/FLAG, DsRed/Myc or DsRed/GFP) or triple-labeled (DsRed/FLAG/Myc or DsRed/FLAG/GFP) cortical neurons were measured using the line tool function of ImageJ by an investigator blinded to each condition.